Publications by authors named "Mikael Mathot"

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GRIN2A null variants confer a high risk for early-onset schizophrenia and other mental disorders and potentially enable precision therapy.
Johannes R Lemke, Andrea Eoli, Ilona Krey, Bernt Popp, Vincent Strehlow, Mikael Mathot

Mol Psychiatry· January 2026

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Functional and clinical studies reveal pathophysiological complexity of CLCN4-related neurodevelopmental condition.
Elizabeth E Palmer, Michael Pusch, Alessandra Picollo, Caitlin Forwood, Matthew H Nguyen, Mikaël Mathot

Mol Psychiatry· February 2023

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A novel RAD21 mutation in a boy with mild Cornelia de Lange presentation: Further delineation of the phenotype.
Sarah Dorval, Maura Masciadri, Mikaël Mathot, Silvia Russo, Nicole Revencu

Eur J Med Genet· January 2020

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Biallelic mutations in RTTN are associated with microcephaly, short stature and a wide range of brain malformations.
Katrien Stouffs, Stéphanie Moortgat, Tim Vanderhasselt, Laura Vandervore, Alice Dica, Mikaël Mathot

Eur J Med Genet· December 2018

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Hypomyelination and congenital cataract: broadening the clinical phenotype.
Roberta Biancheri, Federico Zara, Andrea Rossi, Mikael Mathot, Marie Cecile Nassogne

Arch Neurol· September 2011

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Meningitis with subdural empyema due to non-typhoid Salmonella in a 9-month-old girl.
Ahmad Ghais, Ruth Armano, Renaud Menten, Mikaël Mathot, Francis Zech

Eur J Pediatr· December 2009

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Pseudo-Bartter syndrome in a pregnant mother and her fetus.
Mikael Mathot, Pierre Maton, Elisabeth Henrion, Anne François-Adant, Arnaud Marguglio

Pediatr Nephrol· July 2006

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