导师姓名： 章振林 专业代码： 100201
性别： 男 专业名称： 内科学
培养单位： 附属第六人民医院 三级学科/
专业领域： 内分泌与代谢病
导师类型： 博士生导师 专业学位导师： 兼
联系方式： 电子邮箱：zhangzl@sjtu.edu.cn/zzl2002@medmail.com.cn
邮编： 200233 邮箱地址： zhangzl@sjtu.edu.cn

研究方向 (点击浏览详细信息)
代谢性及遗传性骨病的分子机制研究

社会任职
中华医学会骨质疏松和骨矿盐疾病分会主任委员
《中华骨质疏松和骨矿盐疾病杂志》副总编辑
《中国实用内科杂志》常务编委
《上海医学》常务编委
上海市医学会骨质疏松专科分会前任主任委员
《Acta Pharmacologica Sinica》（SCI收录）编委

科研项目 项目编号项目名称课题来源起止年月批准经费承担职责
2018YFA** 钙磷代谢障碍疾病遗传资源库建立与新致病基因克隆及突变基因谱的构建 国家重点研发计划 2019-07~2024-06 503万元 课题负责人
SHDC** 骨发育不良类疾病临床确诊和干预体系的建立 上海申康医院发展中心临床科技创新项目 2018-11~2021-11 80万元 课题负责人
** 药物转运体基因深度测序鉴定阿德福韦酯致低磷性骨软化症的风险基因型和功能研究 国家自然科学基金面上项目 2018-01~2021-12 52万元 课题负责人
** 骨质疏松三级防治网络的运作及以社区为基地开展胸腰椎脆性骨折的早期筛查 上海市科委医学领域项目 2016-07~2019-09 50万元 课题负责人
** 性腺激素调控SLCO2A1突变导致原发性肥大性骨关节病发病的分子机制研究 国家自然科学基金面上项目 2016-01~2019-12 58万元 课题负责人
2015SQ00072 常见骨代谢疾病诊疗规范与防治关键技术的建立及应用 公益性行业基金子课题 2015-01~2017-12 52.81万元 子课题负责人
2014ZYJB0009 原发性肥大性骨关节病因鉴定和临床治疗研究 上海市卫生系统重要疾病联合攻关项目 2015-01~2017-12 50万元 课题负责人
14JC** 常见单基因遗传性骨病家系资源库建立和致病基因的鉴定 上海市科委重点项目 2014-09~2017-08 50万元 课题负责人
** BCOR基因突变致X-连锁骨质疏松伴肢端骨溶解综合征发病机制的研究 国家自然科学基金面上项目 2014-01~2017-12 70万元 课题负责人
CSTC2013jcyjC00009 几种常见骨骼遗传病及防治策略的研究 重庆市基础与前沿研究计划项目 2014-01~2016-12 30万元 子课题负责人
2014CB942903 脊柱稳态维持的细胞分子机制研究 科技部973重大研究项目子课题 2014-01~2018-08 235万元 子课题负责人
SHDC** 新骨转换指标在骨质疏松诊治中的应用及临床推广研究 上海市市级医院新兴前沿技术联合攻关项目 2013-01~2016-12 100万元 课题负责人
051 上海市领军人才 上海市人力资源和社会保障局 2012-11~2014-10 50万元 课题负责人
** 骨量和肌肉双变量复杂性状与11个候选基因68个SNP和单倍型的核心家系连锁和群体关联分析 国家自然科学基金面上项目 2012-01~2015-12 55万元 课题负责人
XBR** 阿仑膦酸钠对绝经后妇女骨质疏松疗效与其作用关键靶点基因群标签单核苷酸多态性的关系 上海市卫生系统优秀学科带头人培养计划 2011-01~2014-12 50万元 课题负责人
** 阿仑膦酸钠作用10个基因67个标签SNP和单倍型与骨质疏松疗效关系的研究 国家自然科学基金面上项目 2011-01~2013-12 32万元 课题负责人
10DZ** 以社区为基地骨质疏松防治模式的推广与应用 上海市科委重大科技专题攻关专项 2010-01~2013-12 50万元 课题负责人
** 骨代谢相关基因26个标签SNP和单倍型与女性峰值骨量的家系连锁分析 国家自然基金委,面上项目 2008-01~2010-12 30万元 课题负责人
** 男性峰值骨量与骨代谢相关候选基因10个SNP的家系连锁分析 国家自然科学基金面上项目 2006-01~2008-12 24万元 课题负责人

学术论文 作者论文标题期刊名出版年卷期页码
Cao YJ, Zhang H, Zhang ZL （通讯作者） Novel mutations in the WNT1, TMEM38B, P4HB, ad PLS3 genes in four unrelated Chinese families with osteogenesis imperfecta Endocr Pract 2019 25(3):230-241
Gao C, Xu Y, Li L, Gu WQ, Yi CT, Zhu Q, Gu HA, Chen BH, Wang QQ, Tang F, Xu JL, Hou JM, Song HJ, Wang H, Wang ZL, Zhang ZL （通讯作者） Prevalence of osteoporotic vertebral fracture among community-dwelling elderly in Shanghai Chin Med J (Engl) 2019 132(14):1749-1751
