Léon-Charles Tranchevent

4.9k total citations · 1 hit paper
44 papers, 3.1k citations indexed

About

Léon-Charles Tranchevent is a scholar working on Molecular Biology, Genetics and Neurology. According to data from OpenAlex, Léon-Charles Tranchevent has authored 44 papers receiving a total of 3.1k indexed citations (citations by other indexed papers that have themselves been cited), including 37 papers in Molecular Biology, 12 papers in Genetics and 4 papers in Neurology. Recurrent topics in Léon-Charles Tranchevent's work include Bioinformatics and Genomic Networks (18 papers), Gene expression and cancer classification (13 papers) and Genomic variations and chromosomal abnormalities (7 papers). Léon-Charles Tranchevent is often cited by papers focused on Bioinformatics and Genomic Networks (18 papers), Gene expression and cancer classification (13 papers) and Genomic variations and chromosomal abnormalities (7 papers). Léon-Charles Tranchevent collaborates with scholars based in Belgium, France and United Kingdom. Léon-Charles Tranchevent's co-authors include Yves Moreau, Bart De Moor, Peter Van Loo, Stein Aerts, Bert Coessens, Shi Yu, Bassem A. Hassan, Frederik De Smet, Sunit Maity and Peter Carmeliet and has published in prestigious journals such as Nucleic Acids Research, Nature Biotechnology and Bioinformatics.

In The Last Decade

Léon-Charles Tranchevent

43 papers receiving 3.0k 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 prioritization through genomic data fusion

2006 661 citations Stein Aerts, Peter Van Loo et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Léon-Charles Tranchevent Belgium	27	2.4k	750	299	278	187	44	3.1k
Jun Sese Japan	27	1.9k 0.8×	334 0.4×	226 0.8×	518 1.9×	280 1.5×	82	3.6k
Jianhua Xuan United States	22	1.4k 0.6×	176 0.2×	303 1.0×	219 0.8×	175 0.9×	126	2.2k
Marc Fiume Canada	9	1.5k 0.6×	410 0.5×	426 1.4×	303 1.1×	82 0.4×	11	2.2k
Semyon Kruglyak United States	13	2.0k 0.8×	1.1k 1.4×	452 1.5×	233 0.8×	80 0.4×	20	3.1k
Barbara E. Engelhardt United States	26	3.1k 1.3×	1.8k 2.4×	622 2.1×	424 1.5×	101 0.5×	79	5.1k
Christof Angermueller United Kingdom	9	2.0k 0.9×	288 0.4×	406 1.4×	245 0.9×	77 0.4×	9	2.7k
Xianghong Jasmine Zhou United States	35	3.7k 1.6×	424 0.6×	1.1k 3.7×	230 0.8×	104 0.6×	88	4.7k
Leo J. Lee Canada	11	4.3k 1.8×	443 0.6×	830 2.8×	201 0.7×	59 0.3×	16	5.1k
Duygu Ucar United States	25	1.9k 0.8×	352 0.5×	219 0.7×	134 0.5×	60 0.3×	55	3.1k
Fereydoun Hormozdiari United States	23	2.2k 0.9×	1.4k 1.9×	468 1.6×	205 0.7×	57 0.3×	42	3.1k

Countries citing papers authored by Léon-Charles Tranchevent

Since Specialization

Citations

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

Fields of papers citing papers by Léon-Charles Tranchevent

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Léon-Charles Tranchevent. 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 Léon-Charles Tranchevent. The network helps show where Léon-Charles Tranchevent may publish in the future.

Co-authorship network of co-authors of Léon-Charles Tranchevent

This figure shows the co-authorship network connecting the top 25 collaborators of Léon-Charles Tranchevent. A scholar is included among the top collaborators of Léon-Charles Tranchevent 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 Léon-Charles Tranchevent. Léon-Charles Tranchevent 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

Tranchevent, Léon-Charles, Francisco Azuaje, & Jagath C. Rajapakse. (2019). A deep neural network approach to predicting clinical outcomes of neuroblastoma patients. BMC Medical Genomics. 12(S8). 178–178. 20 indexed citations

Tranchevent, Léon-Charles, Petr V. Nazarov, Tony Kaoma, et al.. (2018). Predicting clinical outcome of neuroblastoma patients using an integrative network-based approach. Biology Direct. 13(1). 12–12. 13 indexed citations

