D. Perucca‐Lostanlen

402 total citations
12 papers, 330 citations indexed

About

D. Perucca‐Lostanlen is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, D. Perucca‐Lostanlen has authored 12 papers receiving a total of 330 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 4 papers in Genetics and 3 papers in Oncology. Recurrent topics in D. Perucca‐Lostanlen's work include Genomic variations and chromosomal abnormalities (4 papers), RNA modifications and cancer (3 papers) and Genomics and Chromatin Dynamics (3 papers). D. Perucca‐Lostanlen is often cited by papers focused on Genomic variations and chromosomal abnormalities (4 papers), RNA modifications and cancer (3 papers) and Genomics and Chromatin Dynamics (3 papers). D. Perucca‐Lostanlen collaborates with scholars based in France, United States and United Kingdom. D. Perucca‐Lostanlen's co-authors include Patrick Gaudray, A Franchi, J. Pouysségur, Josiane Grosgeorge, Pierre Szepetowski, Daniel Birnbaum, Charles Theillet, M.-J. Pébusque, François‐Xavier Caroli‐Bosc and Soumeya Bekri and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Biochemical and Biophysical Research Communications and Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease.

In The Last Decade

D. Perucca‐Lostanlen

12 papers receiving 325 citations

Peers

Countries citing papers authored by D. Perucca‐Lostanlen

Since Specialization

Citations

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

Fields of papers citing papers by D. Perucca‐Lostanlen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of D. Perucca‐Lostanlen

This figure shows the co-authorship network connecting the top 25 collaborators of D. Perucca‐Lostanlen. A scholar is included among the top collaborators of D. Perucca‐Lostanlen 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 D. Perucca‐Lostanlen. D. Perucca‐Lostanlen is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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12 of 12 papers shown

#	Work	Indexed citations
1	Distinct MDM2 and P14ARF expression and centrosome amplification in well‐differentiated liposarcomas 2003 ·Genes Chromosomes and Cancer ·D. Perucca‐Lostanlen, Philippe Rostagno, Josiane Grosgeorge, S. Marcié, Patrick Gaudray, Claude Turc‐Carel	9
2	Molecular and functional effects of the T14709C point mutation in the mitochondrial DNA of a patient with maternally inherited diabetes and deafness 2002 ·Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·D. Perucca‐Lostanlen, Robert W. Taylor, H Narbonne, (unknown), Christine Hayes, (unknown), Véronique Paquis‐Flucklinger, Douglass M. Turnbull, B. Vialettes, Claude Desnuelle	20
3	Mitochondrial DNA Variations in Patients with Maternally Inherited Diabetes and Deafness Syndrome 2000 ·Biochemical and Biophysical Research Communications ·D. Perucca‐Lostanlen, H Narbonne, (unknown), Pascal Staccini, (unknown), Véronique Paquis‐Flucklinger, B. Vialettes, Claude Desnuelle	18
4	Mapping FRA11A, a folate-sensitive fragile site in human chromosome band 11q13.3 1997 ·Cytogenetic and Genome Research ·D. Perucca‐Lostanlen, (unknown), Adeline Courseaux, Josiane Grosgeorge, Frederick Hecht, Patrick Gaudray	11
5	Detailed map of a region commonly amplified at 11q13→q14 in human breast carcinoma 1997 ·Cytogenetic and Genome Research ·Soumeya Bekri, José Adélaı̈de, Sandra Merscher, Josiane Grosgeorge, François‐Xavier Caroli‐Bosc, D. Perucca‐Lostanlen, (unknown), M.-J. Pébusque, Charles Theillet, Daniel Birnbaum, Patrick Gaudray	132
6	Framework YAC Contig Anchored into a 3.2-Mb High-Resolution Physical Map in Proximal 11q13 1997 ·Genomics ·(unknown), Pierre Szepetowski, Marie Fernandes, Carine Serizet, Yoshihiko Kawaguchi, Josiane Grosgeorge, D. Perucca‐Lostanlen, Thomas B. Shows, John A. Todd, Norma J. Nowak, Patrick Gaudray	22
7	Description of a 700-kb yeast artificial chromosome contig containing the BCL1 translocation breakpoint region at 11q13 1995 ·Cytogenetic and Genome Research ·Pierre Szepetowski, D. Perucca‐Lostanlen, Josiane Grosgeorge, Denis Le Paslier, Bernard H. Brownstein, Georges F. Carle, Patrick Gaudray	14
8	Mapping Genes According to Their Amplification Status in Tumor Cells: Contribution to the Map of 11ql3 1993 ·Genomics ·Pierre Szepetowski, D. Perucca‐Lostanlen, Patrick Gaudray	26
9	D11S146 and BCL1 are physically linked but can be discriminated by their amplification status in human breast cancer 1991 ·Genomics ·Pierre Szepetowski, Catherine Nguyen, D. Perucca‐Lostanlen, Georges F. Carle, (unknown), Daniel Birnbaum, Charles Theillet, Patrick Gaudray	15
10	Amplification, proto-oncogènes et cancers humains 1991 ·médecine/sciences ·Pierre Szepetowski, D. Perucca‐Lostanlen, Patrick Gaudray	2
11	Functional expression of a human Na+/H+ antiporter gene transfected into antiporter-deficient mouse L cells. 1986 ·Proceedings of the National Academy of Sciences ·A Franchi, D. Perucca‐Lostanlen, J. Pouysségur	58
12	Structure of mouse interferon-beta cDNA clones: sequence rearrangements in a cloned cDNA. 1985 ·PubMed ·(unknown), (unknown), (unknown), D. Perucca‐Lostanlen, Claude L. Gallien, Janine Doly	3

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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