FOXP2 (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "FOXP2" in English language version.

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84nih.gov

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biolinguistics.eu

Benítez-Burraco A, Longa VM, Lorenzo G, Uriagereka J (November 2008). "Also sprach Neanderthalis... Or Did She?". Biolinguistics. 2 (2–3): 225–232. doi:10.5964/bioling.8643. S2CID 60864520.

books.google.com

Cowie F (1999). What's Within?: Nativism Reconsidered. New York, US: Oxford University Press. pp. 290–291. ISBN 978-0-19-515978-3.
Jenkins L (2000). Biolinguistics: Exploring the Biology of Language (Revised ed.). Cambridge, UK: Cambridge University Press. pp. 98–99. ISBN 978-0-521-00391-9.

doi.org

Fisher SE, Vargha-Khadem F, Watkins KE, Monaco AP, Pembrey ME (February 1998). "Localisation of a gene implicated in a severe speech and language disorder". Nature Genetics. 18 (2): 168–70. doi:10.1038/ng0298-168. hdl:11858/00-001M-0000-0012-CBD9-5. PMID 9462748. S2CID 3190318.
Lai CS, Fisher SE, Hurst JA, Levy ER, Hodgson S, Fox M, et al. (August 2000). "The SPCH1 region on human 7q31: genomic characterization of the critical interval and localization of translocations associated with speech and language disorder". American Journal of Human Genetics. 67 (2): 357–68. doi:10.1086/303011. PMC 1287211. PMID 10880297.
Lai CS, Fisher SE, Hurst JA, Vargha-Khadem F, Monaco AP (October 2001). "A forkhead-domain gene is mutated in a severe speech and language disorder". Nature. 413 (6855): 519–23. Bibcode:2001Natur.413..519L. doi:10.1038/35097076. hdl:11858/00-001M-0000-0012-CB9C-F. PMID 11586359. S2CID 4421562.
MacDermot KD, Bonora E, Sykes N, Coupe AM, Lai CS, Vernes SC, et al. (June 2005). "Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits". American Journal of Human Genetics. 76 (6): 1074–80. doi:10.1086/430841. PMC 1196445. PMID 15877281.
Groszer M, Keays DA, Deacon RM, de Bono JP, Prasad-Mulcare S, Gaub S, et al. (March 2008). "Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficits". Current Biology. 18 (5): 354–62. Bibcode:2008CBio...18..354G. doi:10.1016/j.cub.2008.01.060. PMC 2917768. PMID 18328704.
Haesler S, Rochefort C, Georgi B, Licznerski P, Osten P, Scharff C (December 2007). "Incomplete and inaccurate vocal imitation after knockdown of FoxP2 in songbird basal ganglia nucleus Area X". PLOS Biology. 5 (12): e321. doi:10.1371/journal.pbio.0050321. PMC 2100148. PMID 18052609.
Fisher SE, Scharff C (April 2009). "FOXP2 as a molecular window into speech and language". Trends in Genetics. 25 (4): 166–77. doi:10.1016/j.tig.2009.03.002. hdl:11858/00-001M-0000-0012-CA31-7. PMID 19304338.
Shu W, Lu MM, Zhang Y, Tucker PW, Zhou D, Morrisey EE (May 2007). "Foxp2 and Foxp1 cooperatively regulate lung and esophagus development". Development. 134 (10): 1991–2000. doi:10.1242/dev.02846. PMID 17428829. S2CID 22896384.
Nudel R, Newbury DF (September 2013). "FOXP2". Wiley Interdisciplinary Reviews. Cognitive Science. 4 (5): 547–560. doi:10.1002/wcs.1247. PMC 3992897. PMID 24765219.
