Imaging-genetics in dyslexia: connecting risk genetic variants to brain neuroimaging and ultimately to reading impairments.

[1]  John D. Eicher,et al.  Alleles of a polymorphic ETV6 binding site in DCDC2 confer risk of reading and language impairment. , 2013, American journal of human genetics.

[2]  Shyamala K Venkatesh,et al.  Analysis of genetic variants of dyslexia candidate genes KIAA0319 and DCDC2 in Indian population , 2013, Journal of Human Genetics.

[3]  John D. Eicher,et al.  Associations of Prenatal Nicotine Exposure and the Dopamine Related Genes ANKK1 and DRD2 to Verbal Language , 2013, PloS one.

[4]  Roslyn H. Fitch,et al.  The effects of Kiaa0319 knockdown on cortical and subcortical anatomy in male rats , 2013, International Journal of Developmental Neuroscience.

[5]  Carsten O. Daub,et al.  Molecular Networks of DYX1C1 Gene Show Connection to Neuronal Migration Genes and Cytoskeletal Proteins , 2013, Biological Psychiatry.

[6]  C. Barr,et al.  A family‐based association analysis and meta‐analysis of the reading disabilities candidate gene DYX1C1 , 2013, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

[7]  N. Kraus,et al.  Unstable Representation of Sound: A Biological Marker of Dyslexia , 2013, The Journal of Neuroscience.

[8]  Simon E Fisher,et al.  Decoding the genetics of speech and language , 2013, Current Opinion in Neurobiology.

[9]  X. Miao,et al.  Meta-analysis of the Association Between DCDC2 Polymorphisms and Risk of Dyslexia , 2013, Molecular Neurobiology.

[10]  D. Kaplan,et al.  FoxP2 Regulates Neurogenesis during Embryonic Cortical Development , 2013, The Journal of Neuroscience.

[11]  T. Stearns,et al.  Transcriptional Program of Ciliated Epithelial Cells Reveals New Cilium and Centrosome Components and Links to Human Disease , 2012, PloS one.

[12]  Wei Chen,et al.  Genetic variant in KIAA0319, but not in DYX1C1, is associated with risk of dyslexia: An integrated meta‐analysis , 2012, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

[13]  Dianne F. Newbury,et al.  The Dyslexia Candidate Locus on 2p12 Is Associated with General Cognitive Ability and White Matter Structure , 2012, PloS one.

[14]  R. Todd Constable,et al.  Variants in the DYX2 locus are associated with altered brain activation in reading-related brain regions in subjects with reading disability , 2012, NeuroImage.

[15]  Torkel Klingberg,et al.  Three Dyslexia Susceptibility Genes, DYX1C1, DCDC2, and KIAA0319, Affect Temporo-Parietal White Matter Structure , 2012, Biological Psychiatry.

[16]  M. Kronbichler,et al.  Distinct patterns of brain function in children with isolated spelling impairment: New insights , 2012, Neuropsychologia.

[17]  Glenn D. Rosen,et al.  Neocortical disruption and behavioral impairments in rats following in utero RNAi of candidate dyslexia risk gene Kiaa0319 , 2012, International Journal of Developmental Neuroscience.

[18]  B. Pennington,et al.  Developmental dyslexia , 2012, The Lancet.

[19]  T. Lachmann,et al.  Neural correlates of temporal auditory processing in developmental dyslexia during German vowel length discrimination: An fMRI study , 2012, Brain and Language.

[20]  M. Nöthen,et al.  The Aromatase Gene CYP19A1: Several Genetic and Functional Lines of Evidence Supporting a Role in Reading, Speech and Language , 2012, Behavior genetics.

[21]  J. Wouters,et al.  A tractography study in dyslexia: neuroanatomic correlates of orthographic, phonological and speech processing. , 2012, Brain : a journal of neurology.

[22]  Suzanne E. Welcome,et al.  Individual differences in skilled adult readers reveal dissociable patterns of neural activity associated with component processes of reading , 2012, Brain and Language.

