DECIPHER : Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources von FIRTH, Helen V, RICHARDS, Shola M, BEVAN, A. Paul, CLAYTON, Stephen, CORPAS, Manuel, RAJAN, Diana, VAN VOOREN, Steven, MOREAU, Yves, PETTETT, Roger M, CARTER, Nigel P

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Endeavour update: a web resource for gene prioritization in multiple species von Tranchevent, Léon-Charles, Barriot, Roland, Yu, Shi, Van Vooren, Steven, Van Loo, Peter, Coessens, Bert, De Moor, Bart, Aerts, Stein, Moreau, Yves

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Critical points for an accurate human genome analysis von White, Stefan J., Laros, Jeroen F.J., Bakker, Egbert, Cambon‐Thomsen, Anne, Eden, Martin, Leonard, Samantha, Lochmüller, Hanns, Matthijs, Gert, Mattocks, Christopher, Patton, Simon, Payne, Katherine, Scheffer, Hans, Souche, Erica, Thomassen, Ellen, Thompson, Rachel, Traeger‐Synodinos, Jan, Vooren, Steven, Janssen, Bart, den Dunnen, Johan T.

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Comparison of vocabularies, representations and ranking algorithms for gene prioritization by text mining von Yu, Shi, Van Vooren, Steven, Tranchevent, Leon-Charles, De Moor, Bart, Moreau, Yves

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Reliable and Scalable SARS-CoV-2 qPCR Testing at a High Sample Throughput: Lessons Learned from the Belgian Initiative von Van Vooren, Steven, Grayson, James, Van Ranst, Marc, Dequeker, Elisabeth, Laenen, Lies, Janssen, Reile, Gillet, Laurent, Bureau, Fabrice, Coppieters, Wouter, Devos, Nathalie, Hengchen, Benjamin, Wattiau, Pierre, Méhauden, Sibylle, Verlinden, Yvan, Van Baelen, Kurt, Pattery, Theresa, Valentin, Jean-Pierre, Janssen, Kris, Geraerts, Martine, Smeraglia, John, Hellemans, Jan, Wytynck, Pieter, Mestdagh, Pieter, Besbrugge, Nienke, Höfer, René, Nollet, Friedel, Vandesompele, Jo, De Smet, Pieter, Lebon, John, Vandewynckele, Emmanuel, Verstrepen, Steven, Uten, Wouter, Capron, Arnaud, Malonne, Hugues, Poels, Jeroen, André, Emmanuel

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Autosomal-Dominant Microtia Linked to Five Tandem Copies of a Copy-Number-Variable Region at Chromosome 4p16 von Balikova, Irina, Martens, Kevin, Melotte, Cindy, Amyere, Mustapha, Van Vooren, Steven, Moreau, Yves, Vetrie, David, Fiegler, Heike, Carter, Nigel P., Liehr, Thomas, Vikkula, Miikka, Matthijs, Gert, Fryns, Jean-Pierre, Casteels, Ingele, Devriendt, Koen, Vermeesch, Joris Robert

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arrayCGHbase: an analysis platform for comparative genomic hybridization microarrays von Menten, Björn, Pattyn, Filip, De Preter, Katleen, Robbrecht, Piet, Michels, Evi, Buysse, Karen, Mortier, Geert, De Paepe, Anne, van Vooren, Steven, Vermeesch, Joris, Moreau, Yves, De Moor, Bart, Vermeulen, Stefan, Speleman, Frank, Vandesompele, Jo

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Mapping biomedical concepts onto the human genome by mining literature on chromosomal aberrations von Van Vooren, Steven, Thienpont, Bernard, Menten, Björn, Speleman, Frank, Moor, Bart De, Vermeesch, Joris, Moreau, Yves

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An experimental loop design for the detection of constitutional chromosomal aberrations by array CGH von Allemeersch, Joke, Van Vooren, Steven, Hannes, Femke, De Moor, Bart, Vermeesch, Joris Robert, Moreau, Yves

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The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data von Köhler, Sebastian, Doelken, Sandra C, Mungall, Christopher J, Bauer, Sebastian, Firth, Helen V, Bailleul-Forestier, Isabelle, Black, Graeme C M, Brown, Danielle L, Brudno, Michael, Campbell, Jennifer, FitzPatrick, David R, Eppig, Janan T, Jackson, Andrew P, Freson, Kathleen, Girdea, Marta, Helbig, Ingo, Hurst, Jane A, Jähn, Johanna, Jackson, Laird G, Kelly, Anne M, Ledbetter, David H, Mansour, Sahar, Martin, Christa L, Moss, Celia, Mumford, Andrew, Ouwehand, Willem H, Park, Soo-Mi, Riggs, Erin Rooney, Scott, Richard H, Sisodiya, Sanjay, Van Vooren, Steven, Wapner, Ronald J, Wilkie, Andrew O M, Wright, Caroline F, Vulto-van Silfhout, Anneke T, de Leeuw, Nicole, de Vries, Bert B A, Washingthon, Nicole L, Smith, Cynthia L, Westerfield, Monte, Schofield, Paul, Ruef, Barbara J, Gkoutos, Georgios V, Haendel, Melissa, Smedley, Damian, Lewis, Suzanna E, Robinson, Peter N

