Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia.-论文-万方医学网

第一作者： Tom,Walsh

第一单位： Department of Medicine, University of Washington, Seattle, WA 98195, USA.

作者： Tom,Walsh ^[1] ; Jon M,McClellan ; Shane E,McCarthy ; Anjené M,Addington ; Sarah B,Pierce ; Greg M,Cooper ; Alex S,Nord ; Mary,Kusenda ; Dheeraj,Malhotra ; Abhishek,Bhandari ; Sunday M,Stray ; Caitlin F,Rippey ; Patricia,Roccanova ; Vlad,Makarov ; B,Lakshmi ; Robert L,Findling ; Linmarie,Sikich ; Thomas,Stromberg ; Barry,Merriman ; Nitin,Gogtay ; Philip,Butler ; Kristen,Eckstrand ; Laila,Noory ; Peter,Gochman ; Robert,Long ; Zugen,Chen ; Sean,Davis ; Carl,Baker ; Evan E,Eichler ; Paul S,Meltzer ; Stanley F,Nelson ; Andrew B,Singleton ; Ming K,Lee ; Judith L,Rapoport ; Mary-Claire,King ; Jonathan,Sebat

作者单位： Department of Medicine, University of Washington, Seattle, WA 98195, USA. ^[1]

医学主题词青少年(Adolescent);成年人(Adult);发病年龄(Age of Onset);氨基酸序列(Amino Acid Sequence);脑(Brain);病例对照研究(Case-Control Studies);儿童(Child);兴奋性氨基酸转运子1(Excitatory Amino Acid Transporter 1);女(雌)性(Female);基因缺失(Gene Deletion);基因复制(Gene Duplication);疾病遗传易感性(Genetic Predisposition to Disease);基因组, 人(Genome, Human);人类(Humans);男(雄)性(Male);分子序列数据(Molecular Sequence Data);突变(Mutation);神经元(Neurons);寡核苷酸序列分析(Oligonucleotide Array Sequence Analysis);多态性, 单核苷酸(Polymorphism, Single Nucleotide);精神分裂症(Schizophrenia);信号传导(Signal Transduction)

DOI 10.1126/science.1155174

PMID 18369103

发布时间 2022-03-17

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Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia.

Science (New York, N.Y.)

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Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia.

Science (New York, N.Y.)

相似文献

同项目论文

Science (New York, N.Y.)

相关期刊

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