Jinwei He
Yishan Road 600
Shanghai, 200233, China
Shanghai, 200233, China
Last Updated: 09/26/2026
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Found 16 publications
GIPR rs10423928 and bone mineral density in postmenopausal women in Shanghai.
Journal: Endocrine connections
Published: December 22, 2021
Association of HIVEP3 Gene and Lnc RNA with Femoral Neck Bone Mineral Content and Hip Geometry by Genome-Wide Association Analysis in Chinese People.
Journal: International journal of endocrinology
Published: April 08, 2020
Sclerostin and Its Associations With Bone Metabolism Markers and Sex Hormones in Healthy Community-Dwelling Elderly Individuals and Adolescents.
Journal: Frontiers in cell and developmental biology
Published: November 05, 2019
Relationship between glucagon-like peptide-1 receptor gene polymorphism and bone mineral density in postmenopausal women in Shanghai.
Journal: Annals of palliative medicine
Published: October 19, 2019
Five novel NF1 gene pathogenic variants in 10 different Chinese families with neurofibromatosis type 1.
Journal: Molecular genetics & genomic medicine
Published: April 04, 2019
Association of SOST gene polymorphisms with peak bone mineral density in Chinese nuclear families with male-offspring.
Journal: Acta biochimica et biophysica Sinica
Published: December 03, 2018
Fibroblast Growth Factor 21 Is Associated With Bone Mineral Density, but not With Bone Turnover Markers and Fractures in Chinese Postmenopausal Women.
Journal: Journal of clinical densitometry : the official journal of the International Society for Clinical Densitometry
Published: July 16, 2018
No association between the vitamin D pathway gene polymorphisms and bone biomarkers response to calcium and low dose calcitriol supplementation in postmenopausal Chinese women: a one-year prospective study.
Journal: Biomarkers : biochemical indicators of exposure, response, and susceptibility to chemicals
Published: May 08, 2018
Targeted resequencing of phosphorus metabolism‑related genes in 86 patients with hypophosphatemic rickets/osteomalacia.
Journal: International journal of molecular medicine
Published: February 16, 2018
Novel mutations of CLCN7 cause autosomal dominant osteopetrosis type II (ADOII) and intermediate autosomal recessive osteopetrosis (ARO) in seven Chinese families.
Journal: Postgraduate medicine
Published: October 05, 2017
Novel mutations of the SERPINF1 and FKBP10 genes in Chinese families with autosomal recessive osteogenesis imperfecta.
Journal: International journal of molecular medicine
Published: September 17, 2017
Last Updated: 09/26/2026