190 related articles for article (PubMed ID: 24507884)
1. Combined analysis of exon splicing and genome wide polymorphism data predict schizophrenia risk loci.
Oldmeadow C; Mossman D; Evans TJ; Holliday EG; Tooney PA; Cairns MJ; Wu J; Carr V; Attia JR; Scott RJ
J Psychiatr Res; 2014 May; 52():44-9. PubMed ID: 24507884
[TBL] [Abstract][Full Text] [Related]
2. Genome-wide identification of splicing QTLs in the human brain and their enrichment among schizophrenia-associated loci.
Takata A; Matsumoto N; Kato T
Nat Commun; 2017 Feb; 8():14519. PubMed ID: 28240266
[TBL] [Abstract][Full Text] [Related]
3. Association of NPAS3 exonic variation with schizophrenia.
Macintyre G; Alford T; Xiong L; Rouleau GA; Tibbo PG; Cox DW
Schizophr Res; 2010 Jul; 120(1-3):143-9. PubMed ID: 20466522
[TBL] [Abstract][Full Text] [Related]
4. Schizophrenia risk variants influence multiple classes of transcripts of sorting nexin 19 (SNX19).
Ma L; Semick SA; Chen Q; Li C; Tao R; Price AJ; Shin JH; Jia Y; ; Brandon NJ; Cross AJ; Hyde TM; Kleinman JE; Jaffe AE; Weinberger DR; Straub RE
Mol Psychiatry; 2020 Apr; 25(4):831-843. PubMed ID: 30635639
[TBL] [Abstract][Full Text] [Related]
5. Expression analysis of the genes identified in GWAS of the postmortem brain tissues from patients with schizophrenia.
Umeda-Yano S; Hashimoto R; Yamamori H; Weickert CS; Yasuda Y; Ohi K; Fujimoto M; Ito A; Takeda M
Neurosci Lett; 2014 May; 568():12-6. PubMed ID: 24686180
[TBL] [Abstract][Full Text] [Related]
6. DOCK4 and CEACAM21 as novel schizophrenia candidate genes in the Jewish population.
Alkelai A; Lupoli S; Greenbaum L; Kohn Y; Kanyas-Sarner K; Ben-Asher E; Lancet D; Macciardi F; Lerer B
Int J Neuropsychopharmacol; 2012 May; 15(4):459-69. PubMed ID: 21682944
[TBL] [Abstract][Full Text] [Related]
7. Role of DISC1 interacting proteins in schizophrenia risk from genome-wide analysis of missense SNPs.
Costas J; Suárez-Rama JJ; Carrera N; Paz E; Páramo M; Agra S; Brenlla J; Ramos-Ríos R; Arrojo M
Ann Hum Genet; 2013 Nov; 77(6):504-12. PubMed ID: 23909765
[TBL] [Abstract][Full Text] [Related]
8. Functional investigation of a schizophrenia GWAS signal at the CDC42 gene.
Gilks WP; Hill M; Gill M; Donohoe G; Corvin AP; Morris DW
World J Biol Psychiatry; 2012 Oct; 13(7):550-4. PubMed ID: 22385474
[TBL] [Abstract][Full Text] [Related]
9. Common variants on 17q25 and gene-gene interactions conferring risk of schizophrenia in Han Chinese population and regulating gene expressions in human brain.
Guan L; Wang Q; Wang L; Wu B; Chen Y; Liu F; Ye F; Zhang T; Li K; Yan B; Lu C; Su L; Jin G; Wang H; Tian H; Wang L; Chen Z; Wang Y; Chen J; Yuan Y; Cong W; Zheng J; Wang J; Xu X; Liu H; Xiao W; Han C; Zhang Y; Jia F; Qiao X; ; Zhang D; Zhang M; Ma H
Mol Psychiatry; 2016 Sep; 21(9):1244-50. PubMed ID: 26728569
[TBL] [Abstract][Full Text] [Related]
10. Association of polymorphisms in the haplotype block spanning the alternatively spliced exons of the NTNG1 gene at 1p13.3 with schizophrenia in Japanese populations.