Cao YJ, Wei Z, Zhang H, Zhang ZL （通讯作者） Expanding the Clinical Spectrum of Osteogenesis Imperfecta Type V: 13 Additional Patients and Review Front Endocrinol (Lausanne) 2019 10:375
Li L, Lv SS, Wang C, Yue H, Zhang ZL （通讯作者） Novel CLCN7 mutations cause autosomal dominant osteopetrosis type II and intermediate autosomal recessive osteopetrosis Mol Med Rep 2019 19(6):5030-5038
Shao C, Wang YW, He JW, Fu WZ, Wang C, Zhang ZL （通讯作者） Genetic variants in the PLS3 gene are associated with osteoporotic fractures in postmenopausal Chinese women Acta Pharmacol Sin 2019 Epub ahead of print
Wang WJ, Fu WZ, He JW, Wang C, Zhang ZL （通讯作者） Association between SOST gene polymorphisms and response to alendronate treatment in postmenopausal Chinese women with low bone mineral density Pharmacogenomics J 2018 Epub ahead of print]
Wei Z, Sun B, Wang ZP, He JW, Fu WZ, Fan YB, Zhang ZL （通讯作者） Whole-Exome Sequencing Identifies Novel Recurrent Somatic Mutations in Sporadic Parathyroid Adenomas Endocrinology 2018 159(8):3061-3068
Xu Y, Kang QL, Zhang ZL （通讯作者） A MYH3 mutation identified for the first time in a Chinese family with Sheldon-Hall syndrome (DA2B) Neuromus Disor 2018 28(5):456-462
Zhang H, Xu Y, Yue H, Wang C, Gu JM, He JW, Fu WZ, Hu WW, Zhang ZL （通讯作者） Novel mutations of the SERPINF1 and FKBP10 gene in Chinese families with autosomal recessive osteogenesis imperfecta Int J Mol Med 2018 41(6):3662-3670
Yu WJ, He JW, Fu WZ, Wang C, Zhang ZL. （通讯作者） Reports of 17 Chinese patients with tumor-induced osteomalacia. J Bone Miner Metab 2017 35(3):298-307
Zhang XY, He JW, Fu WZ, Wang C, Zhang ZL （通讯作者） Novel mutations of TCIRG1 cause a malignant and mild phenotype of autosomal recessive osteopetrosis (ARO) in four Chinese families Acta Pharm Sinic 2017 38(11):1456-1465
Li SS, He JW, Fu WZ, Liu YJ, Hu YQ, Zhang ZL. （通讯作者） 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. J Bone Miner Res 2017 32(8):1659-1666
Zhang XY, Wei ZY, He JW, Wang C, Zhang ZL （通讯作者） Novel mutations of CLCN7 cause autosomal dominant osteopetrosis type II (ADOII) and intermediate autosomal recessive osteopetrosis (ARO) in seven Chinese families Postgra Med 2017 129(8):934-942
Xiong A, Yao Q, He J, Fu W, Yu J, Zhang Z. （通讯作者） 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. Osteoporos Int 2016 27(3):1031-1039
