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DNA methylation and obesity traits: An epigenome-wide association study. The REGICOR study

Epigenetics, 2017-10, Vol.12 (10), p.909-916

2017

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Pathogenesis of coronary artery disease: focus on genetic risk factors and identification of genetic variants

Application of clinical genetics, 2014-01, Vol.7 (default), p.15-32

2014

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Genetically Confirmed Familial Hypercholesterolemia in Patients With Acute Coronary Syndrome

Journal of the American College of Cardiology, 2017-10, Vol.70 (14), p.1732-1740

2017

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Identification of a new locus and validation of previously reported loci showing differential methylation associated with smoking. The REGICOR study

Epigenetics, 2015-12, Vol.10 (12), p.1156-1165

2015

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Analysis of gene-gene interactions among common variants in candidate cardiovascular genes in coronary artery disease

PloS one, 2015-02, Vol.10 (2), p.e0117684-e0117684

2015

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Cardiovascular Risk Factors and Ischemic Heart Disease: Is the Confluence of Risk Factors Greater Than the Parts? A Genetic Approach

Circulation. Cardiovascular genetics, 2016-06, Vol.9 (3), p.279

2016

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Hypothesis-based analysis of gene-gene interactions and risk of myocardial infarction

PloS one, 2012-08, Vol.7 (8), p.e41730-e41730

2012

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Qualitative assessment of previous evidence and an updated meta-analysis confirms lack of association between the ESR1 rs2234693 ( PvuII ) variant and coronary heart disease in men and women

Atherosclerosis, 2009-12, Vol.207 (2), p.480-486

2009

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Post-genomic update on a classical candidate gene for coronary artery disease: ESR1

Circulation. Cardiovascular genetics, 2011-12, Vol.4 (6), p.647

2011

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Additive effect of multiple genetic variants on the risk of coronary artery disease

Revista española de cardiologia, 2010-08, Vol.63 (8), p.925-933

2010

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Update in Cardiology: Vascular Risk and Cardiac Rehabilitation

Revista española de cardiología (English ed.), 2014-03, Vol.67 (3), p.203-210

2014

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Weighted Multi-marker Genetic Risk Scores for Incident Coronary Heart Disease among Individuals of African, Latino and East-Asian Ancestry

Scientific reports, 2018-05, Vol.8 (1), p.6853-13, Article 6853

2018

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Identification and validation of seven new loci showing differential DNA methylation related to serum lipid profile: an epigenome-wide approach. The REGICOR study

Human molecular genetics, 2016-10, Vol.25 (20), p.4556-4565

2016

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Assessment of the value of a genetic risk score in improving the estimation of coronary risk

Atherosclerosis, 2012-06, Vol.222 (2), p.456-463

2012

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Temas de actualidad en cardiología: riesgo vascular y rehabilitación cardiaca

Revista española de cardiologia, 2014-03, Vol.67 (3), p.203-210

2014

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Meta-analyses of the association between cytochrome CYP2C19 loss- and gain-of-function polymorphisms and cardiovascular outcomes in patients with coronary artery disease treated with clopidogrel

Heart, 2012-01, Vol.98 (2), p.100-108

2012

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Corrigendum. Identification of a new locus and validation of previously reported loci showing differential methylation associated with smoking. The REGICOR study

Epigenetics, 2016, Vol.11 (2), p.174-174

2016

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Effectiveness, safety and discontinuation rates of bictegravir/emtricitabine/tenofovir alafenamide (BIC/FTC/TAF) in people with HIV using real-world data: a systematic review and meta-analysis

Journal of antimicrobial chemotherapy, 2024-05, Vol.79 (8), p.1775

2024

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Efecto aditivo de diferentes variantes genéticas en el riesgo de cardiopatía isquémica

Revista española de cardiologia, 2010-08, Vol.63 (8), p.925-933

2010

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DNA Methylation and High-Density Lipoprotein Functionality-Brief Report: The REGICOR Study (Registre Gironi del Cor)

Arteriosclerosis, thrombosis, and vascular biology, 2017-03, Vol.37 (3), p.567

2017

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Abstract P105: Weighted Multi-marker Genetic Risk Scores for Incident CHD Among Individuals of African, Latino or East-Asian Ancestry

