Steven Van Vooren

A Framework for Elucidating Regulatory Networks Based on Prior Information and Expression Data

Bart De Moor, Olivier Gevaert, Steven Van Vooren, 2007, Annals of the New York Academy of Sciences.

Phenotypic information in genomic variant databases enhances clinical care and research: The international standards for cytogenomic arrays consortium experience

Steven Van Vooren, S. van Vooren, David T. Miller, 2012, Human mutation.

Molecular Karyotyping: Array CGH Quality Criteria for Constitutional Genetic Diagnosis

Bart De Moor, Frank Speleman, Björn Menten, 2005, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

Collaboratively charting the gene-to-phenotype network of human congenital heart defects

Yves Moreau, Marc Gewillig, Roland Barriot, 2010, Genome Medicine.

DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources.

Manuel Corpas, Yves Moreau, Steven Van Vooren, 2009, American journal of human genetics.

Mapping biomedical concepts onto the human genome by mining literature on chromosomal aberrations

Bart De Moor, Yves Moreau, Joris Vermeesch, 2007, Nucleic acids research.