Found: 5

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  • Variant-specific inflation factors for assessing population stratification at the phenotypic variance level.

    Published in:
    Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-23655-2
    By:
    • Sofer, Tamar;
    • Zheng, Xiuwen;
    • Laurie, Cecelia A.;
    • Gogarten, Stephanie M.;
    • Brody, Jennifer A.;
    • Conomos, Matthew P.;
    • Bis, Joshua C.;
    • Thornton, Timothy A.;
    • Szpiro, Adam;
    • O'Connell, Jeffrey R.;
    • Lange, Ethan M.;
    • Gao, Yan;
    • Cupples, L. Adrienne;
    • Psaty, Bruce M.;
    • NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium;
    • Abe, Namiko;
    • Abecasis, Gonçalo;
    • Aguet, Francois;
    • Albert, Christine;
    • Almasy, Laura
    Publication type:
    Article

  • eSCAN: scan regulatory regions for aggregate association testing using whole-genome sequencing data.

    Published in:
    Briefings in Bioinformatics, 2022, v. 23, n. 1, p. 1, doi. 10.1093/bib/bbab497
    By:
    • Yang, Yingxi;
    • Sun, Quan;
    • Huang, Le;
    • Broome, Jai G;
    • Correa, Adolfo;
    • Reiner, Alexander;
    • Consortium, NHLBI Trans-Omics for Precision Medicine (TOPMed);
    • Raffield, Laura M;
    • Yang, Yuchen;
    • Li, Yun
    Publication type:
    Article

  • Whole-exome sequencing study identifies four novel gene loci associated with diabetic kidney disease.

    Published in:
    Human Molecular Genetics, 2023, v. 32, n. 6, p. 1048, doi. 10.1093/hmg/ddac290
    By:
    • Pan, Yang;
    • Sun, Xiao;
    • Mi, Xuenan;
    • Huang, Zhijie;
    • Hsu, Yenchih;
    • Hixson, James E;
    • Munzy, Donna;
    • Metcalf, Ginger;
    • Franceschini, Nora;
    • Tin, Adrienne;
    • Köttgen, Anna;
    • Francis, Michael;
    • Group, NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium TOPMed Kidney Function Working;
    • Brody, Jennifer A;
    • Kestenbaum, Bryan;
    • Sitlani, Colleen M;
    • Mychaleckyj, Josyf C;
    • Kramer, Holly;
    • Lange, Leslie A;
    • Guo, Xiuqing
    Publication type:
    Article

  • FGF20 and PGM2 variants are associated with childhood asthma in family-based whole-genome sequencing studies.

    Published in:
    Human Molecular Genetics, 2023, v. 32, n. 4, p. 696, doi. 10.1093/hmg/ddac258
    By:
    • Hecker, Julian;
    • Chun, Sung;
    • Samiei, Ahmad;
    • Liu, Cuining;
    • Laurie, Cecelia;
    • Kachroo, Priyadarshini;
    • Lutz, Sharon M;
    • Lee, Sanghun;
    • Smith, Albert V;
    • Lasky-Su, Jessica;
    • Cho, Michael H;
    • Sharma, Sunita;
    • Quirós, Manuel Enrique Soto;
    • Avila, Lydiana;
    • Celedón, Juan C;
    • Raby, Benjamin;
    • Zhou, Xiaobo;
    • Silverman, Edwin K;
    • DeMeo, Dawn L;
    • Consortium, NHLBI Trans-Omics for Precision Medicine (TOPMed)
    Publication type:
    Article

  • GAWMerge expands GWAS sample size and diversity by combining array-based genotyping and whole-genome sequencing.

    Published in:
    Communications Biology, 2022, v. 5, n. 1, p. 1, doi. 10.1038/s42003-022-03738-6
    By:
    • Mathur, Ravi;
    • Fang, Fang;
    • Gaddis, Nathan;
    • Hancock, Dana B.;
    • Cho, Michael H.;
    • Hokanson, John E.;
    • Bierut, Laura J.;
    • Lutz, Sharon M.;
    • Young, Kendra;
    • Smith, Albert V.;
    • NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium;
    • Silverman, Edwin K.;
    • Page, Grier P.;
    • Johnson, Eric O.
    Publication type:
    Article