张建国-中国科学院大学-UCAS


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张建国-中国科学院大学-UCAS
[中文]
[English]
招生信息
教育背景
工作经历
专利与奖励
出版信息
科研活动
基本信息
张建国 男 硕导 其他电子邮件: zhangjg@genomics.cn通信地址: 广东省深圳市盐田区洪安三街21号华大综合园7栋邮政编码: 518083
研究领域
2001年至今一直从事基因组学和生物信息学相关研究工作。早期主要从事动植物、微生物的基因组学研究。作为生物信息骨干参加了中国杂交水稻基因组计划,并荣获2003年度中国科学院杰出科技成就集体奖(11/18)(2003-02-02-208)。先后参与了家蚕、家鸡、第一个亚洲人、玉米、家猪等大型基因组研究计划,主持了西瓜基因组的组装和生物信息分析工作。2010年至今研究重点在遗传病基因组研究,基于遗传病临床样本和表型信息,以多组学平台和生物信息技术为主,致力于揭示遗传病的分子基础和生物标志物,促进遗传病的临床筛查、诊断、干预和治疗。开展的研究主要集中在出生缺陷、罕见病、脑病、孕期疾病以及生物信息分析工具与方法的开发。
招生信息
招生专业
0710Z1-基因组学0710J3-生物信息学
招生方向
遗传病基因组研究及其生物信息工具开发
教育背景
2005-09--2011-06 复旦大学 博士研究生1997-09--2001-06 南开大学 本科
工作经历
工作简历
2011-07~现在, 深圳华大生命科学研究院, 实验室负责人/临床科研总监2001-07~2005-08,北京华大基因研究中心, 项目负责人/部门副主管
社会兼职
2020-03-20-2022-12-31,安徽医科大学特聘副教授, 特聘副教授2018-09-13-2023-09-13,中国微循环学会-神经变性病专委会-阿尔茨海默病生物标志物学组副主任委员, 副主任委员2018-07-20-2023-07-20,西北大学兼职教授, 兼职教授
专利与奖励
奖励信息
(1)&nbsp深圳市高层次专业人才,&nbsp一等奖,&nbsp市地级,&nbsp2009(2)&nbsp中国科学院杰出科技成就奖,&nbsp部委级,&nbsp2004
专利成果
[1] 袁永一, 林琼芬, 戴朴, 管李萍, 高雪, 谌于蓝, 张建国. 基因突变体及其应用.&nbsp中国:&nbspCN110878306A,&nbsp2020-03-13.[2] 高雪, 袁永一, 戴朴, 林琼芬, 管李萍, 张建国, 谌于蓝. 基因突变体及其应用.&nbspCN:&nbspCN110878307A,&nbsp2020-03-13.[3] 戴兰兰, 杨勇, 张建国, 林志淼, 刘汉奎, 冯程, 谌于蓝, 汪慧君, 汪建. KLHL24基因突变体及其应用.&nbspCN:&nbspCN107974436B,&nbsp2019-11-08.[4] 何思捷, 张建国, 刘轩竹, 李建康, 徐讯. VPS13B基因突变体及其应用.&nbspCN:&nbspCN105779463B,&nbsp2019-08-09.[5] 布娟, 何思捷, 张建国, 方明艳, 王乐今, 刘敬. EPHA2基因突变型及其应用.&nbspCN:&nbspCN106167800B,&nbsp2019-07-19.[6] 高雪, 戴朴, 袁永一, 林琼芬, 管李萍, 张建国, 党孝. 分离的编码IFNLR1突变体的核酸及其应用.&nbspCN:&nbspCN109943569A,&nbsp2019-06-28.[7] 廖卫平, 周青, 石奕武, 管李萍, 秦兵, 何娜, 张建国. 遗传性癫痫伴热性惊厥附加症SCN1A基因新突变.&nbsp中国:&nbspCN104774841B,&nbsp2018-08-31.
