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European Journal of Cancer (Oxford, England : 1990)|June 24, 2026
Spectrum of double heterozygosity in individuals diagnosed with hereditary breast and ovarian cancerNatalie Herold, Christoph Engel, Dorothee Speiser, et al.
Hemasphere|January 17, 2025
Disease characteristics and outcomes of acute myeloid leukemia in germline RUNX1 deficiency (Familial Platelet Disorder with associated Myeloid Malignancy)Martijn P T Ernst, Jurjen Versluis, Peter J M Valk, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 18, 2019
An alternative approach to establishing unbiased colorectal cancer risk estimation in Lynch syndromeManon Suerink, Mar Rodríguez-Girondo, Heleen M van der Klift, et al.
Gastroenterology|December 31, 2022
Constitutional Microsatellite Instability, Genotype, and Phenotype Correlations in Constitutional Mismatch Repair DeficiencyRichard Gallon, Rachel Phelps, Christine Hayes, et al.
European Journal of Public Health|June 21, 2024
Genetic counselling legislation and practice in cancer in EU Member StatesJ Matt McCrary, Els Van Valckenborgh, Hélène A Poirel, et al.
Nature Communications|February 27, 2020
The complex genetic landscape of familial MDS and AML reveals pathogenic germline variantsAna Rio-Machin, Tom Vulliamy, Nele Hug, et al.
Blood Advances|July 5, 2023
Somatic mutational landscape of hereditary hematopoietic malignancies caused by germline variants in RUNX1, GATA2, and DDX41Claire C Homan, Michael W Drazer, Kai Yu, et al.
American Journal of Medical Genetics. Part A|February 8, 2017
Childhood cancer predisposition syndromes-A concise review and recommendations by the Cancer Predisposition Working Group of the Society for Pediatric Oncology and HematologyTim Ripperger, Stefan S Bielack, Arndt Borkhardt, et al.
European Journal of Human Genetics : EJHG|February 13, 2026
Priority European strategies for sustainable access to high-quality genetic counselling in cancer: A Delphi studyJ Matt McCrary, Els Van Valckenborgh, Denis Horgan, et al.
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