Simon E. Fisher

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