Yves Moreau
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Why Is Yves Moreau Influential?
(Suggest an Edit or Addition)According to Wikipedia, Yves Moreau is a Professor of Engineering at KU Leuven. Moreau was elected a Fellow of the International Society for Computational Biology in 2018 for outstanding contributions to the fields of computational biology and bioinformatics.
Yves Moreau's Published Works
Number of citations in a given year to any of this author's works
Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- PlantCARE, a database of plant cis-acting regulatory elements and a portal to tools for in silico analysis of promoter sequences (2002) (3977)
- BioMart and Bioconductor: a powerful link between biological databases and microarray data analysis (2005) (1593)
- DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources. (2009) (1488)
- A human phenome-interactome network of protein complexes implicated in genetic disorders (2007) (955)
- Gene prioritization through genomic data fusion (2006) (924)
- Chromosome instability is common in human cleavage-stage embryos (2009) (720)
- A higher-order background model improves the detection of promoter regulatory elements by Gibbs sampling (2001) (449)
- A Gibbs sampling method to detect over-represented motifs in the upstream regions of co-expressed genes (2001) (425)
- Computational tools for prioritizing candidate genes: boosting disease gene discovery (2012) (419)
- Emerging patterns of cryptic chromosomal imbalance in patients with idiopathic mental retardation and multiple congenital anomalies: a new series of 140 patients and review of published reports (2006) (399)
- Versatile gene-specific sequence tags for Arabidopsis functional genomics: transcript profiling and reverse genetics applications. (2004) (347)
- Predicting the prognosis of breast cancer by integrating clinical and microarray data with Bayesian networks (2006) (341)
- An expanded evaluation of protein function prediction methods shows an improvement in accuracy (2016) (316)
- Biclustering microarray data by Gibbs sampling (2003) (246)
- Endeavour update: a web resource for gene prioritization in multiple species (2008) (242)
- Adaptive quality-based clustering of gene expression profiles (2002) (225)
- Toucan: deciphering the cis-regulatory logic of coregulated genes. (2003) (223)
- Effective diagnosis of genetic disease by computational phenotype analysis of the disease-associated genome (2014) (221)
- Single-cell chromosomal imbalances detection by array CGH (2006) (217)
- Heterozygous missense mutations in SMARCA2 cause Nicolaides-Baraitser syndrome (2012) (215)
- Optimized Data Fusion for Kernel k-Means Clustering (2012) (214)
- From hype to reality: data science enabling personalized medicine (2018) (203)
- A guide to web tools to prioritize candidate genes (2011) (199)
- Using Ribosomal Protein Genes as Reference: A Tale of Caution (2008) (194)
- GRNBoost2 and Arboreto: efficient and scalable inference of gene regulatory networks (2018) (191)
- Comparison and meta-analysis of microarray data: from the bench to the computer desk. (2003) (177)
- GRU-ODE-Bayes: Continuous modeling of sporadically-observed time series (2019) (176)
- Microarray analysis reveals abnormal chromosomal complements in over 70% of 14 normally developing human embryos. (2013) (174)
- TOUCAN 2: the all-inclusive open source workbench for regulatory sequence analysis (2005) (173)
- eXtasy: variant prioritization by genomic data fusion (2013) (159)
- Kernel-based data fusion for gene prioritization (2007) (150)
- Single-cell paired-end genome sequencing reveals structural variation per cell cycle (2013) (143)
- Computational detection of cis-regulatory modules (2003) (141)
- Repurposing High-Throughput Image Assays Enables Biological Activity Prediction for Drug Discovery. (2018) (139)
- L2-norm multiple kernel learning and its application to biomedical data fusion (2010) (121)
- Microarray screening for target genes of the proto-oncogene PLAG1 (2004) (115)
- Associations of Disease-Modifying Therapies With COVID-19 Severity in Multiple Sclerosis (2021) (103)
- Candidate gene prioritization by network analysis of differential expression using machine learning approaches (2010) (103)
- Benchmarking the CATMA Microarray. A Novel Tool forArabidopsis Transcriptome Analysis1[w] (2005) (97)
- arrayCGHbase: an analysis platform for comparative genomic hybridization microarrays (2005) (96)
- Candidate gene prioritization with Endeavour (2016) (93)
- Haploinsufficiency of TAB2 causes congenital heart defects in humans. (2010) (92)
- Concurrent whole-genome haplotyping and copy-number profiling of single cells. (2015) (90)
- INCLUSive: INtegrated Clustering, Upstream sequence retrieval and motif Sampling (2002) (89)
- Using literature and data to learn Bayesian networks as clinical models of ovarian tumors (2004) (87)
- An unbiased evaluation of gene prioritization tools (2012) (86)
- Analysis of HIV-1 pol sequences using Bayesian Networks: implications for drug resistance (2006) (84)
- TXTGate: profiling gene groups with text-based information (2004) (79)
- Proteomics Analysis of Cytokine-induced Dysfunction and Death in Insulin-producing INS-1E Cells (2007) (78)
