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2016 4
2017 3
2024 0

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Page 1
Motor Stereotypies: A Pathophysiological Review.
Péter Z, Oliphant ME, Fernandez TV. Péter Z, et al. Front Neurosci. 2017 Mar 29;11:171. doi: 10.3389/fnins.2017.00171. eCollection 2017. Front Neurosci. 2017. PMID: 28405185 Free PMC article. Review.
Neurogenetic analysis of childhood disintegrative disorder.
Gupta AR, Westphal A, Yang DYJ, Sullivan CAW, Eilbott J, Zaidi S, Voos A, Vander Wyk BC, Ventola P, Waqar Z, Fernandez TV, Ercan-Sencicek AG, Walker MF, Choi M, Schneider A, Hedderly T, Baird G, Friedman H, Cordeaux C, Ristow A, Shic F, Volkmar FR, Pelphrey KA. Gupta AR, et al. Mol Autism. 2017 Apr 4;8:19. doi: 10.1186/s13229-017-0133-0. eCollection 2017. Mol Autism. 2017. PMID: 28392909 Free PMC article.
Molecular characterization of a patient with 3p deletion syndrome and a review of the literature.
Fernandez TV, García-González IJ, Mason CE, Hernández-Zaragoza G, Ledezma-Rodríguez VC, Anguiano-Alvarez VM, E'Vega R, Gutiérrez-Angulo M, Maya ML, García-Bejarano HE, González-Cruz M, Barrios S, Atorga R, López-Cardona MG, Armendariz-Borunda J, State MW, Dávalos NO. Fernandez TV, et al. Am J Med Genet A. 2008 Nov 1;146A(21):2746-52. doi: 10.1002/ajmg.a.32533. Am J Med Genet A. 2008. PMID: 18837054 Review.
Tourette's syndrome and translational clinical science.
Fernandez TV, King RA, Pittenger C. Fernandez TV, et al. J Am Acad Child Adolesc Psychiatry. 2015 Jan;54(1):6-8. doi: 10.1016/j.jaac.2014.11.004. J Am Acad Child Adolesc Psychiatry. 2015. PMID: 25524784 Free PMC article. No abstract available.
De Novo Coding Variants Are Strongly Associated with Tourette Disorder.
Willsey AJ, Fernandez TV, Yu D, King RA, Dietrich A, Xing J, Sanders SJ, Mandell JD, Huang AY, Richer P, Smith L, Dong S, Samocha KE; Tourette International Collaborative Genetics (TIC Genetics); Tourette Syndrome Association International Consortium for Genetics (TSAICG); Neale BM, Coppola G, Mathews CA, Tischfield JA, Scharf JM, State MW, Heiman GA. Willsey AJ, et al. Neuron. 2017 May 3;94(3):486-499.e9. doi: 10.1016/j.neuron.2017.04.024. Neuron. 2017. PMID: 28472652 Free PMC article.
Whole-exome sequencing in obsessive-compulsive disorder identifies rare mutations in immunological and neurodevelopmental pathways.
Cappi C, Brentani H, Lima L, Sanders SJ, Zai G, Diniz BJ, Reis VN, Hounie AG, Conceição do Rosário M, Mariani D, Requena GL, Puga R, Souza-Duran FL, Shavitt RG, Pauls DL, Miguel EC, Fernandez TV. Cappi C, et al. Transl Psychiatry. 2016 Mar 29;6(3):e764. doi: 10.1038/tp.2016.30. Transl Psychiatry. 2016. PMID: 27023170 Free PMC article.
12 results