基本信息
师咏勇 男 博导 中国科学院脑科学与智能技术卓越创新中心
电子邮件: shiyongyong@ion.ac.cn
通信地址: 上海市徐汇区岳阳路320号,新生命科学实验楼A栋1018室
邮政编码:
电子邮件: shiyongyong@ion.ac.cn
通信地址: 上海市徐汇区岳阳路320号,新生命科学实验楼A栋1018室
邮政编码:
招生信息
招生专业
071007-遗传学0710J3-生物信息学071006-神经生物学
招生方向
精神分裂症为主的脑类疾病
教育背景
2001-09--2006-03 上海交通大学 博士1997-09--2001-06 上海交通大学 理学学士
工作经历
工作简历
2023-06~现在, 中国科学院神经科学研究所, 副主任2022-07~现在, 上海交通大学, Bio-X研究院 院长2019-01~2022-06,上海交通大学, Bio-X研究院副院长&执行院长2019-01~2023-05,上海交通大学, 生命学院副院长2014-01~现在, 上海交通大学, 特聘教授2008-02~2013-12,上海交通大学, 研究员2006-06~2008-01,上海交通大学, 副教授2001-09~2006-03,上海交通大学, 博士1997-09~2001-06,上海交通大学, 理学学士
教授课程
行为遗传学研讨生命科学前沿:脑科学遗传与发育
专利与奖励
奖励信息
(1) 第十七届上海市科技精英, , 省级, 2022(2) 基于连锁不平衡及长单倍型分析的精神疾病关键基因精细定位研究, 二等奖, 国家级, 2019(3) 精神疾病关键基因的精细定位研究, 一等奖, 部委级, 2019(4) 致盲性眼病防治融合体系的创建的精准干预, 二等奖, 部委级, 2018(5) 教育部青年科学奖, 部委级, 2016(6) 上海市科技杰出贡献奖, 省级, 2016(7) 基于全基因组策略的肿瘤遗传易感性, 一等奖, 部委级, 2015(8) 霍英东教育基金会, 其他, 2015(9) 多元、协同生物传感界面的设计组装及生物分析应用研究, 一等奖, 省级, 2014(10) 谈家桢科学创新奖, 其他, 2014(11) 科技部中青年科技领军人才, 部委级, 2014(12) 复杂疾病遗传机制研究中若干关键算法的研究与应用, 一等奖, 省级, 2013
专利成果
( 1 ) Choriogonadotropin alfa在治疗多囊卵巢综合征中的应用, 2020, 第 1 作者, 专利号: CN110841060A( 2 ) 一种基于DNA折纸标记检测乙肝病毒亚型的方法, 2019, 第 1 作者, 专利号: CN110079633A( 3 ) 一种基于有机薄膜晶体管阵列的尿酸传感器及控制方法, 2019, 第 2 作者, 专利号: CN109752423A( 4 ) USP48基因突变在ACTH型垂体腺瘤分子诊断中的应用, 2018, 第 1 作者, 专利号: CN108624683A( 5 ) CDH23基因突变在垂体腺瘤分子诊断中的应用, 2018, 第 3 作者, 专利号: CN108396063A( 6 ) 用于微量DNA超低频突变检测的双分子自校验文库制备及杂交捕获的二代测序方法, 2018, 第 1 作者, 专利号: CN107604046A( 7 ) 特定基因突变在检测垂体腺瘤的分子诊断和靶向治疗中的应用, 2017, 第 2 作者, 专利号: CN106434918A( 8 ) Etonogestrel在制备抗B细胞淋巴瘤产品中的应用, 2016, 第 1 作者, 专利号: CN105816467A( 9 ) BRAF基因检测物在制备ACTH型垂体腺瘤分子病理诊断及分型产品中的应用, 2016, 第 1 作者, 专利号: CN105506116A( 10 ) Promethazine在制备抗肝癌和/或结肠癌和/或肺癌产品中的应用, 2015, 第 1 作者, 专利号: CN105030785A( 11 ) Desogestrel在制备抗结肠癌/ER阴性的Ah受体阳性的乳腺癌产品中的应用, 2015, 第 1 作者, 专利号: CN105030792A( 12 ) Etonogestrel在制备抗前列腺癌产品中的应用, 2015, 第 1 作者, 专利号: CN105012314A( 13 ) Sunlidac在制备抗肺癌产品中的应用, 2015, 第 1 作者, 专利号: CN105012284A( 14 ) Estradiol在制备抗小细胞肺癌和/或卵巢癌和/或骨肉瘤产品中的应用, 2015, 第 1 作者, 专利号: CN104983734A( 15 ) Levonorgestrel在制备抗卵巢癌产品中的应用, 2015, 第 1 作者, 专利号: CN104983736A( 16 ) Nicardipine在制备抗肺癌产品中的应用, 2015, 第 1 作者, 专利号: CN104983733A( 17 ) Estrone在制备抗卵巢癌和/或乳腺癌产品中的应用, 2015, 第 1 作者, 专利号: CN104983735A( 18 ) 单核苷酸多态性rs2359536在检测垂体腺瘤中的应用, 2015, 第 2 作者, 专利号: CN104762389A( 19 ) 单核苷酸多态性rs10763170在检测垂体腺瘤中的应用, 2015, 第 2 作者, 专利号: CN104762388A( 20 ) 单核苷酸多态性rs17083838在检测垂体腺瘤中的应用, 2015, 第 1 作者, 专利号: CN104762387A( 21 ) USP8基因检测物在制备ACTH型垂体腺瘤分子病理诊断及分型产品中的应用, 2015, 第 2 作者, 专利号: CN104593490A( 22 ) 与多囊卵巢综合征相关的SNP标记, 2015, 第 4 作者, 专利号: CN104411824A( 23 ) 一种辅助诊断待测胎儿是否为21-三体综合征患者的试剂盒, 2014, 第 1 作者, 专利号: CN104152553A( 24 ) 与多囊卵巢综合征相关的SNP、包含SNP的芯片及其应用, 2013, 第 3 作者, 专利号: CN102918158A( 25 ) 纳米颗粒分子单倍型分型方法, 2011, 第 1 作者, 专利号: CN102199668A( 26 ) 检测重度抑郁关联基因的试剂盒及其制备方法, 2011, 第 1 作者, 专利号: CN102191329A( 27 ) 用于精神分裂症、双相情感障碍和重性抑郁症关联基因检测的引物、探针及其试剂盒及制备方法, 2011, 第 1 作者, 专利号: CN102146479A( 28 ) 用于双相情感障碍关联基因检测的引物、探针及其试剂盒, 2011, 第 1 作者, 专利号: CN102140520A( 29 ) 检测精神分裂关联基因的试剂盒及其制备方法, 2011, 第 1 作者, 专利号: CN101985659A( 30 ) 一组精神分裂症相关核酸序列, 2008, 第 3 作者, 专利号: CN100365118C( 31 ) 检测单核苷酸多态性的方法, 2005, 第 3 作者, 专利号: CN1706968A
出版信息
发表论文
