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European Journal of Medical Genetics|June 30, 2026
NEW INSIGHTS INTO THE COMPLEX GENETIC ARCHITECTURE OF AGE-RELATED HEARING LOSSCrystel Bonnet, Salim Aiche, Sophie Boucher
Frontiers in Aging Neuroscience|March 18, 2021
Contributions of Age-Related and Audibility-Related Deficits to Aided Consonant Identification in Presbycusis: A Causal-Inference AnalysisLéo Varnet, Agnès C Léger, Sophie Boucher, et al.
Current Opinion in Neurology|December 22, 2011
Usher syndrome (sensorineural deafness and retinitis pigmentosa): pathogenesis, molecular diagnosis and therapeutic approachesCrystel Bonnet, Aziz El-Amraoui
Nature Reviews. Genetics|May 12, 2023
Deafness: from genetic architecture to gene therapyChristine Petit, Crystel Bonnet, Saaïd Safieddine
Proceedings of the National Academy of Sciences of the United States of America|August 30, 2006
A mitotically inheritable unit containing a MAP kinase moduleSébastien Kicka, Crystel Bonnet, Andrew K Sobering, et al.
Human Molecular Genetics|June 9, 2012
Defect in the gene encoding the EAR/EPTP domain-containing protein TSPEAR causes DFNB98 profound deafnessSedigheh Delmaghani, Asadollah Aghaie, Nicolas Michalski, et al.
Biochemical and Biophysical Research Communications|October 3, 2002
Interaction of STOP with neuronal tubulin is independent of polyglutamylationCrystel Bonnet, Eric Denarier, Christophe Bosc, et al.
Molecular Microbiology|September 22, 2006
The peroxisomal import proteins PEX2, PEX5 and PEX7 are differently involved in Podospora anserina sexual cycleCrystel Bonnet, Eric Espagne, Denise Zickler, et al.
Vision Research|September 25, 2012
Fundus autofluorescence and optical coherence tomography in relation to visual function in Usher syndrome type 1 and 2Ana Fakin, Martina Jarc-Vidmar, Damjan Glavač, et al.
RNA (New York, N.Y.)|June 6, 2006
mRNA localization to the mitochondrial surface allows the efficient translocation inside the organelle of a nuclear recoded ATP6 proteinValérie Kaltimbacher, Crystel Bonnet, Gaëlle Lecoeuvre, et al.
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