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Thomas is a neurogeneticist, He completed his MD at Université de Paris - Cité in 2019. He also earned a master’s degree in Human Genetics from University College London (Institute of Neurology, 2016) and a PhD from Sorbonne Université on early onset movement disorders (Paris Brain Institute, 2024). He is currently an assistant professor (Praticien Hospitalo-Universitaire) in the Department of Medical Genomics at Necker-Enfants Malades Hospital, specializing in rare neuropediatric diseases. His primary research focuses in the biological bases of neurodevelopmental disorders by applying genetics and genomics.
Thomas joined the lab in January 2025, he aims at developing innovative methods and models to integrate genomics into patient care, while accelerating translational discoveries by bridging research and clinical practice.
Resources & publications
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Journal (source)Clin Genet
Next Generation Phenotyping and Synthetic Faces in Coffin Siris Syndrome.
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Journal (source)Sci Rep
Next generation phenotyping for diagnosis and phenotype-genotype correlations...
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Journal (source)J Exp Med
Hemifacial myohyperplasia is due to somatic muscular PIK3CA gain-of-function ...