Diana Zélénika

41.9k total citations
50 papers, 3.3k citations indexed

About

Diana Zélénika is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, Diana Zélénika has authored 50 papers receiving a total of 3.3k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 16 papers in Genetics and 10 papers in Immunology. Recurrent topics in Diana Zélénika's work include Genetic Associations and Epidemiology (7 papers), Immune Cell Function and Interaction (7 papers) and T-cell and B-cell Immunology (6 papers). Diana Zélénika is often cited by papers focused on Genetic Associations and Epidemiology (7 papers), Immune Cell Function and Interaction (7 papers) and T-cell and B-cell Immunology (6 papers). Diana Zélénika collaborates with scholars based in France, United States and United Kingdom. Diana Zélénika's co-authors include Stephen Cobbold, Herman Waldmann, Elizabeth Adams, Luís Graça, Simon Heath, Raquel Castejón, Mark Lathrop, Bernard Pessac, Brigitte Grima and Fumihiko Matsuda and has published in prestigious journals such as New England Journal of Medicine, The Lancet and JAMA.

In The Last Decade

Diana Zélénika

50 papers receiving 3.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Diana Zélénika France 29 990 935 627 535 473 50 3.3k
Alexandre Montpetit Canada 33 621 0.6× 1.4k 1.5× 897 1.4× 152 0.3× 403 0.9× 66 3.5k
David E. Harrison United States 37 854 0.9× 1.4k 1.5× 340 0.5× 1.3k 2.4× 1.2k 2.5× 87 4.1k
Richard Person United States 27 885 0.9× 1.4k 1.5× 1.9k 3.1× 448 0.8× 610 1.3× 65 3.5k
Yong Cheng United States 26 879 0.9× 3.5k 3.8× 1.2k 2.0× 353 0.7× 305 0.6× 51 5.2k
Pekka Ellonen Finland 29 521 0.5× 1.3k 1.4× 802 1.3× 167 0.3× 281 0.6× 70 3.1k
Ann P. Chidgey Australia 33 2.0k 2.0× 738 0.8× 285 0.5× 486 0.9× 241 0.5× 64 3.4k
Thomas Serwold United States 24 1.8k 1.8× 2.3k 2.4× 261 0.4× 449 0.8× 563 1.2× 36 4.2k
Janna Saarela Finland 34 839 0.8× 1.5k 1.6× 662 1.1× 158 0.3× 296 0.6× 89 4.0k
Kanji Sugita Japan 27 638 0.6× 720 0.8× 263 0.4× 899 1.7× 105 0.2× 157 2.9k
Jens van den Brandt Germany 28 820 0.8× 923 1.0× 407 0.6× 122 0.2× 350 0.7× 73 2.6k

