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 I Recenti Progressi Nella Genetica Di Compromissione Del Linguaggio 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 E ATP2C2 Modulano Memoria Fonologica a Breve Termine Nella Svalutazione Del Linguaggio 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 Valutare L'impatto Delle Mutazioni FOXP1 Su Disprassia Verbale 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 Un Funzionale Collegamento Genetico Tra I Disturbi Del Linguaggio Di Sviluppo Distinti The New England Journal of Medicine. Nov, 2008 | Pubmed ID: 18987363 Alterata Plasticità Sinaptica E Motore Di Apprendimento Nei Topi Con Una Mutazione Puntiforme Implicata Nel Deficit Di Linguaggio Umano 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 Canto Topi, Uccelli Canori E Più: Modelli Per FOXP2 Funzione E Disfunzione Nel Discorso Umano E Linguaggio 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 Identificazione Di FOXP2 Troncamento Come Una Romanzo Causa Di Deficit Dello Sviluppo Di Linguaggio American Journal of Human Genetics. Jun, 2005 | Pubmed ID: 15877281 Regione Del Cromosoma 6p22.2 77-kilobase è Associata Con Dislessia in Famiglie Dal Regno Unito E Dagli Stati Uniti 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 Familiari E Genetici Effetti Sulla Coordinazione Motoria, Lateralità E Cognizione Lettura-correlati The American Journal of Psychiatry. Nov, 2003 | Pubmed ID: 14594743 Padre Di Origine Effetti Sulla Suscettibilità Di Manualità E Schizofrenia Sul Cromosoma 2 P 12 - Q11 Human Molecular Genetics. Dec, 2003 | Pubmed ID: 14583442 FOXP2 Espressione Durante Lo Sviluppo Del Cervello Coincide Con Siti Per Adulti Della Patologia in Un Discorso Grave E Disturbi Del Linguaggio 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 Una Scansione Di Genomewide Attention-deficit/hyperactivity Disorder in Un Esteso Campione: Suggestivo Collegamento Su 17 P 11 American Journal of Human Genetics. May, 2003 | Pubmed ID: 12687500 Prova Confermativa Per Collegamento Di Abilità Relativa Mano a 2 P 12 - Q11 American Journal of Human Genetics. Feb, 2003 | Pubmed ID: 12596796 Uso Dell'analisi Di Linkage Multivariata Per La Dissezione Di Un Tratto Cognitivo Complesso American Journal of Human Genetics. Mar, 2003 | Pubmed ID: 12587094 Decifrando Le Basi Genetiche Dei Disturbi Del Linguaggio 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 Evoluzione Molecolare Di FOXP2, Un Gene Coinvolto Nel Discorso E Lingua Nature. Aug, 2002 | Pubmed ID: 12192408 Collegamento Genetico Di Attention-deficit/hyperactivity Disorder Sul Cromosoma 16 P 13, in Una Regione Implicata Nell'autismo American Journal of Human Genetics. Oct, 2002 | Pubmed ID: 12187510 Una Scansione Di Genomewide Per Loci Coinvolti Nella Attention-deficit/hyperactivity Disorder American Journal of Human Genetics. May, 2002 | Pubmed ID: 11923911 Fine Mappatura Del Locus Di Suscettibilità Di Cromosoma 2 P 12-16 Dislessia: Analisi Quantitativa Associazione E Geni Candidati Posizionale SEMA4F E OTX1 Psychiatric Genetics. Mar, 2002 | Pubmed ID: 11901358 Una Schermata Di Collegamento Genomewide Per Skill Relativa Mano in Coppie Di Pari Livello American Journal of Human Genetics. Mar, 2002 | Pubmed ID: 11774074 Indipendente Genome-wide Scansioni Identificano Un Locus Quantitative Trait Cromosoma 18 Influenzando La Dislessia Nature Genetics. Jan, 2002 | Pubmed ID: 11743577 Indagare interazioni proteina-proteina in cellule vive utilizzando il trasferimento bioluminescenza Resonance Energy 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
Indagare interazioni proteina-proteina in cellule vive utilizzando il trasferimento bioluminescenza Resonance Energy 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