Atkinson EG, Audesse AJ, Palacios JA, Bobo DM, Webb AE, Ramachandran S, et al. (September 2018). "No Evidence for Recent Selection at FOXP2 among Diverse Human Populations". Cell. 174 (6): 1424–1435.e15. doi:10.1016/j.cell.2018.06.048. PMC 6128738. PMID 30078708.
Shu W, Cho JY, Jiang Y, Zhang M, Weisz D, Elder GA, et al. (July 2005). "Altered ultrasonic vocalization in mice with a disruption in the Foxp2 gene". Proceedings of the National Academy of Sciences of the United States of America. 102 (27): 9643–8. Bibcode:2005PNAS..102.9643S. doi:10.1073/pnas.0503739102. PMC 1160518. PMID 15983371.
Enard W, Przeworski M, Fisher SE, Lai CS, Wiebe V, Kitano T, et al. (August 2002). "Molecular evolution of FOXP2, a gene involved in speech and language" (PDF). Nature. 418 (6900): 869–72. Bibcode:2002Natur.418..869E. doi:10.1038/nature01025. hdl:11858/00-001M-0000-0012-CB89-A. PMID 12192408. S2CID 4416233. Archived from the original (PDF) on 30 August 2006.
Spiteri E, Konopka G, Coppola G, Bomar J, Oldham M, Ou J, et al. (December 2007). "Identification of the transcriptional targets of FOXP2, a gene linked to speech and language, in developing human brain". American Journal of Human Genetics. 81 (6): 1144–57. doi:10.1086/522237. PMC 2276350. PMID 17999357.
Bowers JM, Perez-Pouchoulen M, Edwards NS, McCarthy MM (February 2013). "Foxp2 mediates sex differences in ultrasonic vocalization by rat pups and directs order of maternal retrieval". The Journal of Neuroscience. 33 (8): 3276–83. doi:10.1523/JNEUROSCI.0425-12.2013. PMC 3727442. PMID 23426656.
Clovis YM, Enard W, Marinaro F, Huttner WB, De Pietri Tonelli D (September 2012). "Convergent repression of Foxp2 3'UTR by miR-9 and miR-132 in embryonic mouse neocortex: implications for radial migration of neurons". Development. 139 (18): 3332–42. doi:10.1242/dev.078063. PMID 22874921.
Enard W, Gehre S, Hammerschmidt K, Hölter SM, Blass T, Somel M, et al. (May 2009). "A humanized version of Foxp2 affects cortico-basal ganglia circuits in mice". Cell. 137 (5): 961–71. doi:10.1016/j.cell.2009.03.041. hdl:11858/00-001M-0000-000F-F8C5-2. PMID 19490899. S2CID 667723.
Konopka G, Bomar JM, Winden K, Coppola G, Jonsson ZO, Gao F, et al. (November 2009). "Human-specific transcriptional regulation of CNS development genes by FOXP2". Nature. 462 (7270): 213–7. Bibcode:2009Natur.462..213K. doi:10.1038/nature08549. PMC 2778075. PMID 19907493.
- "Why Can't Chimps Speak? Key Differences In How Human And Chimp Versions Of FOXP2 Gene Work". ScienceDaily (Press release). 12 November 2009.
- Gauthier J, Joober R, Mottron L, Laurent S, Fuchs M, De Kimpe V, et al. (April 2003). "Mutation screening of FOXP2 in individuals diagnosed with autistic disorder". American Journal of Medical Genetics. Part A. 118A (2): 172–5. doi:10.1002/ajmg.a.10105. PMID 12655497. S2CID 39762074.
- Newbury DF, Bonora E, Lamb JA, Fisher SE, Lai CS, Baird G, et al. (May 2002). "FOXP2 is not a major susceptibility gene for autism or specific language impairment". American Journal of Human Genetics. 70 (5): 1318–27. doi:10.1086/339931. PMC 447606. PMID 11894222.