Countries citing papers authored by Diana Zélénika

Since Specialization
Citations

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

Fields of papers citing papers by Diana Zélénika

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Diana Zélénika

This figure shows the co-authorship network connecting the top 25 collaborators of Diana Zélénika. A scholar is included among the top collaborators of Diana Zélénika 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 Diana Zélénika. Diana Zélénika 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.
Costantino, Félicie, Roula Said‐Nahal, Ariane Leboime, et al.. (2016). A family-based genome-wide association study reveals an association of spondyloarthritis with MAPK14. Annals of the Rheumatic Diseases. 76(1). 310–314. 9 indexed citations
2.
Costantino, Félicie, Tifenn Leturcq, Roula Said‐Nahal, et al.. (2015). Whole-genome single nucleotide polymorphism-based linkage analysis in spondyloarthritis multiplex families reveals a new susceptibility locus in 13q13. Annals of the Rheumatic Diseases. 75(7). 1380–1385. 9 indexed citations
3.
Étain, Bruno, Stéphane Jamain, Vanessa Milhiet, et al.. (2014). Association between circadian genes, bipolar disorders and chronotypes. Chronobiology International. 31(7). 807–814. 59 indexed citations
4.
Cacciagli, Pierre, Jean‐Pierre Desvignes, Nadine Girard, et al.. (2013). AP1S2 is mutated in X-linked Dandy–Walker malformation with intellectual disability, basal ganglia disease and seizures (Pettigrew syndrome). European Journal of Human Genetics. 22(3). 363–368. 37 indexed citations
5.
Belot, Marie‐Pierre, Delphine Fradin, Diana Zélénika, et al.. (2013). CpG Methylation Changes within the IL2RA Promoter in Type 1 Diabetes of Childhood Onset. PLoS ONE. 8(7). e68093–e68093. 32 indexed citations
6.
Pinel, Philippe, Fabien Fauchereau, Antonio Moreno, et al.. (2012). Genetic Variants ofFOXP2andKIAA0319/TTRAP/THEM2Locus Are Associated with Altered Brain Activation in Distinct Language-Related Regions. Journal of Neuroscience. 32(3). 817–825. 117 indexed citations
7.
Bonaventure, Audrey, Stéphanie Goujon-Bellec, Jérémie Rudant, et al.. (2011). Maternal smoking during pregnancy, genetic polymorphisms of metabolic enzymes, and childhood acute leukemia: the ESCALE Study (SFCE). Cancer Causes & Control. 23(2). 329–345. 28 indexed citations
8.
Desrivières, Sylvane, Anbarasu Lourdusamy, Francesca Ducci, et al.. (2011). Sex-Specific Role for Adenylyl Cyclase Type 7 in Alcohol Dependence. Biological Psychiatry. 69(11). 1100–1108. 17 indexed citations
9.
Antoni, Guillemette, Pierre‐Emmanuel Morange, He‐Kuan Luo, et al.. (2010). A multi‐stage multi‐design strategy provides strong evidence that the BAI3 locus is associated with early‐onset venous thromboembolism. Journal of Thrombosis and Haemostasis. 8(12). 2671–2679. 28 indexed citations
10.
Reeves, Gillian, Ruth C. Travis, Jane Green, et al.. (2010). Incidence of Breast Cancer and Its Subtypes in Relation to Individual and Multiple Low-Penetrance Genetic Susceptibility Loci. JAMA. 304(4). 426–426. 81 indexed citations
11.
Zinovieva, Elena, Catherine Bourgain, Amir Kadi, et al.. (2009). Comprehensive Linkage and Association Analyses Identify Haplotype, Near to the TNFSF15 Gene, Significantly Associated with Spondyloarthritis. PLoS Genetics. 5(6). e1000528–e1000528. 46 indexed citations
12.
Trégouët, David‐Alexandre, Simon Heath, Noémie Saut, et al.. (2009). Common susceptibility alleles are unlikely to contribute as strongly as the FV and ABO loci to VTE risk: results from a GWAS approach. Blood. 113(21). 5298–5303. 209 indexed citations
13.
Alonso, Santos, Neskuts Izagirre, Isabel Smith Zubiaga, et al.. (2008). Complex signatures of selection for the melanogenic loci TYR, TYRP1 and DCT in humans. BMC Evolutionary Biology. 8(1). 74–74. 51 indexed citations
14.
Bouzigon, Emmanuelle, Eve Corda, Hugues Aschard, et al.. (2008). Effect of 17q21 Variants and Smoking Exposure in Early-Onset Asthma. New England Journal of Medicine. 359(19). 1985–1994. 281 indexed citations
15.
Cobbold, Stephen, Raquel Castejón, Elizabeth Adams, et al.. (2004). Induction of foxP3 + Regulatory T Cells in the Periphery of T Cell Receptor Transgenic Mice Tolerized to Transplants. The Journal of Immunology. 172(10). 6003–6010. 334 indexed citations
16.
Abdulkarim, Bassam, Siham Sabri, Diana Zélénika, et al.. (2003). Antiviral agent Cidofovir decreases Epstein–Barr virus (EBV) oncoproteins and enhances the radiosensitivity in EBV-related malignancies. Oncogene. 22(15). 2260–2271. 44 indexed citations
17.
Zélénika, Diana, Elizabeth Adams, Luís Graça, et al.. (2002). Regulatory T Cells Overexpress a Subset of Th2 Gene Transcripts. The Journal of Immunology. 168(3). 1069–1079. 144 indexed citations
18.
Zélénika, Diana, Elizabeth Adams, Andrew L. Mellor, et al.. (1998). Rejection of H-Y Disparate Skin Grafts by Monospecific CD4+ Th1 and Th2 Cells: No Requirement for CD8+ T Cells or B Cells. The Journal of Immunology. 161(4). 1868–1874. 125 indexed citations
19.
Zélénika, Diana, Brigitte Grima, & Bernard Pessac. (1993). A New Family of Transcripts of the Myelin Basic Protein Gene: Expression in Brain and in Immune System. Journal of Neurochemistry. 60(4). 1574–1577. 53 indexed citations
20.
Grima, Brigitte, Diana Zélénika, & Bernard Pessac. (1992). A Novel Transcript Overlapping the Myelin Basic Protein Gene. Journal of Neurochemistry. 59(6). 2318–2323. 39 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Alexandre Montpetit Breakdown of academic impact, for papers by David E. Harrison Breakdown of academic impact, for papers by Richard Person Breakdown of academic impact, for papers by Yong Cheng Breakdown of academic impact, for papers by Pekka Ellonen Breakdown of academic impact, for papers by Ann P. Chidgey Breakdown of academic impact, for papers by Thomas Serwold Breakdown of academic impact, for papers by Janna Saarela Breakdown of academic impact, for papers by Kanji Sugita Breakdown of academic impact, for papers by Jens van den Brandt
Rankless by CCL
2026