-
1
-
-
42349095075
-
Advances in autism genetics: on the threshold of a new neurobiology
-
Abrahams B.S., Geschwind D.H. Advances in autism genetics: on the threshold of a new neurobiology. Nat. Rev. Genet. 2008, 9:341-355.
-
(2008)
Nat. Rev. Genet.
, vol.9
, pp. 341-355
-
-
Abrahams, B.S.1
Geschwind, D.H.2
-
2
-
-
38849159213
-
A novel mutation in JARID1C/SMCX in a patient with autism spectrum disorder (ASD)
-
Adegbola A., Gao H., Sommer S., Browning M. A novel mutation in JARID1C/SMCX in a patient with autism spectrum disorder (ASD). Am. J. Med. Genet. A 2008, 146A:505-511.
-
(2008)
Am. J. Med. Genet. A
, vol.146 A
, pp. 505-511
-
-
Adegbola, A.1
Gao, H.2
Sommer, S.3
Browning, M.4
-
3
-
-
0028264422
-
A novel X-gene with a widely transcribed Y-linked homolog escapes X-inactivation in mouse and human
-
Agulnik A., Mitchell M., Mattei M., Borsani G., Avner P., Lerner J., Bishop C. A novel X-gene with a widely transcribed Y-linked homolog escapes X-inactivation in mouse and human. Hum. Mol. Genet. 1994, 3:879-884.
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 879-884
-
-
Agulnik, A.1
Mitchell, M.2
Mattei, M.3
Borsani, G.4
Avner, P.5
Lerner, J.6
Bishop, C.7
-
4
-
-
33847654643
-
Progranulin in frontotemporal lobar degeneration and neuroinflammation
-
Ahmed Z., Mackenzie I.R.A., Hutton M.L., Dickson D.W. Progranulin in frontotemporal lobar degeneration and neuroinflammation. J. Neuroinflamm. 2007, 4:7.
-
(2007)
J. Neuroinflamm.
, vol.4
, pp. 7
-
-
Ahmed, Z.1
Mackenzie, I.R.A.2
Hutton, M.L.3
Dickson, D.W.4
-
5
-
-
80052596765
-
Low plasma progranulin levels in children with autism
-
Al-Ayadhi L., Mostafa G. Low plasma progranulin levels in children with autism. J. Neuroinflamm. 2011, 8.
-
(2011)
J. Neuroinflamm.
, vol.8
-
-
Al-Ayadhi, L.1
Mostafa, G.2
-
6
-
-
0030879482
-
Imprinted expression of the murine Angelman syndrome gene, Ube3a, in hippocampal and Purkinje neurons
-
Albrecht U., Sutcliffe J.S., Cattanach B.M., Beechey C.V., Armstrong D., Eichele G., Beaudet A.L. Imprinted expression of the murine Angelman syndrome gene, Ube3a, in hippocampal and Purkinje neurons. Nat. Genet. 1997, 17:75-78.
-
(1997)
Nat. Genet.
, vol.17
, pp. 75-78
-
-
Albrecht, U.1
Sutcliffe, J.S.2
Cattanach, B.M.3
Beechey, C.V.4
Armstrong, D.5
Eichele, G.6
Beaudet, A.L.7
-
7
-
-
77951559056
-
A unified theory of autism revisited: linkage evidence points to chromosome X using a high-risk subset of AGRE families
-
Allen-Brady K., Cannon D., Robison R., McMahon W.M., Coon H. A unified theory of autism revisited: linkage evidence points to chromosome X using a high-risk subset of AGRE families. Autism Res. 2010, 3:47-52.
-
(2010)
Autism Res.
, vol.3
, pp. 47-52
-
-
Allen-Brady, K.1
Cannon, D.2
Robison, R.3
McMahon, W.M.4
Coon, H.5
-
8
-
-
0036813151
-
A novel mechanism of dendritic spine plasticity involving estradiol induction of prostaglandin-E2
-
Amateau S.K., McCarthy M.M. A novel mechanism of dendritic spine plasticity involving estradiol induction of prostaglandin-E2. J. Neurosci. 2002, 22:8586-8596.
-
(2002)
J. Neurosci.
, vol.22
, pp. 8586-8596
-
-
Amateau, S.K.1
McCarthy, M.M.2
-
9
-
-
2542429265
-
Induction of PGE2 by estradiol mediates developmental masculinization of sex behavior
-
Amateau S.K., McCarthy M.M. Induction of PGE2 by estradiol mediates developmental masculinization of sex behavior. Nat. Neurosci. 2004, 7:643-650.
-
(2004)
Nat. Neurosci.
, vol.7
, pp. 643-650
-
-
Amateau, S.K.1
McCarthy, M.M.2
-
10
-
-
33748675306
-
X chromosome-inactivation patterns of 1,005 phenotypically unaffected females
-
Amos-Landgraf J.M., Cottle A., Plenge R.M., Friez M., Schwartz C.E., Longshore J., Willard H.F. X chromosome-inactivation patterns of 1,005 phenotypically unaffected females. Am. J. Hum. Genet. 2006, 79:493-499.
-
(2006)
Am. J. Hum. Genet.
, vol.79
, pp. 493-499
-
-
Amos-Landgraf, J.M.1
Cottle, A.2
Plenge, R.M.3
Friez, M.4
Schwartz, C.E.5
Longshore, J.6
Willard, H.F.7
-
11
-
-
0033358525
-
Polymorphic X-chromosome inactivation of the human TIMP1 gene
-
Anderson C.L., Brown C.J. Polymorphic X-chromosome inactivation of the human TIMP1 gene. Am. J. Hum. Genet. 1999, 65:699-708.
-
(1999)
Am. J. Hum. Genet.
, vol.65
, pp. 699-708
-
-
Anderson, C.L.1
Brown, C.J.2
-
12
-
-
70349601666
-
Brief report: parental age and the sex ratio in autism
-
Anello A., Reichenberg A., Luo X., Schmeidler J., Hollander E., Smith C.J., Puleo C.M., Kryzak L.a., Silverman J.M. Brief report: parental age and the sex ratio in autism. J. Autism Dev. Disord. 2009, 39:1487-1492.
-
(2009)
J. Autism Dev. Disord.
, vol.39
, pp. 1487-1492
-
-
Anello, A.1
Reichenberg, A.2
Luo, X.3
Schmeidler, J.4
Hollander, E.5
Smith, C.J.6
Puleo, C.M.7
Kryzak, L.8
Silverman, J.M.9
-
13
-
-
63549101812
-
Mouse models for evaluating sex chromosome effects that cause sex differences in non-gonadal tissues
-
Arnold A.P. Mouse models for evaluating sex chromosome effects that cause sex differences in non-gonadal tissues. J. Neuroendocrinol. 2009, 21:377-386.
-
(2009)
J. Neuroendocrinol.
, vol.21
, pp. 377-386
-
-
Arnold, A.P.1
-
14
-
-
84856215229
-
The end of gonad-centric sex determination in mammals
-
Arnold A.P. The end of gonad-centric sex determination in mammals. Trends Genet. 2012, 28:55-61.
-
(2012)
Trends Genet.
, vol.28
, pp. 55-61
-
-
Arnold, A.P.1
-
15
-
-
58049173922
-
What does the "four core genotypes" mouse model tell us about sex differences in the brain and other tissues
-
Arnold A.P., Chen X. What does the "four core genotypes" mouse model tell us about sex differences in the brain and other tissues?. Front. Neuroendocrinol. 2009, 30:1-9.
-
(2009)
Front. Neuroendocrinol.
, vol.30
, pp. 1-9
-
-
Arnold, A.P.1
Chen, X.2
-
16
-
-
78549271649
-
Maternal infection requiring hospitalization during pregnancy and autism spectrum disorders
-
Atladóttir H.O., Thorsen P., Østergaard L., Schendel D.E., Lemcke S., Abdallah M., Parner E.T. Maternal infection requiring hospitalization during pregnancy and autism spectrum disorders. J. Autism Dev. Disord. 2010, 40:1423-1430.
-
(2010)
J. Autism Dev. Disord.
, vol.40
, pp. 1423-1430
-
-
Atladóttir, H.O.1
Thorsen, P.2
Østergaard, L.3
Schendel, D.E.4
Lemcke, S.5
Abdallah, M.6
Parner, E.T.7
-
17
-
-
84868089983
-
Traits of ADHD and autism in girls with a twin brother: a Mendelian randomization study
-
Attermann J., Obel C., Bilenberg N., Nordenbæk C.M., Skytthe A., Olsen J. Traits of ADHD and autism in girls with a twin brother: a Mendelian randomization study. Eur. Child Adolesc. Psychiat. 2012, 21:503-509.
-
(2012)
Eur. Child Adolesc. Psychiat.
, vol.21
, pp. 503-509
-
-
Attermann, J.1
Obel, C.2
Bilenberg, N.3
Nordenbæk, C.M.4
Skytthe, A.5
Olsen, J.6
-
18
-
-
0141884303
-
Glial cells and neurotransmission
-
Auld D.S., Robitaille R. Glial cells and neurotransmission. Neuron 2003, 40:389-400.
-
(2003)
Neuron
, vol.40
, pp. 389-400
-
-
Auld, D.S.1
Robitaille, R.2
-
19
-
-
61449207882
-
Fetal testosterone and autistic traits
-
Auyeung B., Baron-Cohen S., Ashwin E., Knickmeyer R., Taylor K., Hackett G. Fetal testosterone and autistic traits. Br. J. Psychol. 2009, 100:1-22.
-
(2009)
Br. J. Psychol.
, vol.100
, pp. 1-22
-
-
Auyeung, B.1
Baron-Cohen, S.2
Ashwin, E.3
Knickmeyer, R.4
Taylor, K.5
Hackett, G.6
-
20
-
-
77956391388
-
Foetal testosterone and autistic traits in 18 to 24-month-old children
-
Auyeung B., Taylor K., Hackett G., Baron-Cohen S. Foetal testosterone and autistic traits in 18 to 24-month-old children. Mol. Autism 2010, 1:11.
-
(2010)
Mol. Autism
, vol.1
, pp. 11
-
-
Auyeung, B.1
Taylor, K.2
Hackett, G.3
Baron-Cohen, S.4
-
21
-
-
84873025855
-
Prenatal versus postnatal sex steroid hormone effects on autistic traits in children at 18 to 24 months of age
-
Auyeung B., Ahluwalia J., Thomson L., Taylor K., Hackett G., O'Donnell K.J., Baron-Cohen S. Prenatal versus postnatal sex steroid hormone effects on autistic traits in children at 18 to 24 months of age. Mol. Autism 2012, 3:17.
-
(2012)
Mol. Autism
, vol.3
, pp. 17
-
-
Auyeung, B.1
Ahluwalia, J.2
Thomson, L.3
Taylor, K.4
Hackett, G.5
O'Donnell, K.J.6
Baron-Cohen, S.7
-
22
-
-
79251552301
-
DIA1R is an X-linked gene related to deleted in autism-1
-
Aziz A., Harrop S.P., Bishop N.E. DIA1R is an X-linked gene related to deleted in autism-1. PLoS One 2011, 6:e14534.
-
(2011)
PLoS One
, vol.6
-
-
Aziz, A.1
Harrop, S.P.2
Bishop, N.E.3
-
23
-
-
0028906338
-
Autism as a strongly genetic disorder: evidence from a British twin study
-
Bailey A., Le Couteur A., Gottesman I., Bolton P., Simonoff E., Yuzda E., Rutter M., et al. Autism as a strongly genetic disorder: evidence from a British twin study. Psychol. Med. 1995, 25:63-78.
-
(1995)
Psychol. Med.
, vol.25
, pp. 63-78
-
-
Bailey, A.1
Le Couteur, A.2
Gottesman, I.3
Bolton, P.4
Simonoff, E.5
Yuzda, E.6
Rutter, M.7
-
24
-
-
14844292638
-
Towards an understanding of unique and shared pathways in the psychopathophysiology of ADHD
-
Banaschewski T., Hollis C., Oosterlaan J., Roeyers H., Rubia K., Willcutt E., Taylor E. Towards an understanding of unique and shared pathways in the psychopathophysiology of ADHD. Dev. Sci. 2005, 8:132-140.
-
(2005)
Dev. Sci.
, vol.8
, pp. 132-140
-
-
Banaschewski, T.1
Hollis, C.2
Oosterlaan, J.3
Roeyers, H.4
Rubia, K.5
Willcutt, E.6
Taylor, E.7
-
25
-
-
0036606475
-
The extreme male brain theory of autism
-
Baron-Cohen S. The extreme male brain theory of autism. Trends Cogn. Sci. 2002, 6:248-254.
-
(2002)
Trends Cogn. Sci.
, vol.6
, pp. 248-254
-
-
Baron-Cohen, S.1
-
26
-
-
3543119581
-
The empathy quotient: an investigation of adults with Asperger syndrome or high functioning autism, and normal sex differences
-
Baron-Cohen S., Wheelwright S. The empathy quotient: an investigation of adults with Asperger syndrome or high functioning autism, and normal sex differences. J. Autism Dev. Disord. 2004, 34:163-175.
-
(2004)
J. Autism Dev. Disord.
, vol.34
, pp. 163-175
-
-
Baron-Cohen, S.1
Wheelwright, S.2
-
27
-
-
0035087628
-
The "reading the mind in the eyes" test revised version: a study with normal adults, and adults with Asperger syndrome or high-functioning autism
-
Baron-Cohen S., Wheelwright S., Hill J., Raste Y., Plumb I. The "reading the mind in the eyes" test revised version: a study with normal adults, and adults with Asperger syndrome or high-functioning autism. J. Child Psychol. Psychiat. 2001, 42:241-251.
-
(2001)
J. Child Psychol. Psychiat.
, vol.42
, pp. 241-251
-
-
Baron-Cohen, S.1
Wheelwright, S.2
Hill, J.3
Raste, Y.4
Plumb, I.5
-
28
-
-
0037470349
-
The systemizing quotient: an investigation of adults with Asperger syndrome or high-functioning autism, and normal sex differences
-
Baron-Cohen S., Richler J., Bisarya D., Gurunathan N., Wheelwright S. The systemizing quotient: an investigation of adults with Asperger syndrome or high-functioning autism, and normal sex differences. Philos. Trans. Roy. Soc. Lond. B. Biol. Sci. 2003, 358:361-374.
-
(2003)
Philos. Trans. Roy. Soc. Lond. B. Biol. Sci.
, vol.358
, pp. 361-374
-
-
Baron-Cohen, S.1
Richler, J.2
Bisarya, D.3
Gurunathan, N.4
Wheelwright, S.5
-
29
-
-
27644506085
-
Sex differences in the brain: implications for explaining autism
-
Baron-Cohen S., Knickmeyer R., Belmonte M.K. Sex differences in the brain: implications for explaining autism. Science 2005, 310:819-823.
-
(2005)
Science
, vol.310
, pp. 819-823
-
-
Baron-Cohen, S.1
Knickmeyer, R.2
Belmonte, M.K.3
-
30
-
-
79959791701
-
Why are autism spectrum conditions more prevalent in males
-
Baron-Cohen S., Lombardo M.V., Auyeung B., Ashwin E., Chakrabarti B., Knickmeyer R. Why are autism spectrum conditions more prevalent in males?. PLoS Biol. 2011, 9:e1001081.
-
(2011)
PLoS Biol.
, vol.9
-
-
Baron-Cohen, S.1
Lombardo, M.V.2
Auyeung, B.3
Ashwin, E.4
Chakrabarti, B.5
Knickmeyer, R.6
-
31
-
-
79251512326
-
Intragenic deletions of IL1RAPL1: report of two cases and review of the literature
-
Behnecke A., Hinderhofer K., Bartsch O., Nümann A., Ipach M.-L., Damatova N., Haaf T., Dufke A., Riess O., Moog U. Intragenic deletions of IL1RAPL1: report of two cases and review of the literature. Am. J. Med. Genet. A 2011, 155A:372-379.
-
(2011)
Am. J. Med. Genet. A
, vol.155 A
, pp. 372-379
-
-
Behnecke, A.1
Hinderhofer, K.2
Bartsch, O.3
Nümann, A.4
Ipach, M.-L.5
Damatova, N.6
Haaf, T.7
Dufke, A.8
Riess, O.9
Moog, U.10
-
32
-
-
0033867110
-
Effect of the androgen receptor CAG repeat polymorphism on transcriptional activity: specificity in prostate and non-prostate cell lines
-
Beilin J. Effect of the androgen receptor CAG repeat polymorphism on transcriptional activity: specificity in prostate and non-prostate cell lines. J. Mol. Endocrinol. 2000, 25:85-96.
-
(2000)
J. Mol. Endocrinol.
, vol.25
, pp. 85-96
-
-
Beilin, J.1
-
33
-
-
21744447595
-
Neurosteroids: endogenous regulators of the GABA(A) receptor
-
Belelli D., Lambert J.J. Neurosteroids: endogenous regulators of the GABA(A) receptor. Nat. Rev. Neurosci. 2005, 6:565-575.
-
(2005)
Nat. Rev. Neurosci.
, vol.6
, pp. 565-575
-
-
Belelli, D.1
Lambert, J.J.2
-
34
-
-
0030722387
-
Early androgen effects on aggression in children and adults with congenital adrenal hyperplasia
-
Berenbaum S., Resnick S. Early androgen effects on aggression in children and adults with congenital adrenal hyperplasia. Psychoneuroendocrinology 1997, 22:505-515.
-
(1997)
Psychoneuroendocrinology
, vol.22
, pp. 505-515
-
-
Berenbaum, S.1
Resnick, S.2
-
35
-
-
33846887598
-
Microglial control of neuronal death and synaptic properties
-
Bessis A., Béchade C., Bernard D., Roumier A. Microglial control of neuronal death and synaptic properties. Glia 2007, 55:233-238.
-
(2007)
Glia
, vol.55
, pp. 233-238
-
-
Bessis, A.1
Béchade, C.2
Bernard, D.3
Roumier, A.4
-
36
-
-
37249045889
-
Disruption of the IL1RAPL1 gene associated with a pericentromeric inversion of the X chromosome in a patient with mental retardation and autism
-
Bhat S.S., Ladd S., Grass F., Spence J.E., Brasington C.K., Simensen R.J., Schwartz C.E., Dupont B.R., Stevenson R.E., Srivastava a.K. Disruption of the IL1RAPL1 gene associated with a pericentromeric inversion of the X chromosome in a patient with mental retardation and autism. Clin. Genet. 2008, 73:94-96.
-
(2008)
Clin. Genet.
