Campbell P, Reep RL, Stoll ML, Ophir AG, Phelps SM (2009) Conservation and diversity of Foxp2 expression in muroid rodents: functional implications. J Comp Neurol 512:84–100

Article  PubMed  PubMed Central  Google Scholar 

Carrion-Castillo A, Franke B, Fisher SE (2013) Molecular genetics of dyslexia: an overview. Dyslexia (Chichester, England) 19:214–240

Article  PubMed  Google Scholar 

Co M, Anderson AG, Konopka G (2020) FOXP transcription factors in vertebrate brain development, function, and disorders. Wiley Interdiscip Rev Dev Biol 9:e375

Article  CAS  PubMed  PubMed Central  Google Scholar 

d’Hennezel E, Bin Dhuban K, Torgerson T, Piccirillo CA (2012) The immunogenetics of immune dysregulation, polyendocrinopathy, enteropathy, X linked (IPEX) syndrome. J Med Genet 49:291–302

Article  CAS  PubMed  Google Scholar 

Enard W, Przeworski M, Fisher SE, Lai CS, Wiebe V, Kitano T, Monaco AP, Pääbo S (2002) Molecular evolution of FOXP2, a gene involved in speech and language. Nature 418:869–872

Article  ADS  CAS  PubMed  Google Scholar 

Ferland RJ, Cherry TJ, Preware PO, Morrisey EE, Walsh CA (2003) Characterization of Foxp2 and Foxp1 mRNA and protein in the developing and mature brain. J Comp Neurol 460:266–279

Article  CAS  PubMed  Google Scholar 

Le Fevre AK, Taylor S, Malek NH, Horn D, Carr CW, Abdul-Rahman OA, O'Donnell S, Burgess T, Shaw M, Gecz J, Bain N, Fagan K, Hunter MF (2013) FOXP1 mutations cause intellectual disability and a recognizable phenotype. Am J Med Genet A 161a:3166–3175

Fisher SE, Scharff C (2009) FOXP2 as a molecular window into speech and language. Trends in Genetics: TIG 25:166–177

Article  CAS  PubMed  Google Scholar 

Haesler S, Wada K, Nshdejan A, Morrisey EE, Lints T, Jarvis ED, Scharff C (2004) FoxP2 expression in avian vocal learners and non-learners. J Neurosci: Off J Soc Neurosci 24:3164–3175

Article  CAS  Google Scholar 

Lai CS, Fisher SE, Hurst JA, Vargha-Khadem F, Monaco AP (2001) A forkhead-domain gene is mutated in a severe speech and language disorder. Nature 413:519–523

Article  ADS  CAS  PubMed  Google Scholar 

Lai CS, Gerrelli D, Monaco AP, Fisher SE, Copp AJ (2003) FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder. Brain: a J. Neuro 126:2455-2462

MacDermot KD, Bonora E, Sykes N, Coupe AM, Lai CS, Vernes SC, Vargha-Khadem F, McKenzie F, Smith RL, Monaco AP, Fisher SE (2005) Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits. Am J Hum Genet 76:1074–1080

Article  CAS  PubMed  PubMed Central  Google Scholar 

Morgan A, Fisher SE, Scheffer I, Hildebrand M. (1993). FOXP2-related speech and language disorder. In: GeneReviews(®), M.P. Adam, J. Feldman, G.M. Mirzaa, R.A. Pagon, S.E. Wallace, L.J.H. Bean, K.W. Gripp, andA. Amemiya, eds. (Seattle (WA), University of Washington, Seattle. Copyright © 1993–2023, University of Washington, Seattle. GeneReviews is a registered trademark of the University of Washington, Seattle

Newbury DF, Monaco AP (2010) Genetic advances in the study of speech and language disorders. Neuron 68:309–320

Article  CAS  PubMed  PubMed Central  Google Scholar 

Newbury DF, Mari F, Sadighi Akha E, Macdermot KD, Canitano R, Monaco AP, Taylor JC, Renieri A, Fisher SE, Knight SJ (2013) Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder. Eur J Hum Genet: EJHG 21:361–365

Article  PubMed  Google Scholar 

Reader RH, Covill LE, Nudel R, Newbury DF (2014) Genome-wide studies of specific language impairment. Curr Behav Neurosci Rep 1:242–250

Article  PubMed  PubMed Central  Google Scholar 

Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL (2015) Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology. Genet Med: Off J Am College Med Genet 17:405–424

Article  Google Scholar 

Shao J, Diamond MI (2007) Polyglutamine diseases: emerging concepts in pathogenesis and therapy. Hum Mol Genet 16(2):R115-123

Article  CAS  PubMed  Google Scholar 

Shu W, Yang H, Zhang L, Lu MM, Morrisey EE (2001) Characterization of a new subfamily of winged-helix/forkhead (Fox) genes that are expressed in the lung and act as transcriptional repressors. J Biol Chem 276:27488–27497

Article  CAS  PubMed  Google Scholar 

Takahashi K, Liu FC, Hirokawa K, Takahashi H (2003) Expression of Foxp2, a gene involved in speech and language, in the developing and adult striatum. J Neurosci Res 73:61–72

Article  CAS  PubMed  Google Scholar 

Teramitsu I, Kudo LC, London SE, Geschwind DH, White SA (2004) Parallel FoxP1 and FoxP2 expression in songbird and human brain predicts functional interaction. J Neurosci: Off J Soc Neurosci 24:3152–3163

Article  CAS  Google Scholar 

Thevenon J, Callier P, Andrieux J, Delobel B, David A, Sukno S, Minot D, Mosca Anne L, Marle N, Sanlaville D, Bonnet M, Masurel-Paulet A, Levy F, Gaunt L, Farrell S, Le Caignec C, Toutain A, Carmignac V, Mugneret F, Clayton-Smith J, Thauvin-Robinet C, Faivre L (2013) 12p13.33 microdeletion including ELKS/ERC1, a new locus associated with childhood apraxia of speech. Eur J Hum Genet: EJHG 21:82–88

Article  CAS  PubMed  Google Scholar 

Tønne E, Due-Tønnessen BJ, Vigeland MD, Amundsen SS, Ribarska T, Åsten PM, Sheng Y, Helseth E, Gilfillan GD, Mero IL, Heimdal KR (2022) Whole-exome sequencing in syndromic craniosynostosis increases diagnostic yield and identifies candidate genes in osteogenic signaling pathways. Am J Med Genet A 188:1464–1475

Article  PubMed  Google Scholar 

Turner SJ, Hildebrand MS, Block S, Damiano J, Fahey M, Reilly S, Bahlo M, Scheffer IE, Morgan AT (2013) Small intragenic deletion in FOXP2 associated with childhood apraxia of speech and dysarthria. Am J Med Genet A 161a: 2321–2326

Wang K, Li M, Hakonarson H (2010) ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data. Nucleic Acids Res 38:e164

Article  PubMed  PubMed Central  Google Scholar