Matthis Synofzik

159PUBLICATIONS
701CO-AUTHORS
Forensic epidemiologyDevelopmental genetics (incl. sex determination)Speech pathologyMolecular evolutionGene mapping
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Publications (159)

|Aug 05, 2026
Educational attainment and sex modulate clinical outcomes in genetic frontotemporal dementia.

|Jun 22, 2026
Trajectories of brain structure and function in young adult carriers of genetic frontotemporal dementia variants.

|Mar 10, 2026
Development and validation of the dysarthria impact scale: a patient-reported outcome for motor speech disorders.

Adam P Vogel, Lisa Graf, Merit Weiß

|Mar 10, 2026
Identification of Biological Subtypes of Friedreich Ataxia with Structural MRI-based Machine Learning.

Giuseppe Pontillo, Simone Penna, Filippo Arrigoni

|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

|Feb 12, 2026
Composite grey matter fingerprints for genetic frontotemporal dementia.

Arabella Bouzigues, Giulia Campana, Matthieu Joulot

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Frequent Collaborators

28 joint publications

Harro Seelaar

28 joint publications

Simon Ducharme

23 joint publications

Rik Vandenberghe

23 joint publications

Caroline Graff