Associated Papers
LGR4: A New Receptor Member in Endocrine and Metabolic Diseases.
Zhang N et al.
Endocrine Reviews, 2023
Genetic analysis and prenatal diagnosis of short-rib thoracic dysplasia 3 with or without polydactyly caused by compound heterozygous variants of DYNC2H1 gene in four Chinese families.
Fang Y et al.
Frontiers in Genetics, 2023
37007936 (PubMed )
Supplement: Table1.XLS › Sheet
LGR4 Gene Polymorphisms Are Associated With Bone and Obesity Phenotypes in Chinese Female Nuclear Families.
Shi SQ et al.
Frontiers in Endocrinology, 2021
Association between LGR4 polymorphisms and peak bone mineral density and body composition.
Yu WJ et al.
Journal of Bone and Mineral Metabolism, 2020
Association of a gain-of-function variant in LGR4 with central obesity.
Zou Y et al.
Obesity (silver Spring, Md.), 2017
Ablation of LGR4 promotes energy expenditure by driving white-to-brown fat switch.
Wang J et al.
Nature Cell Biology, 2013
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