-
1
-
-
84918523899
-
The relationship of HLA class I and II alleles and haplotypes with autism: a case control Study
-
Al-Hakbany M., Awadallah S., Al-Ayadhi L. The relationship of HLA class I and II alleles and haplotypes with autism: a case control Study. Autism Res. Treat. 2014, 2014:242048. 10.1155/2014/242048.
-
(2014)
Autism Res. Treat.
, vol.2014
, pp. 242048
-
-
Al-Hakbany, M.1
Awadallah, S.2
Al-Ayadhi, L.3
-
2
-
-
48949094665
-
Autism and the environment: challenges and opportunities for research
-
Altevogt B.M., Hanson S.L., Leshner A.I. Autism and the environment: challenges and opportunities for research. Pediatrics 2008, 121:1225-1229.
-
(2008)
Pediatrics
, vol.121
, pp. 1225-1229
-
-
Altevogt, B.M.1
Hanson, S.L.2
Leshner, A.I.3
-
3
-
-
84870465485
-
Diagnostic and Statistical Manual of Mental Disorders
-
fourth ed. Washington, DC
-
American Psychiatric Association, 1994. Diagnostic and Statistical Manual of Mental Disorders, fourth ed. Washington, DC.
-
(1994)
-
-
-
4
-
-
79957896374
-
Altered T cell responses in children with autism
-
Ashwood P., Krakowiak P., Hertz-Picciotto I., Pessah I.N., Van de Water J. Altered T cell responses in children with autism. Brain Behav. Immun. 2010, 25:840-849.
-
(2010)
Brain Behav. Immun.
, vol.25
, pp. 840-849
-
-
Ashwood, P.1
Krakowiak, P.2
Hertz-Picciotto, I.3
Pessah, I.N.4
Van de Water, J.5
-
5
-
-
67749109981
-
Association of family history of autoimmune diseases and autism spectrum disorders
-
Atladóttir H.O., Pedersen M.G., Thorsen P., Mortensen P.B., Deleuran B., Eaton W.W., et al. Association of family history of autoimmune diseases and autism spectrum disorders. Pediatrics 2009, 124:687-694.
-
(2009)
Pediatrics
, vol.124
, pp. 687-694
-
-
Atladóttir, H.O.1
Pedersen, M.G.2
Thorsen, P.3
Mortensen, P.B.4
Deleuran, B.5
Eaton, W.W.6
-
6
-
-
27644506085
-
Sex differences in the brain: implications for explaining autism
-
(Review)
-
Baron-Cohen S., Knickmeyer R.C., Belmonte M.K. Sex differences in the brain: implications for explaining autism. Science 2005, 4:819-823. (Review).
-
(2005)
Science
, vol.4
, pp. 819-823
-
-
Baron-Cohen, S.1
Knickmeyer, R.C.2
Belmonte, M.K.3
-
7
-
-
0033431844
-
Prenatal and perinatal risk factors for autism
-
Burd L., Severud R., Kerbeshian J., Klug M.G. Prenatal and perinatal risk factors for autism. J. Perinat. Med. 1999, 27:441-450.
-
(1999)
J. Perinat. Med.
, vol.27
, pp. 441-450
-
-
Burd, L.1
Severud, R.2
Kerbeshian, J.3
Klug, M.G.4
-
8
-
-
0242671604
-
HLA-G molecules: from maternal-fetal tolerance to tissue acceptance
-
(Review)
-
Carosella E.D., Moreau P., Le Maoult J., Le Discorde M., Dausset J., Rouas-Freiss N. HLA-G molecules: from maternal-fetal tolerance to tissue acceptance. Adv. Immunol. 2003, 81:199-252. (Review).
-
(2003)
Adv. Immunol.
, vol.81
, pp. 199-252
-
-
Carosella, E.D.1
Moreau, P.2
Le Maoult, J.3
Le Discorde, M.4
Dausset, J.5
Rouas-Freiss, N.6
-
9
-
-
46749123555
-
Beyond the increasing complexity of the immunomodulatory HLA-G molecule
-
Carosella E.D., Favier B., Rouas-Freiss N., Moreau P., LeMaoult J. Beyond the increasing complexity of the immunomodulatory HLA-G molecule. Blood 2008, 111:4862-4870.
