Juan Gómez

E. Coto, D. Calvo, J. Rubín, 2018, Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology.

An elderly Jervell and Lange‐Nielsen patient heterozygous compound for two new KCNQ1 mutations

E. Coto, D. Calvo, B. Alonso, 2017, American journal of medical genetics. Part A.

The Cw6 and late-cornified envelope genotype plays a significant role in anti-tumor necrosis factor response among psoriatic patients.

E. Coto, P. Coto-Segura, J. Santos-Juanes, 2015, Pharmacogenetics and genomics.

Insights Into Hypertrophic Cardiomyopathy Evaluation Through Follow-up of a Founder Pathogenic Variant.

E. Coto, V. León, I. Pascual, 2019, Revista espanola de cardiologia.

Late-onset Alzheimer's disease is associated with mitochondrial DNA 7028C/haplogroup H and D310 poly-C tract heteroplasmy

V. Álvarez, E. Coto, C. Martínez, 2011, neurogenetics.

Association of the Genetic Variation in the Long Non-Coding RNA FENDRR with the Risk of Developing Hypertrophic Cardiomyopathy

E. Coto, R. Lorca, J. Rodríguez-Reguero, 2022, Life.

Next generation sequencing of the NOTCH3 gene in a cohort of pulmonary hypertension patients.

E. Coto, C. Morís, C. Alvarez, 2016, International journal of cardiology.

Common European mitochondrial haplogroups in the risk for psoriasis and psoriatic arthritis.

V. Álvarez, E. Coto, P. Coto-Segura, 2012, Genetic testing and molecular biomarkers.

Mutation analysis of the main hypertrophic cardiomyopathy genes using multiplex amplification and semiconductor next-generation sequencing.

V. Álvarez, E. Coto, María Martín, 2014, Circulation journal : official journal of the Japanese Circulation Society.

Non Optical Semi-Conductor Next Generation Sequencing of the Main Cardiac QT-Interval Duration Genes in Pooled DNA Samples

V. Álvarez, E. Coto, C. Morís, 2014, Journal of Cardiovascular Translational Research.

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

V. Álvarez, E. Coto, F. Ortega, 2013, Gene.

Clinical Evaluation of Patients with Genetically Confirmed Familial Hypercholesterolemia

E. Coto, C. Martínez-Faedo, Lorena Suárez-Gutiérrez, 2023, Journal of clinical medicine.

Opportunistic Genetic Screening for Familial Hypercholesterolemia in Heart Transplant Patients

E. Coto, P. Avanzas, I. Pascual, 2023, Journal of clinical medicine.

A Next-Generation Sequencing of the NOTCH3 and HTRA1 Genes in CADASIL Patients

E. Coto, B. Alonso, S. Iglesias, 2015, Journal of Molecular Neuroscience.

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

E. Coto, H. Gil-Peña, D. Calvo, 2017, Epigenomics.

Effect of mitochondrial, APOE. ACE and NOS3 gene polymorphisms on cardiovascular risk factors among the Vaqueiros de Alzada, a Northern Spain human isolate

E. Coto, Juan Gómez, A. Corao, 2014, Annals of human biology.

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

E. Coto, P. Coto-Segura, C. López-Larrea, 2018, Human immunology.

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

V. Álvarez, E. Coto, E. Delgado, 2016, Molecular and Cellular Endocrinology.

Renal malignancies in the elderly

Juan Gómez, Juan C. Hernandez, M. U. Avisrror, 1987 .

Screening of the Filamin C Gene in a Large Cohort of Hypertrophic Cardiomyopathy Patients

V. Álvarez, E. Coto, P. Avanzas, 2017, Circulation. Cardiovascular genetics.

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

X. Puente, R. Valdés-Mas, Diana A. Puente, 2014, Nature Communications.

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

E. Coto, P. Avanzas, María Martín, 2018, Epigenomics.

Next generation sequencing search for uromodulin gene variants related with impaired renal function

E. Coto, S. Tranche, B. Alonso, 2015, Molecular Biology Reports.

The donor ABCB1 (MDR-1) C3435T polymorphism is a determinant of the graft glomerular filtration rate among tacrolimus treated kidney transplanted patients

E. Coto, C. López-Larrea, B. Tavira, 2015, Journal of Human Genetics.

Variant-genetic and transcript-expression analysis showed a role for the chemokine-receptor CCR5 in COVID-19 severity

V. Álvarez, E. Coto, H. Gil-Peña, 2021, International Immunopharmacology.

Distal renal tubular acidosis. Clinical manifestations in patients with different underlying gene mutations

E. Coto, F. Santos, H. Gil-Peña, 2018, Pediatric Nephrology.

Primary distal renal tubular acidosis: novel findings in patients studied by next-generation sequencing

E. Coto, F. Santos, H. Gil-Peña, 2016, Pediatric Research.

The FCGR2A rs1801274 polymorphism was associated with the risk of death among COVID-19 patients

V. Álvarez, E. Coto, E. Cuesta-Llavona, 2022, Clinical Immunology.

A labor and cost effective next generation sequencing of PKHD1 in autosomal recessive polycystic kidney disease patients.

V. Álvarez, E. Coto, A. Plasencia, 2015, Gene.

A Common APOE Polymorphism Is an Independent Risk Factor for Reduced Glomerular Filtration Rate in the Spanish RENASTUR Cohort

V. Álvarez, E. Coto, F. Ortega, 2013, Cardiorenal Medicine.

Genetic Variation in the H19-IGF2 Cluster Might Confer Risk of Developing Impaired Renal Function.