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Development, Validation, and Implementation of an Augmented Multiwell, Multitarget Quantitative PCR for the Analysis of Human Papillomavirus Genotyping through Software Automation,... von Pereira, A. Rita, Redzic, Nina, Van Vooren, Steven, Pelak, Kimberly, Broekmans, An, Desloovere, Guus, Vanden Broeck, Davy, Kehoe, Kaat, Bogers, Johannes, Coppens, Astrid, Vreysen, Samme, Mailleux, Jo, Uten, Wouter

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Phenotypic information in genomic variant databases enhances clinical care and research: The international standards for cytogenomic arrays consortium experience von Riggs, Erin Rooney, Jackson, Laird, Miller, David T., Van Vooren, Steven

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Somatic Tumor Variant Filtration Strategies to Optimize Tumor-Only Molecular Profiling Using Targeted Next-Generation Sequencing Panels von Sukhai, Mahadeo A., Misyura, Maksym, Thomas, Mariam, Garg, Swati, Zhang, Tong, Stickle, Natalie, Virtanen, Carl, Bedard, Philippe L., Siu, Lillian L., Smets, Tina, Thijs, Gert, Van Vooren, Steven, Kamel-Reid, Suzanne, Stockley, Tracy L.

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Diagnostic interpretation of array data using public databases and internet sources von de Leeuw, Nicole, Dijkhuizen, Trijnie, Hehir-Kwa, Jayne Y., Carter, Nigel P., Feuk, Lars, Firth, Helen V., Kuhn, Robert M., Ledbetter, David H., Martin, Christa Lese, van Ravenswaaij-Arts, Conny M. A., Scherer, Steven W., Shams, Soheil, Van Vooren, Steven, Sijmons, Rolf, Swertz, Morris, Hastings, Ros

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A novel genomic disorder : a deletion of the SACS gene leading to Spastic Ataxia of Charlevoix-Saguenay von BRECKPOT, Jeroen, TAKIYAMA, Yoshihisa, THIENPONT, Bernard, VAN VOOREN, Steven, VERMEESCH, Joris Robert, ORTIBUS, Els, DEVRIENDT, Koenraad

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Somatic Tumor Variant Filtration Strategies to Optimize Tumor-Only Molecular Profiling Using Targeted Next-Generation Sequencing Panels von Sukhai, Mahadeo A, Misyura, Maksym, Thomas, Mariam, Garg, Swati, Zhang, Tong, Stickle, Natalie, Virtanen, Carl, Bedard, Philippe L, Siu, Lillian L, Smets, Tina, Thijs, Gert, Van Vooren, Steven, Kamel-Reid, Suzanne, Stockley, Tracy L

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Reliable and Scalable SARS-CoV-2 qPCR Testing at a High Sample Throughput: Lessons Learned from the Belgian Initiative von Van Vooren, Steven, Grayson, James, Van Ranst, Marc, Dequeker, Elisabeth, Laenen, Lies, Janssen, Reile, Gillet, Laurent, Bureau, Fabrice, Coppieters, Wouter, Devos, Nathalie, Hengchen, Benjamin, Wattiau, Pierre, Mehauden, Sibylle, Verlinden, Yvan, Van Baelen, Kurt, Pattery, Theresa, Valentin, Jean-Pierre, Janssen, Kris, Geraerts, Martine, Smeraglia, John, Hellemans, Jan, Wytynck, Pieter, Mestdagh, Pieter, Besbrugge, Nienke, Hoefer, Rene, Nollet, Friedel, Vandesompele, Jo, De Smet, Pieter, Lebon, John, Vandewynckele, Emmanuel, Verstrepen, Steven, Uten, Wouter, Capron, Arnaud, Malonne, Hugues, Poels, Jeroen, Andre, Emmanuel

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A Framework for Elucidating Regulatory Networks Based on Prior Information and Expression Data von GEVAERT, OLIVIER, VAN VOOREN, STEVEN, DE MOOR, BART

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Critical points for an accurate human genome analysis von White, Stefan J, Laros, Jeroen F.J, Bakker, Egbert, Cambon-Thomsen, Anne, Eden, Martin, Leonard, Samantha, Lochmüller, Hanns, Matthijs, Gert, Mattocks, Christopher, Patton, Simon, Payne, Katherine, Scheffer, Hans, Souche, Erica, Thomassen, Ellen, Thompson, Rachel, Traeger-Synodinos, Jan, Van Vooren, Steven, Janssen, Bart, den Dunnen, Johan T

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Critical points for an accurate human genome analysis von White, Stefan J, Laros, Jeroen F J, Bakker, Egbert, Cambon-Thomsen, Anne, Eden, Martin, Leonard, Samantha, Lochmüller, Hanns, Matthijs, Gert, Mattocks, Christopher, Patton, Simon, Payne, Katherine, Scheffer, Hans, Souche, Erica, Thomassen, Ellen, Thompson, Rachel, Traeger-Synodinos, Jan, van Vooren, Steven, Janssen, Bart, den Dunnen, Johan T

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