Marc Jeanpierre

8.5k citations

120 papers · 4.7k indexed · h-index 37

Impact in

Molecular Biology top 2%
- Renal and related cancers
- Muscle Physiology and Disorders
- Epigenetics and DNA Methylation
- RNA modifications and cancer
Genetics top 1%

Papers in

Genetics 41
- Genomic variations and chromosomal abnormalities 10
- Genetic Syndromes and Imprinting 9
Molecular Biology 98
- Renal and related cancers 41
- Muscle Physiology and Disorders 19
- Epigenetics and DNA Methylation 14

Co-authors: Claudine Junien E. Viégas-Pèquignot France Leturcq Isabelle Henry Kevin P. Campbell Fédérica Piccolo Corinne Antignac F.M.S. Tomé
Journals: Human Genetics (12 papers)Human Molecular Genetics (6 papers)Neuromuscular Disorders (6 papers)Cytogenetic and Genome Research (6 papers)Nucleic Acids Research (5 papers)
Partner nations: France United States United Kingdom

In The Last Decade

Marc Jeanpierre

116 papers receiving 4.6k citations

Peers

Countries citing papers authored by Marc Jeanpierre

Since Specialization

Citations

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

Fields of papers citing papers by Marc Jeanpierre

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Marc Jeanpierre, 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 Jeanpierre Line = papers co-authored together Marc Jeanpierre links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	RET and GDNF mutations are rare in fetuses with renal agenesis or other severe kidney development defects Journal of Medical Genetics ·Marc Jeanpierre, G. Macé, Mélanie Parisot, Vincent Morinière, A. Pawtowsky, Max E. Benabou, Jelena Martinović, Jeanne Amiel, Tania Attié‐Bitach, Anne‐Lise Delezoide, Philippe Loget, Patricia Blanchet, Dominique Gaillard, M. Gonzalés, Wassila Carpentier, Patrick Nitschké, Frédéric Torès, Laurence Heidet, Corinne Antignac, Rémi Salomon, (unknown)	2011	37
2	Control of the Wnt pathways by nephrocystin-4 is required for morphogenesis of the zebrafish pronephros Human Molecular Genetics ·Céline Burcklé, Helori-Maël Gaudé, Christine Vesque, Flora Silbermann, Rémi Salomon, Marc Jeanpierre, Corinne Antignac, Sophie Saunier, Sylvie Schneider‐Maunoury	2011	46
3	Permanent muscle weakness in MCArdle disease Muscle & Nerve ·Aleksandra Nadaj‐Pakleza, C. Vincitorio, Pascal Laforêt, B. Eymard, Élisabeth Dion, Susana Teijeira, Irene Vietez, Marc Jeanpierre, Carmen Navarro, Tanya Stojkovic	2009	46
4	Molecular cytogenetic anomalies and phenotype alterations in a newly established cell line from Wilms tumor with diffuse anaplasia Cancer Genetics and Cytogenetics ·Marine Faussillon, Ichiro Murakami, Magalie Bichat, Louise Telvi, Marc Jeanpierre, C Nézelof, Francis Jaubert, Jean Gogusev	2008	7
5	Origin of the prevalent SFTPB indel g.1549C > GAA (121ins2) mutation causing surfactant protein B (SP‐B) deficiency American Journal of Medical Genetics Part A ·Mohammed Tredano, D.N. Cooper, Manfred Stuhrmann, John Christodoulou, Nadia Chuzhanova, Françoise Roudot‐Thoraval, Pierre‐Yves Boëlle, Jacques Élion, Marc Jeanpierre, Josué Feingold, Rémy Couderc, Michel Bahuau	2005	16
6	Frequent overexpression of cyclin D2/cyclin-dependent kinase 4 in Wilms' tumor Cancer Letters ·Marine Faussillon, Lucie Monnier, Claudine Junien, Marc Jeanpierre	2004	27
7	Founder Effect in Patients with Unverricht‐Lundborg Disease on Reunion Island Epilepsia ·Bruno Moulard, Françoise Darcel, Didier Mignard, Marc Jeanpierre, Pierre Genton, François Cartault, Jacqueline Yaouanq, Agathe Roubertie, Arnaud Biraben, Catherine Burési, Alain Malafosse	2003	8
8	L'épilepsie myoclonique progressive de type Unverricht-Lundborg sur l'île de la Réunion Bruno Moulard, Françoise Darcel, Didier Mignard, Marc Jeanpierre, Pierre Genton, François Cartault, Jacqueline Yaouanq, Agathe Roubertie, Arnaud Biraben, Catherine Burési, Alain Malafosse	2002	1
9	Assignment<footref rid="foot01"><sup>1</sup></footref> of E-cadherin (CDH1) and KSP-cadherin (CDH16) to chromosome 16q22.1 by radiation hybrid mapping Cytogenetic and Genome Research ·David Baudry, Marc Jeanpierre	2000	1
10	Abnormal methylation does not prevent X inactivation in ICF patients Cytogenetic and Genome Research ·Déborah Bourc’his, Pierre Miniou, Marc Jeanpierre, D. Molina Gomes, Jean‐Michel Dupont, Geneviève de Saint Basile, P Maraschio, L. Tiepolo, E. Viégas-Pèquignot	1999	32
11	Identification of Constitutional WT1 Mutations, in Patients with Isolated Diffuse Mesangial Sclerosis, and Analysis of Genotype/Phenotype Correlations by Use of a Computerized Mutation Database The American Journal of Human Genetics ·Marc Jeanpierre, Érick Denamur, Isabelle Henry, M.-O. Cabanis, Sandrine Luce, A Cécille, Jacques Élion, M. Peuchmaur, Chantal Loirat, Patrick Niaudet, Marie-Claire Gübler, Claudine Junien	1998	164
12	Severe limb girdle muscular dystrophy in Spanish gypsies: further evidence for a founder mutation in the γ-sarcoglycan gene European Journal of Human Genetics ·Adriana Lasa, Fédérica Piccolo, Carles de Diego, Marc Jeanpierre, Jaume Colomer, Maria José Rodríguez, Jon Andoni Urtizberea, Montserrat Baiget, Jean Claude Kaplan, P. Gallano	1998	15
13	Gènes et retards de croissance intra-utérins Archives de Pédiatrie ·Marc Jeanpierre	1998	2
14	Correlations of allelic imbalance of chromosome 14 with adverse prognostic parameters in 148 renal cell carcinomas Genes Chromosomes and Cancer ·Christophe Béroud, Jean‐Christophe Fournet, Marc Jeanpierre, D Droz, Raymonde Bouvier, Delphine Froger, Yves Chrétien, Jean-Marie Maréchal, Jean Weissenbach, Claudine Junlen	1996	41
15	Immunohistochemical analysis of dystrophin-associated proteins in Becker/Duchenne muscular dystrophy with huge in-frame deletions in the NH2-terminal and rod domains of dystrophin. Journal of Clinical Investigation ·Kiichiro Matsumura, Arthur H.M. Burghes, Marina Mora, F.M.S. Tomé, Lucía Morandi, F Cornello, France Leturcq, Marc Jeanpierre, J.‐C. Kaplan, Philippe Reinert	1994	45
16	Specific induction of uncoiling and recombination by azacytidine in classical satellite-containing constitutive heterochromatin Cytogenetic and Genome Research ·Nadja Kokalj-Vokač, Anna Almeida, E. Viégas-Pèquignot, Marc Jeanpierre, Bernard Malfoy, B. Dutrillaux	1993	74
17	A highly informative CACA repeat polymorphism upstream of the human dystrophin gene (DMD) Nucleic Acids Research ·Jean‐Philippe Hugnot, Dominique Récan, Marc Jeanpierre, J.‐C. Kaplan, Aslıhan Tolun	1991	16
18	Constitutional and somatic deletions of two different regions of maternal chromosome 11 in Wilms tumor Genomics ·Marc Jeanpierre, Corinne Antignac, Christophe Béroud, Christian Lavedan, Isabelle Henry, G F Saunders, Bryan Williams, Tom Glaser, Claudine Junien	1990	18
19	Detection of 1q polysomy in interphase nuclei of human solid tumors with a biotinylated probe Human Genetics ·E. Viégas-Pèquignot, Marc Jeanpierre, A.M. Dutrillaux, Michèle Gerbault‐Seureau, Martine Muleris, Bernard Dutrillaux	1989	29
20	A rapid method for the purification of DNA from blood Nucleic Acids Research ·Marc Jeanpierre	1987	278

