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Causality and functional relevance of BRCA1 and BRCA2 pathogenic variants in non-high-grade serous ovarian carcinomas
PredictCBC-2.0: a contralateral breast cancer risk prediction model developed and validated in similar to 200,000 patients (vol 24, 69, 2022)
PredictCBC-2.0: a contralateral breast cancer risk prediction model developed and validated in similar to 200,000 patients
Clinical applicability of the Polygenic Risk Score for breast cancer risk prediction in familial cases
Polygenic risk modeling for prediction of epithelial ovarian cancer risk
Germline BRCA-Associated Endometrial Carcinoma Is a Distinct Clinicopathologic Entity
Families with BAP1-Tumor Predisposition Syndrome in The Netherlands: Path to Identification and a Proposal for Genetic Screening Guidelines
Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer
Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations
A Post Hoc Study on Gene Panel Analysis for the Diagnosis of Dystonia
Uptake of prenatal diagnostic testing for retinoblastoma compared to other hereditary cancer syndromes in the Netherlands
Bias Explains Most of the Parent-of-Origin Effect on Breast Cancer Risk in BRCA1/2 Mutation Carriers
The growth response to GH treatment is greater in patients with SHOX enhancer deletions compared to SHOX defects
Assessing Associations between the AURKA-HMMR-TPX2-TUBG1 Functional Module and Breast Cancer Risk in BRCA1/2 Mutation Carriers
A Study of the Clinical and Radiological Features in a Cohort of 93 Patients with a COL2A1 Mutation Causing Spondyloepiphyseal Dysplasia Congenita or a Related Phenotype
Candidate Genetic Modifiers for Breast and Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers
Variation in Mutation Spectrum Partly Explains Regional Differences in the Breast Cancer Risk of Female BRCA Mutation Carriers in the Netherlands
DNA Glycosylases Involved in Base Excision Repair May Be Associated with Cancer Risk in BRCA1 and BRCA2 Mutation Carriers
Identification of a BRCA2-Specific Modifier Locus at 6p24 Related to Breast Cancer Risk
Genome-Wide Association Study in BRCA1 Mutation Carriers Identifies Novel Loci Associated with Breast and Ovarian Cancer Risk
Phenotypic characterization of patients with deletions in the 3 '-flanking SHOX region
An urgent need for a change in policy revealed by a study on prenatal testing for Duchenne muscular dystrophy
TP53 germline mutation testing in 180 families suspected of Li-Fraumeni syndrome: mutation detection rate and relative frequency of cancers in different familial phenotypes