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Julián R. Reguero

Observed names: J R Reguero, J Rodríguez Reguero, J. R. Reguero, J. Rodriguez Reguero, J.R. Reguero, J.Rodriguez Reguero, Julian R Reguero, Julian R. Reguero, Julián R Reguero, Julián R. Reguero, Julián Rodriguez Reguero, Julián R Reguero, Julián R. REGUERO, Julián R. Reguro, Julián Rodríguez Reguero
Observed institutions: Universidad de Oviedo, Hospital Universitario Central de Asturias, Hospital Universitario De Cabueñes, Foundation for the Promotion of Applied Scientific Research and Technology in Asturias, Instituto de Investigación Sanitaria del Principado de Asturias, Fundación Renal Española, Hospital Vital Álvarez-Buylla
OpenAlex ID: A5111913368
Genetic variation in the renin-angiotensin system and athletic performance
2000 · Ruth Alvarez, Nicolás Terrados, et al. · European Journal of Applied Physiology · 198
Mutations in filamin C cause a new form of familial hypertrophic cardiomyopathy
2014 · Rafael Valdés-Mas, Ana Gutiérrez-Fernández, et al. · Nature Communications · 193
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Association between the NOS3 (−786 T/C) and the ACE (I/D) DNA Genotypes and Early Coronary Artery Disease
2001 · Ruth Álvarez, Pelayo González, et al. · Nitric Oxide · 92
Screening of the Filamin C Gene in a Large Cohort of Hypertrophic Cardiomyopathy Patients
2017 · Juan Gómez, Rebeca Lorca, et al. · Circulation Cardiovascular Genetics · 90
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Synergistic Effect between Apolipoprotein E and Angiotensinogen Gene Polymorphisms in the Risk for Early Myocardial Infarction
2000 · Alberto Batalla, Ruth Alvarez, et al. · Clinical Chemistry · 71
5-Hydroxytryptamine 5-HT2A receptor and 5-hydroxytryptamine transporter polymorphisms in acute myocardial infarction
2003 · Eliecer COTO, Julián R. REGUERO, et al. · Clinical Science · 70
Hypertrophic Cardiomyopathy: Low Frequency of Mutations in the β-Myosin Heavy Chain (MYH7) and Cardiac Troponin T (TNNT2) Genes among Spanish Patients
2003 · Mónica Garcı́a-Castro, Julián R Reguero, et al. · Clinical Chemistry · 63
Mitochondrial DNA haplogroups in Spanish patients with hypertrophic cardiomyopathy
2005 · Mónica G. Castro, Cecilia Huerta, et al. · International Journal of Cardiology · 62
Mutation Analysis of the Main Hypertrophic Cardiomyopathy Genes Using Multiplex Amplification and Semiconductor Next-Generation Sequencing
2014 · Juan Gómez, Julian R. Reguero, et al. · Circulation Journal · 60
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Mitochondrial haplogroup T is negatively associated with the status of elite endurance athlete
2007 · Mónica G. Castro, Nicolás Terrados, et al. · Mitochondrion · 60
Espectro mutacional de los genes sarcoméricos MYH7, MYBPC3, TNNT2, TNNI3 y TPM1 en pacientes con miocardiopatía hipertrófica
2009 · Mónica García-Castro, Eliecer Coto, et al. · Revista Española de Cardiología · 59
Mutations in Sarcomeric Genes MYH7, MYBPC3, TNNT2, TNNI3, and TPM1 in Patients With Hypertrophic Cardiomyopathy
2009 · Mónica García-Castro, Eliecer Coto, et al. · Revista Española de Cardiología (English Edition) · 56
Apolipoprotein A1 Gene Polymorphisms and Risk of Early Coronary Disease
1998 · Julián R. Reguero, Gustavo Iglesias Cubero, et al. · Cardiology · 48
Gene variants in the NF-KB pathway (NFKB1, NFKBIA, NFKBIZ) and their association with type 2 diabetes and impaired renal function
2018 · Eliecer Coto, Carmen Díaz-Corte, et al. · Human Immunology · 47
Mitochondrial DNA and TFAM gene variation in early-onset myocardial infarction: Evidence for an association to haplogroup H
2010 · María Palacín, Victoria Alvarez, et al. · Mitochondrion · 45
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Role of the CDKN1A/p21, CDKN1C/p57, and CDKN2A/p16 Genes in the Risk of Atherosclerosis and Myocardial Infarction
2007 · Isabel Rodríguez, Eliecer Coto, et al. · Cell Cycle · 43
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Gene variants in the NF-KB pathway (NFKB1, NFKBIA, NFKBIZ) and risk for early-onset coronary artery disease
2019 · Eliecer Coto, Julián R. Reguero, et al. · Immunology Letters · 42
Differential Methylation of lncRNA KCNQ1OT1 Promoter Polymorphism was Associated with Symptomatic Cardiac Long QT
2017 · Eliecer Coto, David Calvo, et al. · Epigenomics · 31
Profile of MicroRNAs Differentially Produced in Hearts from Patients with Hypertrophic Cardiomyopathy and Sarcomeric Mutations
2011 · María Palacín, Julián R Reguero, et al. · Clinical Chemistry · 31
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A functional Sp1/Egr1‐tandem repeat polymorphism in the 5‐lipoxygenase gene is not associated with myocardial infarction
2007 · P. González, J. R. Reguero, et al. · International Journal of Immunogenetics · 27
Genetic Variation at the Long Noncoding RNA H19 Gene is Associated with the Risk of Hypertrophic Cardiomyopathy
2018 · Juan Gómez, Rebeca Lorca, et al. · Epigenomics · 26
Hypertrophic cardiomyopathy linked to homozygosity for a new mutation in the myosin-binding protein C gene (A627V) suggests a dosage effect
2004 · Mónica García-Castro, Julián R. Reguero, et al. · International Journal of Cardiology · 26
KCNQ1 gene variants in the risk for type 2 diabetes and impaired renal function in the Spanish Renastur cohort
2016 · Cristina Riobello, Juan Gómez, et al. · Molecular and Cellular Endocrinology · 24
Variation in the lipoprotein receptor-related protein, α2-macroglobulin and lipoprotein receptor-associatedprotein genes in relation to plasma lipid levels and riskof early myocardial infarction
2002 · Pelayo González, Ruth Álvarez, et al. · Coronary Artery Disease · 24
Functional polymorphisms in genes of the Angiotensin and Serotonin systems and risk of hypertrophic cardiomyopathy: AT1R as a potential modifier
2010 · Eliecer Coto, María Palacín, et al. · Journal of Translational Medicine · 23
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Works count: 73
Citation count: 1,875
H-index: 24
I10-index: 41
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