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Author Details

Jan Lubinski
Pomeranian Medical University
1979
737
93
PMIDPaper TitleJournal TitlePublished Year
38030749Risk-reducing mastectomy and breast cancer mortality in women with a BRCA1 or BRCA2 pathogenic variant: an international analysis.Br J Cancer2024
38030749Risk-reducing mastectomy and breast cancer mortality in women with a BRCA1 or BRCA2 pathogenic variant: an international analysis.Br J Cancer2024
38015775Correlates of Circulating Osteoprotegerin in Women with a Pathogenic or Likely Pathogenic Variant in the BRCA1 Gene.Cancer Epidemiol Biomarkers Prev2024
38015775Correlates of Circulating Osteoprotegerin in Women with a Pathogenic or Likely Pathogenic Variant in the BRCA1 Gene.Cancer Epidemiol Biomarkers Prev2024
36824750Association of the CHEK2 c.1100delC variant, radiotherapy, and systemic treatment with contralateral breast cancer risk and breast cancer-specific survival.Res Sq2023
37945903Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants.Nat Genet2023
37752189Analytical sensitivity of a method is critical in detection of low-level BRCA1 constitutional epimutation.Sci Rep2023
38019076Physical Activity During Adolescence and Early-adulthood and Ovarian Cancer Among Women with a BRCA1 or BRCA2 Mutation.Cancer Res Commun2023
37914736MTHFR C677T and A1298C polymorphism's effect on risk of colorectal cancer in Lynch syndrome.Sci Rep2023
37728466Nuclear expression of Ku70/80 is associated with CHEK2 germline mutations in breast cancer.Pol J Pathol2023
37789226Polymorphisms in genes of melatonin biosynthesis and signaling support the light-at-night hypothesis for breast cancer.Eur J Epidemiol2023
36839209An Assessment of Serum Selenium Concentration in Women with Ovarian Cancer.Nutrients2023
37209533Dissecting the genetic heterogeneity of gastric cancer.EBioMedicine2023
37020525<i>IRF6</i> and <i>FGF1</i> polymorphisms in non-syndromic cleft lip with or without cleft palate in the Polish population.Open Med (Wars)2023
36824750Association of the CHEK2 c.1100delC variant, radiotherapy, and systemic treatment with contralateral breast cancer risk and breast cancer-specific survival.Res Sq2023
36707629FANCM missense variants and breast cancer risk: a case-control association study of 75,156 European women.Eur J Hum Genet2023
36572991CCNE1 and survival of patients with tubo-ovarian high-grade serous carcinoma: An Ovarian Tumor Tissue Analysis consortium study.Cancer2023
36948887p53 and ovarian carcinoma survival: an Ovarian Tumor Tissue Analysis consortium study.J Pathol Clin Res2023
36571512The risks of cancer in older women with BRCA pathogenic variants: How far have we come?Cancer2023
37451831Evaluation of European-based polygenic risk score for breast cancer in Ashkenazi Jewish women in Israel.J Med Genet2023
37444426Spectrum and Frequency of Germline <i>FANCM</i> Protein-Truncating Variants in 44,803 European Female Breast Cancer Cases.Cancers (Basel)2023
37312208Genetic testing for hereditary breast cancer in Poland: 1998-2022.Hered Cancer Clin Pract2023
37299574Serum Essential Elements and Survival after Cancer Diagnosis.Nutrients2023
37510234The <i>APOBEC3B</i> c.783delG Truncating Mutation Is Not Associated with an Increased Risk of Breast Cancer in the Polish Population.Genes (Basel)2023
37480624Corrigendum to "Dissecting the genetic heterogeneity of gastric cancer".EBioMedicine2023
37291133Identification of BRCA1/2 mutation female carriers using circulating microRNA profiles.Nat Commun2023
36977412Variants in ATRIP are associated with breast cancer susceptibility in the Polish population and UK Biobank.Am J Hum Genet2023
38019076Physical Activity During Adolescence and Early-adulthood and Ovarian Cancer Among Women with a BRCA1 or BRCA2 Mutation.Cancer Res Commun2023
37914736MTHFR C677T and A1298C polymorphism's effect on risk of colorectal cancer in Lynch syndrome.Sci Rep2023
37752189Analytical sensitivity of a method is critical in detection of low-level BRCA1 constitutional epimutation.Sci Rep2023
37480624Corrigendum to "Dissecting the genetic heterogeneity of gastric cancer".EBioMedicine2023
