-
1
-
-
42349095075
-
Advances in autism genetics: On the threshold of a new neurobiology
-
Abrahams BS, Geschwind DH. 2008. Advances in autism genetics: on the threshold of a new neurobiology. Nat Rev Genet 9: 341-355.
-
(2008)
Nat Rev Genet
, vol.9
, pp. 341-355
-
-
Abrahams, B.S.1
Geschwind, D.H.2
-
2
-
-
66249097733
-
A high-density SNP genome-wide linkage scan in a large autism extended pedigree
-
Allen-Brady K, Miller J, Matsunami N, Stevens J, Block H, Farley M, et al. 2009. A high-density SNP genome-wide linkage scan in a large autism extended pedigree. Mol Psychiatry 14: 590-600.
-
(2009)
Mol Psychiatry
, vol.14
, pp. 590-600
-
-
Allen-Brady, K.1
Miller, J.2
Matsunami, N.3
Stevens, J.4
Block, H.5
Farley, M.6
-
3
-
-
70249150753
-
Examination of association of genes in the serotonin system to autism
-
Anderson BM, Schnetz-Boutaud NC, Bartlett J, Wotawa AM, Wright HH, Abramson RK, et al. 2009. Examination of association of genes in the serotonin system to autism. Neurogenetics 10: 209-216.
-
(2009)
Neurogenetics
, vol.10
, pp. 209-216
-
-
Anderson, B.M.1
Schnetz-Boutaud, N.C.2
Bartlett, J.3
Wotawa, A.M.4
Wright, H.H.5
Abramson, R.K.6
-
4
-
-
0036780698
-
A genomewide screen for autism spectrum disorders: Evidence for a major susceptibility locus on chromosome 3q25-27
-
Auranen M, Vanhala R, Varilo T, Ayers K, Kempas E, Ylisaukko-Oja T, et al. 2002. A genomewide screen for autism spectrum disorders: evidence for a major susceptibility locus on chromosome 3q25-27. Am J Hum Genet 71: 777-790.
-
(2002)
Am J Hum Genet
, vol.71
, pp. 777-790
-
-
Auranen, M.1
Vanhala, R.2
Varilo, T.3
Ayers, K.4
Kempas, E.5
Ylisaukko-Oja, T.6
-
5
-
-
13444269543
-
Haploview: Analysis and visualization of LD and haplotype maps
-
Barrett JC, Fry B, Maller J, Daly MJ. 2005. Haploview: analysis and visualization of LD and haplotype maps. Bioinformatics 21: 263-265.
-
(2005)
Bioinformatics
, vol.21
, pp. 263-265
-
-
Barrett, J.C.1
Fry, B.2
Maller, J.3
Daly, M.J.4
-
6
-
-
0042824074
-
Possible parent-of-origin effect of Dopa decarboxylase in susceptibility to bipolar affective disorder
-
B ø rglum AD, Kirov G, Craddock N, Mors O, Muir W, Murray V, et al. 2003. Possible parent-of-origin effect of Dopa decarboxylase in susceptibility to bipolar affective disorder. Am J Med Genet B Neuropsychiatr Genet 117B: 18-22.
-
(2003)
Am J Med Genet B Neuropsychiatr Genet
, vol.117 B
, pp. 18-22
-
-
Børglum, A.D.1
Kirov, G.2
Craddock, N.3
Mors, O.4
Muir, W.5
Murray, V.6
-
7
-
-
67650750977
-
A synaptic trek to autism
-
Bourgeron T. 2009. A synaptic trek to autism. Curr Opin Neurobiol 19: 231-234.
-
(2009)
Curr Opin Neurobiol
, vol.19
, pp. 231-234
-
-
Bourgeron, T.1
-
9
-
-
0346373654
-
Selecting a maximally informative set of singlenucleotide polymorphisms for association analysis using linkage disequilibrium
-
Carlson CS, Eberle MA, Rieder MJ, Yi Q, Kruglyak L, Nickerson DA. 2004. Selecting a maximally informative set of singlenucleotide polymorphisms for association analysis using linkage disequilibrium. Am J Hum Genet 74: 106-120.
-
(2004)
Am J Hum Genet
, vol.74
, pp. 106-120
-
-
Carlson, C.S.1
Eberle, M.A.2
Rieder, M.J.3
Yi, Q.4
Kruglyak, L.5
Nickerson, D.A.6
-
10
-
-
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, et al. 2009. Genes related to sex steroids, neural growth, and social-emotional behavior are associated with autistic traits, empathy, and Asperger syndrome. Autism Res 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
-
11
-
-
14644394987
-
Significance of abnormalities in developmental trajectory and asymmetry of cortical serotonin synthesis in autism
-
Chandana SR, Behen ME, Juhasz C, Muzik O, Rothermel RD, Mangner TJ, et al. 2005. Significance of abnormalities in developmental trajectory and asymmetry of cortical serotonin synthesis in autism. Int J Dev Neurosci 23: 171-182.