[23]  J. Kere,et al.  The rs3743205 SNP is important for the regulation of the dyslexia candidate gene DYX1C1 by estrogen receptor β and DNA methylation. , 2012, Molecular endocrinology.

[24]  Steve Horvath,et al.  Molecular Microcircuitry Underlies Functional Specification in a Basal Ganglia Circuit Dedicated to Vocal Learning , 2012, Neuron.

[25]  Haiying Meng,et al.  DCDC2 genetic variants and susceptibility to developmental dyslexia , 2012, Psychiatric genetics.

[26]  Nadine Gaab,et al.  Functional characteristics of developmental dyslexia in left-hemispheric posterior brain regions predate reading onset , 2012, Proceedings of the National Academy of Sciences.

[27]  Jean-Baptiste Poline,et al.  Genetic Variants of FOXP2 and KIAA0319/TTRAP/THEM2 Locus Are Associated with Altered Brain Activation in Distinct Language-Related Regions , 2012, The Journal of Neuroscience.

[28]  Heather C Whalley,et al.  Genetic variation in CNTNAP2 alters brain function during linguistic processing in healthy individuals , 2011, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

[29]  J. Loturco,et al.  Mutation of the dyslexia‐associated gene Dcdc2 impairs LTM and visuo‐spatial performance in mice , 2011, Genes, brain, and behavior.

[30]  D. Geschwind,et al.  Absence of CNTNAP2 Leads to Epilepsy, Neuronal Migration Abnormalities, and Core Autism-Related Deficits , 2011, Cell.

[31]  S. Cichon,et al.  Imaging genetics of FOXP2 in dyslexia , 2011, European Journal of Human Genetics.

[32]  Dorothy V.M. Bishop,et al.  DCDC2, KIAA0319 and CMIP Are Associated with Reading-Related Traits , 2011, Biological Psychiatry.

[33]  Kay E. Davies,et al.  Foxp2 Regulates Gene Networks Implicated in Neurite Outgrowth in the Developing Brain , 2011, PLoS genetics.

[34]  G. D. Pearlson,et al.  Genetic influences of cortical gray matter in language-related regions in healthy controls and schizophrenia , 2011, Schizophrenia Research.

[35]  Juha Kere,et al.  Increased Expression of the Dyslexia Candidate Gene DCDC2 Affects Length and Signaling of Primary Cilia in Neurons , 2011, PloS one.

[36]  W. Enard.  FOXP2 and the role of cortico-basal ganglia circuits in speech and language evolution , 2011, Current Opinion in Neurobiology.

[37]  D. Bishop,et al.  CNTNAP2 variants affect early language development in the general population , 2011, Genes, brain, and behavior.

[38]  C. Pennell,et al.  Analysis of dyslexia candidate genes in the Raine cohort representing the general Australian population , 2011, Genes, brain, and behavior.

[39]  S. Pääbo,et al.  Humanized Foxp2 specifically affects cortico-basal ganglia circuits , 2011, Neuroscience.

[40]  Timothy A. Currier,et al.  The effects of embryonic knockdown of the candidate dyslexia susceptibility gene homologue Dyx1c1 on the distribution of GABAergic neurons in the cerebral cortex , 2011, Neuroscience.

[41]  M. Lovett,et al.  Genetic Variation in the KIAA0319 5′ Region as a Possible Contributor to Dyslexia , 2011, Behavior genetics.

[42]  J. B. Talcott,et al.  Investigation of Dyslexia and SLI Risk Variants in Reading- and Language-Impaired Subjects , 2010, Behavior genetics.

[43]  Timothy C. Bates,et al.  Dyslexia and DYX1C1: deficits in reading and spelling associated with a missense mutation , 2010, Molecular Psychiatry.

[44]  Richard S. Frackowiak,et al.  Normal variation in fronto-occipital circuitry and cerebellar structure with an autism-associated polymorphism of CNTNAP2 , 2010, NeuroImage.

[45]  Ellen M. Wijsman,et al.  Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sample , 2010, Journal of Neurodevelopmental Disorders.

