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Steven Van Vooren | Researchclopedia

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Steven Van Vooren

48

Works

4,098

Citations

18

h-index

21

i10-index

Research Topics

Genomic variations and chromosomal abnormalities Genomics and Rare Diseases Bioinformatics and Genomic Networks

Affiliations

Agilent Technologies (United States)2017–2017

University Colleges Leuven-Limburg2013–2013

Agilent Technologies (Australia)2017–2017

Clinical Research Consortium2017–2017

KU Leuven2003–2010

Top Works

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

Helen V. Firth,Shola M. Richards,et al.

20092,072 citations

Biomedical Text Mining and Ontologies

Gene expression and cancer classification

The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data

Sebastian Köhler,Sandra C. Doelken,et al.

2013837 citations

ENDEAVOUR update: a web resource for gene prioritization in multiple species

Léon-Charles Tranchevent,Roland Barriot,et al.

2008214 citations

Molecular Karyotyping: Array CGH Quality Criteria for Constitutional Genetic Diagnosis

Joris Vermeesch,Cindy Melotte,et al.

2005156 citations

Diagnostic interpretation of array data using public databases and internet sources

Nicole de Leeuw,Trijnie Dijkhuizen,et al.

2012108 citations

Autosomal-Dominant Microtia Linked to Five Tandem Copies of a Copy-Number-Variable Region at Chromosome 4p16

Irina Balikova,Kevin Martens,et al.

200887 citations

arrayCGHbase: an analysis platform for comparative genomic hybridization microarrays

Björn Menten,Filip Pattyn,et al.

200586 citations

TXTGate: profiling gene groups with text-based information

Patrick Glenisson,Bert Coessens,et al.

200467 citations

A novel genomic disorder: a deletion of the SACS gene leading to Spastic Ataxia of Charlevoix–Saguenay

Jeroen Breckpot,Yoshihisa Takiyama,et al.

200863 citations