Publicaciones en las que colabora con ELIECER COTO GARCIA (23)

2021

  1. The APOB polymorphism rs1801701 A/G (p.R3638Q) is an independent risk factor for early-onset coronary artery disease: Data from a Spanish cohort

    Nutrition, Metabolism and Cardiovascular Diseases, Vol. 31, Núm. 5, pp. 1564-1568

2020

  1. Characterization of left ventricular non-compaction cardiomyopathy

    Journal of Clinical Medicine, Vol. 9, Núm. 8, pp. 1-16

  2. Clinical implications and gender differences of kcnq1 p.Gly168arg pathogenic variant in long qt syndrome

    Journal of Clinical Medicine, Vol. 9, Núm. 12, pp. 1-12

2018

  1. Variants in cardiac GATA genes associated with bicuspid aortic valve

    European Journal of Clinical Investigation, Vol. 48, Núm. 12

2017

  1. Rare genetic variants in GATA transcription factors in patients with hypertrophic cardiomyopathy

    Journal of Investigative Medicine, Vol. 65, Núm. 5, pp. 926-934

2016

  1. KCNQ1 gene variants in the risk for type 2 diabetes and impaired renal function in the Spanish Renastur cohort

    Molecular and Cellular Endocrinology, Vol. 427, pp. 86-91

2014

  1. Association of matrix Gla protein gene functional polymorphisms with loss of bone mineral density and progression of aortic calcification

    Osteoporosis International, Vol. 25, Núm. 4, pp. 1237-1246

2013

  1. A common APOE polymorphism is an independent risk factor for reduced glomerular filtration rate in the Spanish RENASTUR cohort

    CardioRenal Medicine, Vol. 3, Núm. 2, pp. 113-119

  2. Association between a MYH9 polymorphism (rs3752462) and renal function in the Spanish RENASTUR cohort

    Gene, Vol. 520, Núm. 1, pp. 73-76

2012

  1. New polymorphisms in human MEF2C gene as potential modifier of hypertrophic cardiomyopathy

    Molecular Biology Reports, Vol. 39, Núm. 9, pp. 8777-8785

2011

  1. Mitochondrial DNA and TFAM gene variation in early-onset myocardial infarction: Evidence for an association to haplogroup H

    Mitochondrion, Vol. 11, Núm. 1, pp. 176-181

  2. TGFBR2 gene mutational spectrum in aortic pathology

    Journal of the American College of Cardiology

2010

  1. Polimorfismos de metaloproteasas y válvula aórtica bicúspide

    Revista Espanola de Cardiologia

  2. Residue 826 in the calcium-sensing receptor is implicated in the response to calcium and to R-568 calcimimetic compound

    Calcified Tissue International, Vol. 86, Núm. 3, pp. 227-233

2009

  1. Lack of association between endothelin-1 gene variants and myocardial infarction

    Journal of Atherosclerosis and Thrombosis, Vol. 16, Núm. 4, pp. 388-395

  2. Matrix metalloproteinase 1 promoter polymorphisms and risk of myocardial infarction: A case-control study in a Spanish population

    Coronary Artery Disease, Vol. 20, Núm. 6, pp. 383-386

  3. Mutation analysis of the myocyte enhancer factor 2a gene (MEF2A) in patients with left ventricular hypertrophy/hypertrophic cardiomyopathy

    American Journal of Medical Genetics, Part A

2008

  1. Mitochondrial transcription factor A (TFAM) gene variation in Parkinson's disease

    Neuroscience Letters, Vol. 432, Núm. 1, pp. 79-82

  2. Mitochondrial transcription factor a (TFAM) gene variation and risk of late-onset Alzheimer's disease

    Journal of Alzheimer's Disease, Vol. 13, Núm. 3, pp. 275-280

  3. Mitochondrial transcription factors TFA, TFB1 and TFB2: A search for DNA variants/haplotypes and the risk of cardiac hypertrophy

    Disease Markers, Vol. 25, Núm. 3, pp. 131-139