Gisela Nogales-Gadea

ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2016-2022
Publications (10 Years): 12

Top Venues

Genes

Human mutation

Genetics in medicine : official journal of the American College of Medical Genetics

Biomedicines

Fundació Institut d'Investigació en Ciències de la Salut Germans Trias i Pujol

Universitat de Barcelona (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Fundació Institut d'Investigació en Ciències de la Salut Germans Trias i Pujol Jan 1o 2015

Spain

Investigator :: Neurosciences

Education History

Universitat de Barcelona

Spain

PHD

Publications

Emma Koehorst, Renato Odria, Júlia Capó, Judit Núñez-Manchón, Andrea Arbex, Miriam Almendrote, Ian Linares-Pardo, Daniel Natera-de Benito, Verónica Saez, Andres Nascimento, Carlos Ortez, Miguel Ángel Rubio, Jordi Díaz-Manera, Jorge Alonso-Pérez, Giuseppe Lucente, Agustín Rodriguez-Palmero, Alba Ramos-Fransi, Alicia Martínez-Piñeiro, Gisela Nogales-Gadea, Mònica Suelves
An Integrative Analysis of DNA Methylation Pattern in Myotonic Dystrophy Type 1 Samples Reveals a Distinct DNA Methylation Profile between Tissues and a Novel Muscle-Associated Epigenetic Dysregulation. Biomedicines 10 (6) (2022)
Aitana Almodóvar-Payá, Mónica Villarreal-Salazar, Noemí de Luna, Gisela Nogales-Gadea, Alberto Real-Martínez, Antoni L Andreu, Miguel Angel Martin, Joaquin Arenas, Alejandro Lucia, John Vissing, Thomas O Krag, Tomàs Pinós
Preclinical Research in Glycogen Storage Diseases: A Comprehensive Review of Current Animal Models. International journal of molecular sciences 21 (24) (2020)
Andrea López-Martínez, Patricia Soblechero-Martín, Laura de-la-Puente-Ovejero, Gisela Nogales-Gadea, Virginia Arechavala-Gomeza
An Overview of Alternative Splicing Defects Implicated in Myotonic Dystrophy Type I. Genes 11 (9) (2020)
Emma Koehorst, Alfonsina Ballester-Lopez, Virginia Arechavala-Gomeza, Alicia Martínez-Piñeiro, Gisela Nogales-Gadea
The Biomarker Potential of miRNAs in Myotonic Dystrophy Type I. Journal of clinical medicine 9 (12) (2020)
Alfonsina Ballester-Lopez, Ian Linares-Pardo, Emma Koehorst, Judit Núñez-Manchón, Guillem Pintos-Morell, Jaume Coll-Cantí, Miriam Almendrote, Giuseppe Lucente, Andrea Arbex, Jonathan Javier Magaña, Nadia M Murillo-Melo, Alejandro Lucia, Darren G Monckton, Sarah A Cumming, Alba Ramos-Fransi, Alicia Martínez-Piñeiro, Gisela Nogales-Gadea
The Need for Establishing a Universal CTG Sizing Method in Myotonic Dystrophy Type 1. Genes 11 (7) (2020)
Alfonsina Ballester-Lopez, Emma Koehorst, Ian Linares-Pardo, Judit Núñez-Manchón, Miriam Almendrote, Giuseppe Lucente, Andrea Arbex, Carles Puente, Alejandro Lucia, Darren G Monckton, Sarah A Cumming, Guillem Pintos-Morell, Jaume Coll-Cantí, Alba Ramos-Fransi, Alicia Martínez-Piñeiro, Gisela Nogales-Gadea
Preliminary Findings on CTG Expansion Determination in Different Tissues from Patients with Myotonic Dystrophy Type 1. Genes 11 (11) (2020)
Alfonsina Ballester-Lopez, Emma Koehorst, Miriam Almendrote, Alicia Martínez-Piñeiro, Giuseppe Lucente, Ian Linares-Pardo, Judit Núñez-Manchón, Nicolau Guanyabens, Antoni Cano, Alejandro Lucia, Gayle Overend, Sarah A Cumming, Darren G Monckton, Teresa Casadevall, Irina Isern, Josep Sánchez-Ojanguren, Albert Planas, Agustín Rodriguez-Palmero, Laura Monlleó-Neila, Guillem Pintos-Morell, Alba Ramos-Fransi, Jaume Coll-Cantí, Gisela Nogales-Gadea
A DM1 family with interruptions associated with atypical symptoms and late onset but not with a milder phenotype. Human mutation 41 (2) (2019)
Carmen Fiuza-Luces, Alejandro Santos-Lozano, Francisco Llavero, Rocío Campo, Gisela Nogales-Gadea, Jorge Díez-Bermejo, Carlos Baladrón, África González-Murillo, Joaquín Arenas, Miguel Angel Martin, Antoni L Andreu, Tomàs Pinós, Beatriz G Gálvez, Juan Antonio López, Jesús Vázquez, José L Zugaza, Alejandro Lucia
Muscle molecular adaptations to endurance exercise training are conditioned by glycogen availability: a proteomics-based analysis in the McArdle mouse model. The Journal of physiology 596 (6) (2018)
Inés García-Consuegra, Sara Asensio-Peña, Alfonsina Ballester-Lopez, Rosario Francisco-Velilla, Tomás Pinos, Guillem Pintos-Morell, Jaume Coll-Cantí, Adrián González-Quintana, Antoni L Andreu, Joaquín Arenas, Alejandro Lucia, Gisela Nogales-Gadea, Miguel A Martín
Missense mutations have unexpected consequences: The McArdle disease paradigm. Human mutation 39 (10) (2018)
Judit Núñez-Manchón, Alfonsina Ballester-Lopez, Emma Koehorst, Ian Linares-Pardo, Daniëlle Coenen, Ignacio Ara, Carlos Rodriguez-Lopez, Alba Ramos-Fransi, Alicia Martínez-Piñeiro, Giuseppe Lucente, Miriam Almendrote, Jaume Coll-Cantí, Guillem Pintos-Morell, Alejandro Santos-Lozano, Joaquin Arenas, Miguel Angel Martín, Mauricio de Castro, Alejandro Lucia, Alfredo Santalla, Gisela Nogales-Gadea
Manifesting heterozygotes in McArdle disease: a myth or a reality-role of statins. Journal of inherited metabolic disease 41 (6) (2018)
Gisela Nogales-Gadea, Tomàs Pinós, Antoni L Andreu, Miguel A Martín, Joaquin Arenas, Alejandro Lucia
Next-generation sequencing to estimate the prevalence of a great unknown: McArdle disease. Genetics in medicine : official journal of the American College of Medical Genetics 17 (8) (2016)
Ines Garcia-Consuegra, Alberto Blázquez-Encinar, Juan Carlos Rubio, Joaquín Arenas, Alfonsina Ballester-Lopez, Adrián González-Quintana, Antoni L Andreu, Tomàs Pinós, Jaume Coll-Cantí, Alejandro Lucia, Gisela Nogales-Gadea, Miguel Angel Martin
Taking advantage of an old concept, "illegitimate transcription", for a proposed novel method of genetic diagnosis of McArdle disease. Genetics in medicine : official journal of the American College of Medical Genetics 18 (11) (2016)

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Publication Activity (10 Years)

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Gisela Nogales-Gadea