出版信息
发表论文
[1] Zeng, Zheng, Liu, Hankui, Xu, Huifang, Lu, Haiying, Yu, Yanyan, Xu, Xiaoyuan, Yu, Min, Zhang, Tao, Tian, Xiulan, Xi, Hongli, Guan, Liping, Zhang, Jianguo, OBrien, Stephen J, HBVstudy Consortium. Genome-wide association study identifies new loci associated with risk of HBV infection and disease progression. BMC MEDICAL GENOMICS[J]. 2021, 14(1):&nbsphttps://www.webofscience.com/wos/woscc/full-record/WOS:000631120300001.[2] Liu, HanKui, He, SiJie, Zhang, JianGuo. A bioinformatic study revealed serotonergic neurons are involved in the etiology and therapygenetics of anxiety disorders. TRANSLATIONAL PSYCHIATRY[J]. 2021, 11(1):&nbsphttps://doaj.org/article/7815bcbe295142ae9aa28a4c49a4224b.[3] Zhou, Yingjie, Tariq, Muhammad, He, Sijie, Abdullah, Uzma, Zhang, Jianguo, Baig, Shahid Mahmood. Whole exome sequencing identified mutations causing hearing loss in five consanguineous Pakistani families. BMC MEDICAL GENETICS[J]. 2020, 21(1):&nbsphttp://dx.doi.org/10.1186/s12881-020-01087-x.[4] Yuan, Yongyi, Li, Qi, Su, Yu, Lin, Qiongfen, Gao, Xue, Liu, Hankui, Huang, Shasha, Kang, Dongyang, Todd, N Wendell, Mattox, Douglas, Zhang, Jianguo, Lin, Xi, Dai, Pu. Comprehensive genetic testing of Chinese SNHL patients and variants interpretation using ACMG guidelines and ethnically matched normal controls. EUROPEAN JOURNAL OF HUMAN GENETICS[J]. 2020, 28(2):&nbsp231-243, https://www.webofscience.com/wos/woscc/full-record/WOS:000508939400013.[5] Fan, Mengjie, Wang, Jing, Wang, Sa, Li, Tengyan, Pan, Hong, Liu, Hankui, Xu, Huifang, Zhernakova, Daria, V, OBrien, Stephen J, Feng, Zhenru, Chang, Le, Dai, Erhei, Lu, Jianhua, Xi, Hongli, Yu, Yanyan, Zhang, Jianguo, Wang, Binbin, Zeng, Zheng. New Gene Variants Associated with the Risk of Chronic HBV Infection. VIROLOGICA SINICA[J]. 2020, 35(4):&nbsp378-387, http://lib.cqvip.com/Qikan/Article/Detail?id=7102878171.[6] Broderick, Lori, Yost, Shawn, Li, Dong, McGeough, Matthew D, Booshehri, Laela M, Guaderrama, Marisela, Brydges, Susannah D, Kucharova, Karolina, Patel, Niraj C, Harr, Margaret, Hakonarson, Hakon, Zackai, Elaine, Cowell, Ian G, Austin, Caroline A, Hugle, Boris, Gebauer, Corinna, Zhang, Jianguo, Xu, Xun, Wang, Jian, Croker, Ben A, Frazer, Kelly A, Putnam, Christopher D, Hoffman, Hal M. Mutations in topoisomerase II beta result in a B cell immunodeficiency. NATURE COMMUNICATIONS[J]. 2019, 10: http://dx.doi.org/10.1038/s41467-019-11570-6.[7] He, Sijie, Chen, Weiwei, Liu, Hankui, Li, Shengting, Lei, Dongzhu, Dang, Xiao, Chen, Yulan, Zhang, Xiuqing, Zhang, Jianguo. Gene pathogenicity prediction of Mendelian diseases via the random forest algorithm. HUMAN GENETICS[J]. 2019, 138(6):&nbsp673-679, [8] Huang, Xiaoyan, Liu, Hankui, Li, Xinming, Guan, Liping, Li, Jiankang, Tellier, Laurent Christian Asker M, Yang, Huanming, Wang, Jian, Zhang, Jianguo. Revealing Alzheimer's disease genes spectrum in the whole-genome by machine learning. BMC NEUROLOGY[J]. 