- Comprehensive analysis of the base composition around the transcription start site in Metazoa (2004) (76)
- Bayesian applications of belief networks and multilayer perceptrons for ovarian tumor classification with rejection (2003) (74)
- PINTA: a web server for network-based gene prioritization from expression data (2011) (73)
- Combined mRNA microarray and proteomic analysis of eutopic endometrium of women with and without endometriosis. (2012) (70)
- Network Analysis of Differential Expression for the Identification of Disease-Causing Genes (2009) (70)
- Pan-cancer analysis of homozygous deletions in primary tumours uncovers rare tumour suppressors (2017) (67)
- Bridging the gap between systems biology and medicine (2009) (66)
- Genome-wide copy number profiling of single cells in S-phase reveals DNA-replication domains (2013) (65)
- Predicting the outcome of pregnancies of unknown location: Bayesian networks with expert prior information compared to logistic regression. (2006) (64)
- Weighted hybrid clustering by combining text mining and bibliometrics on a large-scale journal database (2010) (64)
- Challenges of Interpreting Copy Number Variation in Syndromic and Non-Syndromic Congenital Heart Defects (2011) (64)
- CATMA, a comprehensive genome-scale resource for silencing and transcript profiling of Arabidopsis genes (2007) (63)
- Breakage–fusion–bridge cycles leading to inv dup del occur in human cleavage stage embryos (2011) (63)
- Kernel-based Data Fusion for Machine Learning - Methods and Applications in Bioinformatics and Text Mining (2009) (62)
- Beegle: from literature mining to disease-gene discovery (2015) (59)
- Comparison of vocabularies, representations and ranking algorithms for gene prioritization by text mining (2008) (59)
- Functional bioinformatics of microarray data: from expression to regulation (2002) (59)
- Evaluation of the Vector Space Representation in Text-Based Gene Clustering (2002) (58)
- A genetic algorithm for the detection of new cis-regulatory modules in sets of coregulated genes (2004) (58)
- INCLUSive: a web portal and service registry for microarray and regulatory sequence analysis (2003) (58)
- Predicting disease-causing variant combinations (2019) (57)
- Positional gene enrichment analysis of gene sets for high-resolution identification of overrepresented chromosomal regions (2008) (56)
- Proteome analysis demonstrates profound alterations in human dendritic cell nature by TX527, an analogue of vitamin D (2009) (55)
- Easy Hyperparameter Search Using Optunity (2014) (55)
- Chronic lymphocytic leukemia and prolymphocytic leukemia with MYC translocations: a subgroup with an aggressive disease course (2012) (55)
- Unraveling genomic variation from next generation sequencing data (2013) (54)
- Improved detection of chromosomal abnormalities in chronic lymphocytic leukemia by conventional cytogenetics using CpG oligonucleotide and interleukin‐2 stimulation: A Belgian multicentric study (2009) (54)
- Finding the targets of a drug by integration of gene expression data with a protein interaction network. (2013) (54)
- Cluster analysis of microarray data (2004) (53)
- COVID-19 in people with multiple sclerosis: A global data sharing initiative (2020) (48)
- Gene prioritization and clustering by multi-view text mining (2010) (48)
- The genetic heterogeneity and mutational burden of engineered melanomas in zebrafish models (2013) (45)
- Single-cell copy number variation detection (2011) (45)
- Bayesian network analysis of resistance pathways against HIV-1 protease inhibitors. (2007) (43)
- Linking drug target and pathway activation for effective therapy using multi-task learning (2018) (43)
- Autosomal-dominant microtia linked to five tandem copies of a copy-number-variable region at chromosome 4p16. (2008) (43)
- Estimation of an in vivo fitness landscape experienced by HIV-1 under drug selective pressure useful for prediction of drug resistance evolution during treatment (2008) (43)
- Gene profiling of hippocampal neuronal culture (2003) (42)
- ModuleMiner - improved computational detection of cis-regulatory modules: are there different modes of gene regulation in embryonic development and adult tissues? (2008) (40)
- Understanding mutational effects in digenic diseases (2017) (40)
- Mutual inhibition among postmitotic neurons regulates robustness of brain wiring in Drosophila (2013) (39)
- Hybrid Clustering of Text Mining and Bibliometrics Applied to Journal Sets (2009) (37)
- Congenital heart defects in a novel recurrent 22q11.2 deletion harboring the genes CRKL and MAPK1 (2012) (37)
- Associations of DMT therapies with COVID-19 severity in multiple sclerosis (2020) (37)
- YTPdb: a wiki database of yeast membrane transporters. (2010) (36)
- Emerging patterns of cryptic chromosomal imbalances in patients with idiopathic mental retardation and multiple congenital anomalies (2006) (35)
- Collaboratively charting the gene-to-phenotype network of human congenital heart defects (2010) (35)
- Large-scale benchmark of Endeavour using MetaCore maps (2010) (35)
- Microarray analysis of copy number variation in single cells (2012) (33)