(1) Highly accurate protein structure prediction and drug screen of monkeypox virus proteome, JOURNAL OF INFECTION, 2023, 第 5 作者 通讯作者(2) Cancer Cells Enter an Adaptive Persistence to Survive Radiotherapy and Repopulate Tumor, ADVANCED SCIENCE, 2023, 第 21 作者 通讯作者(3) Whole���Exome Sequencing Reveals Distinct Genetic Profiles of Palindromic Rheumatism, 2023, 第 10 作者 通讯作者(4) Multiomics Analyses Reveal Microbiome���Gut���Brain Crosstalk Centered on Aberrant Gamma-Aminobutyric Acid and Tryptophan Metabolism in Drug-Na��ve Patients with First-Episode, 2023, 第 17 作者 通讯作者(5) Genome-Wide Association Study of Obstructive Sleep Apnea and Objective Sleep-related Traits Identifies Novel Risk Loci in Han Chinese Individuals, AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2022, 第 25 作者 通讯作者(6) Structural Comparison and Drug Screening of Spike Proteins of Ten SARS-CoV-2 Variants, Structural Comparison and Drug Screening of Spike Proteins of Ten SARS-CoV-2 Variants, 研究(英文), 2022, 第 14 作者 通讯作者(7) Cigarette smoking and schizophrenia: Mendelian randomisation study, BRITISH JOURNAL OF PSYCHIATRY, 2021, 第 12 作者 通讯作者(8) Structural Analysis of the SARS-CoV-2 Omicron Variant Proteins, Structural Analysis of the SARS-CoV-2 Omicron Variant Proteins, RESEARCH, 2021, 第 4 作者 通讯作者(9) Both HLA class I and II regions identified as genome-wide significant susceptibility loci for adult-onset Still's disease in Chinese individuals, ANNALSOFTHERHEUMATICDISEASES, 2020, 第 37 作者 通讯作者(10) Rare and common variants analysis of the EMB gene in patients with schizophrenia, BMC PSYCHIATRY, 2020, 第 8 作者 通讯作者(11) 医学大数据使用安全及伦理问题探讨, Discussion on the Safety and Ethical Issues of Medical Big Data, 中国医学伦理学, 2019, 第 3 作者(12) ACTN3 is associated with children's physical fitness in Han Chinese, MOLECULAR GENETICS AND GENOMICS, 2019, 第 14 作者 通讯作者(13) Amplicon targeted resequencing for SLC2A9 and SLC22A12 identified novel mutations in hypouricemia subjects, MOLECULAR GENETICS & GENOMIC MEDICINE, 2019, 第 15 作者 通讯作者(14) Comparative genetic architectures of schizophrenia in East Asian and European populations, NATURE GENETICS, 2019, 第 11 作者(15) Common variants in the SLC28A2 gene are associated with serum uric acid level and hyperuricemia and gout in Han Chinese, HEREDITAS, 2019, 第 7 作者 通讯作者(16) Identification of serum microRNAs as diagnostic biomarkers for schizophrenia, HEREDITAS, 2019, 第 8 作者 通讯作者(17) INCREASING ANCESTRY DIVERSITY IN PSYCHIATRIC GENOMICS RESEARCH, EUROPEAN NEUROPSYCHOPHARMACOLOGY, 2019, 第 13 作者(18) The schizophrenia genetics knowledgebase: a comprehensive update of findings from candidate gene studies, TRANSLATIONAL PSYCHIATRY, 2019, 第 19 作者(19) Polymorphism of the PPARD Gene and Dynamic Balance Performance in Han Chinese Children, HEREDITAS, 2019, 第 15 作者 通讯作者(20) Association study of NDST3 gene for schizophrenia, bipolar disorder, major depressive disorder in the Han Chinese population, AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2018, 第 10 作者 通讯作者(21) 生物芯概念计算——生物信息计算的新概念, Biological data processing based on bio-processor unit (BPU), a new concept for next generation computational biology, 中国科学:生命科学, 2018, 第 6 作者(22) Meta-analysis of GABRB2 polymorphisms and the risk of schizophrenia combined with GWAS