Estelle Fédirko

892 total citations
6 papers, 192 citations indexed

About

Estelle Fédirko is a scholar working on Cellular and Molecular Neuroscience, Genetics and Psychiatry and Mental health. According to data from OpenAlex, Estelle Fédirko has authored 6 papers receiving a total of 192 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Cellular and Molecular Neuroscience, 3 papers in Genetics and 2 papers in Psychiatry and Mental health. Recurrent topics in Estelle Fédirko's work include Genomics and Rare Diseases (2 papers), Epilepsy research and treatment (2 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Estelle Fédirko is often cited by papers focused on Genomics and Rare Diseases (2 papers), Epilepsy research and treatment (2 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Estelle Fédirko collaborates with scholars based in France, Spain and Germany. Estelle Fédirko's co-authors include Christel Depienne, Eric Leguern, Isabelle Gourfinkel‐An, Oriane Trouillard, Rima Nabbout, Michel Baulac, Stéphanie Baulac, Charlotte Dravet, Alexis Arzimanoglou and Cécile Saint‐Martin and has published in prestigious journals such as Clinical Neurophysiology, Human Mutation and Journal of Molecular Medicine.

In The Last Decade

Estelle Fédirko

6 papers receiving 189 citations

Peers

Estelle Fédirko

PMH

GENET

MB

CMN

PPCH

Dora Steel United Kingdom

Giacomo Garone Italy

Fatima Jaffer United Kingdom

Anne Hempelmann Germany

Theresa Scattergood United States

Jenna C. Carpenter United Kingdom

Lia Santulli Italy

Samuel M. Tucker United States

Roberta Epifanio Italy

Kristien Verhaert Belgium

Dora Steel United Kingdom

Estelle Fédirko

105 ×1.2

PMH

107 ×1.3

GENET

131 ×1.8

MB

111 ×1.8

CMN

49 ×2.1

PPCH

Citations per year, relative to Estelle Fédirko Estelle Fédirko (= 1×) peers Dora Steel

Countries citing papers authored by Estelle Fédirko

Since Specialization

Citations

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

Fields of papers citing papers by Estelle Fédirko

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Estelle Fédirko

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

All Works

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6 of 6 papers shown

1.

Couarch, Philippe, Santiago Vernia, Isabelle Gourfinkel‐An, et al.. (2011). Lafora progressive myoclonus epilepsy: NHLRC1 mutations affect glycogen metabolism. Journal of Molecular Medicine. 89(9). 915–925. 19 indexed citations

2.

Piard, Juliette, Christel Depienne, Boris Keren, et al.. (2011). Intragenic deletion of UBE3A gene in 2 sisters with Angelman syndrome detected by MLPA. American Journal of Medical Genetics Part A. 155(12). 3170–3173. 5 indexed citations

3.

Gauvain, Grégory, Isabelle Gourfinkel‐An, Estelle Fédirko, et al.. (2009). Two novelCLCN2mutations accelerating chloride channel deactivation are associated with idiopathic generalized epilepsy. Human Mutation. 30(3). 397–405. 46 indexed citations

4.

Navarro, Vincent, Christel Depienne, Estelle Fédirko, et al.. (2008). K-complex-induced seizures in autosomal dominant nocturnal frontal lobe epilepsy. Clinical Neurophysiology. 119(10). 2201–2204. 21 indexed citations

5.

Ribaı̈, Pascale, Christel Depienne, Estelle Fédirko, et al.. (2007). Mental deficiency in three families with SPG4 spastic paraplegia. European Journal of Human Genetics. 16(1). 97–104. 25 indexed citations

6.

Depienne, Christel, Alexis Arzimanoglou, Oriane Trouillard, et al.. (2006). Parental mosaicism can cause recurrent transmission ofSCN1A mutations associated with severe myoclonic epilepsy of infancy. Human Mutation. 27(4). 389–389. 76 indexed citations

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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