-
(2008)
Blood
, vol.111
, pp. 4862-4870
-
-
Carosella, E.D.1
Favier, B.2
Rouas-Freiss, N.3
Moreau, P.4
LeMaoult, J.5
-
10
-
-
70350702674
-
In silico analysis of microRNAS targeting the HLA-G 3' untranslated region alleles and haplotypes
-
Castelli E.C., Moreau P., Oya e Chiromatzo A., Mendes-Junior C.T., Veiga-Castelli L.C., Yaghi L. In silico analysis of microRNAS targeting the HLA-G 3' untranslated region alleles and haplotypes. Hum. Immunol. 2009, 70:1020-1025.
-
(2009)
Hum. Immunol.
, vol.70
, pp. 1020-1025
-
-
Castelli, E.C.1
Moreau, P.2
Oya e Chiromatzo, A.3
Mendes-Junior, C.T.4
Veiga-Castelli, L.C.5
Yaghi, L.6
-
11
-
-
77649335964
-
The genetic structure of 3' untranslated region of the HLA-G gene: polymorphisms and haplotypes
-
Castelli E.C., Mendes-Junior C.T., Deghaide N.H., de Albuquerque R.S., Muniz Y.C., Simoes R.T., et al. The genetic structure of 3' untranslated region of the HLA-G gene: polymorphisms and haplotypes. Genes Immun. 2010, 11:134-141.
-
(2010)
Genes Immun.
, vol.11
, pp. 134-141
-
-
Castelli, E.C.1
Mendes-Junior, C.T.2
Deghaide, N.H.3
de Albuquerque, R.S.4
Muniz, Y.C.5
Simoes, R.T.6
-
12
-
-
84862330211
-
Maternal homozygocity for a 14 base pair insertion in exon 8 of the HLA-G gene and carriage of HLA class II alleles restricting HY immunity predispose to unexplained secondary recurrent miscarriage and low birth weight in children born to these patients
-
Christiansen O.B., Kolte A.M., Dahl M., Larsen E.C., Steffensen R., Nielsen H.S., Hviid T.V. Maternal homozygocity for a 14 base pair insertion in exon 8 of the HLA-G gene and carriage of HLA class II alleles restricting HY immunity predispose to unexplained secondary recurrent miscarriage and low birth weight in children born to these patients. Hum. Immunol. 2012, 73:699-705. 10.1016/j.humimm.2012.04.014.
-
(2012)
Hum. Immunol.
, vol.73
, pp. 699-705
-
-
Christiansen, O.B.1
Kolte, A.M.2
Dahl, M.3
Larsen, E.C.4
Steffensen, R.5
Nielsen, H.S.6
Hviid, T.V.7
-
13
-
-
0032989380
-
Familial clustering of autoimmune disorders and evaluation of medical risk factors in autism
-
Comi A.M., Zimmerman A.W., Frye V.H., Law P.A., Peeden J.N. Familial clustering of autoimmune disorders and evaluation of medical risk factors in autism. J. Child Neurol. 1999, 14:388-394.
-
(1999)
J. Child Neurol.
, vol.14
, pp. 388-394
-
-
Comi, A.M.1
Zimmerman, A.W.2
Frye, V.H.3
Law, P.A.4
Peeden, J.N.5
-
14
-
-
13244275092
-
Maternal autoimmune diseases, asthma and allergies, and childhood autism spectrum disorders: a case-control study
-
Croen L.A., Grether J.K., Yoshida C.K., Odouli R., van de Water J.V. Maternal autoimmune diseases, asthma and allergies, and childhood autism spectrum disorders: a case-control study. Arch. Pediatr. Adolesc. Med. 2005, 159:151-157.
-
(2005)
Arch. Pediatr. Adolesc. Med.
, vol.159
, pp. 151-157
-
-
Croen, L.A.1
Grether, J.K.2
Yoshida, C.K.3
Odouli, R.4
van de Water, J.V.5
-
15
-
-
79951550728
-
Implications of the polymorphism of HLA-G on its function, regulation, evolution and disease association
-
Donadi E.A., Castelli E.C., Arnaiz-Villena A., Roger M., Rey D., Moreau P. Implications of the polymorphism of HLA-G on its function, regulation, evolution and disease association. Cell. Mol. Life Sci. 2011, 68:369-395.