- Drug repositioning or target repositioning: A structural perspective of drug-target-indication relationship for available repurposed drugs (2020) (33)
- Mapping biomedical concepts onto the human genome by mining literature on chromosomal aberrations (2007) (33)
- Integrating Computational Biology and Forward Genetics in Drosophila (2009) (33)
- Interactogeneous: Disease Gene Prioritization Using Heterogeneous Networks and Full Topology Scores (2012) (32)
- DNA methylation analysis of Homeobox genes implicates HOXB7 hypomethylation as risk factor for neural tube defects (2015) (31)
- Query-driven module discovery in microarray data (2007) (31)
- Macau: Scalable Bayesian factorization with high-dimensional side information using MCMC (2017) (31)
- Annotate-it: a Swiss-knife approach to annotation, analysis and interpretation of single nucleotide variation in human disease (2012) (29)
- Protein fold recognition using geometric kernel data fusion (2014) (29)
- Estimating the Relative Contribution of dNTP Pool Imbalance and APOBEC3G/3F Editing to HIV Evolution In Vivo (2007) (29)
- Computational identification of prion-like RNA-binding proteins that form liquid phase-separated condensates (2019) (28)
- Towards practical privacy-preserving genome-wide association study (2018) (28)
- Gene prioritization using Bayesian matrix factorization with genomic and phenotypic side information (2018) (28)
- Peripheral Blood RNA Levels of QSOX1 and PLBD1 Are New Independent Predictors of Left Ventricular Dysfunction After Acute Myocardial Infarction (2019) (25)
- ChemGrapher: Optical Graph Recognition of Chemical Compounds by Deep Learning (2020) (25)
- In vitro screening of embryos by whole-genome sequencing: now, in the future or never? (2014) (25)
- Detecting cis-regulatory binding sites for cooperatively binding proteins (2008) (24)
- Insight into the protein solubility driving forces with neural attention (2020) (24)
- The t(4;8) is mediated by homologous recombination between olfactory receptor gene clusters, but other 4p16 translocations occur at random. (2007) (24)
- Modelled in vivo HIV Fitness under drug Selective Pressure and Estimated Genetic Barrier Towards Resistance are Predictive for Virological Response (2008) (24)
- Macau: Scalable Bayesian Multi-relational Factorization with Side Information using MCMC (2015) (23)
- ACE-inhibition induces a cardioprotective transcriptional response in the metabolic syndrome heart (2018) (23)
- Optimized data fusion for K-means Laplacian clustering (2010) (23)
- BMPR1A is a candidate gene for congenital heart defects associated with the recurrent 10q22q23 deletion syndrome. (2012) (23)
- Balancing false positives and false negatives for the detection of differential expression in malignancies (2004) (23)
- The use of polygenic risk scores in pre-implantation genetic testing: an unproven, unethical practice (2021) (23)
- Novel insights into the global proteome responses of insulin-producing INS-1E cells to different degrees of endoplasmic reticulum stress. (2010) (23)
- Concordance of gene expression in human protein complexes reveals tissue specificity and pathology (2013) (23)
- pBRIT: gene prioritization by correlating functional and phenotypic annotations through integrative data fusion (2018) (22)
- Clustering by heterogeneous data fusion : framework and applications (2008) (22)
- NGS-Logistics: federated analysis of NGS sequence variants across multiple locations (2014) (22)
- Crack down on genomic surveillance (2019) (21)
- Methylome analysis for spina bifida shows SOX18 hypomethylation as a risk factor with evidence for a complex (epi)genetic interplay to affect neural tube development (2016) (21)
- Topological Graph Neural Networks (2021) (20)
- Interphase fluorescence in situ hybridization on selected plasma cells is superior in the detection of cytogenetic aberrations in plasma cell dyscrasia (2010) (18)
- Array comparative genomic hybridization and computational genome annotation in constitutional cytogenetics: suggesting candidate genes for novel submicroscopic chromosomal imbalance syndromes (2007) (17)
- An experimental loop design for the detection of constitutional chromosomal aberrations by array CGH (2009) (16)
- Importing MAGE-ML format microarray data into BioConductor (2004) (16)
- Structure-based drug repositioning explains ibrutinib as VEGFR2 inhibitor (2019) (16)
- Advances in Cluster Analysis of Microarray Data (2005) (15)
- Protein‐induced changes during the maturation process of human dendritic cells: A 2‐D DIGE approach (2008) (15)
- Biological knowledge bases using Wikis: combining the flexibility of Wikis with the structure of databases (2010) (14)
- Detection of novel 3' untranslated region extensions with 3' expression microarrays (2010) (14)
- Exploring the limitations of biophysical propensity scales coupled with machine learning for protein sequence analysis (2019) (14)
- Probabilistic Graphical Models for Computational Biomedicine (2003) (14)
- Estimating the individualized HIV-1 genetic barrier to resistance using a nelfinavir fitness landscape (2010) (14)
- Galahad: a web server for drug effect analysis from gene expression (2015) (13)
