Browsing by author "Gómez, Juan"

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

Lorca Gutiérrez, Rebeca

; Pannone, L.; Cuesta Llavona, Elías; Bocchinfuso, G.; Rodríguez Reguero, José Julián

; Carpentieri, G.; Hernando, Inés; Flex, E.; Tartaglia, M.; Coto García, Eliecer

; Gómez, Juan; Martinelli, S. (2021)

Concealed inherited cardiomyopathies detected in cardio-oncology screening

Lorca Gutiérrez, Rebeca

; Pascual Calleja, Isaac

; Fernández, M.; Álvarez Velasco, Rut; Colunga, Santiago; Muñiz, M.; Izquierdo, M.; Fernández, Y.; Esteban, E.; Gómez, Juan; Avanzas Fernández, Pablo

; López Fernández, Teresa (2024)

Epigenetic study of cohort of monozygotic twins with hypertrophic cardiomyopathy due to MYBPC3 (Cardiac Myosin-Binding protein C)

Peñarroya, A.; Lorca Gutiérrez, Rebeca

; Rodríguez Reguero, Juan Ramón; Gómez, Juan; Avanzas Fernández, Pablo

; Tejedor Vaquero, Juan Ramón

; Fernández Fernández, Agustín

; Fernández Fraga, Mario

(2024)

Gene Variant in the NF- κ B Pathway Inhibitor NFKBIA Distinguishes Patients with Psoriatic Arthritis within the Spectrum of Psoriatic Disease

Coto Segura, Pablo

; Coto García, Eliecer

; González Lara, Leire; Alonso, Belén; Gómez, Juan; Cuesta Llavona, Elías; Queiro Silva, Rubén

(2019)

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

Coto García, Eliecer

; Rodríguez Reguero, José Julián

; Avanzas Fernández, Pablo

; Pascual Calleja, Isaac

; Martín, M.; Hevia Nava, Sergio

; Morís de la Tassa, César

; Díaz Molina, Beatriz

; Rodríguez Lambert, José Luis

; Alonso González, Belén

; Cuesta Llavona, Elías; Díaz Corte, María del Carmen

; Gómez, Juan (2019)

IL17RA in early-onset coronary artery disease: total leukocyte transcript analysis and promoter polymorphism (rs4819554) association

Coto García, Eliecer

; Pascual Calleja, Isaac

; Avanzas Fernández, Pablo

; Cuesta Llavona, Elías; Lorca Gutiérrez, Rebeca

; Martín, María; Vázquez Coto, Daniel; Díaz Corte, María del Carmen

; Morís de la Tassa, César

; Rodríguez Reguero, José Julián

; Gómez, Juan (2020)

Mechanical Stretch Induces Senescence of Lung Epithelial Cells and Drives Fibroblast Activation by Paracrine Mechanisms

Martín Vicente, Paula; López Martínez, Cecilia; López Alonso, Inés

; Exojo Ramírez, Sara M.; Duarte Herrera, Israel David; Amado Rodríguez, Laura

; Ordoñez, Irene; Cuesta Llavona, Elías; Gómez, Juan; Campo, Natalia; O’Kane, Cecilia M.; McAuley, Daniel F .; Huidobro Fernández, Covadonga

; Muñiz Albaiceta, Guillermo

(2025-02)

Mitochondrial heteroplasmy as a marker for premature coronary artery disease: analysis of the poly-C tract of the control region sequence

Lorca Gutiérrez, Rebeca

; Aparicio, A.; Gómez, Juan; Álvarez Velasco, Rut; Pascual Calleja, Isaac

; Avanzas Fernández, Pablo

; González Urbistondo, F.; Alen, A.; Vázquez Coto, D.; González Fernández, M.; García Lago, C.; Cuesta Llavona, Elías; Morís de la Tassa, César

; Coto García, Eliecer

(2023)

Neurocognition functioning as a prerequisite to intact social cognition in schizophrenia

Fernández Modamio, Mar; Gil Sanz, David; Arrieta Rodríguez, Marta; Santacoloma Cabero, Iciar; Bengochea Seco, Rosario; González Fraile, Eduardo; Muñiz Fernández, José

; Gómez, Juan; Pérez, Silvia; Palacios, Mariola; Novoa, Teresa; Domínguez, Ana I.; Sáez de Ibarra, Alfonso (2020-01-23)

Survival analysis and gender differences in hypertrophic cardiomyopathy proband patients referred for genetic testing