, vol.73
, pp. 94-96
-
-
Bhat, S.S.1
Ladd, S.2
Grass, F.3
Spence, J.E.4
Brasington, C.K.5
Simensen, R.J.6
Schwartz, C.E.7
Dupont, B.R.8
Stevenson, R.E.9
Srivastava, A.10
-
37
-
-
0033981995
-
Distinctive patterns of memory function in subgroups of females with Turner syndrome: evidence for imprinted loci on the X-chromosome affecting neurodevelopment
-
Bishop D.V.M., Canning E., Elgar K., Morris E., Jacobs P.A., Skuse D.H. Distinctive patterns of memory function in subgroups of females with Turner syndrome: evidence for imprinted loci on the X-chromosome affecting neurodevelopment. Neuropsychologia 2000, 38:712-721.
-
(2000)
Neuropsychologia
, vol.38
, pp. 712-721
-
-
Bishop, D.V.M.1
Canning, E.2
Elgar, K.3
Morris, E.4
Jacobs, P.A.5
Skuse, D.H.6
-
38
-
-
80052827372
-
Autism, language and communication in children with sex chromosome trisomies
-
Bishop D., Jacobs P., Lachlan K., Wellesley D., Barnicoat A., Boyd P., Fryer A., Middlemiss P., Smithson S., Metcalfe K., Shears D., Leggett V., Nation K., Scerif G. Autism, language and communication in children with sex chromosome trisomies. Arch. Dis. Childh. 2011, 96:954-959.
-
(2011)
Arch. Dis. Childh.
, vol.96
, pp. 954-959
-
-
Bishop, D.1
Jacobs, P.2
Lachlan, K.3
Wellesley, D.4
Barnicoat, A.5
Boyd, P.6
Fryer, A.7
Middlemiss, P.8
Smithson, S.9
Metcalfe, K.10
Shears, D.11
Leggett, V.12
Nation, K.13
Scerif, G.14
-
39
-
-
0042706143
-
A stain upon the silence: genes escaping X inactivation
-
Brown C.J., Greally J.M. A stain upon the silence: genes escaping X inactivation. Trends Genet. 2003, 19:432-438.
-
(2003)
Trends Genet.
, vol.19
, pp. 432-438
-
-
Brown, C.J.1
Greally, J.M.2
-
40
-
-
66049159361
-
Psychiatric characteristics in a self-selected sample of boys with Klinefelter syndrome
-
Bruining H., Swaab H., Kas M., van Engeland H. Psychiatric characteristics in a self-selected sample of boys with Klinefelter syndrome. Pediatrics 2009, 123:e865-e870.
-
(2009)
Pediatrics
, vol.123
-
-
Bruining, H.1
Swaab, H.2
Kas, M.3
van Engeland, H.4
-
41
-
-
0029654179
-
The genetic basis of XX-XY differences present before gonadal sex differentiation in the mouse
-
discussion 260-1
-
Burgoyne P.S., Thornhill A.R., Boudrean S.K., Darling S.M., Bishop C.E., Evans E.P. The genetic basis of XX-XY differences present before gonadal sex differentiation in the mouse. Philos. Trans. Roy. Soc. Lond. B.: Biol. Sci. 1995, 350:253-260. discussion 260-1.
-
(1995)
Philos. Trans. Roy. Soc. Lond. B.: Biol. Sci.
, vol.350
, pp. 253-260
-
-
Burgoyne, P.S.1
Thornhill, A.R.2
Boudrean, S.K.3
Darling, S.M.4
Bishop, C.E.5
Evans, E.P.6
-
42
-
-
0033594960
-
Heterogeneous gene expression from the inactive X chromosome: an X-linked gene that escapes X inactivation in some human cell lines but is inactivated in others
-
Carrel L., Willard H.F. Heterogeneous gene expression from the inactive X chromosome: an X-linked gene that escapes X inactivation in some human cell lines but is inactivated in others. Proc. Natl. Acad. Sci. 1999, 96:7364-7369.
-
(1999)
Proc. Natl. Acad. Sci.
, vol.96
, pp. 7364-7369
-
-
Carrel, L.1
Willard, H.F.2
-
43
-
-
15244353967
-
X-inactivation profile reveals extensive variability in X-linked gene expression in females
-
Carrel L., Willard H.F. X-inactivation profile reveals extensive variability in X-linked gene expression in females. Nature 2005, 434:400-404.
-
(2005)
Nature
, vol.434
, pp. 400-404
-
-
Carrel, L.1
Willard, H.F.2
-
44
-
-
33749407724
-
Genomic environment predicts expression patterns on the human inactive X chromosome
-
Carrel L., Park C., Tyekucheva S., Dunn J., Chiaromonte F., Makova K.D. Genomic environment predicts expression patterns on the human inactive X chromosome. PLoS Genet. 2006, 2:e151.
-
(2006)
PLoS Genet.
, vol.2
-
-
Carrel, L.1
Park, C.2
Tyekucheva, S.3
Dunn, J.4
Chiaromonte, F.5
Makova, K.D.6
-
45
-
-
0036785889
-
Sex chromosome genes directly affect brain sexual differentiation
-
Carruth L.L., Reisert I., Arnold A.P. Sex chromosome genes directly affect brain sexual differentiation. Nat. Neurosci. 2002, 5:933-934.
-
(2002)
Nat. Neurosci.
, vol.5
, pp. 933-934
-
-
Carruth, L.L.1
Reisert, I.2
Arnold, A.P.3
-
46
-
-
0034672159
-
Familial-skewed X-chromosome inactivation as a predisposing factor for late-onset X-linked sideroblastic anemia in carrier females
-
Cazzola M., May A., Bergamaschi G. Familial-skewed X-chromosome inactivation as a predisposing factor for late-onset X-linked sideroblastic anemia in carrier females. Blood 2000, 96:4363-4365.
-
(2000)
Blood
, vol.96
, pp. 4363-4365
-
-
Cazzola, M.1
May, A.2
Bergamaschi, G.3
-
47
-
-
67651213461
-
Genes related to sex steroids, neural growth, and social-emotional behavior are associated with autistic traits, empathy, and Asperger syndrome
-
Chakrabarti B., Dudbridge F., Kent L., Wheelwright S., Hill-Cawthorne G., Allison C., Banerjee-Basu S., Baron-Cohen S. Genes related to sex steroids, neural growth, and social-emotional behavior are associated with autistic traits, empathy, and Asperger syndrome. Autism Res. 2009, 2:157-177.
-
(2009)
Autism Res.
, vol.2
, pp. 157-177
-
-
Chakrabarti, B.1
Dudbridge, F.2
Kent, L.3
Wheelwright, S.4
Hill-Cawthorne, G.5
Allison, C.6
Banerjee-Basu, S.7
Baron-Cohen, S.8
-
48
-
-
0028033594
-
The length and location of CAG trinucleotide repeats in the androgen receptor N-terminal domain affect transactivation function
-
Chamberlain N.L., Driver E.D., Miesfeld R.L. The length and location of CAG trinucleotide repeats in the androgen receptor N-terminal domain affect transactivation function. Nucleic Acids Res. 1994, 22:3181-3186.
-
(1994)
Nucleic Acids Res.
, vol.22
, pp. 3181-3186
-
-
Chamberlain, N.L.1
Driver, E.D.2
Miesfeld, R.L.3
-
49
-
-
34447620077
-
Fetal testosterone and empathy: evidence from the empathy quotient (EQ) and the "reading the mind in the eyes" test
-
Chapman E., Baron-Cohen S., Auyeung B., Knickmeyer R., Taylor K., Hackett G. Fetal testosterone and empathy: evidence from the empathy quotient (EQ) and the "reading the mind in the eyes" test. Soc. Neurosci. 2006, 1:135-148.
-
(2006)
Soc. Neurosci.
, vol.1
, pp. 135-148
-
-
Chapman, E.1
Baron-Cohen, S.2
Auyeung, B.3
Knickmeyer, R.4
Taylor, K.5
Hackett, G.6
-
50
-
-
0017809273
-
Behavioral consequences of congenital rubella
-
Chess S., Fernandez P., Korn S. Behavioral consequences of congenital rubella. J. Pediatr. 1978, 93:699-703.
-
(1978)
J. Pediatr.
, vol.93
, pp. 699-703
-
-
Chess, S.1
Fernandez, P.2
Korn, S.3
-
51
-
-
33644849965
-
Molecular cytogenetic analysis of a familial interstitial deletion Xp22.2-22.3 with a highly variable phenotype in female carriers
-
Chocholska S., Rossier E., Barbi G., Kehrer-sawatzki H. Molecular cytogenetic analysis of a familial interstitial deletion Xp22.2-22.3 with a highly variable phenotype in female carriers. Am. J. Med. Genet. A 2006, 140A(6):604-610.
-
(2006)
Am. J. Med. Genet. A
, vol.140 A
, Issue.6
, pp. 604-610
-
-
Chocholska, S.1
Rossier, E.2
Barbi, G.3
Kehrer-sawatzki, H.4
-
52
-
-
33947245128
-
RBP2 belongs to a family of demethylases, specific for tri-and dimethylated lysine 4 on histone 3
-
Christensen J., Agger K., Cloos P.A.C., Pasini D., Rose S., Sennels L., Rappsilber J., Hansen K.H., Salcini A.E., Helin K. RBP2 belongs to a family of demethylases, specific for tri-and dimethylated lysine 4 on histone 3. Cell 2007, 128:1063-1076.
-
(2007)
Cell
, vol.128
, pp. 1063-1076
-
-
Christensen, J.1
Agger, K.2
Cloos, P.A.C.3
Pasini, D.4
Rose, S.5
Sennels, L.6
Rappsilber, J.7
Hansen, K.H.8
Salcini, A.E.9
Helin, K.10
-
53
-
-
84860582461
-
An X chromosome-wide association study in autism families identifies TBL1X as a novel autism spectrum disorder candidate gene in males
-
Chung R.-H., Ma D., Wang K., Hedges D.J., Jaworski J.M., Gilbert J.R., Cuccaro M.L., Wright H.H., Abramson R.K., Konidari I., Whitehead P.L., Schellenberg G.D., Hakonarson H., Haines J.L., Pericak-Vance M.a., Martin E.R. An X chromosome-wide association study in autism families identifies TBL1X as a novel autism spectrum disorder candidate gene in males. Mol. Autism 2011, 2:18.
-
(2011)
Mol. Autism
, vol.2
, pp. 18
-
-
Chung, R.-H.1
Ma, D.2
Wang, K.3
Hedges, D.J.4
Jaworski, J.M.5
Gilbert, J.R.6
Cuccaro, M.L.7
Wright, H.H.8
Abramson, R.K.9
Konidari, I.10
Whitehead, P.L.11
Schellenberg, G.D.12
Hakonarson, H.13
Haines, J.L.14
Pericak-Vance, M.15
Martin, E.R.16
-
54
-
-
0027769559
-
The human SRY transcript
-
Clepet C., Schater A.J., Sinclair A.H., Palmer M.S., Lovell-Badge R., Goodfellow P.N. The human SRY transcript. Hum. Mol. Genet. 1993, 2:2007-2012.
-
(1993)
Hum. Mol. Genet.
, vol.2
, pp. 2007-2012
-
-
Clepet, C.1
Schater, A.J.2
Sinclair, A.H.3
Palmer, M.S.4
Lovell-Badge, R.5
Goodfellow, P.N.6
-
55
-
-
79952213669
-
Autism severity is associated with child and maternal MAOA genotypes
-
Cohen I.L., Liu X., Lewis M.E.S., Chudley a., Forster-Gibson C., Gonzalez M., Jenkins E.C., Brown W.T., Holden J.J.a. Autism severity is associated with child and maternal MAOA genotypes. Clin. Genet. 2011, 79:355-362.
-
(2011)
Clin. Genet.
, vol.79
, pp. 355-362
-
-
Cohen, I.L.1
Liu, X.2
Lewis, M.E.S.3
Chudley, A.4
Forster-Gibson, C.5
Gonzalez, M.6
Jenkins, E.C.7
Brown, W.T.8
Holden, J.9
-
56
-
-
33645232376
-
Immunological findings in autism
-
Cohly H., Panja A. Immunological findings in autism. Int. Rev. Neurobiol. 2005, 71:317-341.
-
(2005)
Int. Rev. Neurobiol.
, vol.71
, pp. 317-341
-
-
Cohly, H.1
Panja, A.2
-
57
-
-
78349291914
-
Sibling recurrence and the genetic epidemiology of autism
-
Constantino J.N., Zhang Y., Frazier T., Abbacchi A.M., Law P. Sibling recurrence and the genetic epidemiology of autism. Am. J. Psychiat. 2010, 167:1349-1356.
-
(2010)
Am. J. Psychiat.
, vol.167
, pp. 1349-1356
-
-
Constantino, J.N.1
Zhang, Y.2
Frazier, T.3
Abbacchi, A.M.4
Law, P.5
-
58
-
-
84903779624
-
Increased BDNF levels and association with the NTRK2 gene suggest a disruption of BDNF/TRKB signaling in autism
-
Correia C., Sequeira A.F., Almeida J., Gallagher L., Oliveira G., Vicente A.M. Increased BDNF levels and association with the NTRK2 gene suggest a disruption of BDNF/TRKB signaling in autism. Int. J. Dev. Neurosci. 2010, 28:713.
-
(2010)
Int. J. Dev. Neurosci.
, vol.28
, pp. 713
-
-
Correia, C.1
Sequeira, A.F.2
Almeida, J.3
Gallagher, L.4
Oliveira, G.5
Vicente, A.M.6
-
59
-
-
0033374463
-
Autism in association with Turner syndrome: genetic implications for male vulnerability to pervasive developmental disorders
-
Creswell C.S., Skuse D.H. Autism in association with Turner syndrome: genetic implications for male vulnerability to pervasive developmental disorders. Neurocase 1999, 5:511-518.
-
(1999)
Neurocase
, vol.5
, pp. 511-518
-
-
Creswell, C.S.1
Skuse, D.H.2
-
60
-
-
77957864989
-
Serum testosterone concentration in male autistic youngsters
-
Croonenberghs J., Van Grieken S., Wauters A., Van West D., Brouw L., Maes M., Deboutte D. Serum testosterone concentration in male autistic youngsters. Neuroendocrinol. Lett. 2010, 31(4):483-488.
-
(2010)
Neuroendocrinol. Lett.
, vol.31
, Issue.4
, pp. 483-488
-
-
Croonenberghs, J.1
Van Grieken, S.2
Wauters, A.3
Van West, D.4
Brouw, L.5
Maes, M.6
Deboutte, D.7
-
61
-
-
41249089087
-
Loss of progranulin function in frontotemporal lobar degeneration
-
Cruts M., Van Broeckhoven C. Loss of progranulin function in frontotemporal lobar degeneration. Trends Genet. 2008, 24:186-194.
-
(2008)
Trends Genet.
, vol.24
, pp. 186-194
-
-
Cruts, M.1
Van Broeckhoven, C.2
-
62
-
-
84874586343
-
Microglia regulate the number of neural precursor cells in the developing cerebral cortex
-
Cunningham C.L., Martínez-Cerdeño V., Noctor S.C. Microglia regulate the number of neural precursor cells in the developing cerebral cortex. J. Neurosci. 2013, 33:4216-4233.
-
(2013)
J. Neurosci.
, vol.33
, pp. 4216-4233
-
-
Cunningham, C.L.1
Martínez-Cerdeño, V.2
Noctor, S.C.3
-
63
-
-
70350571767
-
Autism and nonsyndromic mental retardation associated with a de novo mutation in the NLGN4X gene promoter causing an increased expression level
-
Daoud H., Bonnet-Brilhault F., Védrine S., Demattéi M.-V., Vourc'h P., Bayou N., Andres C.R., Barthélémy C., Laumonnier F., Briault S. Autism and nonsyndromic mental retardation associated with a de novo mutation in the NLGN4X gene promoter causing an increased expression level. Biol. Psychiat. 2009, 66:906-910.
-
(2009)
Biol. Psychiat.
, vol.66
, pp. 906-910
-
-
Daoud, H.1
Bonnet-Brilhault, F.2
Védrine, S.3
Demattéi, M.-V.4
Vourc'h, P.5
Bayou, N.6
Andres, C.R.7
Barthélémy, C.8
Laumonnier, F.9
Briault, S.10
-
65
-
-
0038434285
-
Anatomy, development and function of sexually dimorphic neural circuits in the mammalian brain
-
Academic, New York, D. Pfaff, A. Arnold, A. Etgen, S. Fahrbach, R. Rubin (Eds.)
-
De Vries G., Simerly R. Anatomy, development and function of sexually dimorphic neural circuits in the mammalian brain. Hormones, brain and behavior 2002, 137-192. Academic, New York. D. Pfaff, A. Arnold, A. Etgen, S. Fahrbach, R. Rubin (Eds.).
-
(2002)
Hormones, brain and behavior
, pp. 137-192
-
-
De Vries, G.1
Simerly, R.2
-
66
-
-
38049013294
-
Gabrb3 gene deficient mice exhibit impaired social and exploratory behaviors, deficits in non-selective attention and hypoplasia of cerebellar vermal lobules: a potential model of autism spectrum disorder
-
DeLorey T.M., Sahbaie P., Hashemi E., Homanics G.E., Clark J.D. Gabrb3 gene deficient mice exhibit impaired social and exploratory behaviors, deficits in non-selective attention and hypoplasia of cerebellar vermal lobules: a potential model of autism spectrum disorder. Behav. Brain Res. 2008, 187:207-220.
-
(2008)
Behav. Brain Res.
, vol.187
, pp. 207-220
-
-
DeLorey, T.M.1
Sahbaie, P.2
Hashemi, E.3
Homanics, G.E.4
Clark, J.D.5
-
67
-
-
84859256941
-
Critical evaluation of imprinted gene expression by RNA-Seq: a new perspective
-
DeVeale B., van der Kooy D., Babak T. Critical evaluation of imprinted gene expression by RNA-Seq: a new perspective. PLoS Genet. 2012, 8:e1002600.
-
(2012)
PLoS Genet.
, vol.8
-
-
DeVeale, B.1
van der Kooy, D.2
Babak, T.3
-
68
-
-
0141888333
-
Sexually dimorphic gene expression in mouse brain precedes gonadal differentiation
-
Dewing P., Shi T., Horvath S. Sexually dimorphic gene expression in mouse brain precedes gonadal differentiation. Mol. Brain Res. 2003, 118:82-90.
-
(2003)
Mol. Brain Res.
, vol.118
, pp. 82-90
-
-
Dewing, P.1
Shi, T.2
Horvath, S.3
-
69
-
-
32944479204
-
Direct regulation of adult brain function by the male-specific factor SRY
-
Dewing P., Chiang C.W.K., Sinchak K., Sim H., Fernagut P.-O., Kelly S., Chesselet M.-F., Micevych P.E., Albrecht K.H., Harley V.R., Vilain E. Direct regulation of adult brain function by the male-specific factor SRY. Curr. Biol. 2006, 16:415-420.
-
(2006)
Curr. Biol.
