Works matching AU Ronemus, Michael

Results: 16
    1

    Rates of contributory de novo mutation in high and low-risk autism families.

    Published in:
    Communications Biology, 2021, v. 4, n. 1, p. 1, doi. 10.1038/s42003-021-02533-z
    By:
    • Yoon, Seungtai;
    • Munoz, Adriana;
    • Yamrom, Boris;
    • Lee, Yoon-ha;
    • Andrews, Peter;
    • Marks, Steven;
    • Wang, Zihua;
    • Reeves, Catherine;
    • Winterkorn, Lara;
    • Krieger, Abba M.;
    • Buja, Andreas;
    • Pradhan, Kith;
    • Ronemus, Michael;
    • Baldwin, Kristin K.;
    • Levy, Dan;
    • Wigler, Michael;
    • Iossifov, Ivan
    Publication type:
    Article
    2
    3

    Breaking point.

    Published in:
    Nature Medicine, 2000, v. 6, n. 5, p. 503, doi. 10.1038/74974
    By:
    • Ronemus, Michael
    Publication type:
    Article
    4

    A new match-maker.

    Published in:
    Nature Medicine, 2000, v. 6, n. 1, p. 19, doi. 10.1038/71475
    By:
    • Ronemus, Michael
    Publication type:
    Article
    5

    Spring back?or forward?

    Published in:
    Nature Genetics, 2000, v. 24, n. 3, p. 323, doi. 10.1038/73571
    By:
    • Ronemus, Michael
    Publication type:
    Article
    6

    Stocking stuffers.

    Published in:
    Nature Genetics, 1999, v. 23, n. 4, p. 479, doi. 10.1038/70607
    By:
    • Ronemus, Michael
    Publication type:
    Article
    7

    Flower power.

    Published in:
    Nature Genetics, 1999, v. 23, n. 2, p. 132, doi. 10.1038/13757
    By:
    • Ronemus, Michael
    Publication type:
    Article
    8

    Summer array.

    Published in:
    Nature Genetics, 1999, v. 22, n. 2, p. 207, doi. 10.1038/9731
    By:
    • Ronemus, Michael
    Publication type:
    Article
    9

    Shuffling viral tropism.

    Published in:
    Nature Biotechnology, 2000, v. 18, n. 9, p. 913, doi. 10.1038/79331
    By:
    • Ronemus, Michael
    Publication type:
    Article
    10
    11
    12
    13

    Indel variant analysis of short-read sequencing data with Scalpel.

    Published in:
    Nature Protocols, 2016, v. 11, n. 12, p. 2529, doi. 10.1038/nprot.2016.150
    By:
    • Fang, Han;
    • Bergmann, Ewa A;
    • Arora, Kanika;
    • Vacic, Vladimir;
    • Zody, Michael C;
    • Iossifov, Ivan;
    • O'Rawe, Jason A;
    • Wu, Yiyang;
    • Jimenez Barron, Laura T;
    • Rosenbaum, Julie;
    • Ronemus, Michael;
    • Lee, Yoon-ha;
    • Wang, Zihua;
    • Dikoglu, Esra;
    • Jobanputra, Vaidehi;
    • Lyon, Gholson J;
    • Wigler, Michael;
    • Schatz, Michael C;
    • Narzisi, Giuseppe
    Publication type:
    Article
    14
    15

    The contribution of de novo coding mutations to autism spectrum disorder.

    Published in:
    Nature, 2014, v. 515, n. 7526, p. 216, doi. 10.1038/nature13908
    By:
    • Iossifov, Ivan;
    • Ronemus, Michael;
    • Levy, Dan;
    • Yamrom, Boris;
    • Lee, Yoon-ha;
    • Wang, Zihua;
    • Marks, Steven;
    • Andrews, Peter;
    • Leotta, Anthony;
    • Kendall, Jude;
    • Hakker, Inessa;
    • Rosenbaum, Julie;
    • Ma, Beicong;
    • Rodgers, Linda;
    • Troge, Jennifer;
    • Yoon, Seungtai;
    • Schatz, Michael C.;
    • McCombie, W. Richard;
    • Wigler, Michael;
    • Grabowska, Ewa
    Publication type:
    Article
    16

    The contribution of de novo and rare inherited copy number changes to congenital heart disease in an unselected sample of children with conotruncal defects or hypoplastic left heart disease.

    Published in:
    Human Genetics, 2014, v. 133, n. 1, p. 11, doi. 10.1007/s00439-013-1353-9
    By:
    • Warburton, Dorothy;
    • Ronemus, Michael;
    • Kline, Jennie;
    • Jobanputra, Vaidehi;
    • Williams, Ismee;
    • Anyane-Yeboa, Kwame;
    • Chung, Wendy;
    • Yu, Lan;
    • Wong, Nancy;
    • Awad, Danielle;
    • Yu, Chih-yu;
    • Leotta, Anthony;
    • Kendall, Jude;
    • Yamrom, Boris;
    • Lee, Yoon-ha;
    • Wigler, Michael;
    • Levy, Dan
    Publication type:
    Article