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Tomas Zima

Showing results (71-80 of 76) with videos related to

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Cancers|January 8, 2023
Low Frequency of Cancer-Predisposition Gene Mutations in Liver Transplant Candidates with Hepatocellular CarcinomaKlara Horackova, Sona Frankova, Petra Zemankova, et al.
Cancer|May 8, 2024
Population-specific validation and comparison of the performance of 77- and 313-variant polygenic risk scores for breast cancer risk predictionMilena Hovhannisyan, Petra Zemankova, Petr Nehasil, et al.
Oncology Letters|May 8, 2023
Germline multigene panel testing of patients with endometrial cancerJan Kral, Sandra Jelinkova, Petra Zemankova, et al.
Cancer Medicine|August 16, 2024
A comprehensive study evaluating germline FANCG variants in predisposition to breast and ovarian cancerJana Soukupova, Barbora Stastna, Madiha Kanwal, et al.
Breast (Edinburgh, Scotland)|March 30, 2024
A deep intronic recurrent CHEK2 variant c.1009-118_1009-87delinsC affects pre-mRNA splicing and contributes to hereditary breast cancer predispositionPetra Zemankova, Marta Cerna, Klara Horackova, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|July 14, 2023
ENIGMA CHEK2gether Project: A Comprehensive Study Identifies Functionally Impaired CHEK2 Germline Missense Variants Associated with Increased Breast Cancer RiskLenka Stolarova, Petra Kleiblova, Petra Zemankova, et al.
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Showing results (71-80 of 76) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 76 results.
Cancers|January 8, 2023
Low Frequency of Cancer-Predisposition Gene Mutations in Liver Transplant Candidates with Hepatocellular CarcinomaKlara Horackova, Sona Frankova, Petra Zemankova, et al.
Cancer|May 8, 2024
Population-specific validation and comparison of the performance of 77- and 313-variant polygenic risk scores for breast cancer risk predictionMilena Hovhannisyan, Petra Zemankova, Petr Nehasil, et al.
Oncology Letters|May 8, 2023
Germline multigene panel testing of patients with endometrial cancerJan Kral, Sandra Jelinkova, Petra Zemankova, et al.
Cancer Medicine|August 16, 2024
A comprehensive study evaluating germline FANCG variants in predisposition to breast and ovarian cancerJana Soukupova, Barbora Stastna, Madiha Kanwal, et al.
Breast (Edinburgh, Scotland)|March 30, 2024
A deep intronic recurrent CHEK2 variant c.1009-118_1009-87delinsC affects pre-mRNA splicing and contributes to hereditary breast cancer predispositionPetra Zemankova, Marta Cerna, Klara Horackova, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|July 14, 2023
ENIGMA CHEK2gether Project: A Comprehensive Study Identifies Functionally Impaired CHEK2 Germline Missense Variants Associated with Increased Breast Cancer RiskLenka Stolarova, Petra Kleiblova, Petra Zemankova, et al.
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