贺林院士集【2025|PDF|Epub|mobi|kindle电子书版本百度云盘下载】

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第一部分 奋斗历程1

贺林小传3

贺林传记5

第二部分 学术贡献17

一、贺林院士的主要学术论文19

精神分裂症的基因组学研究进展19

精神分裂症中拷贝数变异的研究新进展30

转化医学：从基础科研到临床应用36

Mutations in IHH，Encoding Indian Hedgehog，Cause Brachydactyly Type A-142

A Family-Based and Case-Control Association Study of the NOTCH4 Gene and Schizophrenia47

Family-Based Association Studies of COMT Gene Polymorphisms and Schizophrenia in the Chinese Population52

Family-Based Association Study of DTNBP1 in 6 p22.3 and Schizophrenia54

Polymorphisms within 5′End of the Neuregulin 1 Gene are Genetically Associated with Schizophrenia in the Chinese Population56

Association of SNPs and Haplotypes in GABAA Receptor β2 Gene with Schizophrenia58

No Association Between Polymorphisms of Methylenetetrahydrofolate Reductase Gene and Schizophrenia in Both Chinese and Scottish Populations66

SHEsis，a Powerful Software Platform for Analyses of Linkage Disequilibrium,Haplotype Construction，and Genetic Association at Polymorphism Loci69

Rates of Adult Schizophrenia Following Prenatal Exposure to the Chinese Famine of 1959-196171

Further Evidence for the Association Between G72/G30 Genes and Schizophrenia in Two Ethnically Distinct Populations78

Family-Based Association Study of Epsin 4 and Schizophrenia88

MPZL1/PZR,a Novel Candidate Predisposing Schizophrenia in Han Chinese93

Meta-Analysis Supports Association Between Serotonin transporter（5-HTT）and Suicidal Behavior98

A Study of Rare Structural Variants in Schizophrenia Patients and Normal Controls from Chinese Han Population107

Identification of Loci Associated with Schizophrenia by Genome-wide Association and Follow-up110

A Mutation in Ihh that Causes Digit Abnormalities Alters its Signalling Capacity and range115

A Partition-Ligation-Combination-Subdivision EM Algorithm for Haplotype Inference with Multiallelic Markers：Update of the SHEsis（http：//analysis.bio-x.cn）125

Copy-Number Mutations on Chromosome 17q24.2-q24.3 in Congenital Generalized Hypertrichosis Terminalis with or without Gingival Hyperplasia129

The Sequence and de Novo Assembly of the Giant Panda Genome137

Asymmetric DNA Origami for Spatially Addressable and Index-Free Solution-Phase DNA Chips147

SHEsisEpi,A GPU-Enhanced Genome-Wide SNP-SNP Interaction Scanning Algorithm,Efficiently Reveals the Risk Genetic Epistasis in Bipolar Disorder153

Analysis of 10 Independent Samples Provides Evidence for Association Between Schizop-hrenia and a SNP Flanking Fibroblast Growth Factor Receptor 2（FGFR2）157

Common Variants in Major Histocompatibility Complex Region and TCF4 Gene are Significantly Associated with Schizophrenia in Han Chinese165

A Positive Role for c-Abl in Atm and Atr Activation in DNA Damage Response169

Genome-Wide Association Study Identifies Susceptibility Loci for Polycystic Ovary Syndrome on Chromosome 2p16.3,2p21 and 9q33.3184

Common Variants in the BCL9 Gene Conferring Risk of Schizophrenia192

Common SNPs and Haplotypes in DGK H are Associated with Bipolar Disorder and Schizophrenia in the Chinese Han Population203

A Genome-Wide Association Study Reveals Association Between Common Variants in An Intergenic Region of 4q25 and High-Grade Myopia in the Chinese Han Population206

Indian Hedgehog Mutations Causing Brachydactyly Type A1 Impair Hedgehog Signal Transduction at Multiple Levels215

Gold Nanoparticles for High-Throughput Genotyping of Long-Range Haplotypes229

Common Variants on 8p12 and lq24.2 Confer Risk of Schizophrenia237

NMDA Receptor Hypofunction Induces Dysfunctions of Energy Metabolism and Semaphorin Signaling in Rats：A Synaptic Proteome Study243

GWAS Identifies Novel Susceptibility Loci on 6p21.32 and 21q21.3 for Hepatocellular Carcinoma in Chronic Hepatitis B Virus Carriers257

Genome-wide Association Study in Han Chinese Identifies four New Susceptibility Loci for Coronary Artery Disease268

Genome-Wide Association Study Identifies Eight New Risk Loci for Polycystic Ovary Syndrome275

Genetic Variants at 6p21.1 and 7p15.3 Are Associated with Risk of Multiple Cancers in Han Chinese283

ORIGINAL ARTICLE Potential metabolite markers of schizophrenia291

二、贺林院士学术年表304

（一）代表论文304

（二）论文总目录304

（三）参与的学术会议350

（四）主要成绩360

（五）承担课题361

（六）专利申请362

第三部分 治学之道365

贺林“既然要做，为什么不做得最好？”367

贺林院士：做一件事，就要努力做到最好372

第四部分 大师风范377

在科学的殿堂里实现自己的梦想379

贺林：遗传生物学家的X魅力383

中国出生缺陷问题的探讨387

破译中国人的“遗传密码”389

第五部分 社会影响393

临床转化医学研究中心无锡成立395

大熊猫钟情竹子的原因有答案396

基因“失活”大熊猫不爱吃肉397

2001年中国医药科技十大新闻揭晓398

人类短指症病因终被揭开400

上海交大破解短指症病因402

2011年上海科技奖揭晓交大获奖数十年居首贺林院士荣获2011年度上海市科技功臣奖［图］403

［交大两会代表言论］政协委员贺林：加强出生缺陷研究405

Bio-X研究院贺林院士应邀演讲于世博名人堂407

贺林教授当选为中国侨联特聘科技专家、中国侨联科技专家委员会副主任408

贺林院士当选为第二十届TWAS发展中国家科学2009年度生物奖的贺词（1）409

贺林院士当选为第二十届TWAS发展中国家科学2009年度生物奖的贺词（2）410

贺林院士当选为第二十一届TWAS院士的贺词411

两成果入选2009年度中国基础科学研究十大新闻［图］412

不仅是个头衔更是一份责任414

基因定位［步步快半拍］416

上海市科技功臣、上海交通大学Bio-X研究院院长贺林快乐科学418

快乐“帅才”420

“创新是城市活力和后劲所在”422

上海科学技术奖公布 周良辅、贺林获“科技功臣奖”424

周良辅、贺林获科技功臣奖425

感谢信426

第六部分 人生风采427

家庭431

海外留学、工作432

科研、教学、社会活动435

国际交流443

业余生活446