Flores R - Search Results

1

Mutational mechanisms of Williams-Beuren syndrome deletions.

Bayés M, Magano LF, Rivera N, Flores R, Pérez Jurado LA. Bayés M, et al. Among authors: flores r. Am J Hum Genet. 2003 Jul;73(1):131-51. doi: 10.1086/376565. Epub 2003 Jun 9. Am J Hum Genet. 2003. PMID: 12796854 Free PMC article.

2

Lateral preference in Williams-Beuren syndrome is associated with cognition and language.

Pérez-García D, Flores R, Brun-Gasca C, Pérez-Jurado LA. Pérez-García D, et al. Among authors: flores r. Eur Child Adolesc Psychiatry. 2015 Sep;24(9):1025-33. doi: 10.1007/s00787-014-0652-6. Epub 2014 Nov 28. Eur Child Adolesc Psychiatry. 2015. PMID: 25431039

3

[Williams syndrome: its clinical aspects and molecular bases].

Antonell A, Del Campo M, Flores R, Campuzano V, Perez-Jurado LA. Antonell A, et al. Among authors: flores r. Rev Neurol. 2006 Jan 7;42 Suppl 1:S69-75. Rev Neurol. 2006. PMID: 16506136 Free article. Review. Spanish.

4

Partial 7q11.23 deletions further implicate GTF2I and GTF2IRD1 as the main genes responsible for the Williams-Beuren syndrome neurocognitive profile.

Antonell A, Del Campo M, Magano LF, Kaufmann L, de la Iglesia JM, Gallastegui F, Flores R, Schweigmann U, Fauth C, Kotzot D, Pérez-Jurado LA. Antonell A, et al. Among authors: flores r. J Med Genet. 2010 May;47(5):312-20. doi: 10.1136/jmg.2009.071712. Epub 2009 Nov 5. J Med Genet. 2010. PMID: 19897463

5

Copy number variation at the 7q11.23 segmental duplications is a susceptibility factor for the Williams-Beuren syndrome deletion.

Cuscó I, Corominas R, Bayés M, Flores R, Rivera-Brugués N, Campuzano V, Pérez-Jurado LA. Cuscó I, et al. Among authors: flores r. Genome Res. 2008 May;18(5):683-94. doi: 10.1101/gr.073197.107. Epub 2008 Feb 21. Genome Res. 2008. PMID: 18292220 Free PMC article.

6

Visual phenotype in Williams-Beuren syndrome challenges magnocellular theories explaining human neurodevelopmental visual cortical disorders.

Castelo-Branco M, Mendes M, Sebastião AR, Reis A, Soares M, Saraiva J, Bernardes R, Flores R, Pérez-Jurado L, Silva E. Castelo-Branco M, et al. Among authors: flores r. J Clin Invest. 2007 Dec;117(12):3720-9. doi: 10.1172/JCI32556. J Clin Invest. 2007. PMID: 18037993 Free PMC article.

7

Hemizygosity at the NCF1 gene in patients with Williams-Beuren syndrome decreases their risk of hypertension.

Del Campo M, Antonell A, Magano LF, Muñoz FJ, Flores R, Bayés M, Pérez Jurado LA. Del Campo M, et al. Among authors: flores r. Am J Hum Genet. 2006 Apr;78(4):533-42. doi: 10.1086/501073. Epub 2006 Jan 31. Am J Hum Genet. 2006. PMID: 16532385 Free PMC article.

8

Metabolic abnormalities in Williams-Beuren syndrome.

Palacios-Verdú MG, Segura-Puimedon M, Borralleras C, Flores R, Del Campo M, Campuzano V, Pérez-Jurado LA. Palacios-Verdú MG, et al. Among authors: flores r. J Med Genet. 2015 Apr;52(4):248-55. doi: 10.1136/jmedgenet-2014-102713. Epub 2015 Feb 6. J Med Genet. 2015. PMID: 25663682

9

Association of common copy number variants at the glutathione S-transferase genes and rare novel genomic changes with schizophrenia.

Rodríguez-Santiago B, Brunet A, Sobrino B, Serra-Juhé C, Flores R, Armengol L, Vilella E, Gabau E, Guitart M, Guillamat R, Martorell L, Valero J, Gutiérrez-Zotes A, Labad A, Carracedo A, Estivill X, Pérez-Jurado LA. Rodríguez-Santiago B, et al. Among authors: flores r. Mol Psychiatry. 2010 Oct;15(10):1023-33. doi: 10.1038/mp.2009.53. Epub 2009 Jun 16. Mol Psychiatry. 2010. PMID: 19528963

10

DNA methylation abnormalities in congenital heart disease.

Serra-Juhé C, Cuscó I, Homs A, Flores R, Torán N, Pérez-Jurado LA. Serra-Juhé C, et al. Among authors: flores r. Epigenetics. 2015;10(2):167-77. doi: 10.1080/15592294.2014.998536. Epigenetics. 2015. PMID: 25587870 Free PMC article.

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