, vol.16
, pp. 415-420
-
-
Dewing, P.1
Chiang, C.W.K.2
Sinchak, K.3
Sim, H.4
Fernagut, P.-O.5
Kelly, S.6
Chesselet, M.-F.7
Micevych, P.E.8
Albrecht, K.H.9
Harley, V.R.10
Vilain, E.11
-
70
-
-
0033460319
-
Escapees on the X chromosome
-
Disteche C.M. Escapees on the X chromosome. Proc. Natl. Acad. Sci. 1999, 96:14180-14182.
-
(1999)
Proc. Natl. Acad. Sci.
, vol.96
, pp. 14180-14182
-
-
Disteche, C.M.1
-
71
-
-
84859887139
-
Prenatal stress causes alterations in the morphology of microglia and the inflammatory response of the hippocampus of adult female mice
-
Diz-Chaves Y., Pernía O., Carrero P., Garcia-Segura L.M. Prenatal stress causes alterations in the morphology of microglia and the inflammatory response of the hippocampus of adult female mice. J. Neuroinflamm. 2012, 9:71.
-
(2012)
J. Neuroinflamm.
, vol.9
, pp. 71
-
-
Diz-Chaves, Y.1
Pernía, O.2
Carrero, P.3
Garcia-Segura, L.M.4
-
72
-
-
57149100947
-
Advanced parental age and the risk of autism spectrum disorder
-
Durkin M.S., Maenner M.J., Newschaffer C.J., Lee L.-C., Cunniff C.M., Daniels J.L., Kirby R.S., Leavitt L., Miller L., Zahorodny W., Schieve L.A. Advanced parental age and the risk of autism spectrum disorder. Am. J. Epidemiol. 2008, 168:1268-1276.
-
(2008)
Am. J. Epidemiol.
, vol.168
, pp. 1268-1276
-
-
Durkin, M.S.1
Maenner, M.J.2
Newschaffer, C.J.3
Lee, L.-C.4
Cunniff, C.M.5
Daniels, J.L.6
Kirby, R.S.7
Leavitt, L.8
Miller, L.9
Zahorodny, W.10
Schieve, L.A.11
-
73
-
-
50049129101
-
Chronic maternal stress affects growth, behaviour and hypothalamo-pituitary-adrenal function in juvenile offspring
-
Emack J., Kostaki A., Walker C.-D., Matthews S.G. Chronic maternal stress affects growth, behaviour and hypothalamo-pituitary-adrenal function in juvenile offspring. Horm. Behav. 2008, 54:514-520.
-
(2008)
Horm. Behav.
, vol.54
, pp. 514-520
-
-
Emack, J.1
Kostaki, A.2
Walker, C.-D.3
Matthews, S.G.4
-
74
-
-
0037131025
-
New insights into neuron-glia communication
-
Fields R.D., Stevens-Graham B. New insights into neuron-glia communication. Science 2002, 298:556-562.
-
(2002)
Science
, vol.298
, pp. 556-562
-
-
Fields, R.D.1
Stevens-Graham, B.2
-
75
-
-
78649992249
-
Deletion in Xp22.11: PTCHD1 is a candidate gene for X-linked intellectual disability with or without autism
-
Filges I., Röthlisberger B., Blattner A., Boesch N., Demougin P., Wenzel F., Huber A.R., Heinimann K., Weber P., Miny P. Deletion in Xp22.11: PTCHD1 is a candidate gene for X-linked intellectual disability with or without autism. Clin. Genet. 2011, 79:79-85.
-
(2011)
Clin. Genet.
, vol.79
, pp. 79-85
-
-
Filges, I.1
Röthlisberger, B.2
Blattner, A.3
Boesch, N.4
Demougin, P.5
Wenzel, F.6
Huber, A.R.7
Heinimann, K.8
Weber, P.9
Miny, P.10
-
76
-
-
84877099960
-
Dissociation of frontotemporal dementia-related deficits and neuroinflammation in progranulin haploinsufficient mice
-
Filiano A.J., Martens L.H., Young A.H., Warmus B.a., Zhou P., Diaz-Ramirez G., Jiao J., Zhang Z., Huang E.J., Gao F.-B., Farese R.V., Roberson E.D. Dissociation of frontotemporal dementia-related deficits and neuroinflammation in progranulin haploinsufficient mice. J. Neurosci. 2013, 33:5352-5361.
-
(2013)
J. Neurosci.
, vol.33
, pp. 5352-5361
-
-
Filiano, A.J.1
Martens, L.H.2
Young, A.H.3
Warmus, B.4
Zhou, P.5
Diaz-Ramirez, G.6
Jiao, J.7
Zhang, Z.8
Huang, E.J.9
Gao, F.-B.10
Farese, R.V.11
Roberson, E.D.12
-
77
-
-
0017530988
-
Infantile autism: a genetic study of 21 twin pairs
-
Folstein S., Rutter M. Infantile autism: a genetic study of 21 twin pairs. J. Child Psychol. Psychiat. 1977, 18:297-321.
-
(1977)
J. Child Psychol. Psychiat.
, vol.18
, pp. 297-321
-
-
Folstein, S.1
Rutter, M.2
-
78
-
-
0141427915
-
Epidemiological surveys of autism and other pervasive developmental disorders: an update
-
Fombonne E. Epidemiological surveys of autism and other pervasive developmental disorders: an update. J. Autism Dev. Disord. 2003, 33:365-382.
-
(2003)
J. Autism Dev. Disord.
, vol.33
, pp. 365-382
-
-
Fombonne, E.1
-
79
-
-
84929281115
-
Epigenetic mechanisms: DNA methylation and histone protein modification
-
Springer Verlag, Heidelberg, D. Pfaff (Ed.)
-
Gagnidze K., Pfaff D. Epigenetic mechanisms: DNA methylation and histone protein modification. Neuroscience in the 21st century 2012, 1939-1979. Springer Verlag, Heidelberg. D. Pfaff (Ed.).
-
(2012)
Neuroscience in the 21st century
, pp. 1939-1979
-
-
Gagnidze, K.1
Pfaff, D.2
-
80
-
-
84878827703
-
Hormone-dependent chromatin modifications related to sexually differentiated behaviors
-
Springer Verlag, Berlin-Heidelberg, D.W. Pfaff, Y. Christen (Eds.)
-
Gagnidze K., Pfaff D.W. Hormone-dependent chromatin modifications related to sexually differentiated behaviors. Multiple Origins of Sex Differences in Brain 2013, 1-20. Springer Verlag, Berlin-Heidelberg. D.W. Pfaff, Y. Christen (Eds.).
-
(2013)
Multiple Origins of Sex Differences in Brain
, pp. 1-20
-
-
Gagnidze, K.1
Pfaff, D.W.2
-
81
-
-
78649241823
-
Gene expression in neuroendocrine cells during the critical period for sexual differentiation of the brain
-
Gagnidze K., Pfaff D.W., Mong J.A. Gene expression in neuroendocrine cells during the critical period for sexual differentiation of the brain. Prog. Brain Res. 2010, 186:97-111.
-
(2010)
Prog. Brain Res.
, vol.186
, pp. 97-111
-
-
Gagnidze, K.1
Pfaff, D.W.2
Mong, J.A.3
-
82
-
-
43849112803
-
Immune transcriptome alterations in the temporal cortex of subjects with autism
-
Garbett K., Ebert P.J., Mitchell A., Lintas C., Manzi B., Mirnics K., Persico A.M. Immune transcriptome alterations in the temporal cortex of subjects with autism. Neurobiol. Dis. 2008, 30:303-311.
-
(2008)
Neurobiol. Dis.
, vol.30
, pp. 303-311
-
-
Garbett, K.1
Ebert, P.J.2
Mitchell, A.3
Lintas, C.4
Manzi, B.5
Mirnics, K.6
Persico, A.M.7
-
83
-
-
80051539002
-
Perinatal and neonatal risk factors for autism: a comprehensive meta-analysis
-
Gardener H., Spiegelman D., Buka S.L. Perinatal and neonatal risk factors for autism: a comprehensive meta-analysis. Pediatrics 2011, 344-355.
-
(2011)
Pediatrics
, pp. 344-355
-
-
Gardener, H.1
Spiegelman, D.2
Buka, S.L.3
-
84
-
-
0034723366
-
AIDS:HIV infection and dementia
-
Gartner S. AIDS:HIV infection and dementia. Science 2000, 287:602-604.
-
(2000)
Science
, vol.287
, pp. 602-604
-
-
Gartner, S.1
-
85
-
-
11244334274
-
NLGN3/NLGN4 gene mutations are not responsible for autism in the Quebec population
-
Gauthier J., Bonnel A., St-Onge J., Karemera L., Laurent S., Mottron L., Fombonne E., Joober R., Rouleau G.A. NLGN3/NLGN4 gene mutations are not responsible for autism in the Quebec population. Am. J. Med. Genet. B. Neuropsychiatr. Genet. 2005, 132B:74-75.
-
(2005)
Am. J. Med. Genet. B. Neuropsychiatr. Genet.
, vol.132 B
, pp. 74-75
-
-
Gauthier, J.1
Bonnel, A.2
St-Onge, J.3
Karemera, L.4
Laurent, S.5
Mottron, L.6
Fombonne, E.7
Joober, R.8
Rouleau, G.A.9
-
86
-
-
0141756141
-
The XYY syndrome: a follow-up study on 38 boys
-
Geerts M., Steyaert J., Fryns J. The XYY syndrome: a follow-up study on 38 boys. Genet. Couns. 2003, 14:267-279.
-
(2003)
Genet. Couns.
, vol.14
, pp. 267-279
-
-
Geerts, M.1
Steyaert, J.2
Fryns, J.3
-
87
-
-
33748774908
-
A clinical and laboratory evaluation of methionine cycle-transsulfuration and androgen pathway markers in children with autistic disorders
-
20905
-
Geier D., Geier M. A clinical and laboratory evaluation of methionine cycle-transsulfuration and androgen pathway markers in children with autistic disorders. Horm. Res. Paediatr. 2006, 20905:182-188.
-
(2006)
Horm. Res. Paediatr.
, pp. 182-188
-
-
Geier, D.1
Geier, M.2
-
88
-
-
37849023607
-
A prospective assessment of androgen levels in patients with autistic spectrum disorders: biochemical underpinnings and suggested therapies
-
Geier D.A., Geier M.R. A prospective assessment of androgen levels in patients with autistic spectrum disorders: biochemical underpinnings and suggested therapies. Neuroendocrinol. Lett. 2007, 28:565-573.
-
(2007)
Neuroendocrinol. Lett.
, vol.28
, pp. 565-573
-
-
Geier, D.A.1
Geier, M.R.2
-
90
-
-
77949488475
-
Sex differences in the evaluation and diagnosis of autism spectrum disorders among children
-
Giarelli E., Wiggins L.D., Rice C.E., Levy S.E., Kirby R.S., Pinto-Martin J., Mandell D. Sex differences in the evaluation and diagnosis of autism spectrum disorders among children. Disab. Health J. 2010, 3:107-116.
-
(2010)
Disab. Health J.
, vol.3
, pp. 107-116
-
-
Giarelli, E.1
Wiggins, L.D.2
Rice, C.E.3
Levy, S.E.4
Kirby, R.S.5
Pinto-Martin, J.6
Mandell, D.7
-
91
-
-
33744803185
-
Brief report: "the autism epidemic". The registered prevalence of autism in a Swedish urban area
-
Gillberg C., Cederlund M., Lamberg K., Zeijlon L. Brief report: "the autism epidemic". The registered prevalence of autism in a Swedish urban area. J. Autism Dev. Disord. 2006, 36:429-435.
-
(2006)
J. Autism Dev. Disord.
, vol.36
, pp. 429-435
-
-
Gillberg, C.1
Cederlund, M.2
Lamberg, K.3
Zeijlon, L.4
-
92
-
-
79958035893
-
Rare de novo variants associated with autism implicate a large functional network of genes involved in formation and function of synapses
-
Gilman S.R., Iossifov I., Levy D., Ronemus M., Wigler M., Vitkup D. Rare de novo variants associated with autism implicate a large functional network of genes involved in formation and function of synapses. Neuron 2011, 70:898-907.
-
(2011)
Neuron
, vol.70
, pp. 898-907
-
-
Gilman, S.R.1
Iossifov, I.2
Levy, D.3
Ronemus, M.4
Wigler, M.5
Vitkup, D.6
-
93
-
-
0035879378
-
Microglia in HIV-associated neurological diseases
-
Glass J.D., Wesselingh S.L. Microglia in HIV-associated neurological diseases. Microsc. Res. Tech. 2001, 54:95-105.
-
(2001)
Microsc. Res. Tech.
, vol.54
, pp. 95-105
-
-
Glass, J.D.1
Wesselingh, S.L.2
-
94
-
-
67349182343
-
Autism genome-wide copy number variation reveals ubiquitin and neuronal genes
-
Glessner J.T., Wang K., Cai G., Korvatska O., Kim C.E., et al. Autism genome-wide copy number variation reveals ubiquitin and neuronal genes. Nature 2009, 459:569-573.
-
(2009)
Nature
, vol.459
, pp. 569-573
-
-
Glessner, J.T.1
Wang, K.2
Cai, G.3
Korvatska, O.4
Kim, C.E.5
-
95
-
-
84875892696
-
Opinion: sex, gender and the diagnosis of autism - a biosocial view of the male preponderance
-
Goldman S. Opinion: sex, gender and the diagnosis of autism - a biosocial view of the male preponderance. Res. Autism Spectr. Disord. 2013, 7:675-679.
-
(2013)
Res. Autism Spectr. Disord.
, vol.7
, pp. 675-679
-
-
Goldman, S.1
-
96
-
-
0035574679
-
From brain determination to testis determination: evolution of the mammalian sex-determining gene
-
Graves J. From brain determination to testis determination: evolution of the mammalian sex-determining gene. Reprod. Fertil. Dev. 2001, 13:665-672.
-
(2001)
Reprod. Fertil. Dev.
, vol.13
, pp. 665-672
-
-
Graves, J.1
-
97
-
-
77955285002
-
Sex-specific parent-of-origin allelic expression in the mouse brain
-
Gregg C., Zhang J., Butler J.E., Haig D., Dulac C. Sex-specific parent-of-origin allelic expression in the mouse brain. Science 2010, 329:682-685.
-
(2010)
Science
, vol.329
, pp. 682-685
-
-
Gregg, C.1
Zhang, J.2
Butler, J.E.3
Haig, D.4
Dulac, C.5
-
98
-
-
80051944739
-
Genetic heritability and shared environmental factors among twin pairs with autism
-
Hallmayer J., Cleveland S., Torres A., Phillips J., Cohen B., Torigoe T., Miller J., Fedele A., Collins J., Smith K., Lotspeich L., Croen L.a., Ozonoff S., Lajonchere C., Grether J.K., Risch N. Genetic heritability and shared environmental factors among twin pairs with autism. Arch. Gen. Psychiat. 2011, 68:1095-1102.
-
(2011)
Arch. Gen. Psychiat.
, vol.68
, pp. 1095-1102
-
-
Hallmayer, J.1
Cleveland, S.2
Torres, A.3
Phillips, J.4
Cohen, B.5
Torigoe, T.6
Miller, J.7
Fedele, A.8
Collins, J.9
Smith, K.10
Lotspeich, L.11
Croen, L.12
Ozonoff, S.13
Lajonchere, C.14
Grether, J.K.15
Risch, N.16
-
99
-
-
0031822169
-
Spatial reasoning in children with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
-
Hampson E., Rovet J.F., Altmann D. Spatial reasoning in children with congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Dev. Neuropsychol. 1998, 14:299-320.
-
(1998)
Dev. Neuropsychol.
, vol.14
, pp. 299-320
-
-
Hampson, E.1
Rovet, J.F.2
Altmann, D.3
-
100
-
-
4143149688
-
Distribution of androgen receptor immunoreactivity in the brainstem of male rats
-
Hamson D.K., Jones B.A., Watson N.V. Distribution of androgen receptor immunoreactivity in the brainstem of male rats. Neuroscience 2004, 127:797-803.
-
(2004)
Neuroscience
, vol.127
, pp. 797-803
-
-
Hamson, D.K.1
Jones, B.A.2
Watson, N.V.3
-
101
-
-
70450230588
-
Sex differences in autism spectrum disorder: an examination of developmental functioning, autistic symptoms, and coexisting behavior problems in toddlers
-
Hartley S.L., Sikora D.M. Sex differences in autism spectrum disorder: an examination of developmental functioning, autistic symptoms, and coexisting behavior problems in toddlers. J. Autism Dev. Disord. 2009, 39:1715-1722.
-
(2009)
J. Autism Dev. Disord.
, vol.39
, pp. 1715-1722
-
-
Hartley, S.L.1
Sikora, D.M.2
-
102
-
-
34247641659
-
Steroid modulation of GABAA receptor-mediated transmission in the hypothalamus: effects on reproductive function
-
Henderson L.P. Steroid modulation of GABAA receptor-mediated transmission in the hypothalamus: effects on reproductive function. Neuropharmacology 2007, 52:1439-1453.
-
(2007)
Neuropharmacology
, vol.52
, pp. 1439-1453
-
-
Henderson, L.P.1
-
103
-
-
10744229158
-
Presence of dendritic cells, MCP-1, and activated microglia/macrophages in amyotrophic lateral sclerosis spinal cord tissue
-
Henkel J.S., Engelhardt J.I., Siklós L., Simpson E.P., Kim S.H., Pan T., Goodman J.C., Siddique T., Beers D.R., Appel S.H. Presence of dendritic cells, MCP-1, and activated microglia/macrophages in amyotrophic lateral sclerosis spinal cord tissue. Ann. Neurol. 2004, 55:221-235.
-
(2004)
Ann. Neurol.
, vol.55
, pp. 221-235
-
-
Henkel, J.S.1
Engelhardt, J.I.2
Siklós, L.3
Simpson, E.P.4
Kim, S.H.5
Pan, T.6
Goodman, J.C.7
Siddique, T.8
Beers, D.R.9
Appel, S.H.10
-
104
-
-
64449087475
-
Possible association between the androgen receptor gene and autism spectrum disorder
-
Henningsson S., Jonsson L., Ljunggren E., Westberg L., Gillberg Carina., Råstam M., Anckarsäter H., Nygren G., Landén M., Thuresson K., Betancur C., Leboyer M., Gillberg Christopher., Eriksson E., Melke J. Possible association between the androgen receptor gene and autism spectrum disorder. Psychoneuroendocrinology 2009, 34:752-761.
-
(2009)
Psychoneuroendocrinology
, vol.34
, pp. 752-761
-
-
Henningsson, S.1
Jonsson, L.2
Ljunggren, E.3
Westberg, L.4
Gillberg, C.5
Råstam, M.6
Anckarsäter, H.7
Nygren, G.8
Landén, M.9
Thuresson, K.10
Betancur, C.11
Leboyer, M.12
Gillberg, C.13
Eriksson, E.14
Melke, J.15
-
105
-
-
79959236375
-
Gender development and the human brain
-
Hines M. Gender development and the human brain. Annu. Rev. Neurosci. 2011, 34:69-88.
