Simon Fisher | Academic Influence

Simon Fisher's AcademicInfluence.com Rankings

Simon Fisher

Biology

#1623

World Rank

#2667

Historical Rank

Molecular Biology

#318

World Rank

#323

Historical Rank

Genetics

#296

World Rank

#349

Historical Rank

biology Degrees

Download Badge

Biology

Simon Fisher's Degrees

Bachelors Biochemistry University of Oxford

Why Is Simon Fisher Influential?

(Suggest an Edit or Addition)

According to Wikipedia, Simon E. Fisher is a British geneticist and neuroscientist who has pioneered research into the genetic basis of human speech and language. He is a director of the Max Planck Institute for Psycholinguistics and Professor of language and genetics at the Donders Institute for Brain, Cognition and Behaviour in Nijmegen, The Netherlands.

(See a Problem?)

Simon Fisher's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

A forkhead-domain gene is mutated in a severe speech and language disorder (2001) (1850)
Molecular evolution of FOXP2, a gene involved in speech and language (2002) (1358)
Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations (2011) (1025)
Common genetic variants influence human subcortical brain structures (2015) (731)
A common molecular basis for three inherited kidney stone diseases (1996) (696)
A functional genetic link between distinct developmental language disorders. (2008) (662)
The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data (2014) (646)
Localisation of a gene implicated in a severe speech and language disorder (1997) (546)
FOXP2 as a molecular window into speech and language. (2009) (472)
A Humanized Version of Foxp2 Affects Cortico-Basal Ganglia Circuits in Mice (2009) (465)
Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits. (2005) (407)
Developmental dyslexia: genetic dissection of a complex cognitive trait (2002) (375)
The genetic architecture of the human cerebral cortex (2018) (355)
FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder. (2003) (347)
LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia (2007) (334)
The eloquent ape: genes, brains and the evolution of language (2006) (320)
A genomewide scan for loci involved in attention-deficit/hyperactivity disorder. (2002) (315)
A quantitative-trait locus on chromosome 6p influences different aspects of developmental dyslexia. (1999) (301)
ENIGMA and global neuroscience: A decade of large-scale studies of the brain in health and disease across more than 40 countries (2019) (288)
Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia (2002) (285)
Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations (2012) (283)
A genomewide scan identifies two novel loci involved in specific language impairment. (2002) (282)
Identification of the transcriptional targets of FOXP2, a gene linked to speech and language, in developing human brain. (2007) (280)
Impaired Synaptic Plasticity and Motor Learning in Mice with a Point Mutation Implicated in Human Speech Deficits (2008) (274)
Foxp2 Regulates Gene Networks Implicated in Neurite Outgrowth in the Developing Brain (2011) (270)
A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States. (2004) (253)
Genetic linkage of attention-deficit/hyperactivity disorder on chromosome 16p13, in a region implicated in autism. (2002) (244)
High-throughput analysis of promoter occupancy reveals direct neural targets of FOXP2, a gene mutated in speech and language disorders. (2007) (242)
On the other hand: including left-handers in cognitive neuroscience and neurogenetics (2014) (240)
Novel genetic loci associated with hippocampal volume (2017) (238)
A genomewide scan for attention-deficit/hyperactivity disorder in an extended sample: suggestive linkage on 17p11. (2003) (233)
FOXP2 in focus: what can genes tell us about speech and language? (2003) (231)
FOXP2 is not a major susceptibility gene for autism or specific language impairment. (2002) (228)
The SPCH1 region on human 7q31: genomic characterization of the critical interval and localization of translocations associated with speech and language disorder. (2000) (212)
Novel genetic loci underlying human intracranial volume identified through genome-wide association (2016) (192)
Patterns of Gray Matter Abnormalities in Schizophrenia Based on an International Mega-analysis. (2015) (180)
CNTNAP2 variants affect early language development in the general population (2011) (180)
A major susceptibility locus for leprosy in India maps to chromosome 10p13 (2001) (179)
CMIP and ATP2C2 Modulate Phonological Short-Term Memory in Language Impairment (2009) (176)
Deciphering the genetic basis of speech and language disorders. (2003) (169)
Mapping cortical brain asymmetry in 17,141 healthy individuals worldwide via the ENIGMA Consortium (2017) (168)
ENIGMA and the individual: Predicting factors that affect the brain in 35 countries worldwide☆☆☆★ (2015) (168)
Functional genetic analysis of mutations implicated in a human speech and language disorder. (2006) (167)
Tangled webs: Tracing the connections between genes and cognition (2006) (167)
Isolation and partial characterization of a chloride channel gene which is expressed in kidney and is a candidate for Dent's disease (an X-linked hereditary nephrolithiasis). (1994) (157)
Characterisation of renal chloride channel, CLCN5, mutations in hypercalciuric nephrolithiasis (kidney stones) disorders. (1997) (149)
Cloning and characterization of CLCN5, the human kidney chloride channel gene implicated in Dent disease (an X-linked hereditary nephrolithiasis). (1995) (148)
Genetic architecture of subcortical brain structures in 38,851 individuals (2019) (148)
Common Variants in Left/Right Asymmetry Genes and Pathways Are Associated with Relative Hand Skill (2013) (141)
Attention deficit hyperactivity disorder: fine mapping supports linkage to 5p13, 6q12, 16p13, and 17p11. (2004) (138)
Molecular genetics of dyslexia: an overview. (2013) (137)
Use of multivariate linkage analysis for dissection of a complex cognitive trait. (2003) (136)
Humanized Foxp2 accelerates learning by enhancing transitions from declarative to procedural performance (2014) (135)
Genes, cognition and dyslexia: learning to read the genome (2006) (134)
Decoding the genetics of speech and language (2013) (130)
Altered structural brain asymmetry in autism spectrum disorder in a study of 54 datasets (2019) (123)
Human subcortical brain asymmetries in 15,847 people worldwide reveal effects of age and sex (2016) (120)
A genomewide linkage screen for relative hand skill in sibling pairs. (2002) (116)
