Simon E. Fisher

Language and Genetics Department, Max Planck Institute for Psycholinguistics

Affiliated withMax Planck Institute for Psycholinguistics Donders Institute for Brain, Cognition and Behaviour Max Planck Institute for Psycholinguistics

Research Area

Biology

Biography

Simon E. Fisher has not added Biography.
If you are Simon E. Fisher and would like to personalize this page please email our Author Liaison for assistance.

JoVE Journal Publications

ArticleTotal : 1	Year
Publication title Cited by 25	2014

Other Publications

Article	Year
Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia. Nature genetics\| PubMed ID: 11743577	2002
A genomewide linkage screen for relative hand skill in sibling pairs. American journal of human genetics\| PubMed ID: 11774074	2002
Fine mapping of the chromosome 2p12-16 dyslexia susceptibility locus: quantitative association analysis and positional candidate genes SEMA4F and OTX1. Psychiatric genetics\| PubMed ID: 11901358	2002
A genomewide scan for loci involved in attention-deficit/hyperactivity disorder. American journal of human genetics\| PubMed ID: 11923911	2002
Genetic linkage of attention-deficit/hyperactivity disorder on chromosome 16p13, in a region implicated in autism. American journal of human genetics\| PubMed ID: 12187510	2002
Molecular evolution of FOXP2, a gene involved in speech and language. Nature\| PubMed ID: 12192408	2002
Developmental dyslexia: genetic dissection of a complex cognitive trait. Nature reviews. Neuroscience\| PubMed ID: 12360321	2002
Deciphering the genetic basis of speech and language disorders. Annual review of neuroscience\| PubMed ID: 12524432	2003
Use of multivariate linkage analysis for dissection of a complex cognitive trait. American journal of human genetics\| PubMed ID: 12587094	2003
Confirmatory evidence for linkage of relative hand skill to 2p12-q11. American journal of human genetics\| PubMed ID: 12596796	2003
A genomewide scan for attention-deficit/hyperactivity disorder in an extended sample: suggestive linkage on 17p11. American journal of human genetics\| PubMed ID: 12687500	2003
FOXP2 in focus: what can genes tell us about speech and language? Trends in cognitive sciences\| PubMed ID: 12804692	2003
FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder. Brain : a journal of neurology\| PubMed ID: 12876151	2003
Parent-of-origin effects on handedness and schizophrenia susceptibility on chromosome 2p12-q11. Human molecular genetics\| PubMed ID: 14583442	2003
Familial and genetic effects on motor coordination, laterality, and reading-related cognition. The American journal of psychiatry\| PubMed ID: 14594743	2003
Attention deficit hyperactivity disorder: fine mapping supports linkage to 5p13, 6q12, 16p13, and 17p11. American journal of human genetics\| PubMed ID: 15297934	2004
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\| PubMed ID: 15514892	2004
Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits. American journal of human genetics\| PubMed ID: 15877281	2005
On genes, speech, and language. The New England journal of medicine\| PubMed ID: 16236736	2005
The eloquent ape: genes, brains and the evolution of language. Nature reviews. Genetics\| PubMed ID: 16369568	2006
Genes, cognition and dyslexia: learning to read the genome. Trends in cognitive sciences\| PubMed ID: 16675285	2006
Tangled webs: tracing the connections between genes and cognition. Cognition\| PubMed ID: 16764847	2006
Functional genetic analysis of mutations implicated in a human speech and language disorder. Human molecular genetics\| PubMed ID: 16984964	2006
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\| PubMed ID: 17035521	2006
Molecular windows into speech and language disorders. Folia phoniatrica et logopaedica : official organ of the International Association of Logopedics and Phoniatrics (IALP)\| PubMed ID: 17556856	2007
Generation of mice with a conditional Foxp2 null allele. Genesis (New York, N.Y. : 2000)\| PubMed ID: 17619227	2007
Identification of the transcriptional targets of FOXP2, a gene linked to speech and language, in developing human brain. American journal of human genetics\| PubMed ID: 17999357	2007
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\| PubMed ID: 17999362	2007
Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficits. Current biology : CB\| PubMed ID: 18328704	2008
A functional genetic link between distinct developmental language disorders. The New England journal of medicine\| PubMed ID: 18987363	2008
FOXP2 as a molecular window into speech and language. Trends in genetics : TIG\| PubMed ID: 19304338	2009
Assessing the impact of FOXP1 mutations on developmental verbal dyspraxia. European journal of human genetics : EJHG\| PubMed ID: 19352412	2009
A humanized version of Foxp2 affects cortico-basal ganglia circuits in mice. Cell\| PubMed ID: 19490899	2009
Modified sound-evoked brainstem potentials in Foxp2 mutant mice. Brain research\| PubMed ID: 19596273	2009
CMIP and ATP2C2 modulate phonological short-term memory in language impairment. American journal of human genetics\| PubMed ID: 19646677	2009
Unravelling neurogenetic networks implicated in developmental language disorders. Biochemical Society transactions\| PubMed ID: 19909259	2009
Genetic susceptibility to stuttering. The New England journal of medicine\| PubMed ID: 20147708	2010
Recent advances in the genetics of language impairment. Genome medicine\| PubMed ID: 20193051	2010
Molecular networks implicated in speech-related disorders: FOXP2 regulates the SRPX2/uPAR complex. Human molecular genetics\| PubMed ID: 20858596	2010
Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations. Nature genetics\| PubMed ID: 21572417	2011
Foxp2 regulates gene networks implicated in neurite outgrowth in the developing brain. PLoS genetics\| PubMed ID: 21765815	2011
Foxp2 mutations impair auditory-motor association learning. PloS one\| PubMed ID: 22412993	2012
The DISC1 promoter: characterization and regulation by FOXP2. Human molecular genetics\| PubMed ID: 22434823	2012
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\| PubMed ID: 22909776	2013
Decoding the genetics of speech and language. Current opinion in neurobiology\| PubMed ID: 23228431	2013
Persistence and transmission of recessive deafness and sign language: new insights from village sign languages. European journal of human genetics : EJHG\| PubMed ID: 23321624	2013
Absolute pitch exhibits phenotypic and genetic overlap with synesthesia. Human molecular genetics\| PubMed ID: 23406871	2013
Neurogenomics of speech and language disorders: the road ahead. Genome biology\| PubMed ID: 23597266	2013
FOXP2 targets show evidence of positive selection in European populations. American journal of human genetics\| PubMed ID: 23602712	2013
Evolution. Culture, genes, and the human revolution. Science (New York, N.Y.)\| PubMed ID: 23704558	2013
Common variants in left/right asymmetry genes and pathways are associated with relative hand skill. PLoS genetics\| PubMed ID: 24068947	2013
Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia. Developmental medicine and child neurology\| PubMed ID: 24117048	2014
Molecular genetics of dyslexia: an overview. Dyslexia (Chichester, England)\| PubMed ID: 24133036	2013
Is synaesthesia more common in autism? Molecular autism\| PubMed ID: 24252644	2013
The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data. Brain imaging and behavior\| PubMed ID: 24399358	2014
Associations of HLA alleles with specific language impairment. Journal of neurodevelopmental disorders\| PubMed ID: 24433325	2014
On the other hand: including left-handers in cognitive neuroscience and neurogenetics. Nature reviews. Neuroscience\| PubMed ID: 24518415	2014
Differences in cerebral cortical anatomy of left- and right-handers. Frontiers in psychology\| PubMed ID: 24734025	2014
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\| PubMed ID: 24801482	2014
Measurement and genetics of human subcortical and hippocampal asymmetries in large datasets. Human brain mapping\| PubMed ID: 24827550	2013