189 related articles for article (PubMed ID: 36002455)
1. Splicing QTL analysis focusing on coding sequences reveals mechanisms for disease susceptibility loci.
Yamaguchi K; Ishigaki K; Suzuki A; Tsuchida Y; Tsuchiya H; Sumitomo S; Nagafuchi Y; Miya F; Tsunoda T; Shoda H; Fujio K; Yamamoto K; Kochi Y
Nat Commun; 2022 Aug; 13(1):4659. PubMed ID: 36002455
[TBL] [Abstract][Full Text] [Related]
2. Subcutaneous adipose tissue splice quantitative trait loci reveal differences in isoform usage associated with cardiometabolic traits.
Brotman SM; Raulerson CK; Vadlamudi S; Currin KW; Shen Q; Parsons VA; Iyengar AK; Roman TS; Furey TS; Kuusisto J; Collins FS; Boehnke M; Laakso M; Pajukanta P; Mohlke KL
Am J Hum Genet; 2022 Jan; 109(1):66-80. PubMed ID: 34995504
[TBL] [Abstract][Full Text] [Related]
3. Genome-Wide Splicing Quantitative Expression Locus Analysis Identifies Causal Risk Variants for Non-Small Cell Lung Cancer.
Jin M; Liu B; Chen C; Huang Y; Zhang H; Chen B; Song G; Zhao D; Duan L; Liu W; Yang H; Yue F; Liu P; Yuan X; Chu Q; Tian J; Hu K
Cancer Res; 2023 May; 83(10):1742-1756. PubMed ID: 36939399
[TBL] [Abstract][Full Text] [Related]
4. Identification of common genetic variants controlling transcript isoform variation in human whole blood.
Zhang X; Joehanes R; Chen BH; Huan T; Ying S; Munson PJ; Johnson AD; Levy D; O'Donnell CJ
Nat Genet; 2015 Apr; 47(4):345-52. PubMed ID: 25685889
[TBL] [Abstract][Full Text] [Related]
5. Integrative splicing-quantitative-trait-locus analysis reveals risk loci for non-small-cell lung cancer.
Wang Y; Ding Y; Liu S; Wang C; Zhang E; Chen C; Zhu M; Zhang J; Zhu C; Ji M; Dai J; Jin G; Hu Z; Shen H; Ma H
Am J Hum Genet; 2023 Sep; 110(9):1574-1589. PubMed ID: 37562399
[TBL] [Abstract][Full Text] [Related]
6. Long-read sequencing for 29 immune cell subsets reveals disease-linked isoforms.
Inamo J; Suzuki A; Ueda MT; Yamaguchi K; Nishida H; Suzuki K; Kaneko Y; Takeuchi T; Hatano H; Ishigaki K; Ishihama Y; Yamamoto K; Kochi Y
Nat Commun; 2024 May; 15(1):4285. PubMed ID: 38806455
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Aberrant RNA Splicing Is a Primary Link between Genetic Variation and Pancreatic Cancer Risk.
Tian J; Chen C; Rao M; Zhang M; Lu Z; Cai Y; Ying P; Li B; Wang H; Wang L; Li Y; Huang J; Fan L; Cai X; Ning C; Li Y; Zhang F; Wang W; Jiang Y; Liu Y; Wang M; Li H; Huang C; Yang Z; Chang J; Zhu Y; Yang X; Miao X
Cancer Res; 2022 Jun; 82(11):2084-2096. PubMed ID: 35363263
[TBL] [Abstract][Full Text] [Related]
9. Genome-wide identification of splicing QTLs in the human brain and their enrichment among schizophrenia-associated loci.
Takata A; Matsumoto N; Kato T
Nat Commun; 2017 Feb; 8():14519. PubMed ID: 28240266
[TBL] [Abstract][Full Text] [Related]
10. Identification of Candidate mRNA Isoforms for Prostate Cancer-Risk SNPs Utilizing Iso-eQTL and sQTL Methods.
Moradi A; Sharma H; Sharma RD; Fernando A; Barrero RA; Batra J
Int J Mol Sci; 2022 Oct; 23(20):. PubMed ID: 36293264
[TBL] [Abstract][Full Text] [Related]
11. Analysis of genetically driven alternative splicing identifies FBXO38 as a novel COPD susceptibility gene.
Saferali A; Yun JH; Parker MM; Sakornsakolpat P; Chase RP; Lamb A; Hobbs BD; Boezen MH; Dai X; de Jong K; Beaty TH; Wei W; Zhou X; Silverman EK; Cho MH; Castaldi PJ; Hersh CP; ;
PLoS Genet; 2019 Jul; 15(7):e1008229. PubMed ID: 31269066
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Long-read proteogenomics to connect disease-associated sQTLs to the protein isoform effectors of disease.
Abood A; Mesner LD; Jeffery ED; Murali M; Lehe M; Saquing J; Farber CR; Sheynkman GM
bioRxiv; 2023 Mar; ():. PubMed ID: 36993769
[TBL] [Abstract][Full Text] [Related]
14. Genetic control of RNA splicing and its distinct role in complex trait variation.
Qi T; Wu Y; Fang H; Zhang F; Liu S; Zeng J; Yang J
Nat Genet; 2022 Sep; 54(9):1355-1363. PubMed ID: 35982161
[TBL] [Abstract][Full Text] [Related]
15. Bridging the splicing gap in human genetics with long-read RNA sequencing: finding the protein isoform drivers of disease.
Castaldi PJ; Abood A; Farber CR; Sheynkman GM
Hum Mol Genet; 2022 Oct; 31(R1):R123-R136. PubMed ID: 35960994
[TBL] [Abstract][Full Text] [Related]
16. Identification of eQTLs and sQTLs associated with meat quality in beef.
Leal-Gutiérrez JD; Elzo MA; Mateescu RG
BMC Genomics; 2020 Jan; 21(1):104. PubMed ID: 32000679
[TBL] [Abstract][Full Text] [Related]
17. Genome-Wide Association Analyses Reveal the Importance of Alternative Splicing in Diversifying Gene Function and Regulating Phenotypic Variation in Maize.
Chen Q; Han Y; Liu H; Wang X; Sun J; Zhao B; Li W; Tian J; Liang Y; Yan J; Yang X; Tian F
Plant Cell; 2018 Jul; 30(7):1404-1423. PubMed ID: 29967286
[TBL] [Abstract][Full Text] [Related]
18. Genome variants associated with RNA splicing variations in bovine are extensively shared between tissues.
Xiang R; Hayes BJ; Vander Jagt CJ; MacLeod IM; Khansefid M; Bowman PJ; Yuan Z; Prowse-Wilkins CP; Reich CM; Mason BA; Garner JB; Marett LC; Chen Y; Bolormaa S; Daetwyler HD; Chamberlain AJ; Goddard ME
BMC Genomics; 2018 Jul; 19(1):521. PubMed ID: 29973141
[TBL] [Abstract][Full Text] [Related]
19. Splicing annotation of endometrial cancer GWAS risk loci reveals potentially causal variants and supports a role for
Canson DM; O'Mara TA; Spurdle AB; Glubb DM
HGG Adv; 2023 Apr; 4(2):100185. PubMed ID: 36908940
[TBL] [Abstract][Full Text] [Related]
20. Genome-Wide Identification of Splicing Quantitative Trait Loci (sQTLs) in Diverse Ecotypes of
Khokhar W; Hassan MA; Reddy ASN; Chaudhary S; Jabre I; Byrne LJ; Syed NH
Front Plant Sci; 2019; 10():1160. PubMed ID: 31632417
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