BCL11A Haploinsufficiency Causes an Intellectual Disability Syndrome and Dysregulates Transcription (2016) (113)
De novo TBR1 mutations in sporadic autism disrupt protein functions (2014) (113)
A novel forkhead-domain gene is mutated in a severe speech and language disorder (2001) (112)
Asymmetry within and around the human planum temporale is sexually dimorphic and influenced by genes involved in steroid hormone receptor activity (2015) (110)
Bivariate linkage scan for reading disability and attention-deficit/hyperactivity disorder localizes pleiotropic loci. (2005) (108)
Genome-wide screening for DNA variants associated with reading and language traits (2014) (108)
Putative functional alleles of DYX1C1 are not associated with dyslexia susceptibility in a large sample of sibling pairs from the UK (2004) (106)
Is synaesthesia more common in autism? (2013) (106)
Molecular networks implicated in speech-related disorders: FOXP2 regulates the SRPX2/uPAR complex. (2010) (104)
Understanding Language from a Genomic Perspective. (2015) (102)
A set of regulatory genes co-expressed in embryonic human brain is implicated in disrupted speech development (2018) (99)
The structure of innate vocalizations in Foxp2-deficient mouse pups (2010) (96)
Recent advances in the genetics of language impairment (2010) (95)
Generation of mice with a conditional Foxp2 null allele (2007) (95)
Differences in cerebral cortical anatomy of left- and right-handers (2014) (94)
Genome-wide scan of reading ability in affected sibling pairs with attention-deficit/hyperactivity disorder: unique and shared genetic effects (2004) (92)
Associations of HLA alleles with specific language impairment (2014) (92)
Genetic and phenotypic effects of phonological short‐term memory and grammatical morphology in specific language impairment (2008) (91)
An aetiological Foxp2 mutation causes aberrant striatal activity and alters plasticity during skill learning (2011) (89)
Singing Mice, Songbirds, and More: Models for FOXP2 Function and Dysfunction in Human Speech and Language (2006) (88)
A Foxp2 Mutation Implicated in Human Speech Deficits Alters Sequencing of Ultrasonic Vocalizations in Adult Male Mice (2016) (85)
Cortical thickness across the lifespan: Data from 17,075 healthy individuals aged 3–90 years (2021) (84)
Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes (2018) (81)
Fine mapping of the chromosome 2p12-16 dyslexia susceptibility locus: quantitative association analysis and positional candidate genes SEMA4F and OTX1 (2002) (78)
Shared genetic influences between dimensional ASD and ADHD symptoms during child and adolescent development (2017) (76)
Foxp2 Mutations Impair Auditory-Motor Association Learning (2012) (75)
Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment (2014) (75)
Neandertal Introgression Sheds Light on Modern Human Endocranial Globularity (2018) (74)
Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment (2017) (71)
FOXP2-Related Speech and Language Disorders (2016) (68)
Confirmatory evidence for linkage of relative hand skill to 2p12-q11. (2003) (68)
Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia (2018) (67)
Identification and functional characterization of de novo FOXP1 variants provides novel insights into the etiology of neurodevelopmental disorder. (2016) (66)
Absolute pitch exhibits phenotypic and genetic overlap with synesthesia. (2013) (65)
Parent-of-origin effects on handedness and schizophrenia susceptibility on chromosome 2p12-q11. (2003) (64)
Defining the biological bases of individual differences in musicality (2015) (62)
FOXP2 targets show evidence of positive selection in European populations. (2013) (62)
Familial and genetic effects on motor coordination, laterality, and reading-related cognition. (2003) (61)
What can mice tell us about Foxp2 function? (2014) (60)
Culture, Genes, and the Human Revolution (2013) (59)
Pooled genome-wide linkage data on 424 ADHD ASPs suggests genetic heterogeneity and a common risk locus at 5p13 (2006) (58)
A highly penetrant form of childhood apraxia of speech due to deletion of 16p11.2 (2015) (57)
Greater male than female variability in regional brain structure across the lifespan (2020) (57)
FOXP 2 Is Not a Major Susceptibility Gene for Autism or Specific Language Impairment (2002) (56)
Mapping brain asymmetry in health and disease through the ENIGMA consortium (2019) (54)
Mapping the X chromosome breakpoint in two papillary renal cell carcinoma cell lines with a t(X;1)(p11.2;q21.2) and the first report of a female case. (1995) (53)
Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language (2018) (52)
Foxp1/2/4 regulate endochondral ossification as a suppresser complex. (2015) (51)
CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language (2018) (51)
Speech and Language: Translating the Genome. (2017) (50)
Left–Right Asymmetry of Maturation Rates in Human Embryonic Neural Development (2017) (49)
Genome-wide analysis identifies a role for common copy number variants in specific language impairment (2015) (49)
Exome Sequencing in an Admixed Isolated Population Indicates NFXL1 Variants Confer a Risk for Specific Language Impairment (2015) (48)
Dissection of molecular mechanisms underlying speech and language disorders (2005) (47)
Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition. (2020) (47)
Subcortical volumes across the lifespan: Data from 18,605 healthy individuals aged 3–90 years (2021) (47)
Measurement and genetics of human subcortical and hippocampal asymmetries in large datasets (2014) (47)
Ultrasonic vocalizations of adult male Foxp2‐mutant mice: behavioral contexts of arousal and emotion (2016) (47)
A de novo FOXP1 variant in a patient with autism, intellectual disability and severe speech and language impairment (2015) (46)
The genetic architecture of structural left–right asymmetry of the human brain (2020) (46)
Subtle left-right asymmetry of gene expression profiles in embryonic and foetal human brains (2018) (46)
Assessing the impact of FOXP1 mutations on developmental verbal dyspraxia (2009) (45)
Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia (2020) (45)
The DISC1 promoter: characterization and regulation by FOXP2. (2012) (45)
Investigation of Quantitative Measures Related to Reading Disability in a Large Sample of Sib-Pairs from the UK (2001) (44)
Explorer CMIP and ATP 2 C 2 Modulate Phonological Short-Term Memory in Language Impairment (2009) (43)
Next-gen sequencing identifies non-coding variation disrupting miRNA-binding sites in neurological disorders (2017) (42)