Tranchevent, Léon-Charles, Fabien Aubé, Clara Benoit‐Pilven, et al.. (2017). Identification of protein features encoded by alternative exons using Exon Ontology. Genome Research. 27(6). 1087–1097. 44 indexed citations

Tranchevent, Léon-Charles, Amin Ardeshirdavani, Sarah ElShal, et al.. (2016). Candidate gene prioritization with Endeavour. Nucleic Acids Research. 44(W1). W117–W121. 72 indexed citations

ElShal, Sarah, Léon-Charles Tranchevent, Alejandro Sifrim, et al.. (2015). Beegle:from literature mining to disease-gene discovery. Nucleic Acids Research. 44(2). e18–e18. 47 indexed citations

Dardenne, Étienne, Micaela Polay Espinoza, Laurent Fattet, et al.. (2014). RNA Helicases DDX5 and DDX17 Dynamically Orchestrate Transcription, miRNA, and Splicing Programs in Cell Differentiation. Cell Reports. 7(6). 1900–1913. 156 indexed citations

Breckpot, Jeroen, Bernard Thienpont, Marijke Bauters, et al.. (2013). Congenital heart defects in a novel recurrent 22q11.2 deletion harboring the genes CRKL and MAPK1. 24(1). 126–127.

Sifrim, Alejandro, Dušan Popović, Léon-Charles Tranchevent, et al.. (2013). eXtasy: variant prioritization by genomic data fusion. Nature Methods. 10(11). 1083–1084. 125 indexed citations

Villemin, Jean-Philippe, Hussein Mortada, Micaela Polay Espinoza, et al.. (2013). Endothelial, epithelial, and fibroblast cells exhibit specific splicing programs independently of their tissue of origin. Genome Research. 24(3). 511–521. 52 indexed citations

10.

Tranchevent, Léon-Charles, et al.. (2012). Visualizing high dimensional datasets using parallel coordinaties : application to gene prioritization. International Conference on Bioinformatics. 52–57. 1 indexed citations

11.

Moreau, Yves & Léon-Charles Tranchevent. (2012). Computational tools for prioritizing candidate genes: boosting disease gene discovery. Nature Reviews Genetics. 13(8). 523–536. 309 indexed citations

12.

Breckpot, Jeroen, Bernard Thienpont, Marijke Bauters, et al.. (2012). Congenital heart defects in a novel recurrent 22q11.2 deletion harboring the genes CRKL and MAPK1. American Journal of Medical Genetics Part A. 158A(3). 574–580. 32 indexed citations

13.

Sifrim, Alejandro, Léon-Charles Tranchevent, Beata Nowakowska, et al.. (2012). Annotate-it: a Swiss-knife approach to annotation, analysis and interpretation of single nucleotide variation in human disease. Genome Medicine. 4(9). 73–73. 26 indexed citations

14.

Breckpot, Jeroen, Léon-Charles Tranchevent, Bernard Thienpont, et al.. (2011). BMPR1A is a candidate gene for congenital heart defects associated with the recurrent 10q22q23 deletion syndrome. European Journal of Medical Genetics. 55(1). 12–16. 22 indexed citations

15.

Thorrez, Lieven, et al.. (2010). Detection of novel 3' untranslated region extensions with 3' expression microarrays. BMC Genomics. 11(1). 205–205. 11 indexed citations

16.

Tranchevent, Léon-Charles, et al.. (2010). A guide to web tools to prioritize candidate genes. Briefings in Bioinformatics. 12(1). 22–32. 150 indexed citations

17.

Yu, Shi, Tillmann Falck, Anneleen Daemen, et al.. (2010). L2-norm multiple kernel learning and its application to biomedical data fusion. BMC Bioinformatics. 11(1). 309–309. 90 indexed citations

18.

Thienpont, Bernard, Litu Zhang, Alex V. Postma, et al.. (2010). Haploinsufficiency of TAB2 Causes Congenital Heart Defects in Humans. The American Journal of Human Genetics. 86(6). 839–849. 72 indexed citations

19.

Aerts, Stein, Sven Vilain, Shu Hu, et al.. (2009). Integrating Computational Biology and Forward Genetics in Drosophila. PLoS Genetics. 5(1). e1000351–e1000351. 22 indexed citations

20.

Thorrez, Lieven, Katrijn Van Deun, Léon-Charles Tranchevent, et al.. (2008). Using Ribosomal Protein Genes as Reference: A Tale of Caution. PLoS ONE. 3(3). e1854–e1854. 165 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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