Associated Papers
Frequency of Founder Mutations in BRCA1 and BRCA2 Genes in Hereditary Breast Cancers in Poland vs. Other Countries.
Kulikowska B et al.
Cancers, 2026
BRCA1 founder mutations do not contribute to increased risk of gastric cancer in the Polish population.
Ławniczak M et al.
Hereditary Cancer in Clinical Practice, 2016
A novel BRCA2 in frame deletion in a Tunisian woman with early onset sporadic breast cancer.
Hadiji-Abbes N et al.
Pathologie-biologie, 2015
Recurrent mutations of BRCA1 and BRCA2 in Poland: an update.
Szwiec M et al.
Clinical Genetics, 2015
Common low-penetrance risk variants associated with breast cancer in Polish women.
Ledwoń JK et al.
Bmc Cancer, 2013
High frequency of BRCA1 founder mutations in Polish women with nonfamilial breast cancer.
Gaj P et al.
Familial Cancer, 2012
Novel germline mutations in BRCA2 gene among breast and breast-ovarian cancer families from Poland.
Balabas A et al.
Familial Cancer, 2010
Selected Aspects of Molecular Diagnostics of Constitutional Alterations in BRCA1 and BRCA2 Genes Associated with Increased Risk of Breast Cancer in the Polish Population.
Górski B
Hereditary Cancer in Clinical Practice, 2006
A high proportion of founder BRCA1 mutations in Polish breast cancer families.
Górski B et al.
International Journal of Cancer, 2004
Cancer variation associated with the position of the mutation in the BRCA2 gene.
Lubinski J et al.
Familial Cancer, 2004
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