Hernan I - Search Results

1

The interaction effect between BDNF val66met polymorphism and obesity on executive functions and frontal structure.

Marqués-Iturria I, Garolera M, Pueyo R, Segura B, Hernan I, García-García I, Sánchez-Garre C, Vernet-Vernet M, Sender-Palacios MJ, Narberhaus A, Ariza M, Junqué C, Jurado MÁ. Marqués-Iturria I, et al. Among authors: hernan i. Am J Med Genet B Neuropsychiatr Genet. 2014 Apr;165B(3):245-53. doi: 10.1002/ajmg.b.32229. Epub 2014 Mar 12. Am J Med Genet B Neuropsychiatr Genet. 2014. PMID: 24619555

2

Dopamine genes (DRD2/ANKK1-TaqA1 and DRD4-7R) and executive function: their interaction with obesity.

Ariza M, Garolera M, Jurado MA, Garcia-Garcia I, Hernan I, Sánchez-Garre C, Vernet-Vernet M, Sender-Palacios MJ, Marques-Iturria I, Pueyo R, Segura B, Narberhaus A. Ariza M, et al. Among authors: hernan i. PLoS One. 2012;7(7):e41482. doi: 10.1371/journal.pone.0041482. Epub 2012 Jul 25. PLoS One. 2012. PMID: 22848508 Free PMC article. Clinical Trial.

3

Effect of the catechol-O-methyltransferase Val ¹⁵⁸ Met polymorphism on theory of mind in obesity.

Caldú X, Ottino-González J, Sánchez-Garre C, Hernan I, Tor E, Sender-Palacios MJ, Dreher JC, Garolera M, Jurado MÁ. Caldú X, et al. Among authors: hernan i. Eur Eat Disord Rev. 2019 Jul;27(4):401-409. doi: 10.1002/erv.2665. Epub 2019 Feb 13. Eur Eat Disord Rev. 2019. PMID: 30761671

4

Detection of novel mutations that cause autosomal dominant retinitis pigmentosa in candidate genes by long-range PCR amplification and next-generation sequencing.

de Sousa Dias M, Hernan I, Pascual B, Borràs E, Mañé B, Gamundi MJ, Carballo M. de Sousa Dias M, et al. Among authors: hernan i. Mol Vis. 2013;19:654-64. Epub 2013 Mar 21. Mol Vis. 2013. PMID: 23559859 Free PMC article.

5

Mutations in the pre-mRNA splicing-factor genes PRPF3, PRPF8, and PRPF31 in Spanish families with autosomal dominant retinitis pigmentosa.

Martínez-Gimeno M, Gamundi MJ, Hernan I, Maseras M, Millá E, Ayuso C, García-Sandoval B, Beneyto M, Vilela C, Baiget M, Antiñolo G, Carballo M. Martínez-Gimeno M, et al. Among authors: hernan i. Invest Ophthalmol Vis Sci. 2003 May;44(5):2171-7. doi: 10.1167/iovs.02-0871. Invest Ophthalmol Vis Sci. 2003. PMID: 12714658

6

Sequence variations in the retinal fascin FSCN2 gene in a Spanish population with autosomal dominant retinitis pigmentosa or macular degeneration.

Gamundi MJ, Hernan I, Maseras M, Baiget M, Ayuso C, Borrego S, Antiñolo G, Millán JM, Valverde D, Carballo M. Gamundi MJ, et al. Among authors: hernan i. Mol Vis. 2005 Nov 2;11:922-8. Mol Vis. 2005. PMID: 16280978 Free article.

7

Three novel and the common Arg677Ter RP1 protein truncating mutations causing autosomal dominant retinitis pigmentosa in a Spanish population.

Gamundi MJ, Hernan I, Martínez-Gimeno M, Maseras M, García-Sandoval B, Ayuso C, Antiñolo G, Baiget M, Carballo M. Gamundi MJ, et al. Among authors: hernan i. BMC Med Genet. 2006 Apr 5;7:35. doi: 10.1186/1471-2350-7-35. BMC Med Genet. 2006. PMID: 16597330 Free PMC article.

8

Novel LMX1B mutation in familial nail-patella syndrome with variable expression of open angle glaucoma.

Millá E, Hernan I, Gamundi MJ, Martínez-Gimeno M, Carballo M. Millá E, et al. Among authors: hernan i. Mol Vis. 2007 Apr 27;13:639-48. Mol Vis. 2007. PMID: 17515884 Free PMC article.

9

High prevalence of mutations in peripherin/RDS in autosomal dominant macular dystrophies in a Spanish population.

Gamundi MJ, Hernan I, Muntanyola M, Trujillo MJ, García-Sandoval B, Ayuso C, Baiget M, Carballo M. Gamundi MJ, et al. Among authors: hernan i. Mol Vis. 2007 Jun 28;13:1031-7. Mol Vis. 2007. PMID: 17653047 Free PMC article.

10

Transcriptional expression of cis-acting and trans-acting splicing mutations cause autosomal dominant retinitis pigmentosa.

Gamundi MJ, Hernan I, Muntanyola M, Maseras M, López-Romero P, Alvarez R, Dopazo A, Borrego S, Carballo M. Gamundi MJ, et al. Among authors: hernan i. Hum Mutat. 2008 Jun;29(6):869-78. doi: 10.1002/humu.20747. Hum Mutat. 2008. PMID: 18412284

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