Ohtsuki T; Horiuchi Y; Koga M; Ishiguro H; Inada T; Iwata N; Ozaki N; Ujike H; Watanabe Y; Someya T; Arinami T
Neurosci Lett; 2008 Apr; 435(3):194-7. PubMed ID: 18384956
[TBL] [Abstract][Full Text] [Related]
11. Multivariate eQTL mapping uncovers functional variation on the X-chromosome associated with complex disease traits.
Brumpton BM; Ferreira MA
Hum Genet; 2016 Jul; 135(7):827-39. PubMed ID: 27155841
[TBL] [Abstract][Full Text] [Related]
12. Families with the risk allele of DISC1 reveal a link between schizophrenia and another component of the same molecular pathway, NDE1.
Hennah W; Tomppo L; Hiekkalinna T; Palo OM; Kilpinen H; Ekelund J; Tuulio-Henriksson A; Silander K; Partonen T; Paunio T; Terwilliger JD; Lönnqvist J; Peltonen L
Hum Mol Genet; 2007 Mar; 16(5):453-62. PubMed ID: 17185386
[TBL] [Abstract][Full Text] [Related]
13. Whole-genome association studies of alcoholism with loci linked to schizophrenia susceptibility.
Namkung J; Kim Y; Park T
BMC Genet; 2005 Dec; 6 Suppl 1(Suppl 1):S9. PubMed ID: 16451705
[TBL] [Abstract][Full Text] [Related]
14. Identification and expression pattern of two novel alternative splicing variants of EEF1D gene of dairy cattle.
Xie Y; Yang S; Cui X; Jiang L; Zhang S; Zhang Q; Zhang Y; Sun D
Gene; 2014 Jan; 534(2):189-96. PubMed ID: 24239553
[TBL] [Abstract][Full Text] [Related]
15. Chromosome conformation elucidates regulatory relationships in developing human brain.
Won H; de la Torre-Ubieta L; Stein JL; Parikshak NN; Huang J; Opland CK; Gandal MJ; Sutton GJ; Hormozdiari F; Lu D; Lee C; Eskin E; Voineagu I; Ernst J; Geschwind DH
Nature; 2016 Oct; 538(7626):523-527. PubMed ID: 27760116
[TBL] [Abstract][Full Text] [Related]
16. Schizophrenia genetics: advancing on two fronts.
Owen MJ; Williams HJ; O'Donovan MC
Curr Opin Genet Dev; 2009 Jun; 19(3):266-70. PubMed ID: 19345090
[TBL] [Abstract][Full Text] [Related]
17. Common variants of IRF3 conferring risk of schizophrenia.
Li X; Zhang W; Lencz T; Darvasi A; Alkelai A; Lerer B; Jiang HY; Zhang DF; Yu L; Xu XF; Li M; Yao YG
J Psychiatr Res; 2015 May; 64():67-73. PubMed ID: 25843157
[TBL] [Abstract][Full Text] [Related]
18. Regional Variation of Splicing QTLs in Human Brain.
Zhang Y; Yang HT; Kadash-Edmondson K; Pan Y; Pan Z; Davidson BL; Xing Y
Am J Hum Genet; 2020 Aug; 107(2):196-210. PubMed ID: 32589925
[TBL] [Abstract][Full Text] [Related]
19. Identification of novel loci for bipolar I disorder in a multi-stage genome-wide association study.
Kuo PH; Chuang LC; Liu JR; Liu CM; Huang MC; Lin SK; Sunny Sun H; Hsieh MH; Hung H; Lu RB
Prog Neuropsychopharmacol Biol Psychiatry; 2014 Jun; 51():58-64. PubMed ID: 24444492
[TBL] [Abstract][Full Text] [Related]
20. Association at SYNE1 in both bipolar disorder and recurrent major depression.
Green EK; Grozeva D; Forty L; Gordon-Smith K; Russell E; Farmer A; Hamshere M; Jones IR; Jones L; McGuffin P; Moran JL; Purcell S; Sklar P; Owen MJ; O'Donovan MC; Craddock N
Mol Psychiatry; 2013 May; 18(5):614-7. PubMed ID: 22565781
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
