D. Depétris

2.2k citations

44 papers · 1.5k indexed · h-index 23

Impact in

Aging top 10%
Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities

Papers in

Genetics 16
- Genomic variations and chromosomal abnormalities 7
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 6
- Genetics and Neurodevelopmental Disorders 6
Molecular Biology 34
- Genomics and Chromatin Dynamics 6
- Epigenetics and DNA Methylation 4
- RNA Research and Splicing 4

Co-authors: Marie‐Geneviève Mattéi Nicolas Lévy Catherine Metzler‐Guillemain Annachiara De Sandre‐Giovannoli Claire Navarro Cécile Mignon‐Ravix Michael Mitchell Judith Luciani
Journals: European Journal of Human Genetics (5 papers)Cytogenetic and Genome Research (5 papers)Chromosome Research (5 papers)Genomics (5 papers)Mammalian Genome (3 papers)
Partner nations: France Lebanon United States

In The Last Decade

D. Depétris

44 papers receiving 1.5k citations

Peers

Countries citing papers authored by D. Depétris

Since Specialization

Citations

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

Fields of papers citing papers by D. Depétris

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	MG 132‐induced progerin clearance is mediated by autophagy activation and splicing regulation EMBO Molecular Medicine ·Karim Harhouri, Claire Navarro, D. Depétris, Marie‐Geneviève Mattéi, Xavier Nissan, Pierre Cau, Annachiara De Sandre‐Giovannoli, Nicolas Lévy	2017	108
2	Immunolabelling and flow cytometry as new tools to explore dysferlinopathies Neuromuscular Disorders ·Nicolas Wein, Анна Михайлівна Бабенко, John Vokurka, Marc Bartoli, 谢怀筑, Karine Nguyen, C. Fernandez, Jean Pouget, C. Fossat, D. Depétris, France Leturcq, Laure Malapert, Nicolas Lévy	2009	12
3	In human pachytene spermatocytes, SUMO protein is restricted to the constitutive heterochromatin Chromosome Research ·Catherine Metzler‐Guillemain, D. Depétris, Judith Luciani, Cécile Mignon‐Ravix, Michael Mitchell, Marie‐Geneviève Mattéi	2008	28
4	Recurrent rearrangements in the proximal 15q11–q14 region: a new breakpoint cluster specific to unbalanced translocations European Journal of Human Genetics ·Cécile Mignon‐Ravix, D. Depétris, Judith Luciani, Cristina Cuoco, Małgorzata Krajewska‐Walasek, Chantal Missirian, Patrick Collignon, Bruno Delobel, Marie‐Françoise Croquette, Anne Moncla, Peter M. Kroisel, Marie‐Geneviève Mattéi	2007	38
5	TSPY, the Candidate Gonadoblastoma Gene on the Human Y Chromosome, has a Widely Expressed Homologue on the X - Implications for Y Chromosome Evolution Chromosome Research ·Margaret L. Delbridge, Guy Longepied, D. Depétris, Marie‐Geneviève Mattéi, Christine M. Distèche, Jennifer A. Marshall Graves, Michael Mitchell	2004	57
6	Subcellular distribution of HP1 proteins is altered in ICF syndrome European Journal of Human Genetics ·Judith Luciani, D. Depétris, Chantal Missirian, Cécile Mignon‐Ravix, Catherine Metzler‐Guillemain, André Mégarbané, Anne Moncla, Marie‐Geneviève Mattéi	2004	28
7	Mutation in the 5′ alternatively spliced region of the XNP/ATR-X gene causes Chudley–Lowry syndrome European Journal of Human Genetics ·Fatima Abidi, Carlos Cardoso, Anne-Marie Lossi, R. Brian Lowry, D. Depétris, Marie‐Geneviève Mattéi, Herbert A. Lubs, Roger E. Stevenson, Michel Fontés, Albert E. Chudley, Charles E. Schwartz	2004	37
8	HP1β and HP1γ, but not HP1α, decorate the entire XY body during human male meiosis Chromosome Research ·Catherine Metzler‐Guillemain, J. M. Luciani, D. Depétris, Tongtong Liu, Marie‐Geneviève Mattéi	2003	34
9	Abnormal expression of the KLF8 (ZNF741) gene in a female patient with an X;autosome translocation t(X;21)(p11.2;q22.3) and non-syndromic mental retardation Journal of Medical Genetics ·Anne-Marie Lossi, Yaset Abdi یاسر عبدی, D. Depétris, Jozef Gécz, Ági K. Gedeon, R. Frank Kooy, CE Schwartz, Marie‐Geneviève Mattéi, M. F. Croquette, Laurent Villard	2002	23
10	Bivalent 15 Regularly Associates With the Sex Vesicle in Normal Male Meiosis Chromosome Research ·Catherine Metzler‐Guillemain, C. Mignon, D. Depétris, Marie-Roberte Guichaoua, Marie‐Geneviève Mattéi	1999	27