-
(2011)
Cell. Mol. Life Sci.
, vol.68
, pp. 369-395
-
-
Donadi, E.A.1
Castelli, E.C.2
Arnaiz-Villena, A.3
Roger, M.4
Rey, D.5
Moreau, P.6
-
16
-
-
84892771719
-
The role of prenatal immune activation in the pathogenesis of autism and schizophrenia: a literature review
-
Easson A., Woodbury-Smith M. The role of prenatal immune activation in the pathogenesis of autism and schizophrenia: a literature review. Res. Autism Spect. Dis. 2014, 8:312-316.
-
(2014)
Res. Autism Spect. Dis.
, vol.8
, pp. 312-316
-
-
Easson, A.1
Woodbury-Smith, M.2
-
17
-
-
0021054170
-
Parental reproductive problems and gestational hormonal exposure in autistic and schizophrenic children
-
Funderburk S.J., Carter J., Tanguay P., Freeman B.J., Westlake J.R. Parental reproductive problems and gestational hormonal exposure in autistic and schizophrenic children. J. Autism Dev. Disord. 1983, 1:325-332.
-
(1983)
J. Autism Dev. Disord.
, vol.1
, pp. 325-332
-
-
Funderburk, S.J.1
Carter, J.2
Tanguay, P.3
Freeman, B.J.4
Westlake, J.R.5
-
18
-
-
84905582433
-
Most genetic risk for autism resides with common variation
-
(Epub)
-
Gaugler T., Klei L., Sanders S.J., Bodea C.A., Goldberg A.P., Lee A.B., et al. Most genetic risk for autism resides with common variation. Nat. Genet. 2014, 46:881-885. (Epub). 10.1038/ng.3039.
-
(2014)
Nat. Genet.
, vol.46
, pp. 881-885
-
-
Gaugler, T.1
Klei, L.2
Sanders, S.J.3
Bodea, C.A.4
Goldberg, A.P.5
Lee, A.B.6
-
19
-
-
84881375626
-
Immunological and autoimmune considerations of autism spectrum disorders
-
Gesundheit B., Rosenzweig J.P., Naor D., Lerer B., Zachor D.A., Procházka V., et al. Immunological and autoimmune considerations of autism spectrum disorders. J. Autoimmun. 2013, 44:1-7. 10.1016/j.jaut.2013.05.005. Review.
-
(2013)
J. Autoimmun.
, vol.44
, pp. 1-7
-
-
Gesundheit, B.1
Rosenzweig, J.P.2
Naor, D.3
Lerer, B.4
Zachor, D.A.5
Procházka, V.6
-
20
-
-
61549105327
-
Family-based transmission analysis of HLA genetic markers in Sardinian children with autistic spectrum disorders
-
Guerini F.R., Bolognesi E., Manca S., Sotgiu S., Zanzottera M., Agliardi C., et al. Family-based transmission analysis of HLA genetic markers in Sardinian children with autistic spectrum disorders. Hum. Immunol. 2009, 70:184-190.
-
(2009)
Hum. Immunol.
, vol.70
, pp. 184-190
-
-
Guerini, F.R.1
Bolognesi, E.2
Manca, S.3
Sotgiu, S.4
Zanzottera, M.5
Agliardi, C.6
-
21
-
-
78650991968
-
HLA polymorphisms in Italian children with autism spectrum disorders: results of a family based linkage study
-
Guerini F.R., Bolognesi E., Chiappedi M., De Silvestri A., Ghezzo A., Zanette M., et al. HLA polymorphisms in Italian children with autism spectrum disorders: results of a family based linkage study. J. Neuroimmunol. 2011, 230:135-142.
-
(2011)
J. Neuroimmunol.
, vol.230
, pp. 135-142
-
-
Guerini, F.R.1
Bolognesi, E.2
Chiappedi, M.3
De Silvestri, A.4
Ghezzo, A.5
Zanette, M.6
-
22
-
-
84891826729
-
Activating KIR molecules and their cognate ligands prevail in children with a diagnosis of ASD and in their mothers
-
Guerini F.R., Bolognesi E., Chiappedi M., Manca S., Ghezzo A., Agliardi C., et al. Activating KIR molecules and their cognate ligands prevail in children with a diagnosis of ASD and in their mothers. Brain Behav. Immun. 2014, 36:54-60. 10.1016/j.bbi.2013.10.006.
