Isabelle Callebaut

19.3k total citations · 2 hit papers
239 papers, 12.9k citations indexed

About

Isabelle Callebaut is a scholar working on Molecular Biology, Immunology and Physiology. According to data from OpenAlex, Isabelle Callebaut has authored 239 papers receiving a total of 12.9k indexed citations (citations by other indexed papers that have themselves been cited), including 149 papers in Molecular Biology, 36 papers in Immunology and 31 papers in Physiology. Recurrent topics in Isabelle Callebaut's work include Cystic Fibrosis Research Advances (28 papers), RNA and protein synthesis mechanisms (24 papers) and Protein Structure and Dynamics (23 papers). Isabelle Callebaut is often cited by papers focused on Cystic Fibrosis Research Advances (28 papers), RNA and protein synthesis mechanisms (24 papers) and Protein Structure and Dynamics (23 papers). Isabelle Callebaut collaborates with scholars based in France, United States and Belgium. Isabelle Callebaut's co-authors include Jean‐Paul Mornon, Alain Fischer, J.-P. Mornon, Jean‐Pierre de Villartay, Philippe Monget, Jean‐Claude Courvalin, Gilles Labesse, Françoise Le Deist, Despina Moshous and Pierre Lehn and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Isabelle Callebaut

236 papers receiving 12.7k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Munc13-4 Is Essential for Cytolytic Granules Fusion and Is Mutated in a Form of Familial Hemophagocytic Lymphohistiocytosis (FHL3)

2003 684 citations Isabelle Callebaut, Alain Fischer et al. profile →
Artemis, a Novel DNA Double-Strand Break Repair/V(D)J Recombination Protein, Is Mutated in Human Severe Combined Immune Deficiency

2001 680 citations Isabelle Callebaut, Alain Fischer et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Isabelle Callebaut France	59	7.9k	2.5k	1.7k	1.3k	1.3k	239	12.9k
Osamu Ohara Japan	67	7.6k 1.0×	5.0k 2.0×	1.7k 1.0×	1.9k 1.4×	1.1k 0.8×	422	15.7k
Ulf Hellman Sweden	63	9.4k 1.2×	1.7k 0.7×	1.1k 0.6×	1.8k 1.3×	1.5k 1.2×	280	14.3k
Toru Nakano Japan	68	12.9k 1.6×	4.6k 1.8×	2.7k 1.6×	1.8k 1.3×	1.4k 1.0×	208	18.9k
Stephen C. Blacklow United States	62	11.1k 1.4×	2.5k 1.0×	899 0.5×	2.2k 1.6×	1.6k 1.2×	156	15.9k
Peter F. Johnson United States	64	11.2k 1.4×	3.4k 1.4×	2.6k 1.6×	2.4k 1.8×	1.3k 1.0×	127	17.0k
Steffan N. Ho United States	31	9.6k 1.2×	2.2k 0.9×	2.0k 1.2×	1.6k 1.2×	1.5k 1.1×	51	14.6k
Richard Tizard United States	41	6.1k 0.8×	3.3k 1.3×	1.7k 1.0×	847 0.6×	846 0.6×	56	11.8k
Roy A. Black United States	50	7.3k 0.9×	3.9k 1.6×	873 0.5×	3.8k 2.8×	1.0k 0.8×	95	14.8k
Douglas Pat Cerretti United States	47	7.1k 0.9×	4.1k 1.6×	1.1k 0.7×	3.0k 2.2×	1.6k 1.2×	82	14.5k
Norma Neff United States	48	9.1k 1.1×	1.6k 0.7×	1.5k 0.9×	1.3k 1.0×	729 0.6×	92	13.4k

Countries citing papers authored by Isabelle Callebaut

Since Specialization

Citations

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

Fields of papers citing papers by Isabelle Callebaut

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Isabelle Callebaut

This figure shows the co-authorship network connecting the top 25 collaborators of Isabelle Callebaut. A scholar is included among the top collaborators of Isabelle Callebaut 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 Isabelle Callebaut. Isabelle Callebaut 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

Gugger, Muriel, Manuela Dezi, Julie Leloup, et al.. (2025). Diel changes in the expression of a marker gene and candidate genes for intracellular amorphous CaCO3 biomineralization in Microcystis. Peer Community Journal. 5.

