196 related articles for article (PubMed ID: 38664746)
1. xWAS analysis in neuropsychiatric disorders by integrating multi-molecular phenotype quantitative trait loci and GWAS summary data.
Luo L; Pang T; Zheng H; Liufu C; Chang S
J Transl Med; 2024 Apr; 22(1):387. PubMed ID: 38664746
[TBL] [Abstract][Full Text] [Related]
2. Pleiotropic Effects of Trait-Associated Genetic Variation on DNA Methylation: Utility for Refining GWAS Loci.
Hannon E; Weedon M; Bray N; O'Donovan M; Mill J
Am J Hum Genet; 2017 Jun; 100(6):954-959. PubMed ID: 28528868
[TBL] [Abstract][Full Text] [Related]
3. Meta-Analyses of Splicing and Expression Quantitative Trait Loci Identified Susceptibility Genes of Glioma.
Patro CPK; Nousome D; ; Lai RK
Front Genet; 2021; 12():609657. PubMed ID: 33936159
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Novel DNA methylation loci and genes showing pleiotropic association with Alzheimer's dementia: a network Mendelian randomization analysis.
Liu D; Wang Y; Jing H; Meng Q; Yang J
Epigenetics; 2022; 17(7):746-758. PubMed ID: 34461811
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Oxidative stress gene expression, DNA methylation, and gut microbiota interaction trigger Crohn's disease: a multi-omics Mendelian randomization study.
Xu S; Li X; Zhang S; Qi C; Zhang Z; Ma R; Xiang L; Chen L; Zhu Y; Tang C; Bourgonje AR; Li M; He Y; Zeng Z; Hu S; Feng R; Chen M
BMC Med; 2023 May; 21(1):179. PubMed ID: 37170220
[TBL] [Abstract][Full Text] [Related]
8. Leveraging lung tissue transcriptome to uncover candidate causal genes in COPD genetic associations.
Lamontagne M; Bérubé JC; Obeidat M; Cho MH; Hobbs BD; Sakornsakolpat P; de Jong K; Boezen HM; ; Nickle D; Hao K; Timens W; van den Berge M; Joubert P; Laviolette M; Sin DD; Paré PD; Bossé Y
Hum Mol Genet; 2018 May; 27(10):1819-1829. PubMed ID: 29547942
[TBL] [Abstract][Full Text] [Related]
9. Integrating genome-wide association study and expression quantitative trait loci data identifies multiple genes and gene set associated with neuroticism.
Fan Q; Wang W; Hao J; He A; Wen Y; Guo X; Wu C; Ning Y; Wang X; Wang S; Zhang F
Prog Neuropsychopharmacol Biol Psychiatry; 2017 Aug; 78():149-152. PubMed ID: 28552732
[TBL] [Abstract][Full Text] [Related]
10. Mendelian Randomization and Transcriptome-Wide Association Analysis Identified Genes That Were Pleiotropically Associated with Intraocular Pressure.
Yang Z; Zhang Z; Zhu Y; Yuan G; Yang J; Yu W
Genes (Basel); 2023 Apr; 14(5):. PubMed ID: 37239387
[TBL] [Abstract][Full Text] [Related]
11. Exploring genes for immunoglobulin A nephropathy: a summary data-based mendelian randomization and FUMA analysis.
Zhang Q; Zhang K; Zhu Y; Yuan G; Yang J; Zhang M
BMC Med Genomics; 2023 Jan; 16(1):16. PubMed ID: 36709307
[TBL] [Abstract][Full Text] [Related]
12. Identifying potential risk genes and pathways for neuropsychiatric and substance use disorders using intermediate molecular mediator information.
Gedik H; Nguyen TH; Peterson RE; Chatzinakos C; Vladimirov VI; Riley BP; Bacanu SA
Front Genet; 2023; 14():1191264. PubMed ID: 37415601
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Single-cell and genome-wide Mendelian randomization identifies causative genes for gout.
Yang Y; Hu P; Zhang Q; Ma B; Chen J; Wang B; Ma J; Liu D; Hao J; Zhou X
Arthritis Res Ther; 2024 Jun; 26(1):114. PubMed ID: 38831441
[TBL] [Abstract][Full Text] [Related]
15. Identification of the primate-specific gene BTN3A2 as an additional schizophrenia risk gene in the MHC loci.
Wu Y; Bi R; Zeng C; Ma C; Sun C; Li J; Xiao X; Li M; Zhang DF; Zheng P; Sheng N; Luo XJ; Yao YG
EBioMedicine; 2019 Jun; 44():530-541. PubMed ID: 31133542
[TBL] [Abstract][Full Text] [Related]
16. Cell-type-specific meQTLs extend melanoma GWAS annotation beyond eQTLs and inform melanocyte gene-regulatory mechanisms.
Zhang T; Choi J; Dilshat R; Einarsdóttir BÓ; Kovacs MA; Xu M; Malasky M; Chowdhury S; Jones K; Bishop DT; Goldstein AM; Iles MM; Landi MT; Law MH; Shi J; Steingrímsson E; Brown KM
Am J Hum Genet; 2021 Sep; 108(9):1631-1646. PubMed ID: 34293285
[TBL] [Abstract][Full Text] [Related]
17. Genetic and functional interaction network analysis reveals global enrichment of regulatory T cell genes influencing basal cell carcinoma susceptibility.
Adolphe C; Xue A; Fard AT; Genovesi LA; Yang J; Wainwright BJ
Genome Med; 2021 Feb; 13(1):19. PubMed ID: 33549134
[TBL] [Abstract][Full Text] [Related]
18. How powerful are summary-based methods for identifying expression-trait associations under different genetic architectures?
Veturi Y; Ritchie MD
Pac Symp Biocomput; 2018; 23():228-239. PubMed ID: 29218884
[TBL] [Abstract][Full Text] [Related]
19. Integrating genome-wide association study and expression quantitative trait loci data identifies NEGR1 as a causal risk gene of major depression disorder.
Wang X; Cheng W; Zhu J; Yin H; Chang S; Yue W; Yu H
J Affect Disord; 2020 Mar; 265():679-686. PubMed ID: 32090785
[TBL] [Abstract][Full Text] [Related]
20. Mendelian Randomization Analysis Identified Potential Genes Pleiotropically Associated with Polycystic Ovary Syndrome.
Sun Q; Gao Y; Yang J; Lu J; Feng W; Yang W
Reprod Sci; 2022 Mar; 29(3):1028-1037. PubMed ID: 34704236
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
