Luke Mansard

4PUBLICATIONS
26CO-AUTHORS
Cell and nuclear divisionEpigenetics (incl. genome methylation and epigenomics)Haematology
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Publications (4)

|Oct 17, 2025
CEP76 impairment at the centrosome-cilium interface contributes to a spectrum of ciliopathies.

Kamal Khan, Erika Tavares, Katherine Bishara

|Jan 21, 2022
Identification of the First Single GSDME Exon 8 Structural Variants Associated with Autosomal Dominant Hearing Loss.

Luke Mansard, Christel Vaché, Julie Bianchi

|Dec 24, 2021
The Study of a 231 French Patient Cohort Significantly Extends the Mutational Spectrum of the Two Major Usher Genes MYO7A and USH2A.

Luke Mansard, David Baux, Christel Vaché

|Sep 28, 2021
When Familial Hearing Loss Means Genetic Heterogeneity: A Model Case Report.

Camille Cenni, Luke Mansard, Catherine Blanchet

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