- Lennon PA, Cooper ML, Peiffer DA, Gunderson KL, Patel A, Peters S, et al. (April 2007). "Deletion of 7q31.1 supports involvement of FOXP2 in language impairment: clinical report and review". American Journal of Medical Genetics. Part A. 143A (8): 791–8. doi:10.1002/ajmg.a.31632. PMID 17330859. S2CID 22021740.
- Rossell S, Tan E, Bozaoglu K, Neill E, Sumner P, Carruthers S, et al. (2017). "Is language Impairment in Schizophrenia related to Language Genes?". European Neuropsychopharmacology. 27: S459–S460. doi:10.1016/j.euroneuro.2016.09.532. S2CID 54316143.
- Reuter MS, Riess A, Moog U, Briggs TA, Chandler KE, Rauch A, et al. (January 2017). "FOXP2 variants in 14 individuals with developmental speech and language disorders broaden the mutational and clinical spectrum". Journal of Medical Genetics. 54 (1): 64–72. doi:10.1136/jmedgenet-2016-104094. PMID 27572252. S2CID 24589445.
- Liégeois F, Baldeweg T, Connelly A, Gadian DG, Mishkin M, Vargha-Khadem F (November 2003). "Language fMRI abnormalities associated with FOXP2 gene mutation". Nature Neuroscience. 6 (11): 1230–7. doi:10.1038/nn1138. PMID 14555953. S2CID 31003547.
- Demontis D, Walters RK, Martin J, Mattheisen M, Als TD, Agerbo E, et al. (January 2019). "Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder". Nature Genetics. 51 (1): 63–75. doi:10.1038/s41588-018-0269-7. PMC 6481311. PMID 30478444.
- Johnson EC, Demontis D, Thorgeirsson TE, Walters RK, Polimanti R, Hatoum AS, et al. (December 2020). "A large-scale genome-wide association study meta-analysis of cannabis use disorder". The Lancet. Psychiatry. 7 (12): 1032–1045. doi:10.1016/S2215-0366(20)30339-4. PMC 7674631. PMID 33096046.
- Preuss TM (June 2012). "Human brain evolution: from gene discovery to phenotype discovery". Proceedings of the National Academy of Sciences of the United States of America. 109 (Suppl 1): 10709–16. Bibcode:2012PNAS..10910709P. doi:10.1073/pnas.1201894109. PMC 3386880. PMID 22723367.
- Vargha-Khadem F, Gadian DG, Copp A, Mishkin M (February 2005). "FOXP2 and the neuroanatomy of speech and language". Nature Reviews. Neuroscience. 6 (2): 131–8. doi:10.1038/nrn1605. PMID 15685218. S2CID 2504002.
- Teramitsu I, Kudo LC, London SE, Geschwind DH, White SA (March 2004). "Parallel FoxP1 and FoxP2 expression in songbird and human brain predicts functional interaction". The Journal of Neuroscience. 24 (13): 3152–63. doi:10.1523/JNEUROSCI.5589-03.2004. PMC 6730014. PMID 15056695.
- Haesler S, Wada K, Nshdejan A, Morrisey EE, Lints T, Jarvis ED, et al. (March 2004). "FoxP2 expression in avian vocal learners and non-learners". The Journal of Neuroscience. 24 (13): 3164–75. doi:10.1523/JNEUROSCI.4369-03.2004. PMC 6730012. PMID 15056696.
- Li G, Wang J, Rossiter SJ, Jones G, Zhang S (September 2007). Ellegren H (ed.). "Accelerated FoxP2 evolution in echolocating bats". PLOS ONE. 2 (9): e900. Bibcode:2007PLoSO...2..900L. doi:10.1371/journal.pone.0000900. PMC 1976393. PMID 17878935.
