Marc Délepine

12.0k total citations · 2 hit papers
28 papers, 3.2k citations indexed

About

Marc Délepine is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Marc Délepine has authored 28 papers receiving a total of 3.2k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 9 papers in Genetics and 7 papers in Cell Biology. Recurrent topics in Marc Délepine's work include Nuclear Structure and Function (6 papers), Pancreatic function and diabetes (5 papers) and RNA Research and Splicing (5 papers). Marc Délepine is often cited by papers focused on Nuclear Structure and Function (6 papers), Pancreatic function and diabetes (5 papers) and RNA Research and Splicing (5 papers). Marc Délepine collaborates with scholars based in France, United Kingdom and United States. Marc Délepine's co-authors include Cécile Julier, G.M. Lathrop, Marc Nicolino, Timothy Barrett, Mark Lathrop, Jocelyne Magré, Jacqueline Capeau, Muriel Meier, Bernard Keavney and Mark Lathrop and has published in prestigious journals such as Nature, New England Journal of Medicine and Proceedings of the National Academy of Sciences.

In The Last Decade

Marc Délepine

28 papers receiving 3.2k 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.

EIF2AK3, encoding translation initiation factor 2-α kinase 3, is mutated in patients with Wolcott-Rallison syndrome

2000 643 citations Marc Délepine, Marc Nicolino et al. Nature Genetics profile →
Identification of the gene altered in Berardinelli–Seip congenital lipodystrophy on chromosome 11q13

2001 560 citations Jocelyne Magré, Marc Délepine et al. Nature Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Marc Délepine France	21	1.5k	1.1k	859	837	529	28	3.2k
Li‐Shin Huang United States	26	1.2k 0.8×	322 0.3×	662 0.8×	266 0.3×	723 1.4×	39	2.8k
Danhong Lu United States	30	1.5k 1.0×	817 0.8×	1.7k 2.0×	386 0.5×	624 1.2×	44	3.1k
Stephan Rust Germany	30	2.0k 1.3×	418 0.4×	1.9k 2.2×	212 0.3×	436 0.8×	63	3.9k
Kathy D. Shelton United States	14	1.5k 0.9×	487 0.5×	1.0k 1.2×	205 0.2×	422 0.8×	19	2.3k
Ramendra K. Kundu United States	27	1.1k 0.7×	355 0.3×	1.1k 1.2×	115 0.1×	421 0.8×	44	3.1k
Ross W. Milne Canada	33	1.2k 0.8×	148 0.1×	938 1.1×	202 0.2×	934 1.8×	69	3.2k
Fabrice Moore Belgium	19	667 0.4×	871 0.8×	1.1k 1.3×	528 0.6×	377 0.7×	25	2.1k
William R. Lagor United States	25	1.1k 0.7×	429 0.4×	440 0.5×	127 0.2×	386 0.7×	57	2.0k
Olivier Lascols France	29	1.9k 1.2×	303 0.3×	276 0.3×	214 0.3×	151 0.3×	86	2.7k
Mats Gåfvels Sweden	26	873 0.6×	283 0.3×	835 1.0×	152 0.2×	348 0.7×	69	2.5k

Countries citing papers authored by Marc Délepine

Since Specialization

Citations

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

Fields of papers citing papers by Marc Délepine

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marc Délepine

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

Shen, Yimin, Antoine Daunay, Marc Délepine, et al.. (2025). A detailed analysis of second and third-generation sequencing approaches for accurate length determination of short tandem repeats and homopolymers. Nucleic Acids Research. 53(5). 4 indexed citations

Jubin, Claire, Marta Rodríguez de Alba, Cristina Villaverde, et al.. (2023). Long-read genome sequencing identifies cryptic structural variants in congenital aniridia cases. Human Genomics. 17(1). 45–45. 13 indexed citations

Auclair, Martine, Faraj Terro, Mona Nemani, et al.. (2016). Maladaptative Autophagy Impairs Adipose Function in Congenital Generalized Lipodystrophy due to Cavin-1 Deficiency. The Journal of Clinical Endocrinology & Metabolism. 101(7). 2892–2904. 13 indexed citations

Llewellyn, Martin, Louisa A. Messenger, Alejandro O. Luquetti, et al.. (2015). Deep Sequencing of the Trypanosoma cruzi GP63 Surface Proteases Reveals Diversity and Diversifying Selection among Chronic and Congenital Chagas Disease Patients. PLoS neglected tropical diseases. 9(4). e0003458–e0003458. 37 indexed citations