Proteomic analysis of FOXP proteins reveals interactions between cortical transcription factors associated with neurodevelopmental disorders (2018) (41)
Deep phenotyping of speech and language skills in individuals with 16p11.2 deletion (2018) (41)
Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia (2018) (40)
Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia (2013) (40)
Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder (2012) (39)
Genetics and the Language Sciences (2015) (39)
The language-related transcription factor FOXP2 is post-translationally modified with small ubiquitin-like modifiers (2016) (39)
Loss of Intercalated Cells (ITCs) in the Mouse Amygdala of Tshz1 Mutants Correlates with Fear, Depression, and Social Interaction Phenotypes (2017) (38)
Assessing the effects of common variation in the FOXP2 gene on human brain structure (2014) (38)
Sequence-based exon prediction around the synaptophysin locus reveals a gene-rich area containing novel genes in human proximal Xp. (1997) (37)
Evolution of language: Lessons from the genome (2016) (36)
The FOXP1, FOXP2 and FOXP4 transcription factors are required for islet alpha cell proliferation and function in mice (2015) (35)
De novo mutations in MED13, a component of the Mediator complex, are associated with a novel neurodevelopmental disorder (2018) (34)
A genome‐wide search for quantitative trait loci affecting the cortical surface area and thickness of Heschl's gyrus (2014) (34)
Rare variants in axonogenesis genes connect three families with sound–color synesthesia (2018) (33)
Molecular cloning of the papillary renal cell carcinoma-associated translocation (X;1)(p11;q21) breakpoint. (1996) (33)
Conserved regulation of neurodevelopmental processes and behavior by FoxP in Drosophila (2019) (32)
De Novo Variants Disturbing the Transactivation Capacity of POU3F3 Cause a Characteristic Neurodevelopmental Disorder. (2019) (30)
Association analysis of dyslexia candidate genes in a Dutch longitudinal sample (2017) (30)
Human Genetics: The Evolving Story of FOXP2 (2019) (30)
Modified sound-evoked brainstem potentials in Foxp2 mutant mice (2009) (29)
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 (2014) (29)
Foxp2 regulates anatomical features that may be relevant for vocal behaviors and bipedal locomotion (2018) (29)
Genetic Architecture of Subcortical Brain Structures in Over 40,000 Individuals Worldwide (2017) (28)
Genetic variants associated with longitudinal changes in brain structure across the lifespan (2021) (27)
Neurogenomics of speech and language disorders: the road ahead (2013) (27)
Equivalent missense variant in the FOXP2 and FOXP1 transcription factors causes distinct neurodevelopmental disorders (2017) (26)
Genetic Determinants of Cortical Structure (Thickness, Surface Area and Volumes) among Disease Free Adults in the CHARGE Consortium (2018) (26)
A Common CYFIP1 Variant at the 15q11.2 Disease Locus Is Associated with Structural Variation at the Language-Related Left Supramarginal Gyrus (2016) (26)
Developmental Changes Within the Genetic Architecture of Social Communication Behavior: A Multivariate Study of Genetic Variance in Unrelated Individuals (2017) (25)
The Forkhead Transcription Factor FOXP2 Is Required for Regulation of p21WAF1/CIP1 in 143B Osteosarcoma Cell Growth Arrest (2015) (25)
Homozygous microdeletion of exon 5 in ZNF277 in a girl with specific language impairment (2014) (25)
Structural asymmetries of the human cerebellum in relation to cerebral cortical asymmetries and handedness (2016) (25)
Early speech development in Koolen de Vries syndrome limited by oral praxis and hypotonia (2017) (25)
Overlapping SETBP1 gain-of-function mutations in Schinzel-Giedion syndrome and hematologic malignancies (2017) (25)
Differential effects of Foxp2 disruption in distinct motor circuits (2018) (24)
Severe childhood speech disorder: gene discovery highlights transcriptional dysregulation (2019) (24)
Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction (2020) (24)
The genetics of situs inversus without primary ciliary dyskinesia (2020) (24)
No effect of schizophrenia risk genes MIR137, TCF4, and ZNF804A on macroscopic brain structure (2014) (24)
Lack of replication for the myosin-18B association with mathematical ability in independent cohorts (2015) (23)
Functional characterization of TBR1 variants in neurodevelopmental disorder (2018) (23)
Foxp transcription factors suppress a non-pulmonary gene expression program to permit proper lung development. (2016) (23)
Insights into the Genetic Foundations of Human Communication (2015) (23)
Multivariate genome-wide association study of rapid automatised naming and rapid alternating stimulus in Hispanic American and African–American youth (2019) (23)
Genetic effects on planum temporale asymmetry and their limited relevance to neurodevelopmental disorders, intelligence or educational attainment (2019) (22)
Low-frequency variation in TP53 has large effects on head circumference and intracranial volume (2018) (22)
Discovery of 42 genome-wide significant loci associated with dyslexia (2021) (22)
Handedness and its genetic influences are associated with structural asymmetries of the cerebral cortex in 31,864 individuals (2021) (22)
Hypomethylation of the paternally inherited LRRTM1 promoter linked to schizophrenia (2014) (22)
Analysis of structural brain asymmetries in Attention-Deficit/Hyperactivity Disorder in 39 datasets (2020) (22)
A Foxp 2 Mutation Implicated in Human Speech Deficits Alters Sequencing of Ultrasonic Vocalizations in Adult Male Mice (2019) (21)
High-resolution comparative mapping of the proximal region of the mouse X chromosome. (1995) (21)
Investigating protein-protein interactions in live cells using bioluminescence resonance energy transfer. (2014) (21)
Severe childhood speech disorder (2020) (21)
A common variant of the CNTNAP2 gene is associated with structural variation in the left superior occipital gyrus (2017) (21)
Functional characterization of rare FOXP2 variants in neurodevelopmental disorder (2016) (20)
Disentangling polygenic associations between attention-deficit/hyperactivity disorder, educational attainment, literacy and language (2019) (20)
1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans (2021) (20)
Unravelling neurogenetic networks implicated in developmental language disorders. (2009) (19)
On genes, speech, and language. (2005) (19)
Investigating the effects of copy number variants on reading and language performance (2016) (19)
