Björn Menten
Björn Menten
Center for Medical Genetics, Ghent University
Verified email at ugent.be - Homepage
Title
Cited by
Cited by
Year
Recurrent rearrangements of chromosome 1q21. 1 and variable pediatric phenotypes
HC Mefford, AJ Sharp, C Baker, A Itsara, Z Jiang, K Buysse, S Huang, ...
New England Journal of Medicine 359 (16), 1685-1699, 2008
7362008
LNCipedia: a database for annotated human lncRNA transcript sequences and structures
PJ Volders, K Helsens, X Wang, B Menten, L Martens, K Gevaert, ...
Nucleic acids research 41 (D1), D246-D251, 2013
4822013
Emerging patterns of cryptic chromosomal imbalance in patients with idiopathic mental retardation and multiple congenital anomalies: a new series of 140 patients and review of …
B Menten, N Maas, B Thienpont, K Buysse, J Vandesompele, C Melotte, ...
Journal of medical genetics 43 (8), 625-633, 2006
4422006
A link between host plant adaptation and pesticide resistance in the polyphagous spider mite Tetranychus urticae
W Dermauw, N Wybouw, S Rombauts, B Menten, J Vontas, M Grbić, ...
Proceedings of the National Academy of Sciences 110 (2), E113-E122, 2013
2982013
Extending the phenotype of recurrent rearrangements of 16p11. 2: deletions in mentally retarded patients without autism and in normal individuals
EK Bijlsma, ACJ Gijsbers, JHM Schuurs-Hoeijmakers, A Van Haeringen, ...
European journal of medical genetics 52 (2-3), 77-87, 2009
2722009
Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome
BWM Van Bon, HC Mefford, B Menten, DA Koolen, AJ Sharp, ...
Journal of medical genetics 46 (8), 511-523, 2009
2662009
Constitutional chromothripsis rearrangements involve clustered double-stranded DNA breaks and nonhomologous repair mechanisms
WP Kloosterman, M Tavakoli-Yaraki, MJ Van Roosmalen, ...
Cell reports 1 (6), 648-655, 2012
1942012
Fourteen new cases contribute to the characterization of the 7q11. 23 microduplication syndrome
N Van der Aa, L Rooms, G Vandeweyer, J van den Ende, E Reyniers, ...
European journal of medical genetics 52 (2-3), 94-100, 2009
1912009
Molecular karyotyping: array CGH quality criteria for constitutional genetic diagnosis
JR Vermeesch, C Melotte, G Froyen, S Van Vooren, B Dutta, N Maas, ...
Journal of Histochemistry & Cytochemistry 53 (3), 413-422, 2005
1862005
The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies
C Redin, H Brand, RL Collins, T Kammin, E Mitchell, JC Hodge, ...
Nature genetics 49 (1), 36-45, 2017
1772017
An integrative genomics screen uncovers ncRNA T-UCR functions in neuroblastoma tumours
P Mestdagh, E Fredlund, F Pattyn, A Rihani, T Van Maerken, J Vermeulen, ...
Oncogene 29 (24), 3583-3592, 2010
1462010
Targeted expression of mutated ALK induces neuroblastoma in transgenic mice
LC Heukamp, T Thor, A Schramm, K De Preter, C Kumps, B De Wilde, ...
Science translational medicine 4 (141), 141ra91-141ra91, 2012
1432012
The H3K27me3 demethylase UTX is a gender-specific tumor suppressor in T-cell acute lymphoblastic leukemia
J Van der Meulen, V Sanghvi, K Mavrakis, K Durinck, F Fang, ...
Blood 125 (1), 13-21, 2015
1422015
Exonic deletions in AUTS2 cause a syndromic form of intellectual disability and suggest a critical role for the C terminus
G Beunders, E Voorhoeve, C Golzio, LM Pardo, JA Rosenfeld, ...
The American Journal of Human Genetics 92 (2), 210-220, 2013
1242013
Challenges for CNV interpretation in clinical molecular karyotyping: lessons learned from a 1001 sample experience
K Buysse, B Delle Chiaie, R Van Coster, B Loeys, A De Paepe, G Mortier, ...
European journal of medical genetics 52 (6), 398-403, 2009
1092009
Alternative routes to induce naive pluripotency in human embryonic stem cells
G Duggal, S Warrier, S Ghimire, D Broekaert, M Van der Jeught, ...
Stem cells 33 (9), 2686-2698, 2015
1082015
arrayCGHbase: an analysis platform for comparative genomic hybridization microarrays
B Menten, F Pattyn, K De Preter, P Robbrecht, E Michels, K Buysse, ...
BMC bioinformatics 6 (1), 1-9, 2005
1062005
Disease-causing 7.4 kb cis-regulatory deletion disrupting conserved non-coding sequences and their interaction with the FOXL2 promotor: implications for mutation screening
B D'haene, C Attanasio, D Beysen, J Dostie, E Lemire, P Bouchard, ...
PLoS Genet 5 (6), e1000522, 2009
1042009
Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly
DA Braun, J Rao, G Mollet, D Schapiro, MC Daugeron, W Tan, ...
Nature genetics 49 (10), 1529, 2017
962017
Mutations in GTPBP3 Cause a Mitochondrial Translation Defect Associated with Hypertrophic Cardiomyopathy, Lactic Acidosis, and Encephalopathy
R Kopajtich, TJ Nicholls, J Rorbach, MD Metodiev, P Freisinger, H Mandel, ...
The American Journal of Human Genetics 95 (6), 708-720, 2014
932014
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