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Results: 1 to 20 of 271

Related Citations for PubMed (Select 12399956)

1.

Reelin gene alleles and susceptibility to autism spectrum disorders.

Zhang H, Liu X, Zhang C, Mundo E, Macciardi F, Grayson DR, Guidotti AR, Holden JJ.

Mol Psychiatry. 2002;7(9):1012-7.

2.

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
3.

Lack of evidence for an association between WNT2 and RELN polymorphisms and autism.

Li J, Nguyen L, Gleason C, Lotspeich L, Spiker D, Risch N, Myers RM.

Am J Med Genet B Neuropsychiatr Genet. 2004 Apr 1;126B(1):51-7.

PMID:
15048648
4.

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
5.

Investigation of potential gene-gene interactions between APOE and RELN contributing to autism risk.

Ashley-Koch AE, Jaworski J, Ma de Q, Mei H, Ritchie MD, Skaar DA, Robert Delong G, Worley G, Abramson RK, Wright HH, Cuccaro ML, Gilbert JR, Martin ER, Pericak-Vance MA.

Psychiatr Genet. 2007 Aug;17(4):221-6.

PMID:
17621165
6.

Absence of association between a polymorphic GGC repeat in the 5' untranslated region of the reelin gene and autism.

Krebs MO, Betancur C, Leroy S, Bourdel MC, Gillberg C, Leboyer M; Paris Autism Research International Sibpair (PARIS) Study.

Mol Psychiatry. 2002;7(7):801-4.

7.

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
8.

The association analysis of RELN and GRM8 genes with autistic spectrum disorder in Chinese Han population.

Li H, Li Y, Shao J, Li R, Qin Y, Xie C, Zhao Z.

Am J Med Genet B Neuropsychiatr Genet. 2008 Mar 5;147B(2):194-200.

PMID:
17955477
9.

Alleles of a reelin CGG repeat do not convey liability to autism in a sample from the CPEA network.

Devlin B, Bennett P, Dawson G, Figlewicz DA, Grigorenko EL, McMahon W, Minshew N, Pauls D, Smith M, Spence MA, Rodier PM, Stodgell C, Schellenberg GD; CPEA Genetics Network.

Am J Med Genet B Neuropsychiatr Genet. 2004 Apr 1;126B(1):46-50.

PMID:
15048647
10.

Reelin gene alleles and haplotypes as a factor predisposing to autistic disorder.

Persico AM, D'Agruma L, Maiorano N, Totaro A, Militerni R, Bravaccio C, Wassink TH, Schneider C, Melmed R, Trillo S, Montecchi F, Palermo M, Pascucci T, Puglisi-Allegra S, Reichelt KL, Conciatori M, Marino R, Quattrocchi CC, Baldi A, Zelante L, Gasparini P, Keller F; Collaborative Linkage Study of Autism.

Mol Psychiatry. 2001 Mar;6(2):150-9.

11.

Analysis of reelin as a candidate gene for autism.

Bonora E, Beyer KS, Lamb JA, Parr JR, Klauck SM, Benner A, Paolucci M, Abbott A, Ragoussis I, Poustka A, Bailey AJ, Monaco AP; International Molecular Genetic Study of Autism (IMGSAC).

Mol Psychiatry. 2003 Oct;8(10):885-92.

PMID:
14515139
12.

The genetics of autism.

Muhle R, Trentacoste SV, Rapin I.

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

PMID:
15121991
13.

Population-based and family-based association study of 5'UTR polymorphism of the reelin gene and schizophrenia.

Goldberger C, Gourion D, Leroy S, Schürhoff F, Bourdel MC, Leboyer M, Krebs MO.

Am J Med Genet B Neuropsychiatr Genet. 2005 Aug 5;137B(1):51-5.

PMID:
15965968
14.

Association of Reelin gene polymorphisms with autism.

Serajee FJ, Zhong H, Mahbubul Huq AH.

Genomics. 2006 Jan;87(1):75-83. Epub 2005 Nov 28.

15.

Polymorphisms of candidate genes in Slovak autistic patients.

Kelemenova S, Schmidtova E, Ficek A, Celec P, Kubranska A, Ostatnikova D.

Psychiatr Genet. 2010 Aug;20(4):137-9. doi: 10.1097/YPG.0b013e32833a1eb3.

PMID:
20436377
16.

Association analysis of polymorphic CGG repeat in 5' UTR of the reelin and VLDLR genes with schizophrenia.

Akahane A, Kunugi H, Tanaka H, Nanko S.

Schizophr Res. 2002 Nov 1;58(1):37-41.

PMID:
12363388
17.

No significant association between RELN polymorphism and autism in case-control and family-based association study in Chinese Han population.

He Y, Xun G, Xia K, Hu Z, Lv L, Deng Z, Zhao J.

Psychiatry Res. 2011 May 30;187(3):462-4. doi: 10.1016/j.psychres.2010.04.051. Epub 2011 Apr 7.

PMID:
20554015
18.

Autism spectrum disorders and attention-deficit/hyperactivity disorder in boys with the fragile X premutation.

Farzin F, Perry H, Hessl D, Loesch D, Cohen J, Bacalman S, Gane L, Tassone F, Hagerman P, Hagerman R.

J Dev Behav Pediatr. 2006 Apr;27(2 Suppl):S137-44.

PMID:
16685180
19.

Genetically determined low maternal serum dopamine beta-hydroxylase levels and the etiology of autism spectrum disorders.

Robinson PD, Schutz CK, Macciardi F, White BN, Holden JJ.

Am J Med Genet. 2001 Apr 15;100(1):30-6.

PMID:
11337745
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