What is he best known for?
The fields of study he is best known for:
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 most cited work include:
- Recurrent Rearrangements of Chromosome 1q21.1 and Variable Pediatric Phenotypes (609 citations)
- LNCipedia: a database for annotated human lncRNA transcript sequences and structures. (362 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 (353 citations)
What are the main themes of his work throughout his whole career to date?
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.
He most often published in these fields:
- Genetics (47.66%)
- Gene (18.72%)
- Comparative genomic hybridization (14.04%)
What were the highlights of his more recent work (between 2017-2021)?
- Cell biology (13.19%)
- Genetics (47.66%)
- Cancer research (9.36%)
In recent papers he was focusing on the following fields of study:
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
- EZH2 and Priming most often made with reference to Apoptosis,
- Chaperone that intertwine with fields like Cell culture,
- Mitochondrion that connect with fields like Disease and Internal medicine.
Between 2017 and 2021, his most popular works were:
- Chromosomal mosaicism in human blastocysts: the ultimate challenge of preimplantation genetic testing? (47 citations)
- Extended in vitro culture of human embryos demonstrates the complex nature of diagnosing chromosomal mosaicism from a single trophectoderm biopsy (36 citations)
- Chromosomal mosaicism in human blastocysts: the ultimate diagnostic dilemma. (30 citations)
In his most recent research, the most cited papers focused on:
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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