Sylviane Marouillat

1.2k citations
35 papers · 732 indexed · h-index 15
  • Neurology top 5%
    • Amyotrophic Lateral Sclerosis Research 14
    • Parkinson's Disease Mechanisms and Treatments 3
    • Neurological diseases and metabolism 2
  • Genetics top 10%
    • Neurogenetic and Muscular Disorders Research 11
    • Genetics and Neurodevelopmental Disorders 10
  • Neurology top 10%
    • Amyotrophic Lateral Sclerosis Research 14
    • Parkinson's Disease Mechanisms and Treatments 3
    • Neurological diseases and metabolism 2
  • Nephrology top 10%
    • Autism Spectrum Disorder Research 6
    • Ubiquitin and proteasome pathways 5
    • Pluripotent Stem Cells Research 2

Sylviane Marouillat

35 papers receiving 729 citations

Peers

Sylviane Marouillat
Comparison fields: 5 of 91
  • Neurology 199
  • Genetics 96
  • Neurology 71
  • Nephrology 59
  • Developmental Neuroscience 28
Replace Lucía Galán with:
Lucía Galán Spain
Guoda Ma China
Mónica Sánchez-Contreras United States
Bruno Maranda Canada
Jiasheng Zhang United States
C. Henrique Alves Netherlands
Ekaterina Zakharova Russia
Barry A. Chioza United Kingdom
Julián Esteve-Rudd United States
Rasim Özgür Rosti United States
Sylviane Marouillat relative to Lucía Galán Spain Lucía Galán's profile →
Citations per field
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Lucía Galán · 1×
Citations per year

Countries citing papers authored by Sylviane Marouillat

Since Specialization
Citations

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

Fields of papers citing papers by Sylviane Marouillat

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Sylviane Marouillat, 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 Sylviane Marouillat Line = papers co-authored together Sylviane Marouillat links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown
#Work
1 20241
2 20245
3 20241
4 20241
5 20233
6 202114
7 201912
8 201923
9 201855
10 20186
11 201641
12 201635
13 201518
14 201526
15 201514
16 200314
17 1997202
18 19964
19 19953
20 19955

About Sylviane Marouillat

Sylviane Marouillat is a scholar working on Genetics, Neurology and Genetics, having authored 35 papers that have together received 732 indexed citations. Recurring topics across this work include Amyotrophic Lateral Sclerosis Research (14 papers), Neurogenetic and Muscular Disorders Research (11 papers), Genetics and Neurodevelopmental Disorders (10 papers), Autism Spectrum Disorder Research (6 papers), Ubiquitin and proteasome pathways (5 papers), Parkinson's Disease Mechanisms and Treatments (3 papers), Neurological diseases and metabolism (2 papers) and Pluripotent Stem Cells Research (2 papers). The work is most often cited by research in Neurology (199 citations), Genetics (96 citations) and Neurology (71 citations). Sylviane Marouillat has collaborated with scholars based in France, Netherlands and Lebanon. Frequent co-authors include Christian Andrés, Patrick Vourc’h, Christelle Monteil, Lorraine C. Racusen, Anita Sgrignoli, Hélène Blasco, Philippe Corcia, Frédéric Laumonnier, Joëlle Martineau and Franck Patin. Their work appears in journals such as International Journal of Molecular Sciences, Neuroscience and The American Journal of Human Genetics.

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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