His main research concerns Genetics, Comparative genomic hybridization, Copy-number variation, Microdeletion syndrome and Autism. His Genetics study focuses mostly on Human genome, Structural variation, Gene rearrangement, Genomics and Gene duplication. His Human genome study combines topics from a wide range of disciplines, such as Genome browser and Computational biology.
His Comparative genomic hybridization research is multidisciplinary, incorporating perspectives in Copy number analysis, Karyotype and Pattern recognition. His Microdeletion syndrome research integrates issues from Clinical significance and Developmental disorder. His research investigates the link between Autism and topics such as Microcephaly that cross with problems in Gene knockdown, Unfolded protein response and DNA repair.
His primary areas of study are Genetics, Gene, Comparative genomic hybridization, Cell biology and Computational biology. His Genetics research focuses on Copy-number variation, Breakpoint, Phenotype, Gene duplication and Chromosome. Björn Menten has included themes like Structural variation, Microdeletion syndrome and Bioinformatics in his Copy-number variation study.
As part of the same scientific family, Björn Menten usually focuses on Gene, concentrating on Neuroblastoma and intersecting with Gene dosage and Regulation of gene expression. The study incorporates disciplines such as Molecular biology, Copy number analysis, Karyotype and Pathology in addition to Comparative genomic hybridization. Björn Menten combines subjects such as Exome sequencing, DNA microarray and Human genome with his study of Computational biology.
His scientific interests lie mostly in Cell biology, Genetics, Cancer research, Gene and Transcription factor. His Cell biology study combines topics in areas such as Chromatin, Embryonic stem cell, Regulation of gene expression and Loss function. His research on Genetics frequently connects to adjacent areas such as Hearing loss.
In Cancer research, he works on issues like Neuroblastoma, which are connected to Gene dosage and Regulator. The various areas that Björn Menten examines in his Gene study include Metastasis, Computational biology and Iris. His research on Transcription factor also deals with topics like
Björn Menten focuses on Cell biology, Embryo, Context, Blastocyst and Andrology. His research integrates issues of Embryonic stem cell, Transcription factor, Gene, Regulation of gene expression and Epigenetics in his study of Cell biology. His Embryonic stem cell research incorporates elements of Transcriptome and Stem cell.
His study in Embryo is interdisciplinary in nature, drawing from both Ovarian reserve and Infertility. Among his Context studies, there is a synthesis of other scientific areas such as Genetic testing, Aneuploidy, Copy-number variation, Pediatrics and Child development. His Copy-number variation research incorporates themes from Microarray, Prenatal diagnosis, Uncertain significance and Database.
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Recurrent Rearrangements of Chromosome 1q21.1 and Variable Pediatric Phenotypes
Heather C Mefford;Andrew J Sharp;Carl Baker;Andy Itsara.
The New England Journal of Medicine (2008)
LNCipedia: a database for annotated human lncRNA transcript sequences and structures.
Pieter-Jan Volders;Kenny Helsens;Xiaowei Wang;Björn Menten.
Nucleic Acids Research (2013)
Loss-of-function mutations in LEMD3 result in osteopoikilosis, Buschke-Ollendorff syndrome and melorheostosis.
Jan Hellemans;Olena Preobrazhenska;Andy Willaert;Philippe Debeer.
Nature Genetics (2004)
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.
Journal of Medical Genetics (2006)
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.
Proceedings of the National Academy of Sciences of the United States of America (2013)
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.
European Journal of Medical Genetics (2009)
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.
Journal of Medical Genetics (2009)
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.
Nature Genetics (2017)
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.
Cell Reports (2012)
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.
European Journal of Medical Genetics (2009)
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