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Year | Number of Results |
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2023 | 2 |
2024 | 1 |
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A phenome-wide scan reveals convergence of common and rare variant associations.
Genome Med. 2023 Nov 28;15(1):101. doi: 10.1186/s13073-023-01253-9.
Genome Med. 2023.
PMID: 38017547
Free PMC article.
Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variants.
Einson J, Glinos D, Boerwinkle E, Castaldi P, Darbar D, de Andrade M, Ellinor P, Fornage M, Gabriel S, Germer S, Gibbs R, Hersh CP, Johnsen J, Kaplan R, Konkle BA, Kooperberg C, Nassir R, Loos RJF, Meyers DA, Mitchell BD, Psaty B, Vasan RS, Rich SS, Rienstra M, Rotter JI, Saferali A, Shoemaker MB, Silverman E, Smith AV; NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium; Mohammadi P, Castel SE, Iossifov I, Lappalainen T.
Einson J, et al.
Genetics. 2023 Aug 9;224(4):iyad115. doi: 10.1093/genetics/iyad115.
Genetics. 2023.
PMID: 37348055
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Transcriptome-Wide Association Studies (TWAS): Methodologies, Applications, and Challenges.
Evans P, Nagai T, Konkashbaev A, Zhou D, Knapik EW, Gamazon ER.
Evans P, et al.
Curr Protoc. 2024 Feb;4(2):e981. doi: 10.1002/cpz1.981.
Curr Protoc. 2024.
PMID: 38314955
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