369 related articles for article (PubMed ID: 32442411)
1. Systems Genetics in Human Endothelial Cells Identifies Non-coding Variants Modifying Enhancers, Expression, and Complex Disease Traits.
Stolze LK; Conklin AC; Whalen MB; López Rodríguez M; Õunap K; Selvarajan I; Toropainen A; Örd T; Li J; Eshghi A; Solomon AE; Fang Y; Kaikkonen MU; Romanoski CE
Am J Hum Genet; 2020 Jun; 106(6):748-763. PubMed ID: 32442411
[TBL] [Abstract][Full Text] [Related]
2. Integrative analysis of liver-specific non-coding regulatory SNPs associated with the risk of coronary artery disease.
Selvarajan I; Toropainen A; Garske KM; López Rodríguez M; Ko A; Miao Z; Kaminska D; Õunap K; Örd T; Ravindran A; Liu OH; Moreau PR; Jawahar Deen A; Männistö V; Pan C; Levonen AL; Lusis AJ; Heikkinen S; Romanoski CE; Pihlajamäki J; Pajukanta P; Kaikkonen MU
Am J Hum Genet; 2021 Mar; 108(3):411-430. PubMed ID: 33626337
[TBL] [Abstract][Full Text] [Related]
3. A non-coding genetic variant associated with abdominal aortic aneurysm alters ERG gene regulation.
Marsman J; Gimenez G; Day RC; Horsfield JA; Jones GT
Hum Mol Genet; 2020 Mar; 29(4):554-565. PubMed ID: 31691800
[TBL] [Abstract][Full Text] [Related]
4. The Transcription Factor ERG Regulates Super-Enhancers Associated With an Endothelial-Specific Gene Expression Program.
Kalna V; Yang Y; Peghaire CR; Frudd K; Hannah R; Shah AV; Osuna Almagro L; Boyle JJ; Göttgens B; Ferrer J; Randi AM; Birdsey GM
Circ Res; 2019 Apr; 124(9):1337-1349. PubMed ID: 30892142
[TBL] [Abstract][Full Text] [Related]
5. Multiple Functional Variants at 13q14 Risk Locus for Osteoporosis Regulate RANKL Expression Through Long-Range Super-Enhancer.
Zhu DL; Chen XF; Hu WX; Dong SS; Lu BJ; Rong Y; Chen YX; Chen H; Thynn HN; Wang NN; Guo Y; Yang TL
J Bone Miner Res; 2018 Jul; 33(7):1335-1346. PubMed ID: 29528523
[TBL] [Abstract][Full Text] [Related]
6. 9p21 DNA variants associated with coronary artery disease impair interferon-γ signalling response.
Harismendy O; Notani D; Song X; Rahim NG; Tanasa B; Heintzman N; Ren B; Fu XD; Topol EJ; Rosenfeld MG; Frazer KA
Nature; 2011 Feb; 470(7333):264-8. PubMed ID: 21307941
[TBL] [Abstract][Full Text] [Related]
7. Joint Bayesian inference of risk variants and tissue-specific epigenomic enrichments across multiple complex human diseases.
Li Y; Kellis M
Nucleic Acids Res; 2016 Oct; 44(18):e144. PubMed ID: 27407109
[TBL] [Abstract][Full Text] [Related]
8. Functional noncoding SNPs in human endothelial cells fine-map vascular trait associations.
Toropainen A; Stolze LK; Örd T; Whalen MB; Torrell PM; Link VM; Kaikkonen MU; Romanoski CE
Genome Res; 2022 Mar; 32(3):409-424. PubMed ID: 35193936
[TBL] [Abstract][Full Text] [Related]
9. Enhancer variants associated with Alzheimer's disease affect gene expression via chromatin looping.
Kikuchi M; Hara N; Hasegawa M; Miyashita A; Kuwano R; Ikeuchi T; Nakaya A
BMC Med Genomics; 2019 Sep; 12(1):128. PubMed ID: 31500627
[TBL] [Abstract][Full Text] [Related]
10. Putative enhancer sites in the bovine genome are enriched with variants affecting complex traits.
Wang M; Hancock TP; MacLeod IM; Pryce JE; Cocks BG; Hayes BJ
Genet Sel Evol; 2017 Jul; 49(1):56. PubMed ID: 28683716
[TBL] [Abstract][Full Text] [Related]
11. ETS-dependent enhancers for endothelial-specific expression of serum/glucocorticoid-regulated kinase 1 during mouse embryo development.