-
(2011)
Annu. Rev. Neurosci.
, vol.34
, pp. 69-88
-
-
Hines, M.1
-
106
-
-
0642337128
-
Spatial abilities following prenatal androgen abnormality: targeting and mental rotations performance in individuals with congenital adrenal hyperplasia
-
Hines M., Fane B., Pasterski V., Mathews G., Conway G., Brook C. Spatial abilities following prenatal androgen abnormality: targeting and mental rotations performance in individuals with congenital adrenal hyperplasia. Psychoneuroendocrinology 2003, 28:1010-1026.
-
(2003)
Psychoneuroendocrinology
, vol.28
, pp. 1010-1026
-
-
Hines, M.1
Fane, B.2
Pasterski, V.3
Mathews, G.4
Conway, G.5
Brook, C.6
-
107
-
-
66349137661
-
Gene expression profiling differentiates autism case-controls and phenotypic variants of autism spectrum disorders: evidence for circadian rhythm dysfunction in severe
-
Hu V., Sarachana T., Kim K. Gene expression profiling differentiates autism case-controls and phenotypic variants of autism spectrum disorders: evidence for circadian rhythm dysfunction in severe. Autism Res. 2009, 2:78-97.
-
(2009)
Autism Res.
, vol.2
, pp. 78-97
-
-
Hu, V.1
Sarachana, T.2
Kim, K.3
-
108
-
-
0347357614
-
Inheritance of a pre-inactivated paternal X chromosome in early mouse embryos
-
Huynh K.D., Lee J.T. Inheritance of a pre-inactivated paternal X chromosome in early mouse embryos. Nature 2003, 426:857-862.
-
(2003)
Nature
, vol.426
, pp. 857-862
-
-
Huynh, K.D.1
Lee, J.T.2
-
109
-
-
34248640836
-
Elevated rates of testosterone-related disorders in women with autism spectrum conditions
-
Ingudomnukul E., Baron-Cohen S., Wheelwright S., Knickmeyer R. Elevated rates of testosterone-related disorders in women with autism spectrum conditions. Horm. Behav. 2007, 51:597-604.
-
(2007)
Horm. Behav.
, vol.51
, pp. 597-604
-
-
Ingudomnukul, E.1
Baron-Cohen, S.2
Wheelwright, S.3
Knickmeyer, R.4
-
110
-
-
0037656313
-
Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism
-
Jamain S., Quach H., Betancur C., Råstam M., Colineaux C., Gillberg I.C., Soderstrom H., Giros B., Leboyer M., Gillberg C., Bourgeron T. Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism. Nat. Genet. 2003, 34:27-29.
-
(2003)
Nat. Genet.
, vol.34
, pp. 27-29
-
-
Jamain, S.1
Quach, H.2
Betancur, C.3
Råstam, M.4
Colineaux, C.5
Gillberg, I.C.6
Soderstrom, H.7
Giros, B.8
Leboyer, M.9
Gillberg, C.10
Bourgeron, T.11
-
111
-
-
0031798509
-
A study of females with deletions of the short arm of the X chromosome
-
James R.S., Coppin B., Dalton P., Dennis N.R., Mitchell C., Sharp a.J., Skuse D.H., Thomas N.S., Jacobs P.a. A study of females with deletions of the short arm of the X chromosome. Hum. Genet. 1998, 102:507-516.
-
(1998)
Hum. Genet.
, vol.102
, pp. 507-516
-
-
James, R.S.1
Coppin, B.2
Dalton, P.3
Dennis, N.R.4
Mitchell, C.5
Sharp, A.6
Skuse, D.H.7
Thomas, N.S.8
Jacobs, P.9
-
113
-
-
0030595097
-
Nonfamiliality of the sex ratio in autism
-
Jones M., Szatmari P., Piven J. Nonfamiliality of the sex ratio in autism. Am. J. Med. Gen. 1996, 500:499-500.
-
(1996)
Am. J. Med. Gen.
, vol.500
, pp. 499-500
-
-
Jones, M.1
Szatmari, P.2
Piven, J.3
-
114
-
-
77952327341
-
The androgen receptor governs the execution, but not programming, of male sexual and territorial behaviors
-
Juntti S.A., Tollkuhn J., Wu M.V., Fraser E.J., Soderborg T., Tan S., Honda S.-I., Harada N., Shah N.M. The androgen receptor governs the execution, but not programming, of male sexual and territorial behaviors. Neuron 2010, 66:260-272.
-
(2010)
Neuron
, vol.66
, pp. 260-272
-
-
Juntti, S.A.1
Tollkuhn, J.2
Wu, M.V.3
Fraser, E.J.4
Soderborg, T.5
Tan, S.6
Honda, S.-I.7
Harada, N.8
Shah, N.M.9
-
115
-
-
0034750434
-
Proinflammatory and regulatory cytokine production associated with innate and adaptive immune responses in children with autism spectrum disorders and developmental regression
-
Jyonouchi H., Sun S., Le H. Proinflammatory and regulatory cytokine production associated with innate and adaptive immune responses in children with autism spectrum disorders and developmental regression. J. Neuroimmunol. 2001, 120:170-179.
-
(2001)
J. Neuroimmunol.
, vol.120
, pp. 170-179
-
-
Jyonouchi, H.1
Sun, S.2
Le, H.3
-
116
-
-
35448929818
-
Alteration of behavioural phenotype in mice by targeted disruption of the progranulin gene
-
Kayasuga Y., Chiba S., Suzuki M., Kikusui T., Matsuwaki T., Yamanouchi K., Kotaki H., Horai R., Iwakura Y., Nishihara M. Alteration of behavioural phenotype in mice by targeted disruption of the progranulin gene. Behav. Brain Res. 2007, 185:110-118.
-
(2007)
Behav. Brain Res.
, vol.185
, pp. 110-118
-
-
Kayasuga, Y.1
Chiba, S.2
Suzuki, M.3
Kikusui, T.4
Matsuwaki, T.5
Yamanouchi, K.6
Kotaki, H.7
Horai, R.8
Iwakura, Y.9
Nishihara, M.10
-
117
-
-
50049104212
-
X-linked ichthyosis (steroid sulfatase deficiency) is associated with increased risk of attention deficit hyperactivity disorder, autism and social communication deficits
-
Kent L., Emerton J., Bhadravathi V., Weisblatt E., Pasco G., Willatt L.R., McMahon R., Yates J.R.W. X-linked ichthyosis (steroid sulfatase deficiency) is associated with increased risk of attention deficit hyperactivity disorder, autism and social communication deficits. J. Med. Genet. 2008, 45:519-524.
-
(2008)
J. Med. Genet.
, vol.45
, pp. 519-524
-
-
Kent, L.1
Emerton, J.2
Bhadravathi, V.3
Weisblatt, E.4
Pasco, G.5
Willatt, L.R.6
McMahon, R.7
Yates, J.R.W.8
-
118
-
-
0242348826
-
Effects of X-monosomy and X-linked imprinting on superior temporal gyrus morphology in Turner syndrome
-
Kesler S.R., Blasey C.M., Brown W.E., Yankowitz J., Zeng S.M., Bender B.G., Reiss A.L. Effects of X-monosomy and X-linked imprinting on superior temporal gyrus morphology in Turner syndrome. Biol. Psychiat. 2003, 54:636-646.
-
(2003)
Biol. Psychiat.
, vol.54
, pp. 636-646
-
-
Kesler, S.R.1
Blasey, C.M.2
Brown, W.E.3
Yankowitz, J.4
Zeng, S.M.5
Bender, B.G.6
Reiss, A.L.7
-
119
-
-
25444495866
-
Microglia in health and disease
-
Kim S.U., de Vellis J. Microglia in health and disease. J. Neurosci. Res. 2005, 81:302-313.
-
(2005)
J. Neurosci. Res.
, vol.81
, pp. 302-313
-
-
Kim, S.U.1
de Vellis, J.2
-
120
-
-
52049113008
-
Prenatal stress and risk for autism
-
Kinney D.K., Munir K.M., Crowley D.J., Miller M. Prenatal stress and risk for autism. Neurosci. Biobehav. Rev. 2008, 32:1519-1532.
-
(2008)
Neurosci. Biobehav. Rev.
, vol.32
, pp. 1519-1532
-
-
Kinney, D.K.1
Munir, K.M.2
Crowley, D.J.3
Miller, M.4
-
121
-
-
15844431969
-
Foetal testosterone, social relationships, and restricted interests in children
-
Knickmeyer R., Baron-Cohen S., Raggatt P., Taylor K. Foetal testosterone, social relationships, and restricted interests in children. J. Child Psychol. Psychiat. 2005, 46:198-210.
-
(2005)
J. Child Psychol. Psychiat.
, vol.46
, pp. 198-210
-
-
Knickmeyer, R.1
Baron-Cohen, S.2
Raggatt, P.3
Taylor, K.4
-
122
-
-
33747136225
-
Androgens and autistic traits: a study of individuals with congenital adrenal hyperplasia
-
Knickmeyer R., Baron-Cohen S., Fane B.a., Wheelwright S., Mathews G.a., Conway G.S., Brook C.G.D., Hines M. Androgens and autistic traits: a study of individuals with congenital adrenal hyperplasia. Horm. Behav. 2006, 50:148-153.
-
(2006)
Horm. Behav.
, vol.50
, pp. 148-153
-
-
Knickmeyer, R.1
Baron-Cohen, S.2
Fane, B.3
Wheelwright, S.4
Mathews, G.5
Conway, G.S.6
Brook, C.G.D.7
Hines, M.8
-
123
-
-
0024619007
-
Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion
-
Knoll J.H., Nicholls R.D., Magenis R.E., Graham J.M., Lalande M., Latt S.A. Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion. Am. J. Med. Genet. 1989, 32:285-290.
-
(1989)
Am. J. Med. Genet.
, vol.32
, pp. 285-290
-
-
Knoll, J.H.1
Nicholls, R.D.2
Magenis, R.E.3
Graham, J.M.4
Lalande, M.5
Latt, S.A.6
-
124
-
-
34147174017
-
Prenatal and perinatal risk factors for autism - a review and integration of findings
-
Kolevzon A., Gross R., Reichenberg A. Prenatal and perinatal risk factors for autism - a review and integration of findings. Arch. Pediatr. Adolesc. Med. 2007, 161:326-333.
-
(2007)
Arch. Pediatr. Adolesc. Med.
, vol.161
, pp. 326-333
-
-
Kolevzon, A.1
Gross, R.2
Reichenberg, A.3
-
125
-
-
0025243412
-
Expression of a candidate sex-determining gene during mouse testis differentiation
-
Koopman P., Münsterberg A., Capel B., Vivian N., Lovell-Badge R. Expression of a candidate sex-determining gene during mouse testis differentiation. Nature 1990, 348:450-452.
-
(1990)
Nature
, vol.348
, pp. 450-452
-
-
Koopman, P.1
Münsterberg, A.2
Capel, B.3
Vivian, N.4
Lovell-Badge, R.5
-
126
-
-
0036195694
-
Genetic and immunologic considerations in autism
-
Korvatska E., Van de Water J., Anders T.F., Gershwin M.E. Genetic and immunologic considerations in autism. Neurobiol. Dis. 2002, 9:107-125.
-
(2002)
Neurobiol. Dis.
, vol.9
, pp. 107-125
-
-
Korvatska, E.1
Van de Water, J.2
Anders, T.F.3
Gershwin, M.E.4
-
127
-
-
0141615600
-
Double oestrogen receptor α and β knockout mice reveal differences in neural oestrogen-mediated progestin receptor induction and female sexual behaviour
-
Kudwa A.E., Rissman E.F. Double oestrogen receptor α and β knockout mice reveal differences in neural oestrogen-mediated progestin receptor induction and female sexual behaviour. J. Neuroendocrinol. 2003, 15:978-983.
-
(2003)
J. Neuroendocrinol.
, vol.15
, pp. 978-983
-
-
Kudwa, A.E.1
Rissman, E.F.2
-
128
-
-
0029126575
-
Transcription of the Y chromosomal gene, Sry, in adult mouse brain
-
Lahr G., Maxson S.C., Mayer A., Just W., Pilgrim C., Reisert I. Transcription of the Y chromosomal gene, Sry, in adult mouse brain. Mol. Brain Res. 1995, 33:179-182.
-
(1995)
Mol. Brain Res.
, vol.33
, pp. 179-182
-
-
Lahr, G.1
Maxson, S.C.2
Mayer, A.3
Just, W.4
Pilgrim, C.5
Reisert, I.6
-
129
-
-
12144291350
-
X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family
-
Laumonnier F., Bonnet-Brilhault F., Gomot M., Blanc R., David A., Moizard M.-P., Raynaud M., Ronce N., Lemonnier E., Calvas P., Laudier B., Chelly J., Fryns J.-P., Ropers H.-H., Hamel B.C.J., Andres C., Barthélémy C., Moraine C., Briault S. X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family. Am. J. Hum. Genet. 2004, 74:552-557.
-
(2004)
Am. J. Hum. Genet.
, vol.74
, pp. 552-557
-
-
Laumonnier, F.1
Bonnet-Brilhault, F.2
Gomot, M.3
Blanc, R.4
David, A.5
Moizard, M.-P.6
Raynaud, M.7
Ronce, N.8
Lemonnier, E.9
Calvas, P.10
Laudier, B.11
Chelly, J.12
Fryns, J.-P.13
Ropers, H.-H.14
Hamel, B.C.J.15
Andres, C.16
Barthélémy, C.17
Moraine, C.18
Briault, S.19
-
130
-
-
33846619125
-
The role of neuronal complexes in human X-linked brain diseases
-
Laumonnier F., Cuthbert P.C., Grant S.G.N. The role of neuronal complexes in human X-linked brain diseases. Am. J. Hum. Genet. 2007, 80:205-220.
-
(2007)
Am. J. Hum. Genet.
, vol.80
, pp. 205-220
-
-
Laumonnier, F.1
Cuthbert, P.C.2
Grant, S.G.N.3
-
131
-
-
84873693906
-
Microglia are essential to masculinization of brain and behavior
-
Lenz K.M., Nugent B.M., Haliyur R., McCarthy M.M. Microglia are essential to masculinization of brain and behavior. J. Neurosci. 2013, 33:2761-2772.
-
(2013)
J. Neurosci.
, vol.33
, pp. 2761-2772
-
-
Lenz, K.M.1
Nugent, B.M.2
Haliyur, R.3
McCarthy, M.M.4
-
132
-
-
0345448863
-
Dissection of an inverted X(p21.3q27.1) chromosome associated with mental retardation
-
Lepretre F., Delannoy V., Froguel P. Dissection of an inverted X(p21.3q27.1) chromosome associated with mental retardation. Cytogen. Genome Res. 2003, 101:124-129.
-
(2003)
Cytogen. Genome Res.
, vol.101
, pp. 124-129
-
-
Lepretre, F.1
Delannoy, V.2
Froguel, P.3
-
133
-
-
0029817825
-
Characterization of the promoter region of human steroid sulfatase: a gene which escapes X inactivation
-
Li X.-M., Alperin E.S., Salido E., Gong Y., Yen P., Shapiro L.J. Characterization of the promoter region of human steroid sulfatase: a gene which escapes X inactivation. Somat. Cell Mol. Genet. 1996, 22:105-117.
-
(1996)
Somat. Cell Mol. Genet.
, vol.22
, pp. 105-117
-
-
Li, X.-M.1
Alperin, E.S.2
Salido, E.3
Gong, Y.4
Yen, P.5
Shapiro, L.J.6
-
134
-
-
60149103359
-
Elevated immune response in the brain of autistic patients
-
Li X., Chauhan A., Sheikh A.M., Patil S., Chauhan V., Li X.-M., Ji L., Brown T., Malik M. Elevated immune response in the brain of autistic patients. J. Neuroimmunol. 2009, 207:111-116.
-
(2009)
J. Neuroimmunol.
, vol.207
, pp. 111-116
-
-
Li, X.1
Chauhan, A.2
Sheikh, A.M.3
Patil, S.4
Chauhan, V.5
Li, X.-M.6
Ji, L.7
Brown, T.8
Malik, M.9
-
135
-
-
20444403730
-
GABAA receptor beta3 subunit gene-deficient heterozygous mice show parent-of-origin and gender-related differences in beta3 subunit levels, EEG, and behavior
-
Liljelund P., Handforth A., Homanics G.E., Olsen R.W. GABAA receptor beta3 subunit gene-deficient heterozygous mice show parent-of-origin and gender-related differences in beta3 subunit levels, EEG, and behavior. Brain Res. Dev. Brain Res. 2005, 157:150-161.
-
(2005)
Brain Res. Dev. Brain Res.
, vol.157
, pp. 150-161
-
-
Liljelund, P.1
Handforth, A.2
Homanics, G.E.3
Olsen, R.W.4
-
136
-
-
0027958509
-
Microphthalmia with linear skin defects (MLS) syndrome: clinical, cytogenetic, and molecular characterization
-
Lindsay E.A., Grillo A., Ferrero G.B., Roth E.J., Magenis E., Grompe M., Hultén M., Gould C., Baldini A., Zoghbi H.Y. Microphthalmia with linear skin defects (MLS) syndrome: clinical, cytogenetic, and molecular characterization. Am. J. Med. Genet. 1994, 49:229-234.
-
(1994)
Am. J. Med. Genet.
, vol.49
, pp. 229-234
-
-
Lindsay, E.A.1
Grillo, A.2
Ferrero, G.B.3
Roth, E.J.4
Magenis, E.5
Grompe, M.6
Hultén, M.7
Gould, C.8
Baldini, A.9
Zoghbi, H.Y.10
-
137
-
-
78651239869
-
CCL3L1 copy number variation and susceptibility to HIV-1 infection: a meta-analysis
-
Liu S., Yao L., Ding D., Zhu H. CCL3L1 copy number variation and susceptibility to HIV-1 infection: a meta-analysis. PLoS One 2010, 5:e15778.
-
(2010)
PLoS One
, vol.5
-
-
Liu, S.1
Yao, L.2
Ding, D.3
Zhu, H.4
-
138
-
-
0036428871
-
Foetal testosterone and eye contact in 12-month-old human infants
-
Lutchmaya S., Baron-Cohen S., Raggatt P. Foetal testosterone and eye contact in 12-month-old human infants. Infant Behav. Dev. 2002, 25:327-335.
-
(2002)
Infant Behav. Dev.
, vol.25
, pp. 327-335
-
-
Lutchmaya, S.1
Baron-Cohen, S.2
Raggatt, P.3
-
139
-
-
0021320709
-
Steroid sulphatase in man: a non inactivated X-locus with partial gene dosage compensation
-
Lykkesfeldt G., Lykkesfeldt A.E., Skakkeb□k N.E. Steroid sulphatase in man: a non inactivated X-locus with partial gene dosage compensation. Hum. Genet. 1984, 65:355-357.
