Sébastien Küry

10.3k total citations
48 papers, 1.3k citations indexed

About

Sébastien Küry is a scholar working on Molecular Biology, Nutrition and Dietetics and Plant Science. According to data from OpenAlex, Sébastien Küry has authored 48 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 19 papers in Nutrition and Dietetics and 13 papers in Plant Science. Recurrent topics in Sébastien Küry's work include Trace Elements in Health (19 papers), Aluminum toxicity and tolerance in plants and animals (13 papers) and Heavy Metal Exposure and Toxicity (9 papers). Sébastien Küry is often cited by papers focused on Trace Elements in Health (19 papers), Aluminum toxicity and tolerance in plants and animals (13 papers) and Heavy Metal Exposure and Toxicity (9 papers). Sébastien Küry collaborates with scholars based in France, United States and Germany. Sébastien Küry's co-authors include Stéphane Bezieau, Monia Kharfi, Brigitte Dréno, Jean‐Paul Moisan, R. Kamoun, Sébastien Schmitt, Graham Christie, Peter M. Taylor, John C. Mathers and Siôn R. Phillips and has published in prestigious journals such as Journal of Biological Chemistry, Nature Genetics and SHILAP Revista de lepidopterología.

In The Last Decade

Sébastien Küry

43 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sébastien Küry France 17 687 422 316 281 193 48 1.3k
T. Tønnesen Denmark 17 784 1.1× 729 1.7× 273 0.9× 161 0.6× 198 1.0× 43 1.5k
Aiko Hasegawa Japan 11 490 0.7× 291 0.7× 190 0.6× 94 0.3× 77 0.4× 18 920
Andrew Grimes Australia 15 850 1.2× 513 1.2× 423 1.3× 148 0.5× 257 1.3× 28 1.3k
J D Gitlin United States 23 1.5k 2.2× 809 1.9× 664 2.1× 244 0.9× 745 3.9× 32 2.5k
Casilda V. Mura United States 19 323 0.5× 513 1.2× 132 0.4× 47 0.2× 175 0.9× 35 1.1k
H. J. McArdle United Kingdom 26 489 0.7× 358 0.8× 208 0.7× 52 0.2× 416 2.2× 45 1.5k
Lien H. Ho Australia 11 374 0.5× 430 1.0× 192 0.6× 59 0.2× 62 0.3× 12 1.3k
Ketil Thorstensen Norway 18 384 0.6× 232 0.5× 45 0.1× 62 0.2× 611 3.2× 52 1.2k
Nicolás Montalbetti United States 24 211 0.3× 731 1.7× 76 0.2× 52 0.2× 84 0.4× 51 1.5k
Kazuko Takahashi Japan 13 141 0.2× 936 2.2× 152 0.5× 44 0.2× 39 0.2× 30 1.6k

