Works matching IS 09646906 AND DT 2021 AND VI 30 AND IP 21


Results: 12
    1
    2
    3
    4
    5
    6
    7
    8
    9
    10
    11

    novel somatic mutation in GNB2 provides new insights to the pathogenesis of Sturge–Weber syndrome.

    Published in:
    Human Molecular Genetics, 2021, v. 30, n. 21, p. 1919, doi. 10.1093/hmg/ddab144
    By:
    • Fjær, Roar;
    • Marciniak, Katarzyna;
    • Sundnes, Olav;
    • Hjorthaug, Hanne;
    • Sheng, Ying;
    • Hammarström, Clara;
    • Sitek, Jan Cezary;
    • Vigeland, Magnus Dehli;
    • Backe, Paul Hoff;
    • Øye, Ane-Marte;
    • Fosse, Johanna Hol;
    • Stav-Noraas, Tor Espen;
    • Uchiyama, Yuri;
    • Matsumoto, Naomichi;
    • Comi, Anne;
    • Pevsner, Jonathan;
    • Haraldsen, Guttorm;
    • Selmer, Kaja Kristine
    Publication type:
    Article
    12

    Genome-wide association study of cardiac troponin I in the general population.

    Published in:
    Human Molecular Genetics, 2021, v. 30, n. 21, p. 2027, doi. 10.1093/hmg/ddab124
    By:
    • Moksnes, Marta R;
    • Røsjø, Helge;
    • Richmond, Anne;
    • Lyngbakken, Magnus N;
    • Graham, Sarah E;
    • Hansen, Ailin Falkmo;
    • Wolford, Brooke N;
    • Taliun, Sarah A Gagliano;
    • LeFaive, Jonathon;
    • Rasheed, Humaira;
    • Thomas, Laurent F;
    • Zhou, Wei;
    • Aung, Nay;
    • Surakka, Ida;
    • Douville, Nicholas J;
    • Campbell, Archie;
    • Porteous, David J;
    • Petersen, Steffen E;
    • Munroe, Patricia B;
    • Welsh, Paul
    Publication type:
    Article