基本信息
张昆林男硕导中国科学院心理研究所
电子邮件： zhangkl@psych.ac.cn
通信地址： 北京市朝阳区林萃路16号院
邮政编码： 100101

研究领域

招生信息
招生专业040222-行为遗传学
040220-医学心理学
071021-生物信息学

招生方向生物信息学，遗传学
生物信息学，遗传学


教育背景2005-12--2008-10瑞士洛桑大学医学中心（CHUV,UNIL）、瑞士洛桑联邦理工大学(EPFL)博士后
2000-09--2005-06北京大学生命科学学院博士
1996-09--2000-06北京大学数学科学学院学士

学历
学位

工作经历
工作简历2008-11~现在,中国科学院心理研究所,助理研究员、副研究员

社会兼职

教授课程

专利与奖励
奖励信息
专利成果

出版信息
发表论文（1）A DRD2/ANNK1-COMT interaction, consisting of functional variants, confers risk of post-traumatic stress disorder in traumatized Chinese,Frontiers in Psychiatry,2018,第1作者
（2）Genetic analysis for cognitive flexibility in the trail-making test in attention deficit hyperactivity disorder patients from single nucleotide polymorphism, gene to pathway level,World Journal of Biological Psychiatry,2017,第1作者
（3）Common variants near IKZF1 are associated with primary Sj?gren's syndrome in Han Chinese,PLoS One,2017,通讯作者
（4）An overview of posttraumatic stress disorder genetic studies by analyzing and integrating genetic data into genetic database PTSDgene,Neuroscience and Biobehavioral Reviews,2017,第1作者
（5）Analysis of polymorphisms of genes associated with folate-mediated one-carbon metabolism and neural tube defects in Chinese Han population,Birth Defects Research Part A: Clinical and Molecular Teratology,2016,通讯作者
（6）A combined analysis of genome-wide expression profiling of bipolar disorder in human prefrontal cortex,Journal of Psychiatric Research,2016,第5作者
（7）Network-Based Analysis of Schizophrenia Genome-Wide Association Data to Detect the Joint Functional Association Signals,PLoS ONE,2015,第3作者
（8）Network-assisted analysis of primary Sjogren's syndrome GWAS data in Han Chinese,Scientific Reports,2015,第2作者
（9）Pathway-based analysis for genome-wide association study data of bipolar disorder provides new insights for genetic study,Protein Cell,2015,第3作者
（10）I-GSEA4GWAS v2: a web server for functional analysis of SNPs in trait-associated pathways identified from genome-wide association study,Protein Cell,2015,第1作者
（11）A genome-wide association study in Han Chinese identifies a susceptibility locus for primary Sjogren’s syndrome at 7q11.23,Nature Genetics,2013,第2作者
（12）ADHDgene: a genetic database for attention deficit hyperactivity disorder,Nucleic Acids Research,2012,第4作者
（13）ICSNPathway: identify candidate causal SNPs and pathways from genome-wide association study by one analytical framework,Nucleic Acids Research,2011,第1作者
（14）Pathway-based analysis for genome-wide association studies of schizophrenia to provide new insight in schizophrenia study,Chinese Science Bulletin,2011,第1作者
（15）Systematic evaluation of genome-wide methylated DNA enrichment using a CpG island array,BMC Genomics,2011,第2作者
（16）Exploring the metabolic network of the epidemic pathogen Burkholderia cenocepacia J2315 via genome-scale reconstruction,BMC systems Biology,2011,第6作者
（17）i-GSEA4GWAS: a web server for identification of pathways/gene sets associated with traits by applying an improved gene set enrichment analysis to genome-wide association study,Nucleic Acids Research,2010,第1作者
（18）Common genetic variation and the control of HIV-1 in humans,PLoS Genetics,2009,第8作者
（19）Model Structure of Human APOBEC3G,PLoS ONE,2007,第1作者

发表著作

科研活动
科研项目（ 1 ） 基于全基因组关联研究数据二次分析的肿瘤候选基因变异研究, 主持,国家级,2012-01--2014-12
（ 2 ） 基于芯片的健康评估系统, 主持,院级,2016-10--2018-03

参与会议

合作情况
项目协作单位

指导学生