Genome sequencing for rightward hemispheric language dominance (2019) (19)
Large-Scale Phenomic and Genomic Analysis of Brain Asymmetrical Skew (2019) (18)
Genetic susceptibility to stuttering. (2010) (18)
The Evolutionary History of Common Genetic Variants Influencing Human Cortical Surface Area (2019) (18)
Mapping of Human FOXP2 Enhancers Reveals Complex Regulation (2018) (18)
Molecular windows into speech and language disorders (2006) (18)
Foxp2 loss of function increases striatal direct pathway inhibition via increased GABA release (2018) (18)
Evaluation of results from genome‐wide studies of language and reading in a novel independent dataset (2016) (17)
Progress towards the identification of genes influencing developmental dyslexia (2001) (17)
Neuroimaging genetic analyses of novel candidate genes associated with reading and language (2017) (17)
Dynamics of Brain Structure and its Genetic Architecture over the Lifespan (2020) (16)
Effects of copy number variations on brain structure and risk for psychiatric illness: Large‐scale studies from the ENIGMA working groups on CNVs (2021) (16)
A schizophrenia-associated HLA locus affects thalamus volume and asymmetry (2015) (16)
Subtly altered topological asymmetry of brain structural covariance networks in autism spectrum disorder across 43 datasets from the ENIGMA consortium (2021) (15)
Cortical Thickness Trajectories across the Lifespan: Data from 17,075 healthy individuals aged 3-90 years (2020) (15)
A chromosomal rearrangement in a child with severe speech and language disorder separates FOXP2 from a functional enhancer (2015) (15)
Speech and language deficits are central to SETBP1 haploinsufficiency disorder (2021) (15)
Isolation of the genetic factors underlying speech and language disorders (2002) (14)
Toward Robust Functional Neuroimaging Genetics of Cognition (2019) (13)
Do Candidate Genes Affect the Brain’s White Matter Microstructure? Large-Scale Evaluation of 6,165 Diffusion MRI Scans (2017) (13)
Persistence and transmission of recessive deafness and sign language: new insights from village sign languages (2013) (13)
Genetic pathways involved in human speech disorders. (2020) (13)
Effect of apolipoprotein E polymorphism on cognition and brain in the Cambridge Centre for Ageing and Neuroscience cohort (2020) (13)
Genetics of language (2009) (12)
Gene Expression Correlates of the Cortical Network Underlying Sentence Processing (2018) (12)
Heterozygous variants that disturb the transcriptional repressor activity of FOXP4 cause a developmental disorder with speech/language delays and multiple congenital abnormalities (2020) (12)
Subcortical Volume Trajectories across the Lifespan: Data from 18,605 healthy individuals aged 3-90 years (2020) (12)
Investigating genetic links between grapheme–colour synaesthesia and neuropsychiatric traits (2019) (12)
Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations. (2020) (11)
Attention Deficit Hyperactivity Disorder : Fine Mapping Supports Linkage to 5 p 13 , 6 q 12 , 16 p 13 , and 17 p 11 (2004) (11)
Neandertal Introgression Sheds Light on Modern Human Endocranial Globularity (2019) (11)
The DISC 1 promoter : characterization and regulation by FOXP 2 (2012) (11)
Early developmental gene enhancers affect subcortical volumes in the adult human brain (2016) (11)
Severe speech impairment is a distinguishing feature of FOXP1‐related disorder (2021) (11)
Corrigendum: Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations (Nature Genetics (2011) 43, (585-589)) (2012) (11)
G‐protein genomic association with normal variation in gray matter density (2015) (11)
The Association of Dyslexia and Developmental Speech and Language Disorder Candidate Genes with Reading and Language Abilities in Adults (2020) (11)
Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people (2022) (10)
A Pooled Genome-Wide Association Study of Asperger Syndrome (2015) (10)
Characterization of novel promoter and enhancer elements of the mouse homologue of the Dent disease gene, CLCN5, implicated in X-linked hereditary nephrolithiasis. (1999) (10)
Region-specific Foxp2 deletions in cortex, striatum or cerebellum cannot explain vocalization deficits observed in spontaneous global knockouts (2020) (10)
Correction: Localisation of a gene implicated in a severe speech and language disorder (1998) (10)
A genome-wide search strategy for identifying quantitative trait loci involved in reading and spelling disability (developmental dyslexia) (2009) (10)
The developmental origins of genetic factors influencing language and literacy: Associations with early-childhood vocabulary. (2020) (10)
Molecular networks of the FOXP2 transcription factor in the brain (2021) (9)
Translating the genome in human neuroscience (2015) (9)
Polygenic selection underlies evolution of human brain structure and behavioral traits (2017) (8)
Special Notice to Contributors (1996) (7)
Construction of two YAC contigs in human Xp11.23-p11.22, one encompassing the loci OATL1, GATA, TFE3, and SYP, the other linking DXS255 to DXS146. (1995) (7)
LRRTM1 protein is located in the endoplasmic reticulum (ER) in mammalian cells (2007) (7)
Clinical delineation of SETBP1 haploinsufficiency disorder (2021) (7)
Genome-wide association analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people (2021) (7)
A molecular genetic perspective on speech and language [Invited talk] (2016) (6)
Building bridges between genes, brains and language (2012) (6)
Altered structural brain asymmetry in autism spectrum disorder: large-scale analysis via the ENIGMA Consortium (2019) (6)
Large-scale analysis of structural brain asymmetries in schizophrenia via the ENIGMA consortium (2022) (5)
Missense variants in ANKRD11 cause KBG syndrome by impairment of stability or transcriptional activity of the encoded protein (2021) (5)
Genes and language (2011) (5)
Reply to Pembrey et al: ‘ZNF277 microdeletions, specific language impairment and the meiotic mismatch methylation (3M) hypothesis' (2014) (5)
The Musical Abilities, Pleiotropy, Language, and Environment (MAPLE) Framework for Understanding Musicality-Language Links Across the Lifespan (2021) (5)
Genetic Pathways Implicated in Speech and Language (2013) (5)
CNTNAP2 variants affect early language development in the general population (2012) (5)
Next-generation sequencing identifies novel gene variants and pathways involved in specific language impairment (2016) (5)
A novel transcription factor is mutated in a severe speech and language disorder (2001) (4)
