October 24, 2008 article Open access Sequence variant classification and reporting: recommendations for improving the interpretation of cancer susceptibility genetic test results Human Mutation DOI: 10.1002/humu.20880 Full text (OA) OpenAlex Authors 0 Author list not loaded yet. Cited by 27 stored of 935 Search Sort Most cited Newest Oldest Patent citations Title Any typearticle review book-chapter conference-paper preprint dissertation book dataset other Any fieldAgricultural and Biological Sciences Arts and Humanities Biochemistry, Genetics and Molecular Biology Business, Management and Accounting Chemical Engineering Chemistry Computer Science Decision Sciences Dentistry Earth and Planetary Sciences Economics, Econometrics and Finance Energy Engineering Environmental Science Health Professions Immunology and Microbiology Materials Science Mathematics Medicine Neuroscience Nursing Pharmacology, Toxicology and Pharmaceutics Physics and Astronomy Psychology Social Sciences Veterinary Open access The RECAP Test Rapidly and Reliably Identifies Homologous Recombination-Deficient Ovarian Carcinomas 2020 Cancers article Medicine PARP inhibition in cancer therapy Open access 45 citations Functional Characterization of PALB2 Variants of Uncertain Significance: Toward Cancer Risk and Therapy Response Prediction 2020 Frontiers in Molecular Biosciences article Biochemistry, Genetics and Molecular Biology BRCA gene mutations in cancer Open access 16 citations Functional Categorization of BRCA1 Variants of Uncertain Clinical Significance in Homologous Recombination Repair Complementation Assays 2020 Clinical Cancer Research article Biochemistry, Genetics and Molecular Biology BRCA gene mutations in cancer Open access 39 citations Genotype-phenotype correlations for pancreatic cancer risk in Dutch melanoma families with pathogenic CDKN2A variants 2020 Journal of Medical Genetics article Medicine Pancreatic and Hepatic Oncology Research Open access 31 citations Alternative mRNA splicing can attenuate the pathogenicity of presumed loss-of-function variants in BRCA2 2020 Genetics in Medicine article Biochemistry, Genetics and Molecular Biology BRCA gene mutations in cancer Open access 40 citations Variants of uncertain clinical significance in hereditary breast and ovarian cancer genes: best practices in functional analysis for clinical annotation 2020 Journal of Medical Genetics article Biochemistry, Genetics and Molecular Biology BRCA gene mutations in cancer Open access 48 citations Two integrated and highly predictive functional analysis-based procedures for the classification of MSH6 variants in Lynch syndrome 2020 Genetics in Medicine article Medicine Genetic factors in colorectal cancer Open access cited by 2 patents 27 citations 21–27 of 27 ← Previous Page 2 / 2 References 0