[46]  Russell A. Poldrack,et al.  Altered Functional Connectivity in Frontal Lobe Circuits Is Associated with Variation in the Autism Risk Gene CNTNAP2 , 2010, Science Translational Medicine.

[47]  A. Monaco,et al.  Genetic Advances in the Study of Speech and Language Disorders , 2010, Neuron.

[48]  C. Scharff,et al.  Knockdown of FoxP2 alters spine density in Area X of the zebra finch , 2010, Genes, brain, and behavior.

[49]  Kevin M. Beaver,et al.  Association between the A1 allele of the DRD2 gene and reduced verbal abilities in adolescence and early adulthood , 2010, Journal of Neural Transmission.

[50]  S. Fisher,et al.  The structure of innate vocalizations in Foxp2-deficient mouse pups , 2010, Genes, brain, and behavior.

[51]  A. Galaburda,et al.  The effect of variation in expression of the candidate dyslexia susceptibility gene homolog Kiaa0319 on neuronal migration and dendritic morphology in the rat. , 2010, Cerebral cortex.

[52]  R. Tannock,et al.  Association of reading disabilities with regions marked by acetylated H3 histones in KIAA0319 , 2010, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

[53]  Nicholas G Martin,et al.  Dyslexia and DCDC2: normal variation in reading and spelling is associated with DCDC2 polymorphisms in an Australian population sample , 2010, European Journal of Human Genetics.

[54]  Michael Lachmann,et al.  Linkage disequilibrium extends across putative selected sites in FOXP2. , 2009, Molecular biology and evolution.

[55]  Johannes Schwarz,et al.  A Humanized Version of Foxp2 Affects Cortico-Basal Ganglia Circuits in Mice , 2009, Cell.

[56]  Bertram Müller-Myhsok,et al.  Further evidence for DYX1C1 as a susceptibility factor for dyslexia , 2009, Psychiatric genetics.

[57]  Richard Wade-Martins,et al.  A Common Variant Associated with Dyslexia Reduces Expression of the KIAA0319 Gene , 2009, PLoS genetics.

[58]  P. Ahnert,et al.  The role of gene DCDC2 in German dyslexics , 2009, Annals of dyslexia.

[59]  J. Maisog,et al.  A Meta‐analysis of Functional Neuroimaging Studies of Dyslexia , 2008, Annals of the New York Academy of Sciences.

[60]  R. Tannock,et al.  The KIAA0319-Like (KIAA0319L) Gene on Chromosome 1p34 as a Candidate for Reading Disabilities , 2008, Journal of neurogenetics.

[61]  Jiannis Ragoussis,et al.  Association of the KIAA0319 dyslexia susceptibility gene with reading skills in the general population. , 2008, The American journal of psychiatry.

[62]  M. Nöthen,et al.  Investigation of the DCDC2 intron 2 deletion/compound short tandem repeat polymorphism in a large German dyslexia sample , 2008, Psychiatric genetics.

[63]  D. Geschwind,et al.  A functional genetic link between distinct developmental language disorders. , 2008, The New England journal of medicine.

[64]  B. Shaywitz,et al.  Paying attention to reading: The neurobiology of reading and dyslexia , 2008, Development and Psychopathology.

[65]  J. Gruen,et al.  The human lexinome: genes of language and reading. , 2008, Journal of communication disorders.

[66]  G. Coop,et al.  The Timing of Selection at the Human FOXP2 Gene , 2008, Molecular biology and evolution.

[67]  A. Galaburda,et al.  Postnatal analysis of the effect of embryonic knockdown and overexpression of candidate dyslexia susceptibility gene homolog Dcdc2 in the rat , 2008, Neuroscience.

[68]  Steve D. M. Brown,et al.  Impaired Synaptic Plasticity and Motor Learning in Mice with a Point Mutation Implicated in Human Speech Deficits , 2008, Current Biology.

[69]  J A Veltman,et al.  CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy , 2008, Molecular Psychiatry.

[70]  Vince D. Calhoun,et al.  Polymorphism of DCDC2 Reveals Differences in Cortical Morphology of Healthy Individuals—A Preliminary Voxel Based Morphometry Study , 2008, Brain Imaging and Behavior.

