W. Fu

发表

Identification of one novel mutation in the EVC2 gene in a Chinese family with Ellis-van Creveld syndrome.

Zhenlin Zhang, Jin-wei He, Zeng Zhang, 2012, Gene.

Establishing Reference Intervals for Bone Turnover Markers in the Healthy Shanghai Population and the Relationship with Bone Mineral Density in Postmenopausal Women

Wei-wei Hu, Zhenlin Zhang, Jin-wei He, 2013, International journal of endocrinology.

Identification of a novel mutation in the CLCN5 gene in a Chinese family with Dent‐1 disease

Zhenlin Zhang, Jin-wei He, H. Yue, 2014, Nephrology.

A novel compound mutation of CYP27B1 in a Chinese family with vitamin D-dependent rickets type 1A

Zhenlin Zhang, Jin-wei He, H. Yue, 2014, Journal of pediatric endocrinology & metabolism : JPEM.

Reports of 17 Chinese patients with tumor-induced osteomalacia

Wei Yu, Zhenlin Zhang, Jin-wei He, 2017, Journal of Bone and Mineral Metabolism.

High Prevalence of Vitamin D Insufficiency in China: Relationship with the Levels of Parathyroid Hormone and Markers of Bone Turnover

Zhenlin Zhang, Jin-wei He, Hankui Lu, 2012, PloS one.

OPG, RANKL, and RANK gene polymorphisms and the bone mineral density response to alendronate therapy in postmenopausal Chinese women with osteoporosis or osteopenia

Zhenlin Zhang, Jin-wei He, W. Fu, 2016, Pharmacogenetics and genomics.

Associations of serum sclerostin and polymorphisms in the SOST gene with bone mineral density and markers of bone metabolism in postmenopausal Chinese women.

Wei-wei Hu, Yujuan Liu, Zhenlin Zhang, 2014, The Journal of clinical endocrinology and metabolism.

Serum osteocalcin levels are inversely associated with plasma glucose and body mass index in healthy Chinese women

Di Chen, Zhenlin Zhang, Jin-wei He, 2014, Acta Pharmacologica Sinica.

The A242T mutation in the low-density lipoprotein receptor-related protein 5 gene in one Chinese family with osteosclerosis.

Bao-Hong Zhang, Zhenlin Zhang, Jin-wei He, 2013, Internal medicine.

Whole-Exome Sequencing Identifies Novel Recurrent Somatic Mutations in Sporadic Parathyroid Adenomas.

Zhenlin Zhang, Youben Fan, Jin-wei He, 2018, Endocrinology.

Fibroblast Growth Factor 21 Is Associated With Bone Mineral Density, but not With Bone Turnover Markers and Fractures in Chinese Postmenopausal Women.

Wei-wei Hu, C. Wang, Zhenlin Zhang, 2019, Journal of clinical densitometry : the official journal of the International Society for Clinical Densitometry.

The identification of novel mutations in COL1A1, COL1A2, and LEPRE1 genes in Chinese patients with osteogenesis imperfecta

Zhenlin Zhang, Jin-wei He, H. Yue, 2012, Journal of Bone and Mineral Metabolism.

Genetic Polymorphisms of Nuclear Factor-κB Family Affect the Bone Mineral Density Response to Zoledronic Acid Therapy in Postmenopausal Chinese Women

Zhenlin Zhang, Jin-wei He, W. Fu, 2022, Genes.

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

Wei-wei Hu, Zhenlin Zhang, Jin-wei He, 2018, Biomarkers : biochemical indicators of exposure, response, and susceptibility to chemicals.

Thirteen Chinese patients with sporadic Paget’s disease of bone: clinical features, SQSTM1 mutation identification, and functional analysis

Zhenlin Zhang, Jin-wei He, H. Yue, 2012, Journal of Bone and Mineral Metabolism.

Three novel PHEX gene mutations in four Chinese families with X-linked dominant hypophosphatemic rickets.

Zhenlin Zhang, Jin-wei He, Q. Kang, 2012, Biochemical and biophysical research communications.

A novel mutation (R122Q) in the cathepsin K gene in a Chinese child with Pyknodysostosis.

Zhenlin Zhang, Jin-wei He, Zeng Zhang, 2013, Gene.

Identification of one novel mutation in the C-propeptide of COL2A1 in a Chinese family with spondyloperipheral dysplasia.

