Zhenlin Zhang

发表

Menatetrenone versus alfacalcidol in the treatment of Chinese postmenopausal women with osteoporosis: a multicenter, randomized, double-blinded, double-dummy, positive drug-controlled clinical trial

X. Xing, Yan Jiang, Zhenlin Zhang, 2014, Clinical interventions in aging.

Association of JAG1 with bone mineral density and osteoporotic fractures: a genome-wide association study and follow-up replication studies.

Bjarni V. Halldórsson, D. Kiel, T. Spector, 2010, American journal of human genetics.

Expanding the Clinical Spectrum of Osteogenesis Imperfecta Type V: 13 Additional Patients and Review

Zhenlin Zhang, Yang-Jia Cao, Zhe Wei, 2019, Front. Endocrinol..

Identification of novel mutations in WISP3 gene in two unrelated Chinese families with progressive pseudorheumatoid dysplasia.

Zhenlin Zhang, Jin-wei He, H. Yue, 2009, Bone.

Calcifediol (25-hydroxyvitamin D) improvement and calcium-phosphate metabolism of alendronate sodium/vitamin D3 combination in Chinese women with postmenopausal osteoporosis: a post hoc efficacy analysis and safety reappraisal

E. Liao, W. Xia, Zhenlin Zhang, 2018, BMC Musculoskeletal Disorders.

Pathogenic Mutations in the Valosin-containing Protein/p97(VCP) N-domain Inhibit the SUMOylation of VCP and Lead to Impaired Stress Response*

Zhenlin Zhang, Tao Wang, Wangchao Xu, 2016, The Journal of Biological Chemistry.

Chinese Bone Turnover Marker Study: Reference Ranges for C-Terminal Telopeptide of Type I Collagen and Procollagen I N-Terminal Peptide by Age and Gender

W. Xia, Ling Xu, Mei Li, 2014, PloS one.

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.

Sclerostin and Its Associations With Bone Metabolism Markers and Sex Hormones in Healthy Community-Dwelling Elderly Individuals and Adolescents

Zhenlin Zhang, Jin-wei He, H. Yue, 2020, Frontiers in Cell and Developmental Biology.

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.

Association of bone turnover markers with glucose metabolism in Chinese population

Y. Bao, Cheng Hu, X. Hou, 2017, Acta Pharmacologica Sinica.

Prevalence of Vitamin D Inadequacy Among Chinese Postmenopausal Women: A Nationwide, Multicenter, Cross-Sectional Study

J. Chandler, W. Xia, Zhenlin Zhang, 2019, Front. Endocrinol..

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.

Identification of mutations in EXT1 and EXT2 genes in six Chinese families with multiple osteochondromas.

Zhenlin Zhang, Q. Kang, Yang Xu, 2017, Molecular medicine reports.

Clinical characteristics associated with bone mineral density improvement after 1-year alendronate/vitamin d3 or calcitriol treatment

E. Liao, W. Xia, Zhenlin Zhang, 2018, Medicine.

[Association of polymorphisms of vitamin D receptor gene start codon and 3'-end region with bone mineral density in postmenopausal women].

X. Xing, W. Xia, Zhenlin Zhang, 2003, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

[Association of Apa I polymorphism of vitamin D receptor gene with bone mass in men].

Qi Zhou, Zhenlin Zhang, Jin-wei He, 2003, Zhongguo yi xue ke xue yuan xue bao. Acta Academiae Medicinae Sinicae.

Association of estrogen receptor-alpha and vitamin D receptor genotypes with therapeutic response to calcium in postmenopausal Chinese women.

Qi Zhou, Zhenlin Zhang, Jin-wei He, 2004, Acta pharmacologica Sinica.

The influence of rs139416141 in Neighbor of Brca1 gene (NBR1) on bone mineral density in postmenopausal Chinese women.

Zhenlin Zhang, Yang Zhang, Zinan Zhang, 2020, Acta biochimica et biophysica Sinica.

Association of HIVEP3 Gene and Lnc RNA with Femoral Neck Bone Mineral Content and Hip Geometry by Genome-Wide Association Analysis in Chinese People

Wei-wei Hu, Zhenlin Zhang, Jin-wei He, 2020, International journal of endocrinology.

Effect of low-dose alendronate treatment on bone mineral density and bone turnover markers in Chinese postmenopausal women with osteopenia and osteoporosis

E. Liao, Z. Sheng, W. Xia, 2013, Menopause.

Efficacy of Yigu® versus Aclasta® in Chinese postmenopausal women with osteoporosis: a multicenter prospective study

Shi-gui Yan, Zhenlin Zhang, Q. Cheng, 2022, Archives of Osteoporosis.

Zhenlin Zhang, Jin-wei He, Hao Zhang, 2008, Acta Pharmacologica Sinica.

Associations of Serum Cathepsin K and Polymorphisms in CTSK Gene With Bone Mineral Density and Bone Metabolism Markers in Postmenopausal Chinese Women

Shan-shan Li, Zhenlin Zhang, H. Yue, 2020, Frontiers in Endocrinology.

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.