- Webb DM, Zhang J (2005). "FoxP2 in song-learning birds and vocal-learning mammals". The Journal of Heredity. 96 (3): 212–6. doi:10.1093/jhered/esi025. PMID 15618302.
- Scharff C, Haesler S (December 2005). "An evolutionary perspective on FoxP2: strictly for the birds?". Current Opinion in Neurobiology. 15 (6): 694–703. doi:10.1016/j.conb.2005.10.004. PMID 16266802. S2CID 11350165.
- Krause J, Lalueza-Fox C, Orlando L, Enard W, Green RE, Burbano HA, et al. (November 2007). "The derived FOXP2 variant of modern humans was shared with Neandertals". Current Biology. 17 (21): 1908–12. Bibcode:2007CBio...17.1908K. doi:10.1016/j.cub.2007.10.008. hdl:11858/00-001M-0000-000F-FED3-1. PMID 17949978. S2CID 9518208.
  - Nicholas Wade (19 October 2007). "Neanderthals Had Important Speech Gene, DNA Evidence Shows". The New York Times.
  - Benítez-Burraco A, Longa VM, Lorenzo G, Uriagereka J (November 2008). "Also sprach Neanderthalis... Or Did She?". Biolinguistics. 2 (2–3): 225–232. doi:10.5964/bioling.8643. S2CID 60864520.
  - Toda M, Okubo S, Ikigai H, Suzuki T, Suzuki Y, Hara Y, et al. (1992). "The protective activity of tea catechins against experimental infection by Vibrio cholerae O1". Microbiology and Immunology. 36 (9): 999–1001. doi:10.1111/j.1348-0421.1992.tb02103.x. PMID 1461156. S2CID 34400234.
  - Li S, Weidenfeld J, Morrisey EE (January 2004). "Transcriptional and DNA binding activity of the Foxp1/2/4 family is modulated by heterotypic and homotypic protein interactions". Molecular and Cellular Biology. 24 (2): 809–22. doi:10.1128/MCB.24.2.809-822.2004. PMC 343786. PMID 14701752.
  - Smith RS, Kenny CJ, Ganesh V, Jang A, Borges-Monroy R, Partlow JN, et al. (September 2018). "Sodium Channel SCN3A (Na_V1.3) Regulation of Human Cerebral Cortical Folding and Oral Motor Development". Neuron. 99 (5): 905–913.e7. doi:10.1016/j.neuron.2018.07.052. PMC 6226006. PMID 30146301.
  - Vernes SC, Spiteri E, Nicod J, Groszer M, Taylor JM, Davies KE, et al. (December 2007). "High-throughput analysis of promoter occupancy reveals direct neural targets of FOXP2, a gene mutated in speech and language disorders". American Journal of Human Genetics. 81 (6): 1232–50. doi:10.1086/522238. PMC 2276341. PMID 17999362.
  - Vernes SC, Newbury DF, Abrahams BS, Winchester L, Nicod J, Groszer M, et al. (November 2008). "A functional genetic link between distinct developmental language disorders". The New England Journal of Medicine. 359 (22): 2337–45. doi:10.1056/NEJMoa0802828. PMC 2756409. PMID 18987363.
  - Sia GM, Clem RL, Huganir RL (November 2013). "The human language-associated gene SRPX2 regulates synapse formation and vocalization in mice". Science. 342 (6161): 987–91. Bibcode:2013Sci...342..987S. doi:10.1126/science.1245079. PMC 3903157. PMID 24179158.
  - Smith K (11 November 2009). "Evolution of a single gene linked to language". Nature. doi:10.1038/news.2009.1079. ISSN 1744-7933.
  - Holy TE, Guo Z (December 2005). "Ultrasonic songs of male mice". PLOS Biology. 3 (12): e386. doi:10.1371/journal.pbio.0030386. PMC 1275525. PMID 16248680.
