What is he best known for?
The fields of study he is best known for:
Magnus Nordenskjöld mostly deals with Genetics, Molecular biology, Locus, Loss of heterozygosity and Chromosome.
Chromosome 22, Allele, Mutation, Chromosome 13 and Genetic linkage are the primary areas of interest in his Genetics study.
His Molecular biology research integrates issues from Cell, Carcinogenesis, Complementary DNA and Telomerase, Telomerase reverse transcriptase.
His work carried out in the field of Locus brings together such families of science as Autosome, Deletion mapping, Autosomal dominant trait and Multiple endocrine neoplasia, MEN1.
His Loss of heterozygosity research includes elements of Germline mutation, Birt–Hogg–Dubé syndrome, Genotype and Pathology.
To a larger extent, he studies Gene with the aim of understanding Chromosome.
His most cited work include:
- Human estrogen receptor β-gene structure, chromosomal localization, and expression pattern (1046 citations)
- The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2. International RET mutation consortium analysis. (977 citations)
- Multiple endocrine neoplasia type 1 gene maps to chromosome 11 and is lost in insulinoma (852 citations)
What are the main themes of his work throughout his whole career to date?
Genetics, Gene, Molecular biology, Immunology and Cancer research are his primary areas of study.
Chromosome, Locus, Mutation, Chromosome 22 and Karyotype are the subjects of his Genetics studies.
The various areas that Magnus Nordenskjöld examines in his Locus study include Genetic marker, Genetic linkage, MEN1 and Allele.
His studies deal with areas such as Complementary DNA and DNA, Cosmid as well as Molecular biology.
His research integrates issues of Hemophagocytic lymphohistiocytosis and Internal medicine in his study of Immunology.
Pathology is closely connected to Cancer in his research, which is encompassed under the umbrella topic of Cancer research.
He most often published in these fields:
- Genetics (55.77%)
- Gene (23.94%)
- Molecular biology (16.62%)
What were the highlights of his more recent work (between 2012-2021)?
- Genetics (55.77%)
- Gene (23.94%)
- Mutation (16.06%)
In recent papers he was focusing on the following fields of study:
His scientific interests lie mostly in Genetics, Gene, Mutation, Phenotype and Immunology.
His study in Bioinformatics extends to Genetics with its themes.
Magnus Nordenskjöld has included themes like Molecular biology, Autism, Mutant and Copy-number variation in his Mutation study.
His studies in Molecular biology integrate themes in fields like Zebrafish, Morpholino, Molecular genetics, Hypotonia and Sanger sequencing.
The study incorporates disciplines such as Brachydactyly, Chronic pain, Platyspondyly and Scoliosis in addition to Phenotype.
His Chromosome 21 study which covers Cancer research that intersects with Lymphoma, B cell and Cancer.
Between 2012 and 2021, his most popular works were:
- Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases (241 citations)
- Clonal culturing of human embryonic stem cells on laminin-521/E-cadherin matrix in defined and xeno-free environment (190 citations)
- A genome-wide association study of atopic dermatitis identifies loci with overlapping effects on asthma and psoriasis (137 citations)
In his most recent research, the most cited papers focused on:
His primary areas of investigation include Genetics, Mutation, Gene, Missense mutation and Immunology.
His is involved in several facets of Genetics study, as is seen by his studies on Genetic heterogeneity, Exome sequencing, Point mutation, Intellectual disability and Breakpoint.
His Mutation study incorporates themes from Phenotype, Molecular biology and Allele.
His research on Phenotype also deals with topics like
- Neurodevelopmental disorder together with GRID2 and Neuroscience,
- Chromosome most often made with reference to Candidate gene.
His Missense mutation study combines topics from a wide range of disciplines, such as Familial haemophagocytic lymphohistiocytosis, Intron and UNC13D.
Magnus Nordenskjöld interconnects Hemophagocytic lymphohistiocytosis, Genome-wide association study and Nonsense mutation in the investigation of issues within Immunology.
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