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Author Details

Steven Van Vooren
Katholieke Universiteit Leuven
2004
24
17
PMIDPaper TitleJournal TitlePublished Year
35207446Reliable and Scalable SARS-CoV-2 qPCR Testing at a High Sample Throughput: Lessons Learned from the Belgian Initiative.Life (Basel)2022
30576869Somatic Tumor Variant Filtration Strategies to Optimize Tumor-Only Molecular Profiling Using Targeted Next-Generation Sequencing Panels.J Mol Diagn2019
28471515Critical points for an accurate human genome analysis.Hum Mutat2017
24217912The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data.Nucleic Acids Res2014
23851227An update on ECARUCA, the European Cytogeneticists Association Register of Unbalanced Chromosome Aberrations.Eur J Med Genet2013
22331816Phenotypic information in genomic variant databases enhances clinical care and research: the International Standards for Cytogenomic Arrays Consortium experience.Hum Mutat2012
26285306Diagnostic interpretation of array data using public databases and internet sources.Hum Mutat2012
20193066Collaboratively charting the gene-to-phenotype network of human congenital heart defects.Genome Med2010
19344873DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources.Am J Hum Genet2009
19925645An experimental loop design for the detection of constitutional chromosomal aberrations by array CGH.BMC Bioinformatics2009
18179897Autosomal-dominant microtia linked to five tandem copies of a copy-number-variable region at chromosome 4p16.Am J Hum Genet2008
18508807ENDEAVOUR update: a web resource for gene prioritization in multiple species.Nucleic Acids Res2008
18689812Comparison of vocabularies, representations and ranking algorithms for gene prioritization by text mining.Bioinformatics2008
18271954Text-mining assisted regulatory annotation.Genome Biol2008
18229693Integration of microarray and textual data improves the prognosis prediction of breast, lung and ovarian cancer patients.Pac Symp Biocomput2008
18398442A novel genomic disorder: a deletion of the SACS gene leading to spastic ataxia of Charlevoix-Saguenay.Eur J Hum Genet2008
17403693Mapping biomedical concepts onto the human genome by mining literature on chromosomal aberrations.Nucleic Acids Res2007
18286816The t(4;8) is mediated by homologous recombination between olfactory receptor gene clusters, but other 4p16 translocations occur at random.Genet Couns2007
17925352A framework for elucidating regulatory networks based on prior information and expression data.Ann N Y Acad Sci2007
17873653Array comparative genomic hybridization and computational genome annotation in constitutional cytogenetics: suggesting candidate genes for novel submicroscopic chromosomal imbalance syndromes.Genet Med2007
16490798Emerging 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.J Med Genet2006
15750031Molecular karyotyping: array CGH quality criteria for constitutional genetic diagnosis.J Histochem Cytochem2005
15910681arrayCGHbase: an analysis platform for comparative genomic hybridization microarrays.BMC Bioinformatics2005
15186494TXTGate: profiling gene groups with text-based information.Genome Biol2004
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Collaborators

Yves Moreau
KU Leuven - University of Leuven
Co-authored papers 12
Bart De Moor
STADIUS Center for Dynamical Systems
Co-authored papers 11
Bert Coessens
Katholieke Universiteit Leuven
Co-authored papers 4
Nicole de Leeuw
Radboud University Medical Center
Co-authored papers 3
Nigel P Carter
4Wellcome Trust Sanger Institute
Co-authored papers 3
Jo Vandesompele
Co-authored papers 3
Helen V Firth
Clinical Genetics, Addenbrooke's Hospital, Cambridge University Hospitals
Co-authored papers 3
L??on-Charles Tranchevent
University of Luxembourg
Co-authored papers 3
Anneke T Vulto-van Silfhout
Radboud University Medical Center
Co-authored papers 2
Bert B A de Vries
Radboud University Medical Center
Co-authored papers 2
David H Ledbetter
University of Florida, College of Medicine-Jacksonville
Co-authored papers 2
Christa Lese Martin
Autism and Developmental Medicine Institute
Co-authored papers 2
Jayne Y Hehir-Kwa
Princess Maxima Center for Pediatric Oncology
Co-authored papers 2
Gert Matthijs
Center for Human Genetics, KU Leuven and University Hospitals Leuven
Co-authored papers 2
Laird G Jackson
The Children's Hospital of Philadelphia
Co-authored papers 2
Erin Rooney Riggs
Geisinger Autism & Developmental Medicine Institute
Co-authored papers 2
Peter Van Loo
The Francis Crick Institute
Co-authored papers 2
Hanns Lochm??ller
Children's Hospital of Eastern Ontario Research Institute
Co-authored papers 1
Andrew D Mumford
University of Bristol
Co-authored papers 1
Lillian L Siu
Princess Margaret Cancer Centre, University Ave
Co-authored papers 1
Caroline F Wright
University of Exeter, Royal Devon and Exeter Hospital
Co-authored papers 1
Steven J M Jones
University of British Columbia
Co-authored papers 1
Jane A Hurst
Great Ormond Street Hospital NHS Foundation Trust
Co-authored papers 1
Paul N Schofield
University of Cambridge
Co-authored papers 1
Rachel Thompson
Children's Hospital of Eastern Ontario Research Institute
Co-authored papers 1
Jeff Campbell
Co-authored papers 1
Sahar Mansour
St George's University Hospitals NHS Foundation Trust
Co-authored papers 1
Erika Souche
Center for Human Genetics
Co-authored papers 1
Philippe L Bedard
Princess Margaret Cancer Centre, University Health Network
Co-authored papers 1
Suzanne Kamel-Reid
Toronto General Hospital, University Health Network, University of Toronto
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