Works by Musolf, Anthony M.


Results: 14
    1

    Linear mixed models for association analysis of quantitative traits with next‐generation sequencing data.

    Published in:
    Genetic Epidemiology, 2019, v. 43, n. 2, p. 189, doi. 10.1002/gepi.22177
    By:
    • Chiu, Chi‐yang;
    • Yuan, Fang;
    • Zhang, Bing‐song;
    • Yuan, Ao;
    • Li, Xin;
    • Fang, Hong‐Bin;
    • Lange, Kenneth;
    • Weeks, Daniel E.;
    • Wilson, Alexander F.;
    • Bailey‐Wilson, Joan E.;
    • Musolf, Anthony M.;
    • Stambolian, Dwight;
    • Lakhal‐Chaieb, M'Hamed Lajmi;
    • Cook, Richard J.;
    • McMahon, Francis J.;
    • Amos, Christopher I.;
    • Xiong, Momiao;
    • Fan, Ruzong
    Publication type:
    Article
    2

    Association analyses of rare variants identify two genes associated with refractive error.

    Published in:
    PLoS ONE, 2022, v. 17, n. 9, p. 1, doi. 10.1371/journal.pone.0272379
    By:
    • Patasova, Karina;
    • Haarman, Annechien E. G.;
    • Musolf, Anthony M.;
    • Mahroo, Omar A.;
    • Rahi, Jugnoo S.;
    • Falchi, Mario;
    • Verhoeven, Virginie J. M.;
    • Bailey-Wilson, Joan E.;
    • Klaver, Caroline C. W.;
    • Duggal, Priya;
    • Klein, Alison;
    • Guggenheim, Jeremy A.;
    • Hammond, Chris J.;
    • Hysi, Pirro G.
    Publication type:
    Article
    3

    Myopia in Chinese families shows linkage to 10q26.13.

    Published in:
    Molecular Vision, 2018, v. 24, p. 29
    By:
    • Musolf, Anthony M.;
    • Simpson, Claire L.;
    • Long, Kyle A.;
    • Moiz, Bilal A.;
    • Lewis, Deyana D.;
    • Middlebrooks, Candace D.;
    • Portas, Laura;
    • Murgia, Federico;
    • Ciner, Elise B.;
    • Bailey-Wilson, Joan E.;
    • Stambolian, Dwight
    Publication type:
    Article
    4

    Whole genome sequencing identifies associations for nonsyndromic sagittal craniosynostosis with the intergenic region of BMP2 and noncoding RNA gene LINC01428.

    Published in:
    Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-58343-w
    By:
    • Musolf, Anthony M.;
    • Justice, Cristina M.;
    • Erdogan-Yildirim, Zeynep;
    • Goovaerts, Seppe;
    • Cuellar, Araceli;
    • Shaffer, John R.;
    • Marazita, Mary L.;
    • Claes, Peter;
    • Weinberg, Seth M.;
    • Li, Jae;
    • Senders, Craig;
    • Zwienenberg, Marike;
    • Simeonov, Emil;
    • Kaneva, Radka;
    • Roscioli, Tony;
    • Di Pietro, Lorena;
    • Barba, Marta;
    • Lattanzi, Wanda;
    • Cunningham, Michael L.;
    • Romitti, Paul A.
    Publication type:
    Article
    5
    6

    Whole exome sequence analysis in 51 624 participants identifies novel genes and variants associated with refractive error and myopia.

    Published in:
    Human Molecular Genetics, 2022, v. 31, n. 11, p. 1909, doi. 10.1093/hmg/ddac004
    By:
    • Guggenheim, Jeremy A;
    • Clark, Rosie;
    • Cui, Jiangtian;
    • Terry, Louise;
    • Patasova, Karina;
    • Haarman, Annechien E G;
    • Musolf, Anthony M;
    • Verhoeven, Virginie J M;
    • Klaver, Caroline C W;
    • Bailey-Wilson, Joan E;
    • Hysi, Pirro G;
    • Williams, Cathy;
    • Consortium, CREAM;
    • Consortium, UK Biobank Eye Vision
    Publication type:
    Article
    7
    8
    9
    10
    11
    12
    13

    Rare variant analyses across multiethnic cohorts identify novel genes for refractive error.

    Published in:
    Communications Biology, 2023, v. 6, n. 1, p. 1, doi. 10.1038/s42003-022-04323-7
    By:
    • Musolf, Anthony M.;
    • Haarman, Annechien E. G.;
    • Luben, Robert N.;
    • Ong, Jue-Sheng;
    • Patasova, Karina;
    • Trapero, Rolando Hernandez;
    • Marsh, Joseph;
    • Jain, Ishika;
    • Jain, Riya;
    • Wang, Paul Zhiping;
    • Lewis, Deyana D.;
    • Tedja, Milly S.;
    • Iglesias, Adriana I.;
    • Li, Hengtong;
    • Cowan, Cameron S.;
    • Consortium for Refractive Error and Myopia (CREAM);
    • Baird, Paul Nigel;
    • Veluchamy, Amutha Barathi;
    • Burdon, Kathryn P.;
    • Campbell, Harry
    Publication type:
    Article
    14