Steven Van Vooren

4.1k citations

25 papers · 2.0k indexed · 1 hit paper · h-index 16

Genetics top 1%
Molecular Biology top 10%
Pediatrics, Perinatology and Child Health top 5%
Cancer Research top 10%
Plant Science top 10%

Co-authors: Yves Moreau Nigel P. Carter Helen V. Firth A. Paul Bevan Shola M. Richards Manuel Corpas Diana Rajan Stephen Clayton
Topics: Genomic variations and chromosomal abnormalities (11 papers)Genomics and Rare Diseases (9 papers)Bioinformatics and Genomic Networks (8 papers)
Cited by: Genetics Molecular Biology Cancer Research
Journals: Nucleic Acids Research Bioinformatics Annals of the New York Academy of Sciences
Partner nations: Belgium United Kingdom United States

In The Last Decade

Steven Van Vooren

25 papers receiving 2.0k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

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

2009 1.2k citations Helen V. Firth, Shola M. Richards et al. The American Journal of Human Genetics profile →

Peers

Countries citing papers authored by Steven Van Vooren

Since Specialization

Citations

This map shows the geographic impact of Steven Van Vooren's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Steven Van Vooren with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Steven Van Vooren more than expected).

Fields of papers citing papers by Steven Van Vooren

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Steven Van Vooren. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Steven Van Vooren. The network helps show where Steven Van Vooren may publish in the future.

