376 related articles for article (PubMed ID: 32090785)
21. Shared genetics between classes of obesity and psychiatric disorders: A large-scale genome-wide cross-trait analysis.
Ding H; Ouyang M; Wang J; Xie M; Huang Y; Yuan F; Jia Y; Zhang X; Liu N; Zhang N
J Psychosom Res; 2022 Nov; 162():111032. PubMed ID: 36137488
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. Genome-wide Regional Heritability Mapping Identifies a Locus Within the TOX2 Gene Associated With Major Depressive Disorder.
Zeng Y; Navarro P; Shirali M; Howard DM; Adams MJ; Hall LS; Clarke TK; Thomson PA; Smith BH; Murray A; Padmanabhan S; Hayward C; Boutin T; MacIntyre DJ; Lewis CM; Wray NR; Mehta D; Penninx BWJH; Milaneschi Y; Baune BT; Air T; Hottenga JJ; Mbarek H; Castelao E; Pistis G; Schulze TG; Streit F; Forstner AJ; Byrne EM; Martin NG; Breen G; Müller-Myhsok B; Lucae S; Kloiber S; Domenici E; ; Deary IJ; Porteous DJ; Haley CS; McIntosh AM
Biol Psychiatry; 2017 Sep; 82(5):312-321. PubMed ID: 28153336
[TBL] [Abstract][Full Text] [Related]
24. 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]
25. 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]
26. meQTL and ncRNA functional analyses of 102 GWAS-SNPs associated with depression implicate HACE1 and SHANK2 genes.
Ciuculete DM; Voisin S; Kular L; Jonsson J; Rask-Andersen M; Mwinyi J; Schiöth HB
Clin Epigenetics; 2020 Jul; 12(1):99. PubMed ID: 32616021
[TBL] [Abstract][Full Text] [Related]
27. Shared Genetic Liability Between Major Depressive Disorder and Atopic Diseases.
Cao H; Li S; Baranova A; Zhang F
Front Immunol; 2021; 12():665160. PubMed ID: 34566951
[TBL] [Abstract][Full Text] [Related]
28. 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]
29. 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]
30. 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]
31. GWAS Meta-Analysis Reveals Shared Genes and Biological Pathways between Major Depressive Disorder and Insomnia.
Lin YS; Wang CC; Chen CY
Genes (Basel); 2021 Sep; 12(10):. PubMed ID: 34680902
[TBL] [Abstract][Full Text] [Related]
32. Major depressive disorder plays a vital role in the pathway from gastroesophageal reflux disease to chronic obstructive pulmonary disease: a Mendelian randomization study.
Zou M; Zhang W; Shen L; Xu Y; Zhu Y
Front Genet; 2023; 14():1198476. PubMed ID: 37404328
[No Abstract] [Full Text] [Related]
33. Integrative analyses of major histocompatibility complex loci in the genome-wide association studies of major depressive disorder.
Li H; Chang H; Song X; Liu W; Li L; Wang L; Yang Y; Zhang L; Li W; Zhang Y; Zhou DS; Li X; Zhang C; Fang Y; Sun Y; Dai JP; Luo XJ; Yao YG; Xiao X; Lv L; Li M
Neuropsychopharmacology; 2019 Aug; 44(9):1552-1561. PubMed ID: 30771788
[TBL] [Abstract][Full Text] [Related]
34. Integration of summary data from GWAS and eQTL studies identified novel causal BMD genes with functional predictions.
Meng XH; Chen XD; Greenbaum J; Zeng Q; You SL; Xiao HM; Tan LJ; Deng HW
Bone; 2018 Aug; 113():41-48. PubMed ID: 29763751
[TBL] [Abstract][Full Text] [Related]
35. 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]
36. 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]
37. The genome-wide risk alleles for psychiatric disorders at 3p21.1 show convergent effects on mRNA expression, cognitive function, and mushroom dendritic spine.
Yang Z; Zhou D; Li H; Cai X; Liu W; Wang L; Chang H; Li M; Xiao X
Mol Psychiatry; 2020 Jan; 25(1):48-66. PubMed ID: 31723243
[TBL] [Abstract][Full Text] [Related]
38. Landscape of Conditional eQTL in Dorsolateral Prefrontal Cortex and Co-localization with Schizophrenia GWAS.
Dobbyn A; Huckins LM; Boocock J; Sloofman LG; Glicksberg BS; Giambartolomei C; Hoffman GE; Perumal TM; Girdhar K; Jiang Y; Raj T; Ruderfer DM; Kramer RS; Pinto D; ; Akbarian S; Roussos P; Domenici E; Devlin B; Sklar P; Stahl EA; Sieberts SK
Am J Hum Genet; 2018 Jun; 102(6):1169-1184. PubMed ID: 29805045
[TBL] [Abstract][Full Text] [Related]
39. 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]
40. The Gene Encoding Protocadherin 9 (PCDH9), a Novel Risk Factor for Major Depressive Disorder.
Xiao X; Zheng F; Chang H; Ma Y; Yao YG; Luo XJ; Li M
Neuropsychopharmacology; 2018 Apr; 43(5):1128-1137. PubMed ID: 28990594
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
