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Author Details
Full Name
L??on-Charles Tranchevent
Affiliation
University of Luxembourg
ORCID
Career Start Year
2006
Papers
40
H Index
25
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36681675
Systems level analysis of sex-dependent gene expression changes in Parkinson's disease.
NPJ Parkinsons Dis
2023
37420093
A multi-omics integrative approach unravels novel genes and pathways associated with senescence escape after targeted therapy in NRAS mutant melanoma.
Cancer Gene Ther
2023
34805149
iPSC-Derived Microglia as a Model to Study Inflammation in Idiopathic Parkinson's Disease.
Front Cell Dev Biol
2021
30962178
Interplay between coding and exonic splicing regulatory sequences.
Genome Res
2019
31856829
A deep neural network approach to predicting clinical outcomes of neuroblastoma patients.
BMC Med Genomics
2019
29632713
CD47 is a direct target of SNAI1 and ZEB1 and its blockade activates the phagocytosis of breast cancer cells undergoing EMT.
Oncoimmunology
2018
29880025
Predicting clinical outcome of neuroblastoma patients using an integrative network-based approach.
Biol Direct
2018
28420690
Identification of protein features encoded by alternative exons using Exon Ontology.
Genome Res
2017
27131783
Candidate gene prioritization with Endeavour.
Nucleic Acids Res
2016
26384564
Beegle: from literature mining to disease-gene discovery.
Nucleic Acids Res
2016
27604469
An expanded evaluation of protein function prediction methods shows an improvement in accuracy.
Genome Biol
2016
24275493
The Ddx5 and Ddx17 RNA helicases are cornerstones in the complex regulatory array of steroid hormone-signaling pathways.
Nucleic Acids Res
2014
24910439
RNA helicases DDX5 and DDX17 dynamically orchestrate transcription, miRNA, and splicing programs in cell differentiation.
Cell Rep
2014
24307554
Endothelial, epithelial, and fibroblast cells exhibit specific splicing programs independently of their tissue of origin.
Genome Res
2014
24076761
eXtasy: variant prioritization by genomic data fusion.
Nat Methods
2013
22067610
BMPR1A is a candidate gene for congenital heart defects associated with the recurrent 10q22q23 deletion syndrome.
Eur J Med Genet
2012
22962483
ReLiance: a machine learning and literature-based prioritization of receptor--ligand pairings.
Bioinformatics
2012
23013645
Annotate-it: a Swiss-knife approach to annotation, analysis and interpretation of single nucleotide variation in human disease.
Genome Med
2012
23047555
An unbiased evaluation of gene prioritization tools.
Bioinformatics
2012
22751426
Computational tools for prioritizing candidate genes: boosting disease gene discovery.
Nat Rev Genet
2012
22442124
Optimized data fusion for kernel k-means clustering.
IEEE Trans Pattern Anal Mach Intell
2012
22318985
Congenital heart defects in a novel recurrent 22q11.2 deletion harboring the genes CRKL and MAPK1.
Am J Med Genet A
2012
20980271
Optimized data fusion for K-means Laplacian clustering.
Bioinformatics
2011
21921585
Challenges of interpreting copy number variation in syndromic and non-syndromic congenital heart defects.
Cytogenet Genome Res
2011
21602267
PINTA: a web server for network-based gene prioritization from expression data.
Nucleic Acids Res
2011
21278374
A guide to web tools to prioritize candidate genes.
Brief Bioinform
2011
20074336
Gene prioritization and clustering by multi-view text mining.
BMC Bioinformatics
2010
20493459
Haploinsufficiency of TAB2 causes congenital heart defects in humans.
Am J Hum Genet
2010
20538729
Large-scale benchmark of Endeavour using MetaCore maps.
Bioinformatics
2010
20529363
L2-norm multiple kernel learning and its application to biomedical data fusion.
BMC Bioinformatics
2010
20193066
Collaboratively charting the gene-to-phenotype network of human congenital heart defects.
Genome Med
2010
20346121
Detection of novel 3' untranslated region extensions with 3' expression microarrays.
BMC Genomics
2010
19165344
Integrating computational biology and forward genetics in Drosophila.
PLoS Genet
2009
19436755
Network analysis of differential expression for the identification of disease-causing genes.
PLoS One
2009
18365009
Using ribosomal protein genes as reference: a tale of caution.
PLoS One
2008
18508807
ENDEAVOUR update: a web resource for gene prioritization in multiple species.
Nucleic Acids Res
2008
18689812
Comparison of vocabularies, representations and ranking algorithms for gene prioritization by text mining.
Bioinformatics
2008
17646288
Kernel-based data fusion for gene prioritization.
Bioinformatics
2007
16680138
Gene prioritization through genomic data fusion.
Nat Biotechnol
2006
17092029
Physical-chemistry-based analysis of affymetrix microarray data.
J Phys Chem B
2006
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