Browsing by author "Gómez de Oña, Juan"

Entendimiento de la miocardiopatía hipertrófica mediante el estudio de una variante patogénica fundadora

Lorca Gutiérrez, Rebeca

; Gómez de Oña, Juan

; Martín, María; Cabanillas Farpón, Rubén

; Calvo Blanco, Juan

; León, Víctor; Pascual Calleja, Isaac

; Morís de la Tassa, César

; Coto García, Eliecer

; Rodríguez Reguero, José Julián

(2019)

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

Rodríguez Reguero, José Julián

; Gómez de Oña, Juan

; Martín Fernández, María

; Flórez Muñoz, Juan Pablo; Morís de la Tassa, César

; Iglesias, Sara; Alonso González, Belén

; Álvarez Martínez, María Victoria

; Coto García, Eliecer

(2013)

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 de Oña, Juan

; Cuesta Llavona, E.; 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, E.; Díaz Corte, María del Carmen

; Gómez de Oña, Juan

(2019)

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

Coto García, Eliecer

; Díaz Corte, María del Carmen

; Tranche Iparraguirre, Salvador

; Gómez de Oña, Juan

; Alonso González, Belén

; Iglesias, Sara; Rodríguez Reguero, José Julián

; López Larrea, Carlos

; Coto Segura, Pablo

(2018)

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

Gómez de Oña, Juan

; Lorca Gutiérrez, Rebeca

; Rodríguez Reguero, José Julián

; Martín Fernández, María

; Morís de la Tassa, César

; Alonso González, Belén

; Iglesias, Sara; Díaz Molina, Beatriz

; Avanzas Fernández, Pablo

; Coto García, Eliecer

(2018)

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

Coto García, Eliecer

; Díaz Corte, María del Carmen

; Tranche Iparraguirre, Salvador

; Gómez de Oña, Juan

; Rodríguez Reguero, José Julián

; Alonso González, Belén

; Iglesias, Sara; Gil Peña, Helena

; Yin, Xueqian; Coto Segura, Pablo

(2018-10-08)

Genética Mitocondrial y Riesgo de Diabetes Post Trasplante

Gómez de Oña, Juan

(2012-06-22)

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

Lorca Gutiérrez, Rebeca

; Martín Fernández, María

; Gómez de Oña, Juan

; Santamarta Liébana, Elena

; Morís de la Tassa, César

; Rodríguez Reguero, José Julián

; Coto García, Eliecer

(2015)

Hypertrophic cardiomyopathy and sudden cardiac death: Molecular genetics aspects

Coto García, Eliecer

; Gómez de Oña, Juan

; León, D.; Rodríguez Reguero, José Julián

(Nova Science Publishers; Inc., 2013)

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

Riobello Suárez, Cristina; Gómez de Oña, Juan

; Gil Peña, Helena

; Rodríguez Reguero, José Julián

; Hera Galarza, Jesús María de la

; Calvo Temprano, David

; Morís de la Tassa, César

; Santos Rodríguez, Fernando

; Coto Segura, Pablo

; Coto García, Eliecer

(2016)

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

Tavira Iglesias, Beatriz

; Gómez de Oña, Juan

; Málaga Guerrero, Serafín

; Santos Rodríguez, Fernando

; Fernández Aracama, Javier; Alonso González, Belén

; Iglesias, Sara; Benavides, Ana; Hernando, Inés; Plasencia, Ana; Álvarez Martínez, María Victoria

; Coto García, Eliecer

(2015)

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

Tavira Iglesias, Beatriz

; Gómez de Oña, Juan

; Santos Rodríguez, Fernando

; Gil Peña, Helena

; Álvarez Martínez, María Victoria

; Coto García, Eliecer

(2014)

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

Coto García, Eliecer

; Gómez de Oña, Juan

; Alonso González, Belén

; Corao Trueba, Ana Isabel

; Díaz González, Marta Elvira

; Menéndez González, Manuel

; Martínez Rodríguez, Carmen

; Calatayud Noguera, María Teresa

; Morís de la Tassa, Germán

; Álvarez Martínez, María Victoria

(2011)

Miocardiopatía hipertrófica: Identificación de nuevos genes mediante técnicas de secuenciación masiva

Gómez de Oña, Juan

(2017-02-16)

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

Tavira Iglesias, Beatriz

; Gómez de Oña, Juan

; Díaz Corte, María del Carmen

; Llobet, Laura; Ruiz Pesini, Eduardo; Ortega, Francisco Gabriel; Coto García, Eliecer

(2014)

Mutation analysis of the main hypertrophic cardiomyopathy genes using multiplex amplification and semiconductor Next-Generation sequencing

Gómez de Oña, Juan

; Rodríguez Reguero, José Julián

; Morís de la Tassa, César

; Martín Fernández, María

; Álvarez Martínez, María Victoria

; Alonso, Belén; Iglesias, Sara; Coto García, Eliecer

(2014)

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

Valdés Mas, Rafael María

; Gutiérrez Fernández, Ana Yolanda

; Gómez de Oña, Juan

; Coto García, Eliecer

; Astudillo González, María Aurora

; Álvarez Puente, Diana

; Rodríguez Reguero, José Julián

(2014)

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

Gómez de Oña, Juan

; Rodríguez Reguero, José Julián

; Junquera, Manuel R.; Álvarez, Celso; Morís de la Tassa, César

; Alonso González, Belén

; Iglesias, Sara; Coto García, Eliecer

(2016)

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

Gómez de Oña, Juan

; Díaz Corte, María del Carmen

; Tranche Iparraguirre, Salvador

; Álvarez, Fancisco; Iglesias, Sara; Alonso González, Belén

; Coto García, Eliecer

(2015)

Browsing by author "Gómez de Oña, Juan"

Entendimiento de la miocardiopatía hipertrófica mediante el estudio de una variante patogénica fundadora ﻿

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

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 ﻿

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

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

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

Genética Mitocondrial y Riesgo de Diabetes Post Trasplante ﻿

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

Hypertrophic cardiomyopathy and sudden cardiac death: Molecular genetics aspects ﻿

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

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

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 ﻿

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

Miocardiopatía hipertrófica: Identificación de nuevos genes mediante técnicas de secuenciación masiva ﻿

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

Mutation analysis of the main hypertrophic cardiomyopathy genes using multiplex amplification and semiconductor Next-Generation sequencing ﻿

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

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

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

Entendimiento de la miocardiopatía hipertrófica mediante el estudio de una variante patogénica fundadora

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

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

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

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

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

Genética Mitocondrial y Riesgo de Diabetes Post Trasplante

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

Hypertrophic cardiomyopathy and sudden cardiac death: Molecular genetics aspects

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

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

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

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

Miocardiopatía hipertrófica: Identificación de nuevos genes mediante técnicas de secuenciación masiva

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

Mutation analysis of the main hypertrophic cardiomyopathy genes using multiplex amplification and semiconductor Next-Generation sequencing

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

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

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