导师姓名： 张静澜 专业代码： 071000
性别： 男 专业名称： 生物学
培养单位： 附属国际和平妇幼保健院 三级学科/
专业领域：
导师类型： 博士生导师 专业学位导师：
联系方式：
邮编： 邮箱地址： jinglanzhang@foxmail.com

研究方向 (点击浏览详细信息)
医学分子遗传学

社会任职

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
CR201903 胎儿游离DNA的生物学特性研究与临床应用 国际妇幼保健院2019年度院内临床研究 2020-01~2022-12 30万元 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
Anastasia M. Fedick, Jinglan Zhang, Lisa Edelmann, Ruth Kornreich Prenatal Diagnosis of Cystic Fibrosis Methods of Molecular Biology 2019 1885:221-231
Jinglan Zhang, Hongjie Chen, Ruth Kornreich, Chunli Yu Prenatal Diagnosis of Tay-Sachs Disease Methods of Molecular Biology 2019 1885:233-250
Jinglan Zhang （通讯作者）, Jianli Li, Jennifer B. Saucier, Yanming Feng, Yanjun Jiang, Jefferson Sinson, Anne K. McCombs, Eric S. Schmitt, Sandra Peacock, Stella Chen, Hongzheng Dai, Xiaoyan Ge, Guoli Wang, Chad A. Shaw, Hui Mei, Amy Breman, Fan Xia, Yaping Yang, Anne Purgason, Alan Pourpak, Zhao Chen, Xia Wang, Yue Wang, Shashikant Kulkarni, Kwong Wai Choy, Ronald J. Wapner, Ignatia B. Van den Veyver, Arthur Beaudet, Sheetal Parmar, Lee-Jun Wong & Christine M. Eng Non-invasive prenatal sequencing for multiple Mendelian monogenic disorders using circulating cell-free fetal DNA Nature Medicine 2019 25(3):439-447
Makiko Yasuda, Lin Gan, Brenden Chen, Chunli Yu, Jinglan Zhang, Miguel A Gama-Sosa, Daniela D Pollak, Stefanie Berger, John D Phillips, Winfried Edelmann, Robert J Desnick Homozygous hydroxymethylbilane synthase knock-in mice provide pathogenic insights into the severe neurological impairments present in human homozygous dominant acute intermittent porphyria Human Molecular Genetics 2019 28(11):1755–1767
Wenmiao Zhu, Jianli Li, Stella Chen, Jinglan Zhang, Francesco Vetrini, Alicia Braxton, Christine M. Eng, Yaping Yang, Fan Xia, Kory L. Keller, Leila Okinaka‐Hu, Chung Lee, J. Lloyd Holder Jr, Weimin Bi Two de novo novel mutations in one SHANK3 allele in a patient with autism and moderate intellectual disability American Journal of Medical Genetics Part A 2018 176(4):973-979
Shiyu Luo, C. Alexander Valencia, Jinglan Zhang, Ni-Chung Lee, Jesse Slone, Baoheng Gui, Xinjian Wang, Zhuo Li, Sarah Dell, Jenice Brown, Stella Maris Chen, Yin-Hsiu Chien, Wuh-Liang Hwu, Pi-Chuan Fan, Lee-Jun Wong, Paldeep S. Atwal, and Taosheng Huang Biparental Inheritance of Mitochondrial DNA in Humans Proceedings of the National Academy of Sciences of the United States of America 2018 115(51):13039-13044
Daryl A Scott, Andres Hernandez-Garcia, Mahshid S Azamian, Valerie K Jordan, Bum Jun Kim, Molly Starkovich, Jinglan Zhang, Lee-Jun Wong, Sandra A Darilek, Amy M Breman, Yaping Yang, James R Lupski, Amyn K Jiwani, Bibhuti Das, Seema R Lalani, Alejandro D Iglesias, Jill A Rosenfeld, Fan Xia Congenital heart defects and left ventricular non-compaction in males with loss-of-function variants in NONO Journal of Medical Genetics 2017 54(1):47-53
Hui Mei, Hongzheng Dai, Jinglan Zhang, Lee-Jun Wong, Pilar L. Magoulas Application of Next-Generation Sequencing in Noonan Spectrum Disorders Next Generation Sequencing Based Clinical Molecular Diagnosis of Human Genetic Disorders, Springer 2017 155-176