-
(1984)
Hum. Genet.
, vol.65
, pp. 355-357
-
-
Lykkesfeldt, G.1
Lykkesfeldt, A.E.2
Skakkebk, N.E.3
-
140
-
-
33947668880
-
Deletions of VCX-A and NLGN4: a variable phenotype including normal intellect
-
Macarov M., Zeigler M., Newman J.P., Strich D., Sury V., Tennenbaum A., Meiner V. Deletions of VCX-A and NLGN4: a variable phenotype including normal intellect. J. Intellect. Disabil. Res. 2007, 51:329-333.
-
(2007)
J. Intellect. Disabil. Res.
, vol.51
, pp. 329-333
-
-
Macarov, M.1
Zeigler, M.2
Newman, J.P.3
Strich, D.4
Sury, V.5
Tennenbaum, A.6
Meiner, V.7
-
141
-
-
0025173833
-
Comparison of the 15q deletions in Prader-Willi and Angelman syndromes: specific regions, extent of deletions, parental origin, and clinical consequences
-
Magenis R.E., Toth-Fejel S., Allen L.J., Black M., Brown M.G., Budden S., Cohen R., Friedman J.M., Kalousek D., Zonana J. Comparison of the 15q deletions in Prader-Willi and Angelman syndromes: specific regions, extent of deletions, parental origin, and clinical consequences. Am. J. Med. Genet. 1990, 35:333-349.
-
(1990)
Am. J. Med. Genet.
, vol.35
, pp. 333-349
-
-
Magenis, R.E.1
Toth-Fejel, S.2
Allen, L.J.3
Black, M.4
Brown, M.G.5
Budden, S.6
Cohen, R.7
Friedman, J.M.8
Kalousek, D.9
Zonana, J.10
-
142
-
-
77955380361
-
Age of diagnosis among medicaid-enrolled children with autism, 2001-2004
-
Mandell S.D., Morales H.K., Xie M. Age of diagnosis among medicaid-enrolled children with autism, 2001-2004. Psychiat. Serv. 2010, 61:822-829.
-
(2010)
Psychiat. Serv.
, vol.61
, pp. 822-829
-
-
Mandell, S.D.1
Morales, H.K.2
Xie, M.3
-
143
-
-
0142119360
-
The second to fourth digit ratio and variation in the androgen receptor gene
-
Manning J.T., Bundred P.E., Newton D.J., Flanagan B.F. The second to fourth digit ratio and variation in the androgen receptor gene. Evol. Hum. Behav. 2003, 24:399-405.
-
(2003)
Evol. Hum. Behav.
, vol.24
, pp. 399-405
-
-
Manning, J.T.1
Bundred, P.E.2
Newton, D.J.3
Flanagan, B.F.4
-
144
-
-
79957902514
-
Characterization of the cognitive impairments induced by prenatal exposure to stress in the rat
-
Markham J.a., Taylor A.R., Taylor S.B., Bell D.B., Koenig J.I. Characterization of the cognitive impairments induced by prenatal exposure to stress in the rat. Front. Behav. Neurosci. 2010, 4:173.
-
(2010)
Front. Behav. Neurosci.
, vol.4
, pp. 173
-
-
Markham, J.1
Taylor, A.R.2
Taylor, S.B.3
Bell, D.B.4
Koenig, J.I.5
-
145
-
-
40749089626
-
Structural variation of chromosomes in autism spectrum disorder
-
Marshall C.R., Noor A., Vincent J.B., Lionel A.C., Feuk L., Skaug J., Shago M., Moessner R., Pinto D., Ren Y., Thiruvahindrapduram B., Fiebig A., Schreiber S., Friedman J., Ketelaars C.E.J., Vos Y.J., Ficicioglu C., Kirkpatrick S., Nicolson R., Sloman L., Summers A., Gibbons C.A., Teebi A., Chitayat D., Weksberg R., Thompson A., Vardy C., Crosbie V., Luscombe S., Baatjes R., Zwaigenbaum L., Roberts W., Fernandez B., Szatmari P., Scherer S.W. Structural variation of chromosomes in autism spectrum disorder. Am. J. Hum. Genet. 2008, 82:477-488.
-
(2008)
Am. J. Hum. Genet.
, vol.82
, pp. 477-488
-
-
Marshall, C.R.1
Noor, A.2
Vincent, J.B.3
Lionel, A.C.4
Feuk, L.5
Skaug, J.6
Shago, M.7
Moessner, R.8
Pinto, D.9
Ren, Y.10
Thiruvahindrapduram, B.11
Fiebig, A.12
Schreiber, S.13
Friedman, J.14
Ketelaars, C.E.J.15
Vos, Y.J.16
Ficicioglu, C.17
Kirkpatrick, S.18
Nicolson, R.19
Sloman, L.20
Summers, A.21
Gibbons, C.A.22
Teebi, A.23
Chitayat, D.24
Weksberg, R.25
Thompson, A.26
Vardy, C.27
Crosbie, V.28
Luscombe, S.29
Baatjes, R.30
Zwaigenbaum, L.31
Roberts, W.32
Fernandez, B.33
Szatmari, P.34
Scherer, S.W.35
more..
-
147
-
-
0032129443
-
The Y-chromosomal genes SRY and ZFY are transcribed in adult human brain
-
Mayer A., Lahr G., Swaab D.F., Pilgrim C., Reisert I. The Y-chromosomal genes SRY and ZFY are transcribed in adult human brain. Neurogenetics 1998, 1:281-288.
-
(1998)
Neurogenetics
, vol.1
, pp. 281-288
-
-
Mayer, A.1
Lahr, G.2
Swaab, D.F.3
Pilgrim, C.4
Reisert, I.5
-
148
-
-
85047679307
-
Developmental profile of Sry transcripts in mouse brain
-
Mayer A., Mosler G., Just W., Pilgrim C., Reisert I. Developmental profile of Sry transcripts in mouse brain. Neurogenetics 2000, 3:25-30.
-
(2000)
Neurogenetics
, vol.3
, pp. 25-30
-
-
Mayer, A.1
Mosler, G.2
Just, W.3
Pilgrim, C.4
Reisert, I.5
-
149
-
-
38349049457
-
Estradiol and the developing brain
-
McCarthy M.M. Estradiol and the developing brain. Physiol. Rev. 2008, 88:91-124.
-
(2008)
Physiol. Rev.
, vol.88
, pp. 91-124
-
-
McCarthy, M.M.1
-
150
-
-
0027169360
-
Enduring consequences of neonatal treatment with antisense oligodeoxynucleotides to estrogen receptor messenger ribonucleic acid on sexual differentiation of rat brain
-
McCarthy M.M., Schlenker E.H., Pfaff D.W. Enduring consequences of neonatal treatment with antisense oligodeoxynucleotides to estrogen receptor messenger ribonucleic acid on sexual differentiation of rat brain. Endocrinology 1993, 133:433-439.
-
(1993)
Endocrinology
, vol.133
, pp. 433-439
-
-
McCarthy, M.M.1
Schlenker, E.H.2
Pfaff, D.W.3
-
151
-
-
0022657887
-
Psychosocial functioning in girls with Turner's syndrome and short stature: social skills, behavior problems, and self-concept
-
McCauley E., Ito J., Kay T. Psychosocial functioning in girls with Turner's syndrome and short stature: social skills, behavior problems, and self-concept. J. Am. Acad. Child Psychiat. 1986, 25:105-112.
-
(1986)
J. Am. Acad. Child Psychiat.
, vol.25
, pp. 105-112
-
-
McCauley, E.1
Ito, J.2
Kay, T.3
-
152
-
-
0027354835
-
Microglia in degenerative neurological disease
-
McGeer P.L., Kawamata T., Walker D.G., Akiyama H., Tooyama I., McGeer E.G. Microglia in degenerative neurological disease. Glia 1993, 7:84-92.
-
(1993)
Glia
, vol.7
, pp. 84-92
-
-
McGeer, P.L.1
Kawamata, T.2
Walker, D.G.3
Akiyama, H.4
Tooyama, I.5
McGeer, E.G.6
-
153
-
-
0028953529
-
Activation of microglial cells by beta-amyloid protein and interferon-gamma
-
Meda L., Cassatella M.A., Szendrei G.I., Otvos L., Baron P., Villalba M., Ferrari D., Rossi F. Activation of microglial cells by beta-amyloid protein and interferon-gamma. Nature 1995, 374:647-650.
-
(1995)
Nature
, vol.374
, pp. 647-650
-
-
Meda, L.1
Cassatella, M.A.2
Szendrei, G.I.3
Otvos, L.4
Baron, P.5
Villalba, M.6
Ferrari, D.7
Rossi, F.8
-
154
-
-
0019932848
-
Differential expression of steroid sulphatase locus on active and inactive human X chromosome
-
Migeon B.R., Shapiro L.J., Norum R.A., Mohandas T., Axelman J., Dabora R.L. Differential expression of steroid sulphatase locus on active and inactive human X chromosome. Nature 1982, 299:838-840.
-
(1982)
Nature
, vol.299
, pp. 838-840
-
-
Migeon, B.R.1
Shapiro, L.J.2
Norum, R.A.3
Mohandas, T.4
Axelman, J.5
Dabora, R.L.6
-
155
-
-
80053106248
-
Clinically relevant single gene or intragenic deletions encompassing critical neurodevelopmental genes in patients with developmental delay, mental retardation, and/or autism spectrum disorders
-
Mikhail F.M., Lose E.J., Robin N.H., Descartes M.D., Rutledge K.D., Rutledge S.L., Korf B.R., Carroll A.J. Clinically relevant single gene or intragenic deletions encompassing critical neurodevelopmental genes in patients with developmental delay, mental retardation, and/or autism spectrum disorders. Am. J. Med. Genet. A 2011, 155A:2386-2396.
-
(2011)
Am. J. Med. Genet. A
, vol.155 A
, pp. 2386-2396
-
-
Mikhail, F.M.1
Lose, E.J.2
Robin, N.H.3
Descartes, M.D.4
Rutledge, K.D.5
Rutledge, S.L.6
Korf, B.R.7
Carroll, A.J.8
-
156
-
-
0034709291
-
Value of a clinical morphology examination in autism
-
Miles J.H., Hillman R.E. Value of a clinical morphology examination in autism. Am. J. Med. Genet. 2000, 91:245-253.
-
(2000)
Am. J. Med. Genet.
, vol.91
, pp. 245-253
-
-
Miles, J.H.1
Hillman, R.E.2
-
157
-
-
84883809246
-
Gestational flu exposure induces changes in neurochemicals, affiliative hormones and brainstem inflammation, in addition to autism-like behaviors in mice
-
Miller V.M., Zhu Y., Bucher C., McGinnis W., Ryan L.K., Siegel A., Zalcman S. Gestational flu exposure induces changes in neurochemicals, affiliative hormones and brainstem inflammation, in addition to autism-like behaviors in mice. Brain. Behav. Immun. 2013, 33:153-163.
-
(2013)
Brain. Behav. Immun.
, vol.33
, pp. 153-163
-
-
Miller, V.M.1
Zhu, Y.2
Bucher, C.3
McGinnis, W.4
Ryan, L.K.5
Siegel, A.6
Zalcman, S.7
-
158
-
-
4644308233
-
Regulation of tyrosine hydroxylase gene transcription by Sry
-
Milsted A., Serova L., Sabban E.L., Dunphy G., Turner M.E., Ely D.L. Regulation of tyrosine hydroxylase gene transcription by Sry. Neurosci. Lett. 2004, 369:203-207.
-
(2004)
Neurosci. Lett.
, vol.369
, pp. 203-207
-
-
Milsted, A.1
Serova, L.2
Sabban, E.L.3
Dunphy, G.4
Turner, M.E.5
Ely, D.L.6
-
159
-
-
0031985513
-
Microglia as effector cells in brain damage and repair: focus on prostanoids and nitric oxide
-
Minghetti L. Microglia as effector cells in brain damage and repair: focus on prostanoids and nitric oxide. Prog. Neurobiol. 1998, 54:99-125.
-
(1998)
Prog. Neurobiol.
, vol.54
, pp. 99-125
-
-
Minghetti, L.1
-
160
-
-
38549158659
-
Normal intelligence and social interactions in a male patient despite the deletion of NLGN4X and the VCX genes
-
Mochel F., Missirian C., Reynaud R., Moncla A. Normal intelligence and social interactions in a male patient despite the deletion of NLGN4X and the VCX genes. Eur. J. Med. Genet. 2008, 51:68-73.
-
(2008)
Eur. J. Med. Genet.
, vol.51
, pp. 68-73
-
-
Mochel, F.1
Missirian, C.2
Reynaud, R.3
Moncla, A.4
-
161
-
-
77955684004
-
Microglial activation and increased microglial density observed in the dorsolateral prefrontal cortex in autism
-
Morgan J.T., Chana G., Pardo C.A., Achim C., Semendeferi K., Buckwalter J., Courchesne E., Everall I.P. Microglial activation and increased microglial density observed in the dorsolateral prefrontal cortex in autism. Biol. Psychiat. 2010, 68:368-376.
-
(2010)
Biol. Psychiat.
, vol.68
, pp. 368-376
-
-
Morgan, J.T.1
Chana, G.2
Pardo, C.A.3
Achim, C.4
Semendeferi, K.5
Buckwalter, J.6
Courchesne, E.7
Everall, I.P.8
-
162
-
-
77249103482
-
Oxidative stress in Egyptian children with autism: relation to autoimmunity
-
Mostafa G.A., El-Hadidi E.S., Hewedi D.H., Abdou M.M. Oxidative stress in Egyptian children with autism: relation to autoimmunity. J. Neuroimmunol. 2010, 219:114-118.
-
(2010)
J. Neuroimmunol.
, vol.219
, pp. 114-118
-
-
Mostafa, G.A.1
El-Hadidi, E.S.2
Hewedi, D.H.3
Abdou, M.M.4
-
163
-
-
34247255851
-
Early prenatal stress impact on coping strategies and learning performance is sex dependent
-
Mueller B.R., Bale T.L. Early prenatal stress impact on coping strategies and learning performance is sex dependent. Physiol. Behav. 2007, 91:55-65.
-
(2007)
Physiol. Behav.
, vol.91
, pp. 55-65
-
-
Mueller, B.R.1
Bale, T.L.2
-
164
-
-
54049086269
-
Sex-specific programming of offspring emotionality after stress early in pregnancy
-
Mueller B.R., Bale T.L. Sex-specific programming of offspring emotionality after stress early in pregnancy. J. Neurosci. 2008, 28:9055-9065.
-
(2008)
J. Neurosci.
, vol.28
, pp. 9055-9065
-
-
Mueller, B.R.1
Bale, T.L.2
-
165
-
-
0018822890
-
X-linked steroid sulfatase: evidence for different gene-dosage in males and females
-
Mueller C.R., Migl B., Traupe H., Ropers H.H. X-linked steroid sulfatase: evidence for different gene-dosage in males and females. Hum. Genet. 1980, 54:197-199.
-
(1980)
Hum. Genet.
, vol.54
, pp. 197-199
-
-
Mueller, C.R.1
Migl, B.2
Traupe, H.3
Ropers, H.H.4
-
166
-
-
34250893218
-
Defining the cause of skewed X-chromosome inactivation in X-linked mental retardation by use of a mouse model
-
Muers M.R., Sharpe J.a., Garrick D., Sloane-Stanley J., Nolan P.M., Hacker T., Wood W.G., Higgs D.R., Gibbons R.J. Defining the cause of skewed X-chromosome inactivation in X-linked mental retardation by use of a mouse model. Am. J. Hum. Genet. 2007, 80:1138-1149.
-
(2007)
Am. J. Hum. Genet.
, vol.80
, pp. 1138-1149
-
-
Muers, M.R.1
Sharpe, J.2
Garrick, D.3
Sloane-Stanley, J.4
Nolan, P.M.5
Hacker, T.6
Wood, W.G.7
Higgs, D.R.8
Gibbons, R.J.9
-
167
-
-
3042580215
-
Mechanisms of epigenetic variation: polymorphic imprinting
-
Naumova A., Croteau S. Mechanisms of epigenetic variation: polymorphic imprinting. Curr. Genom. 2004, 5:417-429.
-
(2004)
Curr. Genom.
, vol.5
, pp. 417-429
-
-
Naumova, A.1
Croteau, S.2
-
168
-
-
34249735268
-
The epidemiology of autism spectrum disorders
-
Newschaffer C.J., Croen L.a., Daniels J., Giarelli E., Grether J.K., Levy S.E., Mandell D.S., Miller L.a., Pinto-Martin J., Reaven J., Reynolds A.M., Rice C.E., Schendel D., Windham G.C. The epidemiology of autism spectrum disorders. Annu. Rev. Public Health 2007, 28:235-258.
-
(2007)
Annu. Rev. Public Health
, vol.28
, pp. 235-258
-
-
Newschaffer, C.J.1
Croen, L.2
Daniels, J.3
Giarelli, E.4
Grether, J.K.5
Levy, S.E.6
Mandell, D.S.7
Miller, L.8
Pinto-Martin, J.9
Reaven, J.10
Reynolds, A.M.11
Rice, C.E.12
Schendel, D.13
Windham, G.C.14
-
169
-
-
77955563933
-
Disruption at the PTCHD1 Locus on Xp22. 11 in Autism spectrum disorder and intellectual disability
-
Noor A., Whibley A., Marshall C.R., Gianakopoulos P.J., Piton A., et al. Disruption at the PTCHD1 Locus on Xp22. 11 in Autism spectrum disorder and intellectual disability. Sci. Transl. Med. 2010, 2:49ra68.
-
(2010)
Sci. Transl. Med.
, vol.2
-
-
Noor, A.1
Whibley, A.2
Marshall, C.R.3
Gianakopoulos, P.J.4
Piton, A.5
-
170
-
-
84874090406
-
The importance of the intrauterine environment in shaping the human neonatal epigenome
-
Novakovic B., Saffery R. The importance of the intrauterine environment in shaping the human neonatal epigenome. Epigenomics 2013, 5:1-4.
-
(2013)
Epigenomics
, vol.5
, pp. 1-4
-
-
Novakovic, B.1
Saffery, R.2
-
171
-
-
84903766629
-
Effects of estrogen receptor gene disruption on aggressive behaviors in male mice
-
Ogawa S., Lubahn D., Korach K., Pfaff D. Effects of estrogen receptor gene disruption on aggressive behaviors in male mice. Behav. Genet. 1996, 26:593.
-
(1996)
Behav. Genet.
