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教师主页 团队成员 科研项目 研究领域 学术成果 教学 科研分享 新闻动态 疼痛医学中心 成果介绍 软件 毕业去向 加入我们 联系我们 黄捷 Google Scholar 副教授 医学院, 公共卫生及应急管理学院 黄捷，南方科技大学公共卫生及应急管理学院副教授、研究员、博士生导师、公共卫生及应急管理学院应急管理研究中心执行主任。北京大学全球健康发展研究院兼职研究员，深圳市海外高层次人才“孔雀计划”B类人才。曾任哈佛大学医学院讲师、美国退伍军人事务部波士顿荣军医院资深科学家。累计发表SCI论文近百篇，H-指数50，总引用14000+，其中包括在《自然》、《自然通讯》、《血液》、《核酸研究》、《生物信息》等国际一流杂志上发表的第一作者文章。深圳市疾病预防控制事业发展“十四五”规划（2022年），撰稿人。国家重点研发计划项目“健康预期寿命及其价值的测算技术与影响因素研究”，课题“疾病谱分析与疾病对HLE 及其价值的影响研究”，负责人。2018年出版科普著作《基因的名义》，同年入选“中华优秀科普图书榜”。2022年出版科普著作《核酸的前世今生》，同年被推荐参选“中国好书”。 个人简介 个人简介 研究领域 1. 基于人群大队列和分子流行病学（包括全基因组关联分析GWAS、多基因风险评估PRS、孟德尔随机化）的慢性病决定因素研究； 2. 基于个体基因组测序数据的罕见病（包括自闭症）的病因学研究； 3. 基于病原微生物全基因组的系统发生树（phylogeny）方法学和溯源研究； 4. 基于全球大流行性传染病（包括新冠肺炎）大数据的疫情防控策略研究； 学术成果 查看更多 Huang J#*, Döring O, GG Liu. The world needs a “pandamic” solution for a pandemic problem. China CDC Weekly. 4 (52), 1183-1184 Huang J#, Huffman JE#, Huang Y#, Valle ID, Assimes TL, Raghavan S, Voight BF, Liu C, Barabási A, Huang R, Hui Q, Nguyen XT, Ho YL, Djoussé L, Lynch JA, Vujkovic M, Tcheandjieu C, Tang H, Damrauer SM, Reaven PD, Miller D, Phillips LS, Ng MCY, Graff M, Haiman CA, Loos RJF, North KE, Yengo L, Smith GD, Saleheen D, Gaziano JM, Rader DJ, Tsao PS, Cho K, Chang KM, Wilson PWF, VA Million Veteran Program, Sun YV*, O’Donnell CJ. Genomics and phenomics of body mass index reveals a complex disease network. Nature Communications. 2022 Dec 29;13(1):7973. Huang J#*, McLean GR, Dubee FC, Zheng Z. Two pandemics in China, One Health in Chinese. BMJ Global Health. 2022 Mar;7(3).  Huang J#*, Liang ZS, Pallotti S, Ranson JM, Llewellyn DJ, Zheng ZJ, King DA, Zhou Q, Zheng H, Napolioni V*. PAGEANT: personal access to genome and analysis of natural traits. Nucleic Acids Research.2022 Apr 22;50(7):e39.  Wang M, Huang J*, Wu T*, Qi L. Arterial Stiffness, Genetic Risk, and Type 2 Diabetes: A Prospective Cohort Study. Diabetes Care. 2022 Apr 1;45(4):957-964.  Huang J#, Liu J#, Tian R, Liu K, Zhuang P, Sherman HT, Budjan C, Fong M, Jeong MS, Kong XJ. A Next Generation Sequencing-Based Protocol for Screening of Variants of Concern in Autism Spectrum Disorder. Cells. 2021 Dec 21;11(1).  Huang J#*, Pallotti S, Zhou Q, Kleber M, Xin X, King DA, Napolioni V*. PERHAPS: Paired-End short Reads-based HAPlotyping from next-generation Sequencing data. Briefings in Bioinformatics. 2021 Jul 20;22(4).  You C, Zhou Z, Wen J, Li Y, Pang CH, Du H, Wang Z, Zhou XH, King DA, Liu CT, Huang J*. Polygenic Scores and Parental Predictors: An Adult Height Study Based on the United Kingdom Biobank and the Framingham Heart Study. Frontiers in Genetics. 2021;12:669441.  Du Y, Martin JS, McGee J, Yang Y, Liu EY, Sun Y, Geihs M, Kong X, Zhou EL, Li Y, Huang J*. A SNP panel and online tool for checking genotype concordance through comparing QR codes. PLoS One. 2017;12(9):e0182438. Walter K#, Min JL#, Huang J#, Crooks L#, Memari Y, McCarthy S, Perry JR, Xu C, Futema M, Lawson D, Iotchkova V, Schiffels S, Hendricks AE, Danecek P, Li R, Floyd J, Wain LV, Barroso I, Humphries SE, Hurles ME, Zeggini E, Barrett JC, Plagnol V, Richards JB, Greenwood CM, Timpson NJ, Durbin R, Soranzo N. The UK10K project identifies rare variants in health and disease. Nature. 2015 Oct 1;526(7571):82-90. Huang J#, Howie B, McCarthy S, Memari Y, Walter K, Min JL, Danecek P, Malerba G, Trabetti E, Zheng HF, Gambaro G, Richards JB, Durbin R, Timpson NJ, Marchini J, Soranzo N. Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel. Nature Communications. 