128 related articles for article (PubMed ID: 38523169)
1. Correction to: Novel FOXP2 variant associated with speech and language dysfunction in a Chinese family and literature review.
Che F; Li C; Zhang L; Qian C; Mo L; Li B; Wu H; Wang L; Yang Y
J Appl Genet; 2024 May; 65(2):417. PubMed ID: 38523169
[No Abstract] [Full Text] [Related]
2. Small intragenic deletion in FOXP2 associated with childhood apraxia of speech and dysarthria.
Turner SJ; Hildebrand MS; Block S; Damiano J; Fahey M; Reilly S; Bahlo M; Scheffer IE; Morgan AT
Am J Med Genet A; 2013 Sep; 161A(9):2321-6. PubMed ID: 23918746
[TBL] [Abstract][Full Text] [Related]
3. 7q31.2q31.31 deletion downstream of FOXP2 segregating in a family with speech and language disorder.
Rieger M; Krumbiegel M; Reuter MS; Schützenberger A; Reis A; Zweier C
Am J Med Genet A; 2020 Nov; 182(11):2737-2741. PubMed ID: 32885567
[TBL] [Abstract][Full Text] [Related]
4. Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits.
MacDermot KD; Bonora E; Sykes N; Coupe AM; Lai CS; Vernes SC; Vargha-Khadem F; McKenzie F; Smith RL; Monaco AP; Fisher SE
Am J Hum Genet; 2005 Jun; 76(6):1074-80. PubMed ID: 15877281
[TBL] [Abstract][Full Text] [Related]
5. FOXP2 variants in 14 individuals with developmental speech and language disorders broaden the mutational and clinical spectrum.
Reuter MS; Riess A; Moog U; Briggs TA; Chandler KE; Rauch A; Stampfer M; Steindl K; Gläser D; Joset P; ; Krumbiegel M; Rabe H; Schulte-Mattler U; Bauer P; Beck-Wödl S; Kohlhase J; Reis A; Zweier C
J Med Genet; 2017 Jan; 54(1):64-72. PubMed ID: 27572252
[TBL] [Abstract][Full Text] [Related]
6. Identification of the transcriptional targets of FOXP2, a gene linked to speech and language, in developing human brain.
Spiteri E; Konopka G; Coppola G; Bomar J; Oldham M; Ou J; Vernes SC; Fisher SE; Ren B; Geschwind DH
Am J Hum Genet; 2007 Dec; 81(6):1144-57. PubMed ID: 17999357
[TBL] [Abstract][Full Text] [Related]
7. Expression of Foxp2, a gene involved in speech and language, in the developing and adult striatum.
Takahashi K; Liu FC; Hirokawa K; Takahashi H
J Neurosci Res; 2003 Jul; 73(1):61-72. PubMed ID: 12815709
[TBL] [Abstract][Full Text] [Related]
8. Singing mice, songbirds, and more: models for FOXP2 function and dysfunction in human speech and language.
White SA; Fisher SE; Geschwind DH; Scharff C; Holy TE
J Neurosci; 2006 Oct; 26(41):10376-9. PubMed ID: 17035521
[TBL] [Abstract][Full Text] [Related]
9. Human-specific transcriptional regulation of CNS development genes by FOXP2.
Konopka G; Bomar JM; Winden K; Coppola G; Jonsson ZO; Gao F; Peng S; Preuss TM; Wohlschlegel JA; Geschwind DH
Nature; 2009 Nov; 462(7270):213-7. PubMed ID: 19907493
[TBL] [Abstract][Full Text] [Related]
10. Molecular evolution of FOXP2, a gene involved in speech and language.
Enard W; Przeworski M; Fisher SE; Lai CS; Wiebe V; Kitano T; Monaco AP; Pääbo S
Nature; 2002 Aug; 418(6900):869-72. PubMed ID: 12192408
[TBL] [Abstract][Full Text] [Related]
11. Association between FOXP2 gene and speech sound disorder in Chinese population.
Zhao Y; Ma H; Wang Y; Gao H; Xi C; Hua T; Zhao Y; Qiu G
Psychiatry Clin Neurosci; 2010 Oct; 64(5):565-73. PubMed ID: 20923434
[TBL] [Abstract][Full Text] [Related]
12. Case Report: Expressive Speech Disorder in a Family as a Hallmark of 7q31 Deletion Involving the
Nagy O; Kárteszi J; Elmont B; Ujfalusi A
Front Pediatr; 2021; 9():664548. PubMed ID: 34490154
[TBL] [Abstract][Full Text] [Related]
13. Functional characterization of rare FOXP2 variants in neurodevelopmental disorder.
Estruch SB; Graham SA; Chinnappa SM; Deriziotis P; Fisher SE
J Neurodev Disord; 2016; 8():44. PubMed ID: 27933109
[TBL] [Abstract][Full Text] [Related]
14. FOXP2 and the role of cortico-basal ganglia circuits in speech and language evolution.
Enard W
Curr Opin Neurobiol; 2011 Jun; 21(3):415-24. PubMed ID: 21592779
[TBL] [Abstract][Full Text] [Related]
15. Phenotype of FOXP2 haploinsufficiency in a mother and son.
Rice GM; Raca G; Jakielski KJ; Laffin JJ; Iyama-Kurtycz CM; Hartley SL; Sprague RE; Heintzelman AT; Shriberg LD
Am J Med Genet A; 2012 Jan; 158A(1):174-81. PubMed ID: 22106036
[TBL] [Abstract][Full Text] [Related]
16. Early neuroimaging markers of FOXP2 intragenic deletion.
Liégeois FJ; Hildebrand MS; Bonthrone A; Turner SJ; Scheffer IE; Bahlo M; Connelly A; Morgan AT
Sci Rep; 2016 Oct; 6():35192. PubMed ID: 27734906
[TBL] [Abstract][Full Text] [Related]
17. FoxP2 is significantly associated with schizophrenia and major depression in the Chinese Han population.
Li T; Zeng Z; Zhao Q; Wang T; Huang K; Li J; Li Y; Liu J; Wei Z; Wang Y; Feng G; He L; Shi Y
World J Biol Psychiatry; 2013 Mar; 14(2):146-50. PubMed ID: 22404659
[TBL] [Abstract][Full Text] [Related]
18. Enhanced procedural learning of speech sound categories in a genetic variant of FOXP2.
Chandrasekaran B; Yi HG; Blanco NJ; McGeary JE; Maddox WT
J Neurosci; 2015 May; 35(20):7808-12. PubMed ID: 25995468
[TBL] [Abstract][Full Text] [Related]
19. Equivalent missense variant in the FOXP2 and FOXP1 transcription factors causes distinct neurodevelopmental disorders.
Sollis E; Deriziotis P; Saitsu H; Miyake N; Matsumoto N; Hoffer MJV; Ruivenkamp CAL; Alders M; Okamoto N; Bijlsma EK; Plomp AS; Fisher SE
Hum Mutat; 2017 Nov; 38(11):1542-1554. PubMed ID: 28741757
[TBL] [Abstract][Full Text] [Related]
20. The speech and language FOXP2 gene modulates the phenotype of frontotemporal lobar degeneration.
Padovani A; Cosseddu M; Premi E; Archetti S; Papetti A; Agosti C; Bigni B; Cerini C; Paghera B; Bellelli G; Borroni B
J Alzheimers Dis; 2010; 22(3):923-31. PubMed ID: 20858950
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
