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 Recent Advances in the Genetics of Language Impairment 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 and ATP2C2 Modulate Phonological Short-term Memory in Language Impairment 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 Assessing the Impact of FOXP1 Mutations on Developmental Verbal Dyspraxia 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 A Functional Genetic Link Between Distinct Developmental Language Disorders The New England Journal of Medicine. Nov, 2008 | Pubmed ID: 18987363 Impaired Synaptic Plasticity and Motor Learning in Mice with a Point Mutation Implicated in Human Speech Deficits 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 Singing Mice, Songbirds, and More: Models for FOXP2 Function and Dysfunction in Human Speech and Language 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 Identification of FOXP2 Truncation As a Novel Cause of Developmental Speech and Language Deficits American Journal of Human Genetics. Jun, 2005 | Pubmed ID: 15877281 A 77-kilobase Region of Chromosome 6p22.2 is Associated with Dyslexia in Families from the United Kingdom and from the United States 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 Familial and Genetic Effects on Motor Coordination, Laterality, and Reading-related Cognition The American Journal of Psychiatry. Nov, 2003 | Pubmed ID: 14594743 Parent-of-origin Effects on Handedness and Schizophrenia Susceptibility on Chromosome 2p12-q11 Human Molecular Genetics. Dec, 2003 | Pubmed ID: 14583442 FOXP2 Expression During Brain Development Coincides with Adult Sites of Pathology in a Severe Speech and Language Disorder 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 A Genomewide Scan for Attention-deficit/hyperactivity Disorder in an Extended Sample: Suggestive Linkage on 17p11 American Journal of Human Genetics. May, 2003 | Pubmed ID: 12687500 Confirmatory Evidence for Linkage of Relative Hand Skill to 2p12-q11 American Journal of Human Genetics. Feb, 2003 | Pubmed ID: 12596796 Use of Multivariate Linkage Analysis for Dissection of a Complex Cognitive Trait American Journal of Human Genetics. Mar, 2003 | Pubmed ID: 12587094 Deciphering the Genetic Basis of Speech and Language Disorders 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 Molecular Evolution of FOXP2, a Gene Involved in Speech and Language Nature. Aug, 2002 | Pubmed ID: 12192408 Genetic Linkage of Attention-deficit/hyperactivity Disorder on Chromosome 16p13, in a Region Implicated in Autism American Journal of Human Genetics. Oct, 2002 | Pubmed ID: 12187510 A Genomewide Scan for Loci Involved in Attention-deficit/hyperactivity Disorder American Journal of Human Genetics. May, 2002 | Pubmed ID: 11923911 Fine Mapping of the Chromosome 2p12-16 Dyslexia Susceptibility Locus: Quantitative Association Analysis and Positional Candidate Genes SEMA4F and OTX1 Psychiatric Genetics. Mar, 2002 | Pubmed ID: 11901358 A Genomewide Linkage Screen for Relative Hand Skill in Sibling Pairs American Journal of Human Genetics. Mar, 2002 | Pubmed ID: 11774074 Independent Genome-wide Scans Identify a Chromosome 18 Quantitative-trait Locus Influencing Dyslexia Nature Genetics. Jan, 2002 | Pubmed ID: 11743577 Investigating Protein-protein Interactions in Live Cells Using Bioluminescence Resonance Energy Transfer 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
Investigating Protein-protein Interactions in Live Cells Using Bioluminescence Resonance Energy Transfer 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