2018, 18(1):&nbsphttp://www.corc.org.cn/handle/1471x/2374353.[9] Wang, Yun, Garraoui, Abir, Zeng, Liuzhi, Lai, Mingying, He, Fen, Wang, Huaizhou, Jiang, Chongyi, Chen, Yulan, Dai, Lanlan, Fan, Ning, Yang, Huanming, Zhang, Jianguo, Liu, Xuyang. FBN3 gene involved in pathogenesis of a Chinese family with Bardet-Biedl syndrome. ONCOTARGET[J]. 2017, 8(49):&nbsp86718-86725, https://www.webofscience.com/wos/woscc/full-record/WOS:000413077800175.[10] Peng, Wenhui, Li, Miaoxin, L, Hailing, I, Tang, Kai, Zhuang, Jianhui, Zhang, Jianguo, Xiao, Jingjing, Jiang, Hui, Li, Dali, Yu, Yongchun, Sham, Pak C, Nattel, Stanley, Xu, Yawei. Dysfunction of Myosin Light-Chain 4 (MYL4) Leads to Heritable Atrial Cardiomyopathy With Electrical, Contractile, and Structural Components: Evidence From Genetically-Engineered Rats. JOURNAL OF THE AMERICAN HEART ASSOCIATION[J]. 2017, 6(11):&nbsphttp://www.corc.org.cn/handle/1471x/2224518.[11] Lin, Zhimiao, Li, Shuo, Feng, Cheng, Yang, Shang, Wang, Huijun, Ma, Danhui, Zhang, Jing, Gou, Mengting, Bu, Dingfang, Zhang, Tengjiang, Kong, Xiaohui, Wang, Xintong, Sarig, Ofer, Ren, Yali, Dai, Lanlan, Liu, Hankui, Zhang, Jianguo, Li, Fei, Hu, Yongyan, PadalonBrauch, Gilly, Vodo, Dan, Zhou, Feng, Chen, Ting, Deng, Haiteng, Sprecher, Eli, Yang, Yong, Tang, Xu. Stabilizing mutations of KLHL24 ubiquitin ligase cause loss of keratin 14 and human skin fragility. NATURE GENETICS[J]. 2016, 48(12):&nbsp1508-1516, https://www.webofscience.com/wos/woscc/full-record/WOS:000389011100011.[12] Chen, Rong, Shi, Lisong, Hakenberg, Joerg, Naughton, Brian, Sklar, Pamela, Zhang, Jianguo, Zhou, Hanlin, Tian, Lifeng, Prakash, Om, Lemire, Mathieu, Sleiman, Patrick, Cheng, Weiyi, Chen, Wanting, Shah, Hardik, Shen, Yulan, Fromer, Menachem, Omberg, Larsson, Deardorff, Matthew A, Zackai, Elaine, Bobe, Jason R, Levin, Elissa, Hudson, Thomas J, Groop, Leif, Wang, Jun, Hakonarson, Hakon, Wojcicki, Anne, Diaz, George A, Edelmann, Lisa, Schadt, Eric E, Friend, Stephen H. Analysis of 589,306 genomes identifies individuals resilient to severe Mendelian childhood diseases. NATURE BIOTECHNOLOGY[J]. 2016, 34(5):&nbsp531-538, https://www.webofscience.com/wos/woscc/full-record/WOS:000375735000034.[13] Olgiati, Simone, Quadri, Marialuisa, Fang, Mingyan, Rood, Janneke P M A, Saute, Jonas A, Chien, Hsin Fen, Bouwkamp, Christian G, Graafland, Josja, Minneboo, Michelle, Breedveld, Guido J, Zhang, Jianguo, Verheijen, Frans W, Boon, Agnita J W, Kievit, Anneke J A, Jardim, Laura Bannach, Mandemakers, Wim, Barbosa, Egberto Reis, Rieder, Carlos R M, Leenders, Klaus L, Wang, Jun, Bonifati, Vincenzo, van de Warrenburg, B, Delnooz, C, Rietveld, A, Bloem, B, Ferreira, J, Correia Guedes, L, Tolosa, E, Kurtiz, M