S. Iglesias

发表

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

E. Coto, C. Díaz-Corte, P. Avanzas, 2021, Nutrition, metabolism, and cardiovascular diseases : NMCD.

Resequencing the whole MYH7 gene (including the intronic, promoter, and 3' UTR sequences) in hypertrophic cardiomyopathy.

V. Álvarez, E. Coto, María Martín, 2012, The Journal of molecular diagnostics : JMD.

FURIN gene variants (rs6224/rs4702) as potential markers of death and cardiovascular traits in severe COVID‐19

V. Álvarez, E. Coto, G. M. Albaiceta, 2022, Journal of medical virology.

The CCR5-delta32 variant might explain part of the association between COVID-19 and the chemokine-receptor gene cluster

V. Álvarez, E. Coto, J. Gómez, 2020, medRxiv.

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

E. Coto, B. Díaz-Molina, J. Reguero, 2022, Cardiogenetics.

NFKBIZ in Psoriasis: Assessing the association with gene polymorphisms and report of a new transcript variant.

E. Coto, P. Coto-Segura, R. Queiró, 2017, Human immunology.

Ventilation disorders diagnosed preoperatively in patients scheduled for isolated on-pump CABG: Do they increase inflammatory response in the early postoperative period?

Aleks, E. Coto, M. Brykczyński, 2016 .

IL17RA gene variants and anti-TNF response among psoriasis patients

E. Coto, M. Llamas-Velasco, J. Gómez, 2016, The Pharmacogenomics Journal.

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.

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.

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.

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.

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.

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

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

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.

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.

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.

The G263X MYBPC3 mutation is a common and low-penetrant mutation for hypertrophic cardiomyopathy in the region of Asturias (Northern Spain).

V. Álvarez, E. Coto, María Martín, 2013, International journal of cardiology.

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.

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

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

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.

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.

Spectrum of Mutations in Hypertrophic Cardiomyopathy Genes Among Tunisian Patients.

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

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

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

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.