Left-handedness and its genetic influences are associated with structural asymmetries mapped across the cerebral cortex in 31,864 individuals (2021) (4)
A molecular genetic perspective on speech and language [Keynote lecture] (2016) (4)
Uncovering the Genetic Architecture of Broad Antisocial Behavior through a Genome-Wide Association Study Meta-analysis (2021) (4)
Relations between hemispheric asymmetries of grey matter and auditory processing of spoken syllables in 281 healthy adults (2020) (4)
The genetics of situs inversus totalis without primary ciliary dyskinesia (2018) (4)
Erratum: A highly penetrant form of childhood apraxia of speech due to deletion of 16p11.2 (2016) (4)
Polygenic risk for mental disorder reveals distinct association profiles across social behaviour in the general population (2022) (4)
Enhanced self-reported affect and prosocial behaviour without differential physiological responses in mirror-sensory synaesthesia (2019) (4)
Neurogenomics of speech and language (2012) (4)
Self‐reported impact of developmental stuttering across the lifespan (2022) (4)
A sibling-pair based approach for mapping genetic loci that influence quantitative measures of reading disability. (2000) (4)
Multivariate genome-wide association study of rapid automatized naming and rapid alternating stimulus in Hispanic and African American youth (2017) (4)
Topographic divergence of atypical cortical asymmetry and atrophy patterns in temporal lobe epilepsy (2021) (3)
Identification of foxp2 truncation as a novel cause of developmental speech disorder. (2004) (3)
Speech‐language profiles in the context of cognitive and adaptive functioning in SATB2‐associated syndrome (2021) (3)
No clear monogenic links between left-handedness and situs inversus (2018) (3)
ROLE OF A VOLTAGE-GATED CHLORIDE-CHANNEL GENE CLC-5 IN HUMAN AND RAT HYPERCALCIURIA (1995) (3)
Genetic architecture of the white matter connectome of the human brain (2022) (3)
Handedness and Other Variables Associated with Human Brain Asymmetrical Skew (2019) (3)
Whole-genome sequencing identifies functional noncoding variation in SEMA3C that cosegregates with dyslexia in a multigenerational family (2021) (3)
34 LEFT-RIGHT ASYMMETRY OF MATURATION RATES IN HUMAN EMBRYONIC NEURAL DEVELOPMENT (2019) (3)
Mutations in the chloride channel gene (CLCN5) are associated with hypercalciuric rickets and nephrolithiasis. (1996) (3)
Functional Genomic Dissection of Speech and Language Disorders (2011) (3)
Multivariate genome-wide covariance analyses of literacy, language and working memory skills reveal distinct etiologies (2021) (2)
Bridging senses: novel insights from synaesthesia (2019) (2)
Genome-wide search shows association between 10p15.2 and the volume of left Heschl's Gyrus (2013) (2)
In-depth characterisation of a cohort of individuals with missense and loss-of-function variants disrupting FOXP2 (2022) (2)
Proteomic analysis of FOXP proteins reveals interactions between cortical transcription factors associated with neurodevelopmental disorders. (2018) (2)
Planar cell polarity pathway and development of the human visual cortex (2018) (2)
Correction: Exome Sequencing in an Admixed Isolated Population IndicatesNFXL1 Variants Confer a Risk for Specific Language Impairment (2015) (2)
Genes, Brain, and Language: A brief introduction to the Special Issue (2017) (2)
Inherited variants in CHD3 show variable expressivity in Snijders Blok-Campeau syndrome. (2022) (2)
Generalized Structured Component Analysis in candidate gene association studies: applications and limitations (2019) (2)
High-precision spatial analysis of mouse courtship vocalization behavior reveals sex and strain differences (2021) (2)
Disentangling genetically confounded polygenic associations between Attention-Deficit/Hyperactivity Disorder, literacy and language (2018) (2)
Machine learning of large-scale multimodal brain imaging data reveals neural correlates of hand preference (2022) (2)
Molecular genetic methods (2018) (2)
Molecular windows into speech and language (2012) (2)
Generalized Structured Component Analysis in candidate gene association studies: applications and limitations. (2019) (2)
Erratum: Correction: Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia (Molecular psychiatry (2020) 25 3 (584-602)) : Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia (2020) (2)
Genetic aetiologies for childhood speech disorder: novel pathways co-expressed during brain development (2022) (2)
Neurogenomics of speech and language disorders [Keynote lecture] (2013) (1)
Low-frequency variation in TP53 has large effects on head circumference and intracranial volume (2019) (1)
Positional cloning of the gene responsible for dent's disease (1995) (1)
Neurogenomics of speech and language disorders: the road ahead (2013) (1)
Exome sequencing of an isolated Chilean population affected by Specific Language Impairment (SLI) (2012) (1)
The amplification of genetic factors for early vocabulary during children’s language and literacy development (2019) (1)
Birds and brains - what songbirds tell us about language (2016) (1)
Genome-wide screening for DNA variants associated with dyslexia and language impairment (2012) (1)
Genetic architecture of subcortical brain structures in 38,851 individuals (2019) (1)
Instructions for the preparation of gene mapping reports (1995) (1)
A clustering of heterozygous missense variants in the crucial chromatin modifier WDR5 defines a new neurodevelopmental disorder (2022) (1)
Using neuroimaging genomics to investigate the evolution of human brain structure (2022) (1)
Selective deletion of Foxp2 in motor-skill learning circuits (2012) (1)
The Genetic Basis of a Severe Speech and Language Disorder (2003) (1)
Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language (2019) (1)
Evaluating the genetic risk for dyslexia in multi-generation families (2015) (1)
ENIGMA Laterality Working Group (2018). Mapping cortical brain asymmetry in 17,141 healthy individuals worldwide via the ENIGMA Consortium. Proceedings of the National Academy of Sciences of the United States of America , 115 (22), E5154-E5163. (2018) (1)
Correction: Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia (2019) (1)
SETBP1 variants outside the degron disrupt DNA-binding and transcription independent of protein abundance to cause a heterogeneous neurodevelopmental disorder (2022) (1)
Decoding the genetics of speech and language [Abstract] (2013) (1)
Neurogenomics of speech and language disorders (2013) (1)
How can animal studies help to uncover the roles of genes implicated in human speech and language disorders (2006) (1)
Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities (2022) (1)
Foxp 1 / 2 / 4 regulate endochondral ossi fi cation as a suppresser complex (2015) (1)
Cerebellar developmental deficits underlie neurodegenerative disorder spinocerebellar ataxia type 23 (2020) (1)
Human subcortical brain asymmetries in 15,847 people worldwide reveal effects of age and sex (2016) (1)
The Multivariate Genome-wide Architecture of Interrelated Literacy, Language and Working Memory Skills Reveals Distinct Etiologies (2020) (1)
Genetic variations within human gained enhancer elements affect human brain sulcal morphology (2021) (1)
Deep phenotyping of speech and language skills in individuals with 16p11.2 deletion (2018) (0)
Genes, brain and language (2017) (0)
A chromosomal rearrangement in a child with severe speech and language disorder separates FOXP2 from a functional enhancer (2015) (0)
Identification of rare variants from exome sequencing in a large family with dyslexia (2014) (0)
Deciphering the biological basis of speech and language disorders [Keynote lecture] (2016) (0)
Genetics of planum temporale asymmetry: Limited relevance to disorders and cognitive variability (2019) (0)
T15EXPLORING THE GENETIC ARCHITECTURE OF CO-OCCURRING SYMPTOMS IN AUTISM (2019) (0)
Language and reading impairments are associated with increased prevalence of non-right-handedness. (2023) (0)
DISC1 promoter region: Bioinformatic characterisation and functional assessment (2012) (0)
State of the art in CAS genomic research [Keynote lecture] (2013) (0)
Language-Related Gene Activity: From Gene to Brain to Behavior (2016) (0)
Finding functional disease-associated non-coding variation using next-generation sequencing (2016) (0)
Speech and language: Lessons from the genome [Keynote lecture] (2015) (0)
Molecular windows into speech and language disorders [Guest lecture] (2011) (0)
Genome-wide association scanning for asymmetry of the human planum temporale (2013) (0)
A clustering of missense variants in the crucial chromatin modifier WDR5 defines a new neurodevelopmental disorder (2021) (0)
Supplementary material from "Enhanced self-reported affect and prosocial behaviour without differential physiological responses in mirror-sensory synesthesia" (2019) (0)
Normative Modeling of Brain Morphometry Across the Lifespan Using CentileBrain: Algorithm Benchmarking and Model Optimization (2023) (0)
A molecular link between speech and movement disorders revealed by studies of FOXP2 protein-protein interactions (2013) (0)
Molecular windows into speech and language disorders [Plenary lecture] (2012) (0)
FOXP2 in the nucleus accumbens regulates reward signaling and social behavior (2013) (0)
Digging deeper in next generation sequencing data: identification of functional non-coding variants that contribute to neurological disorders (an SLI case study) (2015) (0)
PRELIM II(EDI BOARD) (2014) (0)
A genetic perspective on speech and language development [Keynote lecture] (2012) (0)
PRELIM II(EDI BOARD) (2014) (0)
SA89A GENOME-WIDE ASSOCIATION SCREEN OF QUANTITATIVE SPEECH, LANGUAGE AND READING TRAITS IN >14,000 PEOPLE IN THE GENLANG CONSORTIUM (2019) (0)
Global Asymmetry (2019) (0)
Key issues and future directions: Genes and language (2019) (0)
Building bridges between genes, brains and cognition (2013) (0)
Genetics of brain asymmetries (2012) (0)
Simon Edward Fisher (1970-) (2019) (0)
Brains and birdsong - What birds can tell us about human language (2015) (0)
Neandertal Introgression S heds Light on Modern Human Endocranial Globularity Highlights (2018) (0)
Investigating copy number variants within a cohort of individuals with specific language impairment (2012) (0)
Modelling stability and change in the genetic architecture of language and literacy development (2019) (0)
51 POLYGENIC RISK FOR ADHD IS ASSOCIATED WITH READING AND SPELLING RELATED TRAITS BEYOND PLEIOTROPIC EFFECTS DUE TO EDUCATIONAL ATTAINMENT (2019) (0)
PRELIM II(EDI BOARD) (2015) (0)
Neurogenetic pathways implicated in speech and language disorders (2012) (0)
Altered structural brain asymmetry in autism spectrum disorder: Analysis via the ENIGMA Consortium (2019) (0)
FOXP2 and the search for" language genes (2003) (0)
PRELIM II(EDI BOARD) (2014) (0)
GL.03 Molecular windows into speech and language disorders (2011) (0)
Genes Within The Context of Development: Changes In Genetic Trait Architectures During Childhood and Adolescence (2019) (0)
Speech and language: Lessons from the genome [Guest lecture] (2015) (0)
Whole genome sequencing to investigate genetic variation in "Atypical" language lateralization (2016) (0)
PRELIM II(EDI BOARD) (2015) (0)
Understanding the contribution of FOXP genes in language-related disorders (2015) (0)
FOXPs in neuronal connectivity: Identifying protein-protein interactions using BRET. (2013) (0)
Investigating protein-protein interactions of the language-related transcription factor FOXP2 in live cells with bioluminescence resonance energy transfer (2015) (0)
PRELIM II(EDI BOARD) (2015) (0)
Title : Large-scale Phenomic and Genomic Analysis of Brain Asymmetrical Skew Abbreviated title : Mapping Brain Asymmetrical Skew (2020) (0)
PRELIM II(EDI BOARD) (2015) (0)
Associations of HLA alleles with specific language impairment (2014) (0)
The genetics of situs inversus without primary ciliary dyskinesia (2020) (0)
Conditional disruption of Foxp2 in the mouse brain (2019) (0)
Genome-wide analysis identi fi es a role for common copy number variants in speci fi c language impairment (2015) (0)
Deciphering the genetics of speech and language disorders [Keynote lecture] (2012) (0)
A genome-wide association screen of quantitative reading and language traits in >22,000 people in the GenLang consortium (2019) (0)
Structural asymmetries of the human cerebellum in relation to cerebral cortical asymmetries and handedness (2016) (0)
PRELIM II(EDI BOARD) (2015) (0)
ANALYSIS OF THE GENE ENCODING AN X-LINKED VOLTAGE-GATED CHLORIDE CHANNEL IN IDIOPATHIC HYPERCALIURIA (1995) (0)
PRELIM II(EDI BOARD) (2014) (0)
Language and genetics [Invited talk] (2014) (0)
W14. GENETIC CLUSTERING OF CO-OCCURRING SYMPTOMS IN PEOPLE WITH AUTISM: A MULTIVARIATE GENETIC VARIANCE ANALYSIS OF GENETIC RELATIONSHIP MATRICES IN THE SPARK SAMPLE (2021) (0)
The neglected side of FoxPs - how does FoxP1 affect auditory perception? (2016) (0)
Opposite genetic effects for polygenic ASD risk shared with and independent of ADHD: Evidence for a cancelling-out hypothesis studying genetic overlap with language and literacy (2018) (0)