M, Obeso, J, Emre, M, Hanagasi, H, Bilgic, B, Tufekcioglu, Z, Elibol, B, Lu, ChinSong, WuChou, YahHuei, Yeh, TuHsueh, Atadzhanov, M, Kelly, P, Lopiano, L, Tassorelli, C, Pacchetti, C, Nappi, G, Riboldazzi, G, Bono, G, Comi, C, Padovani, A, Borroni, B, Raudino, F, Fincati, E, Bertolasi, L, Tinazzi, M, Bonizzato, A, Ferracci, C, Libera, A Dalla, Marini, P, Massaro, F, Federico, A, Taglia, I, Battisti, C, Marconi, R, Onofrj, M, Thomas, A, Vanacore, N, Meco, G, Fabbrini, G, Fabrizio, E, Berardelli, A, Stocchi, F, Vacca, L, Picillo, M, De Rosa, A, Criscuolo, C, De Michele, G, Filla, A, Barone, P, De Mari, M, DellAquila, C, Iliceto, G, Lamberti, P, Toni, V, Trianni, G, Gagliardi, M, Annesi, G, Quattrone, A, Saddi, V, Cossu, G, Melis, M, Int Parkinsonism Genetics Network. DNAJC6 Mutations Associated With Early-Onset Parkinson's Disease. ANNALS OF NEUROLOGY[J]. 2016, 79(2):&nbsp244-256, https://www.webofscience.com/wos/woscc/full-record/WOS:000370643100010.[14] Eichler, Florian S, Li, Jiankang, Guo, Yiran, Caruso, Paul A, Bjonnes, Andrew C, Pan, Jessica, Booker, Jessica K, Lane, Jacqueline M, Tare, Archana, Vlasac, Irma, Hakonarson, Hakon, Gusella, James F, Zhang, Jianguo, Keating, Brendan J, Saxena, Richa. CSF1R mosaicism in a family with hereditary diffuse leukoencephalopathy with spheroids. BRAIN[J]. 2016, 139(6):&nbsp1666-1672, http://dx.doi.org/10.1093/brain/aww066.[15] Zhang, J, Barbaro, P, Guo, Y, Alodaib, A, Li, J, Gold, W, Ades, L, Keating, B J, Xu, X, Teo, J, Hakonarson, H, Christodoulou, J. Utility of next-generation sequencing technologies for the efficient genetic resolution of haematological disorders. CLINICAL GENETICS[J]. 2016, 89(2):&nbsp163-172, https://www.webofscience.com/wos/woscc/full-record/WOS:000368806900004.[16] Menezes, Minal J, Guo, Yiran, Zhang, Jianguo, Riley, Lisa G, Cooper, Sandra T, Thorburn, David R, Li, Jiankang, Dong, Daoyuan, Li, Zhijun, Glessner, Joseph, Davis, Ryan L, Sue, Carolyn M, Alexander, Stephen I, Arbuckle, Susan, Kirwan, Paul, Keating, Brendan J, Xu, Xun, Hakonarson, Hakon, Christodoulou, John. Mutation in mitochondrial ribosomal protein S7 (MRPS7) causes congenital sensorineural deafness, progressive hepatic and renal failure and lactic acidemia. HUMAN MOLECULAR GENETICS[J]. 2015, 24(8):&nbsp2297-2307, https://www.webofscience.com/wos/woscc/full-record/WOS:000353066200016.[17] Yuan, Yongyi, Zhang, Jianguo, Chang, Qing, Zeng, Jin, Xin, Feng, Wang, Jianjun, Zhu, Qingyan, Wu, Jing, Lu, Jingqiao, Guo, Weiwei, Yan, Xukun, Jiang, Hui, Zhou, Binfei, Li, Qi, Gao, Xue, Yuan, Huijun, Yang, Shiming, Han, Dongyi, Mao, Zixu, Chen, Ping, Lin, Xi, Dai, Pu. De novo mutation in ATP6V1B2 impairs lysosome acidification and causes dominant deafness-onychodystrophy syndrome. CELL RESEARCHnull. 2014, 24(11):&nbsp1370-1373, https://www.webofscience.com/wos/woscc/full-record/WOS:000344993600013.