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Mutations in filamin C cause a new form of familial hypertrophic cardiomyopathy

Nature communications, 2014-10, Vol.5 (1), p.5326-5326, Article 5326

2014

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

Molecular and cellular endocrinology, 2016-05, Vol.427, p.86-91

2016

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Genetic Screening of a Large Panel of Genes Associated with Cardiac Disease in a Spanish Heart Transplanted Cohort

Cardiogenetics, 2022-06, Vol.12 (2), p.198-205

2022

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The Ups and Downs of Genetic Diagnosis of Hypertrophic Cardiomyopathy

Revista española de cardiología (English ed.), 2016-01, Vol.69 (1), p.61-68

2016

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Profile of microRNAs in the plasma of hypertrophic cardiomyopathy patients compared to healthy controls

International journal of cardiology, 2013-09, Vol.167 (6), p.3075-3076

2013

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Resequencing the Whole MYH7 Gene (Including the Intronic, Promoter, and 3′ UTR Sequences) in Hypertrophic Cardiomyopathy

The Journal of molecular diagnostics : JMD, 2012-09, Vol.14 (5), p.518-524

2012

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Mitochondrial haplogroup T is negatively associated with the status of elite endurance athlete

Mitochondrion, 2007-09, Vol.7 (5), p.354-357

2007

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

Mitochondrion, 2011-01, Vol.11 (1), p.176-181

2011

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Functional polymorphisms in genes of the Angiotensin and Serotonin systems and risk of hypertrophic cardiomyopathy: AT1R as a potential modifier

Journal of translational medicine, 2010-07, Vol.8 (1), p.64-64, Article 64

2010

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Genetic variation in the renin-angiotensin system and athletic performance

European journal of applied physiology, 2000-05, Vol.82 (1-2), p.117-120

2000

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Gene variants in the NF-KB pathway (NFKB1, NFKBIA, NFKBIZ) and their association with type 2 diabetes and impaired renal function

Human immunology, 2018-06, Vol.79 (6), p.494-498

2018

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Role of the CDKN1A/p21, CDKN1C/p57, and CDKN2A/p16 Genes in the Risk of Atherosclerosis and Myocardial Infarction

Cell cycle (Georgetown, Tex.), 2007-03, Vol.6 (5), p.620-625

2007

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Hypertrophic cardiomyopathy: Low frequency of Mutations in the β-myosin heavy chain (MYH7) and cardiac troponin T (TNNT2) genes among Spanish patients

Clinical chemistry (Baltimore, Md.), 2003-08, Vol.49 (8), p.1279-1285

2003

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Mutation Analysis of the Main Hypertrophic Cardiomyopathy Genes Using Multiplex Amplification and Semiconductor Next-Generation Sequencing

Circulation Journal, 2014/11/25, Vol.78(12), pp.2963-2971

2014

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Hypertrophic cardiomyopathy and left ventricular non-compaction: Different manifestations of the same cardiomyopathy spectrum?

International journal of cardiology, 2015-07, Vol.190, p.26-28

2015

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Gene variants in the NF-KB pathway (NFKB1, NFKBIA, NFKBIZ) and risk for early-onset coronary artery disease

Immunology letters, 2019-04, Vol.208, p.39-43

2019

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5-Hydroxytryptamine 5-HT2A receptor and 5-hydroxytryptamine transporter polymorphisms in acute myocardial infarction

Clinical science (1979), 2003-03, Vol.104 (3), p.241

2003

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Lack of Association between Endothelin-1 Gene Variants and Myocardial Infarction

Journal of Atherosclerosis and Thrombosis, 2009, Vol.16(4), pp.388-395

2009

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Luces y sombras en el diagnóstico genético de la miocardiopatía hipertrófica

Revista española de cardiologia, 2016-01, Vol.69 (1), p.61-68

2016

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Genetic variation at the long noncoding RNA H19 gene is associated with the risk of hypertrophic cardiomyopathy

