Laboratory
Rare congenital diseases [33]
Laboratory
Human Developmental Genetics
Kenneth McElreavey
Laboratory
Trypanosome Cell Biology
Philippe Bastin
Permanent Researcher
Benoit Arcangioli
Dynamics of the Genome
Permanent Researcher
Philippe Bastin
Trypanosome Cell Biology
Philippe Bastin grew up in the Belgian countryside where he developed interest for life sciences. He studied biology at Namur, Louvain and Brussels where he completed his doctoral studies in 1993 at the de […]
Permanent Researcher
Pierre Charneau
Institut Pasteur-TheraVectys Joint Laboratory
Permanent Researcher
Kenneth McElreavey
Human Developmental Genetics
Permanent Researcher
Sigolène Meilhac
Heart Morphogenesis
Sigolène MEILHAC is a developmental biologist and INSERM Research Director, leading since 2015 the team of Heart Morphogenesis jointly affiliated to the Institut Pasteur and Institut Imagine. Trained at the Ecole Normale Supérieure, she […]
Permanent Researcher
Aziz El Amraoui
Progressive Sensory Disorders, PathoPhysiology and Therapy
After a PhD in Neuroscience from the University of Lyon-I in 1995, Dr Aziz El-Amraoui joined the Institut Pasteur (Paris) where resorting to dozen identified deafness genes as entry points has enabled him to […]
Permanent Researcher
Nicolas Michalski
Plasticity of central auditory circuits
Permanent Researcher
Christine Petit
Auditory Therapies Innovation Lab
SCIENTIFIC POSITIONS Head of Auditory Therapies Innovation Laboratory at the Hearing Institute (an Institut Pasteur Center), Paris Professor “Classe Exceptionnelle” at Institut Pasteur, Paris Professor Emeritus at Collège de France, Chair of Genetics […]
Permanent Researcher
Uwe Maskos
Integrative Neurobiology of Cholinergic Systems
This is an example of transplanted human iPSC derived cells.
Full Professor
Permanent Researcher
Arnaud Echard
UMR3691 – Physiological and pathological cell biology
Permanent Researcher
Thomas Bourgeron
Human Genetics and Cognitive Functions
Having begun my research career investigating mitochondria in plants and then neurological diseases, I discovered the first mutations of the NLGN3, NLGN4X and SHANK3 genes in autism highlighting the main role of the synapse […]
Laboratory
Human Genetics and Cognitive Functions
Thomas Bourgeron
Laboratory