Diagnosing Autism Spectrum Disorder in Toddlers Born Very Preterm: Estimated Prevalence and Usefulness of Screeners and the Autism Diagnostic Observation Schedule (ADOS)
Vermeirsch, Julie, Verhaeghe, Liedewij, Casaer, Alexandra, Faes, Fran, Oostra, Ann, Roeyers, Herbert
Published in Journal of autism and developmental disorders (01.05.2021)
Published in Journal of autism and developmental disorders (01.05.2021)
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Enhanced cGAS-STING-dependent interferon signaling associated with mutations in ATAD3A
Lepelley, Alice, Della Mina, Erika, Van Nieuwenhove, Erika, Waumans, Lise, Fraitag, Sylvie, Rice, Gillian I, Dhir, Ashish, Frémond, Marie-Louise, Rodero, Mathieu P, Seabra, Luis, Carter, Edwin, Bodemer, Christine, Buhas, Daniela, Callewaert, Bert, de Lonlay, Pascale, De Somer, Lien, Dyment, David A, Faes, Fran, Grove, Lucy, Holden, Simon, Hully, Marie, Kurian, Manju A, McMillan, Hugh J, Suetens, Kristin, Tyynismaa, Henna, Chhun, Stéphanie, Wai, Timothy, Wouters, Carine, Bader-Meunier, Brigitte, Crow, Yanick J
Published in The Journal of experimental medicine (04.10.2021)
Published in The Journal of experimental medicine (04.10.2021)
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Genomic aberrations of the CACNA2D1 gene in three patients with epilepsy and intellectual disability
Vergult, Sarah, Dheedene, Annelies, Meurs, Alfred, Faes, Fran, Isidor, Bertrand, Janssens, Sandra, Gautier, Agnès, Le Caignec, Cédric, Menten, Björn
Published in European journal of human genetics : EJHG (01.05.2015)
Published in European journal of human genetics : EJHG (01.05.2015)
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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
Morris-Rosendahl, Deborah J, Segel, Reeval, Born, A Peter, Conrad, Christoph, Loeys, Bart, Brooks, Susan Sklower, Müller, Laura, Zeschnigk, Christine, Botti, Christina, Rabinowitz, Ron, Uyanik, Gökhan, Crocq, Marc-Antoine, Kraus, Uwe, Degen, Ingrid, Faes, Fran
Published in European journal of human genetics : EJHG (01.10.2010)
Published in European journal of human genetics : EJHG (01.10.2010)
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Congenital Fixed Dilated Pupils Due to ACTA2– Multisystemic Smooth Muscle Dysfunction Syndrome
Roulez, Françoise M J, Faes, Fran, Delbeke, Patricia, Van Bogaert, Patrick, Rodesch, Georges, De Zaeytijd, Julie, Depasse, Fanny, Coucke, Paul J, Meire, Francoise M
Published in Journal of neuro-ophthalmology (01.06.2014)
Published in Journal of neuro-ophthalmology (01.06.2014)
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New mutations in the RAB3GAP1 gene in patients with Warburg MICRO Syndrome and a possible founder effect in the Danish population
Morris-Rosendahl, Deborah J, Segel, Reeval, Born, A. Peter, Conrad, Christoph, Loeys, Bart L., Sklower Brooks, Susan, Müller, Laura, Zeschnigk, Christine, Botti, Christina, Rabinowitz, Ron, Uyanik, Gökhan, Crocq, Marc-Antoine, Kraus, Uwe, Degen, Ingrid, Faes, Fran
Published in European journal of human genetics : EJHG (26.05.2010)
Published in European journal of human genetics : EJHG (26.05.2010)
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Journal Article
Enhanced cGAS-STING-dependent interferon signaling associated with mutations in ATAD3A
Lepelley, Alice, Erika Della Mina, Erika Van Nieuwenhove, Waumans, Lise, Fraitag, Sylvie, Rice, Gilian I, Dhir, Ashish, Marie-Louise Frémond, Rodero, Mathieu P, Seabra, Luis, Carter, Edwin, Bodemer, Christine, Buhas, Daniela, Callewaert, Bert, De Lonlay, Pascale, Lien De Somer, Dyment, David A, Faes, Fran, Grove, Lucy, Holden, Simon, Hully, Marie, Kurian, Manju A, Mcmillan, Hugh J, Suetens, Kristin, Tyynismaa, Henna, Chhun, Stéphanie, Wai, Timothy, Wouters, Carine, Bader-Meunier, Brigitte, Crow, Yanick J
Published in bioRxiv (03.04.2021)
Published in bioRxiv (03.04.2021)
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