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Items: 1 to 20 of 184

1.

Converging evidence for an association of ATP2B2 allelic variants with autism in male subjects.

Carayol J, Sacco R, Tores F, Rousseau F, Lewin P, Hager J, Persico AM.

Biol Psychiatry. 2011 Nov 1;70(9):880-7. doi: 10.1016/j.biopsych.2011.05.020. Epub 2011 Jul 14.

PMID:
21757185
2.

The evidence for association of ATP2B2 polymorphisms with autism in Chinese Han population.

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

PLoS One. 2013 Apr 19;8(4):e61021. doi: 10.1371/journal.pone.0061021. Print 2013.

3.

The genetics of autism.

Muhle R, Trentacoste SV, Rapin I.

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

PMID:
15121991
4.

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
5.

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
6.

Genetic analysis of reelin gene (RELN) SNPs: no association with autism spectrum disorder in the Indian population.

Dutta S, Sinha S, Ghosh S, Chatterjee A, Ahmed S, Usha R.

Neurosci Lett. 2008 Aug 15;441(1):56-60. doi: 10.1016/j.neulet.2008.06.022. Epub 2008 Jun 13.

PMID:
18597938
7.

Identification of significant association and gene-gene interaction of GABA receptor subunit genes in autism.

Ma DQ, Whitehead PL, Menold MM, Martin ER, Ashley-Koch AE, Mei H, Ritchie MD, Delong GR, Abramson RK, Wright HH, Cuccaro ML, Hussman JP, Gilbert JR, Pericak-Vance MA.

Am J Hum Genet. 2005 Sep;77(3):377-88. Epub 2005 Jul 15.

8.

Reelin gene polymorphisms in the Indian population: a possible paternal 5'UTR-CGG-repeat-allele effect on autism.

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

Am J Med Genet B Neuropsychiatr Genet. 2007 Jan 5;144B(1):106-12.

PMID:
16941662
9.

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.

Brain Res. 2007 Mar 30;1139:34-41. Epub 2007 Jan 8.

PMID:
17280648
10.

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
11.

No association between common variants in glyoxalase 1 and autism spectrum disorders.

Rehnström K, Ylisaukko-Oja T, Vanhala R, von Wendt L, Peltonen L, Hovatta I.

Am J Med Genet B Neuropsychiatr Genet. 2008 Jan 5;147B(1):124-7.

PMID:
17722011
12.

An association analysis of microsatellite markers across the Prader-Willi/Angelman critical region on chromosome 15 (q11-13) and autism spectrum disorder.

Curran S, Roberts S, Thomas S, Veltman M, Browne J, Medda E, Pickles A, Sham P, Bolton PF.

Am J Med Genet B Neuropsychiatr Genet. 2005 Aug 5;137B(1):25-8.

PMID:
15952184
13.

Glutamate transporter gene SLC1A1 associated with obsessive-compulsive disorder.

Arnold PD, Sicard T, Burroughs E, Richter MA, Kennedy JL.

Arch Gen Psychiatry. 2006 Jul;63(7):769-76.

PMID:
16818866
14.

Linkage and association of the glutamate receptor 6 gene with autism.

Jamain S, Betancur C, Quach H, Philippe A, Fellous M, Giros B, Gillberg C, Leboyer M, Bourgeron T; Paris Autism Research International Sibpair (PARIS) Study.

Mol Psychiatry. 2002;7(3):302-10.

15.

Family-based studies indicate association of Engrailed 2 gene with autism in an Indian population.

Sen B, Singh AS, Sinha S, Chatterjee A, Ahmed S, Ghosh S, Usha R.

Genes Brain Behav. 2010 Mar 1;9(2):248-55. doi: 10.1111/j.1601-183X.2009.00556.x. Epub 2009 Nov 24.

16.

Protein kinase C-beta 1 gene variants are not associated with autism in the Irish population.

Yang MS, Cochrane L, Conroy J, Hawi Z, Fitzgerald M, Gallagher L, Gill M.

Psychiatr Genet. 2007 Feb;17(1):39-41.

PMID:
17167344
17.

Distinct genetic risk based on association of MET in families with co-occurring autism and gastrointestinal conditions.

Campbell DB, Buie TM, Winter H, Bauman M, Sutcliffe JS, Perrin JM, Levitt P.

Pediatrics. 2009 Mar;123(3):1018-24. doi: 10.1542/peds.2008-0819. Erratum in: Pediatrics. 2009 Apr;123(4):1255.

PMID:
19255034
18.

Transmission disequilibrium studies of the serotonin 5-HT2A receptor gene (HTR2A) in autism.

Veenstra-VanderWeele J, Kim SJ, Lord C, Courchesne R, Akshoomoff N, Leventhal BL, Courchesne E, Cook EH Jr.

Am J Med Genet. 2002 Apr 8;114(3):277-83.

PMID:
11920848
19.

No association between allelic variants of HOXA1/HOXB1 and autism.

Gallagher L, Hawi Z, Kearney G, Fitzgerald M, Gill M.

Am J Med Genet B Neuropsychiatr Genet. 2004 Jan 1;124B(1):64-7.

PMID:
14681917
20.

Analysis of the RELN gene as a genetic risk factor for autism.

Skaar DA, Shao Y, Haines JL, Stenger JE, Jaworski J, Martin ER, DeLong GR, Moore JH, McCauley JL, Sutcliffe JS, Ashley-Koch AE, Cuccaro ML, Folstein SE, Gilbert JR, Pericak-Vance MA.

Mol Psychiatry. 2005 Jun;10(6):563-71.

PMID:
15558079

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