204 related articles for article (PubMed ID: 16941662)
21. Polymorphic GGC repeat differentially regulates human reelin gene expression levels.
Persico AM; Levitt P; Pimenta AF
J Neural Transm (Vienna); 2006 Oct; 113(10):1373-82. PubMed ID: 16604303
[TBL] [Abstract][Full Text] [Related]
22. 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; 147B(2):194-200. PubMed ID: 17955477
[TBL] [Abstract][Full Text] [Related]
23. A pilot Indian family-based association study between dyslexia and Reelin pathway genes, DCDC2 and ROBO1, identifies modest association with a triallelic unit TAT in the gene RELN.
Devasenapathy S; Midha R; Naskar T; Mehta A; Prajapati B; Ummekulsum M; Sagar R; Singh NC; Sinha S
Asian J Psychiatr; 2018 Oct; 37():121-129. PubMed ID: 30199849
[TBL] [Abstract][Full Text] [Related]
24. RELN gene polymorphisms and susceptibility to autism in Chinese Han population.
Tian P
Neurol India; 2012; 60(6):581-4. PubMed ID: 23287318
[TBL] [Abstract][Full Text] [Related]
25. Glutamate receptor 6 gene (GluR6 or GRIK2) polymorphisms in the Indian population: a genetic association study on autism spectrum disorder.
Dutta S; Das S; Guhathakurta S; Sen B; Sinha S; Chatterjee A; Ghosh S; Ahmed S; Ghosh S; Usha R
Cell Mol Neurobiol; 2007 Dec; 27(8):1035-47. PubMed ID: 17712621
[TBL] [Abstract][Full Text] [Related]
26. Reduced blood levels of reelin as a vulnerability factor in pathophysiology of autistic disorder.
Fatemi SH; Stary JM; Egan EA
Cell Mol Neurobiol; 2002 Apr; 22(2):139-52. PubMed ID: 12363196
[TBL] [Abstract][Full Text] [Related]
27. Association and gene-gene interactions study of reelin signaling pathway related genes with autism in the Han Chinese population.
Shen Y; Xun G; Guo H; He Y; Ou J; Dong H; Xia K; Zhao J
Autism Res; 2016 Apr; 9(4):436-42. PubMed ID: 26285919
[TBL] [Abstract][Full Text] [Related]
28. 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. PubMed ID: 20436377
[TBL] [Abstract][Full Text] [Related]
29. The role of reelin gene polymorphisms in the pathogenesis of Alzheimer's disease in a Greek population.
Antoniades D; Katopodi T; Pappa S; Lampropoulos A; Konsta V; Frydas E; Mpalogiannis S; Hatzistilianou M
J Biol Regul Homeost Agents; 2011; 25(3):351-8. PubMed ID: 22023759
[TBL] [Abstract][Full Text] [Related]
30. Association study of RELN polymorphisms with schizophrenia in Han Chinese population.
Li W; Song X; Zhang H; Yang Y; Jiang C; Xiao B; Li W; Yang G; Zhao J; Guo W; Lv L
Prog Neuropsychopharmacol Biol Psychiatry; 2011 Aug; 35(6):1505-11. PubMed ID: 21549172
[TBL] [Abstract][Full Text] [Related]
31. The RELN locus in Alzheimer's disease.
Seripa D; Matera MG; Franceschi M; Daniele A; Bizzarro A; Rinaldi M; Panza F; Fazio VM; Gravina C; D'Onofrio G; Solfrizzi V; Masullo C; Pilotto A
J Alzheimers Dis; 2008 Jul; 14(3):335-44. PubMed ID: 18599960
[TBL] [Abstract][Full Text] [Related]
32. The role of Reelin in pathology of autism.
Fatemi SH
Mol Psychiatry; 2002; 7(9):919-20. PubMed ID: 12399938
[No Abstract] [Full Text] [Related]
33. Reelin gene variants and risk of autism spectrum disorders: an integrated meta-analysis.
Wang Z; Hong Y; Zou L; Zhong R; Zhu B; Shen N; Chen W; Lou J; Ke J; Zhang T; Wang W; Miao X
Am J Med Genet B Neuropsychiatr Genet; 2014 Mar; 165B(2):192-200. PubMed ID: 24453138
[TBL] [Abstract][Full Text] [Related]
34. Reelin signaling is impaired in autism.
Fatemi SH; Snow AV; Stary JM; Araghi-Niknam M; Reutiman TJ; Lee S; Brooks AI; Pearce DA
Biol Psychiatry; 2005 Apr; 57(7):777-87. PubMed ID: 15820235
[TBL] [Abstract][Full Text] [Related]
35. Association of dopamine D4 receptor (DRD4) polymorphisms with attention deficit hyperactivity disorder in Indian population.
Bhaduri N; Das M; Sinha S; Chattopadhyay A; Gangopadhyay PK; Chaudhuri K; Singh M; Mukhopadhyay K
Am J Med Genet B Neuropsychiatr Genet; 2006 Jan; 141B(1):61-6. PubMed ID: 16331654
[TBL] [Abstract][Full Text] [Related]
36. Reelin glycoprotein in autism and schizophrenia.
Fatemi SH
Int Rev Neurobiol; 2005; 71():179-87. PubMed ID: 16512351
[No Abstract] [Full Text] [Related]
37. Serotonin transporter (5-HTT) gene variants associated with autism?
Klauck SM; Poustka F; Benner A; Lesch KP; Poustka A
Hum Mol Genet; 1997 Dec; 6(13):2233-8. PubMed ID: 9361027
[TBL] [Abstract][Full Text] [Related]
38. Two single-nucleotide polymorphisms of the RELN gene and symptom-based and developmental deficits among children and adolescents with autistic spectrum disorders in the Tianjin, China.
Wang GF; Ye S; Gao L; Han Y; Guo X; Dong XP; Su YY; Zhang X
Behav Brain Res; 2018 Sep; 350():1-5. PubMed ID: 29753726
[TBL] [Abstract][Full Text] [Related]
39. 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
Mol Psychiatry; 2002; 7(3):278-88. PubMed ID: 11920155
[TBL] [Abstract][Full Text] [Related]
40. Rare RELN variants affect Reelin-DAB1 signal transduction in autism spectrum disorder.
Sánchez-Sánchez SM; Magdalon J; Griesi-Oliveira K; Yamamoto GL; Santacruz-Perez C; Fogo M; Passos-Bueno MR; Sertié AL
Hum Mutat; 2018 Oct; 39(10):1372-1383. PubMed ID: 29969175
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]