198 related articles for article (PubMed ID: 32765587)
1. ABC-GWAS: Functional Annotation of Estrogen Receptor-Positive Breast Cancer Genetic Variants.
Manjunath M; Zhang Y; Zhang S; Roy S; Perez-Pinera P; Song JS
Front Genet; 2020; 11():730. PubMed ID: 32765587
[TBL] [Abstract][Full Text] [Related]
2. Functional analysis of low-grade glioma genetic variants predicts key target genes and transcription factors.
Manjunath M; Yan J; Youn Y; Drucker KL; Kollmeyer TM; McKinney AM; Zazubovich V; Zhang Y; Costello JF; Eckel-Passow J; Selvin PR; Jenkins RB; Song JS
Neuro Oncol; 2021 Apr; 23(4):638-649. PubMed ID: 33130899
[TBL] [Abstract][Full Text] [Related]
3. Integrative Genomic Analysis Predicts Causative
Zhang Y; Manjunath M; Zhang S; Chasman D; Roy S; Song JS
Cancer Res; 2018 Apr; 78(7):1579-1591. PubMed ID: 29351903
[TBL] [Abstract][Full Text] [Related]
4. KidneyGPS: a user-friendly web application to help prioritize kidney function genes and variants based on evidence from genome-wide association studies.
Stanzick KJ; Stark KJ; Gorski M; Schödel J; Krüger R; Kronenberg F; Warth R; Heid IM; Winkler TW
BMC Bioinformatics; 2023 Sep; 24(1):355. PubMed ID: 37735349
[TBL] [Abstract][Full Text] [Related]
5. Identification of breast cancer associated variants that modulate transcription factor binding.
Liu Y; Walavalkar NM; Dozmorov MG; Rich SS; Civelek M; Guertin MJ
PLoS Genet; 2017 Sep; 13(9):e1006761. PubMed ID: 28957321
[TBL] [Abstract][Full Text] [Related]
6. ezQTL: A Web Platform for Interactive Visualization and Colocalization of QTLs and GWAS Loci.
Zhang T; Klein A; Sang J; Choi J; Brown KM
Genomics Proteomics Bioinformatics; 2022 Jun; 20(3):541-548. PubMed ID: 35643189
[TBL] [Abstract][Full Text] [Related]
7. Functional mapping and annotation of genetic associations with FUMA.
Watanabe K; Taskesen E; van Bochoven A; Posthuma D
Nat Commun; 2017 Nov; 8(1):1826. PubMed ID: 29184056
[TBL] [Abstract][Full Text] [Related]
8. Weighting sequence variants based on their annotation increases the power of genome-wide association studies in dairy cattle.
Cai Z; Guldbrandtsen B; Lund MS; Sahana G
Genet Sel Evol; 2019 May; 51(1):20. PubMed ID: 31077144
[TBL] [Abstract][Full Text] [Related]
9. Massively parallel reporter assays and variant scoring identified functional variants and target genes for melanoma loci and highlighted cell-type specificity.
Long E; Yin J; Funderburk KM; Xu M; Feng J; Kane A; Zhang T; Myers T; Golden A; Thakur R; Kong H; Jessop L; Kim EY; Jones K; Chari R; Machiela MJ; Yu K; ; Iles MM; Landi MT; Law MH; Chanock SJ; Brown KM; Choi J
Am J Hum Genet; 2022 Dec; 109(12):2210-2229. PubMed ID: 36423637
[TBL] [Abstract][Full Text] [Related]
10. Systematic analysis of the effects of genetic variants on chromatin accessibility to decipher functional variants in non-coding regions.
Wang D; Wu X; Jiang G; Yang J; Yu Z; Yang Y; Yang W; Niu X; Tang K; Gong J
Front Oncol; 2022; 12():1035855. PubMed ID: 36330496
[TBL] [Abstract][Full Text] [Related]
11. A comprehensive integrated post-GWAS analysis of Type 1 diabetes reveals enhancer-based immune dysregulation.
Kim SS; Hudgins AD; Yang J; Zhu Y; Tu Z; Rosenfeld MG; DiLorenzo TP; Suh Y
PLoS One; 2021; 16(9):e0257265. PubMed ID: 34529725
[TBL] [Abstract][Full Text] [Related]
12. Predicting regulatory variants using a dense epigenomic mapped CNN model elucidated the molecular basis of trait-tissue associations.
Pei G; Hu R; Dai Y; Manuel AM; Zhao Z; Jia P
Nucleic Acids Res; 2021 Jan; 49(1):53-66. PubMed ID: 33300042
[TBL] [Abstract][Full Text] [Related]
13. HiView: an integrative genome browser to leverage Hi-C results for the interpretation of GWAS variants.
Xu Z; Zhang G; Duan Q; Chai S; Zhang B; Wu C; Jin F; Yue F; Li Y; Hu M
BMC Res Notes; 2016 Mar; 9():159. PubMed ID: 26969411
[TBL] [Abstract][Full Text] [Related]
14. A Comprehensive cis-eQTL Analysis Revealed Target Genes in Breast Cancer Susceptibility Loci Identified in Genome-wide Association Studies.
Guo X; Lin W; Bao J; Cai Q; Pan X; Bai M; Yuan Y; Shi J; Sun Y; Han MR; Wang J; Liu Q; Wen W; Li B; Long J; Chen J; Zheng W
Am J Hum Genet; 2018 May; 102(5):890-903. PubMed ID: 29727689
[TBL] [Abstract][Full Text] [Related]
15. Exploring the effects of genetic variation on gene regulation in cancer in the context of 3D genome structure.
Osman N; Shawky AE; Brylinski M
BMC Genom Data; 2022 Feb; 23(1):13. PubMed ID: 35176995
[TBL] [Abstract][Full Text] [Related]
16. Computational Analysis of Breast Cancer GWAS Loci Identifies the Putative Deleterious Effect of STXBP4 and ZNF404 Gene Variants.
Masoodi TA; Banaganapalli B; Vaidyanathan V; Talluri VR; Shaik NA
J Cell Biochem; 2017 Dec; 118(12):4296-4307. PubMed ID: 28422318
[TBL] [Abstract][Full Text] [Related]
17. Identifying Putative Susceptibility Genes and Evaluating Their Associations with Somatic Mutations in Human Cancers.
Chen Z; Wen W; Beeghly-Fadiel A; Shu XO; Díez-Obrero V; Long J; Bao J; Wang J; Liu Q; Cai Q; Moreno V; Zheng W; Guo X
Am J Hum Genet; 2019 Sep; 105(3):477-492. PubMed ID: 31402092
[TBL] [Abstract][Full Text] [Related]
18. REALGAR: a web app of integrated respiratory omics data.
Kan M; Diwadkar AR; Saxena S; Shuai H; Joo J; Himes BE
Bioinformatics; 2022 Sep; 38(18):4442-4445. PubMed ID: 35863045
[TBL] [Abstract][Full Text] [Related]
19. Snat: a SNP annotation tool for bovine by integrating various sources of genomic information.
Jiang J; Jiang L; Zhou B; Fu W; Liu JF; Zhang Q
BMC Genet; 2011 Oct; 12():85. PubMed ID: 21982513
[TBL] [Abstract][Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]