[71]  Mariko Y Momoi,et al.  Ultrasonic vocalization impairment of Foxp2 (R552H) knockin mice related to speech-language disorder and abnormality of Purkinje cells , 2008, Proceedings of the National Academy of Sciences.

[72]  Katarzyna Chawarska,et al.  Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders. , 2008, American journal of human genetics.

[73]  J. Sebat,et al.  Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene. , 2008, American journal of human genetics.

[74]  Tanya M. Teslovich,et al.  A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism. , 2008, American journal of human genetics.

[75]  D. Geschwind,et al.  High-throughput analysis of promoter occupancy reveals direct neural targets of FOXP2, a gene mutated in speech and language disorders. , 2007, American journal of human genetics.

[76]  D. Geschwind,et al.  Genome-wide analyses of human perisylvian cerebral cortical patterning , 2007, Proceedings of the National Academy of Sciences.

[77]  H. Burbano,et al.  The Derived FOXP2 Variant of Modern Humans Was Shared with Neandertals , 2007, Current Biology.

[78]  Yu Wang,et al.  Disruption of neuronal migration by RNAi of Dyx1c1 results in neocortical and hippocampal malformations. , 2007, Cerebral cortex.

[79]  M. Nobile,et al.  Association of short‐term memory with a variant within DYX1C1 in developmental dyslexia , 2007, Genes, brain, and behavior.

[80]  Margaret J. Wright,et al.  A Haplotype Spanning KIAA0319 and TTRAP Is Associated with Normal Variation in Reading and Spelling Ability , 2007, Biological Psychiatry.

[81]  C. A. French,et al.  Generation of mice with a conditional Foxp2 null allele , 2007, Genesis.

[82]  Ellen M Wijsman,et al.  Evaluation of candidate genes for DYX1 and DYX2 in families with dyslexia , 2007, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

[83]  J. Defries,et al.  Etiology of the Stability of Reading Difficulties: The Longitudinal Twin Study of Reading Disabilities , 2007, Twin Research and Human Genetics.

[84]  Z. Tümer,et al.  Disruption of the CNTNAP2 gene in a t(7;15) translocation family without symptoms of Gilles de la Tourette syndrome , 2007, European Journal of Human Genetics.

[85]  G. Rosen,et al.  Developmental disruptions and behavioral impairments in rats following in utero RNAi of Dyx1c1 , 2007, Brain Research Bulletin.

[86]  Heikki Lyytinen,et al.  A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia. , 2007, Human molecular genetics.

[87]  J. Gabrieli,et al.  Functional and morphometric brain dissociation between dyslexia and reading ability , 2007, Proceedings of the National Academy of Sciences.

[88]  Bruce D. McCandliss,et al.  Left lateralized white matter microstructure accounts for individual differences in reading ability and disability , 2006, Neuropsychologia.

[89]  G. D. Rosen,et al.  DYX1C1 functions in neuronal migration in developing neocortex , 2006, Neuroscience.

[90]  M C O'Donovan,et al.  Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia , 2006, Molecular Psychiatry.

[91]  K. Davies,et al.  Functional genetic analysis of mutations implicated in a human speech and language disorder. , 2006, Human molecular genetics.

[92]  B. Pennington.  From single to multiple deficit models of developmental disorders , 2006, Cognition.

[93]  Richard Wade-Martins,et al.  The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration. , 2006, Human molecular genetics.

[94]  E. Vinckenbosch,et al.  Gray matter alteration in dyslexia: converging evidence from volumetric and voxel-by-voxel MRI analyses , 2005, Neuropsychologia.

[95]  B. Wandell,et al.  Children's Reading Performance is Correlated with White Matter Structure Measured by Diffusion Tensor Imaging , 2005, Cortex.

[96]  P. Skudlarski,et al.  DCDC2 is associated with reading disability and modulates neuronal development in the brain. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[97]  F Fazio,et al.  Brain abnormalities underlying altered activation in dyslexia: a voxel based morphometry study. , 2005, Brain : a journal of neurology.

