Associated Papers
A novel statistical method for interpreting the pathogenicity of rare variants.
Wang J et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2021
32884132 (PubMed )
Supplement: NIHMS1630822-supplement-Supplementary_Tables.xlsx › S10_LRP5_variant
Primary Osteoporosis in Young Adults: Genetic Basis and Identification of Novel Variants in Causal Genes.
Collet C et al.
Jbmr Plus, 2018
Liver cyst gene knockout in cholangiocytes inhibits cilium formation and Wnt signaling.
Wills ES et al.
Human Molecular Genetics, 2017
LRP5 variants may contribute to ADPKD.
Cnossen WR et al.
European Journal of Human Genetics : Ejhg, 2016
Select a paper to view details