- 基本信息
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导师姓名：
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张浩
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学科代码：
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100201
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性别：
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女
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学科名称：
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内科学
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培养单位：
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附属第六人民医院
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三级学科
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内分泌与代谢病
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导师类型：
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硕士生导师
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专业领域名称：
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内科学 专业学位
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联系方式：
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上海交通大学附属第六人民医院门诊5楼骨质疏松与骨病专科
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专业领域代码：
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105101
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邮编：
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200233
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邮箱地址：
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zhanghaozcl@163.com
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- 研究方向 (点击浏览详细信息)
- 社会任职
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中华医学会骨质疏松和骨矿盐分会第六届委员会青年委员会副主任委员
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中国老年保健医学研究会骨质疏松分会委员
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中华医学会骨质疏松和骨矿盐分会第五届委员会继发性骨质疏松学组委员
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中华骨质疏松和骨矿盐疾病杂志编委
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上海市医学会骨质疏松专科分会第七届委员会委员
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中国老年学和老年医学学会骨质疏松分会内分泌专家委员会委员
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- 科研项目
| 81870618 | P4HB基因新突变导致成骨不全Cole-Carpenter综合征的分子机制研究 | 国家自然科学基金面上项目 |
2019-01~2022-12
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57万元
| 课题负责人 |
| 14ZR1431900 | 成骨不全表型多变家系突变基因体细胞镶嵌的检测及外显不全机制研究 | 上海市自然科学基金面上项目 |
2014-07~2017-06
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10万元
| 课题负责人 |
| 30800387 | 成骨不全家系的致病基因突变位点检测及与表型的关系研究 | 国家自然科学基金青年科学基金 |
2009-01~2011-12
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20万元
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- 学术论文
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曹洋嘉,,章振林
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成骨不全的临床表现与分子遗传学
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中华骨质疏松和骨矿盐疾病杂志
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2019
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12(2):199-205
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Cao YJ, Wei Z,, Zhang ZL.
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Expanding the Clinical Spectrum of Osteogenesis Imperfecta Type V: 13 Additional Patients and Review.
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Frontiers in Endocrinology
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2019
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10:375
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Cao YJ,, Zhang ZL.
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Novel mutations in the WNT1, TMEM38B, P4HB, and PLS3 genes in four unrelated chinese families with osteogenesis imperfecta.
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Endocrine Practice
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2019
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25(3):230-241
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, Xu Y, Yue H, Wang C, Gu J, He J, Fu W, Hu W, Zhang Z.
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Novel mutations of the SERPINF1 and FKBP10 genes in Chinese families with autosomal recessive osteogenesis imperfecta.
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International Journal of Molecular Medicine
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2018
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41(6):3662-3670
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, Yue H, Wang C, Gu J, He J, Fu W, Hu W, Zhang Z.
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Novel mutations in the SEC24D gene in Chinese families with autosomal recessive osteogenesis imperfecta.
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Osteoporosis International
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2017
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28(4):1473-1480
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, Yue H, Wang C, Hu W, Gu J, He J, Fu W, Hu Y, Li M, Zhang Z.
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Clinical characteristics and the identification of novel mutations of COL1A1 and COL1A2 in 61 Chinese patients with osteogenesis imperfecta.
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Molecular Medicine Reports
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2016
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14(5):4918-4926
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, Chun Wang, Hua Yue, Wei-Wei Hu, Jie-Mei Gu, Jin-Wei He, Wen-Zhen Fu, Yu-Juan Liu,Zeng Zhang, Zhen-Lin Zhang
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Identification of a novel mutation in the CLCN5 gene in a Chinese
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Nephrology
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2014
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19(2):80-3
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He J,, Wang C, Zhang Z, Yue H, Hu W, Gu J, Fu W, Hu Y, Li M, Liu Y, Zheng H, Zhang Z
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Associations of serum sclerostin and polymorphisms in the SOST gene with bone mineral density and markers of bone metabolism in postmenopausal Chinese women.
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Journal of Clinical Endocrinology Metab
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2014
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99(4):E665-73
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, J. W. He, C. Wang, Z. Zhang, H. Yue, W. W. Hu, J. M. Gu, Y. Q. Hu, M. Li, W. Z. Fu, Z. L. Zhang
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Associations of polymorphisms in the SOST gene and bone mineral density in postmenopausal Chinese Women
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Osteoporosis International
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2014
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25(12)::2797–2803
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, Ke YH, Wang C, Yue H, Hu WW, Gu JM, Zhang ZL
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Identification of the Mutations in the Tissue-nonspecific Alkaline Phosphatase Gene in Two Chinese Families with Hypophosphatasia.
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Archives of Medical Research
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2012
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43(1):21-30
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Zhang ZL,, Ke YH, Yue H, Xiao WJ, Yu JB, Gu JM, Hu WW, Wang C, He JW, Fu WZ
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The identification of novel mutations in COL1A1, COL1A2, and LEPRE1 genes in Chinese patients with osteogenesis imperfecta.
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Journal of Bone and Mineral Metabolism
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2012
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30(1):69-77
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, Huang QR, Gu JM, Hu WW, Liu YJ, Hu YQ, Zhang ZL.
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Comparison of the effects of cholecalciferol and calcitriol on calcium metabolism and bone turnover in Chinese postmenopausal women with vitamin D insufficiency.
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Acta Pharmacol Sin
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2012
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33(4):490-495
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, Hu YQ, Zhang ZL.
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Age trends for hip geometry in Chinese men and women and the association with femoral neck fracture
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Osteoporosis International
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2011
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22(9):2513-22
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, He JW, Gao G, Yue H, Yu JB, Hu WW, Gu JM, Hu YQ, Li M, Fu WZ, Liu YJ, Zhang ZL
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Polymorphisms in the HOXD4 gene are not associated with peak bone mineral density in Chinese nuclear families.
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Acta Pharmacol Sin
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2010
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31(8):977-983
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