- Fast semi-supervised discriminant analysis for binary classification of large data-sets (2017) (12)
- Longitudinal machine learning modeling of MS patient trajectories improves predictions of disability progression (2021) (12)
- ESHG warns against misuses of genetic tests and biobanks for discrimination purposes (2021) (12)
- Complicated legacies: The human genome at 20 (2021) (11)
- Ultra-fast global homology detection with Discrete Cosine Transform and Dynamic Time Warping (2018) (11)
- Plant-Based Microarray Data at the European Bioinformatics Institute. Introducing AtMIAMExpress, a Submission Tool for Arabidopsis Gene Expression Data to ArrayExpress (2005) (11)
- Bioinformatics: Organisms from Venus, Technology from Jupiter, Algorithms from Mars (2003) (11)
- Viva Europa, a Land of Excellence in Research and Innovation for Health and Wellbeing (2017) (10)
- Current cancer driver variant predictors learn to recognize driver genes instead of functional variants (2021) (10)
- Genome-Wide Copy Number Variation Scan Identifies Complement Component C4 as Novel Susceptibility Gene for Crohn's Disease (2016) (9)
- Latent Convergent Cross Mapping (2021) (9)
- Gene prioritization through geometric-inspired kernel data fusion (2015) (9)
- GENESTAT: an information portal for design and analysis of genetic association studies (2009) (9)
- Problems with the nested granularity of feature domains in bioinformatics: the eXtasy case (2015) (9)
- Privacy-Preserving Genome-Wide Association Study is Practical (2017) (9)
- Learning with Heterogenous Data Sets by Weighted Multiple Kernel Canonical Correlation Analysis (2007) (9)
- ReLiance: a machine learning and literature-based prioritization of receptor—ligand pairings (2012) (8)
- An interpretable low-complexity machine learning framework for robust exome-based in-silico diagnosis of Crohn’s disease patients (2020) (8)
- A Genetic Algorithm for Pancreatic Cancer Diagnosis (2013) (8)
- A novel method for data fusion over entity-relation graphs and its application to protein-protein interaction prediction (2021) (8)
- Highlights from the 11th ISCB Student Council Symposium 2015 (2016) (7)
- Meander: visually exploring the structural variome using space-filling curves (2013) (7)
- PyUUL provides an interface between biological structures and deep learning algorithms (2022) (6)
- Large-scale in-silico statistical mutagenesis analysis sheds light on the deleteriousness landscape of the human proteome (2018) (6)
- In silico prediction of in vitro protein liquid-liquid phase separation experiments outcomes with multi-head neural attention (2021) (6)
- DECIPHER : D atabas e of C hromosomal I mbalance and P henotype in H umans Using E nsembl R esources (2009) (6)
- BMPR 1 A is a candidate gene for congenital heart defects associated with the recurrent 10 q 22 q 23 deletion syndrome (2012) (6)
- Rayleigh Quotient-Type Problems in Machine Learning (2011) (6)
- Erratum: Gene prioritization through genomic data fusion (2006) (6)
- Predicting receptor-ligand pairs through kernel learning (2011) (5)
- Detection of cis-acting regulatory elements in plants: a Gibbs sampling approach (2000) (5)
- A Self-Tuning Genetic Algorithm with Applications in Biomarker Discovery (2014) (5)
- Deep Ensemble Tensor Factorization for Longitudinal Patient Trajectories Classification (2018) (5)
- Highly Scalable Tensor Factorization for Prediction of Drug-Protein Interaction Type (2015) (5)
- Splitting chemical structure data sets for federated privacy-preserving machine learning (2021) (5)
- NGS-Logistics: data infrastructure for efficient analysis of NGS sequence variants across multiple centers (2015) (5)
- Updated Results of the COVID-19 in MS Global Data Sharing Initiative (2022) (5)
- Integrating quality-based clustering of microarray data with Gibbs sampling for the discovery of regulatory motifs (2002) (5)
- Ontology Guided Data Integration for Computational Prioritization of Disease Genes (2006) (5)
- Drug repositoning or target repositioning: a structural perspective of drug-target-indication relationship for available repurposed drugs (2019) (5)
- Multiple Sclerosis Data Alliance - A global multi-stakeholder collaboration to scale-up real world data research. (2020) (5)
- A Simple Genetic Algorithm for Biomarker Mining (2012) (5)
- Clinical population genetic analysis of variants in the SARS-CoV-2 receptor ACE2 (2020) (4)
- Web-based data collection for uterine adnexal tumors: a case study (2002) (4)
- HiVA: an integrative wet- and dry-lab platform for haplotype and copy number analysis of single-cell genomes (2019) (4)
- Repurposed high-throughput images enable biological activity prediction for drug discovery (2017) (4)
- mRNA profiling of pancreatic beta-cells: investigating mechanisms of diabetes (2006) (4)
- ECCB 2014: The 13th European Conference on Computational Biology (2014) (4)
- Identification of conserved modes of expression profiles during hippocampal development and neuronal differentiation in vitro (2006) (4)
- Multi-view Text Mining for Disease Gene Prioritization and Clustering (2011) (3)
- SparseChem: Fast and accurate machine learning model for small molecules (2022) (3)