[18] Guo, Shaogui, Zhang, Jianguo, Sun, Honghe, Salse, Jerome, Lucas, William J., Zhang, Haiying, Zheng, Yi, Mao, Linyong, Ren, Yi, Wang, Zhiwen, Min, Jiumeng, Guo, Xiaosen, Murat, Florent, Ham, Byung-Kook, Zhang, Zhaoliang, Gao, Shan, Huang, Mingyun, Xu, Yimin, Zhong, Silin, Bombarely, Aureliano, Mueller, Lukas A., Zhao, Hong, He, Hongju, Zhang, Yan, Zhang, Zhonghua, Huang, Sanwen, Tan, Tao, Pang, Erli, Lin, Kui, Hu, Qun, Kuang, Hanhui, Ni, Peixiang, Wang, Bo, Liu, Jingan, Kou, Qinghe, Hou, Wenju, Zou, Xiaohua, Jiang, Jiao, Gong, Guoyi, Klee, Kathrin, Schoof, Heiko, Huang, Ying, Hu, Xuesong, Dong, Shanshan, Liang, Dequan, Wang, Juan, Wu, Kui, Xia, Yang, Zhao, Xiang, Zheng, Zequn, Xing, Miao, Liang, Xinming, Huang, Bangqing, Lv, Tian, Wang, Junyi, Yin, Ye, Yi, Hongping, Li, Ruiqiang, Wu, Mingzhu, Levi, Amnon, Zhang, Xingping, Giovannoni, James J., Wang, Jun, Li, Yunfu, Fei, Zhangjun, Xu, Yong. The draft genome of watermelon (Citrullus lanatus) and resequencing of 20 diverse accessions. NATURE GENETICS[J]. 2013, 45(1):&nbsp51-+, http://doi.org/10.1038/ng.2470.[19] DansoAbeam, Dina, Zhang, Jianguo, Dooley, James, Staats, Kim A, Van Eyck, Lien, Van Brussel, Thomas, Zaman, Shari, Hauben, Esther, Van de Velde, Marc, Morren, MarieAnne, Renard, Marleen, Van Geet, Christel, Schaballie, Heidi, Lambrechts, Diether, Tao, Jinsheng, Franckaert, Dean, HumbletBaron, Stephanie, Meyts, Isabelle, Liston, Adrian. Olmsted syndrome: exploration of the immunological phenotype. ORPHANET JOURNAL OF RARE DISEASES[J]. 2013, 8(1):&nbsp79-79, http://dx.doi.org/10.1186/1750-1172-8-79.[20] Zhang, Caie, Li, Duanzhuo, Zhang, Jianguo, Chen, Xingping, Huang, Mi, Archacki, Stephen, Tian, Yuke, Ren, Weiping, Mei, Aihua, Zhang, Qingyan, Fang, Mingyan, Su, Zheng, Yin, Ye, Liu, Dongxian, Chen, Yingling, Cui, Xiukun, Li, Chang, Yang, Huanming, Wang, Qing, Wang, Jun, Liu, Mugen, Deng, Yunhua. Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria. JOURNAL OF INVESTIGATIVE DERMATOLOGY[J]. 2013, 133(9):&nbsp2221-2228, https://www.webofscience.com/wos/woscc/full-record/WOS:000323203300020.[21] Groenen, Martien A M, Archibald, Alan L, Uenishi, Hirohide, Tuggle, Christopher K, Takeuchi, Yasuhiro, Rothschild, Max F, RogelGaillard, Claire, Park, Chankyu, Milan, Denis, Megens, HendrikJan, Li, Shengting, Larkin, Denis M, Kim, Heebal, Frantz, Laurent A F, Caccamo, Mario, Ahn, Hyeonju, Aken, Bronwen L, Anselmo, Anna, Anthon, Christian, Auvil, Loretta, Badaoui, Bouabid, Beattie, Craig W, Bendixen, Christian, Berman, Daniel, Blecha, Frank, Blomberg, Jonas, Bolund, Lars, Bosse, Mirte, Botti, Sara, Zhan Bujie, Bystrom, Megan, Capitanu, Boris, CarvalhoSilva, Denise, Chardon, Patrick, Chen, Celine, Cheng, Ryan, Choi, SangHaeng, Chow, William, Clark, Richard C, Clee, Christopher, Crooijmans, Richard P M A, Dawson, Harry D, Dehais, Patrice, De Sapio, Fioravante, Dibbits, Bert, Drou, Nizar, Du, ZhiQiang, Eversole, Kellye, Fadista, Joao, Fairley, Susan, Faraut, Thomas, Faulkner, Geoffrey J, Fowler, Katie E, Fredholm, Merete, Fritz, Eric, Gilbert, James G