-
(2005)
Int J Dev Neurosci
, vol.23
, pp. 171-182
-
-
Chandana, S.R.1
Behen, M.E.2
Juhasz, C.3
Muzik, O.4
Rothermel, R.D.5
Mangner, T.J.6
-
12
-
-
22544469139
-
Are dopaminergic genes involved in a predisposition to pathological aggression? Hypothesizing the importance of " super normal controls " in psychiatricgenetic research of complex behavioral disorders
-
Chen TJ, Blum K, Mathews D, Fisher L, Schnautz N, Braverman ER, et al. 2005. Are dopaminergic genes involved in a predisposition to pathological aggression? Hypothesizing the importance of " super normal controls " in psychiatricgenetic research of complex behavioral disorders. Med Hypotheses 65: 703-707.
-
(2005)
Med Hypotheses
, vol.65
, pp. 703-707
-
-
Chen, T.J.1
Blum, K.2
Mathews, D.3
Fisher, L.4
Schnautz, N.5
Braverman, E.R.6
-
13
-
-
67649661829
-
Association study between BDNF gene polymorphisms and autism by three-dimensional gel-based microarray
-
Cheng L, Ge Q, Xiao P, Sun B, Ke X, Bai Y, Lu Z. 2009. Association study between BDNF gene polymorphisms and autism by three-dimensional gel-based microarray. Int J Mol Sci 10: 2487-2500.
-
(2009)
Int J Mol Sci
, vol.10
, pp. 2487-2500
-
-
Cheng, L.1
Ge, Q.2
Xiao, P.3
Sun, B.4
Ke, X.5
Bai, Y.6
Lu, Z.7
-
14
-
-
33847300921
-
Family-based association study of 5-HTTLPR and the 5-HT2A receptor gene polymorphisms with autism spectrum disorder in Korean trios
-
Cho IH, Yoo HJ, Park M, Lee YS, Kim SA. 2007. Family-based association study of 5-HTTLPR and the 5-HT2A receptor gene polymorphisms with autism spectrum disorder in Korean trios. Brain Res 1139: 34-41.
-
(2007)
Brain Res
, vol.1139
, pp. 34-41
-
-
Cho, I.H.1
Yoo, H.J.2
Park, M.3
Lee, Y.S.4
Kim, S.A.5
-
15
-
-
32544434349
-
Brain-derived neurotrophic factor and autoantibodies to neural antigens in sera of children with autistic spectrum disorders, Landau-Kleffner syndrome, and epilepsy
-
Connolly AM, Chez M, Streif EM, Keeling RM, Golumbek PT, Kwon JM, et al. 2006. Brain-derived neurotrophic factor and autoantibodies to neural antigens in sera of children with autistic spectrum disorders, Landau-Kleffner syndrome, and epilepsy. Biol Psychiatry 59: 354-363.
-
(2006)
Biol Psychiatry
, vol.59
, pp. 354-363
-
-
Connolly, A.M.1
Chez, M.2
Streif, E.M.3
Keeling, R.M.4
Golumbek, P.T.5
Kwon, J.M.6
-
16
-
-
10544234621
-
The serotonin system in autism. A review of the evidence for involvement of the serotonin system in the aetiology of autism
-
Cook E, Leventhal B. 1996. The serotonin system in autism. A review of the evidence for involvement of the serotonin system in the aetiology of autism. Curr Opin Pediatr 8: 348-354.
-
(1996)
Curr Opin Pediatr
, vol.8
, pp. 348-354
-
-
Cook, E.1
Leventhal, B.2
-
17
-
-
33947114826
-
Evidence for epistasis between SLC6A4 and ITGB3 in autism etiology and in the determination of platelet serotonin levels
-
Coutinho AM, Sousa I, Martins M, Correia C, Morgadinho T, Bento C, et al. 2007. Evidence for epistasis between SLC6A4 and ITGB3 in autism etiology and in the determination of platelet serotonin levels. Hum Genet 121: 243-256.
-
(2007)
Hum Genet
, vol.121
, pp. 243-256
-
-
Coutinho, A.M.1
Sousa, I.2
Martins, M.3
Correia, C.4
Morgadinho, T.5
Bento, C.6
-
18
-
-
17144444473
-
Peripheral markers of serotonergic and noradrenergic function in post-pubertal, caucasian males with autistic disorder
-
Croonenberghs J, Delmeire L, Verkerk R, Lin AH, Meskal A, Neels H, et al. 2000. Peripheral markers of serotonergic and noradrenergic function in post-pubertal, caucasian males with autistic disorder. Neuropsychopharmacology 22: 275-283.
