Karen Gaudon

687 citations

6 papers · 88 indexed · h-index 3

Co-authors: Daniel Hantaı̈Pascale Richard B. Eymard Emmanuel Fournier Stéphanie Bauché I. Wargon Damien Sternberg Shahriar Nafissi
Topics: Myasthenia Gravis and Thymoma (4 papers)Ion channel regulation and function (2 papers)Cellular transport and secretion (2 papers)
Cited by: Neurology Cell Biology Genetics
Journals: SHILAP Revista de lepidopterologíaJournal of Medical Genetics Neuromuscular Disorders
Partner nations: France Switzerland Iran

In The Last Decade

Karen Gaudon

6 papers receiving 87 citations

Peers

Countries citing papers authored by Karen Gaudon

Since Specialization

Citations

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

Fields of papers citing papers by Karen Gaudon

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Karen Gaudon

This figure shows the co-authorship network connecting the top 25 collaborators of Karen Gaudon. A scholar is included among the top collaborators of Karen Gaudon 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 Karen Gaudon. Karen Gaudon 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:

6 of 6 papers shown

#	Work	Indexed citations
1	A severe case of PLOD1‐related kyphoscoliotic Ehlers–Danlos syndrome associated with several arterial and venous complications: A case report 2023 ·SHILAP Revista de lepidopterología ·(unknown),Corinne Métay,Michael Frank,Nicolas Denarié,Salma Adham,Clarisse Billon,Anne Debost‐Legrand,Xavier Jeunemaı̂tre,(unknown),Karen Gaudon,Philippe de Mazancourt,Ahmed Mekki,Robert Carlier,Karelle Bénistan	2
2	Novel dominant distal titinopathy phenotype associated with copy number variation 2021 ·Annals of Clinical and Translational Neurology ·Aurélien Perrin,Raúl Juntas Morales,Françoise Chapon,(unknown),(unknown),(unknown),Emmanuelle Uro‐Coste,(unknown),Nicolas Leboucq,Martial Mallaret,É. Lagrange,Valérie Rigau,Karen Gaudon,Pascale Richard,M. Kœnig,Corinne Métay,Mireille Cossée	2
3	Long-term follow-up of patients with congenital myasthenic syndrome caused by COLQ mutations 2011 ·Neuromuscular Disorders ·I. Wargon,Pascale Richard,Thierry Küntzer,Damien Sternberg,Shahriar Nafissi,Karen Gaudon,(unknown),Stéphanie Bauché,Daniel Hantaı̈,Emmanuel Fournier,B. Eymard,Tanya Stojkovic	56
4	P5.17 Congenital Myasthenic Syndromes with COLQ mutations: Long term follow-up 2011 ·Neuromuscular Disorders ·I. Wargon,Pascale Richard,Thierry Küntzer,Shahriar Nafissi,Karen Gaudon,Damien Sternberg,Emmanuel Fournier,(unknown),B. Eymard,T. Stojkovic	1
5	Multiexon deletions account for 15% of congenital myasthenic syndromes with RAPSN mutations after negative DNA sequencing 2010 ·Journal of Medical Genetics ·Karen Gaudon,I. Pénisson-Besnier,B. Chabrol,Françoise Bouhour,L. Demay,Asma Ammar,Stéphanie Bauché,Christophe Vial,Gaël Nicolas,B. Eymard,Daniel Hantaı̈,Pascale Richard	9
6	A synonymous CHRNE mutation responsible for an aberrant splicing leading to congenital myasthenic syndrome 2007 ·Neuromuscular Disorders ·Pascale Richard,Karen Gaudon,Emmanuel Fournier,C. Ellen Jackson,Stéphanie Bauché,(unknown),Jeanine Koenig,Bernard Échenne,Daniel Hantaı̈,B. Eymard	18

About Karen Gaudon

Karen Gaudon is a scholar working on Neurology, Cell Biology and Immunology and Allergy, having authored 6 papers that have together received 88 indexed citations. Recurring topics across this work include Myasthenia Gravis and Thymoma (4 papers), Ion channel regulation and function (2 papers) and Cellular transport and secretion (2 papers). The work is most often cited by research in Neurology (67 citations), Cell Biology (34 citations) and Genetics (12 citations). Karen Gaudon has collaborated with scholars based in France, Switzerland and Iran. Frequent co-authors include Daniel Hantaı̈, Pascale Richard, B. Eymard, Emmanuel Fournier, Stéphanie Bauché, I. Wargon, Damien Sternberg, Shahriar Nafissi, Tanya Stojkovic and Thierry Küntzer. Their work appears in journals such as SHILAP Revista de lepidopterología, Journal of Medical Genetics and Neuromuscular Disorders.

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