Claire Feger

796 total citations
6 papers, 249 citations indexed

About

Claire Feger is a scholar working on Molecular Biology, Genetics and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Claire Feger has authored 6 papers receiving a total of 249 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 4 papers in Genetics and 1 paper in Cardiology and Cardiovascular Medicine. Recurrent topics in Claire Feger's work include Genomics and Rare Diseases (2 papers), Ion channel regulation and function (2 papers) and Bacterial Genetics and Biotechnology (2 papers). Claire Feger is often cited by papers focused on Genomics and Rare Diseases (2 papers), Ion channel regulation and function (2 papers) and Bacterial Genetics and Biotechnology (2 papers). Claire Feger collaborates with scholars based in France, Australia and United States. Claire Feger's co-authors include Johann Böhm, Jocelyn Laporte, Pascal Laforêt, Shahram Attarian, Marc Bartoli, Michel Fardeau, Dominique Figarella‐Branger, Jean Pouget, Karima Ghorab and Daniel Hantaı̈ and has published in prestigious journals such as PLoS ONE, Analytical Biochemistry and The American Journal of Human Genetics.

In The Last Decade

Claire Feger

6 papers receiving 245 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Claire Feger France	5	177	91	67	60	48	6	249
Giovanni Matteo Fratta Italy	7	422 2.4×	44 0.5×	74 1.1×	34 0.6×	32 0.7×	8	463
Sally Prouty United States	5	351 2.0×	23 0.3×	149 2.2×	163 2.7×	29 0.6×	6	440
Christophe Paillart France	8	258 1.5×	26 0.3×	189 2.8×	31 0.5×	50 1.0×	8	357
Aurélie Vandebrouck France	7	257 1.5×	100 1.1×	125 1.9×	99 1.6×	77 1.6×	8	396
Luca Guglielmi Italy	12	224 1.3×	9 0.1×	115 1.7×	55 0.9×	40 0.8×	15	313
Moonkyung Kang South Korea	8	227 1.3×	10 0.1×	47 0.7×	26 0.4×	38 0.8×	15	319
L. Plessers Belgium	6	291 1.6×	71 0.8×	120 1.8×	61 1.0×	13 0.3×	6	353
S. K. Bhattacharya United States	6	266 1.5×	64 0.7×	56 0.8×	165 2.8×	27 0.6×	14	320
H Drac Poland	10	133 0.8×	14 0.2×	183 2.7×	49 0.8×	11 0.2×	38	293
Jacqueline Niu United States	8	225 1.3×	13 0.1×	97 1.4×	100 1.7×	46 1.0×	11	283

Countries citing papers authored by Claire Feger

Since Specialization

Citations

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

Fields of papers citing papers by Claire Feger

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Claire Feger

This figure shows the co-authorship network connecting the top 25 collaborators of Claire Feger. A scholar is included among the top collaborators of Claire Feger 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 Claire Feger. Claire Feger 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.

Feger, Claire, Vincent Laugel, Denys Chaigne, et al.. (2021). Pathogenic variants in KCNQ2 cause intellectual deficiency without epilepsy: Broadening the phenotypic spectrum of a potassium channelopathy. American Journal of Medical Genetics Part A. 185(6). 1803–1815. 12 indexed citations

2.

Quartier, Angélique, Thuong Ha, George McGillivray, et al.. (2019). Novel mutations in NLGN3 causing autism spectrum disorder and cognitive impairment. Human Mutation. 40(11). 2021–2032. 39 indexed citations

3.

Feger, Claire, et al.. (2016). Construction of a compatible Gateway-based co-expression vector set for expressing multiprotein complexes in E. coli. Analytical Biochemistry. 512. 110–113. 5 indexed citations

4.

Feger, Claire, et al.. (2016). Data set for describing the elaboration of a compatible Gateway-based co-expression vector set and supporting its validation. Data in Brief. 9. 946–955. 1 indexed citations

5.

Böhm, Johann, Nasim Vasli, Edoardo Malfatti, et al.. (2013). An Integrated Diagnosis Strategy for Congenital Myopathies. PLoS ONE. 8(6). e67527–e67527. 43 indexed citations

6.

Böhm, Johann, Frédéric Chevessier, Catherine Koch, et al.. (2013). Constitutive Activation of the Calcium Sensor STIM1 Causes Tubular-Aggregate Myopathy. The American Journal of Human Genetics. 92(2). 271–278. 149 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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