Eulalie Lasseaux (E Lasseaux)

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 4

Top Topics

Intellectual Disability

Gene Expression

Human Immunodeficiency Virus

Top Venues

Pigment cell & melanoma research

Ophthalmic genetics

CHU Pellegrin

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

Affiliation History

CHU Pellegrin

France

Praticien Hospitalier :: Génétique Médicale

Publications

Modibo Diallo, Ousmane Sylla, Mohamed Kole Sidibé, Claudio Plaisant, Elina Mercier, Angèle Tingaud-Sequeira, Sophie Javerzat, Abdelaziz Hadid, Eulalie Lasseaux, Vincent Michaud, Benoit Arveiler
Genotypic spectrum of albinism in Mali. Pigment cell & melanoma research (2024)
Vincent Michaud, Angèle Tingaud-Sequeira, Elina Mercier, Eulalie Lasseaux, Claudio Plaisant, Smail Hadj Rabia, Sandra Whalen, Dominique Bonneau, Anne Dieux-Coeslier, Fanny Morice-Picard, Juliette Coursimault, Benoit Arveiler, Sophie Javerzat
Unsuspected consequences of synonymous and missense variants in OCA2 can be detected in blood cell RNA samples of patients with albinism. Pigment cell & melanoma research (2023)
R Lejoyeux, A-S Alonso, J Lafolie, Vincent Michaud, Eulalie Lasseaux, V Vasseur, S Derrien, M P Robert, Y Le Mer, R Tadayoni, Benoit Arveiler, M Mauget-Faÿsse
Foveal hypoplasia in parents of patients with albinism. Ophthalmic genetics (2022)
Vincent Michaud, Mathieu Fiore, Valentine Coste, Yoann Huguenin, Jean Claude Bordet, Claudio Plaisant, Eulalie Lasseaux, Fanny Morice-Picard, Benoit Arveiler
A new case with Hermansky-Pudlak syndrome type 9, a rare cause of syndromic albinism with severe defect of platelets dense bodies. Platelets 32 (3) (2020)