Lionel Coignet

1.4k total citations
42 papers, 1.1k citations indexed

About

Lionel Coignet is a scholar working on Molecular Biology, Genetics and Hematology. According to data from OpenAlex, Lionel Coignet has authored 42 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 12 papers in Genetics and 12 papers in Hematology. Recurrent topics in Lionel Coignet's work include Chronic Lymphocytic Leukemia Research (12 papers), Acute Lymphoblastic Leukemia research (8 papers) and Acute Myeloid Leukemia Research (7 papers). Lionel Coignet is often cited by papers focused on Chronic Lymphocytic Leukemia Research (12 papers), Acute Lymphoblastic Leukemia research (8 papers) and Acute Myeloid Leukemia Research (7 papers). Lionel Coignet collaborates with scholars based in France, United States and United Kingdom. Lionel Coignet's co-authors include Daniel Catovsky, Martin J.S. Dyer, D Jadayel, Tony G. Willis, J. Treleaven, Franck Pellestor, Anne Girardet, B. Andréo, Munah Abdul-Rauf and Hervé Avet‐Loiseau and has published in prestigious journals such as Blood, Cancer Research and Oncogene.

In The Last Decade

Lionel Coignet

42 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Lionel Coignet France 21 530 318 280 262 253 42 1.1k
Sabrina Tosi United Kingdom 20 550 1.0× 578 1.8× 151 0.5× 129 0.5× 180 0.7× 52 1.1k
G.C. Beverstock Netherlands 15 337 0.6× 340 1.1× 131 0.5× 161 0.6× 221 0.9× 20 838
Jack L. Spurbeck United States 17 330 0.6× 342 1.1× 131 0.5× 145 0.6× 244 1.0× 25 1.0k
Lalitha Nagarajan United States 20 690 1.3× 267 0.8× 177 0.6× 143 0.5× 90 0.4× 46 1.0k
A Goodacre United States 14 333 0.6× 438 1.4× 252 0.9× 260 1.0× 329 1.3× 16 845
Mary Callanan France 22 957 1.8× 190 0.6× 431 1.5× 395 1.5× 307 1.2× 67 1.9k
Carin Lassen Sweden 21 642 1.2× 570 1.8× 180 0.6× 101 0.4× 297 1.2× 35 1.3k
Björn Schneider Germany 22 502 0.9× 295 0.9× 242 0.9× 162 0.6× 254 1.0× 63 1.2k
J D Rowley United States 22 761 1.4× 832 2.6× 203 0.7× 207 0.8× 390 1.5× 29 1.6k
Surabhi Kakati United States 18 466 0.9× 442 1.4× 334 1.2× 403 1.5× 273 1.1× 44 1.4k