Trait-specific patterns of common genetic factors influence social communication difficulties and ADHD symptoms during development (2016) (0)
Transcriptional regulation by the language-related protein FOXP2 - a role for sumoylation ? (2014) (0)
How Can Studies of Animals Help to Uncover the Roles of Genes Implicated in Human Speech and Language Disorders ? (2007) (0)
Language, evolution, and the genomics revolution [Invited talk] (2015) (0)
Dissecting FOXPS function in motor-skill learning circuits (2013) (0)
Using brain organoids to uncover the neurobiology of speech and language-related disorders (2019) (0)
Low frequency genetic variation in the TP53 locus has large effects on head circumference and intracranial volume (2018) (0)
The gift of gab: How your genome helps you speak [Presidential Special Lecture] (2012) (0)
Author Correction: Altered structural brain asymmetry in autism spectrum disorder in a study of 54 datasets (2021) (0)
Flying through a molecular window into the neurobiology of language and cognition (2013) (0)
Characterization of the TBR1 interactome: variants associated with neurodevelopmental disorders disrupt novel protein interactions (2022) (0)
PRELIM II(EDI BOARD) (2014) (0)
Correction to ‘Investigating genetic links between grapheme–colour synaesthesia and neuropsychiatric traits’ (2020) (0)
PRELIM II(EDI BOARD) (2015) (0)
(list includes refereed review articles in leading journals, as noted) (2012) (0)
Molecular windows into speech and language disorders [Invited talk] (2015) (0)
Title: Gene Expression Correlates of the Cortical Network Underlying Sentence Processing Abbreviated title: Genes & Sentence Processing Network Authors: Xiang-Zhen Kong (2020) (0)
The Forkhead Transcription Factor FOXP2 Is Required for Regulation of p21 in 143B Osteosarcoma Cell Growth Arrest (2020) (0)
Beyond motor control - Does FoxP1 affect auditory perception? (2016) (0)
The genetics of language [session chair] (2016) (0)
Language genetics and language pathologies [Public lecture] (2014) (0)
Topographic Divergence of Atypical Cortical Asymmetry and Regional Atrophy Patterns in Temporal Lobe Epilepsy: A Worldwide ENIGMA Study (2021) (0)
Inherited variants in CHD3 demonstrate variable expressivity in Snijders Blok-Campeau syndrome (2021) (0)
Understanding the genetic architecture of language- and literacy-related abilities during mid-childhood and adolescence: Evidence for genetically shared factors with early vocabulary (2018) (0)
Measurement and genetics of subcortical asymmetries (2013) (0)
A common variant of the CNTNAP2 gene is associated with structural variation in the dorsal visual stream and language-related regions of the right hemisphere (2015) (0)
The effect of dyslexia candidate genes on reading and language abilities in an adult population cohort (2019) (0)
Asymmetry within and around the planum temporale is sexually dimorphic and influenced by genes involved in steroid biology (2014) (0)
Speech and language: Lessons from the genome [Invited talk] (2014) (0)
Deciphering the 3'UTRome: identification and functional characterization of non-coding variants causing neurodevelopmental disorders (2016) (0)
PRELIM II(EDI BOARD) (2014) (0)
Neurobiology of language: A look forward [invited talk] (2016) (0)
Genes and language: Key issues and ways forward (2018) (0)
The Multivariate Genetic Architecture of Literacy-, Language- and Working Memory-related Abilities as Captured by Genome-wide Variation (2020) (0)
Identification of genetic interactions involved in dyslexia pathogenesis (2017) (0)
Decoding the genetics of speech and language [Invited talk] (2014) (0)
Title: Finding Functional Disease-associated Non-coding Variation Using Next-generation Sequencing (2016) (0)
Effects of Cortical FoxP1 Knockdowns on Learned Song Preference in Female Zebra Finches (2023) (0)
A genetic perspective on speech and language development [Invited talk] (2014) (0)
How does your genome help you speak? [Public lecture] (2016) (0)
The multivariate genetic architecture of language- and literacy-related abilities: Genetic evidence for different cognitive skill sets (2020) (0)
Missense mutations disrupting the ATPase domain of CHD3 cause a novel neurodevelopmental syndrome with intellectual disability, macrocephaly and impaired speech and language (2017) (0)
Heritability analysis of brain laterality indices using the UK biobank dataset (2017) (0)
35OPPOSITE GENETIC EFFECTS FOR POLYGENIC ASD RISK SHARED WITH AND INDEPENDENT OF ADHD: EVIDENCE FOR A CANCELLING-OUT HYPOTHESIS STUDYING GENETIC OVERLAP WITH LANGUAGE AND LITERACY (2019) (0)
Neurogenomics of speech and language disorders [invited talk] (2016) (0)
Functional characterization of a large series of NKX2-1 variants in Brain-Lung-Thyroid syndrome reveals diverse molecular mechanisms of disorder. (2015) (0)
Shared Genetic Variants in Speech and Language Traits (2017) (0)
Decoding the genetics of synaesthesia through studies large and small (2016) (0)
A mouse model for human-specific changes in FOXP2, a gene important for speech and language. (2007) (0)
Motor deficits in developmental verbal dyspraxia: The role of motor-related brain areas (2012) (0)
W58. GENOME-WIDE ASSOCIATION META-ANALYSIS OF EXPRESSIVE AND RECEPTIVE VOCABULARY FROM INFANCY TO EARLY CHILDHOOD: LINKS TO COGNITIVE OUTCOMES AND BEHAVIORAL TRAITS IN LATER LIFE (2021) (0)
Impaired Synaptic Plasticity and Motor t Mutation Implicated in Human Speech Deficits (0)
A genetic perspective on speech and language disorders [Invited Lecture] (2016) (0)
Exploring genetic relationships between early motor, personal-social and language development (2020) (0)
Aberrant striatal activity in mice with a mutation implicated in a developmental speech and language disorder (2010) (0)
Childhood apraxia of speech is caused by genes that control gene expression during fetal brain development (2017) (0)
Identification and functional characterization of de novo FOXP1 variants in cases of autism, intellectual disability and language impairment. (2015) (0)
Neanderthal introgression sheds light on modern human brain globularity (2018) (0)
A Genome-Wide Search for Leprosy Susceptibility Genes (1998) (0)
PRELIM II(EDI BOARD) (2014) (0)
What can genetics tell us about musicality? [Invited talk] (2014) (0)
Functional characterization of coding FOXP1 variants found in individuals with intellectual disability, autism and language impairment (2015) (0)
Polygenic risk for ADHD is associated with reading- and spelling-related traits (2017) (0)
