Journal of Medical Genetics · 2006 · 115 citations · 20 references
A large deletion of exons 9 and 10 of CHEK2 confers an increased risk of prostate cancer in Polish men. The del5395 founder deletion might be present in other Slavic populations, including Ukraine, Belarus, Russia, Baltic and Balkan countries. It will be of interest to see to what extent this deletion is responsible for the burden of prostate cancer in other populations.
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Heterozygous Germ Line <i>hCHK2</i> Mutations in Li-Fraumeni Syndrome
Daphne W. Bell, Jennifer M. Varley, Tara E. Szydlo et al. · Science · 1999 · 899 citations
Spectrum of Mutations in BRCA1, BRCA2, CHEK2, and TP53 in Families at High Risk of Breast Cancer
Tom Walsh, Silvia Casadei, Kathryn Hale Coats et al. · JAMA · 2006 · 662 citations
CHEK2 Is a Multiorgan Cancer Susceptibility Gene
Cezary Cybulski, Bohdan Górski, Tomasz Huzarski et al. · The American Journal of Human Genetics · 2004 · 549 citations · Full text