  - French CA, Fisher SE (October 2014). "What can mice tell us about Foxp2 function?". Current Opinion in Neurobiology. 28: 72–9. doi:10.1016/j.conb.2014.07.003. hdl:11858/00-001M-0000-0019-F62D-4. PMID 25048596. S2CID 17848265.
  - Wilbrecht L, Nottebohm F (2003). "Vocal learning in birds and humans". Mental Retardation and Developmental Disabilities Research Reviews. 9 (3): 135–48. doi:10.1002/mrdd.10073. PMID 12953292.
  - Teramitsu I, White SA (July 2006). "FoxP2 regulation during undirected singing in adult songbirds". The Journal of Neuroscience. 26 (28): 7390–4. doi:10.1523/JNEUROSCI.1662-06.2006. PMC 2683919. PMID 16837586.
  - Heston JB, White SA (February 2015). "Behavior-linked FoxP2 regulation enables zebra finch vocal learning". The Journal of Neuroscience. 35 (7): 2885–94. doi:10.1523/JNEUROSCI.3715-14.2015. PMC 4331621. PMID 25698728.
  - Jarvis ED, Scharff C, Grossman MR, Ramos JA, Nottebohm F (October 1998). "For whom the bird sings: context-dependent gene expression". Neuron. 21 (4): 775–88. doi:10.1016/s0896-6273(00)80594-2. PMID 9808464. S2CID 13893471.
  - Bonkowsky JL, Chien CB (November 2005). "Molecular cloning and developmental expression of foxP2 in zebrafish". Developmental Dynamics. 234 (3): 740–6. doi:10.1002/dvdy.20504. PMID 16028276. S2CID 24771138.
  - Hurst JA, Baraitser M, Auger E, Graham F, Norell S (April 1990). "An extended family with a dominantly inherited speech disorder". Developmental Medicine and Child Neurology. 32 (4): 352–5. doi:10.1111/j.1469-8749.1990.tb16948.x. PMID 2332125. S2CID 2654363.
  - Gopnik M (September 1990). "Genetic basis of grammar defect". Nature. 347 (6288): 26. Bibcode:1990Natur.347...26G. doi:10.1038/347026a0. PMID 2395458. S2CID 4323390.
  - Gopnik M (April 1990). "Feature-blind grammar and dysphagia". Nature. 344 (6268): 715. Bibcode:1990Natur.344..715G. doi:10.1038/344715a0. PMID 2330028. S2CID 4360334.
  - Vargha-Khadem F, Watkins K, Alcock K, Fletcher P, Passingham R (January 1995). "Praxic and nonverbal cognitive deficits in a large family with a genetically transmitted speech and language disorder". Proceedings of the National Academy of Sciences of the United States of America. 92 (3): 930–3. Bibcode:1995PNAS...92..930V. doi:10.1073/pnas.92.3.930. PMC 42734. PMID 7846081.
  - Fisher SE, Lai CS, Monaco AP (2003). "Deciphering the genetic basis of speech and language disorders". Annual Review of Neuroscience. 26: 57–80. doi:10.1146/annurev.neuro.26.041002.131144. hdl:11858/00-001M-0000-0012-CB7E-4. PMID 12524432. S2CID 1276712.
  - Vernes SC, Nicod J, Elahi FM, Coventry JA, Kenny N, Coupe AM, et al. (November 2006). "Functional genetic analysis of mutations implicated in a human speech and language disorder". Human Molecular Genetics. 15 (21): 3154–67. doi:10.1093/hmg/ddl392. hdl:11858/00-001M-0000-0012-CB23-C. PMID 16984964.
  - Feuk L, Kalervo A, Lipsanen-Nyman M, Skaug J, Nakabayashi K, Finucane B, et al. (November 2006). "Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxia". American Journal of Human Genetics. 79 (5): 965–72. doi:10.1086/508902. PMC 1698557. PMID 17033973.

