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Author

Petra Vašíčková

Observed name: Petra Vasickova
ORCID: 0000-0002-4518-5403
Observed ORCID: 0000-0002-4518-5403
OpenAlex ID: A5071996345
Male breast cancer in BRCA1 and BRCA2 mutation carriers: pathology data from the Consortium of Investigators of Modifiers of BRCA1/2
2016 · kConFab Investigators, Valentina Silvestri, et al. · Breast Cancer Research · 119
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Spectrum and characterisation of BRCA1 and BRCA2deleterious mutations in high-risk Czech patients with breast and/or ovarian cancer
2008 · Eva Machackova, Lenka Foretova, et al. · BMC Cancer · 85
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High occurrence of BRCA1 intragenic rearrangements in hereditary breast and ovarian cancer syndrome in the Czech Republic
2007 · Petra Vasickova, Eva Machackova, et al. · BMC Medical Genetics · 57
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GAPPS – Gastric Adenocarcinoma and Proximal Polyposis of the Stomach Syndrome in 8 Families Tested at Masaryk Memorial Cancer Institute – Prevention and Prophylactic Gastrectomies
2019 · Lenka Foretova, Marie Navratilova, et al. · Klinicka onkologie · 46
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Multigene Panel Germline Testing of 1333 Czech Patients with Ovarian Cancer
2020 · Klara Lhotova, Lenka Stolarova, et al. · Cancers · 41
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Recommendations for Preventive Care for Women with Rare Genetic Cause of Breast and Ovarian Cancer
2019 · Lenka Foretová, Marie Navrátilová, et al. · Klinicka onkologie · 25
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Twenty Years of BRCA1 and BRCA2 Molecular Analysis at MMCI – Current Developments for the Classifi cation of Variants
2019 · Eva Machackova, Kathleen Claes, et al. · Klinicka onkologie · 15
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BAP1 Syndrome – Predisposition to Malignant Mesothelioma, Skin and Uveal Melanoma, Renal and Other Cancers
2019 · Lenka Foretová, Marie Navrátilová, et al. · Klinicka onkologie · 10
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Genetic and Preventive Services for Hereditary Breast and Ovarian Cancer in the Czech Republic
2006 · Lenka Foretova, Katarina Petrakova, et al. · Hereditary Cancer in Clinical Practice · 6
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Retrospective NGS Study in High-risk Hereditary Cancer Patients at Masaryk Memorial Cancer Institute
2016 · Eva Macháčková, Jana Házová, et al. · Klinicka onkologie · 5
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BAP1 mutation in a family with malignant mesothelioma and uvealmelanoma
2014 · Lenka Foretová, Marie Navrátilová, et al.
BRCA1/2, CHEK2 and TP53 testing in Czech high-risk families with breast or ovarian cancer
2014 · Lenka Foretová, Marie Navrátilová, et al.
Molekulárně genetické metody používané v diagnostice hereditárních nádorových syndromů v OEGN laboratoři v MOÚ
2014 · Eva Macháčková, Jana Házová, et al.
Sledování výskytu vybraných cizorodých látek v potravinách
2006 · Petra Vašíčková
Works count: 15
Citation count: 409
H-index: 8
I10-index: 8
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