Li SS, Gu JM, Yu WJ, He JW, Fu WZ, Zhang ZL. （通讯作者） Seven novel and six de novo PHEX gene mutations in patients with hypophosphatemic rickets. Int J Mol Med 2016 38(6):1703-1714
Zheng H, Shao C, Zheng Y, He JW, Fu WZ, Wang C, Zhang ZL （通讯作者） Two novel mutations of CLCN7 gene in Chinese families with autosomal dominant osteopetrosis (type II). J Bone Miner Metab 2016 Jul;34(4):440-6
Wei Z, He JW, Fu WZ, Zhang ZL. （通讯作者） Osteomalacia induced by long-term low-dose adefovir dipivoxil: Clinical characteristics and genetic predictors. Bone 2016 93:97-103
Zheng Y, Wang C, Zhang H, Shao C, Gao LH, Li SS, Yu WJ, He JW, Fu WZ, Hu YQ, Li M, Liu YJ, Zhang ZL. （通讯作者） Polymorphisms in Wnt signaling pathway genes are associated with peak bone mineral density, lean mass, and fat mass in Chinese male nuclear families. Osteoporos Int. 2016 27(5):1805-15
Zhang XY, He JW, Fu WZ, Liu YJ, Zhang ZL （通讯作者） Associations of Serum Osteocalcin and Polymorphisms of the Osteocalcin Gene with Bone Mineral Density in Postmenopausal and Elderly Chinese Women JOURNAL OF NUTRIGENETICS AND NUTRIGENOMICS 2016 9(5-6):231-242
Zhang ZL （通讯作者）,Liao EY,Xia WB,Lin H,Cheng Q,Wang L,Hao YQ,Chen DC,Tang H,De Peng Y,You L,He L,Hu ZH,Song CL,Wei F,Wang J,Zhang L,Santora AC. Alendronate sodium/vitamin D3 combination tablet versus calcitriol for osteoporosis in Chinese postmenopausal women： a 6-month, randomized, open-label, active-comparator-controlled study with a 6-month extensi Osteoporos Int（IF=4.169） 2015 26(9):2365-74
Zhang Z,He JW,Fu WZ,Zhang CQ,Zhang ZL. （通讯作者） Calcification of joints and arteries second report with novel NT5E mutations and expansion of the phenotype J Hum Genet（IF=2.462） 2015 60(10):561-4.
Wang C,Zheng H,He JW,Zhang H,Yue H,Hu WW,Gu JM,Shao C,Fu WZ,Hu YQ,Li M,Liu YJ,Zhang ZL （通讯作者） Genetic polymorphisms in the mevalonate pathway affect the therapeutic response to?alendronatetreatment?in postmenopausal Chinese women with low bone mineral density Pharmacogenomics J（IF=4.229） 2015 15(2):158-64
Gu JM,Wang L,Lin H,Chen DC,Tang H,Jin XL,Xia WB,Hu YQ,Fu WZ,He JW,Zhang H,Wang C,Yue H,Hu WW,Liu YJ,Zhang ZL. （通讯作者） The efficacy and safety of weekly 35-mg risedronate dosing regimen for Chinese postmenopausal women with osteoporosis or osteopenia: 1-year data Acta Pharmacol Sin（IF=2.912） 2015 36(7):841-6.?