R, Giuffra, Elisabetta, Gorodkin, Jan, Griffin, Darren K, Harrow, Jennifer L, Hayward, Alexander, Howe, Kerstin, Hu, ZhiLiang, Humphray, Sean J, Hunt, Toby, Hornshoj, Henrik, Jeon, JinTae, Jern, Patric, Jones, Matthew, Jurka, Jerzy, Kanamori, Hiroyuki, Kapetanovic, Ronan, Kim, Jaebum, Kim, JaeHwan, Kim, KyuWon, Kim, TaeHun, Larson, Greger, Lee, Kyooyeol, Lee, KyungTai, Leggett, Richard, Lewin, Harris A, Li, Yingrui, Liu, Wansheng, Loveland, Jane E, Lu, Yao, Lunney, Joan K, Ma, Jian, Madsen, Ole, Mann, Katherine, Matthews, Lucy, McLaren, Stuart, Morozumi, Takeya, Murtaugh, Michael P, Narayan, Jitendra, Dinh Truong Nguyen, Ni, Peixiang, Oh, SongJung, Onteru, Suneel, Panitz, Frank, Park, EungWoo, Park, HongSeog, Pascal, Geraldine, Paudel, Yogesh, PerezEnciso, Miguel, RamirezGonzalez, Ricardo, Reecy, James M, RodriguezZas, Sandra, Rohrer, Gary A, Rund, Lauretta, Sang, Yongming, Schachtschneider, Kyle, Schraiber, Joshua G, Schwartz, John, Scobie, Linda, Scott, Carol, Searle, Stephen, Servin, Bertrand, Southey, Bruce R, Sperber, Goran, Stadler, Peter, Sweedler, Jonathan V, Tafer, Hakim, Thomsen, Bo, Wali, Rashmi, Wang, Jian, Wang, Jun, White, Simon, Xu, Xun, Yerle, Martine, Zhang, Guojie, Zhang, Jianguo, Zhang, Jie, Zhao, Shuhong, Rogers, Jane, Churcher, Carol, Schook, Lawrence B. Analyses of pig genomes provide insight into porcine demography and evolution. NATURE[J]. 2012, 491(7424):&nbsp393-398, https://www.webofscience.com/wos/woscc/full-record/WOS:000311031600036.[22] Lamperti, Costanza, Fang, Mingyan, Invernizzi, Federica, Liu, Xuanzhu, Wang, Hairong, Zhang, Qing, Carrara, Franco, Moroni, Isabella, Zeviani, Massimo, Zhang, Jianguo, Ghezzi, Daniele. A novel homozygous mutation in SUCLA2 gene identified by exome sequencing. MOLECULAR GENETICS AND METABOLISM[J]. 2012, 107(3):&nbsp403-408, http://dx.doi.org/10.1016/j.ymgme.2012.08.020.[23] Guo, BiRong, Zhang, Xin, Chen, Gang, Zhang, JianGuo, Sun, LiangDan, Du, Weidong, Zhang, Qing, Cui, Yong, Zhu, Jun, Tang, XianFa, Xiao, Ruo, Liu, Yuan, Li, Min, Tang, HuaYang, Yang, Xu, Cheng, Hui, Li, Ming, Gao, Min, Li, Ping, Wang, JianBo, Xu, FengPing, Zuo, XianBo, Zheng, XiaoDong, Zhang, XiaoGuang, Yang, Lin, Liu, JianJun, Wang, Jun, Yang, Sen, Zhang, XueJun. Exome sequencing identifies a COL14A1 mutation in a large Chinese pedigree with punctate palmoplantar keratoderma. JOURNAL OF MEDICAL GENETICS[J]. 2012, 49(9):&nbsp563-568, https://www.webofscience.com/wos/woscc/full-record/WOS:000308805200004.[24] Wang, JunLing, Cao, Li, Li, XunHua, Hu, ZhengMao, Li, JiaDa, Zhang, JianGuo, Liang, Yu, SanA, Li, Nan, Chen, SuQin, Guo, JiFeng, Jiang, Hong, Shen, Lu, Zheng, Lan, Mao, Xiao, Yan, WeiQian, Zhou, Ying, Shi, YuTing, Ai, SanXi, Dai, MeiZhi, Zhang, Peng, Xia, Kun, Chen, ShengDi, Tang, BeiSha. Identification of PRRT2 as the causative gene of paroxysmal kinesigenic dyskinesias. BRAIN[J]. 