170 related articles for article (PubMed ID: 38271473)
1. Integration of expression QTLs with fine mapping via SuSiE.
Zhang X; Jiang W; Zhao H
PLoS Genet; 2024 Jan; 20(1):e1010929. PubMed ID: 38271473
[TBL] [Abstract][Full Text] [Related]
2. Integration of Expression QTLs with fine mapping via SuSiE.
Zhang X; Jiang W; Zhao H
medRxiv; 2023 Oct; ():. PubMed ID: 37873337
[TBL] [Abstract][Full Text] [Related]
3. Functionally informed fine-mapping and polygenic localization of complex trait heritability.
Weissbrod O; Hormozdiari F; Benner C; Cui R; Ulirsch J; Gazal S; Schoech AP; van de Geijn B; Reshef Y; Márquez-Luna C; O'Connor L; Pirinen M; Finucane HK; Price AL
Nat Genet; 2020 Dec; 52(12):1355-1363. PubMed ID: 33199916
[TBL] [Abstract][Full Text] [Related]
4. Genetic fine-mapping from summary data using a nonlocal prior improves the detection of multiple causal variants.
Karhunen V; Launonen I; Järvelin MR; Sebert S; Sillanpää MJ
Bioinformatics; 2023 Jul; 39(7):. PubMed ID: 37348543
[TBL] [Abstract][Full Text] [Related]
5. Allele-Specific QTL Fine Mapping with PLASMA.
Wang AT; Shetty A; O'Connor E; Bell C; Pomerantz MM; Freedman ML; Gusev A
Am J Hum Genet; 2020 Feb; 106(2):170-187. PubMed ID: 32004450
[TBL] [Abstract][Full Text] [Related]
6. Improved methods for multi-trait fine mapping of pleiotropic risk loci.
Kichaev G; Roytman M; Johnson R; Eskin E; Lindström S; Kraft P; Pasaniuc B
Bioinformatics; 2017 Jan; 33(2):248-255. PubMed ID: 27663501
[TBL] [Abstract][Full Text] [Related]
7. Leveraging allelic imbalance to refine fine-mapping for eQTL studies.
Zou J; Hormozdiari F; Jew B; Castel SE; Lappalainen T; Ernst J; Sul JH; Eskin E
PLoS Genet; 2019 Dec; 15(12):e1008481. PubMed ID: 31834882
[TBL] [Abstract][Full Text] [Related]
8. SparsePro: An efficient fine-mapping method integrating summary statistics and functional annotations.
Zhang W; Najafabadi H; Li Y
PLoS Genet; 2023 Dec; 19(12):e1011104. PubMed ID: 38153934
[TBL] [Abstract][Full Text] [Related]
9. Identification of potential genetic causal variants for obesity-related traits using statistical fine mapping.
Gong R; Greenbaum J; Lin X; Du Y; Su KJ; Gong Y; Shen J; Deng HW
Mol Genet Genomics; 2023 Nov; 298(6):1309-1319. PubMed ID: 37498361
[TBL] [Abstract][Full Text] [Related]
10. Genome-wide association studies for agronomical traits in a world wide spring barley collection.
Pasam RK; Sharma R; Malosetti M; van Eeuwijk FA; Haseneyer G; Kilian B; Graner A
BMC Plant Biol; 2012 Jan; 12():16. PubMed ID: 22284310
[TBL] [Abstract][Full Text] [Related]
11. The flashfm approach for fine-mapping multiple quantitative traits.
Hernández N; Soenksen J; Newcombe P; Sandhu M; Barroso I; Wallace C; Asimit JL
Nat Commun; 2021 Oct; 12(1):6147. PubMed ID: 34686674
[TBL] [Abstract][Full Text] [Related]
12. An in-depth association analysis of genetic variants within nicotine-related loci: Meeting in middle of GWAS and genetic fine-mapping.
Mo C; Ye Z; Pan Y; Zhang Y; Wu Q; Bi C; Liu S; Mitchell B; Kochunov P; Hong LE; Ma T; Chen S
Mol Cell Neurosci; 2023 Dec; 127():103895. PubMed ID: 37634742
[TBL] [Abstract][Full Text] [Related]
13. Integrating functional data to prioritize causal variants in statistical fine-mapping studies.
Kichaev G; Yang WY; Lindstrom S; Hormozdiari F; Eskin E; Price AL; Kraft P; Pasaniuc B
PLoS Genet; 2014 Oct; 10(10):e1004722. PubMed ID: 25357204
[TBL] [Abstract][Full Text] [Related]
14. Probabilistic fine-mapping of transcriptome-wide association studies.
Mancuso N; Freund MK; Johnson R; Shi H; Kichaev G; Gusev A; Pasaniuc B
Nat Genet; 2019 Apr; 51(4):675-682. PubMed ID: 30926970
[TBL] [Abstract][Full Text] [Related]
15. Effect of all-but-one conditional analysis for eQTL isolation in peripheral blood.
Brown M; Greenwood E; Zeng B; Powell JE; Gibson G
Genetics; 2023 Jan; 223(1):. PubMed ID: 36321965
[TBL] [Abstract][Full Text] [Related]
16. Fine-mapping genetic associations.
Hutchinson A; Asimit J; Wallace C
Hum Mol Genet; 2020 Sep; 29(R1):R81-R88. PubMed ID: 32744321
[TBL] [Abstract][Full Text] [Related]
17. A more accurate method for colocalisation analysis allowing for multiple causal variants.
Wallace C
PLoS Genet; 2021 Sep; 17(9):e1009440. PubMed ID: 34587156
[TBL] [Abstract][Full Text] [Related]
18. A multiple regression method for genomewide association studies using only linkage information.
Mei B; Wang Z
J Genet; 2018 Jun; 97(2):477-482. PubMed ID: 29932068
[TBL] [Abstract][Full Text] [Related]
19. Prioritized candidate causal haplotype blocks in plant genome-wide association studies.
Wu X; Jiang W; Fragoso C; Huang J; Zhou G; Zhao H; Dellaporta S
PLoS Genet; 2022 Oct; 18(10):e1010437. PubMed ID: 36251695
[TBL] [Abstract][Full Text] [Related]
20. ANNORE: genetic fine-mapping with functional annotation.
Fisher V; Sebastiani P; Cupples LA; Liu CT
Hum Mol Genet; 2021 Dec; 31(1):32-40. PubMed ID: 34302344
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]