-
(2000)
Neuropsychopharmacology
, vol.22
, pp. 275-283
-
-
Croonenberghs, J.1
Delmeire, L.2
Verkerk, R.3
Lin, A.H.4
Meskal, A.5
Neels, H.6
-
19
-
-
65449139457
-
Autism-specific copy number variants further implicate the phosphatidylinositol signaling pathway and the glutamatergic synapse in the etiology of the disorder
-
Cusc ó I, Medrano A, Gener B, Vilardell M, Gallastegui F, Villa O, et al. 2009. Autism-specific copy number variants further implicate the phosphatidylinositol signaling pathway and the glutamatergic synapse in the etiology of the disorder. Hum Mol Genet 18: 1795-1804.
-
(2009)
Hum Mol Genet
, vol.18
, pp. 1795-1804
-
-
Cuscó, I.1
Medrano, A.2
Gener, B.3
Vilardell, M.4
Gallastegui, F.5
Villa, O.6
-
20
-
-
61549125385
-
A common variant in DRD3 receptor is associated with autism spectrum disorder
-
de Krom M, Staal WG, Ophoff RA, Hendriks J, Buitelaar J, Franke B, et al. 2009. A common variant in DRD3 receptor is associated with autism spectrum disorder. Biol Psychiatry 65: 625-630.
-
(2009)
Biol Psychiatry
, vol.65
, pp. 625-630
-
-
De Krom, M.1
Staal, W.G.2
Ophoff, R.A.3
Hendriks, J.4
Buitelaar, J.5
Franke, B.6
-
21
-
-
33846804188
-
Extensive linkage disequilibrium mapping at HTR2A and DRD3 for schizophrenia susceptibility genes in the Galician population
-
Dom í nguez E, Loza MI, Pad í n F, Gesteira A, Paz E, P á ramo M, Brenlla J, Pumar E, Iglesias F, Cibeira A, Castro M, Caruncho H, Carracedo A, Costas J. 2007. Extensive linkage disequilibrium mapping at HTR2A and DRD3 for schizophrenia susceptibility genes in the Galician population. Schizophr Res 90: 123-129.
-
(2007)
Schizophr Res
, vol.90
, pp. 123-129
-
-
Domínguez, E.1
Loza, M.I.2
Padín, F.3
Gesteira, A.4
Paz, E.5
Páramo, M.6
Brenlla, J.7
Pumar, E.8
Iglesias, F.9
Cibeira, A.10
Castro, M.11
Caruncho, H.12
Carracedo, A.13
Costas, J.14
-
22
-
-
0041857847
-
Pedigree disequilibrium tests for multilocus haplotypes
-
Dudbridge F. 2003. Pedigree disequilibrium tests for multilocus haplotypes. Genet Epidemiol 25: 115-121.
-
(2003)
Genet Epidemiol
, vol.25
, pp. 115-121
-
-
Dudbridge, F.1
-
23
-
-
33845889998
-
Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders
-
Durand CM, Betancur C, Boeckers TM, Bockmann J, Chaste P, Fauchereau F et al. 2007. Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders. Nat Genet 39: 25-27.
-
(2007)
Nat Genet
, vol.39
, pp. 25-27
-
-
Durand, C.M.1
Betancur, C.2
Boeckers, T.M.3
Bockmann, J.4
Chaste, P.5
Fauchereau, F.6
-
24
-
-
4444320149
-
Neurotrophic factors and the pathophysiology of schizophrenic psychoses
-
Durany N, Thome J. 2004. Neurotrophic factors and the pathophysiology of schizophrenic psychoses. Eur Psychiatry 19: 326-337.
-
(2004)
Eur Psychiatry
, vol.19
, pp. 326-337
-
-
Durany, N.1
Thome, J.2
-
25
-
-
67049118065
-
Epidemiology of pervasive developmental disorders
-
Fombonne E. 2009. Epidemiology of pervasive developmental disorders. Pediatr Res 65: 591-598.
-
(2009)
Pediatr Res
, vol.65
, pp. 591-598
-
-
Fombonne, E.1
-
26
-
-
73949139615
-
A common variant in DRD3 gene is associated with risperidone-induced extrapyramidal symptoms
-
Gass ó P, Mas S, Bernardo M, Alvarez S, Parellada E, Lafuente A. 2009. A common variant in DRD3 gene is associated with risperidone-induced extrapyramidal symptoms. Pharmacogenomics J 9: 404-410.
