Céline Chéry

1.3k total citations
33 papers, 703 citations indexed

About

Céline Chéry is a scholar working on Molecular Biology, Rheumatology and Clinical Biochemistry. According to data from OpenAlex, Céline Chéry has authored 33 papers receiving a total of 703 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 16 papers in Rheumatology and 7 papers in Clinical Biochemistry. Recurrent topics in Céline Chéry's work include Folate and B Vitamins Research (16 papers), Metabolism and Genetic Disorders (7 papers) and Epigenetics and DNA Methylation (6 papers). Céline Chéry is often cited by papers focused on Folate and B Vitamins Research (16 papers), Metabolism and Genetic Disorders (7 papers) and Epigenetics and DNA Methylation (6 papers). Céline Chéry collaborates with scholars based in France, Italy and Switzerland. Céline Chéry's co-authors include Jean‐Louis Guéant, François Feillet, Farès Namour, Antonino Romano, Abderrahim Oussalah, Beat Thöny, Raymond C. Stevens, Johannes Zschocke, Nenad Blau and Alberto Burlina and has published in prestigious journals such as PLoS ONE, American Journal of Clinical Nutrition and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Céline Chéry

33 papers receiving 689 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Céline Chéry France	17	312	225	224	101	96	33	703
Shinji Kitajima Japan	17	260 0.8×	75 0.3×	44 0.2×	75 0.7×	11 0.1×	73	893
Nadia Akawi United Arab Emirates	16	332 1.1×	19 0.1×	39 0.2×	47 0.5×	58 0.6×	41	637
Dorothea M. Heuberger Switzerland	9	122 0.4×	63 0.3×	30 0.1×	37 0.4×	27 0.3×	18	440
Gaël Cobraiville Belgium	16	233 0.7×	166 0.7×	13 0.1×	42 0.4×	39 0.4×	38	613
C. Fernández-López Spain	15	469 1.5×	614 2.7×	30 0.1×	84 0.8×	20 0.2×	33	978
Carmen Segundo Spain	15	228 0.7×	35 0.2×	17 0.1×	108 1.1×	22 0.2×	29	850
Stuart J. Freeman United Kingdom	12	264 0.8×	40 0.2×	35 0.2×	65 0.6×	9 0.1×	29	578
K Furusho Japan	11	103 0.3×	31 0.1×	21 0.1×	128 1.3×	52 0.5×	25	508
Joanna Renke Poland	12	74 0.2×	142 0.6×	12 0.1×	85 0.8×	121 1.3×	48	480
Nikolai A. Maianski Netherlands	8	400 1.3×	73 0.3×	12 0.1×	111 1.1×	57 0.6×	8	896

Countries citing papers authored by Céline Chéry

Since Specialization

Citations

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

Fields of papers citing papers by Céline Chéry

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Céline Chéry

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

All Works

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20 of 20 papers shown

Chéry, Céline, Thomas Josse, Jean–Pierre Bronowicki, et al.. (2023). Predictors of the utility of clinical exome sequencing as a first-tier genetic test in patients with Mendelian phenotypes: results from a referral center study on 603 consecutive cases. Human Genomics. 17(1). 5–5. 6 indexed citations

Guéant, Jean‐Louis, Céline Chéry, Guillaume Schmitt, et al.. (2022). Epimutation in inherited metabolic disorders: the influence of aberrant transcription in adjacent genes. Human Genetics. 141(7). 1309–1325. 6 indexed citations

Namour, Farès, et al.. (2022). Stemness of Normal and Cancer Cells: The Influence of Methionine Needs and SIRT1/PGC-1α/PPAR-α Players. Cells. 11(22). 3607–3607. 7 indexed citations

Guéant, Jean‐Louis, Rosa‐Maria Guéant‐Rodriguez, Julien Fromonot, et al.. (2021). Elastase and exacerbation of neutrophil innate immunity are involved in multi‐visceral manifestations of COVID‐19. Allergy. 76(6). 1846–1858. 65 indexed citations

Wiedemann, Arnaud, Céline Chéry, Jean‐Marie Ravel, et al.. (2021). Diagnostic yield of clinical exome sequencing as a first-tier genetic test for the diagnosis of genetic disorders in pediatric patients: results from a referral center study. Human Genetics. 141(7). 1269–1278. 12 indexed citations

Chéry, Céline, Sébastien Hergalant, Aurélie François, et al.. (2021). Ionizing radiations induce shared epigenomic signatures unraveling adaptive mechanisms of cancerous cell lines with or without methionine dependency. Clinical Epigenetics. 13(1). 212–212. 1 indexed citations