Countries citing papers authored by Sébastien Küry

Since Specialization
Citations

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

Fields of papers citing papers by Sébastien Küry

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sébastien Küry

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

All Works

20 of 20 papers shown
1.
Fournier, Benjamin, Vincent Abramowski, Étienne Merlin, et al.. (2025). Novel de novo dominant PSMB10 variants in three patients with immune deficiency and liver disease. SHILAP Revista de lepidopterología. 2(1).
2.
Sun, Yi‐Qian, Ben Brumpton, Yafang Li, et al.. (2024). Sex hormones and risk of lung and colorectal cancers in women: a Mendelian randomization study. Scientific Reports. 14(1). 23891–23891. 2 indexed citations
3.
Bezieau, Stéphane, Wallid Deb, Sandra Mercier, et al.. (2023). Understanding neurodevelopmental proteasomopathies as new rare disease entities: A review of current concepts, molecular biomarkers, and perspectives. Genes & Diseases. 11(6). 101130–101130. 2 indexed citations
4.
Zuber, Verena, Erik G. Jönsson, Oleksandr Frei, et al.. (2018). Identification of shared genetic variants between schizophrenia and lung cancer. Scientific Reports. 8(1). 674–674. 23 indexed citations
5.
Bou‐Hanna, Chantal, Anne Jarry, Laurence Lodé, et al.. (2015). Acute cytotoxicity of MIRA-1/NSC19630, a mutant p53-reactivating small molecule, against human normal and cancer cells via a caspase-9-dependent apoptosis. Cancer Letters. 359(2). 211–217. 38 indexed citations
6.
Küry, Sébastien, Monia Kharfi, Eric Blouin, Sébastien Schmitt, & Stéphane Bezieau. (2015). Clinical utility gene card for: acrodermatitis enteropathica – update 2015. European Journal of Human Genetics. 24(5). 779–779. 9 indexed citations
7.
Küry, Sébastien, Sandra Mercier, Gasnat Shaboodien, et al.. (2015). CUGC for hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis (POIKTMP). European Journal of Human Genetics. 24(5). 779–779. 8 indexed citations
8.
Küry, Sébastien. (2014). Evaluation of the colorectal cancer risk conferred by rareUNC5Calleles. World Journal of Gastroenterology. 20(1). 204–204. 9 indexed citations
9.
Mercier, Sandra, Christel Thauvin, Sébastien Küry, et al.. (2014). Mutation dans le gène FAM111B : une nouvelle cause de poïkilodermie héréditaire. Annales de Dermatologie et de Vénéréologie. 141(12). S380–S380.
10.
Biervliet, Stéphanie Van, Sébastien Küry, Ruth De Bruyne, et al.. (2014). Clinical Zinc Deficiency as Early Presentation of Wilson Disease. Journal of Pediatric Gastroenterology and Nutrition. 60(4). 457–459. 8 indexed citations
11.
Küry, Sébastien, V. Ramaekers, Stéphane Bezieau, & Barry Wolf. (2012). Clinical utility gene card for: Biotinidase deficiency. European Journal of Human Genetics. 20(5). 4–4. 7 indexed citations
12.
Küry, Sébastien, Monia Kharfi, Sébastien Schmitt, & Stéphane Bezieau. (2011). Clinical utility gene card for: acrodermatitis enteropathica. European Journal of Human Genetics. 20(3). 3–4. 7 indexed citations
13.
Kharfi, Monia, et al.. (2011). Transient symptomatic zinc deficiency in a breast-fed infant: Relevance of a genetic study. Nutrition. 27(10). 1087–1089. 11 indexed citations
14.
Caignec, Cédric Le, David J. Kwiatkowski, Sébastien Küry, et al.. (2009). Three independent mutations in the TSC2 gene in a family with tuberous sclerosis. European Journal of Human Genetics. 17(9). 1165–1170. 7 indexed citations
15.
Guaguère, Éric, Emmanuel Bensignor, Sébastien Küry, et al.. (2009). Clinical, histopathological and genetic data of ichthyosis in the golden retriever: a prospective study. Journal of Small Animal Practice. 50(5). 227–235. 12 indexed citations
16.
Küry, Sébastien, Bruno Buecher, Sébastien Robiou-du-Pont, et al.. (2007). The Thorough Screening of the MUTYH Gene in a Large French Cohort of Sporadic Colorectal Cancers. PubMed. 11(4). 373–380. 12 indexed citations
17.
Giraud, Marion, et al.. (2007). A novel mutation of the SLC39A4 gene causing acrodermatitis enteropathica. British Journal of Dermatology. 157(2). 386–387. 8 indexed citations
18.
Kharfi, Monia, I. Zarâa, Sébastien Küry, Jean‐Paul Moisan, & Mohamed Ridha Kamoun. (2005). Acrodermatite entéropathique chez un nourrisson né à terme nourri exclusivement au sein. Annales de Dermatologie et de Vénéréologie. 132(3). 246–248. 6 indexed citations
19.
Küry, Sébastien, Monia Kharfi, R. Kamoun, et al.. (2003). Mutation spectrum of humanSLC39A4in a panel of patients with acrodermatitis enteropathica. Human Mutation. 22(4). 337–338. 52 indexed citations
20.
Küry, Sébastien, Brigitte Dréno, Stéphane Bezieau, et al.. (2002). Identification of SLC39A4, a gene involved in acrodermatitis enteropathica. Nature Genetics. 31(3). 239–240. 377 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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