Associated Papers
Genetic contributors to osteoporosis in pregnancy and lactation associated osteoporosis (PLO).
Lynch L et al.
Bone, 2026
Domain mapping of disease mutations reveals pathogenic SORL1 variants in Alzheimer's disease.
Andersen OM et al.
Molecular Neurodegeneration, 2025
41327266 (PubMed )
Supplement: 13024_2025_907_MOESM2_ESM.pdf
An LRP6 mutation (Arg360His) associated with low bone mineral density but not cardiovascular events in a Caucasian family.
Puente N et al.
Osteoporosis International : a Journal Established as Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the Usa, 2022
Regulation of the Low-Density Lipoprotein Receptor-Related Protein LRP6 and Its Association With Disease: Wnt/β-Catenin Signaling and Beyond.
Jeong W et al.
Frontiers in Cell and Developmental Biology, 2021
The interplay of canonical and noncanonical Wnt signaling in metabolic syndrome.
Abou Ziki MD et al.
Nutrition Research (new York, N.y.), 2019
The association of LRP6 rs2302685 (V1062I) polymorphism with the risk of hyperlipidemia in Iranian children and adolescents.
Montazeri-Najafabady N et al.
Annals of Human Genetics, 2018
Harnessing low-density lipoprotein receptor protein 6 (LRP6) genetic variation and Wnt signaling for innovative diagnostics in complex diseases.
Wang ZM et al.
The Pharmacogenomics Journal, 2018
Mutant LRP6 Impairs Endothelial Cell Functions Associated with Familial Normolipidemic Coronary Artery Disease.
Guo J et al.
International Journal of Molecular Sciences, 2016
27455246 (PubMed )
Supplement: ijms-17-01173-s001.pdf
Metabolic syndrome: genetic insights into disease pathogenesis.
Abou Ziki MD et al.
Current Opinion in Lipidology, 2016
Rare nonconservative LRP6 mutations are associated with metabolic syndrome.
Singh R et al.
Human Mutation, 2013
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