Esther Kott

657 total citations
5 papers, 270 citations indexed

About

Esther Kott is a scholar working on Genetics, Pulmonary and Respiratory Medicine and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Esther Kott has authored 5 papers receiving a total of 270 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Genetics, 3 papers in Pulmonary and Respiratory Medicine and 2 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Esther Kott's work include Cystic Fibrosis Research Advances (3 papers), Genetic and Kidney Cyst Diseases (3 papers) and Neonatal Respiratory Health Research (1 paper). Esther Kott is often cited by papers focused on Cystic Fibrosis Research Advances (3 papers), Genetic and Kidney Cyst Diseases (3 papers) and Neonatal Respiratory Health Research (1 paper). Esther Kott collaborates with scholars based in France, Switzerland and Belgium. Esther Kott's co-authors include Philippe Duquesnoy, Estelle Escudier, A. Coste, Bruno Copin, Aline Tamalet, Jean‐François Papon, Marie Legendre, Guy Montantin, Serge Amselem and Ludovic Jeanson and has published in prestigious journals such as SHILAP Revista de lepidopterología, The American Journal of Human Genetics and Fertility and Sterility.

In The Last Decade

Esther Kott

5 papers receiving 270 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Esther Kott France	5	187	117	112	56	51	5	270
Ludovic Jeanson France	5	165 0.9×	149 1.3×	121 1.1×	39 0.7×	34 0.7×	5	292
Isabella Aprea Germany	5	143 0.8×	89 0.8×	99 0.9×	39 0.7×	32 0.6×	7	231
Guy Montantin France	6	297 1.6×	198 1.7×	182 1.6×	59 1.1×	50 1.0×	6	418
Inga M. Höben Germany	3	104 0.6×	69 0.6×	74 0.7×	25 0.4×	19 0.4×	5	163
Ana Grangeia Portugal	9	73 0.4×	88 0.8×	90 0.8×	18 0.3×	18 0.4×	30	300
Michael W. Leihy Australia	10	206 1.1×	281 2.4×	62 0.6×	113 2.0×	17 0.3×	11	451
Rim Hjeij Germany	4	113 0.6×	67 0.6×	145 1.3×	10 0.2×	10 0.2×	12	223
Anita Becker-Heck Germany	2	102 0.5×	78 0.7×	75 0.7×	14 0.3×	11 0.2×	3	148
Tabea Nöthe-Menchen Germany	4	78 0.4×	44 0.4×	44 0.4×	30 0.5×	26 0.5×	5	127
Laïla El Khattabi France	11	133 0.7×	156 1.3×	16 0.1×	42 0.8×	34 0.7×	25	343

Countries citing papers authored by Esther Kott

Since Specialization

Citations

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

Fields of papers citing papers by Esther Kott

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Esther Kott

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

All Works

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5 of 5 papers shown

1.

Kerlan, V., Brigitte Delemer, Sophie Catteau-Jonard, et al.. (2022). Whole exome sequencing in a cohort of familial premature ovarian insufficiency cases reveals a broad array of pathogenic or likely pathogenic variants in 50% of families. Fertility and Sterility. 117(4). 843–853. 13 indexed citations

2.

Jeanson, Ludovic, Bruno Copin, Jean‐François Papon, et al.. (2015). RSPH3 Mutations Cause Primary Ciliary Dyskinesia with Central-Complex Defects and a Near Absence of Radial Spokes. The American Journal of Human Genetics. 97(1). 153–162. 66 indexed citations

3.

Lavillaureix, Alinoë, Capucine Hyon, Solveig Heide, et al.. (2014). Nuclear volume differences between balanced and unbalanced spermatozoa in chromosomal translocation carriers. Reproductive BioMedicine Online. 30(3). 290–295. 7 indexed citations

4.

Kott, Esther, Philippe Duquesnoy, Bruno Copin, et al.. (2012). Loss-of-Function Mutations in LRRC6 , a Gene Essential for Proper Axonemal Assembly of Inner and Outer Dynein Arms, Cause Primary Ciliary Dyskinesia. The American Journal of Human Genetics. 91(5). 958–964. 124 indexed citations

5.

Legendre, Marie, Sylvain Blanchon, Bruno Copin, et al.. (2012). Delineation of CCDC39/CCDC40 mutation spectrum and associated phenotypes in primary ciliary dyskinesia. SHILAP Revista de lepidopterología. 1(S1). 410–6. 60 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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