[98]  Juha Kere,et al.  The Axon Guidance Receptor Gene ROBO1 Is a Candidate Gene for Developmental Dyslexia , 2005, PLoS genetics.

[99]  B. Pennington,et al.  TDT-association analysis of EKN1 and dyslexia in a Colorado twin cohort , 2005, Human Genetics.

[100]  J. Buxbaum,et al.  Altered ultrasonic vocalization in mice with a disruption in the Foxp2 gene. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[101]  N. Sykes,et al.  Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits. , 2005, American journal of human genetics.

[102]  Luis Concha,et al.  Imaging brain connectivity in children with diverse reading ability , 2005, NeuroImage.

[103]  Peter Holmans,et al.  Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia. , 2005, American journal of human genetics.

[104]  Maria Luisa Lorusso,et al.  A family-based association study does not support DYX1C1 on 15q21.3 as a candidate gene in developmental dyslexia , 2005, European Journal of Human Genetics.

[105]  M W Lovett,et al.  Support for EKN1 as the susceptibility locus for dyslexia on 15q21 , 2004, Molecular Psychiatry.

[106]  C. Francks,et al.  A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States. , 2004, American journal of human genetics.

[107]  Elior Peles,et al.  Mechanisms and Roles of Axon-Schwann Cell Interactions , 2004, The Journal of Neuroscience.

[108]  D. Perani,et al.  Regional reductions of gray matter volume in familial dyslexia , 2004, Neurology.

[109]  B. Pennington,et al.  Refinement of the 6p21.3 quantitative trait locus influencing dyslexia: linkage and association analyses , 2004, Human Genetics.

[110]  J. Kere,et al.  Fine mapping of the 2p11 dyslexia locus and exclusion of TACR1 as a candidate gene , 2004, Human Genetics.

[111]  M. Mishkin,et al.  Language fMRI abnormalities associated with FOXP2 gene mutation , 2003, Nature Neuroscience.

[112]  Colin L. Stewart,et al.  Juxtaparanodal clustering of Shaker-like K+ channels in myelinated axons depends on Caspr2 and TAG-1 , 2003, The Journal of cell biology.

[113]  P. Heutink,et al.  CNTNAP2 is disrupted in a family with Gilles de la Tourette syndrome and obsessive compulsive disorder. , 2003, Genomics.

[114]  J. Kere,et al.  A genome scan for developmental dyslexia confirms linkage to chromosome 2p11 and suggests a new locus on 7q32 , 2003, Journal of medical genetics.

[115]  Faraneh Vargha-Khadem,et al.  Bilateral brain abnormalities associated with dominantly inherited verbal and orofacial dyspraxia , 2003, Human brain mapping.

[116]  A. Monaco,et al.  Molecular evolution of FOXP2, a gene involved in speech and language , 2002, Nature.

[117]  D E Kaplan,et al.  Evidence for linkage and association with reading disability on 6p21.3-22. , 2002, American journal of human genetics.

[118]  Karl J. Friston,et al.  MRI analysis of an inherited speech and language disorder: structural brain abnormalities. , 2002, Brain : a journal of neurology.

[119]  F. Vargha-Khadem,et al.  Behavioural analysis of an inherited speech and language disorder: comparison with acquired aphasia. , 2002, Brain : a journal of neurology.

[120]  O. Rascol,et al.  A genome wide scan for familial high myopia suggests a novel locus on chromosome 7q36 , 2002, Journal of medical genetics.

[121]  Joseph K. Torgesen,et al.  Critical Elements of Classroom and Small–Group Instruction Promote Reading Success in All Children , 2001 .

[122]  A. Monaco,et al.  A forkhead-domain gene is mutated in a severe speech and language disorder , 2001, Nature.

[123]  V. Menon,et al.  Preliminary evidence of widespread morphological variations of the brain in dyslexia , 2001, Neurology.

[124]  U. Frith,et al.  Dyslexia: Cultural Diversity and Biological Unity , 2001, Science.

[125]  J. Kere,et al.  Two translocations of chromosome 15q associated with dyslexia , 2000, Journal of medical genetics.