Comparing Clinical and Genetic Characteristics of De Novo and Inherited COL1A1/COL1A2 Variants in a Large Chinese Cohort of Osteogenesis Imperfecta

H. Zhang, Zhenlin Zhang, Yazhao Mei, 2022, Frontiers in Endocrinology.

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.

Association of serum uric acid levels with osteoporosis and bone turnover markers in a Chinese population

Y. Bao, Cheng Hu, W. Jia, 2017, Acta Pharmacologica Sinica.

Association of polymorphisms in low-density lipoprotein receptor-related protein 5 gene with bone mineral density in postmenopausal Chinese women

Zhenlin Zhang, Jin-wei He, Yu-juan Liu, 2005, Acta Pharmacologica Sinica.

Clinical and genetic analysis in 185 Chinese probands of osteogenesis imperfecta

Zhenlin Zhang, Hao Zhang, Lei Xi, 2020, Journal of Bone and Mineral Metabolism.

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.

Clinical and genetic characteristics of 29 Chinese patients with X-linked hypophosphatemia

Zhenlin Zhang, H. Yue, Xiaohui Tao, 2022, Frontiers in Endocrinology.

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.

Clinical and Genetic Characteristics of 153 Chinese Patients With X-Linked Hypophosphatemia

Shan-shan Li, Zhenlin Zhang, H. Yue, 2021, Frontiers in Cell and Developmental Biology.

Comparison of the effects of cholecalciferol and calcitriol on calcium metabolism and bone turnover in Chinese postmenopausal women with vitamin D insufficiency

Zhenlin Zhang, Hao Zhang, Jie-mei Gu, 2012, Acta Pharmacologica Sinica.

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.

Exploring and expanding the phenotype and genotype diversity in seven Chinese families with spondylo-epi-metaphyseal dysplasia

H. Zhang, Shan-shan Li, C. Wang, 2022, Frontiers in Genetics.

[Osteoprotegerin gene polymorphism and therapeutic response to alendronate in postmenopausal women with osteoporosis].

Zhenlin Zhang, Jin-wei He, Hao Zhang, 2009, Zhonghua yi xue za zhi.

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.

Identification of a novel mutation of the NTRK1 gene in patients with congenital insensitivity to pain with anhidrosis (CIPA).

Zhenlin Zhang, Yang-Jia Cao, Wenbo Wang, 2018, Gene.

A phase III randomized, double-blind, placebo-controlled trial of the denosumab biosimilar QL1206 in postmenopausal Chinese women with osteoporosis and high fracture risk

Guang Wang, Y. Huo, Han Yang, 2022, Acta Pharmacologica Sinica.

Clinical and Molecular Characterization and Discovery of Novel Genetic Mutations of Chinese Patients with COL2A1-related Dysplasia

Wei-wei Hu, Zhenlin Zhang, H. Yue, 2020, International journal of biological sciences.

Clinical Diagnosis of X-Linked Spondyloepiphyseal Dysplasia Tarda and a Novel Missense Mutation in the Sedlin Gene (SEDL)

Chengsheng Zhang, Shan-shan Li, F. Jing, 2018, International journal of endocrinology.

NOVEL MUTATIONS IN THE WNT1, TMEM38B, P4HB, AND PLS3 GENES IN FOUR UNRELATED CHINESE FAMILIES WITH OSTEOGENESIS IMPERFECTA.

Zhenlin Zhang, Yang-Jia Cao, Hao Zhang, 2019, Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists.

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.

Efficacy and safety of 2 g/day of strontium ranelate in Asian women with postmenopausal osteoporosis.

Jian-min Liu, Ling Xu, Zhenlin Zhang, 2009, Bone.

Glucagon-like peptide-1 receptor gene polymorphism is associated with fat mass in Chinese nuclear families with male offspring.

F. Hua, Zhenlin Zhang, S. Xiang, 2019, Acta biochimica et biophysica Sinica.

17β-estradiol attenuates ovariectomy-induced bone deterioration through the suppression of the ephA2/ephrinA2 signaling pathway

Lin Zhou, Zhenlin Zhang, Lianyong Liu, 2017, Molecular medicine reports.

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.

Hip axis length changes in 10,554 males and females and the association with femoral neck fracture.

Zhenlin Zhang, Jin-wei He, Hao Zhang, 2008, Journal of clinical densitometry : the official journal of the International Society for Clinical Densitometry.

Clinical Characteristics and Pathogenic Gene Identification in Chinese Patients With Paget’s Disease of Bone

Zhenlin Zhang, H. Yue, Zhe Wei, 2022, Frontiers in Endocrinology.

Identification of the mutations in the tissue-nonspecific alkaline phosphatase gene in two Chinese families with hypophosphatasia.

Zhenlin Zhang, H. Yue, Hao Zhang, 2012, Archives of medical research.

Case report: Clinical characteristics and treatment of secondary osteoporosis induced by X-linked congenital adrenal dysplasia

Zhenlin Zhang, H. Yue, Xiaoyun Lin, 2022, Frontiers in Endocrinology.