Zhenlin Zhang, Jin-wei He, Shichang Zhao, 2013, Gene.

Osteomalacia induced by long-term low-dose adefovir dipivoxil: Clinical characteristics and genetic predictors.

Zhenlin Zhang, Jin-wei He, Zhe Wei, 2016, Bone.

Mutations in the SLCO2A1 gene and primary hypertrophic osteoarthropathy: a clinical and biochemical characterization.

Zhenlin Zhang, Jin-wei He, Zeng Zhang, 2013, The Journal of clinical endocrinology and metabolism.

Five novel NF1 gene pathogenic variants in 10 different Chinese families with neurofibromatosis type 1

Zhenlin Zhang, Jin-wei He, Jia Xu, 2019, Molecular genetics & genomic medicine.

Targeted resequencing of phosphorus metabolism‑related genes in 86 patients with hypophosphatemic rickets/osteomalacia.

Wei-wei Hu, Zhenlin Zhang, Jin-wei He, 2018, International journal of molecular medicine.

Seven novel and six de novo PHEX gene mutations in patients with hypophosphatemic rickets

Shan-shan Li, Zhenlin Zhang, Jin-wei He, 2016, International journal of molecular medicine.

Mutation screening for the EXT1 and EXT2 genes in Chinese patients with multiple osteochondromas.

Zhenlin Zhang, Jin-wei He, Q. Kang, 2013, Archives of medical research.

Clinical, Biochemical, and Genetic Features of 41 Han Chinese Families With Primary Hypertrophic Osteoarthropathy, and Their Therapeutic Response to Etoricoxib: Results From a Six‐Month Prospective Clinical Intervention

Shan-shan Li, Zhenlin Zhang, W. Fu, 2017, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Exome sequencing identifies SLCO2A1 mutations as a cause of primary hypertrophic osteoarthropathy.

Wei-wei Hu, Yujuan Liu, W. Xia, 2012, American journal of human genetics.

No association of the polymorphisms of the frizzled-related protein gene with peak bone mineral density in Chinese nuclear families

Zhenlin Zhang, Jin-wei He, H. Yue, 2010, BMC Medical Genetics.

LOX gene polymorphisms are associated with osteoporotic vertebral compression fracture in postmenopausal Chinese women.

Youjia Xu, Zhenlin Zhang, Jin-wei He, 2020, Gene.

Clinical characteristics and the identification of novel mutations of COL1A1 and COL1A2 in 61 Chinese patients with osteogenesis imperfecta.

Wei-wei Hu, Zhenlin Zhang, Jin-wei He, 2016, Molecular medicine reports.

Identification of Two Novel Mutations in the PHEX Gene in Chinese Patients with Hypophosphatemic Rickets/Osteomalacia

Wei-wei Hu, Zhenlin Zhang, Jin-wei He, 2014, PloS one.

Phenotype and Genotype Analysis of Chinese Patients with Osteogenesis Imperfecta Type V

Zhenlin Zhang, Jin-wei He, Zeng Zhang, 2013, PloS one.

Polymorphisms in the HOXD4 gene are not associated with peak bone mineral density in Chinese nuclear families

Zhenlin Zhang, Jin-wei He, H. Yue, 2010, Acta Pharmacologica Sinica.

Susceptibility genes for osteoporotic fracture in postmenopausal chinese women

Zhenlin Zhang, Jin-wei He, H. Yue, 2012, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Genetically Low Vitamin D Levels, Bone Mineral Density, and Bone Metabolism Markers: a Mendelian Randomisation Study

Shan-shan Li, Zhenlin Zhang, W. Fu, 2016, Scientific Reports.

An analysis of the association between the vitamin D pathway and serum 25‐hydroxyvitamin D levels in a healthy Chinese population

Zhenlin Zhang, Jin-wei He, Zeng Zhang, 2013, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

A novel VCP mutation as the cause of atypical IBMPFD in a Chinese family.

Zhenlin Zhang, Jin-wei He, H. Yue, 2013, Bone.

Genetic variants in the PLS3 gene are associated with osteoporotic fractures in postmenopausal Chinese women

Zhenlin Zhang, Jin-wei He, C. Shao, 2019, Acta Pharmacologica Sinica.

LGR4 Gene Polymorphisms Are Associated With Bone and Obesity Phenotypes in Chinese Female Nuclear Families

Shan-shan Li, Zhenlin Zhang, Jin-wei He, 2021, Frontiers in Endocrinology.

