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Björn Menten

Research Profile

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Publications

TOP 3
Hannah Verdin; Diane Beysen; Claudia M B Carvalho; Barbara D'haene; Pablo Lapunzina; James R Lupski; Björn Menten; Julian Nevado; Yana Novikova; Tom Sante; Elfride De Baere
Microhomology-mediated mechanisms underlie non-recurrent disease-causing microdeletions of the FOXL2 gene or its regulatory domain.
Sarah Vergult; Joke B G M Verheij; Geert Mortier; Antonio Perez-Aytes; Tom Sante; Yves Sznajer; Christian Thiel; Hilde Van Esch; Daniela Q C M Barge-Schaapveld; Emilia K Bijlsma; Bram De Wilde; A Jeannette M Hoogeboom; Marjolijn Jongmans; Eva Klopocki; Alma Kuechler; Björn Menten
Complex genetics of radial ray deficiencies: screening of a cohort of 54 patients.
Wannes Dermauw; René Feyereisen; Miodrag Grbic; Björn Menten; Stephane Rombauts; John Vontas; Nicky Wybouw; Richard M Clark; Thomas Van Leeuwen
A link between host plant adaptation and pesticide resistance in the polyphagous spider mite Tetranychus urticae.

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All Publications

2013: Hannah Verdin; Diane Beysen; Claudia M B Carvalho; Barbara D'haene; Pablo Lapunzina; James R Lupski; Björn Menten; Julian Nevado; Yana Novikova; Tom Sante; Elfride De Baere
Microhomology-mediated mechanisms underlie non-recurrent disease-causing microdeletions of the FOXL2 gene or its regulatory domain.
PLoS genetics 2013;9(3):e1003358.
2013: Sarah Vergult; Joke B G M Verheij; Geert Mortier; Antonio Perez-Aytes; Tom Sante; Yves Sznajer; Christian Thiel; Hilde Van Esch; Daniela Q C M Barge-Schaapveld; Emilia K Bijlsma; Bram De Wilde; A Jeannette M Hoogeboom; Marjolijn Jongmans; Eva Klopocki; Alma Kuechler; Björn Menten
Complex genetics of radial ray deficiencies: screening of a cohort of 54 patients.
Genetics in medicine : official journal of the American College of Medical Genetics 2013;15(3):195-202.
2013: Wannes Dermauw; René Feyereisen; Miodrag Grbic; Björn Menten; Stephane Rombauts; John Vontas; Nicky Wybouw; Richard M Clark; Thomas Van Leeuwen
A link between host plant adaptation and pesticide resistance in the polyphagous spider mite Tetranychus urticae.
Proceedings of the National Academy of Sciences of the United States of America 2013;110(2):E113-22.
2013: Sarah Vergult; Ilse Claerhout; Bart Leroy; Björn Menten
Familial cases of a submicroscopic Xp22.2 deletion: genotype-phenotype correlation in microphthalmia with linear skin defects syndrome.
Molecular vision 2013;19():311-8.
2013: Candy Kumps; Geneviève Laureys; Steve Lefever; Björn Menten; Pieter Mestdagh; Rosa Noguera; Filip Pattyn; Tom Sante; Alexander Schramm; Johannes H Schulte; Valérie Combaret; Sara De Brouwer; Katleen De Preter; Christine Devalck; Angelika Eggert; Annelies Fieuw; Tom Van Maerken; Nadine Van Roy; Jo Vandesompele; Frank Westermann; Frank Speleman
Focal DNA copy number changes in neuroblastoma target MYCN regulated genes.
PloS one 2013;8(1):e52321.
2013: Pieter-Jan Volders; Xiaowei Wang; Jo Vandesompele; Kris Gevaert; Kenny Helsens; Lennart Martens; Björn Menten; Pieter Mestdagh
LNCipedia: a database for annotated human lncRNA transcript sequences and structures.
Nucleic acids research 2013;41(Database issue):D246-51.