data of the Han Chinese population and psychiatric genomics consortium, PLOS ONE, 2018, 第 4 作者(23) Genome-wide association study identifies two risk loci for tuberculosis in Han Chinese, NATURE COMMUNICATIONS, 2018, 第 32 作者 通讯作者(24) Biological data processing based on bio-processor unit(BPU), a new concept for next generation computational biology, Biological data processing based on bio-processor unit(BPU), a new concept for next generation computational biology, 中国科学:生命科学英文版, 2018, 第 6 作者(25) Biological data processing based on bio-processor unit (bpu), a new concept for next generation computational biology, SCIENCE CHINA-LIFE SCIENCES, 2018, 第 6 作者(26) Identification of recurrent USP48 and BRAF mutations in Cushing's disease, NATURE COMMUNICATIONS, 2018, 第 40 作者 通讯作者(27) CD40-1C/T基因多态性与中国汉族人群脑卒中遗传易感性的研究(英文), Significant Association of CD40-1C���T Polymorphism and Stroke in the Han Chinese Population, 复旦学报:自然科学版, 2018, 第 7 作者(28) RETRACTED: Association between peroxisome proliferator-activated receptor, UCP3 and lipoprotein lipase gene polymorphisms and obesity in Chinese adolescents, OBESITY RESEARCH & CLINICAL PRACTICE, 2017, 第 3 作者(29) Association between the variability of the ABCA13 gene and the risk of major depressive disorder and schizophrenia in the Han Chinese population, WORLD JOURNAL OF BIOLOGICAL PSYCHIATRY, 2017, 第 12 作者 通讯作者(30) META-ANALYSIS OF GENOME WIDE ASSOCIATION STUDIES SHOWED POLYMORPHISMS ON 2P16.1, 6P22.1 AND 10Q24.32 ASSOCIATED WITH SCHIZOPHRENIA IN CHINESE HAN POPULATION, EUROPEAN NEUROPSYCHOPHARMACOLOGY, 2017, 第 8 作者(31) Genome-wide two-locus interaction analysis identifies multiple epistatic SNP pairs that confer risk of prostate cancer: A cross-population study, INTERNATIONAL JOURNAL OF CANCER, 2017, 第 5 作者 通讯作者(32) Replication of Gout/Urate Concentrations GWAS Susceptibility Loci Associated with Gout in a Han Chinese Population, SCIENTIFIC REPORTS, 2017, 第 24 作者 通讯作者(33) Germline Mutations in CDH23, Encoding Cadherin-Related 23, Are Associated with Both Familial and Sporadic Pituitary Adenomas, AMERICAN JOURNAL OF HUMAN GENETICS, 2017, 第 32 作者(34) The YWHAE gene confers risk to major depressive disorder in the male group of Chinese Han population, PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY, 2017, 第 9 作者 通讯作者(35) ADH1B基因启动子区多态性和结直肠癌易感性关联分析, An association between single nucleotide polymorphisms in the promoter region of alcohol dehydrogenase 1B and the risk of developing colorectal carcinoma in the Chinese Han population, 中国科学. 生命科学, 2017, 第 8 作者(36) Genetics of schizophrenia: A consensus paper of the WFSBP Task Force on Genetics, WORLD JOURNAL OF BIOLOGICAL PSYCHIATRY, 2017, 第 23 作者(37) 中国汉族2型糖尿病人群中UCP基因单核苷酸多态性与视网膜病变的关联分析, Associations of single nucleotide polymorphisms of UCP genes with diabetic retinopathy in Chinese Han population, 中华实验眼科杂志, 2017, 第 13 作者(38) DNA origami-based shape IDs for single-molecule nanomechanical genotyping, NATURE COMMUNICATIONS, 2017, 第 13 作者 通讯作者(39) Consensus paper of the WFSBP Task Force on Genetics: Genetics, epigenetics and gene expression markers of major depressive disorder and antidepressant response, WORLD JOURNAL OF