2015 Sep 14;6:8111. Huang J#, Huffman JE#, Yamakuchi M, Trompet S, Asselbergs FW, Sabater-Lleal M, Trégouët DA, Chen WM, Smith NL, Kleber ME, Shin SY, Becker DM, Tang W, Dehghan A, Johnson AD, Truong V, Folkersen L, Yang Q, Oudot-Mellkah T, Buckley BM, Moore JH, Williams FM, Campbell H, Silbernagel G, Vitart V, Rudan I, Tofler GH, Navis GJ, Destefano A, Wright AF, Chen MH, de Craen AJ, Worrall BB, Rudnicka AR, Rumley A, Bookman EB, Psaty BM, Chen F, Keene KL, Franco OH, Böhm BO, Uitterlinden AG, Carter AM, Jukema JW, Sattar N, Bis JC, Ikram MA, Sale MM, McKnight B, Fornage M, Ford I, Taylor K, Slagboom PE, McArdle WL, Hsu FC, Franco-Cereceda A, Goodall AH, Yanek LR, Furie KL, Cushman M, Hofman A, Witteman JC, Folsom AR, Basu S, Matijevic N, van Gilst WH, Wilson JF, Westendorp RG, Kathiresan S, Reilly MP, Tracy RP, Polasek O, Winkelmann BR, Grant PJ, Hillege HL, Cambien F, Stott DJ, Lowe GD, Spector TD, Meigs JB, Marz W, Eriksson P, Becker LC, Morange PE, Soranzo N, Williams SM, Hayward C, van der Harst P, Hamsten A, Lowenstein CJ, Strachan DP, O’Donnell CJ. Genome-wide association study for circulating tissue plasminogen activator levels and functional follow-up implicates endothelial STXBP5 and STX2.  Arteriosclerosis, Thrombosis, and Vascular Biology (ATVB). 2014 May;34(5):1093-101. Huang J#, Liu EY, Welch R, Willer C, Hindorff LA, Li Y. WikiGWA: an open platform for collecting and using genome-wide association results. Eur J Hum Genet. 2013 Apr;21(4):471-3. Huang J#, Sabater-Lleal M, Asselbergs FW, Tregouet D, Shin SY, Ding J, Baumert J, Oudot-Mellakh T, Folkersen L, Johnson AD, Smith NL, Williams SM, Ikram MA, Kleber ME, Becker DM, Truong V, Mychaleckyj JC, Tang W, Yang Q, Sennblad B, Moore JH, Williams FM, Dehghan A, Silbernagel G, Schrijvers EM, Smith S, Karakas M, Tofler GH, Silveira A, Navis GJ, Lohman K, Chen MH, Peters A, Goel A, Hopewell JC, Chambers JC, Saleheen D, Lundmark P, Psaty BM, Strawbridge RJ, Boehm BO, Carter AM, Meisinger C, Peden JF, Bis JC, McKnight B, Öhrvik J, Taylor K, Franzosi MG, Seedorf U, Collins R, Franco-Cereceda A, Syvänen AC, Goodall AH, Yanek LR, Cushman M, Müller-Nurasyid M, Folsom AR, Basu S, Matijevic N, van Gilst WH, Kooner JS, Hofman A, Danesh J, Clarke R, Meigs JB, Kathiresan S, Reilly MP, Klopp N, Harris TB, Winkelmann BR, Grant PJ, Hillege HL, Watkins H, Spector TD, Becker LC, Tracy RP, März W, Uitterlinden AG, Eriksson P, Cambien F, Morange PE, Koenig W, Soranzo N, van der Harst P, Liu Y, O’Donnell CJ, Hamsten A. Genome-wide association study for circulating levels of PAI-1 provides novel insights into its regulation. Blood. 2012 Dec 6;120(24):4873-81. Huang J#, Ellinghaus D, Franke A, Howie B, Li Y. 1000 Genomes-based imputation identifies novel and refined associations for the Wellcome Trust Case Control Consortium phase 1 Data. Eur J Hum Genet. 2012 Jul;20(7):801-5. Huang J#, Johnson AD, O’Donnell CJ. PRIMe: a method for characterization and evaluation of pleiotropic regions from multiple genome-wide association studies. Bioinformatics. 2011 May 1;27(9):1201-6. Huang J#, Perlis RH, Lee PH, Rush AJ, Fava M, Sachs GS, Lieberman J, Hamilton SP, Sullivan P, Sklar P, Purcell S, Smoller JW. Cross-disorder genomewide analysis of schizophrenia, bipolar disorder, and depression. American Journal of Psychiatry. 2010 Oct;167(10):1254-63. 加入团队 查看更多 联系我们 联系地址 南方科技大学公共卫生及应急管理学院 办公电话 电子邮箱 huangj@sustech.edu.cn