Holger Hengel

20PUBLICATIONS
175CO-AUTHORS
Neurology and neuromuscular diseasesGene mappingEpigenetics (incl. genome methylation and epigenomics)Psychology of ageingAerospace structures
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Publications (20)

|Mar 31, 2026
Natural History of Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia (ALSP): A Retrospective Patient Cohort Study.

Stefanie N Hayer, Donald G McLaren, Robin M Nance

|Feb 14, 2026
Loss-of-function variants in the CAPN1 activator CD99L2 cause X-linked spastic ataxia.

Benita Menden, Rana D Incebacak Eltemur, German Demidov

|Aug 02, 2025
ARSA Variants Associated With Cognitive Decline and Long-Term Preservation of Motor Function in Metachromatic Leukodystrophy.

Shanice Beerepoot, Daphne H Schoenmakers, Francesca Fumagalli

|Jan 17, 2025
Genomic reanalysis of a pan-European rare-disease resource yields new diagnoses.

Steven Laurie, Wouter Steyaert, Elke de Boer

|May 15, 2024
Unravelling undiagnosed rare disease cases by HiFi long-read genome sequencing.

Wouter Steyaert, Lydia Sagath, German Demidov

|Mar 21, 2024
FARS-ADL across Ataxias: Construct Validity, Sensitivity to Change, and Minimal Important Change.

Andreas Traschütz, Zofia Fleszar, Holger Hengel

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Frequent Collaborators

9 joint publications

Matthis Synofzik

5 joint publications

Ludger Schöls

4 joint publications

Stephan Ossowski

3 joint publications

Kiran Polavarapu