Circulation (New York, N.Y.), 2017-03, Vol.135 (suppl_1)

2017

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IMPROVING THE CLINICAL UTILITY OF THE FRAMINGHAM RISK FUNCTION FOR INCIDENT CORONARY HEART DISEASE BY THE ADDITION OF WEIGHTED MULTI-MARKER GENETIC RISK SCORES IN MORE THAN 40,000 INDIVIDUALS OF CAUCASIAN ANCESTRY

Journal of the American College of Cardiology, 2016-04, Vol.67 (13), p.468-468

2016

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Additive Effects of Multiple Genetic Variants on the Risk of Coronary Artery Disease

Revista española de cardiología (English ed.), 2010, Vol.63 (8), p.925-933

2010

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Clinical Utility of Multimarker Genetic Risk Scores for Prediction of Incident Coronary Heart Disease: A Cohort Study Among Over 51 000 Individuals of European Ancestry

Circulation. Cardiovascular genetics, 2016-12, Vol.9 (6), p.531

2016

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Genetics and Cardiovascular Risk Prediction: A Step Toward Personalized Medicine?

Current cardiovascular risk reports, 2013-02, Vol.7 (1), p.33-45

2013

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DNA methylation and obesity traits: An epigenome-wide association study. The REGICOR study

Pathogenesis of coronary artery disease: focus on genetic risk factors and identification of genetic variants

Genetically Confirmed Familial Hypercholesterolemia in Patients With Acute Coronary Syndrome

Identification of a new locus and validation of previously reported loci showing differential methylation associated with smoking. The REGICOR study

Analysis of gene-gene interactions among common variants in candidate cardiovascular genes in coronary artery disease

Cardiovascular Risk Factors and Ischemic Heart Disease: Is the Confluence of Risk Factors Greater Than the Parts? A Genetic Approach

Hypothesis-based analysis of gene-gene interactions and risk of myocardial infarction

Qualitative assessment of previous evidence and an updated meta-analysis confirms lack of association between the ESR1 rs2234693 ( PvuII ) variant and coronary heart disease in men and women

Post-genomic update on a classical candidate gene for coronary artery disease: ESR1

Additive effect of multiple genetic variants on the risk of coronary artery disease

Update in Cardiology: Vascular Risk and Cardiac Rehabilitation

Weighted Multi-marker Genetic Risk Scores for Incident Coronary Heart Disease among Individuals of African, Latino and East-Asian Ancestry

Identification and validation of seven new loci showing differential DNA methylation related to serum lipid profile: an epigenome-wide approach. The REGICOR study

Assessment of the value of a genetic risk score in improving the estimation of coronary risk

Temas de actualidad en cardiología: riesgo vascular y rehabilitación cardiaca

Meta-analyses of the association between cytochrome CYP2C19 loss- and gain-of-function polymorphisms and cardiovascular outcomes in patients with coronary artery disease treated with clopidogrel

Corrigendum. Identification of a new locus and validation of previously reported loci showing differential methylation associated with smoking. The REGICOR study

Effectiveness, safety and discontinuation rates of bictegravir/emtricitabine/tenofovir alafenamide (BIC/FTC/TAF) in people with HIV using real-world data: a systematic review and meta-analysis

Efecto aditivo de diferentes variantes genéticas en el riesgo de cardiopatía isquémica

DNA Methylation and High-Density Lipoprotein Functionality-Brief Report: The REGICOR Study (Registre Gironi del Cor)

Abstract P105: Weighted Multi-marker Genetic Risk Scores for Incident CHD Among Individuals of African, Latino or East-Asian Ancestry

IMPROVING THE CLINICAL UTILITY OF THE FRAMINGHAM RISK FUNCTION FOR INCIDENT CORONARY HEART DISEASE BY THE ADDITION OF WEIGHTED MULTI-MARKER GENETIC RISK SCORES IN MORE THAN 40,000 INDIVIDUALS OF CAUCASIAN ANCESTRY

Additive Effects of Multiple Genetic Variants on the Risk of Coronary Artery Disease

Clinical Utility of Multimarker Genetic Risk Scores for Prediction of Incident Coronary Heart Disease: A Cohort Study Among Over 51 000 Individuals of European Ancestry

Genetics and Cardiovascular Risk Prediction: A Step Toward Personalized Medicine?

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