2012: Lukas Heukamp; Katharina König; Steffi Kuhfittig-Kulle; Candy Kumps; Annette Künkele; Sven Lindner; Lydia Meder; Björn Menten; Pieter Mestdagh; Andrea Odersky; Filip Pattyn; Martin Peifer; Alexander Schramm; Reinhard Büttner; Sampurna Chatterjee; Katleen De Preter; Bram De Wilde; Angelika Eggert; Stefanie Schulte; Frank Speleman; Annika Spruessel; Theresa Thor; Roland T Ullrich; Jo Vandesompele; Johannes H Schulte
Targeted expression of mutated ALK induces neuroblastoma in transgenic mice.
Science translational medicine 2012;4(141):141ra91.
2012: Wigard P Kloosterman; Lidia Larizza; Björn Menten; Eberhard Passarge; Martin Poot; Ivo Renkens; Claudia Ruivenkamp; Masoumeh Tavakoli-Yaraki; Ellen van Binsbergen; Arie van Haeringen; Markus J van Roosmalen; Sarah Vergult; Karen J Duran; Daniela Giardino; Victor Guryev; Thomas Haaf; Kerstin Hansson; Ron Hochstenbach; Elly F Ippel; Myrthe Jager; Lucia Ballarati; Edwin Cuppen
Constitutional chromothripsis rearrangements involve clustered double-stranded DNA breaks and nonhomologous repair mechanisms.
Cell reports 2012;1(6):648-55.
2012: Annelies Fieuw; Candy Kumps; Björn Menten; Rosa Noguera; Filip Pattyn; Alexander Schramm; Johannes H Schulte; Francesca Antonacci; Patrick Buckley; Anne De Paepe; Katleen De Preter; Angelika Eggert; Raymond L Stallings; Peter Sudmant; Nadine Van Roy; Jo Vandesompele; Sarah Vergult; Rogier Versteeg; Frank Speleman
Identification of a novel recurrent 1q42.2-1qter deletion in high risk MYCN single copy 11q deleted neuroblastomas.
International journal of cancer. Journal international du cancer 2012;130(11):2599-606.
2012: Sarah Vergult; Barbara Delle Chiaie; John Crolla; Andrew Dauber; Joel Hirschhorn; Bart Loeys; Shehla Mohammed; Geert Mortier; Caroline Ogilvie; Jean Pfotenhauer; John A Phillips; Ali Rihani; Marleen Simon; Elke Van Oudenhove; Björn Menten
17q24.2 microdeletions: a new syndromal entity with intellectual disability, truncal obesity, mood swings and hallucinations.
European journal of human genetics : EJHG 2012;20(5):534-9.
2011: Sarah Vergult; Geert Mortier; Freddie Sharkey; Britt-Marie Anderlid; Shelagh Joss; Danijela Krgovic; Agne Liedén; Bart Loeys; Stanislas Lyonnet; Björn Menten
Nasal speech and hypothyroidism are common hallmarks of 12q15 microdeletions.
European journal of human genetics : EJHG 2011;19(10):1032-7.
2011: Thomas O'Leary; Björn Heindryckx; Sylvie Lierman; Margot Van der Jeught; Björn Menten; Dieter Deforce; Ria Cornelissen; Susana Chuva de Sousa Lopes; Petra De Sutter
The influence of early embryo traits on human embryonic stem cell derivation efficiency.
Stem cells and development 2011;20(5):785-93.
2011: Helene Verhelst; Patrick Verloo; Karlien Dhondt; Boel De Paepe; Björn Menten; Josep Dalmau; Rudy Van Coster
Anti-NMDA-receptor encephalitis in a 3 year old patient with chromosome 6p21.32 microdeletion including the HLA cluster.
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society 2011;15(2):163-6.
2011: Adrien Inoubli; Griet De Cuypere; Robert Rubens; Gunter Heylens; Els Elaut; Eva Van Caenegem; Björn Menten; Guy T'Sjoen
Karyotyping, is it worthwhile in transsexualism?
