Marco Toffoli

946 total citations
20 papers, 258 citations indexed

About

Marco Toffoli is a scholar working on Neurology, Physiology and Cell Biology. According to data from OpenAlex, Marco Toffoli has authored 20 papers receiving a total of 258 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Neurology, 11 papers in Physiology and 9 papers in Cell Biology. Recurrent topics in Marco Toffoli's work include Lysosomal Storage Disorders Research (11 papers), Cellular transport and secretion (9 papers) and Parkinson's Disease Mechanisms and Treatments (9 papers). Marco Toffoli is often cited by papers focused on Lysosomal Storage Disorders Research (11 papers), Cellular transport and secretion (9 papers) and Parkinson's Disease Mechanisms and Treatments (9 papers). Marco Toffoli collaborates with scholars based in United Kingdom, United States and Italy. Marco Toffoli's co-authors include Anthony H.V. Schapira, Stephen Mullin, Elisa Menozzi, Derralynn Hughes, Micol Avenali, Fabio Blandini, Fritz J. Sedlazeck, Atul Mehta, Christos Proukakis and Laura Smith and has published in prestigious journals such as Journal of Neurochemistry, Journal of Neurology Neurosurgery & Psychiatry and Pharmacology & Therapeutics.

In The Last Decade

Marco Toffoli

18 papers receiving 255 citations

Peers

Marco Toffoli

NEURO

PHYSI

CMN

Jenny Do United States

Nandkishore R. Belur United States

Elina Makino United States

Petra Oliva United States

Melissa A. Hayes United States

Jennifer L. Badger United Kingdom

Nicholas Toker United States

Neil Kulkarni United States

Monia Hammer United States

Anneke J.A. Kievit Netherlands

Jenny Do United States

Marco Toffoli

172 ×1.2

NEURO

168 ×1.3

PHYSI

71 ×0.9

111 ×1.5

59 ×1.8

CMN

Citations per year, relative to Marco Toffoli Marco Toffoli (= 1×) peers Jenny Do

Countries citing papers authored by Marco Toffoli

Since Specialization

Citations

This map shows the geographic impact of Marco Toffoli's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Marco Toffoli with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Marco Toffoli more than expected).

Fields of papers citing papers by Marco Toffoli

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marco Toffoli. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Marco Toffoli. The network helps show where Marco Toffoli may publish in the future.

Co-authorship network of co-authors of Marco Toffoli

This figure shows the co-authorship network connecting the top 25 collaborators of Marco Toffoli. A scholar is included among the top collaborators of Marco Toffoli based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Marco Toffoli. Marco Toffoli is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Macnaughtan, Jane, Kai‐Yin Chau, Marco Toffoli, et al.. (2025). Mitochondrial function is impaired in long COVID patients. Annals of Medicine. 57(1). 2528167–2528167. 2 indexed citations

Avenali, Micol, Silvia Paola Caminiti, Matthew E. Gegg, et al.. (2025). Combined assessment of blood glucocerebrosidase activity and α-synuclein levels in GBA1 mutation carriers: A novel potential biomarker. Parkinsonism & Related Disorders. 135. 107854–107854. 1 indexed citations

Kalef-Ezra, Ester, Dominic W. Horner, Xinchang Zheng, et al.. (2025). Single cell long read whole genome sequencing reveals somatic transposon activity in human brain. Communications Biology. 8(1). 1627–1627.

Menozzi, Elisa, Jane Macnaughtan, Linda L. Gallo, et al.. (2025). Severe GBA1 variants drive the GBA1-PD clinical phenotype: implications for counselling and clinical trials. npj Parkinson s Disease. 11(1). 281–281.

