Marc Délepine

12.0k citations

28 papers · 3.2k indexed · 2 hit papers · h-index 21

Impact in

Cell Biology top 1%
- Endoplasmic Reticulum Stress and Disease
Biochemistry top 1%
- Lipid metabolism and biosynthesis

Papers in ⓘ

Cell Biology 7
- Endoplasmic Reticulum Stress and Disease 4
Genetics 9
- Genetics and Neurodevelopmental Disorders 4

Co-authors: Cécile Julier (7 shared papers)G.M. Lathrop (3 shared papers)Marc Nicolino (1 shared paper)Timothy Barrett (1 shared paper)Mark Lathrop (4 shared papers)Jocelyne Magré (7 shared papers)Jacqueline Capeau (6 shared papers)Muriel Meier (3 shared papers)
Journals: Diabetes (3 papers)Nature Genetics (2 papers)Human Molecular Genetics (2 papers)The Journal of Clinical Endocrinology & Metabolism (2 papers)The Lancet (2 papers)
Partner nations: France United Kingdom United States

In The Last Decade

Marc Délepine

28 papers receiving 3.2k citations

Hit Papers

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Identification of the gene altered in Berardinelli–Seip congenital lipodystrophy on chromosome 11q13 2001 · 560 citations

Peers

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-authors

The 25 scholars most cited alongside Marc Délepine, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Marc Délepine Line = papers co-authored together Marc Délepine links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 28 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	EIF2AK3, encoding translation initiation factor 2-α kinase 3, is mutated in patients with Wolcott-Rallison syndrome Nature Genetics ·Marc Délepine, Marc Nicolino, Timothy Barrett, Mahamadee Golamaully, G.M. Lathrop, Cécile Julier Hit paper breakdown →	2000	643
2	Identification of the gene altered in Berardinelli–Seip congenital lipodystrophy on chromosome 11q13 Nature Genetics ·Jocelyne Magré, Marc Délepine, Eliane Khallouf, Tobias Gedde‐Dahl, Lionel Van Maldergem, Eric M. Sobel, Jeanette C. Papp, Muriel Meier, André Mégarbané, (unknown), Mark Lathrop, Jacqueline Capeau Hit paper breakdown →	2001	560
3	Genetic mapping of a susceptibility locus for insulin-dependent diabetes mellitus on chromosome llq Nature ·L. Hashimoto, C Habita, Jean-Paul Beressi, Marc Délepine, Christoph W. Basse, Anne Cambon‐Thomsen, I Deschamps, Jerome I. Rotter, S. Djoulah, Michael R. James, Philippe Froguel, J. Weissenbach, G.M. Lathrop, Cécile Julier	1994	312
4	Association of a Homozygous Nonsense Caveolin-1 Mutation with Berardinelli-Seip Congenital Lipodystrophy The Journal of Clinical Endocrinology & Metabolism ·Chong Ae Kim, Marc Délepine, Emilie Boutet, Haquima El Mourabit, Soazig Le Lay, Muriel Meier, Mona Nemani, E. Bridel, Claudia C. Leite, Débora Romeo Bertola, Robert K. Semple, Stephen O’Rahilly, Isabelle Dugail, Jacqueline Capeau, Mark Lathrop, Jocelyne Magré	2008	296
5	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 ·Bernard Keavney, Colin A. McKenzie, Sarah Parish, A. W. Palmer, Sarah J. Clark, Linda Youngman, Marc Délepine, Mark Lathrop, Richard Peto, Rory Collins	2000	284
6	Perilipin Deficiency and Autosomal Dominant Partial Lipodystrophy New England Journal of Medicine ·Sheetal Gandotra, Caroline Le Dour, William Bottomley, Pascale Cervera, Philippe Giral, Yves Reznik, G. Charpentier, Martine Auclair, Marc Délepine, Inês Barroso, Robert K. Semple, Mark Lathrop, Olivier Lascols, Jacqueline Capeau, Stephen O’Rahilly, Jocelyne Magré, David B. Savage, Corinne Vigouroux	2011	210
7	Genetic Susceptibility for Human Familial Essential Hypertension in a Region of Homology with Blood Pressure Linkage on Rat Chromosome 10 Human Molecular Genetics ·Cécile Julier, Marc Délepine, Bernard Keavney, Joseph D. Terwilliger, Sean Davis, Daniel E. Weeks, Thuỳ Anh Bùi, Xavier Jeunemaı̂tre, Gilberto Velho, Philippe Froguel, Peter J. Ratcliffe, Pierre Corvol, Florent Soubrier, G. Mark Lathrop	1997	139
8	Fibrinogen and coronary heart disease: test of causality by ‘Mendelian randomization’ International Journal of Epidemiology ·Bernard Keavney, John Danesh, Sarah Parish, A. W. Palmer, Sarah L. Clark, Linda Youngman, Marc Délepine, Mark Lathrop, Richard Peto, Rory Collins	2006	104
9	Evidence of a non-MHC susceptibility locus in type I diabetes linked to HLA on chromosome 6. PubMed ·Marc Délepine, Flemming Pociot, C Habita, L. Hashimoto, Philippe Froguel, Jerome I. Rotter, Anne Cambon‐Thomsen, I Deschamps, S. Djoulah, J. Weissenbach, Jørn Nerup, Mark Lathrop, Cécile Julier	1997	79
10	Prevalence of Mutations in AGPAT2 Among Human Lipodystrophies Diabetes ·Jocelyne Magré, Marc Délepine, Lionel Van Maldergem, Jean‐Jacques Robert, J. Antonie Maassen, Muriel Meier, Vanessa R. Panz, Chong Ae Kim, Nadia Tubiana‐Rufi, Paul Czernichow, E Seemanová, Charles Buchanan, Didier Lacombe, Corinne Vigouroux, Olivier Lascols, C. Ronald Kahn, Jacqueline Capeau, Mark Lathrop	2003	68