About Marc Jeanpierre

Marc Jeanpierre is a scholar working on Genetics, Molecular Biology, Urology, Cellular and Molecular Neuroscience and Pediatrics, Perinatology and Child Health, having authored 120 papers that have together received 4.7k indexed citations. Recurring topics across this work include Renal and related cancers (41 papers), Renal cell carcinoma treatment (19 papers), Muscle Physiology and Disorders (19 papers), Epigenetics and DNA Methylation (14 papers), Genetic Neurodegenerative Diseases (11 papers), Genomic variations and chromosomal abnormalities (10 papers), Prenatal Screening and Diagnostics (10 papers) and Genetic Syndromes and Imprinting (9 papers). The work is most often cited by research in Molecular Biology (3.8k citations), Genetics (1.3k citations), Genetics (366 citations), Urology (205 citations) and Cellular and Molecular Neuroscience (533 citations). Marc Jeanpierre has collaborated with scholars based in France, United States and United Kingdom. Frequent co-authors include Claudine Junien, E. Viégas-Pèquignot, France Leturcq, Isabelle Henry, Kevin P. Campbell, Fédérica Piccolo, Corinne Antignac, F.M.S. Tomé, Michel Fardeau and C Turleau. Their work appears in journals such as Human Genetics, Human Molecular Genetics, Neuromuscular Disorders, Cytogenetic and Genome Research and Nucleic Acids Research.

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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