129 related articles for article (PubMed ID: 22990015)
1. A genome-wide association study identifies a gene network of ADAMTS genes in the predisposition to pediatric stroke.
Arning A; Hiersche M; Witten A; Kurlemann G; Kurnik K; Manner D; Stoll M; Nowak-Göttl U
Blood; 2012 Dec; 120(26):5231-6. PubMed ID: 22990015
[TBL] [Abstract][Full Text] [Related]
2. Rare Variants in the ADAMTS13 Von Willebrand Factor-Binding Domain Contribute to Pediatric Stroke.
Stoll M; Rühle F; Witten A; Barysenka A; Arning A; Strauss C; Nowak-Göttl U
Circ Cardiovasc Genet; 2016 Aug; 9(4):357-67. PubMed ID: 27412500
[TBL] [Abstract][Full Text] [Related]
3. ADAMTS12, a new candidate gene for pediatric stroke.
Witten A; Rühle F; de Witt M; Barysenka A; Stach M; Junker R; Nowak-Göttl U; Stoll M
PLoS One; 2020; 15(8):e0237928. PubMed ID: 32817637
[TBL] [Abstract][Full Text] [Related]
4. Pediatric stroke and ADAMTS genes.
Rosendaal FR; Peyvandi F
Blood; 2012 Dec; 120(26):5097-8. PubMed ID: 23258900
[No Abstract] [Full Text] [Related]
5. Insights on ADAMTS proteases and ADAMTS-like proteins from mammalian genetics.
Dubail J; Apte SS
Matrix Biol; 2015; 44-46():24-37. PubMed ID: 25770910
[TBL] [Abstract][Full Text] [Related]
6. ADAMTS genes and the risk of cerebral aneurysm.
Arning A; Jeibmann A; Köhnemann S; Brokinkel B; Ewelt C; Berger K; Wellmann J; Nowak-Göttl U; Stummer W; Stoll M; Holling M
J Neurosurg; 2016 Aug; 125(2):269-74. PubMed ID: 26745484
[TBL] [Abstract][Full Text] [Related]
7. Rare genetic variants in SMAP1, B3GAT2, and RIMS1 contribute to pediatric venous thromboembolism.
Rühle F; Witten A; Barysenka A; Huge A; Arning A; Heller C; Krümpel A; Mesters R; Franke A; Lieb W; Riemenschneider M; Hiersche M; Limperger V; Nowak-Göttl U; Stoll M
Blood; 2017 Feb; 129(6):783-790. PubMed ID: 28011674
[TBL] [Abstract][Full Text] [Related]
8. Systems-level analysis of genome-wide association data.
Farber CR
G3 (Bethesda); 2013 Jan; 3(1):119-29. PubMed ID: 23316444
[TBL] [Abstract][Full Text] [Related]
9. Identification of susceptibility modules for coronary artery disease using a genome wide integrated network analysis.
Duan S; Luo X; Dong C
Gene; 2013 Dec; 531(2):347-54. PubMed ID: 23994195
[TBL] [Abstract][Full Text] [Related]
10. Gene network analysis in a pediatric cohort identifies novel lung function genes.
Ong BA; Li J; McDonough JM; Wei Z; Kim C; Chiavacci R; Mentch F; Caboot JB; Spergel J; Allen JL; Sleiman PM; Hakonarson H
PLoS One; 2013; 8(9):e72899. PubMed ID: 24023788
[TBL] [Abstract][Full Text] [Related]
11. Association between genetic variation at the ADAMTS13 locus and ischemic stroke.
Hanson E; Jood K; Nilsson S; Blomstrand C; Jern C
J Thromb Haemost; 2009 Dec; 7(12):2147-8. PubMed ID: 19765208
[No Abstract] [Full Text] [Related]
12. Gene network and biological pathways associated with susceptibility to differentiated thyroid carcinoma.
Kulkarni O; Sugier PE; Guibon J; Boland-Augé A; Lonjou C; Bacq-Daian D; Olaso R; Rubino C; Souchard V; Rachedi F; Lence-Anta JJ; Ortiz RM; Xhaard C; Laurent-Puig P; Mulot C; Guizard AV; Schvartz C; Boutron-Ruault MC; Ostroumova E; Kesminiene A; Deleuze JF; Guénel P; De Vathaire F; Truong T; Lesueur F
Sci Rep; 2021 Apr; 11(1):8932. PubMed ID: 33903625
[TBL] [Abstract][Full Text] [Related]
13. [Association of ADAMTS-1 gene polymorphisms with ischemic stroke caused by large artery atherosclerosis].