Association between LGR4 polymorphisms and peak bone mineral density and body composition

Zhenlin Zhang, Jin-wei He, Zeng Zhang, 2020, Journal of Bone and Mineral Metabolism.

Identification of the CLCN7 gene mutations in two Chinese families with autosomal dominant osteopetrosis (type II)

Zhenlin Zhang, Jin-wei He, Hao Zhang, 2009, Journal of Bone and Mineral Metabolism.

Two novel mutations of CLCN7 gene in Chinese families with autosomal dominant osteopetrosis (type II)

Zhenlin Zhang, Jin-wei He, C. Shao, 2016, Journal of Bone and Mineral Metabolism.

Natural History of Type II Autosomal Dominant Osteopetrosis: A Single Center Retrospective Study

Xia Li, C. Wang, Zhenlin Zhang, 2022, Frontiers in Endocrinology.

Calcification of joints and arteries: second report with novel NT5E mutations and expansion of the phenotype

Zhenlin Zhang, Jin-wei He, Zeng Zhang, 2015, Journal of Human Genetics.

Novel mutations of TCIRG1 cause a malignant and mild phenotype of autosomal recessive osteopetrosis (ARO) in four Chinese families

Zhenlin Zhang, Jin-wei He, W. Fu, 2017, Acta Pharmacologica Sinica.

The virulence gene and clinical phenotypes of osteopetrosis in the Chinese population: six novel mutations of the CLCN7 gene in twelve osteopetrosis families

Zhenlin Zhang, Jin-wei He, H. Yue, 2012, Journal of Bone and Mineral Metabolism.

The rs1634330 Polymorphisms in the SOST Gene Are Associated with Body Composition in Chinese Nuclear Families with Male Offspring

Youjia Xu, Wei-wei Hu, Zhenlin Zhang, 2021, International journal of endocrinology.

Association between SNPs and haplotypes in the METTL21C gene and peak bone mineral density and body composition in Chinese male nuclear families

Shan-shan Li, Zhenlin Zhang, Jin-wei He, 2017, Journal of Bone and Mineral Metabolism.

Association between VDR and ESR1 gene polymorphisms with bone and obesity phenotypes in Chinese male nuclear families

Zhenlin Zhang, Jin-wei He, H. Yue, 2009, Acta Pharmacologica Sinica.

Association of ALOX15 gene polymorphisms with obesity-related phenotypes in Chinese nuclear families with male offspring

Zhenlin Zhang, Jin-wei He, H. Yue, 2012, Acta Pharmacologica Sinica.

Identification of two novel mutations in the OCRL1 gene in two Chinese families with Lowe syndrome

Zhenlin Zhang, Jin-wei He, W. Fu, 2012, Nephrology.

BMP7 gene polymorphisms are not associated with bone mineral density or osteoporotic fractures in postmenopausal Chinese women

Shan-shan Li, Zhenlin Zhang, Jin-wei He, 2016, Acta Pharmacologica Sinica.

Association of ALOX12 and ALOX15 gene polymorphisms with age at menarche and natural menopause in Chinese women

Wei-wei Hu, Yujuan Liu, Zhenlin Zhang, 2012, Menopause.

Two novel mutations in the SLCO2A1 gene in a Chinese patient with primary hypertrophic osteoarthropathy.

Zhenlin Zhang, Jin-wei He, Zeng Zhang, 2014, Gene.

A novel mutation in the SLCO2A1 gene in a Chinese family with primary hypertrophic osteoarthropathy.

Zhenlin Zhang, Jin-wei He, Zeng Zhang, 2013, Gene.

Association of serum 25-hydroxyvitamin D with insulin resistance and β-cell function in a healthy Chinese female population

Zhenlin Zhang, Jin-wei He, Zeng Zhang, 2013, Acta Pharmacologica Sinica.

Contribution of Myostatin gene polymorphisms to normal variation in lean mass, fat mass and peak BMD in Chinese male offspring

Zhenlin Zhang, Jin-wei He, H. Yue, 2012, Acta Pharmacologica Sinica.

The efficacy and safety of weekly 35-mg risedronate dosing regimen for Chinese postmenopausal women with osteoporosis or osteopenia: 1-year data

W. Xia, Zhenlin Zhang, Jin-wei He, 2015, Acta Pharmacologica Sinica.

Associations of Serum Osteocalcin and Polymorphisms of the Osteocalcin Gene with Bone Mineral Density in Postmenopausal and Elderly Chinese Women

Zhenlin Zhang, Jin-wei He, W. Fu, 2016, Lifestyle Genomics.

