Lenka Foretová

Biochemistry, Genetics and Molecular Biology · Life Sciences

84h-index31.0kcitations600works4.12yr avg
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Research Topics

BRCA gene mutations in cancer(153), Cancer Genomics and Diagnostics(69), Lymphoma Diagnosis and Treatment(63), Genetic factors in colorectal cancer(56), Nutrition, Genetics, and Disease(55)

Publications573 total

Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies.
Archive ouverte UNIGE (University of Geneva)·2026Open Access
Genetic and molecular factors in the development of bladder cancer - a geneticist's view
Urologie pro praxi·2025
Data from B-Cell NHL Subtype Risk Associated with Autoimmune Conditions and PRS
2025Open Access
Data from Occupational Exposure to Polycyclic Aromatic Hydrocarbons and Lung Cancer Risk: Results from a Pooled Analysis of Case–Control Studies (SYNERGY)
2025Open Access
Supplementary Data from B-Cell NHL Subtype Risk Associated with Autoimmune Conditions and PRS
2025Open Access
Supplementary Figure from Occupational Exposure to Polycyclic Aromatic Hydrocarbons and Lung Cancer Risk: Results from a Pooled Analysis of Case–Control Studies (SYNERGY)
2025Open Access
Supplementary Methods S1 from Application of Genomic Sequencing to Refine Patient Stratification for Adjuvant Therapy in Renal Cell Carcinoma
2025Open Access
Supplementary Table S1 from Application of Genomic Sequencing to Refine Patient Stratification for Adjuvant Therapy in Renal Cell Carcinoma
2025Open Access
Table S2 from ENIGMA <i>CHEK2</i>gether Project: A Comprehensive Study Identifies Functionally Impaired <i>CHEK2</i> Germline Missense Variants Associated with Increased Breast Cancer Risk
2025Open Access
Figure S1 from Application of Genomic Sequencing to Refine Patient Stratification for Adjuvant Therapy in Renal Cell Carcinoma
2025Open Access
Figure S2 from Application of Genomic Sequencing to Refine Patient Stratification for Adjuvant Therapy in Renal Cell Carcinoma
2025Open Access
Supplementary Tables S3-S13 from Application of Genomic Sequencing to Refine Patient Stratification for Adjuvant Therapy in Renal Cell Carcinoma
2025Open Access
Table S1 from ENIGMA <i>CHEK2</i>gether Project: A Comprehensive Study Identifies Functionally Impaired <i>CHEK2</i> Germline Missense Variants Associated with Increased Breast Cancer Risk
2025Open Access
Figure S3 from Application of Genomic Sequencing to Refine Patient Stratification for Adjuvant Therapy in Renal Cell Carcinoma
2025Open Access
Table S3 from ENIGMA <i>CHEK2</i>gether Project: A Comprehensive Study Identifies Functionally Impaired <i>CHEK2</i> Germline Missense Variants Associated with Increased Breast Cancer Risk
2025Open Access
Supplementary Table S2 from Application of Genomic Sequencing to Refine Patient Stratification for Adjuvant Therapy in Renal Cell Carcinoma
2025Open Access
Supplementary Methods 1 from ENIGMA <i>CHEK2</i>gether Project: A Comprehensive Study Identifies Functionally Impaired <i>CHEK2</i> Germline Missense Variants Associated with Increased Breast Cancer Risk
2025Open Access
Genome-wide association study of 398,238 women unveils seven loci associated with high-grade serous ovarian cancer
npj Genomic Medicine·2025Open Access
Using Mendelian randomization to investigate etiologic heterogeneity across renal cell carcinoma subtypes
International Journal of Epidemiology·2025
Leveraging transdiagnostic genetic liability to psychiatric disorders to dissect clinical outcomes of anorexia nervosa
Molecular Psychiatry·2025Open Access
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Frequent Co-authors

Vladimí­r Janout(23), Paul Brennan(23), Vladimír Bencko(21), Jolanta Lissowska(20), Eleonóra Fabiánová(20), Paolo Boffetta(17), Péter Rudnai(17), Rayjean J. Hung(14), Давид Заридзе(14), Dana Mateș(14), Ivana Holcátová(14), Esther M. John(13), James McKay(13), Valérie Gaborieau(10), John K. Field(10), Simone Benhamou(10), Anthony Staines(10), Neonila Szeszenia‐Dąbrowska(10), Lars J. Vatten(9), Ghislaine Scélo(9)