, vol.26
, pp. 593
-
-
Ogawa, S.1
Lubahn, D.2
Korach, K.3
Pfaff, D.4
-
172
-
-
0030475567
-
Reversal of sex roles in genetic female mice by disruption of estrogen receptor gene
-
Ogawa S., Taylor J.A., Lubahn D.B., Korach K.S., Pfaff D.W. Reversal of sex roles in genetic female mice by disruption of estrogen receptor gene. Neuroendocrinology 1996, 64:467-470.
-
(1996)
Neuroendocrinology
, vol.64
, pp. 467-470
-
-
Ogawa, S.1
Taylor, J.A.2
Lubahn, D.B.3
Korach, K.S.4
Pfaff, D.W.5
-
173
-
-
0031037365
-
Behavioral effects of estrogen receptor gene disruption in male mice
-
Ogawa S., Lubahn D.B., Korach K.S., Pfaff D.W. Behavioral effects of estrogen receptor gene disruption in male mice. Proc. Natl. Acad. Sci. 1997, 94:1476-1481.
-
(1997)
Proc. Natl. Acad. Sci.
, vol.94
, pp. 1476-1481
-
-
Ogawa, S.1
Lubahn, D.B.2
Korach, K.S.3
Pfaff, D.W.4
-
174
-
-
0031724077
-
Roles of estrogen receptor-gene expression in reproduction-related behaviors in female mice
-
Ogawa S., Eng V., Taylor L., Lubahn D., Korach K., Pfaff D. Roles of estrogen receptor-gene expression in reproduction-related behaviors in female mice. Endocrinology 1998, 139:5070-5081.
-
(1998)
Endocrinology
, vol.139
, pp. 5070-5081
-
-
Ogawa, S.1
Eng, V.2
Taylor, L.3
Lubahn, D.4
Korach, K.5
Pfaff, D.6
-
175
-
-
0031785604
-
Modifications of testosterone-dependent behaviors by estrogen receptor-gene disruption in male mice
-
Ogawa S., Washburn T., Taylor J., Lubahn D., Korach K., Pfaff D. Modifications of testosterone-dependent behaviors by estrogen receptor-gene disruption in male mice. Endocrinology 1998, 139:5058-5069.
-
(1998)
Endocrinology
, vol.139
, pp. 5058-5069
-
-
Ogawa, S.1
Washburn, T.2
Taylor, J.3
Lubahn, D.4
Korach, K.5
Pfaff, D.6
-
176
-
-
0034687647
-
Abolition of male sexual behaviors in mice lacking estrogen receptors alpha and beta (alpha beta ERKO)
-
Ogawa S., Chester A.E., Hewitt S.C., Walker V.R., Gustafsson J.A., Smithies O., Korach K.S., Pfaff D.W. Abolition of male sexual behaviors in mice lacking estrogen receptors alpha and beta (alpha beta ERKO). Proc. Natl. Acad. Sci. U.S.A. 2000, 97:14737-14741.
-
(2000)
Proc. Natl. Acad. Sci. U.S.A.
, vol.97
, pp. 14737-14741
-
-
Ogawa, S.1
Chester, A.E.2
Hewitt, S.C.3
Walker, V.R.4
Gustafsson, J.A.5
Smithies, O.6
Korach, K.S.7
Pfaff, D.W.8
-
177
-
-
4644232615
-
Microglia initiate central nervous system innate and adaptive immune responses through multiple TLRs
-
Olson J.K., Miller S.D. Microglia initiate central nervous system innate and adaptive immune responses through multiple TLRs. J. Immunol. 2004, 173:3916-3924.
-
(2004)
J. Immunol.
, vol.173
, pp. 3916-3924
-
-
Olson, J.K.1
Miller, S.D.2
-
178
-
-
84860741138
-
Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations
-
O'Roak B.J., Vives L., Girirajan S., Karakoc E., Krumm N., Coe B.P., Levy R., Ko A., Lee C., Smith J.D., Turner E.H., Stanaway I.B., Vernot B., Malig M., Baker C., Reilly B., Akey J.M., Borenstein E., Rieder M.J., Nickerson D.a., Bernier R., Shendure J., Eichler E.E. Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations. Nature 2012, 1-7.
-
(2012)
Nature
, pp. 1-7
-
-
O'Roak, B.J.1
Vives, L.2
Girirajan, S.3
Karakoc, E.4
Krumm, N.5
Coe, B.P.6
Levy, R.7
Ko, A.8
Lee, C.9
Smith, J.D.10
Turner, E.H.11
Stanaway, I.B.12
Vernot, B.13
Malig, M.14
Baker, C.15
Reilly, B.16
Akey, J.M.17
Borenstein, E.18
Rieder, M.J.19
Nickerson, D.20
Bernier, R.21
Shendure, J.22
Eichler, E.E.23
more..
-
179
-
-
74049086148
-
A substitution involving the NLGN4 gene associated with autistic behavior in the Greek population
-
Pampanos A., Volaki K., Kanavakis E., Papandreou O., Youroukos S., Thomaidis L., Karkelis S., Tzetis M., Kitsiou-Tzeli S. A substitution involving the NLGN4 gene associated with autistic behavior in the Greek population. Genet. Test. Mol. Biomark. 2009, 13:611-615.
-
(2009)
Genet. Test. Mol. Biomark.
, vol.13
, pp. 611-615
-
-
Pampanos, A.1
Volaki, K.2
Kanavakis, E.3
Papandreou, O.4
Youroukos, S.5
Thomaidis, L.6
Karkelis, S.7
Tzetis, M.8
Kitsiou-Tzeli, S.9
-
180
-
-
77958117538
-
Strong purifying selection at genes escaping X chromosome inactivation
-
Park C., Carrel L., Makova K.D. Strong purifying selection at genes escaping X chromosome inactivation. Mol. Biol. Evol. 2010, 27:2446-2450.
-
(2010)
Mol. Biol. Evol.
, vol.27
, pp. 2446-2450
-
-
Park, C.1
Carrel, L.2
Makova, K.D.3
-
181
-
-
77955400675
-
Amyloid beta precursor protein regulates male sexual behavior
-
Park J.H., Bonthius P.J., Tsai H.-W., Bekiranov S., Rissman E.F. Amyloid beta precursor protein regulates male sexual behavior. J. Neurosci. 2010, 30:9967-9972.
-
(2010)
J. Neurosci.
, vol.30
, pp. 9967-9972
-
-
Park, J.H.1
Bonthius, P.J.2
Tsai, H.-W.3
Bekiranov, S.4
Rissman, E.F.5
-
182
-
-
67749114055
-
Immune involvement in schizophrenia and autism: etiology, pathology and animal models
-
Patterson P.H. Immune involvement in schizophrenia and autism: etiology, pathology and animal models. Behav. Brain Res. 2009, 204:313-321.
-
(2009)
Behav. Brain Res.
, vol.204
, pp. 313-321
-
-
Patterson, P.H.1
-
184
-
-
0014981679
-
Neonatal androgen effects on sexual and non-sexual behavior of adult rats tested under various hormone regimes
-
Pfaff D., Zigmond R. Neonatal androgen effects on sexual and non-sexual behavior of adult rats tested under various hormone regimes. Neuroendocrinology 1971, 7:129-145.
-
(1971)
Neuroendocrinology
, vol.7
, pp. 129-145
-
-
Pfaff, D.1
Zigmond, R.2
-
185
-
-
79958106998
-
Male predominance in autism: neuroendocrine influences on arousal and social anxiety
-
Pfaff D.W., Rapin I., Goldman S. Male predominance in autism: neuroendocrine influences on arousal and social anxiety. Autism Res. Off. J. Int. Soc. Autism Res. 2011, 4:163-176.
-
(2011)
Autism Res. Off. J. Int. Soc. Autism Res.
, vol.4
, pp. 163-176
-
-
Pfaff, D.W.1
Rapin, I.2
Goldman, S.3
-
186
-
-
57049170205
-
Mutations in the calcium-related gene IL1RAPL1 are associated with autism
-
Piton A., Michaud J.L., Peng H., Aradhya S., Gauthier J., Mottron L., Champagne N., Lafrenière R.G., Hamdan F.F., Joober R., Fombonne E., Marineau C., Cossette P., Dubé M.-P., Haghighi P., Drapeau P., Barker P.A., Carbonetto S., Rouleau G.A. Mutations in the calcium-related gene IL1RAPL1 are associated with autism. Hum. Mol. Genet. 2008, 17:3965-3974.
-
(2008)
Hum. Mol. Genet.
, vol.17
, pp. 3965-3974
-
-
Piton, A.1
Michaud, J.L.2
Peng, H.3
Aradhya, S.4
Gauthier, J.5
Mottron, L.6
Champagne, N.7
Lafrenière, R.G.8
Hamdan, F.F.9
Joober, R.10
Fombonne, E.11
Marineau, C.12
Cossette, P.13
Dubé, M.-P.14
Haghighi, P.15
Drapeau, P.16
Barker, P.A.17
Carbonetto, S.18
Rouleau, G.A.19
-
187
-
-
0036306870
-
Skewed X-chromosome inactivation is a common feature of X-linked mental retardation disorders
-
Plenge R.M., Stevenson R.A., Lubs H.A., Schwartz C.E., Willard H.F. Skewed X-chromosome inactivation is a common feature of X-linked mental retardation disorders. Am. J. Hum. Genet. 2002, 71:168-173.
-
(2002)
Am. J. Hum. Genet.
, vol.71
, pp. 168-173
-
-
Plenge, R.M.1
Stevenson, R.A.2
Lubs, H.A.3
Schwartz, C.E.4
Willard, H.F.5
-
188
-
-
65549120393
-
Conditional inactivation of androgen receptor gene in the nervous system: effects on male behavioral and neuroendocrine responses
-
Raskin K., de Gendt K., Duittoz A., Liere P., Verhoeven G., Tronche F., Mhaouty-Kodja S. Conditional inactivation of androgen receptor gene in the nervous system: effects on male behavioral and neuroendocrine responses. J. Neurosci. 2009, 29:4461-4470.
-
(2009)
J. Neurosci.
, vol.29
, pp. 4461-4470
-
-
Raskin, K.1
de Gendt, K.2
Duittoz, A.3
Liere, P.4
Verhoeven, G.5
Tronche, F.6
Mhaouty-Kodja, S.7
-
189
-
-
0000542870
-
Early hormonal influences on cognitive functioning in congenital adrenal hyperplasia
-
Resnick S.M., Berenbaum S.A., Gottesman I.I., Bouchard T.J. Early hormonal influences on cognitive functioning in congenital adrenal hyperplasia. Dev. Psychol. 1986, 22:191-198.
-
(1986)
Dev. Psychol.
, vol.22
, pp. 191-198
-
-
Resnick, S.M.1
Berenbaum, S.A.2
Gottesman, I.I.3
Bouchard, T.J.4
-
190
-
-
0033564675
-
Colonisation of the developing human brain and spinal cord by microglia: a review
-
Rezaie P., Male D. Colonisation of the developing human brain and spinal cord by microglia: a review. Mircrosc. Res. Tech. 1999, 45:359-382.
-
(1999)
Mircrosc. Res. Tech.
, vol.45
, pp. 359-382
-
-
Rezaie, P.1
Male, D.2
-
191
-
-
39049113401
-
The importance of physician knowledge of autism spectrum disorder: results of a parent survey
-
Rhoades R.A., Scarpa A., Salley B. The importance of physician knowledge of autism spectrum disorder: results of a parent survey. BMC Pediatr. 2007, 7:37.
-
(2007)
BMC Pediatr.
, vol.7
, pp. 37
-
-
Rhoades, R.A.1
Scarpa, A.2
Salley, B.3
-
192
-
-
0021368651
-
Gonadal-steroid concentrations in serum and hypothalamus of the rat at birth - aromatization of testosterone to 17-beta-estradiol
-
Rhoda J., Corbier P., Roffi J. Gonadal-steroid concentrations in serum and hypothalamus of the rat at birth - aromatization of testosterone to 17-beta-estradiol. Endocrinology 1984, 114:1754-1760.
-
(1984)
Endocrinology
, vol.114
, pp. 1754-1760
-
-
Rhoda, J.1
Corbier, P.2
Roffi, J.3
-
193
-
-
84871448593
-
Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders
-
Roak B.J.O., Vives L., Fu W., Egertson J.D., Stanaway I.B., Ian G., Carvill G., Kumar A., Lee C., Ankenman K., Munson J., Hiatt J.B., Turner E.H., Levy R., Day D.R.O., Krumm N., Bradley P., Martin B.K., Borenstein E., Nickerson D.A., Heather C., Doherty D., Akey J.M., Bernier R., Eichler E.E., Shendure J. Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders. Science 2012, 338:1619-1622.
-
(2012)
Science
, vol.338
, pp. 1619-1622
-
-
Roak, B.J.O.1
Vives, L.2
Fu, W.3
Egertson, J.D.4
Stanaway, I.B.5
Ian, G.6
Carvill, G.7
Kumar, A.8
Lee, C.9
Ankenman, K.10
Munson, J.11
Hiatt, J.B.12
Turner, E.H.13
Levy, R.14
Day, D.R.O.15
Krumm, N.16
Bradley, P.17
Martin, B.K.18
Borenstein, E.19
Nickerson, D.A.20
Heather, C.21
Doherty, D.22
Akey, J.M.23
Bernier, R.24
Eichler, E.E.25
Shendure, J.26
more..
-
194
-
-
33744821617
-
Genetic heterogeneity between the three components of the autism spectrum: a twin study
-
Ronald A., Happé F., Bolton P., Butcher L.M., Price T.S., Wheelwright S., Baron-Cohen S., Plomin R. Genetic heterogeneity between the three components of the autism spectrum: a twin study. J. Am. Acad. Child Adolesc. Psychiat. 2006, 45:691-699.
-
(2006)
J. Am. Acad. Child Adolesc. Psychiat.
, vol.45
, pp. 691-699
-
-
Ronald, A.1
Happé, F.2
Bolton, P.3
Butcher, L.M.4
Price, T.S.5
Wheelwright, S.6
Baron-Cohen, S.7
Plomin, R.8
-
195
-
-
52949098733
-
Genetics of intellectual disability
-
Ropers H.H. Genetics of intellectual disability. Curr. Opin. Genet. Dev. 2008, 18:241-250.
-
(2008)
Curr. Opin. Genet. Dev.
, vol.18
, pp. 241-250
-
-
Ropers, H.H.1
-
197
-
-
70349753233
-
Characteristics and concordance of autism spectrum disorders among 277 twin pairs
-
Rosenberg R.E., Law J.K., Yenokyan G., McGready J., Kaufmann W.E., Law P.A. Characteristics and concordance of autism spectrum disorders among 277 twin pairs. Arch. Pediatr. Adolesc. Med. 2009, 163:907-914.
-
(2009)
Arch. Pediatr. Adolesc. Med.
, vol.163
, pp. 907-914
-
-
Rosenberg, R.E.1
Law, J.K.2
Yenokyan, G.3
McGready, J.4
Kaufmann, W.E.5
Law, P.A.6
-
198
-
-
15244363491
-
The DNA sequence of the human X chromosome
-
Ross M., Grafham D., Coffey A., Scherer S., McLay K., Muzny D., Platzer M., Howell G. The DNA sequence of the human X chromosome. Nature 2005, 434:325-337.
-
(2005)
Nature
, vol.434
, pp. 325-337
-
-
Ross, M.1
Grafham, D.2
Coffey, A.3
Scherer, S.4
McLay, K.5
Muzny, D.6
Platzer, M.7
Howell, G.8
-
199
-
-
84859005372
-
A review of research trends in physiological abnormalities in autism spectrum disorders: immune dysregulation, inflammation, oxidative stress, mitochondrial dysfunction and environmental toxicant exposures
-
Rossignol D.A., Frye R.E. A review of research trends in physiological abnormalities in autism spectrum disorders: immune dysregulation, inflammation, oxidative stress, mitochondrial dysfunction and environmental toxicant exposures. Mol. Psychiat. 2012, 17:389-401.
-
(2012)
Mol. Psychiat.
, vol.17
, pp. 389-401
-
-
Rossignol, D.A.1
Frye, R.E.2
-
200
-
-
77951452950
-
Gender differences in attention-deficit/hyperactivity disorder
-
Rucklidge J. Gender differences in attention-deficit/hyperactivity disorder. Psychiatr. Clin. North Am. 2010, 33:357-373.
-
(2010)
Psychiatr. Clin. North Am.
, vol.33
, pp. 357-373
-
-
Rucklidge, J.1
-
201
-
-
83655165272
-
Social and demographic factors that influence the diagnosis of autistic spectrum disorders
-
Russell G., Steer C., Golding J. Social and demographic factors that influence the diagnosis of autistic spectrum disorders. Social Psychiat. Psychiatr. Epidemiol. 2011, 46:1283-1293.
-
(2011)
Social Psychiat. Psychiatr. Epidemiol.
, vol.46
, pp. 1283-1293
-
-
Russell, G.1
Steer, C.2
Golding, J.3
-
202
-
-
79959788002
-
Increased serum androstenedione in adults with autism spectrum conditions
-
Ruta L., Ingudomnukul E., Taylor K., Chakrabarti B., Baron-Cohen S. Increased serum androstenedione in adults with autism spectrum conditions. Psychoneuroendocrinology 2011, 36:1154-1163.
-
(2011)
Psychoneuroendocrinology
, vol.36
, pp. 1154-1163
-
-
Ruta, L.1
Ingudomnukul, E.2
Taylor, K.3
Chakrabarti, B.4
Baron-Cohen, S.5
-
203
-
-
78649244968
-
Genes and brain sex differences
-
Sánchez F.J., Vilain E. Genes and brain sex differences. Prog. Brain Res. 2010, 186:65-76.
-
(2010)
Prog. Brain Res.
, vol.186
, pp. 65-76
-
-
Sánchez, F.J.1
Vilain, E.2
-
204
-
-
77957559100
-
Polymorphisms in genes involved in testosterone metabolism in Slovak autistic boys
-
Schmidtova E., Kelemenova S., Celec P., Ficek A., Ostatnikova D. Polymorphisms in genes involved in testosterone metabolism in Slovak autistic boys. Endocrinologist 2010, 20:245-249.
-
(2010)
Endocrinologist
, vol.20
, pp. 245-249
-
-
Schmidtova, E.1
Kelemenova, S.2
Celec, P.3
Ficek, A.4
Ostatnikova, D.5
-
205
-
-
70449946841
-
Telomere shortening relaxes X chromosome inactivation and forces global transcriptome alterations
-
Schoeftner S., Blanco R., Lopez de Silanes I., Muñoz P., Gómez-López G., Flores J.M., Blasco M.A. Telomere shortening relaxes X chromosome inactivation and forces global transcriptome alterations. Proc. Natl. Acad. Sci. U.S.A. 2009, 106:19393-19398.
-
(2009)
Proc. Natl. Acad. Sci. U.S.A.
