126 related articles for article (PubMed ID: 12476324)
1. Mutation screening and LD mapping in the VCFS deleted region of chromosome 22q11 in schizophrenia using a novel DNA pooling approach.
Williams NM; Spurlock G; Norton N; Williams HJ; Hamshere ML; Krawczak M; Kirov G; Nikolov I; Georgieva L; Jones S; Cardno AG; O'Donovan MC; Owen MJ
Mol Psychiatry; 2002; 7(10):1092-100. PubMed ID: 12476324
[TBL] [Abstract][Full Text] [Related]
2. Association of ZNF74 gene genotypes with age-at-onset of schizophrenia.
Takase K; Ohtsuki T; Migita O; Toru M; Inada T; Yamakawa-Kobayashi K; Arinami T
Schizophr Res; 2001 Dec; 52(3):161-5. PubMed ID: 11705709
[TBL] [Abstract][Full Text] [Related]
3. Detailed analysis of PRODH and PsPRODH reveals no association with schizophrenia.
Williams HJ; Williams N; Spurlock G; Norton N; Zammit S; Kirov G; Owen MJ; O'Donovan MC
Am J Med Genet B Neuropsychiatr Genet; 2003 Jul; 120B(1):42-6. PubMed ID: 12815738
[TBL] [Abstract][Full Text] [Related]
4. Polymorphism in SNAP29 gene promoter region associated with schizophrenia.
Saito T; Guan F; Papolos DF; Rajouria N; Fann CS; Lachman HM
Mol Psychiatry; 2001 Mar; 6(2):193-201. PubMed ID: 11317222
[TBL] [Abstract][Full Text] [Related]
5. Characterization and mutation analysis of goosecoid-like (GSCL), a homeodomain-containing gene that maps to the critical region for VCFS/DGS on 22q11.
Funke B; Saint-Jore B; Puech A; Sirotkin H; Edelmann L; Carlson C; Raft S; Pandita RK; Kucherlapati R; Skoultchi A; Morrow BE
Genomics; 1997 Dec; 46(3):364-72. PubMed ID: 9441739
[TBL] [Abstract][Full Text] [Related]
6. Family-based linkage disequilibrium mapping using SNP marker haplotypes: application to a potential locus for schizophrenia at chromosome 22q11.
Li T; Ball D; Zhao J; Murray RM; Liu X; Sham PC; Collier DA
Mol Psychiatry; 2000 Jan; 5(1):77-84. PubMed ID: 10673772
[TBL] [Abstract][Full Text] [Related]
7. A transmission disequilibrium and linkage analysis of D22S278 marker alleles in 574 families: further support for a susceptibility locus for schizophrenia at 22q12. Schizophrenia Collaborative Linkage Group for Chromosome 22.
Schizophr Res; 1998 Jul; 32(2):115-21. PubMed ID: 9713907
[TBL] [Abstract][Full Text] [Related]
8. Structural and mutational analysis of a conserved gene (DGSI) from the minimal DiGeorge syndrome critical region.
Gong W; Emanuel BS; Galili N; Kim DH; Roe B; Driscoll DA; Budarf ML
Hum Mol Genet; 1997 Feb; 6(2):267-76. PubMed ID: 9063747
[TBL] [Abstract][Full Text] [Related]
9. No evidence for the presence of genetic variants predisposing to psychotic disorders on the non-deleted 22q11.2 allele of VCFS patients.
Guipponi M; Santoni F; Schneider M; Gehrig C; Bustillo XB; Kates WR; Morrow B; Armando M; Vicari S; Sloan-Béna F; Gagnebin M; Shashi V; Hooper SR; Eliez S; Antonarakis SE
Transl Psychiatry; 2017 Feb; 7(2):e1039. PubMed ID: 28221368
[TBL] [Abstract][Full Text] [Related]