37789226Polymorphisms in genes of melatonin biosynthesis and signaling support the light-at-night hypothesis for breast cancer.Eur J Epidemiol2023
37510234The <i>APOBEC3B</i> c.783delG Truncating Mutation Is Not Associated with an Increased Risk of Breast Cancer in the Polish Population.Genes (Basel)2023
37945903Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants.Nat Genet2023
37728466Nuclear expression of Ku70/80 is associated with CHEK2 germline mutations in breast cancer.Pol J Pathol2023
37291133Identification of BRCA1/2 mutation female carriers using circulating microRNA profiles.Nat Commun2023
37020525<i>IRF6</i> and <i>FGF1</i> polymorphisms in non-syndromic cleft lip with or without cleft palate in the Polish population.Open Med (Wars)2023
36948887p53 and ovarian carcinoma survival: an Ovarian Tumor Tissue Analysis consortium study.J Pathol Clin Res2023
37451831Evaluation of European-based polygenic risk score for breast cancer in Ashkenazi Jewish women in Israel.J Med Genet2023
37312208Genetic testing for hereditary breast cancer in Poland: 1998-2022.Hered Cancer Clin Pract2023
37444426Spectrum and Frequency of Germline <i>FANCM</i> Protein-Truncating Variants in 44,803 European Female Breast Cancer Cases.Cancers (Basel)2023
37209533Dissecting the genetic heterogeneity of gastric cancer.EBioMedicine2023
36977412Variants in ATRIP are associated with breast cancer susceptibility in the Polish population and UK Biobank.Am J Hum Genet2023
37299574Serum Essential Elements and Survival after Cancer Diagnosis.Nutrients2023
36839209An Assessment of Serum Selenium Concentration in Women with Ovarian Cancer.Nutrients2023
36572991CCNE1 and survival of patients with tubo-ovarian high-grade serous carcinoma: An Ovarian Tumor Tissue Analysis consortium study.Cancer2023
36707629FANCM missense variants and breast cancer risk: a case-control association study of 75,156 European women.Eur J Hum Genet2023
36571512The risks of cancer in older women with BRCA pathogenic variants: How far have we come?Cancer2023
34897700Validated biomarker assays confirm that ARID1A loss is confounded with MMR deficiency, CD8<sup>+</sup> TIL infiltration, and provides no independent prognostic value in endometriosis-associated ovarian carcinomas.J Pathol2022
35396580Mapping genomic loci implicates genes and synaptic biology in schizophrenia.Nature2022
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Collaborators

International Hereditary Cancer Center, Pomeranian Medical University
Co-authored papers 292
International Hereditary Cancer Center, Pomeranian Medical University
Co-authored papers 259
Center for Cancer Genetic Epidemiology, University of Cambridge
Co-authored papers 153
University of Cambridge
Co-authored papers 148
QIMR Berghofer Medical Research Institute
Co-authored papers 131
Otto-Friedrich-University Bamberg
Co-authored papers 126
German Cancer Research Center (DKFZ)
Co-authored papers 125
Mayo Clinic
Co-authored papers 114
Co-authored papers 112
Co-authored papers 107
Instituto de Salud Carlos III
Co-authored papers 102
University of Toronto
Co-authored papers 102
University of California irvine
Co-authored papers 102
Co-authored papers 101
David Geffen School of Medicine, University of California los angeles
Co-authored papers 100
Co-authored papers 97
National Cancer Institute
Co-authored papers 96
Ospedale Circolo e Fondazione Macchi
Co-authored papers 90
Co-authored papers 86
University of Southern California
Co-authored papers 82
Co-authored papers 82
The M. Sklodowska-Curie Cancer Center and Institute of Oncology
Co-authored papers 80
University of Southern California
Co-authored papers 79
National Cancer Institute, National Institutes of Health
Co-authored papers 74
School of Clinical Medicine, University of NSW Sydney, Lowy Cancer Research Centre
Co-authored papers 72
The Usher Institute, The University of Edinburgh
Co-authored papers 71
Faculty of Clinical Medicine, University of Oslo
Co-authored papers 70
Co-authored papers 70
Co-authored papers 68
Segal Cancer Centre, Jewish General Hospital
Co-authored papers 66