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Anke Van Dijck

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Doctor-assistant

University of Antwerp

Belgium

Research Interests

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Professors in Belgium

Recent Grants

Grant: Close

Improving healthcare and well-being in people with intellectual disabilities through professional skills training with simulation patients

Open Date: 2023-10-01

Close Date: 2025-09-01

Grant: Close

A Double Blind Crossover Trial of Ganaxolone in Patients with Fragile X Syndrome

Open Date: 2013-01-01

Close Date: 2015-01-01

Grant: Close

GABAerge behandeling van het fragiele X syndroom

Open Date: 2012-01-01

Close Date: 2013-01-01

Articles (13)

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2026

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2025

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2025

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2025

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2025

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2025

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2025

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2024

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2024

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2024

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2023

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2023

Year:

2023

Collaborators (12)

Frank Kooy

Professor

University of Antwerp

BELGIUM

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Anna Jansen

University of Antwerp

BELGIUM

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Marc Buehler

Professor in Molecular Biology

University of Basel

SWITZERLAND

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Michele Gabriele

Group Leader

San Raffaele Telethon Institute for Gene Therapy

ITALY

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Joe Ibrahim

University of Antwerp

BELGIUM

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Marije Meuwissen

BELGIUM

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David J. Amor

University of Melbourne

AUSTRALIA

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laïla el khattabi

Sorbonne Université Faculté de Médecine

FRANCE

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Siddharth Banka

The University of Manchester

UNITED KINGDOM

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Ann Hallemans

Associate Research Professor

University of Antwerp

BELGIUM

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Corrado Romano

Docenti di ruolo di IIa fascia

University of Catania

ITALY

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Claudia Vingerhoets

Assistant Professor

University of Maastricht

NETHERLANDS

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Anke Van Dijck

Research Interests

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Recent Grants

Articles (13)

Correction: A missense variant in the KH0-domain of FMRP downregulates the protein in a patient with the clinical hallmarks of fragile X syndrome

Genetic modifiers and ascertainment drive variable expressivity of complex disorders

A Systematic Review Illustrates the Expanding Clinical and Molecular Landscape of Helsmoortel-Van der Aa Syndrome

A missense variant in the KH0-domain of FMRP downregulates the protein in a patient with the clinical hallmarks of fragile X syndrome

ADNP Exhibits Methyltransferase Activity in Overexpression Systems and Modulates DNA and Histone Methylation

A frameshift variant in activity-dependent neuroprotective protein (ADNP) causes nucleocytoskeletal alterations in a dizygotic male twin: a case study

Investigation of gait characteristics and kinematic deviations in rare genetic disorders with instrumented gait analysis

ADNP dysregulates methylation and mitochondrial gene expression in the cerebellum of a Helsmoortel–Van der Aa syndrome autopsy case

Tracing the invisible mutant ADNP protein in Helsmoortel-Van der Aa syndrome patients

Correction to: ADNP dysregulates methylation and mitochondrial gene expression in the cerebellum of a Helsmoortel–Van Der Aa syndrome autopsy case

Assortative mating and parental genetic relatedness contribute to the pathogenicity of variably expressive variants.

Chromatin remodeler Activity-Dependent Neuroprotective Protein (ADNP) contributes to syndromic autism

‘Puzzelstukjes vallen op hun plaats’

Collaborators (12)

Frank Kooy

Anna Jansen

Marc Buehler

Michele Gabriele

Joe Ibrahim

Marije Meuwissen

David J. Amor

laïla el khattabi

Siddharth Banka

Ann Hallemans

Corrado Romano

Claudia Vingerhoets

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