Works by Hunker, Kristina L.


Results: 9
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    Grxcr2 is required for stereocilia morphogenesis in the cochlea.

    Published in:
    PLoS ONE, 2018, v. 13, n. 8, p. 1, doi. 10.1371/journal.pone.0201713
    By:
    • Avenarius, Matthew R.;
    • Jung, Jae-Yun;
    • Askew, Charles;
    • Jones, Sherri M.;
    • Hunker, Kristina L.;
    • Azaiez, Hela;
    • Rehman, Atteeq U.;
    • Schraders, Margit;
    • Najmabadi, Hossein;
    • Kremer, Hannie;
    • Smith, Richard J. H.;
    • Géléoc, Gwenaëlle S. G.;
    • Dolan, David F.;
    • Raphael, Yehoash;
    • Kohrman, David C.
    Publication type:
    Article
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    Chromosome 1q21.2 and additional loci influence risk of spontaneous coronary artery dissection and myocardial infarction.

    Published in:
    Nature Communications, 2020, v. 11, n. 1, p. N.PAG, doi. 10.1038/s41467-020-17558-x
    By:
    • Saw, Jacqueline;
    • Yang, Min-Lee;
    • Trinder, Mark;
    • Tcheandjieu, Catherine;
    • Xu, Chang;
    • Starovoytov, Andrew;
    • Birt, Isabelle;
    • Mathis, Michael R.;
    • Hunker, Kristina L.;
    • Schmidt, Ellen M.;
    • Jackson, Linda;
    • Fendrikova-Mahlay, Natalia;
    • Zawistowski, Matthew;
    • Brummett, Chad M.;
    • Zoellner, Sebastian;
    • Katz, Alexander;
    • Coleman, Dawn M.;
    • Swan, Kirby;
    • O'Donnell, Christopher J.;
    • Million Veteran Program
    Publication type:
    Article
    7

    Author Correction: Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseases.

    Published in:
    2022
    By:
    • Georges, Adrien;
    • Yang, Min-Lee;
    • Berrandou, Takiy-Eddine;
    • Bakker, Mark K.;
    • Dikilitas, Ozan;
    • Kiando, Soto Romuald;
    • Ma, Lijiang;
    • Satterfield, Benjamin A.;
    • Sengupta, Sebanti;
    • Yu, Mengyao;
    • Deleuze, Jean-François;
    • Dupré, Delia;
    • Hunker, Kristina L.;
    • Kyryachenko, Sergiy;
    • Liu, Lu;
    • Sayoud-Sadeg, Ines;
    • Amar, Laurence;
    • Brummett, Chad M.;
    • Coleman, Dawn M.;
    • d'Escamard, Valentina
    Publication type:
    Correction Notice
    8

    Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseases.

    Published in:
    Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-26174-2
    By:
    • Georges, Adrien;
    • Yang, Min-Lee;
    • Berrandou, Takiy-Eddine;
    • Bakker, Mark K.;
    • Dikilitas, Ozan;
    • Kiando, Soto Romuald;
    • Ma, Lijiang;
    • Satterfield, Benjamin A.;
    • Sengupta, Sebanti;
    • Yu, Mengyao;
    • Deleuze, Jean-François;
    • Dupré, Delia;
    • Hunker, Kristina L.;
    • Kyryachenko, Sergiy;
    • Liu, Lu;
    • Sayoud-Sadeg, Ines;
    • Amar, Laurence;
    • Brummett, Chad M.;
    • Coleman, Dawn M.;
    • d'Escamard, Valentina
    Publication type:
    Article
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