-
(2009)
Pharmacogenomics J
, vol.9
, pp. 404-410
-
-
Gassó, P.1
Mas, S.2
Bernardo, M.3
Alvarez, S.4
Parellada, E.5
Lafuente, A.6
-
27
-
-
42149172589
-
Dopa decarboxylase and tyrosine hydroxylase gene variants in suicidal behavior
-
Giegling I, Moreno-De-Luca D, Rujescu D, Schneider B, Hartmann AM, Schnabel A, et al. 2008. Dopa decarboxylase and tyrosine hydroxylase gene variants in suicidal behavior. Am J Med Genet B Neuropsychiatr Genet 147: 308-315.
-
(2008)
Am J Med Genet B Neuropsychiatr Genet
, vol.147
, pp. 308-315
-
-
Giegling, I.1
Moreno-De-Luca, D.2
Rujescu, D.3
Schneider, B.4
Hartmann, A.M.5
Schnabel, A.6
-
28
-
-
34047179603
-
SNPassoc: An R package to perform whole genome association studies
-
Gonzalez JR, Armengol L, Sole X, Guino E, Mercader JM, Estivill X, et al. 2007. SNPassoc: an R package to perform whole genome association studies. Bioinformatics 23: 644-645.
-
(2007)
Bioinformatics
, vol.23
, pp. 644-645
-
-
Gonzalez, J.R.1
Armengol, L.2
Sole, X.3
Guino, E.4
Mercader, J.M.5
Estivill, X.6
-
29
-
-
46749136096
-
Mutations in human monoamine- related neurotransmitter pathway genes
-
Haavik J, Blau N, Thöny B. 2007. Mutations in human monoamine- related neurotransmitter pathway genes. Hum Mutat 29: 891-902.
-
(2007)
Hum Mutat
, vol.29
, pp. 891-902
-
-
Haavik, J.1
Blau, N.2
Thöny, B.3
-
30
-
-
12144270390
-
Relationship of brain-derived neurotrophic factor and its receptor TrkB to altered inhibitory prefrontal circuitry in schizophrenia
-
Hashimoto T, Bergen SE, Nguyen QL, Xu B, Monteggia LM, Pierri JN, et al. 2005. Relationship of brain-derived neurotrophic factor and its receptor TrkB to altered inhibitory prefrontal circuitry in schizophrenia. J Neurosci 25: 372-383.
-
(2005)
J Neurosci
, vol.25
, pp. 372-383
-
-
Hashimoto, T.1
Bergen, S.E.2
Nguyen, Q.L.3
Xu, B.4
Monteggia, L.M.5
Pierri, J.N.6
-
31
-
-
46949092750
-
A DRD1 haplotype is associated with risk for autism spectrum disorders in male-only affected sib-pair families
-
Hettinger JA, Liu X, Schwartz CE, Michaelis RC, Holden JJ. 2008. A DRD1 haplotype is associated with risk for autism spectrum disorders in male-only affected sib-pair families. Am J Med Genet B Neuropsychiatr Genet 147B: 628-636.
-
(2008)
Am J Med Genet B Neuropsychiatr Genet
, vol.147 B
, pp. 628-636
-
-
Hettinger, J.A.1
Liu, X.2
Schwartz, C.E.3
Michaelis, R.C.4
Holden, J.J.5
-
32
-
-
51449089163
-
Autism and serotonin transporter gene polymorphisms: A systematic review and metaanalysis
-
Huang CH, Santangelo SL. 2008. Autism and serotonin transporter gene polymorphisms: a systematic review and metaanalysis. Am J Med Genet B Neuropsychiatr Genet 147B: 903-913.
-
(2008)
Am J Med Genet B Neuropsychiatr Genet
, vol.147 B
, pp. 903-913
-
-
Huang, C.H.1
Santangelo, S.L.2
-
33
-
-
0037656313
-
Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism
-
Jamain S, Quach H, Betancur C, Rastam M, Colineaux C, Gillberg IC et al. 2003. Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism. Nat Genet 34: 27-29.
-
(2003)
Nat Genet
, vol.34
, pp. 27-29
-
-
Jamain, S.1
Quach, H.2
Betancur, C.3
Rastam, M.4
Colineaux, C.5
Gillberg, I.C.6
-
34
-
-
57349087863
-
Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations
-
Lasky-Su J, Neale BM, Franke B, Anney RJ, Zhou K, Maller JB, et al. 2008. Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. Am J Med Genet B Neuropsychiatr Genet 147B: 1345-1354.
-
(2008)
Am J Med Genet B Neuropsychiatr Genet
, vol.147 B
, pp. 1345-1354
-
-
Lasky-Su, J.1
Neale, B.M.2
Franke, B.3
Anney, R.J.4
Zhou, K.5
Maller, J.B.6
-
35
-
-
0037042110
-
Investigation of two variants in the DOPA decarboxylase gene in patients with autism
-
Lauritsen MB, B ø rglum AD, Betancur C, Philippe A, Kruse TA, Leboyer M, et al. 2002. Investigation of two variants in the DOPA decarboxylase gene in patients with autism. Am J Med Genet 114: 466-470.
