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Genetic advances in the study of speech and language disorders.
Newbury DF, Monaco AP. Newbury DF, et al. Among authors: monaco ap. Neuron. 2010 Oct 21;68(2):309-20. doi: 10.1016/j.neuron.2010.10.001. Neuron. 2010. PMID: 20955937 Free PMC article. Review.
Normal radial migration and lamination are maintained in dyslexia-susceptibility candidate gene homolog Kiaa0319 knockout mice.
Martinez-Garay I, Guidi LG, Holloway ZG, Bailey MA, Lyngholm D, Schneider T, Donnison T, Butt SJ, Monaco AP, Molnár Z, Velayos-Baeza A. Martinez-Garay I, et al. Among authors: monaco ap. Brain Struct Funct. 2017 Apr;222(3):1367-1384. doi: 10.1007/s00429-016-1282-1. Epub 2016 Aug 10. Brain Struct Funct. 2017. PMID: 27510895 Free PMC article.
The dyslexia-associated KIAA0319 protein undergoes proteolytic processing with {gamma}-secretase-independent intramembrane cleavage.
Velayos-Baeza A, Levecque C, Kobayashi K, Holloway ZG, Monaco AP. Velayos-Baeza A, et al. Among authors: monaco ap. J Biol Chem. 2010 Dec 17;285(51):40148-62. doi: 10.1074/jbc.M110.145961. Epub 2010 Oct 13. J Biol Chem. 2010. PMID: 20943657 Free PMC article.
Association of the KIAA0319 dyslexia susceptibility gene with reading skills in the general population.
Paracchini S, Steer CD, Buckingham LL, Morris AP, Ring S, Scerri T, Stein J, Pembrey ME, Ragoussis J, Golding J, Monaco AP. Paracchini S, et al. Among authors: monaco ap. Am J Psychiatry. 2008 Dec;165(12):1576-84. doi: 10.1176/appi.ajp.2008.07121872. Epub 2008 Oct 1. Am J Psychiatry. 2008. PMID: 18829873
Alternative splicing in the dyslexia-associated gene KIAA0319.
Velayos-Baeza A, Toma C, da Roza S, Paracchini S, Monaco AP. Velayos-Baeza A, et al. Among authors: monaco ap. Mamm Genome. 2007 Sep;18(9):627-34. doi: 10.1007/s00335-007-9051-3. Epub 2007 Sep 11. Mamm Genome. 2007. PMID: 17846832
Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairments.
Leblond CS, Nava C, Polge A, Gauthier J, Huguet G, Lumbroso S, Giuliano F, Stordeur C, Depienne C, Mouzat K, Pinto D, Howe J, Lemière N, Durand CM, Guibert J, Ey E, Toro R, Peyre H, Mathieu A, Amsellem F, Rastam M, Gillberg IC, Rappold GA, Holt R, Monaco AP, Maestrini E, Galan P, Heron D, Jacquette A, Afenjar A, Rastetter A, Brice A, Devillard F, Assouline B, Laffargue F, Lespinasse J, Chiesa J, Rivier F, Bonneau D, Regnault B, Zelenika D, Delepine M, Lathrop M, Sanlaville D, Schluth-Bolard C, Edery P, Perrin L, Tabet AC, Schmeisser MJ, Boeckers TM, Coleman M, Sato D, Szatmari P, Scherer SW, Rouleau GA, Betancur C, Leboyer M, Gillberg C, Delorme R, Bourgeron T. Leblond CS, et al. Among authors: monaco ap. PLoS Genet. 2014 Sep 4;10(9):e1004580. doi: 10.1371/journal.pgen.1004580. eCollection 2014 Sep. PLoS Genet. 2014. PMID: 25188300 Free PMC article.
Individual common variants exert weak effects on the risk for autism spectrum disorders.
