Matthis Synofzik

158PUBLICATIONS

700CO-AUTHORS

Developmental genetics (incl. sex determination)Speech pathologyMolecular evolutionDiagnostic radiographyGene mapping

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Publications (158)

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|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

|Mar 10, 2026

Teaching NeuroImage: Superior Cerebellar Peduncle Tract Sign in SCA27B.

Benjamin Roeben, David Pellerin, Benjamin Bender

|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

27 joint publications

Harro Seelaar

27 joint publications

Simon Ducharme

22 joint publications

Rik Vandenberghe

22 joint publications

Caroline Graff

22 joint publications

Alexander Gerhard

21 joint publications

Andreas Traschütz

20 joint publications

Barbara Borroni

19 joint publications

Daniela Galimberti

19 joint publications

Raquel Sanchez-Valle

18 joint publications

Elizabeth Finger

Frequent Collaborators

27 joint publications

Harro Seelaar

27 joint publications

Simon Ducharme

22 joint publications

Rik Vandenberghe

22 joint publications

Caroline Graff