Epigenomics, 2018-07, Vol.10 (7), p.865-873

2018

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Diagnostic impact of genetic testing in hypertrophic cardiomyopathy: The story of two families

International journal of cardiology, 2016-02, Vol.205, p.161-162

2016

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Left Ventricle Non-compaction: the still misdiagnosed cardiomyopathy

International journal of cardiology, 2016-11, Vol.223, p.420-421

2016

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Differential methylation of lncRNA KCNQ1OT1 promoter polymorphism was associated with symptomatic cardiac long QT

Epigenomics, 2017-08, Vol.9 (8), p.1049-1057

2017

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Synergistic Effect between Apolipoprotein E and Angiotensinogen Gene Polymorphisms in the Risk for Early Myocardial Infarction

Clinical chemistry (Baltimore, Md.), 2000-12, Vol.46 (12), p.1910-1915

2000

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Profile of MicroRNAs Differentially Produced in Hearts from Patients with Hypertrophic Cardiomyopathy and Sarcomeric Mutations

Clinical chemistry (Baltimore, Md.), 2011-11, Vol.57 (11), p.1614-1616

2011

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Mutations in filamin C cause a new form of familial hypertrophic cardiomyopathy

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

Genetic Screening of a Large Panel of Genes Associated with Cardiac Disease in a Spanish Heart Transplanted Cohort

The Ups and Downs of Genetic Diagnosis of Hypertrophic Cardiomyopathy

Profile of microRNAs in the plasma of hypertrophic cardiomyopathy patients compared to healthy controls

Resequencing the Whole MYH7 Gene (Including the Intronic, Promoter, and 3′ UTR Sequences) in Hypertrophic Cardiomyopathy

Mitochondrial haplogroup T is negatively associated with the status of elite endurance athlete

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

Functional polymorphisms in genes of the Angiotensin and Serotonin systems and risk of hypertrophic cardiomyopathy: AT1R as a potential modifier

Genetic variation in the renin-angiotensin system and athletic performance

Gene variants in the NF-KB pathway (NFKB1, NFKBIA, NFKBIZ) and their association with type 2 diabetes and impaired renal function

Role of the CDKN1A/p21, CDKN1C/p57, and CDKN2A/p16 Genes in the Risk of Atherosclerosis and Myocardial Infarction

Hypertrophic cardiomyopathy: Low frequency of Mutations in the β-myosin heavy chain (MYH7) and cardiac troponin T (TNNT2) genes among Spanish patients

Mutation Analysis of the Main Hypertrophic Cardiomyopathy Genes Using Multiplex Amplification and Semiconductor Next-Generation Sequencing

Hypertrophic cardiomyopathy and left ventricular non-compaction: Different manifestations of the same cardiomyopathy spectrum?

Gene variants in the NF-KB pathway (NFKB1, NFKBIA, NFKBIZ) and risk for early-onset coronary artery disease

5-Hydroxytryptamine 5-HT2A receptor and 5-hydroxytryptamine transporter polymorphisms in acute myocardial infarction

Lack of Association between Endothelin-1 Gene Variants and Myocardial Infarction

Luces y sombras en el diagnóstico genético de la miocardiopatía hipertrófica

Genetic variation at the long noncoding RNA H19 gene is associated with the risk of hypertrophic cardiomyopathy

Diagnostic impact of genetic testing in hypertrophic cardiomyopathy: The story of two families

Left Ventricle Non-compaction: the still misdiagnosed cardiomyopathy

Differential methylation of lncRNA KCNQ1OT1 promoter polymorphism was associated with symptomatic cardiac long QT

Synergistic Effect between Apolipoprotein E and Angiotensinogen Gene Polymorphisms in the Risk for Early Myocardial Infarction

Profile of MicroRNAs Differentially Produced in Hearts from Patients with Hypertrophic Cardiomyopathy and Sarcomeric Mutations

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