Vincent Dion

2.4k citations
34 papers · 1.8k · h-index 19

Impact in

    • Genetic Neurodegenerative Diseases
    • DNA Repair Mechanisms
    • Genomics and Chromatin Dynamics
    • RNA Research and Splicing
    • Mitochondrial Function and Pathology
    • CRISPR and Genetic Engineering
    • Nuclear Structure and Function

Papers in

    • DNA Repair Mechanisms 16
    • Mitochondrial Function and Pathology 12
    • Genomics and Chromatin Dynamics 8
    • RNA Research and Splicing 6
    • CRISPR and Genetic Engineering 4
    • Nuclear Structure and Function 4
    • Genetic Neurodegenerative Diseases 19

Vincent Dion

33 papers receiving 1.7k citations

Peers

Vincent Dion
Comparison fields: 5 of 71
  • Cellular and Molecular Neuroscience 453
  • Molecular Biology 1.6k
  • Genetics 209
  • Cell Biology 94
  • Aging 10
Replace Derick G. Wansink with:
Derick G. Wansink Netherlands
Daniele Canzio United States
Andrea N. Ladd United States
Cecilia Zuliani Germany
Susan Clapoff Canada
Benjamin J. Frankfort United States
Kelly P. Smith United States
Shigeki Yoshiura United States
Grace E. Peng United States
Adeela Syed United States
Vincent Dion relative to Derick G. Wansink Netherlands Derick G. Wansink's profile →
Citations per field
00.5×3.3×
Derick G. Wansink · 1×
Citations per year

Countries citing papers authored by Vincent Dion

Since Specialization
Citations

This map shows the geographic impact of Vincent Dion'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 Vincent Dion with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Vincent Dion more than expected).

Fields of papers citing papers by Vincent Dion

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Vincent Dion. 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 Vincent Dion. The network helps show where Vincent Dion may publish in the future.

Co-authors

The 25 scholars most cited alongside Vincent Dion, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Vincent Dion Line = papers co-authored together Vincent Dion links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 34 papers — load more, or switch the sort, to bring in the rest.

#Work
1 2012239
2 2013172
3 2014136
4 2006135
5 2012130
6 2015100
7 201392
8 200990
9 201377
10 200874
11 201661
12 201158
13 200858
14 201056
15 202150
16 201138
17 201432
18 200331
19 201119
20 201418

About Vincent Dion

Vincent Dion is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience, Genetics, Cardiology and Cardiovascular Medicine and Oncology, having authored 34 papers that have together received 1.8k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (19 papers), DNA Repair Mechanisms (16 papers), Mitochondrial Function and Pathology (12 papers), Genomics and Chromatin Dynamics (8 papers), RNA Research and Splicing (6 papers), Genetics and Neurodevelopmental Disorders (5 papers), CRISPR and Genetic Engineering (4 papers) and Nuclear Structure and Function (4 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (453 citations), Molecular Biology (1.6k citations), Genetics (209 citations), Cell Biology (94 citations) and Aging (10 citations). Vincent Dion has collaborated with scholars based in Switzerland, United States and United Kingdom. Frequent co-authors include Susan M. Gasser, John H. Wilson, Yunfu Lin, Chihiro Horigome, Véronique Kalck, Andrew Seeber, Benjamin D. Towbin, Leroy Hubert, Lutz R. Gehlen and Roger Schmid. Their work appears in journals such as Genes & Development, Human Molecular Genetics, Molecular and Cellular Biology, Trends in Genetics and Scientific Reports.

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.

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