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Author

Jana Házová

Observed names: J Hazova, J Házová, Jana Hazova
Observed institution: Masaryk Memorial Cancer Institute
ORCID: 0000-0001-8221-3867
Observed ORCID: 0000-0001-8221-3867
OpenAlex ID: A5085963563
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 testing and prevention of hereditary cancer at the MMCI--over 10 years of experience.
2010 · L Foretova, K Petrakova, et al. · PubMed · 8
A comprehensive analysis of germline predisposition to early-onset ovarian cancer
2024 · Klara Horackova, Petra Zemankova, et al. · Scientific Reports · 7
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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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[The clinical importance of a genetic analysis of moderate-risk cancer susceptibility genes in breast and other cancer patients from the Czech Republic].
2012 · P Pohlreich, Z Kleibl, et al. · PubMed · 3
Genetic Predisposition to Male Breast Cancer
2024 · Markéta Janatová, Marianna Borecká, et al. · Folia Biologica · 2
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BAP1 mutation in a family with malignant mesothelioma and uvealmelanoma
2014 · Lenka Foretová, Marie Navrátilová, et al.
BAP1 syndrom s maligním mesotheliomem a uveálním melanomem
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.
Genetický polymorfismus CYP2D6 u pacientů léčených Paroxetinema modelování mutantních forem CYP2D6
2008 · Eva Flodrová, Jan Juřica, et al.
Detekce mutací v genu CYP2D6 cytochromu P450 - jejich vliv na metabolismus léčiv
2007 · Jana Házová
Molecular genetic detection of alleles of the CYP2D6 gene inpatinets with depression or anxiety disorders
2006 · Barbora Ravčuková, Eva Hadašová, et al.
Works count: 17
Citation count: 162
H-index: 7
I10-index: 5
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