The journal of sexual medicine 2011;8(2):475-8.
2011: Françoise Meire; Björn Menten; Françoise Roulez; Christian Van Nechel; Cecile Brachet; Catherine Christophe; Isabelle Delpierre; Fanny Depasse; Elfride De Baere
Nonsyndromic bilateral and unilateral optic nerve aplasia: first familial occurrence and potential implication of CYP26A1 and CYP26C1 genes.
Molecular vision 2011;17():2072-9.
2011: Barbara D'haene; Françoise Meire; Ilse Claerhout; Hester Y Kroes; Astrid Plomp; Yvonne H Arens; Thomy de Ravel; Ingele Casteels; Sarah De Jaegere; Sally Hooghe; Wim Wuyts; Jenneke van den Ende; Françoise Roulez; Hermine E Veenstra-Knol; Rogier A Oldenburg; Jacques Giltay; Johanna B G M Verheij; Jan-Tjeerd de Faber; Björn Menten; Anne De Paepe; Philippe Kestelyn; Bart P Leroy; Elfride De Baere
Expanding the spectrum of FOXC1 and PITX2 mutations and copy number changes in patients with anterior segment malformations.
Investigative ophthalmology & visual science 2011;52(1):324-33.
2010: Karen Buysse; Sarah Vergult; Silke Mussche; Chantal Ceuterick-de Groote; Frank Speleman; Björn Menten; Willy Lissens; Rudy Van Coster
Giant axonal neuropathy caused by compound heterozygosity for a maternally inherited microdeletion and a paternal mutation within the GAN gene.
American journal of medical genetics. Part A 2010;152A(11):2802-4.
2010: Pieter Mestdagh; E Fredlund; Filip Pattyn; A Rihani; T Van Maerken; J Vermeulen; C Kumps; Björn Menten; Katleen De Preter; Alexander Schramm; J Schulte; R Noguera; G Schleiermacher; Isabelle Janoueix-Lerosey; Geneviève Laureys; R Powel; D Nittner; Jean-Christophe Marine; M Ringnér; F Speleman; Jo Vandesompele
An integrative genomics screen uncovers ncRNA T-UCR functions in neuroblastoma tumours.
Oncogene 2010;29(24):3583-92.
2010: Bernard Thienpont; Litu Zhang; Alex V Postma; Jeroen Breckpot; Léon-Charles Tranchevent; Peter Van Loo; Kjeld Møllgård; Niels Tommerup; Iben Bache; Zeynep Tümer; Klaartje van Engelen; Björn Menten; Geert Mortier; Darrel Waggoner; Marc Gewillig; Yves Moreau; Koen Devriendt; Lars Allan Larsen
Haploinsufficiency of TAB2 causes congenital heart defects in humans.
American journal of human genetics 2010;86(6):839-49.
2010: Bernard Thienpont; Frédérique Béna; Jeroen Breckpot; Nicole Philip; Björn Menten; Hilde Van Esch; Emmanuel Scalais; Jessica M Salamone; Chin-To Fong; Jennifer L Kussmann; Dorothy K Grange; Jerome L Gorski; Farah Zahir; Siu Li Yong; Michael Morris; Stefania Gimelli; Jean-Pierre Fryns; Geert Mortier; Jan M Friedman; Laurent Villard; Armand Bottani; Joris R Vermeesch; Sau Wai Cheung; Koen Devriendt
Duplications of the critical Rubinstein-Taybi deletion region on chromosome 16p13.3 cause a novel recognisable syndrome.
Journal of medical genetics 2010;47(3):155-61.
2010: An De Weer; Bruce Poppe; Sarah Vergult; Pieter Van Vlierberghe; Marjan Petrick; Robrecht De Bock; Yves Benoit; Lucien Noens; Anne De Paepe; Nadine Van Roy; Björn Menten; Frank Speleman
Identification of two critically deleted regions within chromosome segment 7q35-q36 in EVI1 deregulated myeloid leukemia cell lines.