Harada Y; Tanaka T; Arai Y; Isomoto Y; Nakano A; Nakao S; Urasaki A; Watanabe Y; Kawamura T; Nakagawa O
Genes Cells; 2021 Aug; 26(8):611-626. PubMed ID: 34081835
[TBL] [Abstract][Full Text] [Related]
12. Promoter-interacting expression quantitative trait loci are enriched for functional genetic variants.
Chandra V; Bhattacharyya S; Schmiedel BJ; Madrigal A; Gonzalez-Colin C; Fotsing S; Crinklaw A; Seumois G; Mohammadi P; Kronenberg M; Peters B; Ay F; Vijayanand P
Nat Genet; 2021 Jan; 53(1):110-119. PubMed ID: 33349701
[TBL] [Abstract][Full Text] [Related]
13. Chronic lymphocytic leukemia (CLL) risk is mediated by multiple enhancer variants within CLL risk loci.
Yan H; Tian S; Kleinstern G; Wang Z; Lee JH; Boddicker NJ; Cerhan JR; Kay NE; Braggio E; Slager SL
Hum Mol Genet; 2020 Sep; 29(16):2761-2774. PubMed ID: 32744316
[TBL] [Abstract][Full Text] [Related]
14. Genetic Regulatory Mechanisms of Smooth Muscle Cells Map to Coronary Artery Disease Risk Loci.
Liu B; Pjanic M; Wang T; Nguyen T; Gloudemans M; Rao A; Castano VG; Nurnberg S; Rader DJ; Elwyn S; Ingelsson E; Montgomery SB; Miller CL; Quertermous T
Am J Hum Genet; 2018 Sep; 103(3):377-388. PubMed ID: 30146127
[TBL] [Abstract][Full Text] [Related]
15. Endometrial vezatin and its association with endometriosis risk.
Holdsworth-Carson SJ; Fung JN; Luong HT; Sapkota Y; Bowdler LM; Wallace L; Teh WT; Powell JE; Girling JE; Healey M; Montgomery GW; Rogers PA
Hum Reprod; 2016 May; 31(5):999-1013. PubMed ID: 27005890
[TBL] [Abstract][Full Text] [Related]
16. Trans-Ancestral Fine-Mapping and Epigenetic Annotation as Tools to Delineate Functionally Relevant Risk Alleles at
Vyse TJ; Cunninghame Graham DS
Int J Mol Sci; 2020 Nov; 21(21):. PubMed ID: 33182226
[No Abstract] [Full Text] [Related]
17. An integrative functional genomics framework for effective identification of novel regulatory variants in genome-phenome studies.
Zhao J; Cheng F; Jia P; Cox N; Denny JC; Zhao Z
Genome Med; 2018 Jan; 10(1):7. PubMed ID: 29378629
[TBL] [Abstract][Full Text] [Related]
18. Functional Analysis of a Novel Genome-Wide Association Study Signal in SMAD3 That Confers Protection From Coronary Artery Disease.
Turner AW; Martinuk A; Silva A; Lau P; Nikpay M; Eriksson P; Folkersen L; Perisic L; Hedin U; Soubeyrand S; McPherson R
Arterioscler Thromb Vasc Biol; 2016 May; 36(5):972-83. PubMed ID: 26966274
[TBL] [Abstract][Full Text] [Related]
19. Cis-regulatory variations: a study of SNPs around genes showing cis-linkage in segregating mouse populations.
GuhaThakurta D; Xie T; Anand M; Edwards SW; Li G; Wang SS; Schadt EE
BMC Genomics; 2006 Sep; 7():235. PubMed ID: 16978413
[TBL] [Abstract][Full Text] [Related]
20. Integrative functional genomics identifies regulatory mechanisms at coronary artery disease loci.
Miller CL; Pjanic M; Wang T; Nguyen T; Cohain A; Lee JD; Perisic L; Hedin U; Kundu RK; Majmudar D; Kim JB; Wang O; Betsholtz C; Ruusalepp A; Franzén O; Assimes TL; Montgomery SB; Schadt EE; Björkegren JLM; Quertermous T
Nat Commun; 2016 Jul; 7():12092. PubMed ID: 27386823
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