BIOLOGICAL PSYCHIATRY, 2017, 第 25 作者(40) MicroRNA-137 Inhibits EFNB2 Expression Affected by a Genetic Variant and Is Expressed Aberrantly in Peripheral Blood of Schizophrenia Patients, EBIOMEDICINE, 2016, 第 9 作者(41) Analysis of association between common variants in the SLCO6A1 gene with schizophrenia, bipolar disorder and major depressive disorder in the Han Chinese population, WORLD JOURNAL OF BIOLOGICAL PSYCHIATRY, 2016, 第 12 作者 通讯作者(42) The TNF-alpha-308G/A Polymorphism is Not Associated with Ocular Chlamydia trachomatis Infection in Han Chinese Children, OPHTHALMIC GENETICS, 2016, 第 8 作者(43) Association study of the TPH2 Gene with Major Depressive Disorder in the Han Chinese Population, EUROPEAN JOURNAL OF PSYCHIATRY, 2016, 第 6 作者 通讯作者(44) Fine mapping the MHC region identified four independent variants modifying susceptibility to chronic hepatitis B in Han Chinese, HUMAN MOLECULAR GENETICS, 2016, 第 16 作者(45) Genetic association between NRG1 and schizophrenia, major depressive disorder, bipolar disorder in Han Chinese population, AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2016, 第 9 作者 通讯作者(46) The genome-wide mutational landscape of pituitary adenomas, CELL RESEARCH, 2016, 第 14 作者 通讯作者(47) Extraction of Angelica sinensis polysaccharides using ultrasound-assisted way and its bioactivity, INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 2016, 第 2 作者(48) Noninvasive fetal trisomy detection by multiplexed semiconductor sequencing: a barcoding analysis strategy, JOURNAL OF HUMAN GENETICS, 2016, 第 4 作者 通讯作者(49) A modifier screen identifies DNAJB6 as a cardiomyopathy susceptibility gene, JCIINSIGHT, 2016, 第 12 作者(50) 中国汉族人群HLA-DRA基因rs7194位点多态性与非梗阻性无精症易感性的关联性分析, Analysis of the correlation between the polymorphism of locus rs498422 in HLA-DRA gene of Chinese Han population and the hereditary susceptibility of non-obstructive azoospermia, 上海交通大学学报. 医学版, 2016, 第 4 作者(51) Genome-Wide Association Study of Bladder Cancer in a Chinese Cohort Reveals a New Susceptibility Locus at 5q12.3, CANCER RESEARCH, 2016, 第 31 作者 通讯作者(52) Polymorphisms in NRGN are associated with schizophrenia, major depressive disorder and bipolar disorder in the Han Chinese population, JOURNAL OF AFFECTIVE DISORDERS, 2016, 第 9 作者 通讯作者(53) Common variants in QPCT gene confer risk of schizophrenia in the Han Chinese population, AMERICANJOURNALOFMEDICALGENETICSPARTBNEUROPSYCHIATRICGENETICS, 2016, 第 10 作者 通讯作者(54) A new risk locus in the ZEB2 gene for schizophrenia in the Han Chinese population, PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY, 2016, 第 11 作者 通讯作者(55) Identification of a novel susceptibility locus at 16q23.1 associated with childhood acute lymphoblastic leukemia in Han Chinese, HUMAN MOLECULAR GENETICS, 2016, 第 1 作者 通讯作者(56) The NVL gene confers risk for both major depressive disorder and schizophrenia in the Han Chinese population, PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY, 2015, 第 10 作者 通讯作者(57) Polymorphisms of Renin-Angiotensin-Aldosterone System Gene in Chinese Han Patients with Nonfamilial Atrial Fibrillation, PLOS ONE, 2015, 第 8 作者(58) The GSK3B gene confers risk for both major depressive