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 言語障害の遺伝学における最近の進歩。 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 と ATP2C2 の言語障害における音韻的短期記憶を調節します。 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 FOXP1 変異が発達言語的行動不全の影響の評価。 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 異なる発達性言語障害間の機能的遺伝的リンク。 The New England Journal of Medicine. Nov, 2008 | Pubmed ID: 18987363 人間の音声赤字に関与点突然変異マウスの学習障害のシナプス可塑性とモーター 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 歌うマウス、鳴禽類、その他:人間の音声言語におけるFOXP2の機能と機能障害のためのモデル 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 音声や言語の発達の赤字の小説原因として FOXP2 切り捨ての同定 American Journal of Human Genetics. Jun, 2005 | Pubmed ID: 15877281 77 プラスミド地域染色体 6p22.2 の家族イギリスおよびアメリカ合衆国からの失読症に関連付けられています。 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 家族性および遺伝性影響モーターの調整、左右と読書関連認知。 The American Journal of Psychiatry. Nov, 2003 | Pubmed ID: 14594743 染色体 2 P 12 - Q11 上利き手と統合失調症感受性に及ぼす親の起源。 Human Molecular Genetics. Dec, 2003 | Pubmed ID: 14583442 FOXP2 式脳開発中重度のスピーチおよび言語障害の病理のアダルト サイトと一致します。 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 ケースコントロー注意欠陥/多動性障害の拡張サンプル: 17 P 11 に挑発的なリンケージ。 American Journal of Human Genetics. May, 2003 | Pubmed ID: 12687500 相対の手のスキル 2 P 12 - Q11 へのリンケージを確証します。 American Journal of Human Genetics. Feb, 2003 | Pubmed ID: 12596796 郭清複雑な認知的形質の多変量解析の使用。 American Journal of Human Genetics. Mar, 2003 | Pubmed ID: 12587094 音声や言語障害の遺伝的基礎を解読します。 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 スピーチおよび言語に関与する遺伝子 FOXP2 の分子進化。 Nature. Aug, 2002 | Pubmed ID: 12192408 注意欠陥/多動性障害自閉症に関与する地域での 16 の P 13 番染色体の遺伝的連鎖。 American Journal of Human Genetics. Oct, 2002 | Pubmed ID: 12187510 注意欠陥/多動性障害に関与する遺伝子のゲノムワイド スキャン。 American Journal of Human Genetics. May, 2002 | Pubmed ID: 11923911 染色体 2 P 12-16 失読症感受性遺伝子座の精密マッピング: 定量的協会分析と位置指定候補遺伝子 SEMA4F と OTX1。 Psychiatric Genetics. Mar, 2002 | Pubmed ID: 11901358 相対の手のスキル兄弟ペアのためのゲノムワイド リンケージ スクリーン。 American Journal of Human Genetics. Mar, 2002 | Pubmed ID: 11774074 独立したゲノムのスキャンは失読症に影響を及ぼす染色体 18 量的形質遺伝子座を識別します。 Nature Genetics. Jan, 2002 | Pubmed ID: 11743577 生物発光共鳴エネルギー転移を用いて生細胞中のタンパク質 - タンパク質相互作用を調査する 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
生物発光共鳴エネルギー転移を用いて生細胞中のタンパク質 - タンパク質相互作用を調査する 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