Thomas Melot

5.3k total citations · 2 hit papers
28 papers, 4.2k citations indexed

About

Thomas Melot is a scholar working on Pathology and Forensic Medicine, Pulmonary and Respiratory Medicine and Molecular Biology. According to data from OpenAlex, Thomas Melot has authored 28 papers receiving a total of 4.2k indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Pathology and Forensic Medicine, 11 papers in Pulmonary and Respiratory Medicine and 9 papers in Molecular Biology. Recurrent topics in Thomas Melot's work include Sarcoma Diagnosis and Treatment (11 papers), Genetic factors in colorectal cancer (8 papers) and Neurofibromatosis and Schwannoma Cases (7 papers). Thomas Melot is often cited by papers focused on Sarcoma Diagnosis and Treatment (11 papers), Genetic factors in colorectal cancer (8 papers) and Neurofibromatosis and Schwannoma Cases (7 papers). Thomas Melot collaborates with scholars based in France, United States and Austria. Thomas Melot's co-authors include Olivier Delattre, Gilles Thomas, Jessica Zucman‐Rossi, Alain Aurias, Chantal Desmaze, Martine Peter, Béatrice Plougastel-Douglas, Guy A. Rouleau, Pieter de Jong and Claude Turc‐Carel and has published in prestigious journals such as Nature, New England Journal of Medicine and The Lancet.

In The Last Decade

Thomas Melot

27 papers receiving 4.1k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Gene fusion with an ETS DNA-binding domain caused by chromosome translocation in human tumours

1992 1.4k citations Olivier Delattre, Jessica Zucman‐Rossi et al. Nature profile →
The Ewing Family of Tumors -- A Subgroup of Small-Round-Cell Tumors Defined by Specific Chimeric Transcripts

1994 816 citations Olivier Delattre, Jessica Zucman‐Rossi et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Thomas Melot France	16	2.6k	1.6k	1.3k	1.2k	692	28	4.2k
Frédéric Chibon France	39	2.6k 1.0×	1.2k 0.7×	1.5k 1.2×	873 0.7×	667 1.0×	117	4.3k
Franck Tirode France	33	2.1k 0.8×	2.5k 1.5×	1.3k 1.0×	700 0.6×	408 0.6×	112	4.6k
Maija Tarkkanen Finland	28	1.5k 0.6×	1.3k 0.8×	889 0.7×	608 0.5×	249 0.4×	75	3.1k
Stefania Benini Italy	32	1.7k 0.6×	1.4k 0.8×	864 0.7×	415 0.3×	273 0.4×	89	3.1k
Sadafumi Tamiya Japan	36	1.9k 0.7×	1.2k 0.7×	1.2k 0.9×	825 0.7×	219 0.3×	143	3.6k
Jörn Treuner Germany	23	2.0k 0.8×	555 0.3×	831 0.7×	610 0.5×	414 0.6×	44	2.7k
Bodil Bjerkehagen Norway	36	2.2k 0.9×	770 0.5×	846 0.7×	514 0.4×	265 0.4×	117	3.3k
Roberto Tirabosco United Kingdom	35	3.4k 1.3×	1.2k 0.7×	1.0k 0.8×	716 0.6×	326 0.5×	90	5.3k
Henryk A. Domanski Sweden	35	2.4k 0.9×	481 0.3×	1.2k 0.9×	790 0.7×	378 0.5×	123	3.5k
Wei‐Lien Wang United States	40	3.7k 1.4×	1.1k 0.7×	2.1k 1.7×	1.1k 1.0×	626 0.9×	210	6.4k

Countries citing papers authored by Thomas Melot

Since Specialization

Citations

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

Fields of papers citing papers by Thomas Melot

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Thomas Melot

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

All Works

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20 of 20 papers shown

Melot, Thomas, Luce Dauphinot, Nicolas Sévenet, François Radvanyi, & Olivier Delattre. (2001). Characterization of a new brain‐specific isoform of the EWS oncoprotein. European Journal of Biochemistry. 268(12). 3483–3489. 18 indexed citations

Kovar, Heinrich, Dragana Jugović, Thomas Melot, et al.. (1999). Cryptic Exons as a Source of Increased Diversity of Ewing Tumor-Associated EWS–FLI1 Chimeric Products. Genomics. 60(3). 371–374. 10 indexed citations

Bertolotti, Anne, Thomas Melot, Joël Acker, et al.. (1998). EWS, but Not EWS-FLI-1, Is Associated with Both TFIID and RNA Polymerase II: Interactions between Two Members of the TET Family, EWS and hTAF _II 68, and Subunits of TFIID and RNA Polymerase II Complexes. Molecular and Cellular Biology. 18(3). 1489–1497. 219 indexed citations