- Recognition of gene regulatory sequences by bagging of neural networks (1999) (3)
- Splitting chemical structure data sets for federated privacy-preserving machine learning (2021) (3)
- NEWS ON ULTRASONOGRAPHIC TECHNIQUES FOR PELVIC MALIGNANCIES (2003) (3)
- L n -norm Multiple Kernel Learning and Least Squares Support Vector Machines (2011) (3)
- Extended Bayesian Regression Models: A Symbiotic Application of Belief Networks and Multilayer Perceptrons for the Classification of Ovarian Tumors (2001) (3)
- Hybrid Clustering by Integrating Text and Citation Based Graphs in Journal Database Analysis (2009) (3)
- Topic modeling of biomedical text (2016) (3)
- Detection of low-level mosaicisms by array CGH (2009) (3)
- INTEGRATION OF CLINICAL AND MICROARRAY DATA USING BAYESIAN NETWORKS (2006) (3)
- Industry-Scale Orchestrated Federated Learning for Drug Discovery (2022) (3)
- Text-Based Gene Profiling with Domain-Specific Views (2003) (2)
- Gene sets enrichment analysis of chromosomal regions (2008) (2)
- Gene Regulation Bioinformatics of Microarray Data (2007) (2)
- A Comprehensive Comparison of Two MEDLINE Annotators for Disease and Gene Linkage: Sometimes Less is More (2016) (2)
- Yves Moreau and Jaap Heringa, on behalf of the ECCB10 organizing and steering committees (2010) (2)
- AliBiMotif: Integrating alignment and biclustering to unravel transcription factor binding sites in DNA sequences (2012) (2)
- Expressive Graph Informer Networks (2019) (2)
- Splitting chemical structure data sets for federated privacy-preserving machine learning (2021) (2)
- PRE-OPERATIVE PREDICTION OF DEPTH OF MYOMETRIAL INVASION IN PATIENTS WITH ENDOMETRIAL CANCER: EVALUATION OF ULTRASOUND PARAMETERS AND DEVELOPMENT OF A NEW LOGISTIC REGRESSION MODEL (2003) (2)
- Applications of Gibbs sampling in bioinformatics (2006) (2)
- NGS-Logistics: federated analysis of NGS sequence variants across multiple locations (2014) (2)
- Annotate-it: a Swiss-knife approach to annotation, analysis and interpretation of single nucleotide variation in human disease (2012) (2)
- Translating systems biology into medical applications : Report of the 3rd Bertinoro Systems Biology Workshop (2009) (2)
- Towards practical privacy-preserving genome-wide association study (2018) (1)
- Whole exome sequencing reveals de novo variants that affect chromatin remodeling processes in Nicolaides-Baraitser syndrome patients (2011) (1)
- Protein fold recognition and protein sub-nuclear localization using geometric kernel data fusion (2014) (1)
- Two‐level preconditioning for Ridge Regression (2018) (1)
- NGS-Logistics: data infrastructure for efficient analysis of NGS sequence variants across multiple centers (2012) (1)
- Corrigendum to Longitudinal machine learning modeling of MS patient trajectories improves predictions of disability progression: [Computer Methods and Programs in Biomedicine, Volume 208, (September 2021) 106180] (2021) (1)
- Chromosomal rearrangements arise at high frequency during early human embryogenesis (2008) (1)
- A Hybrid Approach to Feature Ranking for Microarray Data Classification (2013) (1)
- Weighted Multiple Kernel Canonical Correlation (2011) (1)
- From genotype to phenotype in Arabidopsis thaliana: in-silico genome interpretation predicts 288 phenotypes from sequencing data (2021) (1)
- Gene Prioritization through Bayesian matrix factorization (2015) (1)
- Plasma cell selection improves detection of cytogenetic aberrations by interphase fluorescence in situ hybridization in plasma cell dyscrasia. Comparison of results obtained on whole bone marrow culture versus immunologically identified or sorted plasma cells (2010) (1)
- Reply to Letter by Tellier et al., ‘Scientific refutation of ESHG statement on embryo selection’ (2022) (1)
- A bioinformatics e-dating story: computational prediction and prioritization of receptor-ligand pairs (2012) (1)
- Predicting ordered accumulation of mutations of HIV under treatment using an estimate of the HIV in vivo fitness function during treatment (2006) (1)
- Structure learning of Bayesian networks with MCMC : extension to incomplete data and decision trees as local models (2009) (1)
- HPMPdb: A machine learning-ready database of protein molecular phenotypes associated to human missense variants (2022) (1)
- Network-Based Disease Candidate Gene Prioritization: Towards Global Diffusion in Heterogeneous Association Networks (2010) (1)
- Unraveling genomic variation from next generation sequencing data (2013) (1)
- Mining therapeutic insights from large scale drug screenings with transfer learning (2017) (1)
- eXtasy simplified-towards opening the black box (2013) (1)
- Improving performance of the eXtasy model by hierarchical sampling (2014) (1)
- Computational Approaches to Elucidating Transient Protein-Protein Interactions, Predicting Receptor-Ligand Pairings (2012) (1)
- Graph Informer Networks for Molecules (2019) (1)
- Longitudinal modeling of MS patient trajectories improves predictions of disability progression (2020) (1)
- Multilevel preconditioning for Ridge Regression (2018) (1)
- Application of geometric kernel data fusion in protein fold recognition and protein sub-nuclear localization (2014) (1)
- Haplotyping of single human cells (2009) (1)
