Familial cases of a submicroscopic Xp22.2 deletion: genotype-phenotype correlation in microphthalmia with linear skin defects syndrome

por Vergult, Sarah, Leroy, Bart, Claerhout, Ilse, Menten, Björn
Publicado 2013

WisecondorX: improved copy number detection for routine shallow whole-genome sequencing

por Raman, Lennart, Dheedene, Annelies, De Smet, Matthias, Van Dorpe, Jo, Menten, Björn
Publicado 2019

Flexible analysis of digital PCR experiments using generalized linear mixed models

por Vynck, Matthijs, Vandesompele, Jo, Nijs, Nele, Menten, Björn, De Ganck, Ariane, Thas, Olivier
Publicado 2016

PREFACE: In silico pipeline for accurate cell‐free fetal DNA fraction prediction

por Raman, Lennart, Baetens, Machteld, De Smet, Matthias, Dheedene, Annelies, Van Dorpe, Jo, Menten, Björn
Publicado 2019

Expanding the Phenotype of B3GALNT2-Related Disorders

por D’haenens, Erika, Vergult, Sarah, Menten, Björn, Dheedene, Annelies, Kooy, R. Frank, Callewaert, Bert
Publicado 2022

Array comparative genomic hybridization and flow cytometry analysis of spontaneous abortions and mors in utero samples

por Menten, Björn, Swerts, Katrien, Chiaie, Barbara Delle, Janssens, Sandra, Buysse, Karen, Philippé, Jan, Speleman, Frank
Publicado 2009

Mapping biomedical concepts onto the human genome by mining literature on chromosomal aberrations

por Van Vooren, Steven, Thienpont, Bernard, Menten, Björn, Speleman, Frank, Moor, Bart De, Vermeesch, Joris, Moreau, Yves
Publicado 2007

Identification of long non-coding RNAs involved in neuronal development and intellectual disability

por D’haene, Eva, Jacobs, Eva Z., Volders, Pieter-Jan, De Meyer, Tim, Menten, Björn, Vergult, Sarah
Publicado 2016

LNCipedia: a database for annotated human lncRNA transcript sequences and structures

por Volders, Pieter-Jan, Helsens, Kenny, Wang, Xiaowei, Menten, Björn, Martens, Lennart, Gevaert, Kris, Vandesompele, Jo, Mestdagh, Pieter
Publicado 2013

Performance of a TthPrimPol-based whole genome amplification kit for copy number alteration detection using massively parallel sequencing

por Deleye, Lieselot, De Coninck, Dieter, Dheedene, Annelies, De Sutter, Petra, Menten, Björn, Deforce, Dieter, Van Nieuwerburgh, Filip
Publicado 2016

Targeted Genomic Screen Reveals Focal Long Non-Coding RNA Copy Number Alterations in Cancer Cell Lines

por Volders, Pieter-Jan, Lefever, Steve, Baute, Shalina, Nuytens, Justine, Vanderheyden, Katrien, Menten, Björn, Mestdagh, Pieter, Vandesompele, Jo
Publicado 2018

BATCH-GE: Batch analysis of Next-Generation Sequencing data for genome editing assessment

por Boel, Annekatrien, Steyaert, Woutert, De Rocker, Nina, Menten, Björn, Callewaert, Bert, De Paepe, Anne, Coucke, Paul, Willaert, Andy
Publicado 2016

Implementation of non‐invasive prenatal testing by semiconductor sequencing in a genetic laboratory

por Dheedene, Annelies, Sante, Tom, De Smet, Matthias, Vanbellinghen, Jean‐François, Grisart, Bernard, Vergult, Sarah, Janssens, Sandra, Menten, Björn
Publicado 2016

Publisher Correction: BATCH-GE: Batch analysis of Next-Generation Sequencing data for genome editing assessment

por Boel, Annekatrien, Steyaert, Wouter, De Rocker, Nina, Menten, Björn, Callewaert, Bert, De Paepe, Anne, Coucke, Paul, Willaert, Andy
Publicado 2018

Nonsyndromic bilateral and unilateral optic nerve aplasia: first familial occurrence and potential implication of CYP26A1 and CYP26C1 genes

por Meire, Françoise, Delpierre, Isabelle, Brachet, Cecile, Roulez, Françoise, Van Nechel, Christian, Depasse, Fanny, Christophe, Catherine, Menten, Björn, De Baere, Elfride
Publicado 2011

Pushing the boundaries. Concurrent Hodgkin lymphoma and breast cancer treatment with preservation of pregnancy: A case report

por LeJeune, Charlotte, Dierickx, Daan, Wildiers, Hans, Lannoo, Lore, Van Calsteren, Kristel, Vandecaveye, Vincent, Menten, Björn, Vermeesch, Joris, Amant, Frédéric
Publicado 2022

Combined subtractive cDNA cloning and array CGH: an efficient approach for identification of overexpressed genes in DNA amplicons

por De Preter, Katleen, Pattyn, Filip, Berx, Geert, Strumane, Kristin, Menten, Björn, Van Roy, Frans, De Paepe, Anne, Speleman, Frank, Vandesompele, Jo
Publicado 2004

Severe hepatopathy and neurological deterioration after start of valproate treatment in a 6-year-old child with mitochondrial tryptophanyl-tRNA synthetase deficiency

por Vantroys, Elise, Smet, Joél, Vanlander, Arnaud V., Vergult, Sarah, De Bruyne, Ruth, Roels, Frank, Stepman, Hedwig, Roeyers, Herbert, Menten, Björn, Van Coster, Rudy
Publicado 2018

Leigh syndrome followed by parkinsonism in an adult with homozygous c.626C>T mutation in MTFMT

por Hemelsoet, Dimitri M., Vanlander, Arnaud V., Smet, Joél, Vantroys, Elise, Acou, Marjan, Goethals, Ingeborg, Sante, Tom, Seneca, Sara, Menten, Bjorn, Van Coster, Rudy
Publicado 2018

ViVar: A Comprehensive Platform for the Analysis and Visualization of Structural Genomic Variation

por Sante, Tom, Vergult, Sarah, Volders, Pieter-Jan, Kloosterman, Wigard P., Trooskens, Geert, De Preter, Katleen, Dheedene, Annelies, Speleman, Frank, De Meyer, Tim, Menten, Björn
Publicado 2014