Lorca Gutiérrez, Rebeca

; Salgado, M.; Álvarez Velasco, Rut; Reguro, J. R.; Alonso, V.; Gómez, Juan; Coto García, Eliecer

; Cuesta Llavona, Elías; López Negrete, E.; Pascual Calleja, Isaac

; Avanzas Fernández, Pablo

; Tome, Maite (2024)

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

Coto García, Eliecer

; Lorca Gutiérrez, Rebeca

; Rodríguez Reguero, José Julián

; Martín Fernández, María

; Pascual Calleja, Isaac

; Avanzas Fernández, Pablo

; Cuesta Llavona, Elías; Vázquez Coto, Daniel; Díaz Corte, C.; Tranche, S.; Alonso, B.; Iglesias, S.; Morís de la Tassa, César

; Gómez, Juan (2021)

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

López Martínez, Rocío; Muñiz Albaiceta, Guillermo

; Amado Rodríguez, Laura

; Cuesta Llavona, Elías; Gómez, Juan; García Clemente, Marta María

; Vázquez Coto, Daniel; Álvarez, V.; Coto García, Eliecer

(2022)

The Interferon-induced transmembrane protein 3 gene (IFITM3) rs12252 C variant is associated with COVID-19

Gómez, Juan; Muñiz Albaiceta, Guillermo

; Cuesta Llavona, Elías; García Clemente, Marta María

; López Larrea, Carlos

; Amado Rodríguez, Laura

; López Alonso, Inés

; Melón García, Santiago

; Alvarez Argüelles, Marta Elena; Gil Peña, Helena

; Vidal Castiñeira, José Ramón

; Corte Iglesias, V.; Saiz, M. L.; Alvarez, V.; Coto García, Eliecer

(2021)

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

Calvo, David; Rubín, José M.; Pérez, Diego; Gómez, Juan; Flórez, Juan Pablo; Avanzas, Pablo; García-Ruíz, José Manuel; Hera, Jesús María de la; Reguero, Julián; Coto, Eliecer; Morís, César (2015)

Browsing by author "Gómez, Juan"

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

Concealed inherited cardiomyopathies detected in cardio-oncology screening ﻿

Epigenetic study of cohort of monozygotic twins with hypertrophic cardiomyopathy due to MYBPC3 (Cardiac Myosin-Binding protein C) ﻿

Gene Variant in the NF- κ B Pathway Inhibitor NFKBIA Distinguishes Patients with Psoriatic Arthritis within the Spectrum of Psoriatic Disease ﻿

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

IL17RA in early-onset coronary artery disease: total leukocyte transcript analysis and promoter polymorphism (rs4819554) association ﻿

Mechanical Stretch Induces Senescence of Lung Epithelial Cells and Drives Fibroblast Activation by Paracrine Mechanisms ﻿

Mitochondrial heteroplasmy as a marker for premature coronary artery disease: analysis of the poly-C tract of the control region sequence ﻿

Neurocognition functioning as a prerequisite to intact social cognition in schizophrenia ﻿

Survival analysis and gender differences in hypertrophic cardiomyopathy proband patients referred for genetic testing ﻿

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

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

The Interferon-induced transmembrane protein 3 gene (IFITM3) rs12252 C variant is associated with COVID-19 ﻿

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

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

Concealed inherited cardiomyopathies detected in cardio-oncology screening

Epigenetic study of cohort of monozygotic twins with hypertrophic cardiomyopathy due to MYBPC3 (Cardiac Myosin-Binding protein C)

Gene Variant in the NF- κ B Pathway Inhibitor NFKBIA Distinguishes Patients with Psoriatic Arthritis within the Spectrum of Psoriatic Disease

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

IL17RA in early-onset coronary artery disease: total leukocyte transcript analysis and promoter polymorphism (rs4819554) association

Mechanical Stretch Induces Senescence of Lung Epithelial Cells and Drives Fibroblast Activation by Paracrine Mechanisms

Mitochondrial heteroplasmy as a marker for premature coronary artery disease: analysis of the poly-C tract of the control region sequence

Neurocognition functioning as a prerequisite to intact social cognition in schizophrenia

Survival analysis and gender differences in hypertrophic cardiomyopathy proband patients referred for genetic testing

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

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

The Interferon-induced transmembrane protein 3 gene (IFITM3) rs12252 C variant is associated with COVID-19

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