-
(2014)
Brain Behav. Immun.
, vol.36
, pp. 54-60
-
-
Guerini, F.R.1
Bolognesi, E.2
Chiappedi, M.3
Manca, S.4
Ghezzo, A.5
Agliardi, C.6
-
23
-
-
0036075527
-
Sharing of a conserved haplotype suggests a susceptibility gene for multiple sclerosis at chromosome 17p11
-
He B., Giedraitis V., Ligers A., Binzer M., Andersen P.M., Forsgren L., et al. Sharing of a conserved haplotype suggests a susceptibility gene for multiple sclerosis at chromosome 17p11. Eur. J. Hum. Genet. 2002, 10:271-275.
-
(2002)
Eur. J. Hum. Genet.
, vol.10
, pp. 271-275
-
-
He, B.1
Giedraitis, V.2
Ligers, A.3
Binzer, M.4
Andersen, P.M.5
Forsgren, L.6
-
24
-
-
0036702469
-
HLA-G polymorphisms in couples with recurrent spontaneous abortions
-
Hviid T.V., Hylenius S., Hoegh A.M., Kruse C., Christiansen O.B. HLA-G polymorphisms in couples with recurrent spontaneous abortions. Tissue Antigens 2002, 60:122-132.
-
(2002)
Tissue Antigens
, vol.60
, pp. 122-132
-
-
Hviid, T.V.1
Hylenius, S.2
Hoegh, A.M.3
Kruse, C.4
Christiansen, O.B.5
-
25
-
-
3042698491
-
Association between human leukocyte antigen-G genotype and success of in vitro fertilization and pregnancy outcome
-
Hviid T.V., Hylenius S., Lindhard A., Christiansen O.B. Association between human leukocyte antigen-G genotype and success of in vitro fertilization and pregnancy outcome. Tissue Antigens 2004, 64:66-69.
-
(2004)
Tissue Antigens
, vol.64
, pp. 66-69
-
-
Hviid, T.V.1
Hylenius, S.2
Lindhard, A.3
Christiansen, O.B.4
-
26
-
-
1842428164
-
Association between HLA-G genotype and risk of pre-eclampsia: a case-control study using family triads
-
Hylenius S., Andersen A.M., Melbye M., Hviid T.V. Association between HLA-G genotype and risk of pre-eclampsia: a case-control study using family triads. Mol. Hum. Reprod. 2004, 10:237-246.
-
(2004)
Mol. Hum. Reprod.
, vol.10
, pp. 237-246
-
-
Hylenius, S.1
Andersen, A.M.2
Melbye, M.3
Hviid, T.V.4
-
27
-
-
0141886193
-
KIR2DL4 is an IL-2-regulated NK cell receptor that exhibits limited expression in humans but triggers strong IFN-gamma production
-
Kikuchi-Maki A., Yusa S., Catina T.L., Campbell K.S. KIR2DL4 is an IL-2-regulated NK cell receptor that exhibits limited expression in humans but triggers strong IFN-gamma production. J. Immunol. 2003, 171:3415-3425.
-
(2003)
J. Immunol.
, vol.171
, pp. 3415-3425
-
-
Kikuchi-Maki, A.1
Yusa, S.2
Catina, T.L.3
Campbell, K.S.4
-
28
-
-
84900867577
-
Activating killer cell Ig-like receptors in health and disease
-
Martin A.I., Michaëlsson J., Fauriat C. Activating killer cell Ig-like receptors in health and disease. Front. Immunol. 2014, 5:184.
-
(2014)
Front. Immunol.
, vol.5
, pp. 184
-
-
Martin, A.I.1
Michaëlsson, J.2
Fauriat, C.3
-
29
-
-
0029759714
-
Characterization of type 1 and type 2 cytokine production profile in physiologic and pathologic human pregnancy
-
Marzi M., Vigano A., Trabattoni D., Villa M.L., Salvaggio A., Clerici E., Clerici M. Characterization of type 1 and type 2 cytokine production profile in physiologic and pathologic human pregnancy. Clin. Exp. Immunol. 1996, 106:127-133.