No association between polymorphisms and haplotypes of COL1A1 and COL1A2 genes and osteoporotic fracture in postmenopausal Chinese women

Zhenlin Zhang, Jin-wei He, H. Yue, 2011, Acta Pharmacologica Sinica.

Genetics Evaluation of Targeted Exome Sequencing in 223 Chinese Probands With Genetic Skeletal Dysplasias

Shan-shan Li, Wei-wei Hu, Zhenlin Zhang, 2021, Frontiers in Cell and Developmental Biology.

Lean mass predicts hip geometry and bone mineral density in chinese men and women and age comparisons of body composition.

Wei-wei Hu, Zhenlin Zhang, H. Yue, 2012, Journal of clinical densitometry : the official journal of the International Society for Clinical Densitometry.

Identification of two novel mutations in the SLC4A1 gene in two unrelated Chinese families with distal renal tubular acidosis.

Zhenlin Zhang, Jin-wei He, H. Yue, 2012, Archives of medical research.

Association between NF-κB Signal Pathway-Related Gene Polymorphisms and Response to Alendronate Treatment in Postmenopausal Chinese Women with Low Bone Mineral Density

F. Hua, C. Wang, Li Liu, 2022, Evidence-based complementary and alternative medicine : eCAM.

Novel mutations of the SERPINF1 and FKBP10 genes in Chinese families with autosomal recessive osteogenesis imperfecta.

Wei-wei Hu, Zhenlin Zhang, Jin-wei He, 2018, International journal of molecular medicine.

Association of single nucleotide polymorphism Rs2236518 in PRDM16 gene with BMI in Chinese males

Zhenlin Zhang, Jin-wei He, H. Yue, 2013, Acta Pharmacologica Sinica.

Association between Low Density Lipoprotein Receptor- Related Protein 2 Gene Polymorphisms and Bone Mineral Density Variation in Chinese Population

Y. Hu, Zhenlin Zhang, Jin-wei He, 2011 .

Identification of three novel mutations in the COL2A1 gene in four unrelated Chinese families with spondyloepiphyseal dysplasia congenita.

Zhenlin Zhang, Jin-wei He, Zeng Zhang, 2011, Biochemical and biophysical research communications.

Clinical and genetic profiles of 985 Chinese families with skeletal dysplasia

Shan-shan Li, Zhenlin Zhang, H. Yue, 2023, Chinese medical journal.

Polymorphisms in Wnt signaling pathway genes are associated with peak bone mineral density, lean mass, and fat mass in Chinese male nuclear families

H. Zhang, Wenxian Yu, Maolan Li, 2016, Osteoporosis International.

ALOX12 polymorphisms are associated with fat mass but not peak bone mineral density in Chinese nuclear families

H. Zhang, Congrong Wang, Jin-wei He, 2010, International Journal of Obesity.

No causal effect of serum urate on bone-related outcomes among a population of postmenopausal women and elderly men of Chinese Han ethnicity—a Mendelian randomization study

J. Yu, J.-W. He, W. Fu, 2016, Osteoporosis International.

Clinical characteristics and the identification of novel mutations of COL1A1 and COL1A2 in 61 Chinese patients with osteogenesis imperfecta

Wei-wei Hu, Zhenlin Zhang, Jin-wei He, 2016, Molecular medicine reports.

Association of SOST gene polymorphisms with peak bone mineral density in Chinese nuclear families with male-offspring.

Zhenlin Zhang, Jin-wei He, S. Xiang, 2019, Acta biochimica et biophysica Sinica.

No association between LRP5 gene polymorphisms and bone and obesity phenotypes in Chinese male-offspring nuclear families

Zhenlin Zhang, Jin-wei He, H. Yue, 2010, Acta Pharmacologica Sinica.

Identification of two novel CLCN7 gene mutations in three Chinese families with autosomal dominant osteopetrosis type II.

Zhenlin Zhang, Jin-wei He, Zeng Zhang, 2014, Joint, bone, spine : revue du rhumatisme.

Novel mutations in the SEC24D gene in Chinese families with autosomal recessive osteogenesis imperfecta

H. Zhang, H. Yue, C. Wang, 2017, Osteoporosis International.