Flores R - Search Results

1

[Blood cell chimerism in dizygotic twins conceived by in vitro fertilization].

Martos-Moreno GÁ, Campos C, Flores R, Yturriaga R, Pérez-Jurado LA, Argente J. Martos-Moreno GÁ, et al. Among authors: flores r. An Pediatr (Barc). 2013 Oct;79(4):248-52. doi: 10.1016/j.anpedi.2013.04.005. Epub 2013 May 30. An Pediatr (Barc). 2013. PMID: 23726690 Free article. Spanish.

2

Defective minor spliceosome mRNA processing results in isolated familial growth hormone deficiency.

Argente J, Flores R, Gutiérrez-Arumí A, Verma B, Martos-Moreno GÁ, Cuscó I, Oghabian A, Chowen JA, Frilander MJ, Pérez-Jurado LA. Argente J, et al. Among authors: flores r. EMBO Mol Med. 2014 Mar;6(3):299-306. doi: 10.1002/emmm.201303573. Epub 2014 Jan 30. EMBO Mol Med. 2014. PMID: 24480542 Free PMC article.

3

Novel genes involved in severe early-onset obesity revealed by rare copy number and sequence variants.

Serra-Juhé C, Martos-Moreno GÁ, Bou de Pieri F, Flores R, González JR, Rodríguez-Santiago B, Argente J, Pérez-Jurado LA. Serra-Juhé C, et al. Among authors: flores r. PLoS Genet. 2017 May 10;13(5):e1006657. doi: 10.1371/journal.pgen.1006657. eCollection 2017 May. PLoS Genet. 2017. PMID: 28489853 Free PMC article.

4

Heterozygous rare genetic variants in non-syndromic early-onset obesity.

Serra-Juhé C, Martos-Moreno GÁ, Bou de Pieri F, Flores R, Chowen JA, Pérez-Jurado LA, Argente J. Serra-Juhé C, et al. Among authors: flores r. Int J Obes (Lond). 2020 Apr;44(4):830-841. doi: 10.1038/s41366-019-0357-5. Epub 2019 Mar 29. Int J Obes (Lond). 2020. PMID: 30926952 Free PMC article.

5

[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.

6

Generation of induced pluripotent stem cells (iPSCs) by retroviral transduction of skin fibroblasts from four patients suffering Williams-Beuren syndrome (7q11.23 deletion).

Kuebler B, Aran B, Flores R, Pérez-Jurado LA, Veiga A, Corominas R, Cuscó I. Kuebler B, et al. Among authors: flores r. Stem Cell Res. 2020 Dec;49:102087. doi: 10.1016/j.scr.2020.102087. Epub 2020 Nov 16. Stem Cell Res. 2020. PMID: 33370870 Free article.

7

Derivation of induced pluripotent stem cells (iPSCs) by retroviral transduction of skin fibroblasts from four patients suffering 7q11.23 microduplication syndrome.

Kuebler B, Aran B, Flores R, Pérez-Jurado LA, Veiga A, Cuscó I, Corominas R. Kuebler B, et al. Among authors: flores r. Stem Cell Res. 2020 Dec;49:102092. doi: 10.1016/j.scr.2020.102092. Epub 2020 Nov 19. Stem Cell Res. 2020. PMID: 33254092 Free article.

8

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

9

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

10

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

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