Laëtitia Gressin

1.4k total citations
11 papers, 675 citations indexed

About

Laëtitia Gressin is a scholar working on Molecular Biology, Cell Biology and Genetics. According to data from OpenAlex, Laëtitia Gressin has authored 11 papers receiving a total of 675 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 3 papers in Cell Biology and 3 papers in Genetics. Recurrent topics in Laëtitia Gressin's work include RNA modifications and cancer (3 papers), Skin and Cellular Biology Research (2 papers) and Chromosomal and Genetic Variations (2 papers). Laëtitia Gressin is often cited by papers focused on RNA modifications and cancer (3 papers), Skin and Cellular Biology Research (2 papers) and Chromosomal and Genetic Variations (2 papers). Laëtitia Gressin collaborates with scholars based in France, Australia and Latvia. Laëtitia Gressin's co-authors include M Mauchauffé, Thomas Mercher, Olivier Bernard, Richard Monni, Roland Berger, Daniel Birnbaum, Claude Preudhomme, Valérie Soenen, Max Chaffanet and Thierry Leblanc and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Oncogene and Scientific Reports.

In The Last Decade

Laëtitia Gressin

11 papers receiving 668 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Laëtitia Gressin France 8 438 224 135 87 79 11 675
Vijay P.S. Rawat Germany 14 614 1.4× 334 1.5× 83 0.6× 74 0.9× 78 1.0× 29 811
IR Kirsch United States 9 304 0.7× 212 0.9× 162 1.2× 123 1.4× 43 0.5× 17 603
Elizabeth J. Heller United States 6 541 1.2× 147 0.7× 222 1.6× 90 1.0× 83 1.1× 6 856
Paul Sinclair United Kingdom 16 306 0.7× 474 2.1× 218 1.6× 57 0.7× 137 1.7× 24 827
MC Heinrich United States 7 452 1.0× 133 0.6× 52 0.4× 105 1.2× 97 1.2× 8 648
Christopher Slape United States 15 691 1.6× 513 2.3× 92 0.7× 104 1.2× 64 0.8× 29 970
Emily Whisenant United States 7 734 1.7× 719 3.2× 159 1.2× 75 0.9× 66 0.8× 11 990
Hélia Neves Portugal 11 499 1.1× 111 0.5× 36 0.3× 90 1.0× 86 1.1× 23 729
Todd Ashworth United States 12 622 1.4× 175 0.8× 117 0.9× 134 1.5× 52 0.7× 13 851
Denise Gibbs United States 7 1.1k 2.4× 382 1.7× 84 0.6× 213 2.4× 116 1.5× 9 1.4k

Countries citing papers authored by Laëtitia Gressin

Since Specialization
Citations

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

Fields of papers citing papers by Laëtitia Gressin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Laëtitia Gressin

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

All Works

11 of 11 papers shown
1.
Bouyacoub, Yosra, Antoine Daunay, Mourad Sahbatou, et al.. (2022). A high-throughput real-time PCR tissue-of-origin test to distinguish blood from lymphoblastoid cell line DNA for (epi)genomic studies. Scientific Reports. 12(1). 4684–4684. 3 indexed citations
2.
Mourra, Najat, Guy Zeitoun, G. Portier, et al.. (2008). High-resolution Genotyping of Chromosome 8 in Colon Adenocarcinomas Reveals Recurrent Break Point But No Gene Mutation in the 8p21 Region. Diagnostic Molecular Pathology. 17(2). 90–93. 5 indexed citations
3.
Bernard, Olivier, Paola Ballerini, M Mauchauffé, et al.. (2001). A new recurrent and specific cryptic translocation, t(5;14)(q35;q32), is associated with expression of the Hox11L2 gene in T acute lymphoblastic leukemia. Leukemia. 15(10). 1495–1504. 174 indexed citations
4.
Yakıcıer, M. Cengiz, Patricia Legoix, Christelle Vaury, et al.. (2001). Identification of homozygous deletions at chromosome 16q23 in Aflatoxin B1 exposed hepatocellular carcinoma. Oncogene. 20(37). 5232–5238. 45 indexed citations
5.
Parseval, Nathalie de, Jean-François Casella, Laëtitia Gressin, & Thiérry Heidmann. (2001). Characterization of the Three HERV-H Proviruses with an Open Envelope Reading Frame Encompassing the Immunosuppressive Domain and Evolutionary History in Primates. Virology. 279(2). 558–569. 62 indexed citations
6.
Bardet, Valérie, Nathalie Couque, Laurence Cattolico, et al.. (2001). Molecular analysis of nonrandom 8q12 deletions in acute lymphoblastic leukemia: Identification of two candidate genes. Genes Chromosomes and Cancer. 33(2). 178–187. 7 indexed citations
7.
Mercher, Thomas, Maryvonne Busson‐Le Coniat, Richard Monni, et al.. (2001). Involvement of a human gene related to the Drosophila spen gene in the recurrent t(1;22) translocation of acute megakaryocytic leukemia. Proceedings of the National Academy of Sciences. 98(10). 5776–5779. 172 indexed citations
8.
Chaffanet, Max, et al.. (2000). MOZ is fused top300 in an acute monocytic leukemia with t(8;22). Genes Chromosomes and Cancer. 28(2). 138–144. 140 indexed citations
9.
Cavalier, L, Rim Amouri, Samir Belal, et al.. (2000). Giant axonal neuropathy locus refinement to a < 590 kb critical interval. European Journal of Human Genetics. 8(7). 527–534. 18 indexed citations
10.
Thoreau, Vincent, Thierry Bergès, Isabelle Callebaut, et al.. (1999). Molecular Cloning, Expression Analysis, and Chromosomal Localization of Human Syntaxin 8 (STX8). Biochemical and Biophysical Research Communications. 257(2). 577–583. 21 indexed citations
11.
Charbonnier, Frédéric, J.-P. Périn, Marie‐Geneviève Mattéi, et al.. (1998). Genomic Organization of the Human SPOCK Gene and Its Chromosomal Localization to 5q31. Genomics. 48(3). 377–380. 28 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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