-
(2002)
Am J Med Genet
, vol.114
, pp. 466-470
-
-
Lauritsen, M.B.1
Børglum, A.D.2
Betancur, C.3
Philippe, A.4
Kruse, T.A.5
Leboyer, M.6
-
36
-
-
34447339103
-
Maternally inherited duplication of chromosome 7, dup(7)(p11.2p12), associated with mild cognitive deficit without features of Silver-Russell syndrome
-
Leach NT, Chudoba I, Stewart TV, Holmes LB, Weremowicz S. 2007. Maternally inherited duplication of chromosome 7, dup(7)(p11.2p12), associated with mild cognitive deficit without features of Silver-Russell syndrome. Am J Med Genet A 143A: 1489-1493.
-
(2007)
Am J Med Genet A
, vol.143 A
, pp. 1489-1493
-
-
Leach, N.T.1
Chudoba, I.2
Stewart, T.V.3
Holmes, L.B.4
Weremowicz, S.5
-
37
-
-
60749135051
-
Aromatic L-amino acid decarboxylase deficiency in Taiwan
-
Lee HF, Tsai CR, Chi CS, Chang TM, Lee HJ. 2009. Aromatic L-amino acid decarboxylase deficiency in Taiwan. Eur J Paediatr Neurol 13: 135-140.
-
(2009)
Eur J Paediatr Neurol
, vol.13
, pp. 135-140
-
-
Lee, H.F.1
Tsai, C.R.2
Chi, C.S.3
Chang, T.M.4
Lee, H.J.5
-
38
-
-
33745046679
-
Preliminary evidence for an association between a dopamine D3 receptor gene variant and obsessive-compulsive personality disorder in patients with major depression
-
Light KJ, Joyce PR, Luty SE, Mulder RT, Frampton CM, Joyce LR, et al. 2006. Preliminary evidence for an association between a dopamine D3 receptor gene variant and obsessive-compulsive personality disorder in patients with major depression. Am J Med Genet B Neuropsychiatr Genet 141B: 409-413.
-
(2006)
Am J Med Genet B Neuropsychiatr Genet
, vol.141 B
, pp. 409-413
-
-
Light, K.J.1
Joyce, P.R.2
Luty, S.E.3
Mulder, R.T.4
Frampton, C.M.5
Joyce, L.R.6
-
39
-
-
0027997172
-
Autism Diagnostic Interview- Revised: A revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders
-
Lord C, Rutter M, Le Couteur A. 1994. Autism Diagnostic Interview- Revised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders. J Autism Dev Disord 24: 659-685.
-
(1994)
J Autism Dev Disord
, vol.24
, pp. 659-685
-
-
Lord, C.1
Rutter, M.2
Le Couteur, A.3
-
41
-
-
0033802632
-
The autism diagnostic observation schedule-generic: A standard measure of social and communication deficits associated with the spectrum of autism
-
Lord C, Risi S, Lambrecht L. 2000b. The autism diagnostic observation schedule-generic: a standard measure of social and communication deficits associated with the spectrum of autism. J Autism Dev Disord 30: 205-223.
-
(2000)
J Autism Dev Disord
, vol.30
, pp. 205-223
-
-
Lord, C.1
Risi, S.2
Lambrecht, L.3
-
42
-
-
24144452995
-
Genome-wide and Ordered-Subset linkage analyses provide support for autism loci on 17q and 19p with evidence of phenotypic and interlocus genetic correlates
-
McCauley JL, Li C, Jiang L, Olson LM, Crockett G, Gainer K, et al. 2005. Genome-wide and Ordered-Subset linkage analyses provide support for autism loci on 17q and 19p with evidence of phenotypic and interlocus genetic correlates. BMC Med Genet 6: 1.
-
(2005)
BMC Med Genet
, vol.6
, pp. 1
-
-
McCauley, J.L.1
Li, C.2
Jiang, L.3
Olson, L.M.4
Crockett, G.5
Gainer, K.6
-
44
-
-
0024284028
-
A simple salting out procedure for extracting DNA from human nucleated cells
-
Miller SA, Dykes DD, Polesky HF. 1998. A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res 16: 1215.
-
(1998)
Nucleic Acids Res
, vol.16
, pp. 1215
-
-
Miller, S.A.1
Dykes, D.D.2
Polesky, H.F.3
-
45
-
-
2542503520
-
Serum neurotrophin concentrations in autism and mental retardation: A pilot study
-
Miyazaki K, Narita N, Sakuta R, Miyahara T, Naruse H, Okado N, et al. 2004. Serum neurotrophin concentrations in autism and mental retardation: a pilot study. Brain Dev 26: 292-295.