- Gene prioritization by genomic data fusion (2007) (1)
- Fast and accurate inference of gene regulatory networks through robust precision matrix estimation (2022) (1)
- Estimating an In Vivo Fitness Landscape During Protease and Reverse Transcriptase Treatment from Observed Genetic Evolution to Predict Accumulation of Mutations under Selective Pressure (2007) (1)
- Self-Labeling of Fully Mediating Representations by Graph Alignment (2021) (1)
- ECCB 2018: The 17th European Conference on Computational Biology (2018) (1)
- Integrating heterogeneous data sets for Clustering Analysis (2008) (1)
- Improved detection of recurrent cytogenetic aberrations using interphase fish on immunologically identified or sorted plasma cells compared to cultured whole bone marrow cells (2010) (1)
- A bioinformatics e-dating story: computational prediction and prioritization of receptor-ligand pairs (2012) (1)
- Inferring Causal Dependencies between Chaotic Dynamical Systems from Sporadic Time Series (2020) (1)
- An experimental loop design improves the detection of constitutional chromosomal aberrations by array CGH (2007) (0)
- Detection of extended UTRs with 3' expression microarrays (2008) (0)
- O12: Text Mining for Constitutional Cytogenetics (2005) (0)
- High resolution screening of blastomeres from human embryos (2008) (0)
- Matrix factorization with features for drug activity modeling (2015) (0)
- Topic modeling of biomedical text: from words and topics to disease and gene links (2016) (0)
- Cross-Species Candidate Gene Prioritization with MerKator (2011) (0)
- Author Correction: Pan-cancer analysis of homozygous deletions in primary tumours uncovers rare tumour suppressors (2019) (0)
- Correction: ESHG warns against misuses of genetic tests and biobanks for discrimination purposes (2021) (0)
- Gene expression Query-driven module discovery in microarray data (2007) (0)
- Critical Assessment of Microarray Data Analysis Contest Datasets Emerald Dataset : a Microarray Experiment to Study the Relative Magnitudes of Technical and Biological Variation Talks Keynote towards Cracking the Code of Transcription and Chromatin Regulation Analysis of Comparative Genomic Hybridiz (0)
- Author response: Mutual inhibition among postmitotic neurons regulates robustness of brain wiring in Drosophila (2013) (0)
- An experimental loop design improves the detection of congenital chromosomal aberrati (2009) (0)
- Proof-of-principle evaluation of predictive performance for therapy outcome of baseline estimated fitness and genetic barrier towards resistance in a clinical cohort of HIV-1-treated patients (2007) (0)
- A guide through the labyrinth of gene prioritization tools (2009) (0)
- Single cell genomics from the cell cycle perspective (2012) (0)
- Congenital heart defects in a novel recurrent 22q11.2 deletion syndrome harboring the genes CRKL and MAPK1 (2011) (0)
- Next Generation Genetic Tests: from artisan genetic testing to uniform, streamlined, fully quality assured and automated processing of genetic tests using Next Generation Sequencing (2010) (0)
- DOP31 Serum protein markers for early and differential IBD diagnosis validated by machine learning approaches (2020) (0)
- WiNGS: Widely integrated NGS platform for whole genome sequencing (2019) (0)
- Annotate-it: a framework and web-interface for the archival, management and interpretation of single nucleotide variants obtained by next generation sequencing (2011) (0)
- An ontology describing congenital heart defects data (2013) (0)
- Methylome analysis for spina bifida shows SOX18 hypomethylation as a risk factor with evidence for a complex (epi)genetic interplay to affect neural tube development (2016) (0)
- Kernel Data Fusion (2015) (0)
- Augmenting THerapeutic Effectiveness Through Novel Analytics (ATHENA) - A Public and Private Partnership Project Funded by the Flemish Government (VLAIO) (2022) (0)
- Preimplantation Genetics Diagnosis using Single Cell 60-mer oligo arrayCGH platform (2011) (0)
- Genome-wide SNP-, CNV- and haplo-typing of single human cells (2010) (0)
- Computational annotation and interpretation of single nucleotide variation to identify disease-causing variants by next-generation sequencing (2012) (0)
- Evaluation of existing motif detection tools on their ability to retrieve regulatory motifs in sequence data (2009) (0)
- O4: Detection of structural low-grade mosaicism by array CGH (2005) (0)
- Text mining for constitutional cytogenetics (2005) (0)
- Clinical applications of the CHDWIKI: a portal to manage and gather Cardiogenetic data (2009) (0)
- In silico prediction of cis-regulatory features associated with common patterns of gene expression during hippocampal development (2004) (0)
- 00055 PREDICTING THE CLINICAL BEHAVIOR OF OVARIAN CANCER FROM GENE EXPRESSION PROFILES (2005) (0)
- Extension of Healthy Life Using Preventive Genomics (2012) (0)
- Galahad - a web server for gene expression data analysis in support of drug development (2013) (0)
- Information management for constitutional cytogenetics: tools for ArrayCGH in a clinical diagnostic context (2008) (0)
- Somatic variation in early development (2011) (0)
