(list includes refereed review articles in leading journals, as noted)

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

[2]  C. Francks,et al.  Pooled genome-wide linkage data on 424 ADHD ASPs suggests genetic heterogeneity and a common risk locus at 5p13 , 2006, Molecular Psychiatry.

[3]  S. Fisher.  On genes, speech, and language. , 2005, The New England journal of medicine.

[4]  C. Francks,et al.  A sibling-pair based approach for mapping genetic loci that influence quantitative measures of reading disability. , 2000, Prostaglandins, leukotrienes, and essential fatty acids.

[5]  C. Francks,et al.  Fine mapping of the chromosome 2p12-16 dyslexia susceptibility locus: quantitative association analysis and positional candidate genes SEMA4F and OTX1 , 2002, Psychiatric genetics.

[6]  A. Monaco,et al.  The SPCH1 region on human 7q31: genomic characterization of the critical interval and localization of translocations associated with speech and language disorder. , 2000, American journal of human genetics.

[7]  C. Francks,et al.  Parent-of-origin effects on handedness and schizophrenia susceptibility on chromosome 2p12-q11. , 2003, Human molecular genetics.

[8]  S. Fisher,et al.  Cloning and characterization of CLCN5, the human kidney chloride channel gene implicated in Dent disease (an X-linked hereditary nephrolithiasis). , 1995, Genomics.

[9]  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.

[10]  C. Francks,et al.  Bivariate linkage scan for reading disability and attention-deficit/hyperactivity disorder localizes pleiotropic loci. , 2005, Journal of child psychology and psychiatry, and allied disciplines.

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

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

[13]  Edouard Hirsch,et al.  Molecular networks implicated in speech-related disorders: FOXP2 regulates the SRPX2/uPAR complex. , 2010, Human molecular genetics.

[14]  A. Monaco,et al.  Recent advances in the genetics of language impairment , 2010, Genome Medicine.

[15]  Simon E Fisher,et al.  Unravelling neurogenetic networks implicated in developmental language disorders. , 2009, Biochemical Society transactions.

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

[17]  S. Fisher,et al.  Functional Genomic Dissection of Speech and Language Disorders , 2011 .

[18]  Simon E Fisher,et al.  The DISC1 promoter: characterization and regulation by FOXP2. , 2012, Human molecular genetics.

[19]  C. Francks,et al.  A genomewide scan for attention-deficit/hyperactivity disorder in an extended sample: suggestive linkage on 17p11. , 2003, American journal of human genetics.

[20]  Simon E Fisher,et al.  Use of multivariate linkage analysis for dissection of a complex cognitive trait. , 2003, American journal of human genetics.

[21]  Molecular Windows into Speech and Language Disorders , 2007, Folia Phoniatrica et Logopaedica.

[22]  S. Fisher.  How can animal studies help to uncover the roles of genes implicated in human speech and language disorders , 2006 .

[23]  C. Francks,et al.  Attention Deficit Hyperactivity Disorder: Fine Mapping Supports Linkage to 5p13, 6q12, 16p13, and 17p11 , 2022 .

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

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

[26]  E. Hatchwell,et al.  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, Human molecular genetics.

[27]  S. Fisher,et al.  Progress towards the identification of genes influencing developmental dyslexia , 2001 .

[28]  G. Marcus,et al.  FOXP2 in focus: what can genes tell us about speech and language? , 2003, Trends in Cognitive Sciences.

[29]  A. Monaco,et al.  A genome-wide search strategy for identifying quantitative trait loci involved in reading and spelling disability (developmental dyslexia) , 2009, European Child & Adolescent Psychiatry.

[30]  C. Francks,et al.  Genes, cognition and dyslexia: learning to read the genome , 2006, Trends in Cognitive Sciences.

[31]  Simon E Fisher,et al.  Genetic susceptibility to stuttering. , 2010, The New England journal of medicine.

[32]  J. Lamb,et al.  A quantitative-trait locus on chromosome 6p influences different aspects of developmental dyslexia. , 1999, American journal of human genetics.

[33]  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.

[34]  C. Francks,et al.  A genomewide linkage screen for relative hand skill in sibling pairs. , 2002, American journal of human genetics.

[35]  S. Fisher.  Isolation of the genetic factors underlying speech and language disorders , 2002 .

[36]  Simon E. Fisher,et al.  Modified sound-evoked brainstem potentials in Foxp2 mutant mice , 2009, Brain Research.

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

[38]  S. Fisher,et al.  Developmental dyslexia: genetic dissection of a complex cognitive trait , 2002, Nature Reviews Neuroscience.

[39]  C. Francks,et al.  Genome-wide scan of reading ability in affected sibling pairs with attention-deficit/hyperactivity disorder: unique and shared genetic effects , 2004, Molecular Psychiatry.