-
(2004)
Brain Dev
, vol.26
, pp. 292-295
-
-
Miyazaki, K.1
Narita, N.2
Sakuta, R.3
Miyahara, T.4
Naruse, H.5
Okado, N.6
-
46
-
-
33344470869
-
Selected neurotrophins, neuropeptides, and cytokines: Developmental trajectory and concentrations in neonatal blood of children with autism or Down syndrome
-
Nelson PG, Kuddo T, Song EY, Dambrosia JM, Kohler S, Satyanarayana G, et al. 2006. Selected neurotrophins, neuropeptides, and cytokines: developmental trajectory and concentrations in neonatal blood of children with autism or Down syndrome. Int J Dev Neurosci 24: 73-80.
-
(2006)
Int J Dev Neurosci
, vol.24
, pp. 73-80
-
-
Nelson, P.G.1
Kuddo, T.2
Song, E.Y.3
Dambrosia, J.M.4
Kohler, S.5
Satyanarayana, G.6
-
47
-
-
79955465675
-
The role of neurotrophic factors in autism
-
Nickl-Jockschat T, Michel TM. 2011. The role of neurotrophic factors in autism. Mol Psychiatry 16: 478-90.
-
(2011)
Mol Psychiatry
, vol.16
, pp. 478-490
-
-
Nickl-Jockschat, T.1
Michel, T.M.2
-
48
-
-
33745307542
-
Autistic disorder: Current psychopharmacological treatments and areas of interest for future developments
-
Nikolov R, Jonker J, Scahill L. 2006. Autistic disorder: current psychopharmacological treatments and areas of interest for future developments. Rev Bras Psiquiatr 28: 39-46.
-
(2006)
Rev Bras Psiquiatr
, vol.28
, pp. 39-46
-
-
Nikolov, R.1
Jonker, J.2
Scahill, L.3
-
49
-
-
33947106896
-
Genetic analyses of the brain-derived neurotrophic factor (BDNF) gene in autism
-
Nishimura K, Nakamura K, Anitha A, Yamada K, Tsujii M, Iwayama Y, et al. 2007. Genetic analyses of the brain-derived neurotrophic factor (BDNF) gene in autism. Biochem Biophys Res Commun 356: 200-206.
-
(2007)
Biochem Biophys Res Commun
, vol.356
, pp. 200-206
-
-
Nishimura, K.1
Nakamura, K.2
Anitha, A.3
Yamada, K.4
Tsujii, M.5
Iwayama, Y.6
-
50
-
-
77955563933
-
Disruption at the PTCHD1 locus on Xp22.11 in autism spectrum disorder and intellectual disability
-
Noor A, Whibley A, Marshall CR, Gianakopoulos PJ, Piton A, Carson AR, et al. 2010. Disruption at the PTCHD1 locus on Xp22.11 in autism spectrum disorder and intellectual disability. Sci Transl Med 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
Carson, A.R.6
-
51
-
-
71549168918
-
The dopamine D3 receptor (DRD3) gene and risk of schizophrenia: Case-control studies and an updated meta-analysis
-
Nunokawa A, Watanabe Y, Kaneko N, Sugai T, Yazaki S, Arinami T, et al. 2010. The dopamine D3 receptor (DRD3) gene and risk of schizophrenia: case-control studies and an updated meta-analysis. Schizophr Res 116: 61-67.
-
(2010)
Schizophr Res
, vol.116
, pp. 61-67
-
-
Nunokawa, A.1
Watanabe, Y.2
Kaneko, N.3
Sugai, T.4
Yazaki, S.5
Arinami, T.6
-
52
-
-
58149472708
-
HTR1B and HTR2C in autism spectrum disorders in Brazilian families
-
Orabona GM, Griesi-Oliveira K, Vadasz E, Bulc ã o VL, Takahashi VN, Moreira ES, et al. 2008. HTR1B and HTR2C in autism spectrum disorders in Brazilian families. Brain Res 1250: 14-19.
-
(2008)
Brain Res
, vol.1250
, pp. 14-19
-
-
Orabona, G.M.1
Griesi-Oliveira, K.2
Vadasz, E.3
Bulcão, V.L.4
Takahashi, V.N.5
Moreira, E.S.6
-
53
-
-
51449104158
-
Altered expression of neurotrophic factors in patients with major depression
-
Otsuki K, Uchida S, Watanuki T, Wakabayashi Y, Fujimoto M, Matsubara T, et al. 2008. Altered expression of neurotrophic factors in patients with major depression. J Psychiatr Res 42: 1145-1153.
