The cerebellar cognitive affective syndrome

• A Patient-Reported Outcome Measure of Communication Difficulties in Friedreich Ataxia: COMATAX.

  2026 The Cerebellum article Neuroscience Genetic Neurodegenerative Diseases Open access

  1

  citations
• A Severity‐Agnostic Atrophy Pattern in Spinocerebellar Ataxia Type 3: Volumetrics from ENIGMA ‐Ataxia

  2026 Movement Disorders article Neuroscience Genetic Neurodegenerative Diseases Open access

  0

  citations
• Fronto-cerebellar connectivity disruptions and functional reorganization in Friedreich’s Ataxia: A structural and resting-state fMRI study

  2026 NeuroImage article Neuroscience Functional Brain Connectivity Studies Open access

  1

  citations
• Cognitive impairment in SCA3: A multi-center cohort study with demographic, imaging, and biomarker correlates

  2026 Neurobiology of Disease article Neuroscience Genetic Neurodegenerative Diseases Open access

  1

  citations
• A Core Pattern of Cerebellar and Brainstem Degeneration and Reduced Cerebrocerebellar Structural Covariance in Spinocerebellar Ataxia Type 3 (SCA3): MRI Volumetrics from ENIGMA-Ataxia

  2025 bioRxiv (Cold Spring Harbor Laboratory) preprint Neuroscience Genetic Neurodegenerative Diseases Open access

  1

  citations
• Differential Effects of Cerebellar tDCS on Sequential Mentalizing

  2025 The Cerebellum book-chapter Neuroscience Transcranial Magnetic Stimulation Studies Open access

  0

  citations
• Optimizing selectivity of the Cerebellar Cognitive Affective Syndrome Scale by use of correction formulas, and validation of its German version

  2025 Journal of Neurology article Neuroscience Vestibular and auditory disorders Open access

  9

  citations
• Cerebellar Development and the Burden of Prematurity

  2025 The Cerebellum article Medicine Neonatal and fetal brain pathology Open access

  14

  citations
• Subtypes of cognitive impairment in cerebellar disease identified by cross-diagnostic cluster-analysis: results from a German multicenter study

  2024 Journal of Neurology article Medicine Dementia and Cognitive Impairment Research Open access

  6

  citations
• Patient-reported, health economic and psychosocial outcomes in patients with Friedreich ataxia (PROFA): protocol of an observational study using momentary data assessments via mobile health app

  2023 BMJ Open article Neuroscience Genetic Neurodegenerative Diseases Open access

  12

  citations
• cATR Tracing Approach to Identify Individual Intermediary Neurons Based on Their Input and Output: A Proof-of-Concept Study Connecting Cerebellum and Central Hubs Implicated in Developmental Disorders

  2022 Cells article Neuroscience Neuroscience and Neuropharmacology Research Open access

  2

  citations
• The CCAS-scale in hereditary ataxias: helpful on the group level, particularly in SCA3, but limited in individual patients

  2022 Journal of Neurology article Neuroscience Genetic Neurodegenerative Diseases Open access

  32

  citations
• The cognitive profile of Friedreich ataxia: a systematic review and meta-analysis

  2022 BMC Neurology review Neuroscience Genetic Neurodegenerative Diseases Open access

  28

  citations
• Functional connectome of human cerebellum

  2022 NeuroImage article Neuroscience Functional Brain Connectivity Studies Open access

  44

  citations
• Cognitive Decline Is Closely Associated with Ataxia Severity in Spinocerebellar Ataxia Type 2: a Validation Study of the Schmahmann Syndrome Scale

  2021 The Cerebellum article Neuroscience Genetic Neurodegenerative Diseases

  48

  citations
• Reference values for the Cerebellar Cognitive Affective Syndrome Scale: age and education matter

  2020 Brain article Neuroscience Vestibular and auditory disorders Open access

  34

  citations
• Validation of a German version of the Cerebellar Cognitive Affective/ Schmahmann Syndrome Scale: preliminary version and study protocol

  2020 Neurological Research and Practice article Neuroscience Vestibular and auditory disorders Open access

  28

  citations
• Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment

  2020 Genetics in Medicine article Neuroscience Genetic Neurodegenerative Diseases Open access

  51

  citations
• Functional Characterization of Atrophy Patterns Related to Cognitive Impairment

  2020 Frontiers in Neurology article Neuroscience Functional Brain Connectivity Studies Open access

  15

  citations

19 results