Céline Besse

2.2k total citations
14 papers, 332 citations indexed

About

Céline Besse is a scholar working on Molecular Biology, Genetics and Epidemiology. According to data from OpenAlex, Céline Besse has authored 14 papers receiving a total of 332 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 7 papers in Genetics and 3 papers in Epidemiology. Recurrent topics in Céline Besse's work include Epigenetics and DNA Methylation (3 papers), Genetic diversity and population structure (3 papers) and Genetic Syndromes and Imprinting (2 papers). Céline Besse is often cited by papers focused on Epigenetics and DNA Methylation (3 papers), Genetic diversity and population structure (3 papers) and Genetic Syndromes and Imprinting (2 papers). Céline Besse collaborates with scholars based in France, United Kingdom and United States. Céline Besse's co-authors include Rachel E. Jenkins, S.E. HANDFIELD-JONES, D. McGibbon, Sean Whittaker, Jörg Tost, Anne Boland, Pierre Bougnères, Gianpaolo De Filippo, Jean‐François Deleuze and Delphine Fradin and has published in prestigious journals such as Blood, PLoS ONE and Diabetes.

In The Last Decade

Céline Besse

14 papers receiving 326 citations

Peers

Céline Besse

GENET

IMMUN

PHARM

PPCH

Kuang Lin China

Nita Radhakrishnan India

Nisar Ahmed China

George Wendt United States

Fernanda Mafra Brazil

Jasmine Zhao United States

Che‐Wei Ou Taiwan

Jae-Wook Jeong United States

Stephen L. Guthery United States

C H Srivastava United States

Kuang Lin China

Céline Besse

179 ×1.5

184 ×2.1

GENET

117 ×2.2

IMMUN

17 ×0.4

PHARM

10 ×0.3

PPCH

Citations per year, relative to Céline Besse Céline Besse (= 1×) peers Kuang Lin

Countries citing papers authored by Céline Besse

Since Specialization

Citations

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

Fields of papers citing papers by Céline Besse

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Céline Besse

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

All Works

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14 of 14 papers shown

Brucato, Nicolas, Verónica Fernandes, Lauri Saag, et al.. (2020). Papuan mitochondrial genomes and the settlement of Sahul. Journal of Human Genetics. 65(10). 875–887. 34 indexed citations

Soukarieh, Omar, Carole Proust, C. Mouton, et al.. (2020). A novel rare c.-39C>T mutation in the PROS1 5′UTR causing PS deficiency by creating a new upstream translation initiation codon. Clinical Science. 134(10). 1181–1190. 10 indexed citations

Brucato, Nicolas, Verónica Fernandes, Pradiptajati Kusuma, et al.. (2019). Evidence of Austronesian Genetic Lineages in East Africa and South Arabia: Complex Dispersal from Madagascar and Southeast Asia. Genome Biology and Evolution. 11(3). 748–758. 13 indexed citations

Bonaventure, Audrey, Laurent Orsi, Jérémie Rudant, et al.. (2018). Genetic polymorphisms of Th2 interleukins, history of asthma or eczema and childhood acute lymphoid leukaemia: Findings from the ESCALE study (SFCE). Cancer Epidemiology. 55. 96–103. 5 indexed citations

Fradin, Delphine, Pierre‐Yves Boëlle, Marie‐Pierre Belot, et al.. (2017). Genome-Wide Methylation Analysis Identifies Specific Epigenetic Marks In Severely Obese Children. Scientific Reports. 7(1). 46311–46311. 47 indexed citations

Mobuchon, Lenha, Aude Battistella, Claire Bardel, et al.. (2017). A GWAS in uveal melanoma identifies risk polymorphisms in the CLPTM1L locus. npj Genomic Medicine. 2(1). 15 indexed citations

Santos, Reinaldo S. Dos, Anne Philippi, Lorella Marselli, et al.. (2017). dUTPase (DUT) Is Mutated in a Novel Monogenic Syndrome With Diabetes and Bone Marrow Failure. Diabetes. 66(4). 1086–1096. 19 indexed citations

Jabot‐Hanin, Fabienne, Aurélie Cobat, Jacqueline Feinberg, et al.. (2015). Major Loci on Chromosomes 8q and 3q Control Interferon γ Production Triggered by Bacillus Calmette-Guerin and 6-kDa Early Secretory Antigen Target, Respectively, in Various Populations. The Journal of Infectious Diseases. 213(7). 1173–1179. 12 indexed citations

Lepoittevin, Camille, Catherine Bodénès, Émilie Chancerel, et al.. (2015). Single‐nucleotide polymorphism discovery and validation in high‐density SNP array for genetic analysis in European white oaks. Molecular Ecology Resources. 15(6). 1446–1459. 30 indexed citations

10.

Nielsen, Helene Myrtue, Alexandre How‐Kit, Carole Guérin, et al.. (2015). Copy number variations alter methylation and parallel IGF2 overexpression in adrenal tumors. Endocrine Related Cancer. 22(6). 953–967. 18 indexed citations

11.

Yamagata, Yoshiaki, Daniel Stockholm, Guillaume Corre, et al.. (2012). Lentiviral Transduction of CD34+ Cells Induces Genome-Wide Epigenetic Modifications. PLoS ONE. 7(11). e48943–e48943. 19 indexed citations

12.

Caburet, Sandrine, Petra Zavadáková, Ziva Ben‐Neriah, et al.. (2012). Genome-Wide Linkage in a Highly Consanguineous Pedigree Reveals Two Novel Loci on Chromosome 7 for Non-Syndromic Familial Premature Ovarian Failure. PLoS ONE. 7(3). e33412–e33412. 27 indexed citations

13.

Novak, Urban, Elisabeth Oppliger Leibundgut, Jörg Hager, et al.. (2002). A high-resolution allelotype of B-cell chronic lymphocytic leukemia (B-CLL). Blood. 100(5). 1787–1794. 30 indexed citations

14.

HANDFIELD-JONES, S.E., Rachel E. Jenkins, Sean Whittaker, Céline Besse, & D. McGibbon. (1993). The anticonvulsant hypersensitivity syndrome. British Journal of Dermatology. 129(2). 175–177. 53 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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