368 related articles for article (PubMed ID: 19436241)
1. A variant in the reelin gene increases the risk of schizophrenia and schizoaffective disorder but not bipolar disorder.
Pisanté A; Bronstein M; Yakir B; Darvasi A
Psychiatr Genet; 2009 Aug; 19(4):212. PubMed ID: 19436241
[No Abstract] [Full Text] [Related]
2. 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]
3. Potential genetic variants in schizophrenia: a Bayesian analysis.
Hall H; Lawyer G; Sillén A; Jönsson EG; Agartz I; Terenius L; Arnborg S
World J Biol Psychiatry; 2007; 8(1):12-22. PubMed ID: 17366345
[TBL] [Abstract][Full Text] [Related]
4. The human reelin gene: transcription factors (+), repressors (-) and the methylation switch (+/-) in schizophrenia.
Grayson DR; Chen Y; Costa E; Dong E; Guidotti A; Kundakovic M; Sharma RP
Pharmacol Ther; 2006 Jul; 111(1):272-86. PubMed ID: 16574235
[TBL] [Abstract][Full Text] [Related]
5. Association study of the reelin (RELN) gene with Chinese Va schizophrenia.
Yang XB; Kang C; Liu H; Yang J
Psychiatr Genet; 2013 Jun; 23(3):138. PubMed ID: 23277132
[No Abstract] [Full Text] [Related]
6. Identification of a single nucleotide polymorphism at the 5' promoter region of human reelin gene and association study with schizophrenia.
Chen ML; Chen SY; Huang CH; Chen CH
Mol Psychiatry; 2002; 7(5):447-8. PubMed ID: 12082559
[No Abstract] [Full Text] [Related]
7. Reelin mutations in mouse and man: from reeler mouse to schizophrenia, mood disorders, autism and lissencephaly.
Fatemi SH
Mol Psychiatry; 2001 Mar; 6(2):129-33. PubMed ID: 11317213
[No Abstract] [Full Text] [Related]
8. Association of reelin (RELN) single nucleotide polymorphism rs7341475 with prepulse inhibition in the Jewish Israeli population.
Greenbaum L; Levin R; Lerer E; Alkelai A; Kohn Y; Heresco-Levy U; Ebstein RP; Lerer B
Biol Psychiatry; 2011 Mar; 69(5):e17-8; author reply e19. PubMed ID: 21195391
[No Abstract] [Full Text] [Related]
9. 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]
10. Methylation status of the reelin promoter region in the brain of schizophrenic patients.
Tochigi M; Iwamoto K; Bundo M; Komori A; Sasaki T; Kato N; Kato T
Biol Psychiatry; 2008 Mar; 63(5):530-3. PubMed ID: 17870056
[TBL] [Abstract][Full Text] [Related]
11. Reelin and human nodular heterotopia.
Thom M; Garbelli R; Spreafico R
Epilepsia; 2011 Mar; 52(3):650-2. PubMed ID: 21395570
[No Abstract] [Full Text] [Related]
12. Lack of association between SNP rs3914132 of the RELN gene and otosclerosis in India.
Priyadarshi S; Panda KC; Panda AK; Ramchander PV
Genet Mol Res; 2010 Sep; 9(3):1914-20. PubMed ID: 20882487
[TBL] [Abstract][Full Text] [Related]
13. Reelin mouse mutants as models of cortical development disorders.
D'Arcangelo G
Epilepsy Behav; 2006 Feb; 8(1):81-90. PubMed ID: 16266828
[TBL] [Abstract][Full Text] [Related]
14. Replication of linkage on chromosome 7q22 and association of the regional Reelin gene with working memory in schizophrenia families.
Wedenoja J; Loukola A; Tuulio-Henriksson A; Paunio T; Ekelund J; Silander K; Varilo T; Heikkilä K; Suvisaari J; Partonen T; Lönnqvist J; Peltonen L
Mol Psychiatry; 2008 Jul; 13(7):673-84. PubMed ID: 17684500
[TBL] [Abstract][Full Text] [Related]
15. Does originating from a genetic isolate affect the level of cognitive impairments in schizophrenia families?
Torniainen M; Wedenoja J; Varilo T; Partonen T; Suokas J; Häkkinen L; Lönnqvist J; Suvisaari J; Tuulio-Henriksson A
Psychiatry Res; 2013 Jul; 208(2):111-7. PubMed ID: 23083916
[TBL] [Abstract][Full Text] [Related]
16. Neocortical RELN promoter methylation increases significantly after puberty.
Lintas C; Persico AM
Neuroreport; 2010 Jan; 21(2):114-8. PubMed ID: 19952965
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Replication of an association of a common variant in the Reelin gene (RELN) with schizophrenia in Ashkenazi Jewish women.
Liu Y; Chen PL; McGrath J; Wolyniec P; Fallin D; Nestadt G; Liang KY; Pulver A; Valle D; Avramopoulos D
Psychiatr Genet; 2010 Aug; 20(4):184-6. PubMed ID: 20431428
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. What have the genomics ever done for the psychoses?
Gill M; Donohoe G; Corvin A
Psychol Med; 2010 Apr; 40(4):529-40. PubMed ID: 19818200
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
