228 related articles for article (PubMed ID: 31680168)
1. TSEA-DB: a trait-tissue association map for human complex traits and diseases.
Jia P; Dai Y; Hu R; Pei G; Manuel AM; Zhao Z
Nucleic Acids Res; 2020 Jan; 48(D1):D1022-D1030. PubMed ID: 31680168
[TBL] [Abstract][Full Text] [Related]
2. CSEA-DB: an omnibus for human complex trait and cell type associations.
Dai Y; Hu R; Manuel AM; Liu A; Jia P; Zhao Z
Nucleic Acids Res; 2021 Jan; 49(D1):D862-D870. PubMed ID: 33211888
[TBL] [Abstract][Full Text] [Related]
3. Pinpointing miRNA and genes enrichment over trait-relevant tissue network in Genome-Wide Association Studies.
Li B; Dong J; Yu J; Fan Y; Shang L; Zhou X; Bai Y
BMC Med Genomics; 2020 Dec; 13(Suppl 11):191. PubMed ID: 33371893
[TBL] [Abstract][Full Text] [Related]
4. GWAS Atlas: a curated resource of genome-wide variant-trait associations in plants and animals.
Tian D; Wang P; Tang B; Teng X; Li C; Liu X; Zou D; Song S; Zhang Z
Nucleic Acids Res; 2020 Jan; 48(D1):D927-D932. PubMed ID: 31566222
[TBL] [Abstract][Full Text] [Related]
5. Estimating colocalization probability from limited summary statistics.
King EA; Dunbar F; Davis JW; Degner JF
BMC Bioinformatics; 2021 May; 22(1):254. PubMed ID: 34000989
[TBL] [Abstract][Full Text] [Related]
6. Investigation of multi-trait associations using pathway-based analysis of GWAS summary statistics.
Pei G; Sun H; Dai Y; Liu X; Zhao Z; Jia P
BMC Genomics; 2019 Feb; 20(Suppl 1):79. PubMed ID: 30712509
[TBL] [Abstract][Full Text] [Related]
7. Influence of tissue context on gene prioritization for predicted transcriptome-wide association studies.
Li B; Veturi Y; Bradford Y; Verma SS; Verma A; Lucas AM; Haas DW; Ritchie MD
Pac Symp Biocomput; 2019; 24():296-307. PubMed ID: 30864331
[TBL] [Abstract][Full Text] [Related]
8. ncRNA-eQTL: a database to systematically evaluate the effects of SNPs on non-coding RNA expression across cancer types.
Li J; Xue Y; Amin MT; Yang Y; Yang J; Zhang W; Yang W; Niu X; Zhang HY; Gong J
Nucleic Acids Res; 2020 Jan; 48(D1):D956-D963. PubMed ID: 31410488
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Estimating the causal tissues for complex traits and diseases.
Ongen H; Brown AA; Delaneau O; Panousis NI; Nica AC; ; Dermitzakis ET
Nat Genet; 2017 Dec; 49(12):1676-1683. PubMed ID: 29058715
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Inferring the Nature of Missing Heritability in Human Traits Using Data from the GWAS Catalog.
López-Cortegano E; Caballero A
Genetics; 2019 Jul; 212(3):891-904. PubMed ID: 31123044
[TBL] [Abstract][Full Text] [Related]
13. 3'aQTL-atlas: an atlas of 3'UTR alternative polyadenylation quantitative trait loci across human normal tissues.
Cui Y; Peng F; Wang D; Li Y; Li JS; Li L; Li W
Nucleic Acids Res; 2022 Jan; 50(D1):D39-D45. PubMed ID: 34432052
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Probabilistic integration of transcriptome-wide association studies and colocalization analysis identifies key molecular pathways of complex traits.
Okamoto J; Wang L; Yin X; Luca F; Pique-Regi R; Helms A; Im HK; Morrison J; Wen X
Am J Hum Genet; 2023 Jan; 110(1):44-57. PubMed ID: 36608684
[TBL] [Abstract][Full Text] [Related]
16. webTWAS: a resource for disease candidate susceptibility genes identified by transcriptome-wide association study.
Cao C; Wang J; Kwok D; Cui F; Zhang Z; Zhao D; Li MJ; Zou Q
Nucleic Acids Res; 2022 Jan; 50(D1):D1123-D1130. PubMed ID: 34669946
[TBL] [Abstract][Full Text] [Related]
17. CAUSALdb: a database for disease/trait causal variants identified using summary statistics of genome-wide association studies.
Wang J; Huang D; Zhou Y; Yao H; Liu H; Zhai S; Wu C; Zheng Z; Zhao K; Wang Z; Yi X; Zhang S; Liu X; Liu Z; Chen K; Yu Y; Sham PC; Li MJ
Nucleic Acids Res; 2020 Jan; 48(D1):D807-D816. PubMed ID: 31691819
[TBL] [Abstract][Full Text] [Related]
18. QTLbase: an integrative resource for quantitative trait loci across multiple human molecular phenotypes.
Zheng Z; Huang D; Wang J; Zhao K; Zhou Y; Guo Z; Zhai S; Xu H; Cui H; Yao H; Wang Z; Yi X; Zhang S; Sham PC; Li MJ
Nucleic Acids Res; 2020 Jan; 48(D1):D983-D991. PubMed ID: 31598699
[TBL] [Abstract][Full Text] [Related]
19. deTS: tissue-specific enrichment analysis to decode tissue specificity.
Pei G; Dai Y; Zhao Z; Jia P
Bioinformatics; 2019 Oct; 35(19):3842-3845. PubMed ID: 30824912
[TBL] [Abstract][Full Text] [Related]
20. The Beavis Effect in Next-Generation Mapping Panels in
King EG; Long AD
G3 (Bethesda); 2017 Jun; 7(6):1643-1652. PubMed ID: 28592647
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