Gao LH,Zhu WJ,Liu YJ,Gu JM,Zhang ZL （通讯作者）,Wang O,Xing XP,Xu L. Physical performance and life quality in postmenopausal women supplemented with vitamin Da two-year prospective study Acta Pharmacol Sin（IF=2.912） 2015 36(9): 1065–1073
He J, Zhang H, Wang C, Zhang Z, Yue H, Hu W, Gu J, Fu W, Hu Y, Li M, Liu Y, Zheng H, Zhang Z. （通讯作者） Associations of Serum Sclerostin and Polymorphisms in the SOST Gene with Bone Mineral Density and Markers of Bone Metabolism in Postmenopausal Chinese Women. J Clin Endocrinol Metab（IF=6.209） 2014 99(4):E665-73
Zheng H, Zhang Z, He JW, Fu WZ, Wang C, Zhang ZL （通讯作者） Identification of two novel CLCN7 gene mutations in three Chinese families with autosomal dominant osteopetrosis type II Joint Bone Spine（IF=2.901） 2014 81(2):188-9
Yue H,Yu JB,He JW,Zhang Z,Fu WZ,Zhang H,Wang C,Hu WW,Gu JM,Hu YQ,Li M,Liu YJ,Zhang ZL. （通讯作者） Identification of two novel mutations in the?PHEX?gene?in Chinese patients with hypophosphatemic PLoS One（IF=3.234） 2014 9(5):e97830
Hu WW, Ke YH, He JW, Fu WZ, Wang C, Zhang H, Yue H, Gu JM, Zhang ZL （通讯作者） A novel compound mutation of CYP27B1 in a Chinese family with vitamin D-dependent rickets type 1A. J Pediatr Endocrinol Metab（IF=0.995） 2014 27(3-4):335-41
Zhang H, Wang C, Yue H, Hu WW, Gu JM, He JW, Fu WZ, Liu YJ, Zhang Z, Zhang ZL. （通讯作者） Identification of a novel mutation in the CLCN5 gene in a Chinese family with Dent-1 disease Nephrology (IF=2.083) 2014 19(2):80-3
Zhang H,He JW,Wang C,Zhang Z,Yue H,Hu WW,Gu JM,Hu YQ,Li M,Fu WZ,Zhang ZL （通讯作者） Association of polymorphisms in the SOST gene and bone mineral density in postmenopausal Osteoporos Int（IF=4.169） 2014 25(12):2797-803
Hu WW,Ke YH,He JW,Fu WZ,Liu YJ,Chen D,Zhang ZL （通讯作者） Serum?osteocalcin?levels?are inversely associated with plasma glucose and body mass index in healthy Chinese women Acta Pharmacol Sin（IF=2.912） 2014 35(12):1521-6
Zhang Z, He JW, Fu WZ, Zhang CQ, Zhang ZL （通讯作者） Two novel mutations in the SLCO2A1 gene in a Chinese patient with primary hypertrophic osteoarthropathy Gene（IF=2.138） 2014 534(2):421-3
Jiang Y,Zhang ZL （共同第一作者）,Zhang ZL,Zhu HM,Wu YY,Cheng Q,Wu FL,Xing XP,Liu JL,Yu W,Meng XW. Menatetrenone versus alfacalcidol in the treatment of Chinese postmenopausal women with osteoporosis_ a multicenter, randomized, double-blinded, double-dummy, positive drug-controlled clinical trial Clin Interv Aging（IF=2.077） 2014 9:121-7.
