204 related articles for article (PubMed ID: 16941662)
1. 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; 144B(1):106-12. PubMed ID: 16941662
[TBL] [Abstract][Full Text] [Related]
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; 441(1):56-60. PubMed ID: 18597938
[TBL] [Abstract][Full Text] [Related]
3. 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;
Mol Psychiatry; 2002; 7(7):801-4. PubMed ID: 12192627
[TBL] [Abstract][Full Text] [Related]
4. 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;
Mol Psychiatry; 2001 Mar; 6(2):150-9. PubMed ID: 11317216
[TBL] [Abstract][Full Text] [Related]
5. Association of Reelin gene polymorphisms with autism.
Serajee FJ; Zhong H; Mahbubul Huq AH
Genomics; 2006 Jan; 87(1):75-83. PubMed ID: 16311013
[TBL] [Abstract][Full Text] [Related]
6. 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;
Am J Med Genet B Neuropsychiatr Genet; 2004 Apr; 126B(1):46-50. PubMed ID: 15048647
[TBL] [Abstract][Full Text] [Related]
7. 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; 137B(1):51-5. PubMed ID: 15965968
[TBL] [Abstract][Full Text] [Related]
8. 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. PubMed ID: 12399956
[TBL] [Abstract][Full Text] [Related]
9. 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; 126B(1):51-7. PubMed ID: 15048648
[TBL] [Abstract][Full Text] [Related]
10. 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;
Mol Psychiatry; 2003 Oct; 8(10):885-92. PubMed ID: 14515139
[TBL] [Abstract][Full Text] [Related]
11. 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; 58(1):37-41. PubMed ID: 12363388
[TBL] [Abstract][Full Text] [Related]
12. 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. PubMed ID: 15558079
[TBL] [Abstract][Full Text] [Related]
13. Association study between genes in Reelin signaling pathway and autism identifies DAB1 as a susceptibility gene in a Chinese Han population.
Li J; Liu J; Zhao L; Ma Y; Jia M; Lu T; Ruan Y; Li Q; Yue W; Zhang D; Wang L
Prog Neuropsychopharmacol Biol Psychiatry; 2013 Jul; 44():226-32. PubMed ID: 23333377
[TBL] [Abstract][Full Text] [Related]
14. Association of Allelic Variants of the Reelin Gene with Autistic Spectrum Disorder: A Systematic Review and Meta-Analysis of Candidate Gene Association Studies.
Hernández-García I; Chamorro AJ; Ternavasio-de la Vega HG; Carbonell C; Marcos M; Mirón-Canelo JA
Int J Environ Res Public Health; 2020 Oct; 17(21):. PubMed ID: 33143244
[TBL] [Abstract][Full Text] [Related]
15. Absence of association of a polymorphic GGC repeat at the 5' untranslated region of the reelin gene with schizophrenia.
Huang CH; Chen CH
Psychiatry Res; 2006 May; 142(1):89-92. PubMed ID: 16556465
[TBL] [Abstract][Full Text] [Related]
16. 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; 9(2):248-55. PubMed ID: 20050924
[TBL] [Abstract][Full Text] [Related]
17. Investigation of potential gene-gene interactions between APOE and RELN contributing to autism risk.
Ashley-Koch AE; Jaworski J; Ma DQ; 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. PubMed ID: 17621165
[TBL] [Abstract][Full Text] [Related]
18. 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; 187(3):462-4. PubMed ID: 20554015
[TBL] [Abstract][Full Text] [Related]
19. Association analysis of two single-nucleotide polymorphisms of the RELN gene with autism in the South African population.
Sharma JR; Arieff Z; Gameeldien H; Davids M; Kaur M; van der Merwe L
Genet Test Mol Biomarkers; 2013 Feb; 17(2):93-8. PubMed ID: 23216241
[TBL] [Abstract][Full Text] [Related]
20. An association analysis of reelin gene (RELN) polymorphisms with childhood epilepsy in eastern Indian population from West Bengal.
Dutta S; Gangopadhyay PK; Sinha S; Chatterjee A; Ghosh S; Rajamma U
Cell Mol Neurobiol; 2011 Jan; 31(1):45-56. PubMed ID: 20697953
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]