disorder and schizophrenia in the Han Chinese population, JOURNAL OF AFFECTIVE DISORDERS, 2015, 第 13 作者 通讯作者(59) Recurrent gain-of-function USP8 mutations in Cushing's disease, CELL RESEARCH, 2015, 第 45 作者 通讯作者(60) Common variants at 10p12.31, 10q21.1 and 13q12.13 are associated with sporadic pituitary adenoma, NATURE GENETICS, 2015, 第 46 作者 通讯作者(61) Endothelial Nitric Oxide Synthase (eNOS) T-786C, 4a4b, and G894T Polymorphisms and Male Infertility: Study for Idiopathic Asthenozoospermia and Meta-Analysis, BIOLOGY OF REPRODUCTION, 2015, 第 12 作者(62) 基于全基因组关联研究的中国人群肺癌风险预测模型, Genome-wide association study based risk prediction model in predicting lung cancer risk in Chinese, 中华流行病学杂志, 2015, 第 8 作者(63) SHEsisPCA: A GPU-Based Software to Correct for Population Stratification that Efficiently Accelerates the Process for Handling Genome-Wide Datasets, JOURNAL OF GENETICS AND GENOMICS, 2015, 第 3 作者 通讯作者(64) Polymorphisms in GCKR, SLC17A1 and SLC22A12 were associated with phenotype gout in Han Chinese males: a case-control study (vol 16, 66, 2015), BMC MEDICAL GENETICS, 2015, 第 11 作者 通讯作者(65) Comparison of hepatocellular carcinoma (HCC), cholangiocarcinoma (CC), and combined HCC-CC (CHC) with each other based on microarray dataset (Retraction of vol 34, pg 1679, 2013), TUMOR BIOLOGY, 2015, 第 8 作者 通讯作者(66) Genome-wide association analysis identifies three new risk loci for gout arthritis in Han Chinese, NATURE COMMUNICATIONS, 2015, 第 47 作者(67) Association between SREBF2 gene polymorphisms and metabolic syndrome in clozapine-treated patients with schizophrenia, PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY, 2015, 第 12 作者(68) Association Study Between Polymorphisms of PRMT6, PEX10, SOX5, and Nonobstructive Azoospermia in the Han Chinese Population, BIOLOGY OF REPRODUCTION, 2014, 第 19 作者(69) Association analysis of the GRM8 gene with schizophrenia in the Uygur Chinese population, HEREDITAS, 2014, 第 6 作者(70) A Genome-Wide Association Study Identifies a Locus on TERT for Mean Telomere Length in Han Chinese, PLOS ONE, 2014, 第 18 作者(71) Recurrent deletions of ULK4 in schizophrenia: a gene crucial for neuritogenesis and neuronal motility, JOURNAL OF CELL SCIENCE, 2014, 第 10 作者(72) A genome-wide gene���environment interaction analysis for tobacco smoke and lung cancer susceptibility, CARCINOGENESIS, 2014, 第 6 作者(73) Common Variants in the CDH7 Gene are Associated with Major Depressive Disorder in the Han Chinese Population, BEHAVIOR GENETICS, 2014, 第 15 作者 通讯作者(74) The CMYA5 gene confers risk for both schizophrenia and major depressive disorder in the Han Chinese population, WORLDJOURNALOFBIOLOGICALPSYCHIATRY, 2014, 第 11 作者 通讯作者(75) A genome-wide gene-gene interaction analysis identifies an epistatic gene pair for lung cancer susceptibility in Han Chinese, CARCINOGENESIS, 2014, 第 8 作者(76) Comparison of the performance of Ion Torrent chips in noninvasive prenatal trisomy detection, JOURNAL OF HUMAN GENETICS, 2014, 第 8 作者(77) New loci associated with chronic hepatitis B virus infection in Han Chinese, NATURE GENETICS, 2013, 第 26 作者(78) Association of Polymorphism rs198977 in Human Kallikrein-2 Gene (KLK2) with