Kolexia
Lasseaux Eulalie
Pharmacien
Institut Bergonié
Bordeaux, France
73 Activités
450 Followers

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{{person.topmesh1.name}} Albinisme Albinisme oculocutané Prédisposition génétique à une maladie Déficience intellectuelle Syndrome d'Hermanski-Pudlak Albinisme oculaire Épilepsie Microcéphalie Hypopigmentation

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AGILENT TECHNOLOGIES FRANCE
1 collaboration(s)
Dernière en 2017
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Dernières activités

The co-occurrence of genetic variants in the TYR and OCA2 genes confers susceptibility to albinism
Abstracts from the 56th European Society of Human Genetics (ESHG) Conference   01 janvier 2024
Ophthalmologic Phenotype-Genotype Correlations in Patients With Oculocutaneous Albinism Followed in a Reference Center.
Investigative ophthalmology & visual science   15 septembre 2023
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   31 août 2023
A novel compound heterozygous variant in the LLS gene is associated with nonsyndromic hypotrichosis.
Clinical and experimental dermatology   28 août 2023
Characterization of the novel HLA-DRB1*11:01:01:12N allele by sequencing-based typing.
HLA   21 août 2023
A multilayered approach to the analysis of genetic data from individuals with suspected albinism.
Journal of medical genetics   17 juillet 2023
A novel pathogenic variant in the FZD6 gene causes recessive nail dysplasia in a Moroccan family.
Clinical and experimental dermatology   04 juillet 2023
The contribution of common regulatory and protein-coding TYR variants in the genetic architecture of albinism
Abstracts from the 55th European Society of Human Genetics (ESHG) Conference   01 mai 2023
Oculo-Cutaneous Albinism Type 4 (OCA4): Phenotype-Genotype Correlation.
Genes   23 novembre 2022
Syndrome d’Hermansky-Pudlak dans une forme hétérozygote inédite
Journées dermatologiques de Paris, 29 novembre - 3 décembre 2022   01 novembre 2022