178 related articles for article (PubMed ID: 33664438)
1. Shared associations identify causal relationships between gene expression and immune cell phenotypes.
Gasperi C; Chun S; Sunyaev SR; Cotsapas C
Commun Biol; 2021 Mar; 4(1):279. PubMed ID: 33664438
[TBL] [Abstract][Full Text] [Related]
2. Genetic colocalization atlas points to common regulatory sites and genes for hematopoietic traits and hematopoietic contributions to disease phenotypes.
Thom CS; Voight BF
BMC Med Genomics; 2020 Jun; 13(1):89. PubMed ID: 32600345
[TBL] [Abstract][Full Text] [Related]
3. Mendelian randomization integrating GWAS and eQTL data reveals genetic determinants of complex and clinical traits.
Porcu E; Rüeger S; Lepik K; ; ; Santoni FA; Reymond A; Kutalik Z
Nat Commun; 2019 Jul; 10(1):3300. PubMed ID: 31341166
[TBL] [Abstract][Full Text] [Related]
4. Systematic Mendelian randomization framework elucidates hundreds of CpG sites which may mediate the influence of genetic variants on disease.
Richardson TG; Haycock PC; Zheng J; Timpson NJ; Gaunt TR; Davey Smith G; Relton CL; Hemani G
Hum Mol Genet; 2018 Sep; 27(18):3293-3304. PubMed ID: 29893838
[TBL] [Abstract][Full Text] [Related]
5. A transcriptome-wide Mendelian randomization study to uncover tissue-dependent regulatory mechanisms across the human phenome.
Richardson TG; Hemani G; Gaunt TR; Relton CL; Davey Smith G
Nat Commun; 2020 Jan; 11(1):185. PubMed ID: 31924771
[TBL] [Abstract][Full Text] [Related]
6. Multi-trait transcriptome-wide association studies with probabilistic Mendelian randomization.
Liu L; Zeng P; Xue F; Yuan Z; Zhou X
Am J Hum Genet; 2021 Feb; 108(2):240-256. PubMed ID: 33434493
[TBL] [Abstract][Full Text] [Related]
7. Mendelian randomization and genetic colocalization infer the effects of the multi-tissue proteome on 211 complex disease-related phenotypes.
Yang C; Fagan AM; Perrin RJ; Rhinn H; Harari O; Cruchaga C
Genome Med; 2022 Dec; 14(1):140. PubMed ID: 36510323
[TBL] [Abstract][Full Text] [Related]
8. Leveraging genetically simple traits to identify small-effect variants for complex phenotypes.
Kemper KE; Littlejohn MD; Lopdell T; Hayes BJ; Bennett LE; Williams RP; Xu XQ; Visscher PM; Carrick MJ; Goddard ME
BMC Genomics; 2016 Nov; 17(1):858. PubMed ID: 27809761
[TBL] [Abstract][Full Text] [Related]
9. Large-Scale Identification of Common Trait and Disease Variants Affecting Gene Expression.
Hauberg ME; Zhang W; Giambartolomei C; Franzén O; Morris DL; Vyse TJ; Ruusalepp A; ; Sklar P; Schadt EE; Björkegren JLM; Roussos P
Am J Hum Genet; 2017 Jun; 100(6):885-894. PubMed ID: 28552197
[TBL] [Abstract][Full Text] [Related]
10. Mendelian Randomization Analysis Identifies CpG Sites as Putative Mediators for Genetic Influences on Cardiovascular Disease Risk.
Richardson TG; Zheng J; Davey Smith G; Timpson NJ; Gaunt TR; Relton CL; Hemani G
Am J Hum Genet; 2017 Oct; 101(4):590-602. PubMed ID: 28985495
[TBL] [Abstract][Full Text] [Related]
11. Predicting gene targets from integrative analyses of summary data from GWAS and eQTL studies for 28 human complex traits.
Pavlides JM; Zhu Z; Gratten J; McRae AF; Wray NR; Yang J
Genome Med; 2016 Aug; 8(1):84. PubMed ID: 27506385
[TBL] [Abstract][Full Text] [Related]
12. Integrative multiomics analysis highlights immune-cell regulatory mechanisms and shared genetic architecture for 14 immune-associated diseases and cancer outcomes.
Prince C; Mitchell RE; Richardson TG
Am J Hum Genet; 2021 Dec; 108(12):2259-2270. PubMed ID: 34741802
[TBL] [Abstract][Full Text] [Related]
13. An Integrative Genomic Strategy Identifies sRAGE as a Causal and Protective Biomarker of Lung Function.
Keefe J; Yao C; Hwang SJ; Courchesne P; Lee GY; Dupuis J; Mizgerd JP; O'Connor G; Washko GR; Cho MH; Silverman EK; Levy D
Chest; 2022 Jan; 161(1):76-84. PubMed ID: 34237330
[TBL] [Abstract][Full Text] [Related]
14. Leveraging DNA-Methylation Quantitative-Trait Loci to Characterize the Relationship between Methylomic Variation, Gene Expression, and Complex Traits.
Hannon E; Gorrie-Stone TJ; Smart MC; Burrage J; Hughes A; Bao Y; Kumari M; Schalkwyk LC; Mill J
Am J Hum Genet; 2018 Nov; 103(5):654-665. PubMed ID: 30401456
[TBL] [Abstract][Full Text] [Related]
15. Strengthening Causal Inference for Complex Disease Using Molecular Quantitative Trait Loci.
Neumeyer S; Hemani G; Zeggini E
Trends Mol Med; 2020 Feb; 26(2):232-241. PubMed ID: 31718940
[TBL] [Abstract][Full Text] [Related]
16. The impact of cell type and context-dependent regulatory variants on human immune traits.
Mu Z; Wei W; Fair B; Miao J; Zhu P; Li YI
Genome Biol; 2021 Apr; 22(1):122. PubMed ID: 33926512
[TBL] [Abstract][Full Text] [Related]
17. Exploiting horizontal pleiotropy to search for causal pathways within a Mendelian randomization framework.
Cho Y; Haycock PC; Sanderson E; Gaunt TR; Zheng J; Morris AP; Davey Smith G; Hemani G
Nat Commun; 2020 Feb; 11(1):1010. PubMed ID: 32081875
[TBL] [Abstract][Full Text] [Related]
18. Barcoded bulk QTL mapping reveals highly polygenic and epistatic architecture of complex traits in yeast.
Nguyen Ba AN; Lawrence KR; Rego-Costa A; Gopalakrishnan S; Temko D; Michor F; Desai MM
Elife; 2022 Feb; 11():. PubMed ID: 35147078
[TBL] [Abstract][Full Text] [Related]
19. Prioritizing putative influential genes in cardiovascular disease susceptibility by applying tissue-specific Mendelian randomization.
Taylor K; Davey Smith G; Relton CL; Gaunt TR; Richardson TG
Genome Med; 2019 Jan; 11(1):6. PubMed ID: 30704512
[TBL] [Abstract][Full Text] [Related]
20. Causal phenotypic networks for egg traits in an F
Goto T; Fernandes AFA; Tsudzuki M; Rosa GJM
Mol Genet Genomics; 2019 Dec; 294(6):1455-1462. PubMed ID: 31240383
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