, vol.106
, pp. 19393-19398
-
-
Schoeftner, S.1
Blanco, R.2
Lopez de Silanes, I.3
Muñoz, P.4
Gómez-López, G.5
Flores, J.M.6
Blasco, M.A.7
-
206
-
-
80055082702
-
Sex-specific serum biomarker patterns in adults with Asperger's syndrome
-
Schwarz E., Guest P.C., Rahmoune H., Wang L., Levin Y., Ingudomnukul E., Ruta L., Kent L., Spain M., Baron-Cohen S., Bahn S. Sex-specific serum biomarker patterns in adults with Asperger's syndrome. Mol. Psychiat. 2011, 16:1213-1220.
-
(2011)
Mol. Psychiat.
, vol.16
, pp. 1213-1220
-
-
Schwarz, E.1
Guest, P.C.2
Rahmoune, H.3
Wang, L.4
Levin, Y.5
Ingudomnukul, E.6
Ruta, L.7
Kent, L.8
Spain, M.9
Baron-Cohen, S.10
Bahn, S.11
-
207
-
-
0037314806
-
Aggression in male mice lacking functional estrogen receptor α
-
Scordalakes E.M., Rissman E.F. Aggression in male mice lacking functional estrogen receptor α. Behav. Neurosci. 2003, 117:38-45.
-
(2003)
Behav. Neurosci.
, vol.117
, pp. 38-45
-
-
Scordalakes, E.M.1
Rissman, E.F.2
-
208
-
-
0033762221
-
Age- and tissue-specific variation of X chromosome inactivation ratios in normal women
-
Sharp A., Robinson D., Jacobs P. Age- and tissue-specific variation of X chromosome inactivation ratios in normal women. Hum. Genet. 2000, 107:343-349.
-
(2000)
Hum. Genet.
, vol.107
, pp. 343-349
-
-
Sharp, A.1
Robinson, D.2
Jacobs, P.3
-
209
-
-
67650308854
-
Timing of identification among children with an autism spectrum disorder: findings from a population-based surveillance study
-
Shattuck P.T., Durkin M., Maenner M., Newschaffer C., Mandell D.S., Wiggins L., Lee L.-C., Rice C., Giarelli E., Kirby R., Baio J., Pinto-Martin J., Cuniff C. Timing of identification among children with an autism spectrum disorder: findings from a population-based surveillance study. J. Am. Acad. Child Adolesc. Psychiat. 2009, 48:474-483.
-
(2009)
J. Am. Acad. Child Adolesc. Psychiat.
, vol.48
, pp. 474-483
-
-
Shattuck, P.T.1
Durkin, M.2
Maenner, M.3
Newschaffer, C.4
Mandell, D.S.5
Wiggins, L.6
Lee, L.-C.7
Rice, C.8
Giarelli, E.9
Kirby, R.10
Baio, J.11
Pinto-Martin, J.12
Cuniff, C.13
-
211
-
-
66349131004
-
The Xp contiguous deletion syndrome and autism
-
Shinawi M., Patel A., Panichkul P., Zascavage R., Peters S.U., Scaglia F. The Xp contiguous deletion syndrome and autism. Am. J. Med. Genet. A 2009, 149A:1138-1148.
-
(2009)
Am. J. Med. Genet. A
, vol.149 A
, pp. 1138-1148
-
-
Shinawi, M.1
Patel, A.2
Panichkul, P.3
Zascavage, R.4
Peters, S.U.5
Scaglia, F.6
-
212
-
-
0030886961
-
Circulating autoantibodies to neuronal and glial filament proteins in autism
-
Singh V.K., Warren R., Averett R., Ghaziuddin M. Circulating autoantibodies to neuronal and glial filament proteins in autism. Pediatr. Neurol. 1997, 17:88-90.
-
(1997)
Pediatr. Neurol.
, vol.17
, pp. 88-90
-
-
Singh, V.K.1
Warren, R.2
Averett, R.3
Ghaziuddin, M.4
-
213
-
-
0037967242
-
The male-specific region of the human Y chromosome is a mosaic of discrete sequence classes
-
Skaletsky H., Kuroda-Kawaguchi T., Minx P.J., Cordum H.S., Hillier L., Brown L.G., Repping S., Pyntikova T., Ali J., Bieri T., Chinwalla A., Delehaunty A., Delehaunty K., Du H., Fewell G., Fulton L., Fulton R., Graves T., Hou S.-F., Latrielle P., Leonard S., Mardis E., Maupin R., McPherson J., Miner T., Nash W., Nguyen C., Ozersky P., Pepin K., Rock S., Rohlfing T., Scott K., Schultz B., Strong C., Tin-Wollam A., Yang S.-P., Waterston R.H., Wilson R.K., Rozen S., Page D.C. The male-specific region of the human Y chromosome is a mosaic of discrete sequence classes. Nature 2003, 423:825-837.
-
(2003)
Nature
, vol.423
, pp. 825-837
-
-
Skaletsky, H.1
Kuroda-Kawaguchi, T.2
Minx, P.J.3
Cordum, H.S.4
Hillier, L.5
Brown, L.G.6
Repping, S.7
Pyntikova, T.8
Ali, J.9
Bieri, T.10
Chinwalla, A.11
Delehaunty, A.12
Delehaunty, K.13
Du, H.14
Fewell, G.15
Fulton, L.16
Fulton, R.17
Graves, T.18
Hou, S.-F.19
Latrielle, P.20
Leonard, S.21
Mardis, E.22
Maupin, R.23
McPherson, J.24
Miner, T.25
Nash, W.26
Nguyen, C.27
Ozersky, P.28
Pepin, K.29
Rock, S.30
Rohlfing, T.31
Scott, K.32
Schultz, B.33
Strong, C.34
Tin-Wollam, A.35
Yang, S.-P.36
Waterston, R.H.37
Wilson, R.K.38
Rozen, S.39
Page, D.C.40
more..
-
214
-
-
16944366964
-
Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function
-
Skuse D.H., James R., Bishop D., Coppin B. Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function. Nature 1997, 387:705-708.
-
(1997)
Nature
, vol.387
, pp. 705-708
-
-
Skuse, D.H.1
James, R.2
Bishop, D.3
Coppin, B.4
-
215
-
-
0001864544
-
The fetal hormone environment and its effect on the morphogenesis of the genital system
-
Martinus Nijhoff, The Hague, The Netherlands, S.J. Kogan, E.S.E. Hafez (Eds.)
-
Smail P.J., Reyes F.I., Winter J.S.D., Faiman C. The fetal hormone environment and its effect on the morphogenesis of the genital system. Pediatric Andrology 1981, 9-19. Martinus Nijhoff, The Hague, The Netherlands. S.J. Kogan, E.S.E. Hafez (Eds.).
-
(1981)
Pediatric Andrology
, pp. 9-19
-
-
Smail, P.J.1
Reyes, F.I.2
Winter, J.S.D.3
Faiman, C.4
-
216
-
-
84862134180
-
Strikingly different clinicopathological phenotypes determined by progranulin-mutation dosage
-
Smith K.R., Damiano J., Franceschetti S., Carpenter S., Canafoglia L., Morbin M., Rossi G., Pareyson D., Mole S.E., Staropoli J.F., Sims K.B., Lewis J., Lin W.-L., Dickson D.W., Dahl H.-H., Bahlo M., Berkovic S.F. Strikingly different clinicopathological phenotypes determined by progranulin-mutation dosage. Am. J. Hum. Genet. 2012, 90:1102-1107.
-
(2012)
Am. J. Hum. Genet.
, vol.90
, pp. 1102-1107
-
-
Smith, K.R.1
Damiano, J.2
Franceschetti, S.3
Carpenter, S.4
Canafoglia, L.5
Morbin, M.6
Rossi, G.7
Pareyson, D.8
Mole, S.E.9
Staropoli, J.F.10
Sims, K.B.11
Lewis, J.12
Lin, W.-L.13
Dickson, D.W.14
Dahl, H.-H.15
Bahlo, M.16
Berkovic, S.F.17
-
217
-
-
79954627454
-
Autism, Alzheimer disease, and fragile X APP, FMRP, and mGluR5 are molecular links
-
Sokol D.K., Maloney B., Long J.M., Ray B., Lahiri D.K. Autism, Alzheimer disease, and fragile X APP, FMRP, and mGluR5 are molecular links. Neurology 2011, 76:1344-1352.
-
(2011)
Neurology
, vol.76
, pp. 1344-1352
-
-
Sokol, D.K.1
Maloney, B.2
Long, J.M.3
Ray, B.4
Lahiri, D.K.5
-
218
-
-
33746805846
-
CACNA1H mutations in autism spectrum disorders
-
Splawski I., Yoo D.S., Stotz S.C., Cherry A., Clapham D.E., Keating M.T. CACNA1H mutations in autism spectrum disorders. J. Biol. Chem. 2006, 281:22085-22091.
-
(2006)
J. Biol. Chem.
, vol.281
, pp. 22085-22091
-
-
Splawski, I.1
Yoo, D.S.2
Stotz, S.C.3
Cherry, A.4
Clapham, D.E.5
Keating, M.T.6
-
219
-
-
0024523493
-
A twin study of autism in Denmark, Finland, Iceland, Norway and Sweden
-
Steffenburg S., Gillberg C., Hellgren L., Andersson L., Gillberg I.C., Jakobsson G., Bohman M. A twin study of autism in Denmark, Finland, Iceland, Norway and Sweden. J. Child Psychol. Psychiat. 1989, 30:405-416.
-
(1989)
J. Child Psychol. Psychiat.
, vol.30
, pp. 405-416
-
-
Steffenburg, S.1
Gillberg, C.2
Hellgren, L.3
Andersson, L.4
Gillberg, I.C.5
Jakobsson, G.6
Bohman, M.7
-
220
-
-
79953267323
-
Steroid sulfatase is a potential modifier of cognition in attention deficit hyperactivity disorder
-
Stergiakouli E., Langley K., Williams H., Walters J., Williams N.M., Suren S., Giegling I., Wilkinson L.S., Owen M.J., O'Donovan M.C., Rujescu D., Thapar a., Davies W. Steroid sulfatase is a potential modifier of cognition in attention deficit hyperactivity disorder. Genes. Brain Behav. 2011, 10:334-344.
-
(2011)
Genes. Brain Behav.
, vol.10
, pp. 334-344
-
-
Stergiakouli, E.1
Langley, K.2
Williams, H.3
Walters, J.4
Williams, N.M.5
Suren, S.6
Giegling, I.7
Wilkinson, L.S.8
Owen, M.J.9
O'Donovan, M.C.10
Rujescu, D.11
Thapar, A.12
Davies, W.13
-
221
-
-
8844244724
-
Evidence for sex-specific risk alleles in autism spectrum disorder
-
Stone J.L., Merriman B., Cantor R.M., Yonan A.L., Gilliam T.C., Geschwind D.H., Nelson S.F. Evidence for sex-specific risk alleles in autism spectrum disorder. Am. J. Hum. Genet. 2004, 75:1117-1123.
-
(2004)
Am. J. Hum. Genet.
, vol.75
, pp. 1117-1123
-
-
Stone, J.L.1
Merriman, B.2
Cantor, R.M.3
Yonan, A.L.4
Gilliam, T.C.5
Geschwind, D.H.6
Nelson, S.F.7
-
222
-
-
0032548759
-
Identification of a sex steroid-inducible gene in the neonatal rat hypothalamus
-
Suzuki M., Yoshida S., Nishihara M., Takahashi M. Identification of a sex steroid-inducible gene in the neonatal rat hypothalamus. Neurosci. Lett. 1998, 242:127-130.
-
(1998)
Neurosci. Lett.
, vol.242
, pp. 127-130
-
-
Suzuki, M.1
Yoshida, S.2
Nishihara, M.3
Takahashi, M.4
-
223
-
-
0016795487
-
Congenital-rubella and autistic behavior
-
Swisher C., Swisher L. Congenital-rubella and autistic behavior. N. Engl. J. Med. 1975, 293:198.
-
(1975)
N. Engl. J. Med.
, vol.293
, pp. 198
-
-
Swisher, C.1
Swisher, L.2
-
224
-
-
67349208210
-
Chromosome 8p as a potential hub for developmental neuropsychiatric disorders: implications for schizophrenia, autism and cancer
-
Tabarés-Seisdedos R., Rubenstein J.L.R. Chromosome 8p as a potential hub for developmental neuropsychiatric disorders: implications for schizophrenia, autism and cancer. Mol. Psychiat. 2009, 14:563-589.
-
(2009)
Mol. Psychiat.
, vol.14
, pp. 563-589
-
-
Tabarés-Seisdedos, R.1
Rubenstein, J.L.R.2
-
225
-
-
33644863950
-
A truncating mutation in the IL1RAPL1 gene is responsible for X-linked mental retardation in the MRX21 family
-
Tabolacci E., Pomponi M.G., Pietrobono R., Terracciano A., Chiurazzi P., Neri G. A truncating mutation in the IL1RAPL1 gene is responsible for X-linked mental retardation in the MRX21 family. Am. J. Med. Genet. A 2006, 140:482-487.
-
(2006)
Am. J. Med. Genet. A
, vol.140
, pp. 482-487
-
-
Tabolacci, E.1
Pomponi, M.G.2
Pietrobono, R.3
Terracciano, A.4
Chiurazzi, P.5
Neri, G.6
-
226
-
-
34249900454
-
The histone H3K4 demethylase SMCX links REST target genes to X-linked mental retardation
-
Tahiliani M., Mei P., Fang R., Leonor T., Rutenberg M., Shimizu F., Li J., Rao A., Shi Y. The histone H3K4 demethylase SMCX links REST target genes to X-linked mental retardation. Nature 2007, 447:601-605.
-
(2007)
Nature
, vol.447
, pp. 601-605
-
-
Tahiliani, M.1
Mei, P.2
Fang, R.3
Leonor, T.4
Rutenberg, M.5
Shimizu, F.6
Li, J.7
Rao, A.8
Shi, Y.9
-
227
-
-
51449089853
-
Genetic influences on the broad spectrum of autism: study of proband-ascertained twins
-
Taniai H., Nishiyama T., Miyachi T., Imaeda M., Sumi S. Genetic influences on the broad spectrum of autism: study of proband-ascertained twins. Am. J. Med. Genet. B. Neuropsychiatr. Genet. 2008, 147B:844-849.
-
(2008)
Am. J. Med. Genet. B. Neuropsychiatr. Genet.
, vol.147 B
, pp. 844-849
-
-
Taniai, H.1
Nishiyama, T.2
Miyachi, T.3
Imaeda, M.4
Sumi, S.5
-
228
-
-
44849133641
-
A new look at XXYY syndrome: medical and psychological features
-
Tartaglia N., Davis S., Hench A., Nimishakavi S., Beauregard R., Reynolds A., Fenton L., Albrecht L., Ross J., Visootsak J., Hansen R., Hagerman R. A new look at XXYY syndrome: medical and psychological features. Am. J. Med. Genet. A 2008, 146A:1509-1522.
-
(2008)
Am. J. Med. Genet. A
, vol.146 A
, pp. 1509-1522
-
-
Tartaglia, N.1
Davis, S.2
Hench, A.3
Nimishakavi, S.4
Beauregard, R.5
Reynolds, A.6
Fenton, L.7
Albrecht, L.8
Ross, J.9
Visootsak, J.10
Hansen, R.11
Hagerman, R.12
-
229
-
-
79952273325
-
The spectrum of the behavioral phenotype in boys and adolescents 47
-
Tartaglia Nicole., Cordeiro Lisa., Howell Susan. The spectrum of the behavioral phenotype in boys and adolescents 47. XXY (Klinefelter Synd.) 2010, 8(Suppl 1):151-159.
-
(2010)
XXY (Klinefelter Synd.)
, vol.8
, Issue.SUPPL 1
, pp. 151-159
-
-
Tartaglia, N.1
Cordeiro, L.2
Howell, S.3
-
230
-
-
0037294847
-
Pathogenic role of glial cells in Parkinson's disease
-
Teismann P., Tieu K., Cohen O., Choi D.-K., Wu D.C., Marks D., Vila M., Jackson-Lewis V., Przedborski S. Pathogenic role of glial cells in Parkinson's disease. Mov. Disord. 2003, 18:121-129.
-
(2003)
Mov. Disord.
, vol.18
, pp. 121-129
-
-
Teismann, P.1
Tieu, K.2
Cohen, O.3
Choi, D.-K.4
Wu, D.C.5
Marks, D.6
Vila, M.7
Jackson-Lewis, V.8
Przedborski, S.9
-
231
-
-
0032971826
-
Xp deletions associated with autism in three females
-
Thomas N.S., Sharp A.J., Browne C.E., Skuse D.H., Hardie C., Dennis N.R. Xp deletions associated with autism in three females. Hum. Genet. 1999, 43-48.
-
(1999)
Hum. Genet.
, pp. 43-48
-
-
Thomas, N.S.1
Sharp, A.J.2
Browne, C.E.3
Skuse, D.H.4
Hardie, C.5
Dennis, N.R.6
-
232
-
-
0029067398
-
Plasma androgens in autism
-
Tordjman S., Anderson G.M., McBride P.A., Hertzig M.E., Snow M.E., Hall L.M., Ferrari P., Cohen D.J. Plasma androgens in autism. J. Autism Dev. Disord. 1995, 25:295-304.
-
(1995)
J. Autism Dev. Disord.
, vol.25
, pp. 295-304
-
-
Tordjman, S.1
Anderson, G.M.2
McBride, P.A.3
Hertzig, M.E.4
Snow, M.E.5
Hall, L.M.6
Ferrari, P.7
Cohen, D.J.8
-
233
-
-
0030816855
-
Androgenic activity in autism
-
Tordjman S., Ferrari P., Sulmont V., Duyme M., Roubertoux P. Androgenic activity in autism. Am. J. Psychiatry 1997, 154:1626-1627.
-
(1997)
Am. J. Psychiatry
, vol.154
, pp. 1626-1627
-
-
Tordjman, S.1
Ferrari, P.2
Sulmont, V.3
Duyme, M.4
Roubertoux, P.5
-
234
-
-
84888367236
-
Widespread sex differences in gene expression and splicing in the adult human brain
-
Trabzuni D., Ramasamy A., Imran S., Walker R., Smith C., Weale M.E., Hardy J., Ryten M. Widespread sex differences in gene expression and splicing in the adult human brain. Nat. Commun. 2013, 4:2771.
-
(2013)
Nat. Commun.
, vol.4
, pp. 2771
-
-
Trabzuni, D.1
Ramasamy, A.2
Imran, S.3
Walker, R.4
Smith, C.5
Weale, M.E.6
Hardy, J.7
Ryten, M.8
-
235
-
-
80755168115
-
The role of microglia in the healthy brain
-
Tremblay M.-È., Stevens B., Sierra A., Wake H., Bessis A., Nimmerjahn A. The role of microglia in the healthy brain. J. Neurosci. 2011, 31:16064-16069.
