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Items: 1 to 20 of 104

1.

Methyl-CpG-binding protein 2 polymorphisms and vulnerability to autism.

Loat CS, Curran S, Lewis CM, Duvall J, Geschwind D, Bolton P, Craig IW.

Genes Brain Behav. 2008 Oct;7(7):754-60. doi: 10.1111/j.1601-183X.2008.00414.x.

2.

Association of an activity-enhancing variant of IRAK1 and an MECP2-IRAK1 haplotype with increased susceptibility to rheumatoid arthritis.

Han TU, Cho SK, Kim T, Joo YB, Bae SC, Kang C.

Arthritis Rheum. 2013 Mar;65(3):590-8. doi: 10.1002/art.37804.

3.

The expanding role of MBD genes in autism: identification of a MECP2 duplication and novel alterations in MBD5, MBD6, and SETDB1.

Cukier HN, Lee JM, Ma D, Young JI, Mayo V, Butler BL, Ramsook SS, Rantus JA, Abrams AJ, Whitehead PL, Wright HH, Abramson RK, Haines JL, Cuccaro ML, Pericak-Vance MA, Gilbert JR.

Autism Res. 2012 Dec;5(6):385-97. doi: 10.1002/aur.1251. Epub 2012 Oct 10.

4.

Association of the neuronal cell adhesion molecule (NRCAM) gene variants with autism.

Marui T, Funatogawa I, Koishi S, Yamamoto K, Matsumoto H, Hashimoto O, Nanba E, Nishida H, Sugiyama T, Kasai K, Watanabe K, Kano Y, Sasaki T, Kato N.

Int J Neuropsychopharmacol. 2009 Feb;12(1):1-10. doi: 10.1017/S1461145708009127. Epub 2008 Jul 30. Erratum in: Int J Neuropsychopharmacol. 2009 Apr;12(3):439. Sasaki, Tsukasa [added].

PMID:
18664314
5.

Linkage and association analysis at the serotonin transporter (SLC6A4) locus in a rigid-compulsive subset of autism.

McCauley JL, Olson LM, Dowd M, Amin T, Steele A, Blakely RD, Folstein SE, Haines JL, Sutcliffe JS.

Am J Med Genet B Neuropsychiatr Genet. 2004 May 15;127B(1):104-12.

PMID:
15108191
6.

Positive association of the oxytocin receptor gene (OXTR) with autism in the Chinese Han population.

Wu S, Jia M, Ruan Y, Liu J, Guo Y, Shuang M, Gong X, Zhang Y, Yang X, Zhang D.

Biol Psychiatry. 2005 Jul 1;58(1):74-7.

PMID:
15992526
7.

The genetics of autism.

Muhle R, Trentacoste SV, Rapin I.

Pediatrics. 2004 May;113(5):e472-86. Review.

PMID:
15121991
8.

Candidate-gene screening and association analysis at the autism-susceptibility locus on chromosome 16p: evidence of association at GRIN2A and ABAT.

Barnby G, Abbott A, Sykes N, Morris A, Weeks DE, Mott R, Lamb J, Bailey AJ, Monaco AP; International Molecular Genetics Study of Autism Consortium.

Am J Hum Genet. 2005 Jun;76(6):950-66. Epub 2005 Apr 13.

9.

Association of the oxytocin receptor gene (OXTR) in Caucasian children and adolescents with autism.

Jacob S, Brune CW, Carter CS, Leventhal BL, Lord C, Cook EH Jr.

Neurosci Lett. 2007 Apr 24;417(1):6-9. Epub 2007 Feb 3.

10.

Evidence for association between Disrupted-in-Schizophrenia 1 (DISC1) gene polymorphisms and autism in Chinese Han population: a family-based association study.

Zheng F, Wang L, Jia M, Yue W, Ruan Y, Lu T, Liu J, Li J, Zhang D.

Behav Brain Funct. 2011 May 15;7:14. doi: 10.1186/1744-9081-7-14.

11.

MECP2 promoter methylation and X chromosome inactivation in autism.

Nagarajan RP, Patzel KA, Martin M, Yasui DH, Swanberg SE, Hertz-Picciotto I, Hansen RL, Van de Water J, Pessah IN, Jiang R, Robinson WP, LaSalle JM.

Autism Res. 2008 Jun;1(3):169-78. doi: 10.1002/aur.24.

12.

Linkage and association of the mitochondrial aspartate/glutamate carrier SLC25A12 gene with autism.

Ramoz N, Reichert JG, Smith CJ, Silverman JM, Bespalova IN, Davis KL, Buxbaum JD.

Am J Psychiatry. 2004 Apr;161(4):662-9.

PMID:
15056512
13.

Examination of NRCAM, LRRN3, KIAA0716, and LAMB1 as autism candidate genes.

Hutcheson HB, Olson LM, Bradford Y, Folstein SE, Santangelo SL, Sutcliffe JS, Haines JL.

BMC Med Genet. 2004 May 5;5:12.

14.

Autism and other neuropsychiatric symptoms are prevalent in individuals with MeCP2 duplication syndrome.

Ramocki MB, Peters SU, Tavyev YJ, Zhang F, Carvalho CM, Schaaf CP, Richman R, Fang P, Glaze DG, Lupski JR, Zoghbi HY.

Ann Neurol. 2009 Dec;66(6):771-82. doi: 10.1002/ana.21715.

15.

Analysis of MECP2 gene copy number in boys with autism.

Xi CY, Lu Y, Tan YH, Hua TY, Zhao YJ, Liu XM, Gao H.

J Child Neurol. 2011 May;26(5):570-3. doi: 10.1177/0883073810387138.

PMID:
21531908
16.

Reciprocal co-regulation of EGR2 and MECP2 is disrupted in Rett syndrome and autism.

Swanberg SE, Nagarajan RP, Peddada S, Yasui DH, LaSalle JM.

Hum Mol Genet. 2009 Feb 1;18(3):525-34. doi: 10.1093/hmg/ddn380. Epub 2008 Nov 10.

17.

Population-based association study and contrasting linkage disequilibrium pattern reveal genetic association of SLC6A4 with autism in the Indian population from West Bengal.

Guhathakurta S, Sinha S, Ghosh S, Chatterjee A, Ahmed S, Gangopadhyay PK, Usha R.

Brain Res. 2008 Nov 13;1240:12-21. doi: 10.1016/j.brainres.2008.08.063. Epub 2008 Sep 4.

PMID:
18804097
18.

[Mutational analysis of the methyl-CpG-binding protein 2 (MECP2) gene in male autism patients].

Wang SM, Li M, Yang YL, Pan H, Liu J, Pan KF, Bu DF.

Beijing Da Xue Xue Bao. 2013 Apr 18;45(2):197-201. Chinese.

19.

Transmission disequilibrium mapping at the serotonin transporter gene (SLC6A4) region in autistic disorder.

Kim SJ, Cox N, Courchesne R, Lord C, Corsello C, Akshoomoff N, Guter S, Leventhal BL, Courchesne E, Cook EH Jr.

Mol Psychiatry. 2002;7(3):278-88.

20.

A linkage disequilibrium map of the 1-Mb 15q12 GABA(A) receptor subunit cluster and association to autism.

McCauley JL, Olson LM, Delahanty R, Amin T, Nurmi EL, Organ EL, Jacobs MM, Folstein SE, Haines JL, Sutcliffe JS.

Am J Med Genet B Neuropsychiatr Genet. 2004 Nov 15;131B(1):51-9.

PMID:
15389768

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