Liedewei Van de Vondel

11PUBLICATIONS
97CO-AUTHORS
Neurology and neuromuscular diseasesOptometryNeurogeneticsGene expression (incl. microarray and other genome-wide approaches)Medical infection agents (incl. prions)
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Publications (11)

|Jun 22, 2026
Convergent human genetic evidence implicates serine biosynthesis in diabetic peripheral neuropathy.

|Apr 10, 2026
A 5' UTR CCG expansion in TBC1D7 causes oculopharyngodistal myopathy.

Liedewei Van de Vondel, Riccardo Curro, Stefano Facchini

|Sep 25, 2025
A heterozygous 9q34 deletion encompassing SPTAN1 as a cause of distal myopathy.

Liedewei Van de Vondel, Jonathan De Winter, Alice Monticelli

|Sep 09, 2025
The Solve-RD Solvathons as a pan-European interdisciplinary collaboration to diagnose patients with rare disease.

Vicente A Yépez, German Demidov, Kornelia Ellwanger

|Aug 20, 2025
Biallelic variants in COX18 cause a mitochondrial disorder primarily manifesting as peripheral neuropathy.

Camila Armirola-Ricaurte, Laura Morant, Isabelle Adant

|Feb 14, 2025
TBP Repeat Expansion Analysis in Patients Carrying Heterozygous STUB1 Variants.

Jonathan De Winter, Liedewei Van de Vondel, Kristof Van Schil

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Frequent Collaborators

5 joint publications

Steven Laurie

5 joint publications

German Demidov

3 joint publications

Jonathan De Winter

3 joint publications

Kornelia Ellwanger