[126]  Jan C. Frijters,et al.  Remediating the Core Deficits of Developmental Reading Disability , 2000, Journal of learning disabilities.

[127]  S Eliez,et al.  Morphological alteration of temporal lobe gray matter in dyslexia: an MRI study. , 2000, Journal of child psychology and psychiatry, and allied disciplines.

[128]  R. Poldrack,et al.  Microstructure of Temporo-Parietal White Matter as a Basis for Reading Ability Evidence from Diffusion Tensor Magnetic Resonance Imaging , 2000, Neuron.

[129]  Peter Shrager,et al.  Caspr2, a New Member of the Neurexin Superfamily, Is Localized at the Juxtaparanodes of Myelinated Axons and Associates with K+ Channels , 1999, Neuron.

[130]  U. Frith,et al.  Explicit and implicit processing of words and pseudowords by adult developmental dyslexics: A search for Wernicke's Wortschatz? , 1999, Brain : a journal of neurology.

[131]  H. Lubs,et al.  A new gene (DYX3) for dyslexia is located on chromosome 2 , 1999, Journal of medical genetics.

[132]  Karl J. Friston,et al.  Neural basis of an inherited speech and language disorder. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[133]  B. Horwitz,et al.  Functional connectivity of the angular gyrus in normal reading and dyslexia. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[134]  A. Liberman,et al.  Functional disruption in the organization of the brain for reading in dyslexia. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[135]  Simon E. Fisher,et al.  Localisation of a gene implicated in a severe speech and language disorder , 1997, Nature Genetics.

[136]  J. Maisog,et al.  A positron emission tomographic study of impaired word recognition and phonological processing in dyslexic men. , 1997, Archives of neurology.

[137]  Richard S. J. Frackowiak,et al.  Is developmental dyslexia a disconnection syndrome? Evidence from PET scanning. , 1996, Brain : a journal of neurology.

[138]  D W Fulker,et al.  Quantitative trait locus for reading disability on chromosome 6. , 1994, Science.

[139]  J. Rumsey,et al.  Failure to activate the left temporoparietal cortex in dyslexia. An oxygen 15 positron emission tomographic study. , 1992, Archives of neurology.

[140]  D. Fulker,et al.  Evidence for a genetic aetiology in reading disability of twins , 1987, Nature.

[141]  J. Loehlin,et al.  Genotype-environment correlation and IQ , 1987, Behavior genetics.

[142]  R. Wagner,et al.  The nature of phonological processing and its causal role in the acquisition of reading skills. , 1987 .

[143]  D. Shankweiler,et al.  Phonology and the Problems of Learning to Read and Write , 1985 .

[144]  V. Calhoun,et al.  Genetic influences of resting state fMRI activity in language-related brain regions in healthy controls and schizophrenia patients: a pilot study , 2012, Brain Imaging and Behavior.

[145]  Sarah E Medland,et al.  Genetic Variance in a Component of the Language Acquisition Device: ROBO1 Polymorphisms Associated with Phonological Buffer Deficits , 2011, Behavior genetics.

[146]  Grier P Page,et al.  A Dyslexia-Associated Variant in DCDC2 Changes Gene Expression , 2011, Behavior genetics.

[147]  J. J. Chrobak,et al.  Persistent spatial working memory deficits in rats following in utero RNAi of Dyx 1 c 1 , 2010 .

[148]  B. Pennington,et al.  Relations among speech, language, and reading disorders. , 2009, Annual review of psychology.

[149]  Carmela Bravaccio,et al.  No evidence for association between dyslexia and DYX1C1 functional variants in a group of children and adolescents from Southern Italy , 2007, Journal of Molecular Neuroscience.

[150]  Shelley D. Smith.  Genes, language development, and language disorders. , 2007, Mental retardation and developmental disabilities research reviews.

[151]  Andreas Ziegler,et al.  Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia. , 2006, American journal of human genetics.

[152]  L. Cardon,et al.  Quantitative-trait locus for specific language and reading deficits on chromosome 6p. , 1999, American journal of human genetics.