Andreuzzi, Eva, Marco Toffoli, Gabriella Zito, et al.. (2024). P-424 Placental extracellular matrix remodelling in pregnancies by oocyte donation shows similarities with preeclamptic placenta: a pilot study. Human Reproduction. 39(Supplement_1). 1 indexed citations

Toffoli, Marco, Elisa Menozzi, Stephen Mullin, et al.. (2024). Consensus Guidance for Genetic Counseling in GBA1 Variants: A Focus on Parkinson's Disease. Movement Disorders. 39(12). 2144–2154. 3 indexed citations

Agostinis, Chiara, Gabriella Zito, Marco Toffoli, et al.. (2023). Evaluation of levels, specificity and pathophysiology of anti-C1q autoantibodies in pregnancy. Journal of Reproductive Immunology. 159. 104081–104081. 2 indexed citations

Villa, Alessandro, Marco Toffoli, Nicoletta Rizzi, et al.. (2023). Sex-Specific Microglial Responses to Glucocerebrosidase Inhibition: Relevance to GBA1-Linked Parkinson’s Disease. Cells. 12(3). 343–343. 6 indexed citations

Balestrino, Roberta, Tiziana Martone, Marco Toffoli, et al.. (2023). Levodopa-carbidopa intestinal gel infusion (LCIG) in Parkinson disease with genetic mutations. Neurological Sciences. 45(4). 1489–1497. 6 indexed citations

10.

Menozzi, Elisa, Marco Toffoli, & Anthony H.V. Schapira. (2023). Targeting the GBA1 pathway to slow Parkinson disease: Insights into clinical aspects, pathogenic mechanisms and new therapeutic avenues. Pharmacology & Therapeutics. 246. 108419–108419. 33 indexed citations

11.

Blauwendraat, Cornelis, Nahid Tayebi, Grisel Lopez, et al.. (2023). Polygenic Parkinson's Disease Genetic Risk Score as Risk Modifier of Parkinsonism in Gaucher Disease. Movement Disorders. 38(5). 899–903. 11 indexed citations

12.

Toffoli, Marco, Xiaohong Chen, Fritz J. Sedlazeck, et al.. (2022). Comprehensive short and long read sequencing analysis for the Gaucher and Parkinson’s disease-associated GBA gene. Communications Biology. 5(1). 670–670. 17 indexed citations

13.

Toffoli, Marco, et al.. (2021). The Remote Assessment of Parkinsonism Supporting the Ongoing Development of Interventions in Gaucher Disease. Neurodegenerative Disease Management. 11(6). 451–458. 6 indexed citations

14.

Toffoli, Marco, Xiao Chen, Michael A. Eberle, et al.. (2021). Intronic Haplotypes in the GBA Gene Do Not Predict Age at Diagnosis of Parkinson's Disease. Movement Disorders. 36(6). 1456–1460. 4 indexed citations

15.

Toffoli, Marco, Laura Smith, & Anthony H.V. Schapira. (2020). The biochemical basis of interactions between Glucocerebrosidase and alpha‐synuclein in GBA1 mutation carriers. Journal of Neurochemistry. 154(1). 11–24. 14 indexed citations

16.

Toffoli, Marco, et al.. (2020). Genetic causes of PD: A pathway to disease modification. Neuropharmacology. 170. 108022–108022. 26 indexed citations

17.

Toffoli, Marco, et al.. (2020). Biofluid Biomarkers in Parkinson's Disease: Clarity Amid Controversy. Movement Disorders. 35(7). 1128–1133. 7 indexed citations

18.

Avenali, Micol, Marco Toffoli, Stephen Mullin, et al.. (2019). Evolution of prodromal parkinsonian features in a cohort ofGBAmutation-positive individuals: a 6-year longitudinal study. Journal of Neurology Neurosurgery & Psychiatry. 90(10). 1091–1097. 46 indexed citations

19.

Sedlazeck, Fritz J., Marco Toffoli, Stephen Mullin, et al.. (2019). Evaluation of the detection of GBA missense mutations and other variants using the Oxford Nanopore MinION. Molecular Genetics & Genomic Medicine. 7(3). e564–e564. 51 indexed citations

20.

Toffoli, Marco, Eva Dreussi, Erika Cecchin, et al.. (2017). SNCA 3′UTR genetic variants in patients with Parkinson’s disease and REM sleep behavior disorder. Neurological Sciences. 38(7). 1233–1240. 22 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

Explore authors with similar magnitude of impact