- Détection d’aneuploidies à partir d’une cellule unique par la méthode de CGH array (2006) (0)
- Current cancer driver variant predictors learn to recognize driver genes instead of functional variants (2021) (0)
- Genome wide CNV and SNP detection in cleavage stage embryos uncovers chromosomal instability (2009) (0)
- PyUUL provides an interface between biological structures and deep learning algorithms (2022) (0)
- ‘arrayCGHbase’: a freely available and versatile tool for data mining and visualisation of array CGH and SNP chip data (2005) (0)
- Drug profiling using a bioinformatics pipeline (2011) (0)
- Fast and accurate inference of gene regulatory networks through robust precision matrix estimation (2022) (0)
- Galahad – a web server for the functional characterization of drugs from gene expression following treatment (2013) (0)
- Estimating random forest feature importance using a genetic algorithm approach (2014) (0)
- Author Correction: Linking drug target and pathway activation for effective therapy using multi-task learning (2019) (0)
- Secondary use of genomic information: deleterious and disease causing mutations in healthy individuals (2013) (0)
- Using Literature and Data to Annotate and Learn Bayesian Networks (2002) (0)
- Single-cell SNP-array and genome sequence analysis to study individual blastomeres (2014) (0)
- In silico search of plant cis-acting regulatory elements (2001) (0)
- Guest Commentary on Chapter 8: Data Integration: The Next Big Hope? (2010) (0)
- Genome-wide haplotyping of single cells (2009) (0)
- Pan-cancer analysis of homozygous deletions in primary tumours uncovers rare tumour suppressors (2017) (0)
- TRACE: Tennessee Research and Creative TRACE: Tennessee Research and Creative Exchange Exchange Bridging the gap between systems biology and medicine Bridging the gap between systems biology and medicine (2022) (0)
- WHICH FACTOR DOES PREDICT AXILLARY LYMPH NODE STATUS BEST IN OPERABLE BREAST CANCERS? (2003) (0)
- Biomedical text mining for disease-gene discovery (poster) (2013) (0)
- Towards fully streamlined, quality-assured, automated next-generation gene tests (2010) (0)
- Screenshot of the TOUCAN software (2011) (0)
- Author Correction: Linking drug target and pathway activation for effective therapy using multi-task learning (2019) (0)
- Bench and Array-CGH: information modeling for constitutional cytogenetics (2008) (0)
- Involvement of endoplasmic reticulum stress in beta-cell apoptosis : a proteomic approach in INS-1E cells (2009) (0)
- Gene interaction networks boost genetic algorithm performance in biomarker discovery (2014) (0)
- 1.19 Sequential Genomic Analysis of Untreated Patients with Chronic Lymphocytic Leukemia Demonstrates Clonal Evolution (2011) (0)
- High incidence of chromosomal rearrangement sin human pre-implantation embryos of young couples (2008) (0)
- Single-cell genome sequencing to characterize chromosome instability in human cleavage stage embryos (2015) (0)
- Biomedical text mining for disease-gene discovery (2013) (0)
- How normal is a normal human embryo (2009) (0)
- Correction: The use of polygenic risk scores in pre-implantation genetic testing: an unproven, unethical practice (2022) (0)
- Problems with the nested granularity of feature domains in bioinformatics: the eXtasy case (2015) (0)
- Deciphering cis-acting regulatory elements in plant and drosophila promoter sequences (2002) (0)
- O-3 The cell cycle phase influences the accuracy of single cell genome wide array-CGH (2013) (0)
- OC118: Mathematical models to evaluate ovarian masses—can they beat an expert operator? (2003) (0)
- Correction: The use of polygenic risk scores in pre-implantation genetic testing: an unproven, unethical practice (2022) (0)
- IT tools for interpretation of copy number variation in context of the patient phenotype (2010) (0)
- European Mathematical Genetics Meeting, Heidelberg, Germany, 12th–13th April 2007 (2007) (0)
- Su1880 MACHINE LEARNING APPROACHES VALIDATE SEROLOGICAL MARKERS FOR EARLY AND DIFFERENTIAL DIAGNOSIS (2020) (0)
- Genome-wide Haplotyping and Detection of Meiotic Homologous Recombination Sites in Single Cells (2011) (0)
- Author Correction: Pan-cancer analysis of homozygous deletions in primary tumours uncovers rare tumour suppressors (2018) (0)
- Trace: Tennessee Research and Creative Exchange (2009) (0)
- Biomedical Text Mining for Disease Gene Discovery (2012) (0)
- WiNGS: Widely integrated NGS platform for federated genome analysis (2022) (0)
- The genetic heterogeneity and mutational burden of engineered melanomas in zebrafish models (2013) (0)
- Recognition of gene regulatory sequencesby bagging of neural (2007) (0)
- Genome-wide single-cell Haplotyping, a generic method for preimplantation genetic diagnosis (2013) (0)
- Paving the way for preventive genomics - The clinical validity of secondary use of genomic information (2012) (0)
- Invited lectures abstracts (2011) (0)
- Comparison of algorithms for high-resolution array CGH. (2007) (0)
- Towards fully quality-assured complete CFTR gene genetic tests (2010) (0)
- Towards Better Receptor-Ligand Prioritization: How Machine Learning on Protein-Protein Interaction Data Can Provide Insight Into Receptor-Ligand Pairs (2010) (0)