Benzerara, Karim, Élodie Duprat, Tristan Bitard‐Feildel, et al.. (2022). A New Gene Family Diagnostic for Intracellular Biomineralization of Amorphous Ca Carbonates by Cyanobacteria. Genome Biology and Evolution. 14(3). 22 indexed citations

Farinha, Carlos M. & Isabelle Callebaut. (2022). Molecular mechanisms of cystic fibrosis – how mutations lead to misfunction and guide therapy. Bioscience Reports. 42(7). 25 indexed citations

Bitard‐Feildel, Tristan, et al.. (2022). A sequence‐based foldability score combined with AlphaFold2 predictions to disentangle the protein order/disorder continuum. Proteins Structure Function and Bioinformatics. 91(4). 466–484. 13 indexed citations

Callebaut, Isabelle, Jean‐Christophe Gelly, Isabelle Hatin, et al.. (2021). Intergenic ORFs as elementary structural modules of de novo gene birth and protein evolution. Genome Research. 31(12). 2303–2315. 24 indexed citations

O’Donohue, Marie-Françoise, Laëtitia Kermasson, Pierre Frange, et al.. (2019). Impaired telomere integrity and rRNA biogenesis in PARN‐deficient patients and knock‐out models. EMBO Molecular Medicine. 11(7). e10201–e10201. 31 indexed citations

Fournier, Benjamin, Sarah Winter, Kazushi Izawa, et al.. (2019). Concomitant PIK3CD and TNFRSF9 deficiencies cause chronic active Epstein-Barr virus infection of T cells. The Journal of Experimental Medicine. 216(12). 2800–2818. 65 indexed citations

Callebaut, Isabelle, Joël Fontaine, Delphine Logeart‐Avramoglou, et al.. (2017). Thrombospondin-1 (TSP-1), a new bone morphogenetic protein-2 and -4 (BMP-2/4) antagonist identified in pituitary cells. Journal of Biological Chemistry. 292(37). 15352–15368. 9 indexed citations

Gourlaouen, Isabelle, et al.. (2017). Deciphering the molecular basis of ferroportin resistance to hepcidin: Structure/function analysis of rare SLC40A1 missense mutations found in suspected hemochromatosis type 4 patients. Transfusion Clinique et Biologique. 24(4). 462–467. 4 indexed citations

10.

Hinzpeter, Alexandre, Isabelle Callebaut, Cécile Zordan, et al.. (2017). The importance of functional tests to assess the effect of a new CFTR variant when genotype–phenotype correlation is not possible. Clinical Case Reports. 5(5). 658–663. 4 indexed citations

11.

Jeremiah, Nadia, Bénédicte Neven, Matteo Gentili, et al.. (2014). Inherited STING-activating mutation underlies a familial inflammatory syndrome with lupus-like manifestations. Journal of Clinical Investigation. 124(12). 5516–5520. 393 indexed citations

12.

Silvy, Monique, Sylvie Chapel‐Fernandes, Isabelle Callebaut, et al.. (2012). Characterization of novel RHD alleles: relationship between phenotype, genotype, and trimeric architecture. Transfusion. 52(9). 2020–2029. 34 indexed citations

13.

Meslin, Camille, Sylvie Mugnier, Isabelle Callebaut, et al.. (2012). Evolution of Genes Involved in Gamete Interaction: Evidence for Positive Selection, Duplications and Losses in Vertebrates. PLoS ONE. 7(9). e44548–e44548. 43 indexed citations

14.

Chapel‐Fernandes, Sylvie, Isabelle Callebaut, Gregory R. Halverson, et al.. (2009). Dombrock genotyping in a native Congolese cohort reveals two novel alleles. Transfusion. 49(8). 1661–1671. 12 indexed citations

15.

Marcand, Stéphane, et al.. (2008). Multiple pathways inhibit NHEJ at telomeres. Genes & Development. 22(9). 1153–1158. 78 indexed citations

16.

Couprie, Joël, Isabelle Duband‐Goulet, Béatrice Alpha‐Bazin, et al.. (2007). The checkpoint Saccharomyces cerevisiae Rad9 protein contains a tandem tudor domain that recognizes DNA. Nucleic Acids Research. 35(17). 5898–5912. 22 indexed citations

17.

Dentice, Monica, Amitabha Bandyopadhyay, Balázs Gereben, et al.. (2005). The Hedgehog-inducible ubiquitin ligase subunit WSB-1 modulates thyroid hormone activation and PTHrP secretion in the developing growth plate. Nature Cell Biology. 7(7). 698–705. 185 indexed citations

18.

Girault, Jean‐Antoine, et al.. (1999). The N-termini of FAK and JAKs contain divergent band 4.1 domains. Trends in Biochemical Sciences. 24(2). 54–57. 139 indexed citations

19.

Girault, Jean‐Antoine, Gilles Labesse, J.-P. Mornon, & Isabelle Callebaut. (1998). Janus Kinases and Focal Adhesion Kinases Play in the 4.1 Band: A Superfamily of Band 4.1 Domains Important for Cell Structure and Signal Transduction. Molecular Medicine. 4(12). 751–769. 86 indexed citations

20.

Mornon, Jean‐Paul, et al.. (1998). α- C-terminal domain: on the track of an Ig fold. International Journal of Biological Macromolecules. 22(3-4). 219–227. 29 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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