Found: 5

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  • Detectable clonal mosaicism from birth to old age and its relationship to cancer.

    Published in:
    Nature Genetics, 2012, v. 44, n. 6, p. 642, doi. 10.1038/ng.2271
    By:
    • Laurie, Cathy C;
    • Laurie, Cecelia A;
    • Rice, Kenneth;
    • Doheny, Kimberly F;
    • Zelnick, Leila R;
    • McHugh, Caitlin P;
    • Ling, Hua;
    • Hetrick, Kurt N;
    • Pugh, Elizabeth W;
    • Amos, Chris;
    • Wei, Qingyi;
    • Wang, Li-e;
    • Lee, Jeffrey E;
    • Barnes, Kathleen C;
    • Hansel, Nadia N;
    • Mathias, Rasika;
    • Daley, Denise;
    • Beaty, Terri H;
    • Scott, Alan F;
    • Ruczinski, Ingo
    Publication type:
    Article

  • Copy Number Variation in Familial Parkinson Disease.

    Published in:
    PLoS ONE, 2011, v. 6, n. 8, p. 1, doi. 10.1371/journal.pone.0020988
    By:
    • Pankratz, Nathan;
    • Dumitriu, Alexandra;
    • Hetrick, Kurt N.;
    • Mei Sun;
    • Latourelle, Jeanne C.;
    • Wilk, Jemma B.;
    • Halter, Cheryl;
    • Doheny, Kimberly F.;
    • Gusella, James F.;
    • Nichols, William C.;
    • Myers, Richard H.;
    • Foroud, Tatiana;
    • DeStefano, Anita L.
    Publication type:
    Article

  • Genetic Modifiers of Cystic Fibrosis Lung Disease Severity: Whole-Genome Analysis of 7,840 Patients.

    Published in:
    American Journal of Respiratory & Critical Care Medicine, 2023, v. 207, n. 10, p. 1324, doi. 10.1164/rccm.202209-1653OC
    By:
    • Yi-Hui Zhou;
    • Gallins, Paul J.;
    • Pace, Rhonda G.;
    • Hong Dang;
    • Aksit, Melis A.;
    • Blue, Elizabeth E.;
    • Buckingham, Kati J.;
    • Collaco, Joseph M.;
    • Faino, Anna V.;
    • Gordon, William W.;
    • Hetrick, Kurt N.;
    • Hua Ling;
    • Weifang Liu;
    • Onchiri, Frankline M.;
    • Pagel, Kymberleigh;
    • Pugh, Elizabeth W.;
    • Raraigh, Karen S.;
    • Rosenfeld, Margaret;
    • QuanSun;
    • Jia Wen
    Publication type:
    Article

  • R/Bioconductor software for Illumina's Infinium whole-genome genotyping BeadChips.

    Published in:
    Bioinformatics, 2009, v. 25, n. 19, p. 2621, doi. 10.1093/bioinformatics/btp470
    By:
    • Ritchie, Matthew E.;
    • Carvalho, Benilton S.;
    • Hetrick, Kurt N.;
    • Tavaré, Simon;
    • Irizarry, Rafael A.
    Publication type:
    Article

  • Novel Deletion of SERPINF1 Causes Autosomal Recessive Osteogenesis Imperfecta Type VI in Two Brazilian Families.

    Published in:
    Molecular Syndromology, 2014, v. 5, n. 6, p. 268, doi. 10.1159/000369108
    By:
    • Moldenhauer Minillo, Renata;
    • Sobreira, Nara;
    • de Fatima de Faria Soares, Maria;
    • Jurgens, Julie;
    • Ling, Hua;
    • Hetrick, Kurt N.;
    • Doheny, Kimberly F.;
    • Valle, David;
    • Brunoni, Decio;
    • Alvarez Perez, Ana B.
    Publication type:
    Article