-
(1996)
Clin. Exp. Immunol.
, vol.106
, pp. 127-133
-
-
Marzi, M.1
Vigano, A.2
Trabattoni, D.3
Villa, M.L.4
Salvaggio, A.5
Clerici, E.6
Clerici, M.7
-
30
-
-
33745841346
-
The miscarriage-associated HLA-G-725G allele influences transcription rates in JEG-3 cells
-
Ober C., Billstrand C., Kuldanek S., Tan Z. The miscarriage-associated HLA-G-725G allele influences transcription rates in JEG-3 cells. Hum. Reprod. 2006, 21:1743-1748.
-
(2006)
Hum. Reprod.
, vol.21
, pp. 1743-1748
-
-
Ober, C.1
Billstrand, C.2
Kuldanek, S.3
Tan, Z.4
-
31
-
-
0035197109
-
Altered HLA-G transcription in pre-eclampsia is associated with allele specific inheritance: possible role of the HLA-G gene in susceptibility to the disease
-
O'Brien M., McCarthy T., Jenkins D., Paul P., Dausset J., Carosella E.D., et al. Altered HLA-G transcription in pre-eclampsia is associated with allele specific inheritance: possible role of the HLA-G gene in susceptibility to the disease. Cell. Mol. Life Sci. 2001, 58:1943-1949.
-
(2001)
Cell. Mol. Life Sci.
, vol.58
, pp. 1943-1949
-
-
O'Brien, M.1
McCarthy, T.2
Jenkins, D.3
Paul, P.4
Dausset, J.5
Carosella, E.D.6
-
32
-
-
84906848480
-
HLA-G-mediated NK cell senescence promotes vascular remodeling: implications for reproduction
-
Rajagopalan S. HLA-G-mediated NK cell senescence promotes vascular remodeling: implications for reproduction. Cell. Mol. Immunol. 2014, 5:460-466. 10.1038/cmi.2014.53.
-
(2014)
Cell. Mol. Immunol.
, vol.5
, pp. 460-466
-
-
Rajagopalan, S.1
-
33
-
-
70350575737
-
An autistic endophenotype results in complex immune dysfunction in healthy siblings of autistic children
-
Saresella M., Marventano I., Guerini F.R., Mancuso R., Ceresa L., Zanzottera M., et al. An autistic endophenotype results in complex immune dysfunction in healthy siblings of autistic children. Biol. Psychiatry 2009, 66:978-984. 10.1016/j.biopsych.2009.06.020.
-
(2009)
Biol. Psychiatry
, vol.66
, pp. 978-984
-
-
Saresella, M.1
Marventano, I.2
Guerini, F.R.3
Mancuso, R.4
Ceresa, L.5
Zanzottera, M.6
-
34
-
-
48949097186
-
Birth weight and gestational age characteristics of children with autism, including a comparison with other developmental disabilities
-
Schendel D., Bhasin T.K. Birth weight and gestational age characteristics of children with autism, including a comparison with other developmental disabilities. Pediatrics 2008, 121:1155-1164.
-
(2008)
Pediatrics
, vol.121
, pp. 1155-1164
-
-
Schendel, D.1
Bhasin, T.K.2
-
35
-
-
58849104457
-
The HLA genomic loci map: expression, interaction, diversity and disease
-
Shiina T., Hosomichi K., Inoko H., Kulski J.K. The HLA genomic loci map: expression, interaction, diversity and disease. J. Hum. Genet. 2009, 54:15-39.
-
(2009)
J. Hum. Genet.
, vol.54
, pp. 15-39
-
-
Shiina, T.1
Hosomichi, K.2
Inoko, H.3
Kulski, J.K.4
-
36
-
-
0027220071
-
Antibodies to myelin basic protein in children with autistic behavior
-
Singh V.K., Warren R.P., Odell J.D., Warren W.L., Cole P. Antibodies to myelin basic protein in children with autistic behavior. Brain Behav. Immun. 1993, 7:97-103.
-
(1993)
Brain Behav. Immun.
, vol.7
, pp. 97-103
-
-
Singh, V.K.1
Warren, R.P.2
Odell, J.D.3
Warren, W.L.4
Cole, P.5
-
37
-
-
36949009649
-
HLA-G polymorphism in a Polish population and reproductive failure
-
Sipak-Szmigiel O., Cybulski C., Lubinski J., Ronin-Walknowska E. HLA-G polymorphism in a Polish population and reproductive failure. Tissue Antigens 2008, 71:67-71.
