Simon E. Fisher Language and Genetics Department Max Planck Institute for Psycholinguistics Biography Publications Institution JoVE Articles Simon E. Fisher has not added a biography. If you are Simon E. Fisher and would like to personalize this page please email our Author Liaison for assistance. Publications A Genome Wide Association Study of Mathematical Ability Reveals an Association at Chromosome 3q29, a Locus Associated with Autism and Learning Difficulties: a Preliminary Study PloS One. 2014 | Pubmed ID: 24801482 Differences in Cerebral Cortical Anatomy of Left- and Right-handers Frontiers in Psychology. 2014 | Pubmed ID: 24734025 On the Other Hand: Including Left-handers in Cognitive Neuroscience and Neurogenetics Nature Reviews. Neuroscience. Mar, 2014 | Pubmed ID: 24518415 Associations of HLA Alleles with Specific Language Impairment Journal of Neurodevelopmental Disorders. 2014 | Pubmed ID: 24433325 The ENIGMA Consortium: Large-scale Collaborative Analyses of Neuroimaging and Genetic Data Brain Imaging and Behavior. Jan, 2014 | Pubmed ID: 24399358 Increased Prevalence of Sex Chromosome Aneuploidies in Specific Language Impairment and Dyslexia Developmental Medicine and Child Neurology. Apr, 2014 | Pubmed ID: 24117048 Measurement and Genetics of Human Subcortical and Hippocampal Asymmetries in Large Datasets Human Brain Mapping. Nov, 2013 | Pubmed ID: 24827550 Is Synaesthesia More Common in Autism? Molecular Autism. 2013 | Pubmed ID: 24252644 Molecular Genetics of Dyslexia: an Overview Dyslexia (Chichester, England). Nov, 2013 | Pubmed ID: 24133036 Common Variants in Left/right Asymmetry Genes and Pathways Are Associated with Relative Hand Skill PLoS Genetics. 2013 | Pubmed ID: 24068947 Evolution. Culture, Genes, and the Human Revolution Science (New York, N.Y.). May, 2013 | Pubmed ID: 23704558 FOXP2 Targets Show Evidence of Positive Selection in European Populations American Journal of Human Genetics. May, 2013 | Pubmed ID: 23602712 Neurogenomics of Speech and Language Disorders: the Road Ahead Genome Biology. Apr, 2013 | Pubmed ID: 23597266 Absolute Pitch Exhibits Phenotypic and Genetic Overlap with Synesthesia Human Molecular Genetics. May, 2013 | Pubmed ID: 23406871 Persistence and Transmission of Recessive Deafness and Sign Language: New Insights from Village Sign Languages European Journal of Human Genetics : EJHG. Sep, 2013 | Pubmed ID: 23321624 Decoding the Genetics of Speech and Language Current Opinion in Neurobiology. Feb, 2013 | Pubmed ID: 23228431 Dual Copy Number Variants Involving 16p11 and 6q22 in a Case of Childhood Apraxia of Speech and Pervasive Developmental Disorder European Journal of Human Genetics : EJHG. Apr, 2013 | Pubmed ID: 22909776 The DISC1 Promoter: Characterization and Regulation by FOXP2 Human Molecular Genetics. Jul, 2012 | Pubmed ID: 22434823 Foxp2 Mutations Impair Auditory-motor Association Learning PloS One. 2012 | Pubmed ID: 22412993 Foxp2 Regulates Gene Networks Implicated in Neurite Outgrowth in the Developing Brain PLoS Genetics. Jul, 2011 | Pubmed ID: 21765815 Exome Sequencing in Sporadic Autism Spectrum Disorders Identifies Severe De Novo Mutations Nature Genetics. Jun, 2011 | Pubmed ID: 21572417 Molecular Networks Implicated in Speech-related Disorders: FOXP2 Regulates the SRPX2/uPAR Complex Human Molecular Genetics. Dec, 2010 | Pubmed ID: 20858596 语言障碍的遗传学研究的最新进展。 Genome Medicine. 2010 | Pubmed ID: 20193051 Genetic Susceptibility to Stuttering The New England Journal of Medicine. Feb, 2010 | Pubmed ID: 20147708 Unravelling Neurogenetic Networks Implicated in Developmental Language Disorders Biochemical Society Transactions. Dec, 2009 | Pubmed ID: 19909259 CMIP 和 ATP2C2 调节语音短时记忆中的语言障碍。 American Journal of Human Genetics. Aug, 2009 | Pubmed ID: 19646677 Modified Sound-evoked Brainstem Potentials in Foxp2 Mutant Mice Brain Research. Sep, 2009 | Pubmed ID: 19596273 A Humanized Version of Foxp2 Affects Cortico-basal Ganglia Circuits in Mice Cell. May, 2009 | Pubmed ID: 19490899 评估对发展口头 Dyspraxia FOXP1 突变的影响。 