Co-authorship network of co-authors of Steven Van Vooren

This figure shows the co-authorship network connecting the top 25 collaborators of Steven Van Vooren. A scholar is included among the top collaborators of Steven Van Vooren based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Steven Van Vooren. Steven Van Vooren is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Development, Validation, and Implementation of an Augmented Multiwell, Multitarget Quantitative PCR for the Analysis of Human Papillomavirus Genotyping through Software Automation, Data Science, and Artificial Intelligence 2024 ·Journal of Molecular Diagnostics ·(unknown),(unknown),Steven Van Vooren,Kimberly Pelak,A.W. Broekmans,(unknown),Davy Vanden Broeck,(unknown),Johannes Bogers,(unknown),(unknown),(unknown),(unknown)	3
2	Somatic Tumor Variant Filtration Strategies to Optimize Tumor-Only Molecular Profiling Using Targeted Next-Generation Sequencing Panels 2018 ·Journal of Molecular Diagnostics ·Mahadeo A. Sukhai,Maksym Misyura,Mariam Thomas,Swati Garg,Tong Zhang,Natalie Stickle,Carl Virtanen,Philippe L. Bédard,Lillian L. Siu,Tina Smets,Gert Thijs,Steven Van Vooren,Suzanne Kamel‐Reid,Tracy Stockley	29
3	An update on ECARUCA, the European Cytogeneticists Association Register of Unbalanced Chromosome Aberrations 2013 ·European Journal of Medical Genetics ·Anneke T. Vulto‐van Silfhout,Conny M.A. van Ravenswaaij,Jayne Y. Hehir‐Kwa,Eugène T.P. Verwiel,(unknown),Steven Van Vooren,Albert Schinzel,Bert B.A. de Vries,Nicole de Leeuw	23
4	Diagnostic interpretation of array data using public databases and internet sources 2012 ·Human Mutation ·Nicole de Leeuw,Trijnie Dijkhuizen,Jayne Y. Hehir‐Kwa,Nigel P. Carter,Lars Feuk,Helen V. Firth,Robert M. Kuhn,David H. Ledbetter,Alastair J. Martin,Conny M.A. van Ravenswaaij‐Arts,Stephen W. Scherer,Soheil Shams,Steven Van Vooren,Rolf H. Sijmons,Morris A. Swertz,Ros Hastings	83
5	Phenotypic information in genomic variant databases enhances clinical care and research: The international standards for cytogenomic arrays consortium experience 2012 ·Human Mutation ·Erin Rooney Riggs,Laird Jackson,David T. Miller,Steven Van Vooren	41
6	Collaboratively charting the gene-to-phenotype network of human congenital heart defects 2010 ·Genome Medicine ·Roland Barriot,Jeroen Breckpot,Bernard Thienpont,Sylvain Brohée,Steven Van Vooren,Bert Coessens,Léon-Charles Tranchevent,Peter Van Loo,Marc Gewillig,Koenraad Devriendt,Yves Moreau	23
7	An experimental loop design for the detection of constitutional chromosomal aberrations by array CGH 2009 ·BMC Bioinformatics ·Joke Allemeersch,Steven Van Vooren,Femke Hannes,Bart De Moor,Joris Vermeesch,Yves Moreau	12
8	DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resourcesbreakdown → 2009 ·The American Journal of Human Genetics ·Helen V. Firth,Shola M. Richards,A. Paul Bevan,Stephen Clayton,Manuel Corpas,Diana Rajan,Steven Van Vooren,Yves Moreau,(unknown),Nigel P. Carter	1200
9	Autosomal-Dominant Microtia Linked to Five Tandem Copies of a Copy-Number-Variable Region at Chromosome 4p16 2008 ·The American Journal of Human Genetics ·Irina Balikova,Kevin Martens,Cindy Melotte,Mustapha Amyere,Steven Van Vooren,Yves Moreau,David Vetrie,Heike Fiegler,Nigel P. Carter,Thomas Liehr,Miikka Vikkula,Gert Matthijs,Jean‐Pierre Fryns,Ingele Casteels,Koenraad Devriendt,Joris Vermeesch	30
10	A novel genomic disorder: a deletion of the SACS gene leading to Spastic Ataxia of Charlevoix–Saguenay 2008 ·European Journal of Human Genetics ·Jeroen Breckpot,Yoshihisa Takiyama,Bernard Thienpont,Steven Van Vooren,Joris Vermeesch,Els Ortibus,Koenraad Devriendt	41
11	Text-mining assisted regulatory annotation 2008 ·Genome biology ·Stein Aerts,Maximilian Haeussler,Steven Van Vooren,Obi L. Griffith,Paco Hulpiau,Steven J.M. Jones,Stephen B. Montgomery,Casey Bergman	25
12	ENDEAVOUR update: a web resource for gene prioritization in multiple species 2008 ·Nucleic Acids Research ·Léon-Charles Tranchevent,Roland Barriot,Shuguang Yu,Steven Van Vooren,Peter Van Loo,Bert Coessens,Bart De Moor,Stein Aerts,Yves Moreau	160
13	A Framework for Elucidating Regulatory Networks Based on Prior Information and Expression Data 2007 ·Annals of the New York Academy of Sciences ·Olivier Gevaert,Steven Van Vooren,Bart De Moor	14
14	Mapping biomedical concepts onto the human genome by mining literature on chromosomal aberrations 2007 ·Nucleic Acids Research ·Steven Van Vooren,Bernard Thienpont,Björn Menten,Frank Speleman,Bart De Moor,Joris Vermeesch,Yves Moreau	20
15	Array comparative genomic hybridization and computational genome annotation in constitutional cytogenetics: suggesting candidate genes for novel submicroscopic chromosomal imbalance syndromes 2007 ·Genetics in Medicine ·Steven Van Vooren,Bert Coessens,Bart De Moor,Yves Moreau,Joris Vermeesch	12
16	INTEGRATION OF MICROARRAY AND TEXTUAL DATA IMPROVES THE PROGNOSIS PREDICTION OF BREAST, LUNG AND OVARIAN CANCER PATIENTS 2007 ·PubMed ·Olivier Gevaert,Steven Van Vooren,Bart De Moor	4
17	The t(4;8) is mediated by homologous recombination between olfactory receptor gene clusters, but other 4p16 translocations occur at random. 2007 ·PubMed ·Nicole Maas,Steven Van Vooren,Femke Hannes,Griet Van Buggenhout,M. Myśliwiec,Yves Moreau,(unknown),Alina T. Midro,(unknown),(unknown),Michael Parker,Yves Sznajer,Koenraad Devriendt,J P Fryns,Joris Vermeesch	16
18	arrayCGHbase: an analysis platform for comparative genomic hybridization microarrays 2005 ·BMC Bioinformatics ·Björn Menten,Filip Pattyn,Katleen De Preter,(unknown),Evi Michels,Karen Buysse,Geert Mortier,Anne De Paepe,Steven Van Vooren,Joris Vermeesch,Yves Moreau,Bart De Moor,Stefan Vermeulen,Frank Speleman,Jo Vandesompele	65
19	TXTGate: profiling gene groups with text-based information 2004 ·Genome biology ·Patrick Glenisson,Bert Coessens,Steven Van Vooren,Janick Mathys,Yves Moreau,Bart De Moor	48
20	Text-based gene profiling with domain-specific views 2003 ·International Semantic Web Conference ·Patrick Glenisson,Bert Coessens,Steven Van Vooren,Yves Moreau,Bart De Moor	2

About Steven Van Vooren

Steven Van Vooren is a scholar working on Genetics, Molecular Biology and Cancer Research, having authored 25 papers that have together received 2.0k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (11 papers), Genomics and Rare Diseases (9 papers) and Bioinformatics and Genomic Networks (8 papers). The work is most often cited by research in Genetics (1.3k citations), Molecular Biology (1.2k citations) and Cancer Research (195 citations). Steven Van Vooren has collaborated with scholars based in Belgium, United Kingdom and United States. Frequent co-authors include Yves Moreau, Nigel P. Carter, Helen V. Firth, A. Paul Bevan, Shola M. Richards, Manuel Corpas, Diana Rajan, Stephen Clayton, Bart De Moor and Bert Coessens. Their work appears in journals such as Nucleic Acids Research, Bioinformatics and Annals of the New York Academy of Sciences.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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