Publications by authors named "Fran Faes"

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Enhanced cGAS-STING-dependent interferon signaling associated with mutations in ATAD3A.
Alice Lepelley, Erika Della Mina, Erika Van Nieuwenhove, Lise Waumans, Sylvie Fraitag, Fran Faes

J Exp Med· October 2021

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Diagnosing Autism Spectrum Disorder in Toddlers Born Very Preterm: Estimated Prevalence and Usefulness of Screeners and the Autism Diagnostic Observation Schedule (ADOS).
Julie Vermeirsch, Liedewij Verhaeghe, Alexandra Casaer, Fran Faes, Ann Oostra

J Autism Dev Disord· May 2021

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Genomic aberrations of the CACNA2D1 gene in three patients with epilepsy and intellectual disability.
Sarah Vergult, Annelies Dheedene, Alfred Meurs, Fran Faes, Bertrand Isidor

Eur J Hum Genet· May 2015

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Congenital fixed dilated pupils due to ACTA2- multisystemic smooth muscle dysfunction syndrome.
Françoise M J Roulez, Fran Faes, Patricia Delbeke, Patrick Van Bogaert, Georges Rodesch

J Neuroophthalmol· June 2014

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New RAB3GAP1 mutations in patients with Warburg Micro Syndrome from different ethnic backgrounds and a possible founder effect in the Danish.
Deborah J Morris-Rosendahl, Reeval Segel, A Peter Born, Christoph Conrad, Bart Loeys, Fran Faes

Eur J Hum Genet· October 2010

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