Associated Papers
Reply to: Population-Wide Differences in Allele Frequencies of WNT9B E152K and Q47R Genetic Variants Suggest Reassessment of Prostate Cancer Risk.
Dupont WD et al.
Jco Precision Oncology, 2025
Population-Wide Differences in Allele Frequencies of WNT9B E152K and Q47R Genetic Variants Suggest Reassessment of Prostate Cancer Risk.
Raha R et al.
Jco Precision Oncology, 2025
Coding Variants of the Genitourinary Development Gene WNT9B Carry High Risk for Prostate Cancer.
Dupont WD et al.
Jco Precision Oncology, 2025
Accumulation of rare coding variants in genes implicated in risk of human cleft lip with or without cleft palate.
Marini NJ et al.
American Journal of Medical Genetics. Part A, 2019
31063268 (PubMed )
Supplement: AJMG-179-1260-s006.xlsx › Table_S3
Mutations in WNT9B are associated with Mayer-Rokitansky-Küster-Hauser syndrome.
Waschk DE et al.
Clinical Genetics, 2016
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