ensembl.org

May2017.archive.ensembl.org

GRCh38: Ensembl release 89: ENSG00000128573 – Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000029563 – Ensembl, May 2017

handle.net

hdl.handle.net

Fisher SE, Vargha-Khadem F, Watkins KE, Monaco AP, Pembrey ME (February 1998). "Localisation of a gene implicated in a severe speech and language disorder". Nature Genetics. 18 (2): 168–70. doi:10.1038/ng0298-168. hdl:11858/00-001M-0000-0012-CBD9-5. PMID 9462748. S2CID 3190318.
Lai CS, Fisher SE, Hurst JA, Vargha-Khadem F, Monaco AP (October 2001). "A forkhead-domain gene is mutated in a severe speech and language disorder". Nature. 413 (6855): 519–23. Bibcode:2001Natur.413..519L. doi:10.1038/35097076. hdl:11858/00-001M-0000-0012-CB9C-F. PMID 11586359. S2CID 4421562.
Fisher SE, Scharff C (April 2009). "FOXP2 as a molecular window into speech and language". Trends in Genetics. 25 (4): 166–77. doi:10.1016/j.tig.2009.03.002. hdl:11858/00-001M-0000-0012-CA31-7. PMID 19304338.
Enard W, Przeworski M, Fisher SE, Lai CS, Wiebe V, Kitano T, et al. (August 2002). "Molecular evolution of FOXP2, a gene involved in speech and language" (PDF). Nature. 418 (6900): 869–72. Bibcode:2002Natur.418..869E. doi:10.1038/nature01025. hdl:11858/00-001M-0000-0012-CB89-A. PMID 12192408. S2CID 4416233. Archived from the original (PDF) on 30 August 2006.
Enard W, Gehre S, Hammerschmidt K, Hölter SM, Blass T, Somel M, et al. (May 2009). "A humanized version of Foxp2 affects cortico-basal ganglia circuits in mice". Cell. 137 (5): 961–71. doi:10.1016/j.cell.2009.03.041. hdl:11858/00-001M-0000-000F-F8C5-2. PMID 19490899. S2CID 667723.
Krause J, Lalueza-Fox C, Orlando L, Enard W, Green RE, Burbano HA, et al. (November 2007). "The derived FOXP2 variant of modern humans was shared with Neandertals". Current Biology. 17 (21): 1908–12. Bibcode:2007CBio...17.1908K. doi:10.1016/j.cub.2007.10.008. hdl:11858/00-001M-0000-000F-FED3-1. PMID 17949978. S2CID 9518208.
- Nicholas Wade (19 October 2007). "Neanderthals Had Important Speech Gene, DNA Evidence Shows". The New York Times.
- French CA, Fisher SE (October 2014). "What can mice tell us about Foxp2 function?". Current Opinion in Neurobiology. 28: 72–9. doi:10.1016/j.conb.2014.07.003. hdl:11858/00-001M-0000-0019-F62D-4. PMID 25048596. S2CID 17848265.
- Fisher SE, Lai CS, Monaco AP (2003). "Deciphering the genetic basis of speech and language disorders". Annual Review of Neuroscience. 26: 57–80. doi:10.1146/annurev.neuro.26.041002.131144. hdl:11858/00-001M-0000-0012-CB7E-4. PMID 12524432. S2CID 1276712.
- Vernes SC, Nicod J, Elahi FM, Coventry JA, Kenny N, Coupe AM, et al. (November 2006). "Functional genetic analysis of mutations implicated in a human speech and language disorder". Human Molecular Genetics. 15 (21): 3154–67. doi:10.1093/hmg/ddl392. hdl:11858/00-001M-0000-0012-CB23-C. PMID 16984964.