[40]  G Baird,et al.  FOXP2 is not a major susceptibility gene for autism or specific language impairment. , 2002, American journal of human genetics.

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

[42]  R. Pitchappan,et al.  A major susceptibility locus for leprosy in India maps to chromosome 10p13 , 2001, Nature Genetics.

[43]  A. Monaco,et al.  Multivariate Linkage Analysis of Specific Language Impairment (SLI) , 2007, Annals of human genetics.

[44]  Simon E Fisher,et al.  Confirmatory evidence for linkage of relative hand skill to 2p12-q11. , 2003, American journal of human genetics.

[45]  C. Francks,et al.  Investigation of Quantitative Measures Related to Reading Disability in a Large Sample of Sib-Pairs from the UK , 2001, Behavior genetics.

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

[47]  C. Francks,et al.  Genetic linkage of attention-deficit/hyperactivity disorder on chromosome 16p13, in a region implicated in autism. , 2002, American journal of human genetics.

[48]  C. A. French,et al.  An aetiological Foxp2 mutation causes aberrant striatal activity and alters plasticity during skill learning , 2011, Molecular Psychiatry.

[49]  C. Francks,et al.  A genomewide scan for loci involved in attention-deficit/hyperactivity disorder. , 2002, American journal of human genetics.

[50]  Lon R. Cardon,et al.  Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia , 2002, Nature Genetics.

[51]  G. Marcus,et al.  The eloquent ape: genes, brains and the evolution of language , 2006, Nature Reviews Genetics.

[52]  Simon E. Fisher,et al.  Tangled webs: Tracing the connections between genes and cognition , 2006, Cognition.

[53]  S. Fisher.  Dissection of molecular mechanisms underlying speech and language disorders , 2005, Applied Psycholinguistics.

[54]  Dorothy V.M. Bishop,et al.  CMIP and ATP2C2 Modulate Phonological Short-Term Memory in Language Impairment , 2009, American journal of human genetics.

[55]  E. van den Berg,et al.  Molecular cloning of the papillary renal cell carcinoma-associated translocation (X;1)(p11;q21) breakpoint. , 1996, Cytogenetics and cell genetics.

[56]  S. Fisher.  The Genetic Basis of a Severe Speech and Language Disorder , 2003 .

[57]  S. Fisher,et al.  Characterisation of renal chloride channel, CLCN5, mutations in hypercalciuric nephrolithiasis (kidney stones) disorders. , 1997, Human molecular genetics.

[58]  M. Devoto,et al.  A common molecular basis for three inherited kidney stone diseases , 1996, Nature.

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

[60]  F. Ramus,et al.  Genetics of language , 2009 .

[61]  Simon E. Fisher,et al.  Foxp2 Mutations Impair Auditory-Motor Association Learning , 2012, PloS one.

[62]  A. Ciccodicola,et al.  Sequence-based exon prediction around the synaptophysin locus reveals a gene-rich area containing novel genes in human proximal Xp. , 1997, Genomics.

[63]  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.

[64]  Constance Scharff,et al.  FOXP2 as a molecular window into speech and language. , 2009, Trends in genetics : TIG.

[65]  M. Rieder,et al.  Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations , 2011, Nature Genetics.

[66]  A. Monaco,et al.  Deciphering the genetic basis of speech and language disorders. , 2003, Annual review of neuroscience.

[67]  D. Geschwind,et al.  Singing Mice, Songbirds, and More: Models for FOXP2 Function and Dysfunction in Human Speech and Language , 2006, The Journal of Neuroscience.

[68]  C. Francks,et al.  Putative functional alleles of DYX1C1 are not associated with dyslexia susceptibility in a large sample of sibling pairs from the UK , 2004, Journal of Medical Genetics.

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

[70]  A. Monaco,et al.  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, Genomics.

[71]  Wendy Cohen,et al.  Highly significant linkage to the SLI1 locus in an expanded sample of individuals affected by specific language impairment. , 2004, American journal of human genetics.

[72]  A. Monaco,et al.  FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder. , 2003, Brain : a journal of neurology.

[73]  G. Marcus,et al.  Genes and language , 2011 .

[74]  D. Geschwind,et al.  LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia , 2007, Molecular Psychiatry.

[75]  Simon E Fisher,et al.  Familial and genetic effects on motor coordination, laterality, and reading-related cognition. , 2003, The American journal of psychiatry.

[76]  A. Monaco,et al.  Assessing the impact of FOXP1 mutations on developmental verbal dyspraxia , 2009, European Journal of Human Genetics.

[77]  A. Monaco,et al.  High-resolution comparative mapping of the proximal region of the mouse X chromosome. , 1995, Genomics.

[78]  D. Geschwind,et al.  Identification of the transcriptional targets of FOXP2, a gene linked to speech and language, in developing human brain. , 2007, American journal of human genetics.