E. Coto, H. Gil-Peña, P. Coto-Segura, 2018, DNA and cell biology.

A Working-Day Evaluation of Dyslipidaemia in a Spanish Population (JADE Study)

Juan Gómez, J. Martínez, F. Babín, 2000 .

Effect of the FTO rs9930506 Polymorphism on the Main Comorbidities of the Cardiorenal Metabolic Syndrome in an Elderly Spanish Cohort

E. Coto, B. Tavira, S. Tranche, 2014, Cardiorenal Medicine.

Clinical Implications and Gender Differences of KCNQ1 p.Gly168Arg Pathogenic Variant in Long QT Syndrome

E. Coto, P. Avanzas, I. Pascual, 2020, Journal of clinical medicine.

Spectral Analysis of the QT Interval Increases the Prediction Accuracy of Clinical Variables in Brugada Syndrome

E. Coto, D. Calvo, J. Rubín, 2019, Journal of clinical medicine.

Time-dependent responses to provocative testing with flecainide in the diagnosis of Brugada syndrome.

E. Coto, J. M. García-Ruíz, D. Calvo, 2015, Heart rhythm.

The Ups and Downs of Genetic Diagnosis of Hypertrophic Cardiomyopathy.

E. Coto, J. Reguero, Juan Gómez, 2016, Revista espanola de cardiologia.

Mitochondrial DNA haplogroups and risk of new-onset diabetes among tacrolimus-treated renal transplanted patients.

E. Coto, E. Ruiz-Pesini, L. Llobet, 2014, Gene.

Association between the IL17RA rs4819554 polymorphism and reduced renal filtration rate in the Spanish RENASTUR cohort.

E. Coto, A. Ortiz, P. Coto-Segura, 2015, Human immunology.

Lack of association between SNPsrs8176719 (O blood group) and COVID‐19: Data from Spanish age matched patients and controls

E. Coto, Juan Gómez, G. Albaiceta, 2020, Transfusion.

CDKAL1 gene variants affect the anti-TNF response among Psoriasis patients.

E. Coto, P. Coto-Segura, J. Santos-Juanes, 2015, International immunopharmacology.

Mitochondrial Heteroplasmy as a Marker for Premature Coronary Artery Disease: Analysis of the Poly-C Tract of the Control Region Sequence

E. Coto, P. Avanzas, I. Pascual, 2023, Journal of clinical medicine.

A new SLC12A3 founder mutation (p.Val647Met) in Gitelman's syndrome patients of Roma ancestry.

E. Coto, H. Gil-Peña, R. Vargas-Poussou, 2017, Nefrologia : publicacion oficial de la Sociedad Espanola Nefrologia.

A labor- and cost-effective non-optical semiconductor (Ion Torrent) next-generation sequencing of the SLC12A3 and CLCNKA/B genes in Gitelman’s syndrome patients

V. Álvarez, E. Coto, F. Santos, 2014, Journal of Human Genetics.

ABCB1 (MDR-1) pharmacogenetics of tacrolimus in renal transplanted patients: a Next Generation Sequencing approach

E. Coto, M. Arias, C. López-Larrea, 2015, Clinical chemistry and laboratory medicine.

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

E. Coto, J. Cannata-Andía, María Martín, 2017, Journal of Investigative Medicine.

Chromosome Y Haplogroup R Was Associated with the Risk of Premature Myocardial Infarction with ST-Elevation: Data from the CholeSTEMI Registry

E. Coto, P. Avanzas, I. Pascual, 2023, Journal of clinical medicine.

Compound heterozygosity for PTPN11 variants in a subject with Noonan syndrome provides insights into the mechanism of SHP2‐related disorders

E. Coto, M. Tartaglia, G. Bocchinfuso, 2020, Clinical genetics.

KCNH2 p.Gly262AlafsTer98: A New Threatening Variant Associated with Long QT Syndrome in a Spanish Cohort

E. Coto, J. Rubín, I. Pascual, 2022, Life.

Spectrum of Mutations in Hypertrophic Cardiomyopathy Genes Among Tunisian Patients.

E. Coto, S. Kachboura, I. Kammoun, 2016, Genetic testing and molecular biomarkers.

Common and rare CARD14 gene variants affect the antitumour necrosis factor response among patients with psoriasis

E. Coto, J. Gómez, P. Coto-Segura, 2016, The British journal of dermatology.

Next generation sequencing search for uromodulin gene variants related with impaired renal function

E. Coto, S. Tranche, B. Alonso, 2015, Molecular Biology Reports.

Capillary Electrophoresis of PCR fragments with 5’-labelled primers for testing the SARS-Cov-2

V. Álvarez, E. Coto, E. Cuesta-Llavona, 2020, bioRxiv.

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

V. Álvarez, E. Coto, E. Delgado, 2016, Molecular and Cellular Endocrinology.

Primary distal renal tubular acidosis: novel findings in patients studied by next-generation sequencing

E. Coto, F. Santos, H. Gil-Peña, 2018, Pediatric Research.

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

V. Álvarez, E. Coto, F. Ortega, 2013, Gene.

A CLCNKA polymorphism (rs10927887; p.Arg83Gly) previously linked to heart failure is associated with the estimated glomerular filtration rate in the RENASTUR cohort.

M. Sánchez-Niño, E. Coto, A. Ortiz, 2013, Gene.

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

X. Puente, R. Valdés-Mas, Diana A. Puente, 2014, Nature Communications.