Vincenzo Bonifati - Genetic Mutations

Author Information

Vincenzo Bonifati is affiliated with Erasmus MC, University Medical Center, in the Department of Clinical Genetics, Rotterdam, the Netherlands. His research focuses primarily on the genetic underpinnings of Parkinson’s disease and related neurodegenerative disorders. His work involves exploring gene mutations, their pathways, and their clinical implications, contributing significantly to the understanding and potential treatment of these conditions.

Research Contributions

Vincenzo Bonifati has made substantial contributions to the field of genetic research in neurodegenerative diseases, particularly Parkinson's disease. His recent publications include studies on differential gene expression in Parkinson’s disease, the impact of specific gene mutations like AOPEP and WARS2, and the interactions between proteins such as LRP10 and SORL1. His research has also delved into genetic counseling for Parkinson's disease, highlighting the importance of genetic testing and the challenges associated with it. Bonifati’s work is widely recognized and cited, reflecting his influence and the importance of his research in the field.

Aliases

Vincenzo Bonifati is also known by the aliases V Bonifati and V. Bonifati.

Publication and Citation Metrics

Metric Value
Citation Count 20,644
H-index 68
Paper Count 280

Publications:

DOI: 10.3390/cells11020198

Year: 2022

DOI: 10.1002/mds.28928

Year: 2022

DOI: 10.1007/s00401-021-02313-3

Year: 2021

DOI: 10.1016/j.parkreldis.2021.11.030

Year: 2021

DOI: 10.1016/j.parkreldis.2021.06.023

Year: 2021

DOI: 10.1016/j.parkreldis.2021.10.001

Year: 2021

DOI: 10.1002/mdc3.13098

Year: 2021

DOI: 10.1212/WNL.0000000000012705

Year: 2021

DOI: 10.1038/s41598-020-80564-y

Year: 2021

DOI: 10.1002/mds.28517

Year: 2021

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