What is she best known for?
The fields of study she is best known for:
Genetics, Gene, Locus, Molecular biology and Allele are her primary areas of study.
Her Neurofibromatosis, Genetic linkage, Genetic marker, Single-nucleotide polymorphism and Chromosome 17 investigations are all subjects of Genetics research.
Her Candidate gene, Somatic cell and Molecular medicine study in the realm of Gene interacts with subjects such as Leukocyte degranulation and SNARE complex.
Her Locus study integrates concerns from other disciplines, such as Susceptibility locus, Generalized vitiligo, Gene mapping and Exon.
Her Molecular biology study combines topics in areas such as Positional cloning, GTPase, Complementary DNA, Neurofibromin 1 and Sequence analysis.
Her Allele research is multidisciplinary, incorporating perspectives in Mutation, Taste and Receptor.
Her most cited work include:
- A polymorphic DNA marker genetically linked to Huntington's disease (1864 citations)
- Type 1 neurofibromatosis gene: identification of a large transcript disrupted in three NF1 patients (1223 citations)
- Identification of the familial cylindromatosis tumour-suppressor gene. (552 citations)
What are the main themes of her work throughout her whole career to date?
Her primary areas of study are Genetics, Gene, Neurofibromatosis, Molecular biology and Internal medicine.
Genetics is a component of her Chromosome 17, Locus, Genetic marker, Chromosome and Allele studies.
Her Gene research includes elements of Elastin and DNA.
Her work carried out in the field of Neurofibromatosis brings together such families of science as Genetic disorder and Germline mutation.
Margaret R. Wallace combines subjects such as Complementary DNA and Frameshift mutation with her study of Molecular biology.
Her Internal medicine research is multidisciplinary, incorporating elements of Endocrinology and Oncology.
She most often published in these fields:
- Genetics (44.08%)
- Gene (22.75%)
- Neurofibromatosis (23.70%)
What were the highlights of her more recent work (between 2016-2021)?
- Neurofibromatosis (23.70%)
- Cancer research (12.32%)
- Internal medicine (15.64%)
In recent papers she was focusing on the following fields of study:
The scientist’s investigation covers issues in Neurofibromatosis, Cancer research, Internal medicine, Neurofibromin 1 and Single-nucleotide polymorphism.
Her Neurofibromatosis research also works with subjects such as
- Hyperalgesia and Nociception most often made with reference to Genetic disorder,
- Tumor suppressor gene that connect with fields like Molecular biology.
Her Cancer research research is multidisciplinary, relying on both Exome sequencing, CDKN2A, Malignant peripheral nerve sheath tumor and Neurofibroma.
Her Single-nucleotide polymorphism study is concerned with Gene in general.
Proband is the subject of her research, which falls under Genetics.
In the field of Genetics, her study on Mutation overlaps with subjects such as FLNC.
Between 2016 and 2021, her most popular works were:
- Genotype-Phenotype Correlation in NF1: Evidence for a More Severe Phenotype Associated with Missense Mutations Affecting NF1 Codons 844–848 (65 citations)
- The primacy of NF1 loss as the driver of tumorigenesis in neurofibromatosis type 1-associated plexiform neurofibromas (50 citations)
- Versatile and precise gene-targeting strategies for functional studies in mammalian cell lines (26 citations)
In her most recent research, the most cited papers focused on:
Margaret R. Wallace focuses on Cancer research, Neurofibromatosis, Neurofibroma, Genetics and Malignant transformation.
The study incorporates disciplines such as Neurofibromin 1, Malignant peripheral nerve sheath tumor, In vivo and Immortalised cell line in addition to Cancer research.
She focuses mostly in the field of Neurofibromatosis, narrowing it down to matters related to Tumor suppressor gene and, in some cases, Exon, Phenocopy, Mutant, Mutation and Café au lait spot.
She has researched Neurofibroma in several fields, including Cell culture, Exome and Cell growth.
The various areas that Margaret R. Wallace examines in her Genetics study include Periodontitis, Pathogenesis and Bioinformatics.
Her work focuses on many connections between Malignant transformation and other disciplines, such as Germline mutation, that overlap with her field of interest in CDKN2A, Carcinogenesis and Molecular biology.
This overview was generated by a machine learning system which analysed the scientist’s
body of work. If you have any feedback, you can
contact us
here.