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

Cacciagli, Pierre, Jean‐Christophe Roux, Imen Dorboz, et al.. (2013). Mutations in BCAP31 Cause a Severe X-Linked Phenotype with Deafness, Dystonia, and Central Hypomyelination and Disorganize the Golgi Apparatus. The American Journal of Human Genetics. 93(3). 579–586. 48 indexed citations

Gandotra, Sheetal, Caroline Le Dour, William Bottomley, et al.. (2011). Perilipin Deficiency and Autosomal Dominant Partial Lipodystrophy. New England Journal of Medicine. 364(8). 740–748. 210 indexed citations

Roll, Patrice, Damien Sanlaville, Audrey Labalme, et al.. (2010). Infantile Convulsions with Paroxysmal Dyskinesia (ICCA Syndrome) and Copy Number Variation at Human Chromosome 16p11. PLoS ONE. 5(10). e13750–e13750. 10 indexed citations

Kim, Chong Ae, Marc Délepine, Emilie Boutet, et al.. (2008). Association of a Homozygous Nonsense Caveolin-1 Mutation with Berardinelli-Seip Congenital Lipodystrophy. The Journal of Clinical Endocrinology & Metabolism. 93(4). 1129–1134. 296 indexed citations

10.

Keavney, Bernard, John Danesh, Sarah Parish, et al.. (2006). Fibrinogen and coronary heart disease: test of causality by ‘Mendelian randomization’. International Journal of Epidemiology. 35(4). 935–943. 104 indexed citations

11.

Wit, Marie‐Claire Y. de, I.F.M. de Coo, Cécile Julier, et al.. (2006). Microcephaly and simplified gyral pattern of the brain associated with early onset insulin-dependent diabetes mellitus. Neurogenetics. 7(4). 259–263. 25 indexed citations

12.

Keavney, Bernard, Sarah Parish, A. W. Palmer, et al.. (2003). Large-scale evidence that the cardiotoxicity of smoking is not significantly modified by the apolipoprotein E ε2/ε3/ε4 genotype. The Lancet. 361(9355). 396–398. 35 indexed citations

13.

Heathcote, Kirsten, Anna Rajab, Jocelyne Magré, et al.. (2002). Molecular Analysis of Berardinelli-Seip Congenital Lipodystrophy in Oman. Diabetes. 51(4). 1291–1293. 18 indexed citations

14.

Magré, Jocelyne, Marc Délepine, Eliane Khallouf, et al.. (2001). Identification of the gene altered in Berardinelli–Seip congenital lipodystrophy on chromosome 11q13. Nature Genetics. 28(4). 365–370. 560 indexed citations breakdown →

15.

Youngman, Linda, Bernard Keavney, Andrew Palmer, et al.. (2000). Plasma fibrinogen and fibrinogen genotypes in 4685 cases of myocardial infarction and in 6002 controls: Test of causality by "Mendelian randomisation". Circulation. 102. 31–32. 43 indexed citations

16.

Délepine, Marc, et al.. (2000). EIF2AK3, encoding translation initiation factor 2-α kinase 3, is mutated in patients with Wolcott-Rallison syndrome. Nature Genetics. 25(4). 406–409. 643 indexed citations breakdown →

17.

Keavney, Bernard, Colin A. McKenzie, Sarah Parish, et al.. (2000). Large-scale test of hypothesised associations between the angiotensin-converting-enzyme insertion/deletion polymorphism and myocardial infarction in about 5000 cases and 6000 controls. The Lancet. 355(9202). 434–442. 284 indexed citations

18.

Julier, Cécile, Marc Délepine, Bernard Keavney, et al.. (1997). Genetic Susceptibility for Human Familial Essential Hypertension in a Region of Homology with Blood Pressure Linkage on Rat Chromosome 10. Human Molecular Genetics. 6(12). 2077–2085. 139 indexed citations

19.

Hashimoto, L., Jean-Paul Beressi, Marc Délepine, et al.. (1994). Genetic mapping of a susceptibility locus for insulin-dependent diabetes mellitus on chromosome llq. Nature. 371(6493). 161–164. 312 indexed citations

20.

Julier, Cécile, Anneke Lucassen, Marc Délepine, et al.. (1994). Multiple DNA variant association analysis: application to the insulin gene region in type I diabetes.. PubMed. 55(6). 1247–54. 44 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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