10. Genetic variation in the 22q11 locus and susceptibility to schizophrenia.
Liu H; Abecasis GR; Heath SC; Knowles A; Demars S; Chen YJ; Roos JL; Rapoport JL; Gogos JA; Karayiorgou M
Proc Natl Acad Sci U S A; 2002 Dec; 99(26):16859-64. PubMed ID: 12477929
[TBL] [Abstract][Full Text] [Related]
11. Screening the human protocadherin 8 (PCDH8) gene in schizophrenia.
Bray NJ; Kirov G; Owen RJ; Jacobsen NJ; Georgieva L; Williams HJ; Norton N; Spurlock G; Jones S; Zammit S; O'Donovan MC; Owen MJ
Genes Brain Behav; 2002 Aug; 1(3):187-91. PubMed ID: 12884975
[TBL] [Abstract][Full Text] [Related]
12. Molecular definition of 22q11 deletions in 151 velo-cardio-facial syndrome patients.
Carlson C; Sirotkin H; Pandita R; Goldberg R; McKie J; Wadey R; Patanjali SR; Weissman SM; Anyane-Yeboa K; Warburton D; Scambler P; Shprintzen R; Kucherlapati R; Morrow BE
Am J Hum Genet; 1997 Sep; 61(3):620-9. PubMed ID: 9326327
[TBL] [Abstract][Full Text] [Related]
13. High rates of schizophrenia in adults with velo-cardio-facial syndrome.
Murphy KC; Jones LA; Owen MJ
Arch Gen Psychiatry; 1999 Oct; 56(10):940-5. PubMed ID: 10530637
[TBL] [Abstract][Full Text] [Related]
14. An association study between the genetic polymorphisms within TBX1 and schizophrenia in the Chinese population.
Ma G; Shi Y; Tang W; He Z; Huang K; Li Z; He G; Feng G; Li H; He L
Neurosci Lett; 2007 Oct; 425(3):146-50. PubMed ID: 17850965
[TBL] [Abstract][Full Text] [Related]
15. Chromosome 22q11 deletions, velo-cardio-facial syndrome and early-onset psychosis. Molecular genetic study.
Ivanov D; Kirov G; Norton N; Williams HJ; Williams NM; Nikolov I; Tzwetkova R; Stambolova SM; Murphy KC; Toncheva D; Thapar A; O'Donovan MC; Owen MJ
Br J Psychiatry; 2003 Nov; 183():409-13. PubMed ID: 14594915
[TBL] [Abstract][Full Text] [Related]
16. Voltage-gated calcium channel gamma 2 subunit gene is not deleted in velo-cardio-facial syndrome.
Black JL; Krahn LE; Jalal SM
Mol Psychiatry; 2001 Jul; 6(4):461-4. PubMed ID: 11443534
[TBL] [Abstract][Full Text] [Related]
17. Screening for 22q11 deletions in a schizophrenia population.
Arinami T; Ohtsuki T; Takase K; Shimizu H; Yoshikawa T; Horigome H; Nakayama J; Toru M
Schizophr Res; 2001 Dec; 52(3):167-70. PubMed ID: 11705710
[TBL] [Abstract][Full Text] [Related]
18. Molecular definition of the 22q11 deletions in velo-cardio-facial syndrome.
Morrow B; Goldberg R; Carlson C; Das Gupta R; Sirotkin H; Collins J; Dunham I; O'Donnell H; Scambler P; Shprintzen R
Am J Hum Genet; 1995 Jun; 56(6):1391-403. PubMed ID: 7762562
[TBL] [Abstract][Full Text] [Related]
19. Preferential transmission of the high activity allele of COMT in schizophrenia.
Li T; Sham PC; Vallada H; Xie T; Tang X; Murray RM; Liu X; Collier DA
Psychiatr Genet; 1996; 6(3):131-3. PubMed ID: 8902889
[TBL] [Abstract][Full Text] [Related]
20. DNA pooling: a comprehensive, multi-stage association analysis of ACSL6 and SIRT5 polymorphisms in schizophrenia.
Chowdari KV; Northup A; Pless L; Wood J; Joo YH; Mirnics K; Lewis DA; Levitt PR; Bacanu SA; Nimgaonkar VL
Genes Brain Behav; 2007 Apr; 6(3):229-39. PubMed ID: 16827919
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]