Wiedemann, Arnaud, Céline Chéry, David Coelho, et al.. (2019). Mutations in MTHFR and POLG impaired activity of the mitochondrial respiratory chain in 46-year-old twins with spastic paraparesis. Journal of Human Genetics. 65(2). 91–98. 5 indexed citations

Battaglia-Hsu, Shyue-Fang, Sébastien Hergalant, Jean‐Marc Alberto, et al.. (2019). Folate can promote the methionine-dependent reprogramming of glioblastoma cells towards pluripotency. Cell Death and Disease. 10(8). 596–596. 29 indexed citations

Guéant‐Rodriguez, Rosa‐Maria, Jean‐Marc Alberto, Céline Chéry, et al.. (2018). Vitamin B-12 and liver activity and expression of methionine synthase are decreased in fetuses with neural tube defects. American Journal of Clinical Nutrition. 109(3). 674–683. 17 indexed citations

10.

Oussalah, Abderrahim, Paolo Bosco, Guido Anello, et al.. (2015). Exome-Wide Association Study Identifies New Low-Frequency and Rare UGT1A1 Coding Variants and UGT1A6 Coding Variants Influencing Serum Bilirubin in Elderly Subjects. Medicine. 94(22). e925–e925. 14 indexed citations

11.

Romano, Antonino, R.-M. Guéant-Rodriguez, Abderrahim Oussalah, et al.. (2013). Allergy to betalactams and nucleotide-binding oligomerization domain (NOD) gene polymorphisms. Allergy. 68(8). 1076–1080. 17 indexed citations

12.

Oussalah, Abderrahim, Céline Chéry, Élise Jeannesson, et al.. (2012). Helicobacter pylori serologic status has no influence on the association between fucosyltransferase 2 polymorphism (FUT2 461 G→A) and vitamin B-12 in Europe and West Africa. American Journal of Clinical Nutrition. 95(2). 514–521. 20 indexed citations

13.

Namour, Farès, Céline Chéry, Sandra Audonnet, et al.. (2011). Luminal expression of cubilin is impaired in Imerslund-Grasbeck syndrome with compound AMN mutations in intron 3 and exon 7. Haematologica. 96(11). 1715–1719. 23 indexed citations

14.

Forges, Thierry, Céline Chéry, Sandra Audonnet, François Feillet, & Jean‐Louis Guéant. (2010). Life-threatening methylenetetrahydrofolate reductase (MTHFR) deficiency with extremely early onset: Characterization of two novel mutations in compound heterozygous patients. Molecular Genetics and Metabolism. 100(2). 143–148. 19 indexed citations

15.

Pons, Laurent, Shyue-Fang Battaglia-Hsu, Carlos E. Orozco-Barrios, et al.. (2009). Anchoring Secreted Proteins in Endoplasmic Reticulum by Plant Oleosin: The Example of Vitamin B12 Cellular Sequestration by Transcobalamin. PLoS ONE. 4(7). e6325–e6325. 14 indexed citations

16.

Orozco-Barrios, Carlos E., Shyue-Fang Battaglia-Hsu, Martha L. Arango-Rodríguez, et al.. (2009). Vitamin B12-Impaired Metabolism Produces Apoptosis and Parkinson Phenotype in Rats Expressing the Transcobalamin-Oleosin Chimera in Substantia Nigra. PLoS ONE. 4(12). e8268–e8268. 28 indexed citations

17.

Zschocke, Johannes, Martin Lindner, François Feillet, et al.. (2007). Molecular genetics of tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency. Human Mutation. 29(1). 167–175. 144 indexed citations

18.

Pons, L., Céline Chéry, Antonino Romano, et al.. (2002). The 18 kDa peanut oleosin is a candidate allergen for IgE‐mediated reactions to peanuts. Allergy. 57(s72). 88–93. 85 indexed citations

19.

Chéry, Céline, et al.. (2002). Hyperhomocysteinemia Is Related to a Decreased Blood Level of Vitamin B12 in the Second and Third Trimester of Normal Pregnancy. Clinical Chemistry and Laboratory Medicine (CCLM). 40(11). 1105–8. 20 indexed citations

20.

Guéant, Jean‐Louis, et al.. (2001). Overexpression of folate binding protein α is one of the mechanism explaining the adaptation of HT29 cells to high concentration of methotrexate. Cancer Letters. 171(2). 139–145. 16 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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