Björn Menten

Overview

Best Publications

• Recurrent Rearrangements of Chromosome 1q21.1 and Variable Pediatric Phenotypes

  Heather C Mefford;Andrew J Sharp;Carl Baker;Andy Itsara

  852
  Citations

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

  Pieter-Jan Volders;Kenny Helsens;Xiaowei Wang;Björn Menten

  617
  Citations

• Loss-of-function mutations in LEMD3 result in osteopoikilosis, Buschke-Ollendorff syndrome and melorheostosis.

  Jan Hellemans;Olena Preobrazhenska;Andy Willaert;Philippe Debeer

  514
  Citations

• A link between host plant adaptation and pesticide resistance in the polyphagous spider mite Tetranychus urticae.

  Wannes Dermauw;Nicky Wybouw;Stephane Rombauts;Stephane Rombauts;Björn Menten

  420
  Citations

• 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

  B. Menten;N. Maas;B. Thienpont;K. Buysse

  400
  Citations

• Extending the phenotype of recurrent rearrangements of 16p11.2: Deletions in mentally retarded patients without autism and in normal individuals

  E.K. Bijlsma;A.C.J. Gijsbers;J.H.M. Schuurs-Hoeijmakers;A. van Haeringen

  315
  Citations

• Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome

  B W M van Bon;H C Mefford;B Menten;D A Koolen

  314
  Citations

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

  Claire Redin;Claire Redin;Harrison Brand;Harrison Brand;Ryan L Collins;Ryan L Collins;Tammy Kammin

  295
  Citations

• Fourteen new cases contribute to the characterization of the 7q11.23 microduplication syndrome

  Nathalie Van der Aa;Liesbeth Rooms;Geert Vandeweyer;Jenneke van den Ende

  227
  Citations

• Constitutional Chromothripsis Rearrangements Involve Clustered Double-Stranded DNA Breaks and Nonhomologous Repair Mechanisms

  Wigard P Kloosterman;Masoumeh Tavakoli-Yaraki;Markus J van Roosmalen;Ellen van Binsbergen

  222
  Citations

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

  Joni Van der Meulen;Viraj Sanghvi;Konstantinos Mavrakis;Kaat Durinck

  208
  Citations

• Targeted expression of mutated ALK induces neuroblastoma in transgenic mice.

  Lukas C Heukamp;Theresa Thor;Alexander Schramm;Katleen De Preter

  196
  Citations

• Molecular karyotyping: array CGH quality criteria for constitutional genetic diagnosis.

  Joris Vermeesch;Cindy Melotte;Guido Froyen;Steven Van Vooren

  193
  Citations

• Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly.

  Daniela A. Braun;Jia Rao;Geraldine Mollet;Geraldine Mollet;David Schapiro

  190
  Citations

• Exonic Deletions in AUTS2 Cause a Syndromic Form of Intellectual Disability and Suggest a Critical Role for the C Terminus

  Gea Beunders;Els Voorhoeve;Christelle Golzio;Luba M. Pardo

  183
  Citations

• An integrative genomics screen uncovers ncRNA T-UCR functions in neuroblastoma tumours

  P. Mestdagh;Erik Fredlund;Erik Fredlund;F. Pattyn;A. Rihani

  174
  Citations

• Mutations in GTPBP3 Cause a Mitochondrial Translation Defect Associated with Hypertrophic Cardiomyopathy, Lactic Acidosis, and Encephalopathy

  Robert Kopajtich;Thomas J. Nicholls;Joanna Rorbach;Metodi D. Metodiev

  148
  Citations

• Chromosomal mosaicism in human blastocysts: the ultimate diagnostic dilemma.

  Mina Popovic;Lien Dhaenens;Annekatrien Boel;Björn Menten

  142
  Citations

• Alternative Routes to Induce Naïve Pluripotency in Human Embryonic Stem Cells

  Galbha Duggal;Sharat Warrier;Sabitri Ghimire;Dorien Broekaert

  136
  Citations

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

  Karen Buysse;Barbara Delle Chiaie;Rudy Van Coster;Bart Loeys

  135
  Citations