-
(2011)
J. Neurosci.
, vol.31
, pp. 16064-16069
-
-
Tremblay, M.-È.1
Stevens, B.2
Sierra, A.3
Wake, H.4
Bessis, A.5
Nimmerjahn, A.6
-
236
-
-
79955522583
-
Vulnerability for psychopathology in Klinefelter syndrome: age-specific and cognitive-specific risk profiles
-
Van Rijn S., Swaab H. Vulnerability for psychopathology in Klinefelter syndrome: age-specific and cognitive-specific risk profiles. Acta Paediatr. 2011, 100:908-916.
-
(2011)
Acta Paediatr.
, vol.100
, pp. 908-916
-
-
Van Rijn, S.1
Swaab, H.2
-
237
-
-
11144230769
-
Neuroglial activation and neuroinflammation in the brain of patients with autism
-
Vargas D.L., Nascimbene C., Krishnan C., Zimmerman A.W., Pardo C.a. Neuroglial activation and neuroinflammation in the brain of patients with autism. Ann. Neurol. 2005, 57:67-81.
-
(2005)
Ann. Neurol.
, vol.57
, pp. 67-81
-
-
Vargas, D.L.1
Nascimbene, C.2
Krishnan, C.3
Zimmerman, A.W.4
Pardo, C.5
-
238
-
-
33846862008
-
Membrane-initiated actions of estrogens in neuroendocrinology: emerging principles
-
Vasudevan N., Pfaff D.W. Membrane-initiated actions of estrogens in neuroendocrinology: emerging principles. Endocr. Rev. 2007, 28:1-19.
-
(2007)
Endocr. Rev.
, vol.28
, pp. 1-19
-
-
Vasudevan, N.1
Pfaff, D.W.2
-
239
-
-
41549115929
-
Non-genomic actions of estrogens and their interaction with genomic actions in the brain
-
Vasudevan N., Pfaff D.W. Non-genomic actions of estrogens and their interaction with genomic actions in the brain. Front. Neuroendocrinol. 2008, 29:238-257.
-
(2008)
Front. Neuroendocrinol.
, vol.29
, pp. 238-257
-
-
Vasudevan, N.1
Pfaff, D.W.2
-
240
-
-
0035834075
-
Early membrane estrogenic effects required for full expression of slower genomic actions in a nerve cell line
-
Vasudevan N., Kow L.M., Pfaff D.W. Early membrane estrogenic effects required for full expression of slower genomic actions in a nerve cell line. Proc. Natl. Acad. Sci. U.S.A. 2001, 98:12267-12271.
-
(2001)
Proc. Natl. Acad. Sci. U.S.A.
, vol.98
, pp. 12267-12271
-
-
Vasudevan, N.1
Kow, L.M.2
Pfaff, D.W.3
-
241
-
-
3342965856
-
Mutation screening of X-chromosomal neuroligin genes: no mutations in 196 autism probands
-
Vincent J.B., Kolozsvari D., Roberts W.S., Bolton P.F., Gurling H.M.D., Scherer S.W. Mutation screening of X-chromosomal neuroligin genes: no mutations in 196 autism probands. Am. J. Med. Genet. B. Neuropsychiatr. Genet. 2004, 129B:82-84.
-
(2004)
Am. J. Med. Genet. B. Neuropsychiatr. Genet.
, vol.129 B
, pp. 82-84
-
-
Vincent, J.B.1
Kolozsvari, D.2
Roberts, W.S.3
Bolton, P.F.4
Gurling, H.M.D.5
Scherer, S.W.6
-
242
-
-
32844460507
-
Identification of novel autism candidate regions through analysis of reported cytogenetic abnormalities associated with autism
-
Vorstman J.a.S., Staal W.G., van Daalen E., van Engeland H., Hochstenbach P.F.R., Franke L. Identification of novel autism candidate regions through analysis of reported cytogenetic abnormalities associated with autism. Mol. Psychiat. 2006, 11(1):18-28.
-
(2006)
Mol. Psychiat.
, vol.11
, Issue.1
, pp. 18-28
-
-
Vorstman, J.1
Staal, W.G.2
van Daalen, E.3
van Engeland, H.4
Hochstenbach, P.F.R.5
Franke, L.6
-
243
-
-
84891552739
-
Dynamic postnatal developmental and sex-specific neuroendocrine effects of prenatal polychlorinated biphenyls in rats
-
Walker D.M., Goetz B.M., Gore A.C. Dynamic postnatal developmental and sex-specific neuroendocrine effects of prenatal polychlorinated biphenyls in rats. Mol. Endocrinol. 2014, 28:99-115.
-
(2014)
Mol. Endocrinol.
, vol.28
, pp. 99-115
-
-
Walker, D.M.1
Goetz, B.M.2
Gore, A.C.3
-
244
-
-
2542466402
-
Masculinization and defeminization in altricial and precocial mammals: comparative aspects of steroid hormone action
-
Elsevier, New York, D. Pfaff, P. Arnold, A. Etgen, S. Fahrbach, R. Rubin (Eds.)
-
Wallen K., Baum M.J. Masculinization and defeminization in altricial and precocial mammals: comparative aspects of steroid hormone action. Hormones, brain and behavior 2002, 385-423. Elsevier, New York. D. Pfaff, P. Arnold, A. Etgen, S. Fahrbach, R. Rubin (Eds.).
-
(2002)
Hormones, brain and behavior
, pp. 385-423
-
-
Wallen, K.1
Baum, M.J.2
-
245
-
-
0346363764
-
The mouse Murr1 gene is imprinted in the adult brain, presumably due to transcriptional interference by the antisense-oriented U2af1-rs1 gene
-
Wang Y., Joh K., Masuko S., Yatsuki H., Soejima H., Nabetani A., Beechey C.V., Okinami S., Mukai T. The mouse Murr1 gene is imprinted in the adult brain, presumably due to transcriptional interference by the antisense-oriented U2af1-rs1 gene. Mol. Cell. Biol. 2003, 24:270-279.
-
(2003)
Mol. Cell. Biol.
, vol.24
, pp. 270-279
-
-
Wang, Y.1
Joh, K.2
Masuko, S.3
Yatsuki, H.4
Soejima, H.5
Nabetani, A.6
Beechey, C.V.7
Okinami, S.8
Mukai, T.9
-
246
-
-
0023194706
-
Age related reactivation of an X-linked gene
-
Wareham K.A., Lyon M.F., Glenister P.H., Williams E.D. Age related reactivation of an X-linked gene. Nature 1987, 327:725-727.
-
(1987)
Nature
, vol.327
, pp. 725-727
-
-
Wareham, K.A.1
Lyon, M.F.2
Glenister, P.H.3
Williams, E.D.4
-
247
-
-
0037222315
-
Sodium channels SCN1A, SCN2A and SCN3A in familial autism
-
Weiss L.A., Escayg A., Kearney J.A., Trudeau M., MacDonald B.T., Mori M., Reichert J., Buxbaum J.D., Meisler M.H. Sodium channels SCN1A, SCN2A and SCN3A in familial autism. Mol. Psychiat. 2003, 8:186-194.
-
(2003)
Mol. Psychiat.
, vol.8
, pp. 186-194
-
-
Weiss, L.A.1
Escayg, A.2
Kearney, J.A.3
Trudeau, M.4
MacDonald, B.T.5
Mori, M.6
Reichert, J.7
Buxbaum, J.D.8
Meisler, M.H.9
-
248
-
-
39049163023
-
Association between microdeletion and microduplication at 16p11. 2 and autism
-
Weiss L.A., Shen Y., Korn J.M., Arking D.E., Miller D.T., Fossdal R., Saemundsen E., Stefansson H., Ferreira M.A.R., Green T., Platt O.S., Ruderfer D.M., Walsh C.A., Altshuler D., Chakravarti A., Tanzi R.E., Stefansson K., Santangelo S.L., Gusella J.F., Sklar P., Wu B., Daly M.J. Association between microdeletion and microduplication at 16p11. 2 and autism. New Engl. J. Med. 2008, 358:667-675.
-
(2008)
New Engl. J. Med.
, vol.358
, pp. 667-675
-
-
Weiss, L.A.1
Shen, Y.2
Korn, J.M.3
Arking, D.E.4
Miller, D.T.5
Fossdal, R.6
Saemundsen, E.7
Stefansson, H.8
Ferreira, M.A.R.9
Green, T.10
Platt, O.S.11
Ruderfer, D.M.12
Walsh, C.A.13
Altshuler, D.14
Chakravarti, A.15
Tanzi, R.E.16
Stefansson, K.17
Santangelo, S.L.18
Gusella, J.F.19
Sklar, P.20
Wu, B.21
Daly, M.J.22
more..
-
249
-
-
0018921896
-
Plasma testosterone and progesterone titers of pregnant rats, their male and female fetuses, and neonatal offspring
-
Weisz J., Ward I. Plasma testosterone and progesterone titers of pregnant rats, their male and female fetuses, and neonatal offspring. Endocrinology 1980, 106:306-316.
-
(1980)
Endocrinology
, vol.106
, pp. 306-316
-
-
Weisz, J.1
Ward, I.2
-
250
-
-
19244386891
-
Masculine sexual behavior is disrupted in male and female mice lacking a functional estrogen receptor alpha gene
-
Wersinger S.R., Sannen K., Villalba C., Lubahn D.B., Rissman E.F., De Vries G.J. Masculine sexual behavior is disrupted in male and female mice lacking a functional estrogen receptor alpha gene. Horm. Behav. 1997, 32:176-183.
-
(1997)
Horm. Behav.
, vol.32
, pp. 176-183
-
-
Wersinger, S.R.1
Sannen, K.2
Villalba, C.3
Lubahn, D.B.4
Rissman, E.F.5
De Vries, G.J.6
-
251
-
-
84881247952
-
Perinatal testosterone exposure and autistic-like traits in the general population: a longitudinal pregnancy-cohort study
-
Whitehouse A.J., Mattes E., Maybery M.T., Dissanayake C., Sawyer M., Jones R.M., Pennell C.E., Keelan J.A., Hickey M. Perinatal testosterone exposure and autistic-like traits in the general population: a longitudinal pregnancy-cohort study. J. Neurodev. Disord. 2012, 4:25.
-
(2012)
J. Neurodev. Disord.
, vol.4
, pp. 25
-
-
Whitehouse, A.J.1
Mattes, E.2
Maybery, M.T.3
Dissanayake, C.4
Sawyer, M.5
Jones, R.M.6
Pennell, C.E.7
Keelan, J.A.8
Hickey, M.9
-
252
-
-
77956595381
-
Sexual dimorphism in mammalian autosomal gene regulation is determined not only by Sry but by sex chromosome complement as well
-
Wijchers P.J., Yandim C., Panousopoulou E., Ahmad M., Harker N., Saveliev A., Burgoyne P.S., Festenstein R. Sexual dimorphism in mammalian autosomal gene regulation is determined not only by Sry but by sex chromosome complement as well. Dev. Cell 2010, 19:477-484.
-
(2010)
Dev. Cell
, vol.19
, pp. 477-484
-
-
Wijchers, P.J.1
Yandim, C.2
Panousopoulou, E.3
Ahmad, M.4
Harker, N.5
Saveliev, A.6
Burgoyne, P.S.7
Festenstein, R.8
-
253
-
-
70350344681
-
Prostaglandin E2-induced masculinization of brain and behavior requires protein kinase A, AMPA/kainate, and metabotropic glutamate receptor signaling
-
Wright C.L., McCarthy M.M. Prostaglandin E2-induced masculinization of brain and behavior requires protein kinase A, AMPA/kainate, and metabotropic glutamate receptor signaling. J. Neurosci. 2009, 29:13274-13282.
-
(2009)
J. Neurosci.
, vol.29
, pp. 13274-13282
-
-
Wright, C.L.1
McCarthy, M.M.2
-
254
-
-
0028049298
-
Isolation and characterization of XE169, a novel human gene that escapes X-inactivation
-
Wu J., Ellison J., Salido E., Yen P., Mohandas T., Shapiro L. Isolation and characterization of XE169, a novel human gene that escapes X-inactivation. Hum. Mol. Genet. 1994, 3:153-160.
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 153-160
-
-
Wu, J.1
Ellison, J.2
Salido, E.3
Yen, P.4
Mohandas, T.5
Shapiro, L.6
-
255
-
-
70350527351
-
Regulation of monoamine oxidase A by the SRY gene on the Y chromosome
-
Wu J.B., Chen K., Li Y., Lau Y.-F.C., Shih J.C. Regulation of monoamine oxidase A by the SRY gene on the Y chromosome. FASEB J. 2009, 23:4029-4038.
-
(2009)
FASEB J.
, vol.23
, pp. 4029-4038
-
-
Wu, J.B.1
Chen, K.2
Li, Y.3
Lau, Y.-F.C.4
Shih, J.C.5
-
256
-
-
71749101705
-
Sex differences in sex chromosome gene expression in mouse brain
-
Xu J., Burgoyne P.S., Arnold A.P. Sex differences in sex chromosome gene expression in mouse brain. Hum. Mol. Genet. 2002, 11:1409-1419.
-
(2002)
Hum. Mol. Genet.
, vol.11
, pp. 1409-1419
-
-
Xu, J.1
Burgoyne, P.S.2
Arnold, A.P.3
-
257
-
-
49749114829
-
Sex-specific expression of the X-linked histone demethylase gene Jarid1c in brain
-
Xu J., Deng X., Disteche C.M. Sex-specific expression of the X-linked histone demethylase gene Jarid1c in brain. PLoS One 2008, 3:e2553.
-
(2008)
PLoS One
, vol.3
-
-
Xu, J.1
Deng, X.2
Disteche, C.M.3
-
258
-
-
0242432463
-
Neurons but not glial cells show reciprocal imprinting of sense and antisense transcripts of Ube3a
-
Yamasaki K. Neurons but not glial cells show reciprocal imprinting of sense and antisense transcripts of Ube3a. Hum. Mol. Genet. 2003, 12:837-847.
-
(2003)
Hum. Mol. Genet.
, vol.12
, pp. 837-847
-
-
Yamasaki, K.1
-
259
-
-
20144389549
-
Analysis of the neuroligin 3 and 4 genes in autism and other neuropsychiatric patients
-
Yan J., Oliveira G., Coutinho A., Yang C., Feng J., Katz C., Sram J., Bockholt A., Jones I.R., Craddock N., Cook E.H., Vicente A., Sommer S.S. Analysis of the neuroligin 3 and 4 genes in autism and other neuropsychiatric patients. Mol. Psychiat. 2005, 10:329-332.
-
(2005)
Mol. Psychiat.
, vol.10
, pp. 329-332
-
-
Yan, J.1
Oliveira, G.2
Coutinho, A.3
Yang, C.4
Feng, J.5
Katz, C.6
Sram, J.7
Bockholt, A.8
Jones, I.R.9
Craddock, N.10
Cook, E.H.11
Vicente, A.12
Sommer, S.S.13
-
260
-
-
77951794067
-
Global survey of escape from X inactivation by RNA-sequencing in mouse
-
Yang F., Babak T., Shendure J., Disteche C.M. Global survey of escape from X inactivation by RNA-sequencing in mouse. Genome Res. 2010, 20:614-622.
-
(2010)
Genome Res.
, vol.20
, pp. 614-622
-
-
Yang, F.1
Babak, T.2
Shendure, J.3
Disteche, C.M.4
-
261
-
-
0024208474
-
The human X-linked steroid sulfatase gene and a Y-encoded pseudogene: evidence for an inversion of the Y chromosome during primate evolution
-
Yen P.H., Marsh B., Allen E., Tsai S.P., Ellison J., Connolly L., Neiswanger K., Shapiro L.J. The human X-linked steroid sulfatase gene and a Y-encoded pseudogene: evidence for an inversion of the Y chromosome during primate evolution. Cell 1988, 55:1123-1135.
-
(1988)
Cell
, vol.55
, pp. 1123-1135
-
-
Yen, P.H.1
Marsh, B.2
Allen, E.3
Tsai, S.P.4
Ellison, J.5
Connolly, L.6
Neiswanger, K.7
Shapiro, L.J.8
-
262
-
-
80053025841
-
IL-1 receptor accessory protein-like 1 associated with mental retardation and autism mediates synapse formation by trans-synaptic interaction with protein tyrosine phosphatase δ
-
Yoshida T., Yasumura M., Uemura T., Lee S.-J., Ra M., Taguchi R., Iwakura Y., Mishina M. IL-1 receptor accessory protein-like 1 associated with mental retardation and autism mediates synapse formation by trans-synaptic interaction with protein tyrosine phosphatase δ. J. Neurosci. 2011, 31:13485-13499.
-
(2011)
J. Neurosci.
, vol.31
, pp. 13485-13499
-
-
Yoshida, T.1
Yasumura, M.2
Uemura, T.3
Lee, S.-J.4
Ra, M.5
Taguchi, R.6
Iwakura, Y.7
Mishina, M.8
-
263
-
-
0035577350
-
A high density of X-linked genes for general cognitive ability: a run-away process shaping human evolution
-
Zechner U., Wilda M., Kehrer-sawatzki H., Vogel W., Fundele R., Hameister H. A high density of X-linked genes for general cognitive ability: a run-away process shaping human evolution?. Trends Genet. 2001, 17:697-701.
-
(2001)
Trends Genet.
, vol.17
, pp. 697-701
-
-
Zechner, U.1
Wilda, M.2
Kehrer-sawatzki, H.3
Vogel, W.4
Fundele, R.5
Hameister, H.6
-
264
-
-
34547886497
-
A unified genetic theory for sporadic and inherited autism
-
Zhao X., Leotta A., Kustanovich V., Lajonchere C., Geschwind D.H., Law K., Law P., Qiu S., Lord C., Sebat J., Ye K., Wigler M. A unified genetic theory for sporadic and inherited autism. Proc. Natl. Acad. Sci. U.S.A. 2007, 104:12831-12836.
-
(2007)
Proc. Natl. Acad. Sci. U.S.A.
, vol.104
, pp. 12831-12836
-
-
Zhao, X.1
Leotta, A.2
Kustanovich, V.3
Lajonchere, C.4
Geschwind, D.H.5
Law, K.6
Law, P.7
Qiu, S.8
Lord, C.9
Sebat, J.10
Ye, K.11
Wigler, M.12
-
265
-
-
34250652100
-
A Turner syndrome neurocognitive phenotype maps to Xp22.3
-
Zinn A.R., Roeltgen D., Stefanatos G., Ramos P., Elder F.F., Kushner H., Kowal K., Ross J.L. A Turner syndrome neurocognitive phenotype maps to Xp22.3. Behav. Brain Funct. 2007, 3:24.
-
(2007)
Behav. Brain Funct.
, vol.3
, pp. 24
-
-
Zinn, A.R.1
Roeltgen, D.2
Stefanatos, G.3
Ramos, P.4
Elder, F.F.5
Kushner, H.6
Kowal, K.7
Ross, J.L.8
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