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Manuela Basso

Affiliation : University of Trento

2Publications (affiliation in Italy)
106Total publications
3635Citations
32h-index

Research profile

Manuela Basso has 2 indexed publications (2020). Their work appears in “Genetics in Medicine”. Their most cited article, “Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive” (2020), has been cited 49 times. Their work is co-authored with at least 12 researchers.

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Research areas

Amyotrophic Lateral Sclerosis Research
Genetic Neurodegenerative Diseases
Alzheimer's disease research and treatments
Hereditary Neurological Disorders
Extracellular vesicles in disease

Publications (2)

Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment
2020 · Genetics in Medicine · cited 49 times
Correction: Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment
2020 · Genetics in Medicine · cited 2 times

Collaborations

Partner institutions : University of Naples Federico II · IRCCS Eugenio Medea · University of Turin · Federico II University Hospital · University of Padua

Co-authors

Bibliographic data from OpenAlex (open database).