Steven Van Vooren
Publications by Year
Research Areas
Genomic variations and chromosomal abnormalities, Genomics and Rare Diseases, Bioinformatics and Genomic Networks, Biomedical Text Mining and Ontologies, Gene expression and cancer classification
Most-Cited Works
- → DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources(2009)2,072 cited
- → The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data(2013)837 cited
- → ENDEAVOUR update: a web resource for gene prioritization in multiple species(2008)214 cited
- → Molecular Karyotyping: Array CGH Quality Criteria for Constitutional Genetic Diagnosis(2005)156 cited
- → Diagnostic interpretation of array data using public databases and internet sources(2012)108 cited
- → Autosomal-Dominant Microtia Linked to Five Tandem Copies of a Copy-Number-Variable Region at Chromosome 4p16(2008)87 cited
- → arrayCGHbase: an analysis platform for comparative genomic hybridization microarrays(2005)86 cited
- → TXTGate: profiling gene groups with text-based information(2004)67 cited
- → A novel genomic disorder: a deletion of the SACS gene leading to Spastic Ataxia of Charlevoix–Saguenay(2008)63 cited
- → Comparison of vocabularies, representations and ranking algorithms for gene prioritization by text mining(2008)54 cited