11	Polymorphisms in Type II SH2 Domain–Containing Inositol 5-Phosphatase (INPPL1, SHIP2) Are Associated With Physiological Abnormalities of the Metabolic Syndrome Diabetes ·Pamela J. Kaisaki, Marc Délepine, Peng Yeong Woon, Liam Sebag‐Montefiore, Steven P. Wilder, Stephan Menzel, Nathalie Vionnet, Evelyne Marion, Jean‐Pierre Riveline, G. Charpentier, Stéphane Schurmans, J Lévy, Mark Lathrop, Martin Farrall, Dominique Gauguier	2004	67
12	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 ·Pierre Cacciagli, Julie Sutera-Sardo, Ana Borges-Correia, Jean‐Christophe Roux, Imen Dorboz, Jean‐Pierre Desvignes, Catherine Badens, Marc Délepine, Mark Lathrop, Pierre Cau, Nicolas Lévy, Nadine Girard, Pierre Sarda, Odile Boespflug‐Tanguy, Laurent Villard	2013	48
13	Multiple DNA variant association analysis: application to the insulin gene region in type I diabetes. PubMed ·Cécile Julier, Anneke Lucassen, Pascale Villedieu, Marc Délepine, Claire Lévy‐Marchal, Pierre-Marie Danzé, Federico Bianchi, Christian Boîtard, Philippe Froguel, J I Bell	1994	44
14	Plasma fibrinogen and fibrinogen genotypes in 4685 cases of myocardial infarction and in 6002 controls: Test of causality by "Mendelian randomisation" Circulation ·Linda Youngman, Bernard Keavney, Andrew Palmer, Sarah Parish, Sarah L. Clark, John Danesh, Marc Délepine, Mark Lathrop, Richárd Pető, Richard Collins	2000	43
15	WFS1 mutations are frequent monogenic causes of juvenile-onset diabetes mellitus in Lebanon Human Molecular Genetics ·Pierre Zalloua, Sami T. Azar, Marc Délepine, Nadine J. Makhoul, Hervé Blanc, May Sanyoura, Anne Lavergne, Karmen Stankov, Arnaud Lemainque, Patrick Baz, Cécile Julier	2008	42
16	The origin of a developmentally regulatedIghreplicon is located near the border of regulatory domains forIghreplication and expression Proceedings of the National Academy of Sciences ·Jie Zhou, Nasrin Ashouian, Marc Délepine, Fumihiko Matsuda, Christophe Chevillard, Roy Riblet, Carl L. Schildkraut, Barbara K. Birshtein	2002	41
17	AP1S2 is mutated in X-linked Dandy–Walker malformation with intellectual disability, basal ganglia disease and seizures (Pettigrew syndrome) European Journal of Human Genetics ·Pierre Cacciagli, Jean‐Pierre Desvignes, Nadine Girard, Marc Délepine, Diana Zélénika, Mark Lathrop, Nicolas Lévy, David H. Ledbetter, William B. Dobyns, Laurent Villard	2013	37
18	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 ·Martin Llewellyn, Louisa A. Messenger, Alejandro O. Luquetti, Lineth García, Faustino Torrico, Suelene B. N. Tavares, Bachar Cheaib, Nicolas Derôme, Marc Délepine, Céline Baulard, Jean‐François Deleuze, Sascha Sauer, Michael A. Miles	2015	37
19	Performance comparison of three DNA extraction kits on human whole-exome data from formalin-fixed paraffin-embedded normal and tumor samples PLoS ONE ·Éric Bonnet, Marie-Laure Moutet, Céline Baulard, Delphine Bacq‐Daian, Florian Sandron, Lilia Mesrob, Bertrand Fin, Marc Délepine, Marie-Ange Palomares, Claire Jubin, Hélène Blanché, Vincent Meyer, Anne Boland, Robert Olaso, Jean‐François Deleuze	2018	37
20	Large-scale evidence that the cardiotoxicity of smoking is not significantly modified by the apolipoprotein E ε2/ε3/ε4 genotype The Lancet ·Bernard Keavney, Sarah Parish, A. W. Palmer, Sarah L. Clark, Linda Youngman, John Danesh, Colin A. McKenzie, Marc Délepine, Mark Lathrop, Richard Peto, Rory Collins	2003	35

About Marc Délepine

Marc Délepine is a scholar working on Cell Biology, Genetics, Biochemistry, Molecular Biology and Endocrinology, Diabetes and Metabolism, having authored 28 papers that have together received 3.2k indexed citations. Recurring topics across this work include Nuclear Structure and Function (6 papers), Pancreatic function and diabetes (5 papers), RNA Research and Splicing (5 papers), Endoplasmic Reticulum Stress and Disease (4 papers), Genetics and Neurodevelopmental Disorders (4 papers), Metabolism, Diabetes, and Cancer (3 papers), Molecular Biology Techniques and Applications (3 papers) and RNA regulation and disease (3 papers). The work is most often cited by research in Cell Biology (837 citations), Biochemistry (368 citations), Genetics (1.1k citations), Endocrinology, Diabetes and Metabolism (529 citations) and Molecular Biology (1.5k citations). Marc Délepine has collaborated with scholars based in France, United Kingdom and United States. Frequent 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. Their work appears in journals such as Diabetes, Nature Genetics, Human Molecular Genetics, The Journal of Clinical Endocrinology & Metabolism and The Lancet.

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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