Lyu C; Chen Y; Zhu M; Jin X; Liu P; Zheng Z; Li C; Zhu F; Hu X; Wang F; Li W; Wang W
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Dec; 32(6):844-8. PubMed ID: 26663063
[TBL] [Abstract][Full Text] [Related]
14. Pathway analysis supports association of nonsyndromic cryptorchidism with genetic loci linked to cytoskeleton-dependent functions.
Barthold JS; Wang Y; Kolon TF; Kollin C; Nordenskjöld A; Olivant Fisher A; Figueroa TE; BaniHani AH; Hagerty JA; Gonzaléz R; Noh PH; Chiavacci RM; Harden KR; Abrams DJ; Kim CE; Li J; Hakonarson H; Devoto M
Hum Reprod; 2015 Oct; 30(10):2439-51. PubMed ID: 26209787
[TBL] [Abstract][Full Text] [Related]
15. Identification of pleiotropic genes between risk factors of stroke by multivariate metaCCA analysis.
Wang Z; Greenbaum J; Qiu C; Li K; Wang Q; Tang SY; Deng HW
Mol Genet Genomics; 2020 Sep; 295(5):1173-1185. PubMed ID: 32474671
[TBL] [Abstract][Full Text] [Related]
16. Additional common loci associated with stroke and obesity identified using pleiotropic analytical approach.
Wang L; Xu F; Brickell A; Sun N; Mao X; Zhang Q; Wang G; Zhou Q; Yang B; Li F; Yue L; Zhang W; Hao Y; Sun C
Mol Genet Genomics; 2020 Mar; 295(2):439-451. PubMed ID: 31813042
[TBL] [Abstract][Full Text] [Related]
17. Family-based association analyses of imputed genotypes reveal genome-wide significant association of Alzheimer's disease with OSBPL6, PTPRG, and PDCL3.
Herold C; Hooli BV; Mullin K; Liu T; Roehr JT; Mattheisen M; Parrado AR; Bertram L; Lange C; Tanzi RE
Mol Psychiatry; 2016 Nov; 21(11):1608-1612. PubMed ID: 26830138
[TBL] [Abstract][Full Text] [Related]
18. EW_dmGWAS: edge-weighted dense module search for genome-wide association studies and gene expression profiles.
Wang Q; Yu H; Zhao Z; Jia P
Bioinformatics; 2015 Aug; 31(15):2591-4. PubMed ID: 25805723
[TBL] [Abstract][Full Text] [Related]
19. Enhanced Contribution of HLA in Pediatric Onset Ulcerative Colitis.
Venkateswaran S; Prince J; Cutler DJ; Marigorta UM; Okou DT; Prahalad S; Mack D; Boyle B; Walters T; Griffiths A; Sauer CG; LeLeiko N; Keljo D; Markowitz J; Baker SS; Rosh J; Pfefferkorn M; Heyman MB; Patel A; Otley A; Baldassano R; Noe J; Rufo P; Oliva-Hemker M; Davis S; Zwick ME; Gibson G; Denson LA; Hyams J; Kugathasan S
Inflamm Bowel Dis; 2018 Mar; 24(4):829-838. PubMed ID: 29562276
[TBL] [Abstract][Full Text] [Related]
20. Genome-wide association analysis of autism identified multiple loci that have been reported as strong signals for neuropsychiatric disorders.
Xia L; Ou J; Li K; Guo H; Hu Z; Bai T; Zhao J; Xia K; Zhang F
Autism Res; 2020 Mar; 13(3):382-396. PubMed ID: 31647196
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
