Stéphanie Chatel

2.5k citations
29 papers · 1.9k · 1 hit paper · h-index 18

Impact in

Papers in

Stéphanie Chatel

27 papers receiving 1.8k citations

Stéphanie Chatel's Hit Papers

Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death 2013 · 434 citations
4340+4+8Years since publication100200300400

Peers

Stéphanie Chatel
Comparison fields: 5 of 40
  • Cardiology and Cardiovascular Medicine 1.3k
  • Sensory Systems 61
  • Neurology 54
  • Genetics 90
  • Molecular Biology 113
Replace Grażyna Kostrzewa with:
Grażyna Kostrzewa Poland
Stephan Waldmüller Germany
Amir Peleg Israel
Federica Dagradi Italy
Henk J. van der Linde Belgium
Fuyi Xu China
Matteo Pedrazzini Italy
Günter Grupp United States
Sulekha Rajagopalan Australia
Michael A. Makara United States
Stéphanie Chatel relative to Grażyna Kostrzewa Poland Grażyna Kostrzewa's profile →
Citations per field
00.5×2×4×6×8×9.6×
Grażyna Kostrzewa · 1×
Citations per year

Countries citing papers authored by Stéphanie Chatel

Since Specialization
Citations

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

Fields of papers citing papers by Stéphanie Chatel

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 29 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death
Hit paper breakdown →
2013434
2 2014252
3 2008230
4 2013133
5 2015111
6 201699
7 202295
8 201394
9 201584
10 201369
11 201354
12 201646
13 201844
14 201838
15 201625
16 201224
17 201624
18 201723
19 201210
20 202010

About Stéphanie Chatel

Stéphanie Chatel is a scholar working on Cardiology and Cardiovascular Medicine, Neurology, Genetics, Molecular Biology and Nuclear Energy and Engineering, having authored 29 papers that have together received 1.9k indexed citations. Recurring topics across this work include Cardiac electrophysiology and arrhythmias (18 papers), Intracranial Aneurysms: Treatment and Complications (4 papers), Genetic Associations and Epidemiology (2 papers), Forensic and Genetic Research (1 paper), Ubiquitin and proteasome pathways (1 paper) and Genomics and Rare Diseases (1 paper). The work is most often cited by research in Cardiology and Cardiovascular Medicine (1.3k citations), Sensory Systems (61 citations), Neurology (54 citations), Genetics (90 citations) and Molecular Biology (113 citations). Stéphanie Chatel has collaborated with scholars based in France, Netherlands and Germany. Frequent co-authors include Vincent Probst, Jean‐Jacques Schott, Hervé Le Marec, Frédéric Sacher, Michel Haı̈ssaguerre, Yoram Rudy, Stefan Kääb, Rukshen Weerasooriya, Eric Schulze‐Bahr and Arthur A.M. Wilde. Their work appears in journals such as Journal of the American Heart Association, Heart Rhythm, Nature Genetics, The American Journal of Human Genetics and Neurosurgery.

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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