Identification and complete genome sequencing of paramyxoviruses in mallard ducks (Anas platyrhynchos) using random access amplification and next generation sequencing technologies

Por Rosseel, Toon, Lambrecht, Bénédicte, Vandenbussche, Frank, van den Berg, Thierry, Van Borm, Steven
Publicado em 2011

DNase SISPA-Next Generation Sequencing Confirms Schmallenberg Virus in Belgian Field Samples and Identifies Genetic Variation in Europe

Por Rosseel, Toon, Scheuch, Matthias, Höper, Dirk, De Regge, Nick, Caij, Ann Brigitte, Vandenbussche, Frank, Van Borm, Steven
Publicado em 2012

The Origin of Biased Sequence Depth in Sequence-Independent Nucleic Acid Amplification and Optimization for Efficient Massive Parallel Sequencing

Por Rosseel, Toon, Van Borm, Steven, Vandenbussche, Frank, Hoffmann, Bernd, van den Berg, Thierry, Beer, Martin, Höper, Dirk
Publicado em 2013

Complete Genome Sequence of Bovine Polyomavirus Type 1 from Aborted Cattle, Isolated in Belgium in 2014

Por Van Borm, Steven, Rosseel, Toon, Behaeghel, Isabelle, Saulmont, Marc, Delooz, Laurent, Petitjean, Thierry, Mathijs, Elisabeth, Vandenbussche, Frank
Publicado no Genome Announc (2016)

Extensive Genetic Variability Linked to IS26 Insertions in the fljB Promoter Region of Atypical Monophasic Variants of Salmonella enterica Serovar Typhimurium

Por Boland, Cécile, Bertrand, Sophie, Mattheus, Wesley, Dierick, Katelijne, Jasson, Vicky, Rosseel, Toon, Van Borm, Steven, Mahillon, Jacques, Wattiau, Pierre
Publicado no Appl Environ Microbiol (2015)

Complete Coding Sequences of One H9 and Three H7 Low-Pathogenic Influenza Viruses Circulating in Wild Birds in Belgium, 2009 to 2012

Por Van Borm, Steven, Rosseel, Toon, Marché, Sylvie, Steensels, Mieke, Vangeluwe, Didier, Linden, Annick, van den Berg, Thierry, Lambrecht, Bénédicte
Publicado no Genome Announc (2016)

Complete Genome Sequences of Three African Foot-and-Mouth Disease Viruses from Clinical Samples Isolated in 2009 and 2010

Por Van Borm, Steven, Rosseel, Toon, Haegeman, Andy, Fana, Mpolokang Elliot, Seoke, Latoa, Hyera, Joseph, Matlho, George, Vandenbussche, Frank, De Clercq, Kris
Publicado no Genome Announc (2016)

Next-Generation Sequencing in Veterinary Medicine: How Can the Massive Amount of Information Arising from High-Throughput Technologies Improve Diagnosis, Control, and Management of...

Por Van Borm, Steven, Belák, Sándor, Freimanis, Graham, Fusaro, Alice, Granberg, Fredrik, Höper, Dirk, King, Donald P., Monne, Isabella, Orton, Richard, Rosseel, Toon
Publicado no Veterinary Infection Biology: Molecular Diagnostics and High-Throughput Strategies (2014)

NR5A1 is a novel disease gene for 46,XX testicular and ovotesticular disorders of sex development

Por Baetens, Dorien, Stoop, Hans, Peelman, Frank, Todeschini, Anne-Laure, Rosseel, Toon, Coppieters, Frauke, Veitia, Reiner A., Looijenga, Leendert H.J., De Baere, Elfride, Cools, Martine
Publicado no Genet Med (2017)

Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal disease

Por Van de Sompele, Stijn, Smith, Claire, Karali, Marianthi, Corton, Marta, Van Schil, Kristof, Peelman, Frank, Cherry, Timothy, Rosseel, Toon, Verdin, Hannah, Derolez, Julien, Van Laethem, Thalia, Khan, Kamron N., McKibbin, Martin, Toomes, Carmel, Ali, Manir, Torella, Annalaura, Testa, Francesco, Jimenez, Belen, Simonelli, Francesca, De Zaeytijd, Julie, Van den Ende, Jenneke, Leroy, Bart P., Coppieters, Frauke, Ayuso, Carmen, Inglehearn, Chris F., Banfi, Sandro, De Baere, Elfride
Publicado no Genet Med (2018)

Correction: Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal disease

Por Van de Sompele, Stijn, Smith, Claire, Karali, Marianthi, Corton, Marta, Van Schil, Kristof, Peelman, Frank, Cherry, Timothy, Rosseel, Toon, Verdin, Hannah, Derolez, Julien, Van Laethem, Thalia, Khan, Kamron N., McKibbin, Martin, Toomes, Carmel, Ali, Manir, Torella, Annalaura, Testa, Francesco, Jimenez, Belen, Simonelli, Francesca, De Zaeytijd, Julie, Van den Ende, Jenneke, Leroy, Bart P., Coppieters, Frauke, Ayuso, Carmen, Inglehearn, Chris F., Banfi, Sandro, De Baere, Elfride
Publicado no Genet Med (2019)

Functional characterization of the first missense variant in CEP78, a founder allele associated with cone‐rod dystrophy, hearing loss, and reduced male fertility

Por Ascari, Giulia, Peelman, Frank, Farinelli, Pietro, Rosseel, Toon, Lambrechts, Nina, Wunderlich, Kirsten A., Wagner, Matias, Nikopoulos, Konstantinos, Martens, Pernille, Balikova, Irina, Derycke, Lara, Holtappels, Gabriële, Krysko, Olga, Van Laethem, Thalia, De Jaegere, Sarah, Guillemyn, Brecht, De Rycke, Riet, De Bleecker, Jan, Creytens, David, Van Dorpe, Jo, Gerris, Jan, Bachert, Claus, Neuhofer, Christiane, Walraedt, Sophie, Bischoff, Almut, Pedersen, Lotte B., Klopstock, Thomas, Rivolta, Carlo, Leroy, Bart P., De Baere, Elfride, Coppieters, Frauke
Publicado no Hum Mutat (2020)

ABCA4-associated disease as a model for missing heritability in autosomal recessive disorders: novel noncoding splice, cis-regulatory, structural, and recurrent hypomorphic variant...

Por Bauwens, Miriam, Garanto, Alejandro, Sangermano, Riccardo, Naessens, Sarah, Weisschuh, Nicole, De Zaeytijd, Julie, Khan, Mubeen, Sadler, Françoise, Balikova, Irina, Van Cauwenbergh, Caroline, Rosseel, Toon, Bauwens, Jim, De Leeneer, Kim, De Jaegere, Sarah, Van Laethem, Thalia, De Vries, Meindert, Carss, Keren, Arno, Gavin, Fakin, Ana, Webster, Andrew R., de Ravel de l’Argentière, Thomy J. L., Sznajer, Yves, Vuylsteke, Marnik, Kohl, Susanne, Wissinger, Bernd, Cherry, Timothy, Collin, Rob W. J., Cremers, Frans P. M., Leroy, Bart P., De Baere, Elfride
Publicado no Genet Med (2019)