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Detection and localization of early- and late-stage cancers using platelet RNA
Interaction between KDELR2 and HSP47 as a Key Determinant in Osteogenesis Imperfecta Caused by Bi-allelic Variants in KDELR2
Addition of a 161-SNP polygenic risk score to family history-based risk prediction: impact on clinical management in non-BRCA1/2 breast cancer families
Addition of a 161-SNP polygenic risk score to family history-based risk prediction: impact on clinical management in non-BRCA1/2 breast cancer families
Associations of obesity and circulating insulin and glucose with breast cancer risk: a Mendelian randomization analysis
Biallelic loss of function variants in COASY cause prenatal onset pontocerebellar hypoplasia, microcephaly, and arthrogryposis
The Effect of Predictive Testing in Adult-Onset Neurodegenerative Diseases on Social and Personal Life
A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer
The association between cancer family history and ovarian cancer risk in BRCA1/2 mutation carriers: can it be explained by the mutation position?
Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer
Association analysis identifies 65 new breast cancer risk loci
Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer
Uptake of prenatal diagnostic testing for retinoblastoma compared to other hereditary cancer syndromes in the Netherlands
LONG-TERM FOLLOW-UP OF PATIENTS WITH RETINITIS PIGMENTOSA TYPE 12 CAUSED BY CRB1 MUTATIONS A Severe Phenotype With Considerable Interindividual Variability
Genetically Predicted Body Mass Index and Breast Cancer Risk: Mendelian Randomization Analyses of Data from 145,000 Women of European Descent
Effect of predictive testing in adult onset neurodegenerative diseases on social and personal life - a pilot study
A novel Fanconi anaemia subtype associated with a dominant-negative mutation in RAD51
Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer
Relevance and efficacy of breast cancer screening in BRCA1 and BRCA2 mutation carriers above 60 years: A national cohort study
MicroRNA Related Polymorphisms and Breast Cancer Risk
Somatic mutations found in the healthy blood compartment of a 115-yr-old woman demonstrate oligoclonal hematopoiesis
Genome-wide association studies identify four ER negative-specific breast cancer risk loci
Large-scale genotyping identifies 41 new loci associated with breast cancer risk
Exposure to diagnostic radiation and risk of breast cancer among carriers of BRCA1/2 mutations: retrospective cohort study (GENE-RAD-RISK)
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