2011, 134(12):&nbsp3490-3498, https://www.webofscience.com/wos/woscc/full-record/WOS:000298189800008.[25] Jun Wang, Jianguo Zhang, Ruiqiang Li, Hongkun Zheng, Jun Li, Yong Zhang, Heng Li, Peixiang Ni, Songgang Li, Shengting Li, Jingqiang Wang, Dongyuan Liu, Jason McDermott, Ram Samudrala, Siqi Liu, Jian Wang, Huanming Yang, Jun Yu, Gane Ka-Shu Wong. Evolutionary Transients in the Rice Transcriptome. 基因组蛋白质组与生物信息学报:英文版. 2010, 8(4):&nbsp211-228, http://lib.cqvip.com/Qikan/Article/Detail?id=37153302.[26] Lai, Jinsheng, Li, Ruiqiang, Xu, Xun, Jin, Weiwei, Xu, Mingliang, Zhao, Hainan, Xiang, Zhongkai, Song, Weibin, Ying, Kai, Zhang, Mei, Jiao, Yinping, Ni, Peixiang, Zhang, Jianguo, Li, Dong, Guo, Xiaosen, Ye, Kaixiong, Jian, Min, Wang, Bo, Zheng, Huisong, Liang, Huiqing, Zhang, Xiuqing, Wang, Shoucai, Chen, Shaojiang, Li, Jiansheng, Fu, Yan, Springer, Nathan M, Yang, Huanming, Wang, Jian, Dai, Jingrui, Schnable, Patrick S, Wang, Jun. Genome-wide patterns of genetic variation among elite maize inbred lines. NATURE GENETICS[J]. 2010, 42(11):&nbsp1027-+, https://www.webofscience.com/wos/woscc/full-record/WOS:000283540500024.[27] Wang, Jun, Wang, Wei, Li, Ruiqiang, Li, Yingrui, Tian, Geng, Goodman, Laurie, Fan, Wei, Zhang, Junqing, Li, Jun, Zhang, Juanbin, Guo, Yiran, Feng, Binxiao, Li, Heng, Lu, Yao, Fang, Xiaodong, Liang, Huiqing, Du, Zhenglin, Li, Dong, Zhao, Yiqing, Hu, Yujie, Yang, Zhenzhen, Zheng, Hancheng, Hellmann, Ines, Inouye, Michael, Pool, John, Yi, Xin, Zhao, Jing, Duan, Jinjie, Zhou, Yan, Qin, Junjie, Ma, Lijia, Li, Guoqing, Yang, Zhentao, Zhang, Guojie, Yang, Bin, Yu, Chang, Liang, Fang, Li, Wenjie, Li, Shaochuan, Li, Dawei, Ni, Peixiang, Ruan, Jue, Li, Qibin, Zhu, Hongmei, Liu, Dongyuan, Lu, Zhike, Li, Ning, Guo, Guangwu, Zhang, Jianguo, Ye, Jia, Fang, Lin, Hao, Qin, Chen, Quan, Liang, Yu, Su, Yeyang, San, A, Ping, Cuo, Yang, Shuang, Chen, Fang, Li, Li, Zhou, Ke, Zheng, Hongkun, Ren, Yuanyuan, Yang, Ling, Gao, Yang, Yang, Guohua, Li, Zhuo, Feng, Xiaoli, Kristiansen, Karsten, Wong, Gane KaShu, Nielsen, Rasmus, Durbin, Richard, Bolund, Lars, Zhang, Xiuqing, Li, Songgang, Yang, Huanming, Wang, Jian. The diploid genome sequence of an Asian individual. NATURE[J]. 2008, 456(7218):&nbsp60-U1, http://www.corc.org.cn/handle/1471x/2387368.[28] Zou, XinHui, Zhang, FuMin, Zhang, JianGuo, Zang, LiLi, Tang, Liang, Wang, Jun, Sang, Tao, Ge, Song. Analysis of 142 genes resolves the rapid diversification of the rice genus. GENOME BIOLOGY[J]. 2008, 9(3):&nbspR49-R49, http://ir.ibcas.ac.cn/handle/151111/4265.