Anney R, Klei L, Pinto D, Almeida J, Bacchelli E, Baird G, Bolshakova N, Bölte S, Bolton PF, Bourgeron T, Brennan S, Brian J, Casey J, Conroy J, Correia C, Corsello C, Crawford EL, de Jonge M, Delorme R, Duketis E, Duque F, Estes A, Farrar P, Fernandez BA, Folstein SE, Fombonne E, Gilbert J, Gillberg C, Glessner JT, Green A, Green J, Guter SJ, Heron EA, Holt R, Howe JL, Hughes G, Hus V, Igliozzi R, Jacob S, Kenny GP, Kim C, Kolevzon A, Kustanovich V, Lajonchere CM, Lamb JA, Law-Smith M, Leboyer M, Le Couteur A, Leventhal BL, Liu XQ, Lombard F, Lord C, Lotspeich L, Lund SC, Magalhaes TR, Mantoulan C, McDougle CJ, Melhem NM, Merikangas A, Minshew NJ, Mirza GK, Munson J, Noakes C, Nygren G, Papanikolaou K, Pagnamenta AT, Parrini B, Paton T, Pickles A, Posey DJ, Poustka F, Ragoussis J, Regan R, Roberts W, Roeder K, Roge B, Rutter ML, Schlitt S, Shah N, Sheffield VC, Soorya L, Sousa I, Stoppioni V, Sykes N, Tancredi R, Thompson AP, Thomson S, Tryfon A, Tsiantis J, Van Engeland H, Vincent JB, Volkmar F, Vorstman JA, Wallace S, Wing K, Wittemeyer K, Wood S, Zurawiecki D, Zwaigenbaum L, Bailey AJ, Battaglia A, Cantor RM, Coon H, Cuccaro ML, Dawson G, Ennis S, Freitag CM, Geschwind DH, Haines JL, Klauck SM, McMahon WM, Maestrini E, Miller J, Monaco AP, Nelson SF, Nurnberger JI Jr, Oliveira G, Parr JR, Pericak-Vance MA, Piven J, Schellenberg GD, Scherer SW, Vicente AM, Wassink TH, Wijsman EM, Betancur C, Buxbaum JD, Cook EH, Gallagher L, Gill M, Hallmayer J, Paterson AD, Sutcliffe JS, Szatmari P, Vieland VJ, Hakonarson H, Devlin B. Anney R, et al. Among authors: monaco ap. Hum Mol Genet. 2012 Nov 1;21(21):4781-92. doi: 10.1093/hmg/dds301. Epub 2012 Jul 26. Hum Mol Genet. 2012. PMID: 22843504 Free PMC article.
CNVs leading to fusion transcripts in individuals with autism spectrum disorder.
Holt R, Sykes NH, Conceição IC, Cazier JB, Anney RJ, Oliveira G, Gallagher L, Vicente A, Monaco AP, Pagnamenta AT. Holt R, et al. Among authors: monaco ap. Eur J Hum Genet. 2012 Nov;20(11):1141-7. doi: 10.1038/ejhg.2012.73. Epub 2012 May 2. Eur J Hum Genet. 2012. PMID: 22549408 Free PMC article.
Genome-wide analysis of genetic susceptibility to language impairment in an isolated Chilean population.
Villanueva P, Newbury DF, Jara L, De Barbieri Z, Mirza G, Palomino HM, Fernández MA, Cazier JB, Monaco AP, Palomino H. Villanueva P, et al. Among authors: monaco ap. Eur J Hum Genet. 2011 Jun;19(6):687-95. doi: 10.1038/ejhg.2010.251. Epub 2011 Jan 19. Eur J Hum Genet. 2011. PMID: 21248734 Free PMC article.
Assessing the impact of FOXP1 mutations on developmental verbal dyspraxia.
Vernes SC, MacDermot KD, Monaco AP, Fisher SE. Vernes SC, et al. Among authors: monaco ap. Eur J Hum Genet. 2009 Oct;17(10):1354-8. doi: 10.1038/ejhg.2009.43. Epub 2009 Apr 8. Eur J Hum Genet. 2009. PMID: 19352412 Free PMC article.
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