-
(2008)
J Psychiatr Res
, vol.42
, pp. 1145-1153
-
-
Otsuki, K.1
Uchida, S.2
Watanuki, T.3
Wakabayashi, Y.4
Fujimoto, M.5
Matsubara, T.6
-
55
-
-
77954657070
-
Functional impact of global rare copy number variation in autism spectrum disorders
-
Pinto D, Pagnamenta AT, Klei L, Anney R, Merico D, Regan R, et al. 2010. Functional impact of global rare copy number variation in autism spectrum disorders. Nature 466: 368-372.
-
(2010)
Nature
, vol.466
, pp. 368-372
-
-
Pinto, D.1
Pagnamenta, A.T.2
Klei, L.3
Anney, R.4
Merico, D.5
Regan, R.6
-
56
-
-
0034118493
-
Inference of population structure using multilocus genotype data
-
Pritchard JK, Stephens M, Donnelly P. 2000. Inference of population structure using multilocus genotype data. Genetics 155: 945-959.
-
(2000)
Genetics
, vol.155
, pp. 945-959
-
-
Pritchard, J.K.1
Stephens, M.2
Donnelly, P.3
-
57
-
-
33749010358
-
Neurotrophin-regulated signalling pathways
-
Reichardt LF. 2006. Neurotrophin-regulated signalling pathways. Phil Trans R Soc Lond B Biol Sci 361: 1545-1564.
-
(2006)
Phil Trans R Soc Lond B Biol Sci
, vol.361
, pp. 1545-1564
-
-
Reichardt, L.F.1
-
58
-
-
42649105795
-
Association study of 10 genes encoding neurotrophic factors and their receptors in adult and child attention-deficit/hyperactivity disorder
-
Ribasé s M, Hervás A, Ramos-Quiroga JA, Bosch R, Bielsa A, Gastaminza X. et al. 2008. Association study of 10 genes encoding neurotrophic factors and their receptors in adult and child attention-deficit/hyperactivity disorder. Biol Psychiatry 63: 935-945.
-
(2008)
Biol Psychiatry
, vol.63
, pp. 935-945
-
-
Ribasés, M.1
Hervás, A.2
Ramos-Quiroga, J.A.3
Bosch, R.4
Bielsa, A.5
Gastaminza, X.6
-
59
-
-
58049204451
-
Exploration of 19 serotoninergic candidate genes in adults and children with attention-deficit/ hyperactivity disorder identifies association for 5HT2A, DDC and MAOB
-
Ribasé s M, Ramos-Quiroga JA, Hervás A, Bosch R, Bielsa A, Gastaminza X, et al. 2009. Exploration of 19 serotoninergic candidate genes in adults and children with attention-deficit/ hyperactivity disorder identifies association for 5HT2A, DDC and MAOB. Mol Psychiatry 14: 71-85.
-
(2009)
Mol Psychiatry
, vol.14
, pp. 71-85
-
-
Ribasés, M.1
Ramos-Quiroga, J.A.2
Hervás, A.3
Bosch, R.4
Bielsa, A.5
Gastaminza, X.6
-
60
-
-
77950859884
-
Shared heritability of attention-deficit/hyperactivity disorder and autism spectrum disorder
-
Rommelse NN, Franke B, Geurts HM, Hartman CA, Buitelaar JK. 2010. Shared heritability of attention-deficit/hyperactivity disorder and autism spectrum disorder. Eur Child Adolesc Psychiatry 19: 281-295.
-
(2010)
Eur Child Adolesc Psychiatry
, vol.19
, pp. 281-295
-
-
Rommelse, N.N.1
Franke, B.2
Geurts, H.M.3
Hartman, C.A.4
Buitelaar, J.K.5
-
62
-
-
33646557707
-
A multiplex assay with 52 single nucleotide polymorphisms for human identification
-
Sanchez JJ, Phillips C, Borsting C, Balogh K, Bogus M, Fondevila M, et al. 2006. A multiplex assay with 52 single nucleotide polymorphisms for human identification. Electrophoresis 27: 1713-1724.
-
(2006)
Electrophoresis
, vol.27
, pp. 1713-1724
-
-
Sanchez, J.J.1
Phillips, C.2
Borsting, C.3
Balogh, K.4
Bogus, M.5
Fondevila, M.6
-
63
-
-
50049123572
-
Role of serotonin and dopamine system interactions in the neurobiology of impulsive aggression and its comorbidity with other clinical disorders
-
Seo D, Patrick CJ, Kennealy PJ. 2008. Role of serotonin and dopamine system interactions in the neurobiology of impulsive aggression and its comorbidity with other clinical disorders. Aggress Violent Behav 13: 383-395.
