Julie Plaisancie

12PUBLICATIONS
52CO-AUTHORS
NeurogeneticsGene expression (incl. microarray and other genome-wide approaches)Epigenetics (incl. genome methylation and epigenomics)Optical technologyMedical infection agents (incl. prions)
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Publications (12)

|Jun 25, 2025
Comprehensive analysis of CNOT3-related neurodevelopmental disorders: phenotypic and genotypic characterization.

Camille Engel, Michaela Rendek, Jessica Assoumani

|Apr 29, 2025
GJA8-associated developmental eye disorders: a new multicentre study highlights mutational hotspots and genotype-phenotype correlations.

Solomon S Merepa, Linda M Reis, Alejandra Damián

|Oct 25, 2024
Deletion upstream of MAB21L2 highlights the importance of evolutionarily conserved non-coding sequences for eye development.

Fabiola Ceroni, Munevver B Cicekdal, Richard Holt

|Mar 30, 2023
Clinical and genetic analysis further delineates the phenotypic spectrum of ALDH1A3-related anophthalmia and microphthalmia.

Yesim Kesim, Fabiola Ceroni, Alejandra Damián

|Nov 20, 2022
Evaluation of somatic and/or germline mosaicism in congenital malformation of the eye.

Bertrand Chesneau, Véronique Ivashchenko, Christophe Habib

|Jan 08, 2021
Parental mosaicism in Marfan and Ehlers-Danlos syndromes and related disorders.

Bertrand Chesneau, Aurélie Plancke, Guillaume Rolland

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