Zhang Z,He JW,Fu WZ,Zhang ZQ,Zhang ZL. （通讯作者） Mutations in the SLCO2A1 gene and primary hypertrophic osteoarthropathy: a clinical and biochemical characterization J Clin Endocrin Metab(IF=6.31) 2013 98(5):E923-E933
Hu WW, Zhang Z, He JW, Fu WZ, Wang C, Zhang H, Yue H, Gu JM, Zhang ZL （通讯作者） Establishing reference intervals for bone turnover markers in the healthy shanghai population and the relationship with bone mineral density in postmenopausal women Int J Endocrinol（IF=1.515） 2013 2013:513925
Zheng H, Zhang Z, He JW, Fu WZ, Zhang ZL （通讯作者） A novel mutation (R122Q) in the cathepsin K gene in a Chinese child with Pyknodysostosis Gene（IF=2.086） 2013 522(1):107-10
Zhang Z,He JW,Fu WZ,Zhang ZQ,Zhang ZL. （通讯作者） An anlysis of the association between the vitamin D levels in a healthy Chinese population. J Bone Mineral Res(IF=6.589) 2013 28(8):1784-1792
Kang QL, Xu J, Zhang Z, He JW, Fu WZ, Zhang ZL （通讯作者） Mutation screening for the EXT1 and EXT2 genes in Chinese patients with multiple osteochondromas Arch Med Res（IF=2.406） 2013 44(7):542-8
Zhang Z, Li M, He JW, Fu WZ, Zhang CQ, Zhang ZL （通讯作者） Phenotype and genotype analysis of Chinese patients with osteogenesis imperfecta type V PLoS One（IF=3.534） 2013 8(8):e72337
Wang C, Zhang BH, Zhang H, He JW, Hu YQ, Li M, Yue H, Hu WW, Gu JM, Liu YJ, Fu WZ, Zhang ZL （通讯作者） The A242T mutation in the low-density lipoprotein receptor-related protein 5 gene in one Chinese family with osteosclerosis Intern Med（IF=0.967） 2013 52(2):187-92
Wang C, Zhang BH, Liu YJ, Hu YQ, He JW, Zhang ZL （通讯作者） Transforming growth factor-β1 gene mutations and phenotypes in pediatric patients with CamuratiEngelmann disease Mol Med Rep（IF=1.484） 2013 7(5):1695-9
Zhang Z, Zhao SC, He JW, Fu WZ, Zhang CQ,?Zhang ZL （通讯作者） Identification of one novel mutation in the C-propeptide of COL2A1 in a Chinese family with spondyloperipheral dysplasia Gene（IF=2.086） 2013 522(1):107-10
Gu JM, Ke YH, Yue H, Liu YJ, Zhang Z, Zhang H, Hu WW, Wang C, He JW, Hu YQ, Li M, Fu WZ,Zhang ZL （通讯作者） A novel VCP mutation as the cause of atypical IBMPFD in a Chinese family Bone（IF=4.461） 2013 52(1):9-16
Tao MF, Zhang Z, Ke YH, He JW, Fu WZ, Zhang CQ, Zhang ZL （通讯作者） Association of serum 25-hydroxyvitamin D with insulin resistance and β-cell function in a healthy Chinese female population Acta Pharmacol Sin（IF=2.496） 2013 34(8):1070-4
Zhang Z, He JW, Fu WZ, Zhang CQ, Zhang ZL （通讯作者） A novel mutation in the SLCO2A1 gene in a Chinese family with primary hypertrophic osteoarthropathy Gene（IF=2.086） 2013 521(1):191-4
Yue H, He JW, Ke YH, Zhang H, Wang C, Hu WW, Gu JM, Fu WZ, Hu YQ, Li M, Liu YJ, Zhang ZL （通讯作者） Association of single nucleotide polymorphism Rs** in PRDM16 gene with BMI in Chinese males Acta Pharmacol Sin （IF=2.496） 2013 34(5):710-6
Yue H, He JW, Zhang H, Wang C, Hu WW, Gu JM, Ke YH, Fu WZ, Hu YQ, Li M, Liu YJ, Wu SH, Zhang ZL. . Contribution of myostatin gene polymorphisms to normal variation in lean mass, fat mass and peak BMD in Chinese male offspring Acta Pharmacol Sin (IF=1.95) 2012 33(5):660-667.
Zhang Z, Liu KX, He JW, Fu WZ, Yue H, Zhang H, Zhang CQ, Zhang ZL. （通讯作者） Identification of two novel mutations in the SLC4A1 gene in two unrelated Chinese families with distal renal tubular acidosis. Arch Med Res (IF=1.733) 2012 43(4):298-304.
