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上海交通大学医学院研究生导师简介 章振林

上海交通大学 免费考研网/2013-01-10

基本信息
导师姓名: 章振林 专业代码: 100201
性别: 专业名称: 内科学
培养单位: 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:
联系方式: zzl2002@medmail.com.cn 电话13621673716上海第六人民医院骨质疏松和骨病科宜山路600号,200233
研究方向 (点击浏览详细信息)
单基因遗传性骨病的分子机制
社会任职
中华医学会骨质疏松和骨矿盐疾病分会副主任委员
上海市医学会骨质疏松专科分会主任委员
上海市医学会理事
社会任职请输入全称,字数小于50
科研项目
项目编号项目名称课题来源起止时间科研经费承担职责
051上海市领军人才上海市人力资源和社会保障局2012-11~~2014-1050万元课题负责人
81170803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~~2015-1255万元主要责任人
XBR2011014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~~2014-1250万元主要责任人
81070692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~~2013-1232万元主要责任人
10DZ1950100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~~2013-1250万元主要责任人
30771019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~~2010-1230万元课题负责人
30570891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~~2008-1224万元主要责任人
学术论文 (#为通讯作者,*为共同第一作者)

1、Zhang Z#, 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
2、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.#. 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.
3、Zhang ZL#, 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
4、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#. Susceptibility Genes for Osteoporotic Fracture in Postmenopausal Chinese Women. J Bone Mineral Res(IF:6.373),2012;27(12):2582-2591
5、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.#. 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.
6、Wang C, Zhang H, He JW, Gu JM, Hu WW, Hu YQ, Li M, Liu YJ, Fu WZ, Yue H, Ke YH, Zhang ZL. #. 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
7、Zhang Z, Bao K, He JW, Fu WZ, Zhang CQ, Zhang ZL.#. 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
8、Kang QL, Xu J, Zhang Z, He JW, Lu LS, Fu WZ, Zhang ZL.#. 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.
9、Zhang Z, Liu KX, He JW, Fu WZ, Yue H, Zhang H, Zhang CQ, Zhang ZL. #. 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.
10、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.
11、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
12、Ke YH, He JW, Fu WZ, Zhang ZL.#. 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
13、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
14、Xiao WJ, He JW, Zhang H, Hu WW, Gu JM, Yue H, Gao G, Yu JB, Wang C, Ke YH, Fu WZ, Zhang ZL. #. 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.
15、Zhang h, Hu yq, Zhang zl#. 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.
16、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#. 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
17、Zhang Z, He JW, Fu WZ, Zhang CQ, Zhang ZL. #. 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
18、Xiao WJ, He JW, Zhang H, Hu WW, Gu JM, Yue H, Gao G, Yu JB, Wang C, Ke YH, Fu WZ, Zhang ZL. #. 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.
19、Hu WW, He JW, Zhang H, Wang C, Gu JM, Yue H, Ke YH, Hu YQ, Fu WZ, Li M, Liu YJ, Zhang ZL. #. 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
20、Yue H, He JW, Zhang H, Hu WW, Hu YQ, Li M, Liu YJ, Wu SH, Zhang zl#. 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
21、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.
22、Gao G, Zhang ZL#, 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;11:1
23、Yue H, Zhang zl#, 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.
24、Zhang zl#, 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


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