PloS one 2010;5(1):e8676.
2009: Karen Buysse; Barbara Delle Chiaie; Rudy Van Coster; Bart Loeys; Anne De Paepe; Geert R Mortier; Frank Speleman; Björn Menten
Challenges for CNV interpretation in clinical molecular karyotyping: lessons learned from a 1001 sample experience.
European journal of medical genetics 2009;52(6):398-403.
2009: Barbara D'haene; Catia Attanasio; Diane Beysen; Josée Dostie; Edmond Lemire; Philippe Bouchard; Michael Field; Kristie Jones; Birgit Lorenz; Björn Menten; Karen Buysse; Filip Pattyn; Marc Friedli; Catherine Ucla; Colette Rossier; Carine Wyss; Frank Speleman; Anne De Paepe; Job Dekker; Stylianos E Antonarakis; Elfride De Baere
Disease-causing 7.4 kb cis-regulatory deletion disrupting conserved non-coding sequences and their interaction with the FOXL2 promotor: implications for mutation screening.
PLoS genetics 2009;5(6):e1000522.
2009: Karen Buysse; William Reardon; Lakshmi Mehta; Teresa Costa; Carrie Fagerstrom; Daniel J Kingsbury; George Anadiotis; Barbara C McGillivray; Jan Hellemans; Nicole de Leeuw; Bert B A de Vries; Frank Speleman; Björn Menten; Geert R Mortier
The 12q14 microdeletion syndrome: additional patients and further evidence that HMGA2 is an important genetic determinant for human height.
European journal of medical genetics 2009;52(2-3):101-7.
2009: Björn Menten; Katrien Swerts; Barbara Delle Chiaie; Sandra Janssens; Karen Buysse; Jan Philippé; Frank Speleman
Array comparative genomic hybridization and flow cytometry analysis of spontaneous abortions and mors in utero samples.
BMC medical genetics 2009;10():89.
2009: Karen Buysse; Francesca Antonacci; Bert Callewaert; Bart Loeys; Ulrike Fränkel; Victoria Siu; Geert R Mortier; Frank Speleman; Björn Menten
Unusual 8p inverted duplication deletion with telomere capture from 8q.
European journal of medical genetics 2009;52(1):31-6.
2008: Katleen De Preter; Björn Menten; Sara De Brouwer; Candy Kumps; Evi Michels; Nadine Van Roy; Jo Vandesompele; Frank Speleman
Low-cost dedicated mini-arrays for high-throughput analysis of DNA copy-number alterations in neuroblastoma.
Cancer letters 2008;269(1):111-6.
2008: Karen Buysse; Björn Menten; A Oostra; Sylvie Tavernier; Geert R Mortier; Frank Speleman
Delineation of a critical region on chromosome 18 for the del(18)(q12.2q21.1) syndrome.
American journal of medical genetics. Part A 2008;146A(10):1330-4.
2008: Jo Vandesompele; Evi Michels; Katleen De Preter; Björn Menten; Alexander Schramm; Angelika Eggert; Peter F Ambros; Valérie Combaret; Nadine Francotte; Francesca Antonacci; Anne De Paepe; Geneviève Laureys; Frank Speleman; Nadine Van Roy
Identification of 2 putative critical segments of 17q gain in neuroblastoma through integrative genomics.
International journal of cancer. Journal international du cancer 2008;122(5):1177-82.
2008: Frank Speleman; C Kumps; Karen Buysse; Bruce Poppe; Björn Menten; Katleen De Preter
Copy number alterations and copy number variation in cancer: close encounters of the bad kind.
Cytogenetic and genome research 2008;123(1-4):176-82.