Identification of NR0B1 Gene Mutation and Analysis of Bone Damages and Drug Treatment Effect in a Big Family With X-linked Adrenal Hypoplasia Congenita: a Case Report

Zhenlin Zhang, H. Yue, Xiaoyun Lin, 2021 .

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.

Association between SNP and haplotypes in PPARGC1 and adiponectin genes and bone mineral density in Chinese nuclear families

Zhenlin Zhang, Jin-wei He, Hao Zhang, 2007, Acta Pharmacologica Sinica.

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.

Genotypic and Phenotypic Characteristics of 29 Patients With Rare Types of Osteogenesis Imperfecta: Average 5 Years of Follow-Up

Zhenlin Zhang, Hao Zhang, Lei Xi, 2021, Frontiers in Genetics.

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.

Vitamin D pathway gene variation rs3740165 is associated with serological uric acid levels in healthy Chinese women

Wei-wei Hu, C. Wang, Zhenlin Zhang, 2022, Frontiers in Endocrinology.

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.

Clinical Characteristics of Primary Hyperparathyroidism: 15-Year Experience of 457 Patients in a Single Center in China

Zhenlin Zhang, Youben Fan, H. Yue, 2021, Frontiers in Endocrinology.

Clinical characteristics and identification of a novel TGFB1 variant in three unrelated Chinese families with Camurati‐Engelmann disease

Zhenlin Zhang, H. Yue, Xingling Yang, 2022, Molecular genetics & genomic medicine.

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 CLCN7 mutations cause autosomal dominant osteopetrosis type II and intermediate autosomal recessive osteopetrosis.

Zhenlin Zhang, H. Yue, Chun Wang, 2019, Molecular medicine reports.

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.

Novel mutations of CLCN7 cause autosomal dominant osteopetrosis type II (ADOII) and intermediate autosomal recessive osteopetrosis (ARO) in seven Chinese families

Zhenlin Zhang, Jin-wei He, Chun Wang, 2017, Postgraduate medicine.

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.

Transforming growth factor-β1 gene mutations and phenotypes in pediatric patients with Camurati‑Engelmann disease.

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

Mutations in Profilin 1 Cause Early‐Onset Paget's Disease of Bone With Giant Cell Tumors

Baojie Li, Shan-shan Li, Lin Chen, 2021, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Early onset Paget's disease of bone caused by a novel mutation (78dup27) of the TNFRSF11A gene in a Chinese family

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

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.

Contribution of the sclerostin domain-containing protein 1 (SOSTDC1) gene to normal variation of peak bone mineral density in Chinese women and men

Zhenlin Zhang, Jin-wei He, H. Yue, 2011, Journal of Bone and Mineral Metabolism.

SOST polymorphisms and response to alendronate treatment in postmenopausal Chinese women with osteoporosis.

E. Liao, X. Xing, W. Xia, 2015, Pharmacogenomics.

Post-genome wide association studies and functional analyses identify association of MPP7 gene variants with site-specific bone mineral density.

Johnny S. H. Kwan, P. Sham, Zhi-Jie Dai, 2012, Human molecular genetics.

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.

East meets West: current practices and policies in the management of musculoskeletal aging

C. Cooper, J. Reginster, R. Rizzoli, 2019, Aging Clinical and Experimental Research.

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.

A mutation in NOTCH2 gene in a Chinese patient with Hajdu-Cheney syndrome.

Zhenlin Zhang, H. Yue, Hao Zhang, 2013, Joint, bone, spine : revue du rhumatisme.

Undercarboxylated Osteocalcin and Its Associations With Bone Mineral Density, Bone Turnover Markers, and Prevalence of Osteopenia and Osteoporosis in Chinese Population: A Cross-Sectional Study

Wei-wei Hu, Zhenlin Zhang, Yang Xu, 2022, Frontiers in Endocrinology.

Association of vitamin D receptor and estrogen receptor-alpha gene polymorphism with peak bone mass and bone size in Chinese women.

Zhenlin Zhang, Qi Zhao, Yu-juan Liu, 2004, Acta pharmacologica Sinica.

Eldecalcitol increases bone mineral density in Chinese osteoporotic patients without vitamin D or calcium supplementation

Toshio Matsumoto, Xinlong Ma, W. Xia, 2019, Journal of Bone and Mineral Metabolism.

The Assessment of the Osteoporosis Self-Assessment Tool for Asians and Calcaneal Quantitative Ultrasound in Identifying Osteoporotic Fractures and Falls Among Chinese People

Zhenlin Zhang, H. Yue, Huijiang Song, 2021, Frontiers in Endocrinology.

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.

Bone mineral density of the spine and femur in healthy Chinese men.

Zhenlin Zhang, Jin-wei He, Hao Zhang, 2006, Asian journal of andrology.

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.

Identifying therapeutic biomarkers of zoledronic acid by metabolomics

Xia Li, Zhenlin Zhang, Xiang Yu, 2023, Frontiers in Pharmacology.

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.

PFN1 Gene Polymorphisms and the Bone Mineral Density Response to Alendronate Therapy in Postmenopausal Chinese Women with Low Bone Mass

C. Wang, Zhenlin Zhang, H. Yue, 2021, Pharmacogenomics and Personalized Medicine.