European Journal of Human Genetics : EJHG. Oct, 2009 | Pubmed ID: 19352412 FOXP2 As a Molecular Window into Speech and Language Trends in Genetics : TIG. Apr, 2009 | Pubmed ID: 19304338 独特的发展性语言障碍之间的遗传链接功能。 The New England Journal of Medicine. Nov, 2008 | Pubmed ID: 18987363 受损的突触可塑性和电机与人类语音赤字牵连到点突变小鼠学习。 Current Biology : CB. Mar, 2008 | Pubmed ID: 18328704 High-throughput Analysis of Promoter Occupancy Reveals Direct Neural Targets of FOXP2, a Gene Mutated in Speech and Language Disorders American Journal of Human Genetics. Dec, 2007 | Pubmed ID: 17999362 Identification of the Transcriptional Targets of FOXP2, a Gene Linked to Speech and Language, in Developing Human Brain American Journal of Human Genetics. Dec, 2007 | Pubmed ID: 17999357 Generation of Mice with a Conditional Foxp2 Null Allele Genesis (New York, N.Y. : 2000). Jul, 2007 | Pubmed ID: 17619227 Molecular Windows into Speech and Language Disorders Folia Phoniatrica Et Logopaedica : Official Organ of the International Association of Logopedics and Phoniatrics (IALP). 2007 | Pubmed ID: 17556856 歌唱小鼠、 鸣禽,和更多: FOXP2 函数和人类言语和语言功能障碍的模型。 The Journal of Neuroscience : the Official Journal of the Society for Neuroscience. Oct, 2006 | Pubmed ID: 17035521 Functional Genetic Analysis of Mutations Implicated in a Human Speech and Language Disorder Human Molecular Genetics. Nov, 2006 | Pubmed ID: 16984964 Tangled Webs: Tracing the Connections Between Genes and Cognition Cognition. Sep, 2006 | Pubmed ID: 16764847 Genes, Cognition and Dyslexia: Learning to Read the Genome Trends in Cognitive Sciences. Jun, 2006 | Pubmed ID: 16675285 The Eloquent Ape: Genes, Brains and the Evolution of Language Nature Reviews. Genetics. Jan, 2006 | Pubmed ID: 16369568 On Genes, Speech, and Language The New England Journal of Medicine. Oct, 2005 | Pubmed ID: 16236736 作为新型的言语和语言发育赤字原因 FOXP2 截断的标识。 American Journal of Human Genetics. Jun, 2005 | Pubmed ID: 15877281 相关阅读障碍来自联合王国和美国的家庭中的染色体 6p22.2 77 Kilobase 区域。 American Journal of Human Genetics. Dec, 2004 | Pubmed ID: 15514892 Attention Deficit Hyperactivity Disorder: Fine Mapping Supports Linkage to 5p13, 6q12, 16p13, and 17p11 American Journal of Human Genetics. Oct, 2004 | Pubmed ID: 15297934 动作协调、 一侧与阅读相关的认知对家族性和遗传的影响。 The American Journal of Psychiatry. Nov, 2003 | Pubmed ID: 14594743 父的原产地效应对染色体 2 P 12 Q11 惯用手与精神分裂症的易感性。 Human Molecular Genetics. Dec, 2003 | Pubmed ID: 14583442 FOXP2 在大脑发育过程中的表达正值的病理的严重言语和语言障碍的成人网站。 Brain : a Journal of Neurology. Nov, 2003 | Pubmed ID: 12876151 FOXP2 in Focus: What Can Genes Tell Us About Speech and Language? Trends in Cognitive Sciences. Jun, 2003 | Pubmed ID: 12804692 在扩展示例中注意缺陷/多动障碍的全基因组扫描: 17 P 11 日暗示性联系。 American Journal of Human Genetics. May, 2003 | Pubmed ID: 12687500 联系起来的相对手技能到 2 P 12 Q11 的确证证据。 American Journal of Human Genetics. Feb, 2003 | Pubmed ID: 12596796 使用复杂的认知特质剖析多元联动分析。 American Journal of Human Genetics. Mar, 2003 | Pubmed ID: 12587094 破译言语和语言障碍的遗传基础。 Annual Review of Neuroscience. 2003 | Pubmed ID: 12524432 Developmental Dyslexia: Genetic Dissection of a Complex Cognitive Trait Nature Reviews. Neuroscience. Oct, 2002 | Pubmed ID: 12360321 分子进化研究 FOXP2、 言语和语言相关的基因。 Nature. Aug, 2002 | Pubmed ID: 12192408 注意缺陷/多动障碍 16 P 13、 自闭症中受牵连的地区号染色体上的遗传连锁。 American Journal of Human Genetics. Oct, 2002 | Pubmed ID: 12187510 注意缺陷/多动障碍基因位点全基因组扫描。 American Journal of Human Genetics. May, 2002 | Pubmed ID: 11923911 染色体 2 P 12-16 诵读易感位点的精细定位: 定量关联分析和定位候选基因 SEMA4F 和 OTX1。 Psychiatric Genetics. Mar, 2002 | Pubmed ID: 11901358 相对手技能同级成对一个全基因组联系屏幕。 American Journal of Human Genetics. Mar, 2002 | Pubmed ID: 11774074 独立的全基因组扫描找出影响诵读困难 18 号染色体数量性状位点。 Nature Genetics. Jan, 2002 | Pubmed ID: 11743577 研究蛋白质 - 蛋白质相互作用活细胞使用生物发光共振能量转移 Pelagia Deriziotis*1, Sarah A. Graham*1, Sara B. Estruch1, Simon E. Fisher1,2 1Language and Genetics Department, Max Planck Institute for Psycholinguistics, 2Donders Institute for Brain, Cognition and Behaviour JoVE 51438 Biology
研究蛋白质 - 蛋白质相互作用活细胞使用生物发光共振能量转移 Pelagia Deriziotis*1, Sarah A. Graham*1, Sara B. Estruch1, Simon E. Fisher1,2 1Language and Genetics Department, Max Planck Institute for Psycholinguistics, 2Donders Institute for Brain, Cognition and Behaviour JoVE 51438 Biology