Jian-yi Wang
Beijing, 100730, China
Last Updated: 09/26/2026
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Found 9 publications
Characterization of the complete chloroplast genome of Calophaca sinica Rehd.
Journal: Mitochondrial DNA. Part B, Resources
Published: December 28, 2020
Extremely low level of serum pigment epithelium-derived factor is a special biomarker of Chinese osteogenesis imperfecta patients with SERPINF1 mutations.
Journal: Clinica chimica acta; international journal of clinical chemistry
Published: August 24, 2017
Novel Mutations in SERPINF1 Result in Rare Osteogenesis Imperfecta Type VI.
Journal: Calcified tissue international
Published: August 12, 2016
THE CLINICAL CHARACTERISTICS AND EFFICACY OF BISPHOSPHONATES IN AUDLT PATIENTS WITH OSTEOGENESIS IMPERGECTA.
Journal: Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists
Published: August 03, 2016
A cryptic balanced translocation involving COL1A2 gene disruption cause a rare type of osteogenesis imperfecta.
Journal: Clinica chimica acta; international journal of clinical chemistry
Published: April 20, 2016
A novel mutation in CLDN16 results in rare familial hypomagnesaemia with hypercalciuria and nephrocalcinosis in a Chinese family.
Journal: Clinica chimica acta; international journal of clinical chemistry
Published: February 13, 2016
The analysis of DKK1 polymorphisms in relation to skeletal phenotypes and bone response to alendronate treatment in Chinese postmenopausal women.
Journal: Pharmacogenomics
Published: January 19, 2016
Novel mutations in FKBP10 in Chinese patients with osteogenesis imperfecta and their treatment with zoledronic acid.
Journal: Journal of human genetics
Published: January 05, 2016
Two novel mutations in TMEM38B result in rare autosomal recessive osteogenesis imperfecta.
Journal: Journal of human genetics
Published: November 19, 2015
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Last Updated: 09/26/2026