Giovanni Stévanin

21.5k citations
187 papers · 9.8k indexed · 3 hit papers · h-index 55
Topics
Genetic Neurodegenerative Diseases (121 papers)Mitochondrial Function and Pathology (85 papers)Hereditary Neurological Disorders (71 papers)

In The Last Decade

Giovanni Stévanin

186 papers receiving 9.6k citations

Hit Papers

Cloning of the gene for spinocerebellar ataxia 2 reveals ...1995202620052015199619971995200400600

Peers

Giovanni Stévanin
Comparison fields: 5 of 111
  • Cellular and Molecular Neuroscience 7.9k
  • Molecular Biology 6.3k
  • Neurology 3.0k
  • Neurology 2.0k
  • Genetics 1.1k
Replace Garth A. Nicholson with:
Garth A. Nicholson Australia
Stefan M. Pulst United States
Éric Leguern France
Patrick A. Dion Canada
Denise A. Figlewicz United States
Rudolf Martini Germany
Clotilde Lagier‐Tourenne United States
Jeffery L. Twiss United States
Joanna C. Jen United States
Christos Proukakis United Kingdom
Giovanni Stévanin relative to Garth A. Nicholson Australia Garth A. Nicholson's profile →
Citations per field
00.5×1.7×
Garth A. Nicholson · 1×
Citations per year

Countries citing papers authored by Giovanni Stévanin

Since Specialization
Citations

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

Fields of papers citing papers by Giovanni Stévanin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Giovanni Stévanin

This figure shows the co-authorship network connecting the top 25 collaborators of Giovanni Stévanin. A scholar is included among the top collaborators of Giovanni Stévanin 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 Giovanni Stévanin. Giovanni Stévanin is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
#WorkIndexed citations
1 7
2 38
3 6
4 29
5 1
6 148
7 95
8 43
9 9
10 14
11 70
12 30
13 14
14 81
15 76
16 160
17 45
18
The gene for autosomal dominant cerebellar ataxia type II is located in a 5-cM region in 3p12-p13: genetic and physical mapping of the SCA7 locus.
52
19 126
20 5

About Giovanni Stévanin

Giovanni Stévanin is a scholar working on Cellular and Molecular Neuroscience, Neurology and Genetics, having authored 187 papers that have together received 9.8k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (121 papers), Mitochondrial Function and Pathology (85 papers) and Hereditary Neurological Disorders (71 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (7.9k citations), Neurology (2.0k citations) and Neurology (3.0k citations). Giovanni Stévanin has collaborated with scholars based in France, United States and Germany. Frequent co-authors include Alexis Brice, Alexandra Dürr, Yves Agid, Géraldine Cancel‐Tassin, Jean‐Louis Mandel, Gilles David, Georges Imbert, Frédéric Saudou, C. R. Weber and Nacer Abbas. Their work appears in journals such as Nature, Nature Genetics and Journal of Neuroscience.

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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