2007: Evi Michels; Jo Vandesompele; Katleen De Preter; Jasmien Hoebeeck; Joëlle Vermeulen; Alexander Schramm; Jan J Molenaar; Björn Menten; Barbara Marques; Raymond L Stallings; Valérie Combaret; Christine Devalck; Anne De Paepe; Rogier Versteeg; Angelika Eggert; Geneviève Laureys; Nadine Van Roy; Frank Speleman
ArrayCGH-based classification of neuroblastoma into genomic subgroups.
Genes, chromosomes & cancer 2007;46(12):1098-108.
2007: Björn Menten; Karen Buysse; Stefan Vermeulen; Valerie Meersschaut; Jo Vandesompele; Bee Ling Ng; Nigel P Carter; Geert R Mortier; Frank Speleman
Report of a female patient with mental retardation and tall stature due to a chromosomal rearrangement disrupting the OPHN1 gene on Xq12.
European journal of medical genetics 2007;50(6):446-54.
2007: Irina Balikova; Björn Menten; T J L de Ravel; Cédric Le Caignec; Bernard Thienpont; Montse Urbina; Martine Doco-Fenzy; Marjan de Rademaeker; Geert R Mortier; Frank Kooy; Janneke van den Ende; koenraad devriendt; Jean-Pierre Fryns; Frank Speleman; Joris R Vermeesch
Subtelomeric imbalances in phenotypically normal individuals.
Human mutation 2007;28(10):958-67.
2007: Björn Menten; Karen Buysse; Farah Zahir; Jan Hellemans; Sara J Hamilton; Teresa Costa; Carrie Fagerstrom; George Anadiotis; Daniel Kingsbury; Barbara C McGillivray; Marco A Marra; Jan M Friedman; Frank Speleman; Geert R Mortier
Osteopoikilosis, short stature and mental retardation as key features of a new microdeletion syndrome on 12q14.
Journal of medical genetics 2007;44(4):264-8.
2007: Jasmien Hoebeeck; Evi Michels; Björn Menten; Nadine Van Roy; Angelika Eggert; Alexander Schramm; Katleen De Preter; Nurten Yigit; Els De Smet; Anne De Paepe; Geneviève Laureys; Jo Vandesompele; Frank Speleman
High resolution tiling-path BAC array deletion mapping suggests commonly involved 3p21-p22 tumor suppressor genes in neuroblastoma and more frequent tumors.
International journal of cancer. Journal international du cancer 2007;120(3):533-8.
2007: Steven Van Vooren; Bernard Thienpont; Björn Menten; Frank Speleman; Bart De Moor; Joris R Vermeesch; Yves Moreau
Mapping biomedical concepts onto the human genome by mining literature on chromosomal aberrations.
Nucleic acids research 2007;35(8):2533-43.
2006: Björn Menten; Nicole M C Maas; Bernard Thienpont; Karen Buysse; Jo Vandesompele; Cindy Melotte; T J L de Ravel; Steven Van Vooren; Irina Balikova; liesbeth backx; S Janssens; Anne De Paepe; Bart De Moor; Yves Moreau; Peter Marynen; Jean-Pierre Fryns; Geert R Mortier; koenraad devriendt; Frank Speleman; Joris R Vermeesch
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 published reports.
Journal of medical genetics 2006;43(8):625-33.
2006: Nadine Van Roy; Jo Vandesompele; Björn Menten; Helén Nilsson; Els De Smet; Mariano Rocchi; Anne De Paepe; Sven Påhlman; Frank Speleman
Translocation-excision-deletion-amplification mechanism leading to nonsyntenic coamplification of MYC and ATBF1.
Genes, chromosomes & cancer 2006;45(2):107-17.
2006: Evi Michels; Jo Vandesompele; Jasmien Hoebeeck; Björn Menten; Katleen De Preter; Geneviève Laureys; Nadine Van Roy; Frank Speleman
Genome wide measurement of DNA copy number changes in neuroblastoma: dissecting amplicons and mapping losses, gains and breakpoints.
Cytogenetic and genome research 2006;115(3-4):273-82.