Melot, Thomas, et al.. (1997). Production and Characterization of Mouse Monoclonal Antibodies to Wild-Type and Oncogenic FLI-1 Proteins. Hybridoma. 16(5). 457–464. 21 indexed citations

Desmaze, Chantal, Françoise Brizard, Claude Turc‐Carel, et al.. (1997). Multiple chromosomal mechanisms generate an EWS/FLI1 or an EWS/ERG fusion gene in Ewing tumors. Cancer Genetics and Cytogenetics. 97(1). 12–19. 57 indexed citations

Olschwang, Sylviane, Pierre Laurent‐Puig, Thomas Melot, Bénédicte Thuille, & Gilles Thomas. (1995). High resolution genetic map of the adenomatous polyposis coli gene (APC) region. American Journal of Medical Genetics. 56(4). 413–419. 12 indexed citations

Anglard, Patrick, Thomas Melot, Éric Guérin, Gilles Thomas, & Paul Basset. (1995). Structure and Promoter Characterization of the Human Stromelysin-3 Gene. Journal of Biological Chemistry. 270(35). 20337–20344. 56 indexed citations

Desmaze, Chantal, Jessica Zucman‐Rossi, Olivier Delattre, et al.. (1994). Precise localization on chromosome 12 of the ATF-1 gene by fluorescence in situ hybridization. Human Genetics. 93(2). 207–8. 4 indexed citations

Thomas, Gilles, Olivier Delattre, Jessica Zucman‐Rossi, et al.. (1994). Genetic Alterations in the Chromosome 22q12 Region Associated with Development of Neuroectodermal Tumors. Cold Spring Harbor Symposia on Quantitative Biology. 59(0). 555–564. 1 indexed citations

10.

Desmaze, Chantal, Jessica Zucman‐Rossi, Olivier Delattre, et al.. (1994). Interphase molecular cytogenetics of Ewing's sarcoma and peripheral neuroepithelioma t(11;22) with flanking and overlapping cosmid probes. Cancer Genetics and Cytogenetics. 74(1). 13–18. 57 indexed citations

11.

Kurahashi, Hiroki, Ikuo Yana, Thomas Melot, et al.. (1994). Refined mapping of eight cosmid markers on human chromosome 22. The Japanese Journal of Human Genetics. 39(2). 243–248. 2 indexed citations

12.

Hamelin, Richard C., et al.. (1994). p53 mutations in human tumors with chimeric EWS/FLI/1 genes. International Journal of Cancer. 57(3). 336–340. 37 indexed citations

13.

Thomas, Gilles, Marc Sanson, Khê Hoang‐Xuan, et al.. (1994). Neurofibromatosis type 2. European Journal of Cancer. 30(13). 1981–1987. 14 indexed citations

14.

Bijlsma, Emilia K., Olivier Delattre, J. Juyn, et al.. (1993). Regional fine mapping of the β crystallin genes on chromosome 22 excludes these genes as physically linked markers for neurofibromatosis type 2. Genes Chromosomes and Cancer. 8(2). 112–118. 8 indexed citations

15.

Delattre, Olivier, Jessica Zucman‐Rossi, Béatrice Plougastel-Douglas, et al.. (1992). Gene fusion with an ETS DNA-binding domain caused by chromosome translocation in human tumours. Nature. 359(6391). 162–165. 1443 indexed citations breakdown →

16.

Zucman‐Rossi, Jessica, Olivier Delattre, Chantal Desmaze, et al.. (1992). Cloning and characterization of the Ewing's sarcoma and peripheral neuroepithelioma t(11;22) translocation breakpoints. Genes Chromosomes and Cancer. 5(4). 271–277. 238 indexed citations

17.

Delattre, Olivier, Jessica Zucman‐Rossi, Béatrice Plougastel-Douglas, et al.. (1992). Cloning of the (11;22) translocation breakpoints of Ewing's sarcoma & peripheral neuroepithelioma. Cancer Genetics and Cytogenetics. 63(2). 162–162. 1 indexed citations

18.

Olschwang, Sylviane, Barbara Weiffenbach, Pierre Laurent‐Puig, et al.. (1991). Genetic characterization of the APC locus involved in familial adenomatous polyposis. Gastroenterology. 101(1). 154–160. 12 indexed citations

19.

Laurent‐Puig, Pierre, Sylviane Olschwang, Olivier Delattre, et al.. (1991). Association of ki‐ras mutation with differentiation and tumor‐formation pathways in colorectal carcinoma. International Journal of Cancer. 49(2). 220–223. 54 indexed citations

20.

Delattre, Olivier, David Law, Yorghos Remvikos, et al.. (1989). MULTIPLE GENETIC ALTERATIONS IN DISTAL AND PROXIMAL COLORECTAL CANCER. The Lancet. 334(8659). 353–356. 243 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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