Présentation
Boris Chaumette is a psychiatrist at Sainte-Anne hospital, a historic psychiatric hospital, located in the center of Paris, France. His scientific work is conducted at the Institute of Psychiatry and Neuroscience of Paris (INSERM U1266) as well as at McGill University (Montreal, Canada). He is affiliated with the University of Paris.
His clinical and research interests focus on the molecular basis of psychotic disorders. His general aim is to develop personalized therapy in psychiatry, based on the more recent molecular knowledge. He is determined to transfer the scientific knowledge from the bench to the bedside, to improve the clinical care in psychiatry. As a researcher, he explores the epigenetic and transcriptomic mechanisms of the onset of psychosis and the genetic factors associated with extreme phenotypic forms, like childhood-onset schizophrenia. As a clinician, he is involved in the specialized clinic for „Rare Diseases“ (Center of Reference for Rare Psychiatric Diseases) in the GHU Paris Psychiatry and Neurosciences.
Ressources & publications
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Journal (source)Hum. Mol. Genet.
Human IFT52 mutations uncover a novel role for the protein in microtubule dyn...
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Journal (source)Am. J. Hum. Genet.
Mutations in TUBB4B Cause a Distinctive Sensorineural Disease.
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Journal (source)Hum. Mol. Genet.
Constitutively-active FGFR3 disrupts primary cilium length and IFT20 traffick...
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Journal (source)Am J Hum Genet
Mutations in KIAA0586 Cause Lethal Ciliopathies Ranging from a Hydrolethalus ...
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Journal (source)J Med Genet
IFT81, encoding an IFT-B core protein, as a very rare cause of a ciliopathy p...
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Journal (source)Am J Hum Genet
Mutations in TUBB4B Cause a Distinctive Sensorineural Disease.
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Journal (source)Am J Hum Genet
Mutations in TUBB4B Cause a Distinctive Sensorineural Disease.
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Journal (source)Proc Natl Acad Sci U S A
Agonists of prostaglandin E2 receptors as potential first in class treatment ...
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Journal (source)Am J Hum Genet
Mutations in TUBB4B Cause a Distinctive Sensorineural Disease.
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Journal (source)J Med Genet
IFT81, encoding an IFT-B core protein, as a very rare cause of a ciliopathy p...