Chronic lymphocytic leukemia (CLL) is a highly heritable cancer, with a 7.5-fold increased risk in first-degree relatives.1 However, inherited predisposition to CLL remains largely unexplained by traditional linkage or genome-wide association studies. Here, we hypothesized that CLL heritability might arise from rare coding variants not analyzed in previous studies.
Rare Germline Variants in ATM Are Associated with Chronic Lymphocytic Leukemia
G. Tiao,M. R. Improgo,S. Kasar,W. Poh,A. Kamburov,D. Landau,E. Tausch,A. Taylor-Weiner,C. Cibulskis,S. Bahl,S. Fernandes,Kevin Hoang,Esther Rheinbay,Haesook T. Kim,J. Bahlo,S. Robrecht,K. Fischer,M. Hallek,S. Gabriel,E. Lander,S. Stilgenbauer,Catherine J. Wu,Adam Kiezun,G. Getz,Jennifer R. Brown
Published 2017 in Leukemia
ABSTRACT
PUBLICATION RECORD
- Publication year
2017
- Venue
Leukemia
- Publication date
2017-06-13
- Fields of study
Biology, Medicine
- Identifiers
- External record
- Source metadata
Semantic Scholar, PubMed
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