harvard.edu

ui.adsabs.harvard.edu

Lai CS, Fisher SE, Hurst JA, Vargha-Khadem F, Monaco AP (October 2001). "A forkhead-domain gene is mutated in a severe speech and language disorder". Nature. 413 (6855): 519–23. Bibcode:2001Natur.413..519L. doi:10.1038/35097076. hdl:11858/00-001M-0000-0012-CB9C-F. PMID 11586359. S2CID 4421562.
Groszer M, Keays DA, Deacon RM, de Bono JP, Prasad-Mulcare S, Gaub S, et al. (March 2008). "Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficits". Current Biology. 18 (5): 354–62. Bibcode:2008CBio...18..354G. doi:10.1016/j.cub.2008.01.060. PMC 2917768. PMID 18328704.
Shu W, Cho JY, Jiang Y, Zhang M, Weisz D, Elder GA, et al. (July 2005). "Altered ultrasonic vocalization in mice with a disruption in the Foxp2 gene". Proceedings of the National Academy of Sciences of the United States of America. 102 (27): 9643–8. Bibcode:2005PNAS..102.9643S. doi:10.1073/pnas.0503739102. PMC 1160518. PMID 15983371.
Enard W, Przeworski M, Fisher SE, Lai CS, Wiebe V, Kitano T, et al. (August 2002). "Molecular evolution of FOXP2, a gene involved in speech and language" (PDF). Nature. 418 (6900): 869–72. Bibcode:2002Natur.418..869E. doi:10.1038/nature01025. hdl:11858/00-001M-0000-0012-CB89-A. PMID 12192408. S2CID 4416233. Archived from the original (PDF) on 30 August 2006.
Konopka G, Bomar JM, Winden K, Coppola G, Jonsson ZO, Gao F, et al. (November 2009). "Human-specific transcriptional regulation of CNS development genes by FOXP2". Nature. 462 (7270): 213–7. Bibcode:2009Natur.462..213K. doi:10.1038/nature08549. PMC 2778075. PMID 19907493.
- "Why Can't Chimps Speak? Key Differences In How Human And Chimp Versions Of FOXP2 Gene Work". ScienceDaily (Press release). 12 November 2009.
- Preuss TM (June 2012). "Human brain evolution: from gene discovery to phenotype discovery". Proceedings of the National Academy of Sciences of the United States of America. 109 (Suppl 1): 10709–16. Bibcode:2012PNAS..10910709P. doi:10.1073/pnas.1201894109. PMC 3386880. PMID 22723367.
- Li G, Wang J, Rossiter SJ, Jones G, Zhang S (September 2007). Ellegren H (ed.). "Accelerated FoxP2 evolution in echolocating bats". PLOS ONE. 2 (9): e900. Bibcode:2007PLoSO...2..900L. doi:10.1371/journal.pone.0000900. PMC 1976393. PMID 17878935.
- Krause J, Lalueza-Fox C, Orlando L, Enard W, Green RE, Burbano HA, et al. (November 2007). "The derived FOXP2 variant of modern humans was shared with Neandertals". Current Biology. 17 (21): 1908–12. Bibcode:2007CBio...17.1908K. doi:10.1016/j.cub.2007.10.008. hdl:11858/00-001M-0000-000F-FED3-1. PMID 17949978. S2CID 9518208.
  - Nicholas Wade (19 October 2007). "Neanderthals Had Important Speech Gene, DNA Evidence Shows". The New York Times.
  - Sia GM, Clem RL, Huganir RL (November 2013). "The human language-associated gene SRPX2 regulates synapse formation and vocalization in mice". Science. 342 (6161): 987–91. Bibcode:2013Sci...342..987S. doi:10.1126/science.1245079. PMC 3903157. PMID 24179158.
  - Gopnik M (September 1990). "Genetic basis of grammar defect". Nature. 347 (6288): 26. Bibcode:1990Natur.347...26G. doi:10.1038/347026a0. PMID 2395458. S2CID 4323390.
  - Gopnik M (April 1990). "Feature-blind grammar and dysphagia". Nature. 344 (6268): 715. Bibcode:1990Natur.344..715G. doi:10.1038/344715a0. PMID 2330028. S2CID 4360334.
  - Vargha-Khadem F, Watkins K, Alcock K, Fletcher P, Passingham R (January 1995). "Praxic and nonverbal cognitive deficits in a large family with a genetically transmitted speech and language disorder". Proceedings of the National Academy of Sciences of the United States of America. 92 (3): 930–3. Bibcode:1995PNAS...92..930V. doi:10.1073/pnas.92.3.930. PMC 42734. PMID 7846081.

human-brain.org

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