Your account is not claimed yet. You can sign up with ORCID to claim your account.

Aurora Gomez-Duran

Scopus Author ID ResearcherID Loop profile ORCID

Publication Activity (10 Years)

Years Active: 2017-2020
Publications (10 Years): 4

Top Topics

Duchenne Muscular Dystrophy

Mitochondrial Dna

Top Venues

EMBO molecular medicine

Nature communications

Centro de Investigaciones Biológicas

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

Affiliation History

Centro de Investigaciones Biológicas Feb 17o 2020

Spain

Junior Group Leader

Publications

Hannah Steele, Aurora Gomez-Duran, Angela Pyle, Sila Hopton, Jane Newman, Renae J Stefanetti, Sarah J Charman, Jehill D Parikh, Langping He, Carlos Pardo-Hernández, Djordje G Jakovljevic, Kieren G Hollingsworth, Alan J Robinson, Robert W Taylor, Leonardo Bottolo, Rita Horvath, Patrick F Chinnery
Metabolic effects of bezafibrate in mitochondrial disease. EMBO molecular medicine 12 (3) (2020)
Simonetta Andreazza, Colby L Samstag, Alvaro Sanchez-Martinez, Erika Fernández-Vizarra, Aurora Gomez-Duran, Juliette J Lee, Roberta Tufi, Michael J Hipp, Elizabeth K Schmidt, Thomas J Nicholls, Payam A Gammage, Patrick F Chinnery, Michal Minczuk, Leo J Pallanck, Scott R Kennedy, Alexander J Whitworth
Mitochondrially-targeted APOBEC1 is a potent mtDNA mutator affecting mitochondrial function and organismal fitness in Drosophila. Nature communications 10 (1) (2019)
Wei Wei, Aurora Gomez-Duran, Gavin Hudson, Patrick F Chinnery
Background sequence characteristics influence the occurrence and severity of disease-causing mtDNA mutations. PLoS genetics 13 (12) (2017)
Thomas M Connor, Simon Hoer, Andrew Mallett, Daniel P Gale, Aurora Gomez-Duran, Viktor Posse, Robin Antrobus, Pablo Moreno, Marco Sciacovelli, Christian Frezza, Jennifer Duff, Neil S Sheerin, John Andrew Sayer, Margaret Ashcroft, Michael S Wiesener, Gavin Hudson, Claes M Gustafsson, Patrick F Chinnery, Patrick H Maxwell
Mutations in mitochondrial DNA causing tubulointerstitial kidney disease. PLoS genetics 13 (3) (2017)