Countries citing papers authored by Lionel Coignet

Since Specialization
Citations

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

Fields of papers citing papers by Lionel Coignet

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lionel Coignet

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

All Works

20 of 20 papers shown
1.
Pawarode, Attaphol, et al.. (2007). Acute myeloid leukemia developing during imatinib mesylate therapy for chronic myeloid leukemia in the absence of new cytogenetic abnormalities. Leukemia Research. 31(11). 1589–1592. 7 indexed citations
2.
Ghoshal, Pushpankur, Christiane Houde, Timothy R. Johnson, et al.. (2007). SMRT; Not So Smart in Multiple Myeloma.. Blood. 110(11). 4137–4137. 4 indexed citations
3.
Coignet, Lionel, Christiane Houde, Brian N. Bundy, et al.. (2006). The presence of the FRA12E/SMRT fragile site in the genome of prostate cancer patients is a predictor of metastatic development. Clinical Cancer Research. 12. 1 indexed citations
4.
Hasina, Rifat, Lee Martin, Xiaole Qi, et al.. (2005). NOL7 is a nucleolar candidate tumor suppressor gene in cervical cancer that modulates the angiogenic phenotype. Oncogene. 25(4). 588–598. 28 indexed citations
5.
Mikhail, Fady M., et al.. (2003). A novel gene, FGA7, is fused to RUNX1/AML1 in a t(4;21)(q28;q22) in a patient with T‐cell acute lymphoblastic leukemia. Genes Chromosomes and Cancer. 39(2). 110–118. 25 indexed citations
6.
Gazzo, Sophie, Lucile Baseggio, Lionel Coignet, et al.. (2003). Cytogenetic and molecular delineation of a region of chromosome 3q commonly gained in marginal zone B-cell lymphoma.. PubMed. 88(1). 31–8. 25 indexed citations
7.
Mikhail, Fady M., et al.. (2002). A new translocation that rearranges the AML1 gene in a patient with T-cell acute lymphoblastic leukemia. Cancer Genetics and Cytogenetics. 135(1). 96–100. 19 indexed citations
8.
Jiang, Qun, Sylvie Galiègue‐Zouitina, Christophe Roumier, et al.. (2001). Genomic organization and refined mapping of the human nuclear corepressor 2 (NCOR2)/ silencing mediator of retinoid and thyroid hormone receptor (SMRT) gene on chromosome 12q24.3. Cytogenetic and Genome Research. 92(3-4). 217–220. 13 indexed citations
9.
Imbert, Isabelle, Lionel Coignet, & Franck Pellestor. (2001). 6p abnormalities and TNF-α over-expression in retinoblastoma cell line. Cancer Genetics and Cytogenetics. 128(2). 141–147. 7 indexed citations
10.
Matutes, Estella, Lionel Coignet, V Brito-Babapulle, et al.. (1999). FISH analysis for BCL-1 rearrangements and trisomy 12 helps the diagnosis of atypical B cell leukaemias. Leukemia. 13(11). 1721–1726. 34 indexed citations
11.
Gruszka, Alicja, et al.. (1999). The incidence of trisomy 3 in splenic lymphoma with villous lymphocytes: a study by FISH. British Journal of Haematology. 104(3). 600–604. 28 indexed citations
12.
Coignet, Lionel, Carmen Sílvia Passos Lima, Toon Min, et al.. (1999). Myeloid- and lymphoid-specific breakpoint cluster regions in chromosome band 13q14 in acute leukemia. Genes Chromosomes and Cancer. 25(3). 222–229. 25 indexed citations
13.
Coignet, Lionel, et al.. (1998). Molecular characterisation of a new recurrent abnormality of chromosome 12q24 in lymphoid malignancies.. UCL Discovery (University College London). 1 indexed citations
14.
Jadayel, Dalal, Lucy R. Osborne, Lionel Coignet, et al.. (1998). The BCL7 gene family: deletion of BCL7B in Williams syndrome. Gene. 224(1-2). 35–44. 38 indexed citations
15.
Pellestor, Franck, et al.. (1996). Direct detection of disomy in human sperm by the PRINS technique. Human Genetics. 97(1). 21–5. 20 indexed citations
16.
Pellestor, Franck, et al.. (1996). FISH and PRINS, a strategy for rapid chromosome screening: application to the assessment of aneuploidy in human sperm. Cytogenetic and Genome Research. 72(1). 34–36. 27 indexed citations
17.
Coignet, Lionel, et al.. (1996). Double and triple in situ chromosomal labeling of human spermatozoa by PRINS. Cytogenetic and Genome Research. 73(4). 300–303. 14 indexed citations
18.
Pellestor, Franck, et al.. (1996). Assessment of aneuploidy for chromosomes 8, 9, 13, 16, and 21 in human sperm by using primed in situ labeling technique.. PubMed. 58(4). 797–802. 50 indexed citations
19.
Girardet, Anne, et al.. (1995). [Direct analysis of the frequency of disomy in human sperm using the PRINS technique].. PubMed. 38(2). 85–9. 2 indexed citations
20.
Arnoulet, Christine, Régis Costello, Julien Mozziconacci, et al.. (1995). Unbalanced translocation t(5;17) in an atypical acute promyelocytic leukemia. Genes Chromosomes and Cancer. 14(4). 307–312. 22 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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