Björn Menten

发表

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

Tom Sante, Wigard P. Kloosterman, Sarah Vergult, 2014, PloS one.

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

Lennart Martens, Xiaowei Wang, Jo Vandesompele, 2012, Nucleic Acids Res..

A visualization platform for interpretation of structural genomic data

Tom Sante, Sarah Vergult, Björn Menten, 2011 .

Smoothing waves in array CGH tumor profiles

Marieke E. Timmerman, Paul H. C. Eilers, Björn Menten, 2009, Bioinform..

Flexible analysis of digital PCR experiments using generalized linear mixed models

Olivier Thas, Björn Menten, Matthijs Vynck, 2016, Biomolecular detection and quantification.

arrayCGHbase: an analysis platform for comparative genomic hybridization microarrays

Bart De Moor, Yves Moreau, Jo Vandesompele, 2005, BMC Bioinformatics.

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

Björn Menten, Wouter Steyaert, Annekatrien Boel, 2018, Scientific Reports.

Positional and functional mapping of a neuroblastoma differentiation gene on chromosome 11

Frank Speleman, Björn Menten, Wim Waelput, 2005, BMC Genomics.

Translocation–excision–deletion–amplification mechanism leading to nonsyntenic coamplification of MYC and ATBF1

Frank Speleman, Björn Menten, Jo Vandesompele, 2006, Genes, chromosomes & cancer.

Mate pair sequencing for the detection of chromosomal aberrations in patients with intellectual disability and congenital malformations

Edwin Cuppen, Tom Sante, Sarah Vergult, 2013, European Journal of Human Genetics.

ArrayCGH‐based classification of neuroblastoma into genomic subgroups

Frank Speleman, Björn Menten, Rogier Versteeg, 2007, Genes, chromosomes & cancer.

Molecular Karyotyping: Array CGH Quality Criteria for Constitutional Genetic Diagnosis

Bart De Moor, Frank Speleman, Björn Menten, 2005, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

Shallow Whole Genome Sequencing on Circulating Cell-Free DNA Allows Reliable Noninvasive Copy-Number Profiling in Neuroblastoma Patients

Tom Sante, Frank Speleman, Björn Menten, 2017, Clinical Cancer Research.

The H3K27me3 demethylase UTX is a gender-specific tumor suppressor in T-cell acute lymphoblastic leukemia.

Fang Fang, Frank Speleman, Björn Menten, 2014, Blood.

Identification of an unbalanced X-autosome translocation by array CGH in a boy with a syndromic form of chondrodysplasia punctata brachytelephalangic type.

Frank Speleman, Björn Menten, Jo Vandesompele, 2005, European journal of medical genetics.

The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies

Edwin Cuppen, Claire Redin, Ryan L. Collins, 2016, Nature Genetics.

Challenges for CNV interpretation in clinical molecular karyotyping: lessons learned from a 1001 sample experience.

Frank Speleman, Björn Menten, Bart Loeys, 2009, European journal of medical genetics.

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

Bart De Moor, Yves Moreau, Joris Vermeesch, 2007, Nucleic acids research.

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

Tom Sante, Sarah Vergult, Björn Menten, 2016, Prenatal diagnosis.

Disease-Causing 7.4 kb Cis-Regulatory Deletion Disrupting Conserved Non-Coding Sequences and Their Interaction with the FOXL2 Promotor: Implications for Mutation Screening

Stylianos E. Antonarakis, Filip Pattyn, Frank Speleman, 2009, PLoS genetics.