- 4p16 olfactory receptor gene cluster is a promiscuous hotspot for chromosomal rearrangements (2007) (0)
- CHDWiki: a comprehensive tool to gather and manage cardiogenetic data (2008) (0)
- ECCB 2012 Organization (2012) (0)
- Natural Lipid Extracts as an Artificial Membrane for Drug Permeability Assay: In Vitro and In Silico Characterization (2023) (0)
- An R based pipeline for drug profiling based on gene expression data (2012) (0)
- Splitting chemical structure data sets for federated privacy-preserving machine learning (2021) (0)
- P6446Diminished preconditioning potential in the hearts from metabolic syndrome subjects can be partially restored by angiotensin-converting-enzyme inhibitor therapy (2018) (0)
- Single-cell genome sequencing reveals DNA-mutation per cell cycle (2013) (0)
- Genomics: Transcript Profiling and Reverse Genetics Applications Functional Arabidopsis Versatile Gene-Specific Sequence Tags for (2007) (0)
- Applying Kernel Methods on Protein Complexes Detection Problem (2012) (0)
- An aCGH screening study in 150 patients identifies a novel dosage-sensitive gene, TAB2, which is disrupted in multiple patients with cardiac defects (2009) (0)
- Congenital heart defects in a novel rec urrent 22q11.2 deletion harboring CRKL and MAPK1 (2012) (0)
- Applying a genetic algorithm on expression data to reveal the best set of biomarkers (2014) (0)
- Understanding combinatorial effects of variants using machine learning and DIDA, the DIgenic diseases Database (2017) (0)
- A guide to web tools to prioritize candidate genes: How to efficiently choose the tools that match your needs? (2011) (0)
- regionsfor detection of mRNA expression imbalance Expression imbalance map: a new visualization (2015) (0)
- O3: Array CGH findings in a large series of 150 patients with idiopathic mental retardation and congenital anomalies: unexpected findings and implications for future routine diagnostic screening (2005) (0)
- Correction to: Reply to Letter by Tellier et al., ‘Scientific refutation of ESHG statement on embryo selection’ (2022) (0)
- INVITED SESSION, SESSION 42: PARAMEDICAL INVITED SESSION – EMERGING TECHNOLOGIES IN HUMAN IVF LABORATORIES, Tuesday 5 July 2011 14:00 – 15:00 (2011) (0)
- Alu serving as a terminator for gene transcription (2007) (0)
- KSinBIT 2006 PC Co-chairs' Message (2006) (0)
- Microarray technology in PGD (2010) (0)
- Defining Real-World Product Performance Using Survival Analysis and Superivsed Machine Learning (2016) (0)
- Towards a Belgian reference set (2016) (0)
- Array Comparative Genomic Hybridization as a clinical diagnostic tool in syndromic and non-syndromic congenital heart defects (2012) (0)
- Understanding the adenine richness of the HIV genome through the estimation of misincorporation rates in viv (2007) (0)
- Genome-wide detection of genomic variation in single cells (2009) (0)
- Kernel-Based Gene Prioritization Using Late Integration versus Geometric Kernel Fusion (2014) (0)
- Splitting chemical structure data sets for federated privacy-preserving machine learning (2021) (0)
- Weakly Supervised Knowledge Transfer with Probabilistic Logical Reasoning for Object Detection (2023) (0)
- Prediction accuracy for deleterious and disease causing mutations in healthy individuals (2013) (0)
- Accuracy of algorithms and databases for the prediction of deleterious and disease causing mutations in healthy individuals (2013) (0)
- Comparative genomic hybridisation and next-generation sequencing: powerful tools to investigate chromosome number and structure in human embryos (2011) (0)
- Towards Better Prioritization of Epigenetically Modified DNA Regions (2012) (0)
- Contents Vol. 135, 2011 (2011) (0)
- Network analysis of differential expression for drug target prioritization (2011) (0)
- Identifying tissue-specificity of protein-complexes based on a global map of human expression data (2012) (0)
- Multi-task learning for drug activity modeling (2014) (0)
- Splitting chemical structure data sets for federated privacy-preserving machine learning (2021) (0)
- Comparison of aggregation methods for multiphenotype exomic variant prioritization (2016) (0)
- Literature mining for constitutional cytogenetics (2006) (0)
- Combined single-cell FISH and arrayCGH show that segmental aneuploidies do occur in embryos (2009) (0)
- In vitro screening and selection of embryos by whole-genome sequencing and analysis - assessment of its usefulness and ethical implications (2014) (0)
- Multilevel Gibbs Sampling for Bayesian Regression (2020) (0)
- Editorial: Towards genome interpretation: Computational methods to model the genotype-phenotype relationship (2022) (0)
- Integration of gene expression data with a protein interaction network for predicting the targets of a drug (2012) (0)
- Linking drug target and pathway activation for effective therapy using multi-task learning (2018) (0)
- A loop experiment design for the detection of chromosomal aberrations by array CGH (2006) (0)
- Integrating gene expression with protein interactions for drug target prioritization (2012) (0)
- Whole-genome single-cell haplotyping, a generic method for preimplantation genetic diagnosis (2014) (0)
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