Chun Wang, Zeng Zhang, Hao Zhang, Jin-Wei He, Jie-Mei Gu, Wei-Wei Hu, Yun-Qiu Hu, Miao Li,Yu-Juan Liu , Wen-Zhen Fu, Hua Yue, Yao-Hua Ke, and Zhen-Lin Zhang （通讯作者） Susceptibility Genes for Osteoporotic Fracture in Postmenopausal Chinese Women J Bone Mineral Res(IF:6.373) 2012 27(12):2582-2591
Ke YH, Xiao WJ, He JW, Zhang H, Yu JB, Hu WW, Gu JM, Gao G, Yue H, Wang C, Hu YQ, Li M, Liu YJ, Fu WZ, Zhang ZL. Association of ALOX15 gene polymorphisms with obesity-related phenotypes in Chinese nuclear families with male offspring. Acta Pharmacol Sin (IF=1.95) 2012 33(2):201-207
Wang C, Zhang H, He JW, Gu JM, Hu WW, Hu YQ, Li M, Liu YJ, Fu WZ, Yue H, Ke YH, Zhang ZL. （通讯作者） The virulence gene and clinical phenotypes of osteopetrosis in the Chinese population: six novel mutations of the CLCN7 gene in twelve osteopetrosis families. J Bone Miner Metab (IF=2.238） 2012 30(3):338-348
Zhang ZL （通讯作者）, Zhang H, Ke YH, Yue H, Xiao WJ, Yu JB, Gu JM, Hu WW, Wang C, He JW, Fu WZ. The identification of novel mutations in COL1A1, COL1A2, and LEPRE1 genes in Chinese patients with osteogenesis imperfecta. J Bone Miner Metab. (IF=2.238) 2012 30(1):69-77
Zhang Z, Bao K, He JW, Fu WZ, Zhang CQ, Zhang ZL. （通讯作者） Identification of one novel mutation in the EVC2 gene in a Chinese family with Ellis-van Creveld syndrome. Gene (IF=2.341） 2012 511(2):380-382
Ke YH, He JW, Fu WZ, Zhang ZL. （通讯作者） Identification of two novel mutations in the OCRL1 gene in two Chinese families with Lowe syndrome. Nephrology (Carlton) (IF=1.454) 2012 17(1):20-25
Jie-mei Gu,Zhen-Lin Zhang （通讯作者）,Hao Zhang,Wei-wei Hu,Chun Wang,Hua Yue,Yao-hua Ke,Jin-wei He,Yun-qiu Hu,Miao Li,Yu-juan LiuWen-zhen Fu Thirteen Chinese patients with sporadic Paget’s disease of bone:clinical features, SQSTM1 mutation identi?cation, and functionalanalysis J Bone Miner Metab 2012 2012 ;30(5):525-33
Xiao W, Ke Y, He J, Zhang H, Yu J, Hu W, Gu J, Yue H, Wang C, Hu Y, Li M, Fu W, Liu Y, Zhang Z. Association of ALOX12 and ALOX15 gene polymorphisms with age at menarche and natural menopause in Chinese women. Menopause (IF=3.758) 2012 19(9):1029-1036
Xiao WJ, Ke YH, He JW, Zhang H, Yu JB, Hu WW, Gu JM, Gao G, Yue H, Wang C, Hu YQ, Li M, Liu YJ, Fu WZ, Zhang ZL. （通讯作者） Polymorphisms in the human ALOX12 and ALOX15 genes are associated with peak bone mineral density in Chinese nuclear families. Osteoporos Int (IF:4.58) 2012 23(7):1889-1897.
Kang QL, Xu J, Zhang Z, He JW, Lu LS, Fu WZ, Zhang ZL. （通讯作者） Three novel PHEX gene mutations in four Chinese families with X-linked dominant hypophosphatemic rickets. Biochem Biophys Res Commun (IF=2.484) 2012 423(4):793-798.
