Cristina Fenollar-Ferrer

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 6

Top Topics

Dna Methylation

Intellectual Disability

Molecular Dynamics Simulations

Top Venues

Proceedings of the National Academy of Sciences of the United States of America

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

Publications

Peter Rodriguez, Vrinda Kalia, Cristina Fenollar-Ferrer, Chelsea L Gibson, Zayna Gichi, Andre Rajoo, Carson D Matier, Aidan T Pezacki, Tong Xiao, Lucia Carvelli, Christopher J Chang, Gary W Miller, Andy V Khamoui, Jana Boerner, Randy D Blakely
Glial swip-10 controls systemic mitochondrial function, oxidative stress, and neuronal viability via copper ion homeostasis. Proceedings of the National Academy of Sciences of the United States of America 121 (39) (2024)
Isabelle Roux, Cristina Fenollar-Ferrer, Hyun Jae Lee, Parna Chattaraj, Ivan A Lopez, Kyungreem Han, Keiji Honda, Carmen C Brewer, John A Butman, Robert J Morell, Donna M Martin, Andrew J Griffith
CHD7 variants associated with hearing loss and enlargement of the vestibular aqueduct. Human genetics (2023)
Rabia Faridi, Alessandro Rea, Cristina Fenollar-Ferrer, Raymond T O'Keefe, Shoujun Gu, Zunaira Munir, Asma Ali Khan, Sheikh Riazuddin, Michael Hoa, Sadaf Naz, William G Newman, Thomas B Friedman
New insights into Perrault syndrome, a clinically and genetically heterogeneous disorder. Human genetics (2021)
Memoona Ramzan, Christophe Philippe, Inna A Belyantseva, Yoko Nakano, Cristina Fenollar-Ferrer, Risa Tona, Rizwan Yousaf, Rasheeda Bashir, Ayesha Imtiaz, Rabia Faridi, Zunaira Munir, Hafiza Idrees, Midhat Salman, Sophie Nambot, Antonio Vitobello, Souad Kartti, Oumaima Zarrik, P Dane Witmer, Nara Lygia de Macena Sobreira, Azeddine Ibrahimi, Botond Banfi, Sebastien Moutton, Thomas B Friedman, Sadaf Naz
Variants of human CLDN9 cause mild to profound hearing loss. Human mutation 42 (10) (2021)
Kyungreem Han, Richard W Pastor, Cristina Fenollar-Ferrer
PLD2-PI(4,5)P2 interactions in fluid phase membranes: Structural modeling and molecular dynamics simulations. PloS one 15 (7) (2020)
Risa Tona, Ivan A Lopez, Cristina Fenollar-Ferrer, Rabia Faridi, Claudio Anselmi, Asma A Khan, Mohsin Shahzad, Robert J Morell, Shoujun Gu, Michael Hoa, Lijin Dong, Akira Ishiyama, Inna A Belyantseva, Sheikh Riazuddin, Thomas B Friedman
Mouse Models of Human Pathogenic Variants of TBC1D24 Associated with Non-Syndromic Deafness DFNB86 and DFNA65 and Syndromes Involving Deafness. Genes 11 (10) (2020)