[29] Jun Yu, Jun Wang, Wei Lin, Songgang Li, Heng Li, Jun Zhou, Peixiang Ni, Wei Dong, Songnian Hu, Changqing Zeng, Jianguo Zhang, Yong Zhang, Ruiqiang Li, Zuyuan Xu, Shengting Li, Xianran Li, Hongkun Zheng, Lijuan Cong, Liang Lin, Jianning Yin, Jianing Geng, Guangyuan Li, Jianping Shi, Juan Liu, Hong Lv, Jun Li, Jing Wang, Yajun Deng, Longhua Ran, Xiaoli Shi, Xiyin Wang, Qingfa Wu, Changfeng Li, Xiaoyu Ren, Jingqiang Wang, Xiaoling Wang, Dawei Li, Dongyuan Liu, Xiaowei Zhang, Zhendong Ji, Wenming Zhao, Yongqiao Sun, Zhenpeng Zhang, Jingyue Bao, Yujun Han, Lingli Dong, Jia Ji, Peng Chen, Shuming Wu, Jinsong Liu, Ying Xiao, Dongbo Bu, Jianlong Tan, Li Yang, Chen Ye, Jingfen Zhang, Jingyi Xu, Yan Zhou, Yingpu Yu, Bing Zhang, Shulin Zhuang, Haibin Wei, Bin Liu, Meng Lei, Hong Yu, Yuanzhe Li, Hao Xu, Shulin Wei, Ximiao He, Lijun Fang, Zengjin Zhang, Yunze Zhang, Xiangang Huang, Zhixi Su, Wei Tong, Jinhong Li, Zongzhong Tong, Shuangli Li, Jia Ye, Lishun Wang, Lin Fang, Tingting Lei, Chen Chen, Huan Chen, Zhao Xu, Haihong Li, Haiyan Huang, Feng Zhang, Huayong Xu, Na Li, Caifeng Zhao, Shuting Li, Lijun Dong, Yanqing Huang, Long Li, Yan Xi, Qiuhui Qi, Wenjie Li, Bo Zhang, Wei Hu, Yanling Zhang, Xiangjun Tian, Yongzhi Jiao, Xiaohu Liang, Jiao Jin, Lei Gao, Weimou Zheng, Bailin Hao, Siqi Liu, Wen Wang, Longping Yuan, Mengliang Cao, Jason McDermott, Ram Samudrala, Jian Wang, Gane KaShu Wong, Huanming Yang. The Genomes of Oryza sativa: a history of duplications.. PLoS Biology[J]. 2005, 3(2):&nbsp266-281, IR_Article.[30] Hyashizaki, Y. Mouse transcriptome: Neutral evolution of 'non-coding' complementary DNAs Reply. NATUREnull. 2004, 431(7010):&nbsphttps://www.webofscience.com/wos/woscc/full-record/WOS:000224435500029.[31] 陈润生. A draft sequence of the rice genome (Oryza sativa L. ssp indica). SCIENCE[J]. 2002, 296(5565):&nbsp79-92, [32] Wong, GKS, Wang, J, Tao, L, Tan, J, Zhang, JG, Passey, DA, Yu, J. Compositional gradients in Gramineae genes. GENOME RESEARCH[J]. 2002, 12(6):&nbsp851-856, http://dx.doi.org/10.1101/gr.189102.[33] Roland FR Schindler, Chiara Scotton, Jianguo Zhang, Chiara Passarelli, Beatriz OrtizBonnin, Subreena Simrick, Thorsten Schwerte, KarLai Poon, Mingyan Fang, Susanne Rinn, Alexander Froese, Viacheslav O Nikolaev, Christiane Grunert, Thomas Mller, Giorgio Tasca, Padmini Sarathchandra, Fabrizio Drago, Bruno Dallapiccola, Claudio Rapezzi, Eloisa Arbustini, Francesca Romana Di Raimo, Marcella Neri, Rita Selvatici, Francesca Gualandi, Fabiana Fattori, Antonello Pietrangelo, Wenyan Li, Hui Jiang, Xun Xu, Enrico Bertini, Niels Decher, Jun Wang, Thomas Brand, Alessandra Ferlini. POPDC1 S201F causes muscular dystrophy and arrhythmia by affecting protein trafficking. The Journal of Clinical Investigation. 126(1):&nbsp239-253,
科研活动
科研项目
( 1 )&nbsp基于多组学方法的帕金森病发病机制研究, 主持, 省级, 2019-03--2022-03( 2 )&nbsp遗传和环境因素交互作用下神经环路的沉默与早期AD发病, 参与, 国家级, 2016-07--2021-06( 3 )&nbsp阿尔茨海默病遗传机制及生物标记技术的研发, 主持, 省级, 2015-08--2017-08( 4 )&nbsp眼科出生缺陷及遗传性疾病家系收集与珍惜资源复制, 主持, 国家级, 2014-05--2017-04( 5 )&nbspHBV感染相关疾病基因组医学标记物研究, 参与, 国家级, 2014-04--2017-04( 6 )&nbsp眼科单基因病致病基因发现研究及检测技术开发, 主持, 省级, 2013-08--2015-07( 7 )&nbsp西瓜基因组测序及生物信息学分析, 主持, 国家级, 2010-01--2011-12
参与会议
(1)基因组时代的眼科临床与科研 中国研究型医院学会眼科学会与视觉科学专委会2019学术年会 2019-03-22
2013 中国科学院大学,网络信息中心.