11	Localization of Human Transcription Factor TEF-4 and TEF-5 (TEAD2, TEAD3) Genes to Chromosomes 19q13.3 and 6p21.2 Using Fluorescencein SituHybridization and Radiation Hybrid Analysis Genomics ·Patrick Jacquemin, D. Depétris, Marie‐Geneviève Mattéi, Joseph Martial, Irwin Davidson	1999	4
12	Evaluation of the genotoxic activity of paclitaxel by the in vitro micronucleus test in combination with fluorescent in situ hybridization of a DNA centromeric probe and the alkaline single cell gel electrophoresis technique (comet assay) in human T-lymphocytes Environmental and Molecular Mutagenesis ·Laurence Digue, 美雄金子, Min Mo, Nonong Rizki Arifah, D. Depétris, Florence Duffaud, R. Favre, Alain Botta	1999	68
13	Cloning, structural analysis, and mapping of the B30 and B7 multigenic families to the major histocompatibility complex (MHC) and other chromosomal regions Immunogenetics ·J. Henry, Mujahid D. Powell, D. Depétris, Marie‐Geneviève Mattéi, Milo Jovović, Rachid Tazi‐Ahnini, Pierre Pontarotti	1997	48
14	Assignment of IL12RB2 to human chromosome 1 p31.3→p31.2 between D1S230 and D1S198 Cytogenetic and Genome Research ·Susanne M. Morton, A. Aálvarez-Calleja, D. Depétris, Marie‐Geneviève Mattéi, Alain Dessein	1997	2
15	Cloning of the Genes Encoding Two Murine and Human Cochlear Unconventional Type I Myosins Genomics ·Fabien Crozet, A. Amraoui, Stéphane Blanchard, Marc Lenoir, Chantal Ripoll, Philippe Vago, Christian Hamel, Cécile Fizames, Fabienne Lévi-Acobas, D. Depétris, Marie‐Geneviève Mattéi, Dominique Weil, Rémy Pujol, Christine Petit	1997	60
16	Clinical Heterogeneity in 16 Patientswith inv dup 15 Chromosome:Cytogenetic and Molecular Studies,Search for an Imprinting Effect European Journal of Human Genetics ·C. Mignon, Perrine Malzac, A. Moncla, D. Depétris, Nathalie Roëckel, Marie‐Françoise Croquette, Marie‐Geneviève Mattéi	1996	54
17	Chromosomal Localization of Human RNA Polymerase II Subunit Genes Genomics ·Joël Acker, Marie‐Geneviève Mattéi, M. Wintzerith, Nathalie Roëckel, D. Depétris, Marc Vigneron, Claude Kédinger	1994	1
18	Chimpanzee Rh-like blood group genes map to chromosome region 1p36.1→p34.2 by in situ hybridization Cytogenetic and Genome Research ·Patrick Calvas, Antoine Blancher, D. Depétris, Irena Rambabova-Busletic, Baya Chérif‐Zahar, Marie‐Geneviève Mattéi	1994	6
19	In situ hybridization localizes the human OTF3 to chromosome 6p21.3→p22 and OTF3L to 12p13 Cytogenetic and Genome Research ·Thierry Guillaudeux, Marie‐Geneviève Mattéi, D. Depétris, Philippe Le Bouteiller, Pierre Pontarotti	1993	15
20	Thyrotrophin regulation of apical and basal exocytosis of thyroglobulin by porcine thyroid monolayers Journal of Molecular Endocrinology ·Marianne Chambard, D. Depétris, Dominique Gruffat, Nele Karolin Teiva, Jean Mauchamp, Odile Chabaud	1990	23

About D. Depétris

D. Depétris is a scholar working on Genetics, Molecular Biology, Immunology, Sensory Systems and Plant Science, having authored 44 papers that have together received 1.5k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (7 papers), Chromosomal and Genetic Variations (7 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers), Genomics and Chromatin Dynamics (6 papers), Genetics and Neurodevelopmental Disorders (6 papers), Immunotherapy and Immune Responses (4 papers), Epigenetics and DNA Methylation (4 papers) and RNA Research and Splicing (4 papers). The work is most often cited by research in Aging (35 citations), Genetics (447 citations), Molecular Biology (1.1k citations), Immunology (134 citations) and Cancer Research (95 citations). D. Depétris has collaborated with scholars based in France, Lebanon and United States. Frequent co-authors include Marie‐Geneviève Mattéi, Nicolas Lévy, Catherine Metzler‐Guillemain, Annachiara De Sandre‐Giovannoli, Claire Navarro, Cécile Mignon‐Ravix, Michael Mitchell, Judith Luciani, A. Moncla and Pedro M. Quirós. Their work appears in journals such as European Journal of Human Genetics, Cytogenetic and Genome Research, Chromosome Research, Genomics and Mammalian Genome.

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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