Anna Jansen

University of Antwerp

Belgium

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Articles (18)

Year:

2024

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2024

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2024

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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

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2023

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2023

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2022

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2022

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2022

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2022

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2022

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2022

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2022

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2021

Collaborators (24)

Zein Mersini Besharat

Sapienza University of Rome

ITALY

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Annelieke Müller

Assistant professor

Amsterdam UMC

NETHERLANDS

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Kathelijn Keymolen

Vrije Universiteit Brussel

BELGIUM

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Aster Harder

Leiden University Medical Center

NETHERLANDS

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Nicole Tartaglia

Professor

University of Colorado School of Medicine

UNITED STATES

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Christina Engel Høi-Hansen

Professor

University of Copenhagen

DENMARK

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Katrien Stouffs

Vrije Universiteit Brussel

BELGIUM

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Boyan Ivanov Dimitrov

Vrije Universiteit Brussel

BELGIUM

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Terri Finkel

Interim Chair and Pediatrician-in-Chief

UTS

UNITED STATES

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Ellen Rijckmans

Vrije Universiteit Brussel

BELGIUM

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Carola Brussaard

Vrije Universiteit Brussel

BELGIUM

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Tim Vanderhasselt

Vrije Universiteit Brussel

BELGIUM

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Alice Maulisova

Assistant Professor

Charles University

CZECH REPUBLIC

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Ankur Kamdar

UTHealth

UNITED STATES

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Marije Meuwissen

BELGIUM

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Elisabetta Ferretti

Full Professor

Sapienza University of Rome

ITALY

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Peter Janssens

Head of clinics

Universitair Ziekenhuis Antwerpen

BELGIUM

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Berten Ceulemans

BELGIUM

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Eva Cloet

Vrije Universiteit Brussel

BELGIUM

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Mark Fitzgerald

Assistant Professor of Clinical Neurology

UNITED STATES

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Guido Rubboli

Københavns Universitet

DENMARK

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Angeliki Malliri

Professor of Cell Biology

The University of Manchester

UNITED KINGDOM

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Tom H Millard

UNITED KINGDOM

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Małgorzata Urbańska

International Institute of Molecular and Cell Biology in Warsaw

POLAND

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Anna Jansen

Research Interests

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Articles (18)

Diagnostic work-up in malformations of cortical development

Prevalence of Liver Steatosis in Tuberous Sclerosis Complex Patients

Interorganisational collaboration to improve accessibility of diagnostic evaluations for children with a developmental disability

Further characterisation ofARX-related disorders in females due to inherited or de novo variants

Macrocephaly?

From diagnosis to treatment in genetic epilepsies: Implementation of precision medicine in real-world clinical practice

Anti-Sp4 autoantibodies co-occur with anti-TIF1 and are associated with distinct clinical features and immunogenetic risk factors in juvenile myositis

Confirmation of gray matter heterotopia as part of the DDX23 phenotypic spectrum

Overlapping cortical malformations in patients with pathogenic variants in GRIN1 and GRIN2B

Understanding the impact of tuberous sclerosis complex

Activating RAC1 variants in the switch II region cause a developmental syndrome and alter neuronal morphology

Malformations of cerebral development and clues from the peripheral nervous system

Early impact of X- and Y-chromosome variations (XXX, XXY, XYY) on social communication and social emotional development in 1–2-year-old children

Down-regulation of the brain-specific cell-adhesion molecule contactin-3 in tuberous sclerosis complex during the early postnatal period

miRNAs and isomiRs

Evolution of electroencephalogram in infants with tuberous sclerosis complex and neurodevelopmental outcome: a prospective cohort study

Empowering Families Through Technology

Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implications

Collaborators (24)

Zein Mersini Besharat

Annelieke Müller

Kathelijn Keymolen

Aster Harder

Nicole Tartaglia

Christina Engel Høi-Hansen

Katrien Stouffs

Boyan Ivanov Dimitrov

Terri Finkel

Ellen Rijckmans

Carola Brussaard

Tim Vanderhasselt

Alice Maulisova

Ankur Kamdar

Marije Meuwissen

Elisabetta Ferretti

Peter Janssens

Berten Ceulemans

Eva Cloet

Mark Fitzgerald

Guido Rubboli

Angeliki Malliri

Tom H Millard

Małgorzata Urbańska

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