Publications by authors named "I Vandernoot"

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Diagnostic yield of clinical exome sequencing in 868 children with neurodevelopmental disorders.
Sebastian Neuens, Julie Soblet, Aurelie Penninckx, Claire Detry, Cindy Badoer, Isabelle Vandernoot

Eur J Med Genet· August 2025

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Erratum: The G2019S Mutation of Leucine-Rich Repeat Kinase 2 is a Cause of Lewy Body Dementia in Patients with North African Ancestors.
Kurt Segers, Florence Benoit, Levy Sophie, Valérie Martinet, Joachim G Schulz, Isabelle Vandernoot

Alzheimer Dis Assoc Disord· August 2025

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G2019S Mutation of Leucine-Rich Repeat Kinase 2 Is a Cause of Lewy Body Dementia in Patients With North African Ancestors.
Kurt Segers, Florence Benoit, Sophie Levy, Valérie Martinet, Joachim G Schulz, Isabelle Vandernoot

Alzheimer Dis Assoc Disord· November 2024

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Myhre syndrome in adulthood: clinical variability and emerging genotype-phenotype correlations.
Eva Vanbelleghem, Tim Van Damme, Aude Beyens, Sofie Symoens, Kathleen Claes, Isabelle Vandernoot

Eur J Hum Genet· September 2024

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Correction: Myhre syndrome in adulthood: clinical variability and emerging genotype-phenotype correlations.
Eva Vanbelleghem, Tim Van Damme, Aude Beyens, Sofie Symoens, Kathleen Claes, Isabelle Vandernoot

Eur J Hum Genet· September 2024

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