-
(2008)
Tissue Antigens
, vol.71
, pp. 67-71
-
-
Sipak-Szmigiel, O.1
Cybulski, C.2
Lubinski, J.3
Ronin-Walknowska, E.4
-
38
-
-
0032924243
-
Genomic imprinting of the X chromosome: a novel mechanism for the evolution of sexual dimorphism
-
(Review)
-
Skuse D.H. Genomic imprinting of the X chromosome: a novel mechanism for the evolution of sexual dimorphism. J. Lab. Clin. Med. 1999, 133:23-32. (Review).
-
(1999)
J. Lab. Clin. Med.
, vol.133
, pp. 23-32
-
-
Skuse, D.H.1
-
39
-
-
17444421587
-
X-linked genes and mental functioning
-
(Review)
-
Skuse D.H. X-linked genes and mental functioning. Hum. Mol. Genet. 2005, 15(14 Spec No 1):R27-R32. (Review).
-
(2005)
Hum. Mol. Genet.
, vol.15
, Issue.14 SPEC NO. 1
, pp. R27-R32
-
-
Skuse, D.H.1
-
40
-
-
0027377799
-
Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM)
-
Spielman R.S., McGinnis R.E., Ewens W.J. Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM). Am. J. Hum. Genet. 1993, 52:506.
-
(1993)
Am. J. Hum. Genet.
, vol.52
, pp. 506
-
-
Spielman, R.S.1
McGinnis, R.E.2
Ewens, W.J.3
-
41
-
-
82255192290
-
The conundrums of understanding genetic risks for autism spectrum disorders
-
(Review)
-
State M.W., Levitt P. The conundrums of understanding genetic risks for autism spectrum disorders. Nat. Neurosci. 2011, 14:1499-1506. (Review). 10.1038/nn.2924.
-
(2011)
Nat. Neurosci.
, vol.14
, pp. 1499-1506
-
-
State, M.W.1
Levitt, P.2
-
42
-
-
0642343891
-
High blood monocyte counts and neopterin levels in children with autistic disorder
-
Sweeten T.L., Posey D.J., McDougle C.J. High blood monocyte counts and neopterin levels in children with autistic disorder. Am. Psychiatry. 2003, 160:1691-1693.
-
(2003)
Am. Psychiatry.
, vol.160
, pp. 1691-1693
-
-
Sweeten, T.L.1
Posey, D.J.2
McDougle, C.J.3
-
43
-
-
28744446297
-
Evidence of balancing selection at the HLA-G promoter region
-
Tan Z., Shon A.M., Ober C. Evidence of balancing selection at the HLA-G promoter region. Hum. Mol. Genet. 2005, 14:3619-3628.
-
(2005)
Hum. Mol. Genet.
, vol.14
, pp. 3619-3628
-
-
Tan, Z.1
Shon, A.M.2
Ober, C.3
-
44
-
-
35348992063
-
Allele-specific targeting of microRNAs to HLA-G and risk of asthma
-
(Erratum. In: Am J Hum Genet. 2008, 82, 251)
-
Tan Z., Randall G., Fan J., Camoretti-Mercado B., Brockman-Schneider R., Pan L., et al. Allele-specific targeting of microRNAs to HLA-G and risk of asthma. Am. J. Hum. Genet. 2007, 81:829-834. (Erratum. In: Am J Hum Genet. 2008, 82, 251).
-
(2007)
Am. J. Hum. Genet.
, vol.81
, pp. 829-834
-
-
Tan, Z.1
Randall, G.2
Fan, J.3
Camoretti-Mercado, B.4
Brockman-Schneider, R.5
Pan, L.6
-
45
-
-
84865621248
-
Activating killer-cell immunoglobulin-like receptors (KIR) and their cognate HLA ligands are significantly increased in autism
-
Torres A.R., Westover J.B., Gibbons C., Johnson R.C., Ward D.C. Activating killer-cell immunoglobulin-like receptors (KIR) and their cognate HLA ligands are significantly increased in autism. Brain Behav. Immun. 2012, 26:1122-1127. 10.1016/j.bbi.2012.07.014.
