Vanessa Zanette (Aurelio Reyes)

Publication Activity (10 Years)

Years Active: 2020-2023
Publications (10 Years): 5

Top Topics

Cognitive Impairment

Duchenne Muscular Dystrophy

Top Venues

The EMBO journal

Genetics and molecular biology

Journal of medical genetics

Neurology. Genetics

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

Publications

Rebecca Acin-Perez, Cristiane Benincá, Lucia Fernandez Del Rio, Cynthia Shu, Siyouneh Baghdasarian, Vanessa Zanette, Christoph Gerle, Chimari Jiko, Ramzi Khairallah, Shaharyar Khan, David Rincon Fernandez Pacheco, Byourak Shabane, Karel Erion, Ruchi Masand, Sundeep Dugar, Cristina Ghenoiu, George Schreiner, Linsey Stiles, Marc Liesa, Orian S Shirihai
Inhibition of ATP synthase reverse activity restores energy homeostasis in mitochondrial pathologies. The EMBO journal (2023)
Rebecca Acin-Perez, Cristiane Benincá, Lucia Fernandez Del Rio, Cynthia Shu, Siyouneh Baghdasarian, Vanessa Zanette, Christoph Gerle, Chimari Jiko, Ramzi Khairallah, Shaharyar Khan, David Rincon Fernandez Pacheco, Byourak Shabane, Karel Erion, Ruchi Masand, Sundeep Dugar, Cristina Ghenoiu, George Schreiner, Linsey Stiles, Marc Liesa, Orian S Shirihai
Inhibition of ATP synthase reverse activity restores energy homeostasis in mitochondrial pathologies. The EMBO journal (2023)
Vanessa Zanette, Daniel Almeida do Valle, Bruno Augusto Telles, Alan J Robinson, Vaneisse Monteiro, Mara Lucia S F Santos, Ricardo Lehtonen Rodrigues de Souza, Cristiane Benincá
NDUFV1 mutations in complex I deficiency: Case reports and review of symptoms. Genetics and molecular biology 44 (4) (2021)
Cristiane Benincá, Vanessa Zanette, Mark Johnson, Daniel do Valle, Alan J Robinson, Vaneisse Monteiro, Bruno Augusto Telles, Ricardo L R Souza, Mara L S F Santos, Cristiane Benincá, Massimo Zeviani
Neurodevelopmental regression, severe generalized dystonia, and metabolic acidosis caused by POLR3A mutations. Neurology. Genetics 6 (6) (2020)
Cristiane Benincá, Vanessa Zanette, Michele Brischigliaro, Mark Johnson, Aurelio Reyes, Daniel Almeida do Valle, Alan J Robinson, Andrea Degiorgi, Anna Yeates, Bruno Augusto Telles, Julien Prudent, Enrico Baruffini, Mara Lucia S F Santos, Ricardo Lehtonen R de Souza, Erika Fernandez-Vizarra, Alexander J Whitworth, Massimo Zeviani
Mutation in the MICOS subunit gene APOO (MIC26) associated with an X-linked recessive mitochondrial myopathy, lactic acidosis, cognitive impairment and autistic features. Journal of medical genetics 58 (3) (2020)