Michael D. Geschwind

Johns Hopkins University — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

55h-index17.4kcitations253works8.82yr avg
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Research Topics

Prion Diseases and Protein Misfolding(116), Neurological diseases and metabolism(49), Genetic Neurodegenerative Diseases(47), Autoimmune Neurological Disorders and Treatments(38), Neurological disorders and treatments(24)

Publications253 total

Standardizing “Rapid”
Neurology·2025· 1 cited
Creutzfeldt–Jakob Disease and Other Prion Diseases
Cambridge University Press eBooks·2025
Correction: The Natural History Study and Biomarker Collection of the Clinical Research Consortium for the Study of Cerebellar Ataxia (CRC-SCA)
The Cerebellum·2025Open Access
Predictive models for ataxia progression and conversion in spinocerebellar ataxia type 1 and 3
Brain·2025Open Access
Prevalence, Severity, and Progression of Cerebellar Cognitive-Affective Syndrome in Patients With Spinocerebellar Ataxias
Neurology·2025· 2 citedOpen Access
“It may cost you your money, it costs you your life”: a framework for financial hardship in dementia
The Gerontologist·2025Open Access
The Natural History Study and Biomarker Collection of the Clinical Research Consortium for the Study of Cerebellar Ataxia (CRC-SCA)
The Cerebellum·2025
Decoding the Clinical Features that Associate with Progression, Causes, and Outcomes in Patients with Suspected Rapidly Progressive Dementia
Annals of Neurology·2025· 1 citedOpen Access
Suicidal Ideation in Spinocerebellar Ataxia
Journal of Neuropsychiatry·2025
1268 Sleep in Slow and Fast Genetic Carriers of Prion Diseases
SLEEP·2025Open Access
Spinocerebellar Ataxia Progression Measured with the Patient‐Reported Outcome Measure of Ataxia
Movement Disorders·2025· 9 citedOpen Access
“By the Time We Knew …”: Poetic Analysis of End‐of‐Life Caregiving Experiences for Rapidly Progressive and Slower‐Duration Dementia Syndromes
Journal of the American Geriatrics Society·2025· 1 citedOpen Access
Multiomic analyses direct hypotheses for Creutzfeldt-Jakob disease risk genes
Brain·2025· 7 citedOpen Access
TRANSIENT ALTERATIONS IN THALAMO-CEREBELLAR FUNCTIONAL CONNECTIVITY IN PREMANIFEST HUNTINGTON’S DISEASE
2025Open Access
Unraveling the earliest phases of vascular cognitive impairment and dementia by establishing a large USA CADASIL Consortium
Alzheimer s & Dementia·2024Open Access
Dynamic and static functional network connectivity distinguish symptomatic and non‐symptomatic individuals with CADASIL
Alzheimer s & Dementia·2024Open Access
Dynamic and static functional network connectivity distinguish symptomatic and non‐symptomatic individuals with CADASIL
Alzheimer s & Dementia·2024Open Access
A Multi-center Exploration of Efficacious Treatment Approaches in LGI1-Ab Encephalitis
Neurology·2024Open Access
7T MRI Reveals Abnormal Iron Deposition and Microstructure in Premanifest and Manifest Huntington’s Disease
Proceedings on CD-ROM - International Society for Magnetic Resonance in Medicine. Scientific Meeting and Exhibition/Proceedings of the International Society for Magnetic Resonance in Medicine, Scientific Meeting and Exhibition·2024
Genome wide association study of clinical duration and age at onset of sporadic CJD
PLoS ONE·2024· 5 citedOpen Access
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Frequent Co-authors

Bruce L. Miller(16), Jeffrey M. Gelfand(6), Leonel Tadao Takada(6), Sarosh R. Irani(5), Aissa Haman(5), Stephen J. DeArmond(5), Charles C. Torres-Chae(4), Howard J. Rosen(4), Sven Forner(4), Joel H. Kramer(4), Francesc Graus(3), Patrick Waters(3), Josep Dalmau(3), Huidy Shu(3), Gil D. Rabinovici(3), Paul A. Garcia(3), Paolo Vitali(3), David Y. Johnson(3), Jennifer L. Martindale(3), Howard J. Federoff(3)