2005: Björn Menten; Karen Buysse; Jo Vandesompele; Els De Smet; Anne De Paepe; Frank Speleman; Geert R Mortier
Identification of an unbalanced X-autosome translocation by array CGH in a boy with a syndromic form of chondrodysplasia punctata brachytelephalangic type.
European journal of medical genetics 2005;48(3):301-9.
2005: Joris R Vermeesch; Cindy Melotte; Guy Froyen; Steven Van Vooren; Binita Dutta; Nicole M C Maas; Stefan Vermeulen; Björn Menten; Frank Speleman; Bart De Moor; Paul van Hummelen; Peter Marynen; Jean-Pierre Fryns; koenraad devriendt
Molecular karyotyping: array CGH quality criteria for constitutional genetic diagnosis.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 2005;53(3):413-22.
2005: Katleen De Preter; Jo Vandesompele; Björn Menten; Philippa Carr; Heike Fiegler; Anders Edsjö; Nigel P Carter; Nurten Yigit; Wim Waelput; Nadine Van Roy; Scott Bader; Sven Påhlman; Frank Speleman
Positional and functional mapping of a neuroblastoma differentiation gene on chromosome 11.
BMC genomics 2005;6():97.
2005: Björn Menten; Filip Pattyn; Katleen De Preter; Piet Robbrecht; Evi Michels; Karen Buysse; Geert R Mortier; Anne De Paepe; Steven Van Vooren; Joris R Vermeesch; Yves Moreau; Bart De Moor; Stefan Vermeulen; Frank Speleman; Jo Vandesompele
arrayCGHbase: an analysis platform for comparative genomic hybridization microarrays.
BMC bioinformatics 2005;6():124.
2005: Stefan Vermeulen; Frank Speleman; Leen Vanransbeeck; Jasmien Verspeet; Björn Menten; Marie-Rose Verschraegen-Spae; Philippe De Wilde; Ludwine MESSIAEN; Ron C Michaelis; Jules G Leroy
Familial pericentric inversion of chromosome 18: behavioral abnormalities in patients heterozygous for either the dup(18p)/del(18q) or dup(18q)/del(18p) recombinant chromosome.
European journal of human genetics : EJHG 2005;13(1):52-8.
2004: Stefan Vermeulen; Björn Menten; Sylvia De Bie; Paul Coucke; Fransiska Malfait; Julie De Backer; Frank Speleman; Anne De Paepe; Bart Loeys
DUP25 remains unconfirmed.
American journal of medical genetics. Part A 2004;131(3):320-1.
2004: Jan Hellemans; Olena Preobrazhenska; Andy Willaert; Philippe Debeer; Peter C M Verdonk; Teresa Costa; Koen Janssens; Björn Menten; Nadine Van Roy; Stefan Vermeulen; Ravi Savarirayan; Wim Van Hul; Filip Vanhoenacker; Danny Huylebroeck; Anne De Paepe; Jean-Marie Naeyaert; Jo Vandesompele; Frank Speleman; Kristin Verschueren; Paul J Coucke; Geert R Mortier
Loss-of-function mutations in LEMD3 result in osteopoikilosis, Buschke-Ollendorff syndrome and melorheostosis.
Nature genetics 2004;36(11):1213-8.
2004: Katleen De Preter; Filip Pattyn; Geert Berx; Kristin Strumane; Björn Menten; Frans van Roy; Anne De Paepe; Frank Speleman; Jo Vandesompele
Combined subtractive cDNA cloning and array CGH: an efficient approach for identification of overexpressed genes in DNA amplicons.
BMC genomics 2004;5(1):11.
2004: Stefan Vermeulen; Björn Menten; Nadine Van Roy; Heidi Van Limbergen; Anne De Paepe; Geert R Mortier; Frank Speleman
Molecular cytogenetic analysis of complex chromosomal rearrangements in patients with mental retardation and congenital malformations: delineation of 7q21.11 breakpoints.
American journal of medical genetics. Part A 2004;124A(1):10-8.