Yanming Feng, Xiaoyan Ge, Linyan Meng, Jennifer Scull, Jianli Li, Xia Tian, Tao Zhang, Weihong Jin, Hanyin Cheng, Xia Wang, Mari Tokita, Pengfei Liu, Hui Mei, Yue Wang, Fangyuan Li, Eric S. Schmitt, Wei V. Zhang, Donna Muzny, Shu Wen, Zhao Chen, Yaping Yang, Arthur L. Beaudet, Xiaoming Liu, Christine M. Eng, Fan Xia, Lee-Jun Wong, Jinglan Zhang （通讯作者） The Next-Generation of Population-based Spinal Muscular Atrophy Carrier Screening: Comprehensive Pan-ethnic SMN1 Copy Number and Sequence Variant Analysis by Massively Parallel Sequencing Genetics in Medicine 2017 19(8):936-944
Girish N. Nadkarni, Geneviève Galarneau, Stephen B. Ellis, Rajiv Nadukuru, Jinglan Zhang, Stuart A. Scott, Claudia Schurmann, Rongling Li, Laura J. Rasmussen-Torvik, Abel N. Kho, M. Geoffrey Hayes, Jennifer A. Pacheco, Teri A. Manolio, Rex L. Chisholm, Dan M. Roden, Joshua C. Denny, Eimear E. Kenny, Erwin P. Bottinger Apolipoprotein L1 Variants and Blood Pressure Traits in African Americans Journal of the American College of Cardiology 2017 69(12):1564-1574
Daryl A Scott, Andres Hernandez-Garcia, Mahshid S Azamian, Valerie K Jordan, Bum Jun Kim, Molly Starkovich, Jinglan Zhang, Lee-Jun Wong, Sandra A Darilek, Amy M Breman, Yaping Yang, James R Lupski, Amyn K Jiwani, Bibhuti Das, Seema R Lalani, Alejandro D Iglesias, Jill A Rosenfeld, Fan Xia Congenital heart defects and left ventricular non-compaction in males with loss-of-function variants in NONO Journal of Medical Genetics 2017 54(1):47-53
Anastasia Fedick, Jinglan Zhang （通讯作者） Next Generation of Carrier Screening Next Generation Sequencing Based Clinical Molecular Diagnosis of Human Genetic Disorders, Springer 2017 339-354
Jinglan Zhang, Véronik Lachance, Adam Schaffner, Xianting Li, Anastasia Fedick, Lauren E. Kaye, Jun Liao, Jill Rosenfeld, Naomi Yachelevich, Mary-Lynn Chu, Wendy G. Mitchell, Richard G. Boles, Ellen Moran, Mari Tokita, Elizabeth Gorman, Kaytee Bagley, Wei Zhang, Fan Xia, Magalie Leduc, Yaping Yang, Christine Eng, Lee-Jun Wong, Raphael Schiffmann, George A. Diaz, Ruth Kornreich, Ryan Thummel, Melissa Wasserstein, Zhenyu Yue, Lisa Edelmann A Founder Mutation in VPS11 Causes an Autosomal Recessive Leukoencephalopathy Linked to Autophagic Defects PLOS Genetics 2016 12(4):e**
Jinglan Zhang （通讯作者）, Anastasia Fedick, Stephanie Wasserman, Geping Zhao, Lisa Edelmann, Erwin P. Bottinger, Ruth Kornreich, Stuart A. Scott Analytical Validation of a Personalized Medicine APOL1 Genotyping Assay for Nondiabetic Chronic Kidney Disease Risk Assessment Journal of Molecular Diagnostics 2016 18(2):260-6
Jinlian Wang, Jun Liao, Jinglan Zhang, Wei-Yi Cheng, J?rg Hakenberg, Meng Ma, Bryn D. Webb, Rajasekar Ramasamudram-chakravarthi, Lisa Karger, Lakshmi Mehta, Ruth Kornreich, George A. Diaz, Shuyu Li, Lisa Edelmann, Rong Chen ClinLabGeneticist: a tool for clinical management of genetic variants from whole exome sequencing in clinical genetic laboratories Genome Medicine 2015 (2015) 7:77