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Urinary incontinence more than 15 years after premenopausal risk-reducing salpingo-oophorectomy
Spectrum and frequency of germline FANCM protein-truncating variants in 44,803 European female breast cancer cases
BRCA Challenge: BRCA Exchange as a global resource for variants in BRCA1 and BRCA2
SNP association study in PMS2-associated Lynch syndrome
The BRCA1 c. 5096G > A p.Arg1699Gln (R1699Q) intermediate risk variant: breast and ovarian cancer risk estimation and recommendations for clinical management from the ENIGMA consortium
The BRCA1 c. 5096G>A p.Arg1699Gln (R1699Q) intermediate risk variant: breast and ovarian cancer risk estimation and recommendations for clinical management from the ENIGMA consortium
Comprehensive Mutation Analysis of PMS2 in a Large Cohort of Probands Suspected of Lynch Syndrome or Constitutional Mismatch Repair Deficiency Syndrome
The effect of genotypes and parent of origin on cancer risk and age of cancer development in PMS2 mutation carriers
Gastric cancer in three relatives of a patient with a biallelic IL12RB1 mutation
Lynch Syndrome Caused by Germline PMS2 Mutations: Delineating the Cancer Risk
Breast and ovarian cancer risks in a large series of clinically ascertained families with a high proportion of BRCA1 and BRCA2 Dutch founder mutations
Risks of Less Common Cancers in Proven Mutation Carriers With Lynch Syndrome
The counselees' self-reported request for psychological help in genetic counseling for hereditary breast/ovarian cancer: not only psychopathology matters
Quantification of Sequence Exchange Events between PMS2 and PMS2CL Provides a Basis for Improved Mutation Scanning of Lynch Syndrome Patients