Zhang Z （通讯作者）, Xia W, He J, Zhang Z, Ke Y, Yue H, Wang C, Zhang H, Gu J, Hu W, Fu W, Hu Y, Li M, Liu Y. Exome Sequencing Identifies SLCO2A1 Mutations as a Cause of Primary Hypertrophic Osteoarthropathy AM J Human Genetics(IF=10.60) 2012 90（1）：125-132
Wang C, Hu YM, He JW, Gu JM, Zhang H, Hu WW, Yue H, Gao G, Xiao WJ, Yu JB, Ke YH, Hu YQ, Li M, Liu YJ, Fu WZ, Ren Y, Zhang zl （通讯作者） Association between Low Density Lipoprotein Receptor-Related Protein 2 Gene Polymorphisms and Bone Mineral Density Variation in Chinese Population. Plos one (IF=4.441) 2011 6(12): e28874
Zhang Z, He JW, Fu WZ, Zhang CQ, Zhang ZL. （通讯作者） Identification of three novel mutations in the COL2A1 gene in four unrelated Chinese families with spondyloepiphyseal dysplasia congenita. Biochem Biophys Res Commun (IF=2.484) 2011 413(4):504-508
Hu WW, He JW, Zhang H, Wang C, Gu JM, Yue H, Ke YH, Hu YQ, Fu WZ, Li M, Liu YJ, Zhang ZL. （通讯作者） No association between polymorphisms and haplotypes of COL1A1 and COL1A2 genes and osteoporotic fracture in postmenopausal Chinese women. Acta Pharmacol Sin (IF=1.95) 2011 32(7):947-955
Xiao WJ, He JW, Zhang H, Hu WW, Gu JM, Yue H, Gao G, Yu JB, Wang C, Ke YH, Fu WZ, Zhang ZL. （通讯作者） ALOX12 polymorphisms are associated with fat mass but not peak bone mineral density in Chinese nuclear families. Int J Obes (Lond) (IF=4.691) 2011 35(3):378-386.
Xiao WJ, He JW, Zhang H, Hu WW, Gu JM, Yue H, Gao G, Yu JB, Wang C, Ke YH, Fu WZ, Zhang ZL. （通讯作者） ALOX12 polymorphisms are associated with fat mass but not peak bone mineral density in Chinese nuclear families. Int J Obes (Lond) (IF=4.691) 2011 35(3):378-386.
Zhang h, Hu yq, Zhang zl （通讯作者） Age trends for hip geometry in Chinese men and women and the association with femoral neck fracture. Osteoporos Int. (IF=4.58) 2011 22(9):2513-22.
Zhang H, He JW, Gao G, Yue H, Yu JB, Hu WW, Gu JM, Hu YQ, Li M, Fu WZ, Liu YJ, Zhang ZL. Polymorphisms in the HOXD4 gene are not associated with peak bone mineral density in Chinese nuclear families. Acta Pharmacol Sin (IF=1.95) 2010 31(8):977-983.
Yue H, He JW, Zhang H, Hu WW, Hu YQ, Li M, Liu YJ, Wu SH, Zhang zl （通讯作者） No association between polymorphisms of peroxisome proliferator-activated receptor-gamma gene and peak bone mineral density variation in Chinese nuclear Osteoporos Int. (IF=4.58) 2010 21(5):873-582
Gao G, Zhang ZL （通讯作者）, He JW, Zhang H, Yue H, Hu WW, Gu JM, Fu WZ, Hu YQ, Li M, Liu YJ, Yu JB. No association of the polymorphisms of the frizzled-related protein gene with peak bone mineral density in Chinese nuclear families. BMC Med Genet (IF=2.328) 2010
Yue H, Zhang zl （通讯作者）, He JW. Identification of novel mutations in WISP3 gene in two unrelated Chinese families with progressive pseudorheumatoid dysplasia. Bone (IF=4.843) 2009 44(4):547-554.
Zhang zl （通讯作者）, He JW, Qin YJ, Hu YQ, Li M, Zhang H, Hu WW, Liu YJ, Gu JM. Identification of the CLCN7 gene mutations in two Chinese families with autosomal dominant osteopetrosis (type II). J Bone Miner Metab. (IF=2.238) 2009 27(4):444-51