-
(2008)
Aggress Violent Behav
, vol.13
, pp. 383-395
-
-
Seo, D.1
Patrick, C.J.2
Kennealy, P.J.3
-
64
-
-
31744435871
-
Joint analysis is more efficient than replication-based analysis for two-stage genome-wide association studies
-
Skol AD, Scott LJ, Abecasis GR, Boehnke M. 2006. Joint analysis is more efficient than replication-based analysis for two-stage genome-wide association studies. Nat Genet 38: 209-213.
-
(2006)
Nat Genet
, vol.38
, pp. 209-213
-
-
Skol, A.D.1
Scott, L.J.2
Abecasis, G.R.3
Boehnke, M.4
-
65
-
-
0036020892
-
A direct approach to false discovery rates
-
Storey J. 2002. A direct approach to false discovery rates. J R Stat Soc Ser B 64: 479-498.
-
(2002)
J R Stat Soc ser B
, vol.64
, pp. 479-498
-
-
Storey, J.1
-
66
-
-
33847327313
-
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
-
Szatmari P, Paterson AD, Zwaigenbaum L, Roberts W, Brian J, Liu XQ et al. 2007. Mapping autism risk loci using genetic linkage and chromosomal rearrangements. Nat Genet 39: 319-328.
-
(2007)
Nat Genet
, vol.39
, pp. 319-328
-
-
Szatmari, P.1
Paterson, A.D.2
Zwaigenbaum, L.3
Roberts, W.4
Brian, J.5
Liu, X.Q.6
-
67
-
-
33845303175
-
ESPERR: Learning strong and weak signals in genomic sequence alignments to identify functional elements
-
Taylor J, Tyekucheva S, King DC, Hardison RC, Miller W, Chiaromonte F. 2006. ESPERR: learning strong and weak signals in genomic sequence alignments to identify functional elements. Genome Res 16: 1596-1604.
-
(2006)
Genome Res
, vol.16
, pp. 1596-1604
-
-
Taylor, J.1
Tyekucheva, S.2
King, D.C.3
Hardison, R.C.4
Miller, W.5
Chiaromonte, F.6
-
68
-
-
33645741145
-
The SNPlex genotyping system: A flexible and scalable platform for SNP genotyping
-
Tobler AR, Short S, Andersen MR, Paner TM, Briggs JC, Lambert SM, et al. 2005. The SNPlex genotyping system: a flexible and scalable platform for SNP genotyping. J Biomol Tech 16: 398-406.
-
(2005)
J Biomol Tech
, vol.16
, pp. 398-406
-
-
Tobler, A.R.1
Short, S.2
Andersen, M.R.3
Paner, T.M.4
Briggs, J.C.5
Lambert, S.M.6
-
69
-
-
0042413754
-
The role of serotonin in early cortical development
-
Vitalis T, Parnavelas JG. 2003. The role of serotonin in early cortical development. Dev Neurosci 25: 245-256.
-
(2003)
Dev Neurosci
, vol.25
, pp. 245-256
-
-
Vitalis, T.1
Parnavelas, J.G.2
-
71
-
-
0035826462
-
De novo partial duplication of chromosome 7p in a male with autistic disorder
-
Wolpert CM, Donnelly SL, Cuccaro ML, Hedges DJ, Poole CP, Wright HH, et al. 2001. De novo partial duplication of chromosome 7p in a male with autistic disorder. Am J Med Genet 105: 222-225.
-
(2001)
Am J Med Genet
, vol.105
, pp. 222-225
-
-
Wolpert, C.M.1
Donnelly, S.L.2
Cuccaro, M.L.3
Hedges, D.J.4
Poole, C.P.5
Wright, H.H.6
-
72
-
-
0142059641
-
A genomewide screen of 345 families for autismsusceptibility loci
-
Yonan AL, Alarcon M, Cheng R, Magnusson PK, Spence SJ, Palmer AA, et al. 2003. A genomewide screen of 345 families for autismsusceptibility loci. Am J Hum Genet 73: 886-897.
-
(2003)
Am J Hum Genet
, vol.73
, pp. 886-897
-
-
Yonan, A.L.1
Alarcon, M.2
Cheng, R.3
Magnusson, P.K.4
Spence, S.J.5
Palmer, A.A.6
-
73
-
-
60049092473
-
Family- and population-based association studies of monoamine oxidase A and autism spectrum disorders in Korean
-
Yoo HJ, Lee SK, Park M, Cho IH, Hyun SH, Lee JC, et al. 2009. Family- and population-based association studies of monoamine oxidase A and autism spectrum disorders in Korean. Neurosci Res 63: 172-176.
-
(2009)
Neurosci Res
, vol.63
, pp. 172-176
-
-
Yoo, H.J.1
Lee, S.K.2
Park, M.3
Cho, I.H.4
Hyun, S.H.5
Lee, J.C.6
|