Benítez-Burraco A - Search Results

1

Functional characterization of two enhancers located downstream FOXP2.

Torres-Ruiz R, Benítez-Burraco A, Martínez-Lage M, Rodríguez-Perales S, García-Bellido P. Torres-Ruiz R, et al. BMC Med Genet. 2019 May 2;20(1):65. doi: 10.1186/s12881-019-0810-2. BMC Med Genet. 2019. PMID: 31046704 Free PMC article.

2

[FOXP2: from the specific disorder to the molecular biology of language. II. Implications for the ontogenesis and phylogenesis of language].

Benítez-Burraco A. Benítez-Burraco A. Rev Neurol. 2005 Jul 1-15;41(1):37-44. Rev Neurol. 2005. PMID: 15999329 Free article. Review. Spanish.

3

Language impairment in a case of a complex chromosomal rearrangement with a breakpoint downstream of FOXP2.

Moralli D, Nudel R, Chan MT, Green CM, Volpi EV, Benítez-Burraco A, Newbury DF, García-Bellido P. Moralli D, et al. Mol Cytogenet. 2015 Jun 10;8:36. doi: 10.1186/s13039-015-0148-1. eCollection 2015. Mol Cytogenet. 2015. PMID: 26060509 Free PMC article.

4

Narrowing the Genetic Causes of Language Dysfunction in the 1q21.1 Microduplication Syndrome.

Benítez-Burraco A, Barcos-Martínez M, Espejo-Portero I, Fernández-Urquiza M, Torres-Ruiz R, Rodríguez-Perales S, Jiménez-Romero MS. Benítez-Burraco A, et al. Front Pediatr. 2018 Jun 5;6:163. doi: 10.3389/fped.2018.00163. eCollection 2018. Front Pediatr. 2018. PMID: 29922639 Free PMC article.

5

Genes dysregulated in the blood of people with Williams syndrome are enriched in protein-coding genes positively selected in humans.

Benítez-Burraco A. Benítez-Burraco A. Eur J Med Genet. 2020 Apr;63(4):103828. doi: 10.1016/j.ejmg.2019.103828. Epub 2019 Dec 30. Eur J Med Genet. 2020. PMID: 31899327

6

A genetic window to auditory-verbal problems in bipolar disorder.

Benítez-Burraco A. Benítez-Burraco A. Psychiatr Genet. 2020 Dec;30(6):169-173. doi: 10.1097/YPG.0000000000000265. Psychiatr Genet. 2020. PMID: 33165203

7

Human-specific changes in two functional enhancers of FOXP2.

Benítez-Burraco A, Torres-Ruiz R, Gelabert P, Lalueza-Fox C, Rodríguez-Perales S, García-Bellido P. Benítez-Burraco A, et al. Cell Mol Biol (Noisy-le-grand). 2022 Nov 30;68(11):16-19. doi: 10.14715/cmb/2022.68.11.3. Cell Mol Biol (Noisy-le-grand). 2022. PMID: 37114314

8

The Promoter Regions of Intellectual Disability-Associated Genes Are Uniquely Enriched in LTR Sequences of the MER41 Primate-Specific Endogenous Retrovirus: An Evolutionary Connection Between Immunity and Cognition.

Nataf S, Uriagereka J, Benitez-Burraco A. Nataf S, et al. Front Genet. 2019 Apr 12;10:321. doi: 10.3389/fgene.2019.00321. eCollection 2019. Front Genet. 2019. PMID: 31031802 Free PMC article.

9

Communication deficits in a case of a deletion in 7q31.1-q31.33 encompassing FOXP2.

Moreno Campos V, Benítez-Burraco A. Moreno Campos V, et al. Clin Linguist Phon. 2023 Dec 2;37(12):1157-1170. doi: 10.1080/02699206.2022.2085174. Epub 2022 Jun 14. Clin Linguist Phon. 2023. PMID: 35702019

10

[FOXP2 and the molecular biology of language: new evidence. II. Molecular aspects and implications for the ontogenesis and phylogeny of language].

Benítez-Burraco A. Benítez-Burraco A. Rev Neurol. 2008 Mar 16-31;46(6):351-9. Rev Neurol. 2008. PMID: 18368680 Free article. Review. Spanish.

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