Research output per year
Research output per year
Personal profile
Research interests
Vincenzo Bonifati is Professor in Genetics of Movement Disorders at the Erasmus University Rotterdam, The Netherlands. He received his MD and neurology certification from the University of Roma, Italy.
His research focuses on the understanding of molecular mechanisms of Parkinson’s disease and dystonia by the identification of disease-causing genetic variants and the characterization of the involved molecular pathways. His work led to the discovery of genetic defects underlying several forms of hereditary parkinsonism, dystonia, and other more rare movement disorders.
He published more than 230 papers in peer-reviewed journals, and has an H-index of 68.
His work has been cited more than 20,000 times so far.
He was co-Editor in chief of Parkinsonism & Related Disorders (2018-2023).
Education/Academic qualification
PhD, Autosomal recessive, early-onset Parkinson's disease, Erasmus University Rotterdam
Award Date: 10 Dec 2003
Board certification - Clinical Neurology, University of Rome La Sapienza
Award Date: 5 Nov 1992
Bachelor, MD, University of Rome La Sapienza
Award Date: 5 Nov 1988
Fingerprint
Dive into the research topics where Vincenzo Bonifati is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
- 1 Similar Profiles
Collaborations and top research areas from the last five years
Recent external collaboration on country/territory level. Dive into details by clicking on the dots or
-
LRP10 and α-synuclein transmission in Lewy body diseases
Carreras Mascaro, A., Grochowska, M. M., Boumeester, V., Dits, N. F. J., Bilgiҫ, E. N., Breedveld, G. J., Vergouw, L., de Jong, F. J., van Royen, M. E., Bonifati, V. & Mandemakers, W., Dec 2024, In: Cellular and molecular life sciences : CMLS. 81, 1, p. 75 1 p., 75.Research output: Contribution to journal › Article › Academic › peer-review
Open AccessFile2 Citations (Scopus)12 Downloads (Pure) -
Clinical, neuroimaging and genetic findings in Brazilian patients with neurodegeneration with brain iron accumulation
Araújo Salomão, R. P., Rezende Filho, F. M., Borges, V., Kurian, M. A., Ferraz, H. B., Breedveld, G. J., Bonifati, V., Barsottini, O. G. & Pedroso, J. L., Jun 2024, In: Parkinsonism and Related Disorders. 123, 106103.Research output: Contribution to journal › Article › Academic › peer-review
-
Altered TFEB subcellular localization in nigral neurons of subjects with incidental, sporadic and GBA-related Lewy body diseases
Moors, T. E., Morella, M. L., Bertran-Cobo, C., Geut, H., Udayar, V., Timmermans-Huisman, E., Ingrassia, A. M. T., Brevé, J. J. P., Bol, J. G. J. M., Bonifati, V., Jagasia, R. & van de Berg, W. D. J., 6 Apr 2024, In: Acta Neuropathologica. 147, 1, 67.Research output: Contribution to journal › Article › Academic › peer-review
Open AccessFile4 Downloads (Pure) -
Establishing an online resource to facilitate global collaboration and inclusion of underrepresented populations: Experience from the MJFF Global Genetic Parkinson's Disease Project
Vollstedt, E. J., Madoev, H., Aasly, A., Ahmad-Annuar, A., Al-Mubarak, B., Alcalay, R. N., Alvarez, V., Amorin, I., Annesi, G., Arkadir, D., Bardien, S., Barker, R. A., Barkhuizen, M., Basak, A. N., Bonifati, V., Boon, A., Brighina, L., Brockmann, K., Carmine Belin, A. & Carr, J. & 63 others, , 3 Oct 2023, In: PLoS ONE. 18, 10 October, e0292180.Research output: Contribution to journal › Article › Academic › peer-review
Open AccessFile10 Downloads (Pure) -
Genetic Testing in Parkinson's Disease
Pal, G., Cook, L., Schulze, J., Verbrugge, J., Alcalay, R. N., Merello, M., Sue, C. M., Bardien, S., Bonifati, V., Chung, S. J., Foroud, T., Gatto, E., Hall, A., Hattori, N., Lynch, T., Marder, K., Mascalzoni, D., Novaković, I., Thaler, A. & Raymond, D. & 7 others, , Aug 2023, In: Movement Disorders. 38, 8, p. 1384-1396 13 p.Research output: Contribution to journal › Review article › Academic › peer-review
Open AccessFile9 Citations (Scopus)26 Downloads (Pure)