-
(2012)
Brain Behav. Immun.
, vol.26
, pp. 1122-1127
-
-
Torres, A.R.1
Westover, J.B.2
Gibbons, C.3
Johnson, R.C.4
Ward, D.C.5
-
47
-
-
79955769107
-
Association of HLA-G alleles and 3' UTR 14bp haplotypes with recurrent miscarriage in Brazilian couples
-
Vargas R.G., Sarturi P.R., Mattar S.B., Bompeixe E.P., Silva Jdos S., Pirri A., et al. Association of HLA-G alleles and 3' UTR 14bp haplotypes with recurrent miscarriage in Brazilian couples. Hum. Immunol. 2011, 72:479-485.
-
(2011)
Hum. Immunol.
, vol.72
, pp. 479-485
-
-
Vargas, R.G.1
Sarturi, P.R.2
Mattar, S.B.3
Bompeixe, E.P.4
Silva, J.S.5
Pirri, A.6
-
48
-
-
84872668347
-
Association of 14-bp insertion/deletion polymorphism of HLA-G gene with unexplained recurrent spontaneous abortion: a meta-analysis
-
Wang X., Jiang W., Zhang D. Association of 14-bp insertion/deletion polymorphism of HLA-G gene with unexplained recurrent spontaneous abortion: a meta-analysis. Tissue Antigens 2013, 81:108-115. 10.1111/tan.12056.
-
(2013)
Tissue Antigens
, vol.81
, pp. 108-115
-
-
Wang, X.1
Jiang, W.2
Zhang, D.3
-
49
-
-
0030200135
-
Strong association of the third hypervariable region of the HLA-DR1 with autism
-
Warren R.P., Odell J.D., Warren W.L., Burger R.A., Maciulis A., Daniels W.W., et al. Strong association of the third hypervariable region of the HLA-DR1 with autism. J. Neuroimmunol. 1996, 67:97-102.
-
(1996)
J. Neuroimmunol.
, vol.67
, pp. 97-102
-
-
Warren, R.P.1
Odell, J.D.2
Warren, W.L.3
Burger, R.A.4
Maciulis, A.5
Daniels, W.W.6
-
50
-
-
84918515969
-
Immune dysfunction in autism spectrum disorder. In: Valsamma Eapen (Ed.), Autism - A Neurodevelopmental Journey from Genes to Behaviour
-
Available from
-
Westover, J.B., Sweeten, T.L., Benson, M., Bray-Ward, P., Torres, A.R., 2011. Immune dysfunction in autism spectrum disorder. In: Valsamma Eapen (Ed.), Autism - A Neurodevelopmental Journey from Genes to Behaviour. InTech. Available from. http://www.intechopen.com/articles/show/title/immune-dysfunction-inautism-spectrum-disorder.
-
(2011)
InTech
-
-
Westover, J.B.1
Sweeten, T.L.2
Benson, M.3
Bray-Ward, P.4
Torres, A.R.5
-
51
-
-
57649152984
-
A single base-pair mutation in the 3'-untranslated region of HLA-G mRNA is associated with pre-eclampsia
-
Yie S.M., Li L.H., Xiao R., Librach C.L. A single base-pair mutation in the 3'-untranslated region of HLA-G mRNA is associated with pre-eclampsia. Mol. Hum. Reprod. 2008, 14:649-653.
-
(2008)
Mol. Hum. Reprod.
, vol.14
, pp. 649-653
-
-
Yie, S.M.1
Li, L.H.2
Xiao, R.3
Librach, C.L.4
-
52
-
-
34547886497
-
A unified genetic theory for sporadic and inherited autism
-
Zhao X., Leotta A., Kustanovich V., Lajonchere C., Geschwind D.H., Law K., et al. A unified genetic theory for sporadic and inherited autism. Proc. Natl. Acad. Sci. U.S.A. 2007, 31(104):12831-12836.
-
(2007)
Proc. Natl. Acad. Sci. U.S.A.
, vol.31
, Issue.104
, pp. 12831-12836
-
-
Zhao, X.1
Leotta, A.2
Kustanovich, V.3
Lajonchere, C.4
Geschwind, D.H.5
Law, K.6
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