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Machine-learning-based prediction of disability progression in multiple sclerosis : an observational, international, multi-center study
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Genome-wide copy number variation scan identifies complement component C4 as novel susceptibility gene for Crohn's disease
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Haploinsufficiency of TAB2 causes congenital heart defects in humans
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GENESTAT : an information portal for design and analysis of genetic association studies
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Positional gene enrichment analysis of gene sets for high-resolution identification of overrepresented chromosomal regions
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Gene sets enrichment analysis of chromosomal regions
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- Journal Article
- A1
- open access
Using ribosomal protein genes as reference : a tale of caution
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Kernel-based data fusion for gene prioritization
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Gene regulation bioinformatics of microarray data
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Query-driven module discovery in microarray data