De novo mutations in MED13, a component of the Mediator complex, are associated with a novel neurodevelopmental disorder (2018) (0)
University of Groningen Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes Alzheimer’s Disease Neuroimaging Initiative (2018) (0)
Genome sequencing for rightward hemispheric language 1 dominance 2 (2019) (0)
PRELIM II(EDI BOARD) (2015) (0)
PRELIM II(EDI BOARD) (2014) (0)
Testing the antagonistic pleiotropy hypothesis of ApoE with cognitive and brain data from a healthy cohort (2019) (0)
M20 TRAIT-SPECIFIC PATTERNS OF COMMON GENETIC FACTORS INFLUENCE SOCIAL-COMMUNICATION DIFFICULTIES AND ADHD SYMPTOMS DURING CHILD AND ADOLESCENT DEVELOPMENT (2017) (0)
HEREDITARY NEPHROLITHIASIS IS ASSOCIATED WITH MUTATIONS IN AN X-LINKED CHLORIDE CHANNEL GENE (1995) (0)
PRELIM II(EDI BOARD) (2015) (0)
PRELIM II(EDI BOARD) (2015) (0)
Atypical lateralization for sentence production, reading, and listening: detection with multivariate clustering and search for associated rare genetic variants using whole genome sequencing (2018) (0)
VKučinskas-2001-2016 (2016) (0)
Selective deletion of FOXP2 in circuits required for motor-skill learning (2012) (0)
No association of genetic variants of FOXP2 and BOLD response during sentence processing (2015) (0)
A novel method for finding functional variants in whole exome sequencing reveals potential risk factors for specific language impairments (2013) (0)
Exploring structural brain asymmetries in various disorders through the ENIGMA consortium (2018) (0)
Neurogenomics of vocal learning (2014) (0)
Dissociable Cellular and Genetic Mechanisms of Cortical Thinning at Different Life Stages (2022) (0)
Next generation sequencing coupled to functional genomics implicates FOXP pathways in autism and language impairment (2012) (0)
33EXPLORING THE DEVELOPMENTAL GENETIC ARCHITECTURE OF SOCIAL BEHAVIOUR: EVIDENCE FOR GENETIC OVERLAP WITH ASD AND ADHD (2019) (0)
Foxp2 loss of function increases striatal direct pathway inhibition via increased GABA release (2018) (0)
Connecting genes with cognition (2006) (0)
F83PLANUM TEMPORALE ASYMMETRY IS HERITABLE IN THE UK BIOBANK (N=12,236) (2019) (0)
Efficacy in the Dorsal Striatum Activity-Dependent Long-Term Changes in Synaptic Regional and Postnatal Heterogeneity of (2015) (0)
Whole genome sequencing in a multigenerational family with a specific deficit in semantic cognition (2016) (0)
PRELIM II(EDI BOARD) (2015) (0)
De novo BCL11A variants in neurodevelopmental disorder disrupt multiple aspects of protein function. (2015) (0)
PRELIM II(EDI BOARD) (2014) (0)
PRELIM II(EDI BOARD) (2015) (0)
Low frequency genetic variation in TP53 is associated with final head circumference (2017) (0)
Common Polygenic Risk For ASD And ADHD is Associated with Childhood Linguistic Traits within The General Population, But with Opposite Effects (2017) (0)
The genetic architecture of early vocabulary (15-38 months) (2017) (0)
Molecular and cellular windows into speech and language (2013) (0)
PRELIM II(EDI BOARD) (2014) (0)
Functional characterisation of FOXP1 mutations found in patients with intellectual disability (2012) (0)
Effect of APOE polymorphism on cognition and brain in the CamCAN cohort (2020) (0)
Neurogenomic strategies for studying speech and language [Invited talk] (2014) (0)
PRELIM II(EDI BOARD) (2015) (0)
What can genetics tell us about musicality? [Guest lecture] (2015) (0)
Chapter 2 - A Molecular Genetic Perspective on Speech and Language A2 - Hickok, Gregory (2016) (0)
Modelling changes in genetic variances during development - The re-birth of twin modelling strategies in the GWAS era (2017) (0)
Genetic insights into the neurobiology of speech and language (2019) (0)
Alterations of brain laterality in psychiatric, behavioural and developmental disorders (2018) (0)
Language, evolution, and the genomics revolution (2013) (0)
How your genome helps you speak [Public lecture] (2014) (0)
Integrating Molecular Anthropology and Neuroimaging Genomics To Shed New Light On Human Brain Evolution (2019) (0)
Investigating the effects of copy number variants on reading and language performance (2016) (0)
Subtle left-right asymmetry of gene expression profiles in embryonic and foetal human brains (2018) (0)
Author Correction: Discovery of 42 genome-wide significant loci associated with dyslexia (2023) (0)
Insights into the Genetic Foundations of Human Communication (2015) (0)
T10. STRUCTURAL MODELS OF GENOME-WIDE COVARIANCE IDENTIFY MULTIPLE GENETIC INFLUENCES ACROSS ASD SYMPTOMS (2022) (0)
THE GENETIC ARCHITECTURE OF BEAT SYNCHRONIZATION THROUGH A NEURODEVELOPMENTAL AND NEURO-FUNCTIONAL LENS (2022) (0)
Genome-wide analyses of vocabulary size in infancy and toddlerhood: associations with Attention-Deficit/Hyperactivity Disorder and cognition-related traits (2023) (0)
Evolution of language: Lessons from the genome (2016) (0)
Functional characterization of rare FOXP2 variants in neurodevelopmental disorder (2016) (0)
TU78. POLYGENIC RISK FOR PSYCHIATRIC DISORDER REVEALS DISTINCT ASSOCIATION PROFILES ACROSS SOCIAL BEHAVIOUR IN THE GENERAL POPULATION (2021) (0)
Multivariate genome-wide covariance analyses of literacy, language and working memory skills reveal distinct etiologies (2021) (0)
INVESTIGATING THE EVOLUTION OF COMMON DNA VARIANTS ASSOCIATED WITH READING AND RHYTHM TRAITS (2022) (0)
CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language (2018) (0)
Functional characterization of TBR1 variants in neurodevelopmental disorder (2018) (0)
26. GENOME-WIDE ANALYSES OF VOCABULARY SIZE IN INFANCY AND TODDLERHOOD: LINKS WITH ADHD AND COGNITIVE TRAITS (2022) (0)
Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language (2019) (0)
T27. THE GENETICS OF SPEECH PROSODY PERCEPTION: GENETIC ASSOCIATIONS WITH COMMUNICATION-RELATED TRAITS AND SPEECH-LANGUAGE DISORDERS (2022) (0)
Early speech development in Koolen de Vries syndrome limited by oral praxis and hypotonia (2017) (0)
74. STRUCTURAL EQUATION MODELLING IN THE GENOMICS ERA: STATE-OF-THE-ART AND FUTURE DEVELOPMENTS (2021) (0)
Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language (2019) (0)
Correction: Genetic aetiologies for childhood speech disorder: novel pathways co-expressed during brain development (2023) (0)
Meta-analysis of sex and handedness effects on human subcortical asymmetries: ENIGMA-Lateralization (2015) (0)

This paper list is powered by the following services:

Other Resources About Simon Fisher

en.wikipedia.org

What Schools Are Affiliated With Simon Fisher?

Simon Fisher is affiliated with the following schools:

Image Attributions

Image Source for Simon Fisher