Susceptibility of Prostate Cancer: A Meta-Analysis (Retracted article. See vol. 11, e0160298, 2016), PLOS ONE, 2013, 第 10 作者 通讯作者(79) Association of CYP2A6*4 with Susceptibility of Lung Cancer: A Meta-Analysis, PLOS ONE, 2013, (80) A role for c-Abl in cell senescence and spontaneous immortalization, AGE, 2013, 第 10 作者(81) Genetic variants at 5p15 are associated with risk and early onset of gastric cancer in Chinese populations, CARCINOGENESIS, 2013, 第 8 作者(82) MicroRNA Microarray Analysis Combined with Interaction Network Analysis to Investigate the Influence of Clozapine to Metabolic Syndrome, INTERNATIONAL JOURNAL OF PHARMACOLOGY, 2013, 第 9 作者(83) An Evaluation of Association between a Novel Hippocampal Biology Related SNP (rs7294919) and Schizophrenia, PLOS ONE, 2013, 第 17 作者(84) 精神分裂症研究新希望:人体诱导多能干细胞, 中华行为医学与脑科学杂志, 2013, 第 4 作者(85) Genome-wide association study in Han Chinese identifies four new susceptibility loci for coronary artery disease, NATURE GENETICS, 2012, (86) ZNF804A and schizophrenia susceptibility in Asian populations, AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2012, 第 3 作者(87) GWAS Identifies Novel Susceptibility Loci on 6p21.32 and 21q21.3 for Hepatocellular Carcinoma in Chronic Hepatitis B Virus Carriers, PLOS GENETICS, 2012, 第 47 作者(88) Genetic Variants at 6p21.1 and 7p15.3 Are Associated with Risk of Multiple Cancers in Han Chinese, AMERICAN JOURNAL OF HUMAN GENETICS, 2012, 第 6 作者(89) Association of 8q22.3 locus in Chinese Han with idiopathic premature ovarian failure (POF), HUMAN MOLECULAR GENETICS, 2012, 第 4 作者(90) Polymorphisms and Haplotypes in the YWHAE Gene Increase Susceptibility to Bipolar Disorder in Chinese Han Population, JOURNAL OF CLINICAL PSYCHIATRY, 2012, 第 9 作者(91) A genome-wide association study reveals association between common variants in an intergenic region of 4q25 and high-grade myopia in the Chinese Han population, HUMAN MOLECULAR GENETICS, 2011, 第 23 作者 通讯作者(92) The MDGA1 gene confers risk to schizophrenia and bipolar disorder, SCHIZOPHRENIA RESEARCH, 2011, 第 12 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sequence and de novo assembly of the giant panda genome, NATURE, 2010, 第 88 作者(101) 基因分型技术的研究进展, Research Progress in Genotyping Technology, 细胞生物学杂志, 2009, 第 4 作者(102) Association between the PDE4D gene and ischaemic stroke in the Chinese Han population, CLINICAL SCIENCE, 2009, 第 6 作者(103) Copy-Number Mutations on Chromosome 17q24.2-q24.3 in Congenital Generalized Hypertrichosis Terminalis with or without Gingival Hyperplasia, AMERICAN JOURNAL OF HUMAN GENETICS, 2009, 第 8 作者(104) Haplotype analysis confirms association of the serotonin transporter (5-HTT) gene with schizophrenia in the Han Chinese population, NEUROSCIENCELETTERS, 2009, 第 11 作者(105) Association of genetic polymorphisms in the type II deiodinase gene with bipolar disorder in a subset of Chinese population, PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY, 2009, 第 6 作者(106) Positive association between ALDH1A2 and schizophrenia in the Chinese population, PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL 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