What is he best known for?
The fields of study he is best known for:
Stanley F. Nelson mostly deals with Genetics, Gene, Cancer research, Gene expression profiling and Copy-number variation.
His research integrates issues of Autism and Attention deficit hyperactivity disorder in his study of Genetics.
His work is dedicated to discovering how Gene, Cell biology are connected with Endothelial stem cell, Tunicamycin, ATF4 and Unfolded protein response and other disciplines.
His study in Cancer research is interdisciplinary in nature, drawing from both Cancer, Epidermal growth factor receptor, Kinase and Molecular biology.
His Gene expression profiling research incorporates elements of Glioma, Computational biology, Immunology and Bioinformatics.
His studies in Copy-number variation integrate themes in fields like Domestication, Genome-wide association study and Population size.
His most cited work include:
- Melanomas acquire resistance to B-RAF(V600E) inhibition by RTK or N-RAS upregulation (1695 citations)
- Shotgun bisulphite sequencing of the Arabidopsis genome reveals DNA methylation patterning (1683 citations)
- Functional impact of global rare copy number variation in autism spectrum disorders (1592 citations)
What are the main themes of his work throughout his whole career to date?
Stanley F. Nelson focuses on Genetics, Gene, Molecular biology, Exome sequencing and Cancer research.
His Phenotype, Missense mutation, Single-nucleotide polymorphism, Allele and Candidate gene investigations are all subjects of Genetics research.
As part of one scientific family, Stanley F. Nelson deals mainly with the area of Candidate gene, narrowing it down to issues related to the Attention deficit hyperactivity disorder, and often Genetic determinism.
His Gene and Gene expression profiling, Gene expression and Genome investigations all form part of his Gene research activities.
The concepts of his Exome sequencing study are interwoven with issues in Disease, Computational biology, Pediatrics and Bioinformatics.
His research in Cancer research is mostly concerned with Glioma.
He most often published in these fields:
- Genetics (42.86%)
- Gene (14.87%)
- Molecular biology (12.24%)
What were the highlights of his more recent work (between 2015-2021)?
- Genetics (42.86%)
- Phenotype (7.58%)
- Missense mutation (7.87%)
In recent papers he was focusing on the following fields of study:
His primary areas of investigation include Genetics, Phenotype, Missense mutation, Exome sequencing and Pediatrics.
His Genetics study frequently involves adjacent topics like Autism spectrum disorder.
His Phenotype research includes themes of Mutation, Allele, Genotype and Exon.
His Missense mutation research includes elements of Loss function, Myopathy, Neurodevelopmental disorder, Microcephaly and Hypotonia.
His Exome sequencing study incorporates themes from Genetic disorder, Computational biology, DNA sequencing and Bioinformatics.
His Pediatrics research is multidisciplinary, relying on both Intellectual disability, Weakness and Cohort.
Between 2015 and 2021, his most popular works were:
- A Single CRISPR-Cas9 Deletion Strategy that Targets the Majority of DMD Patients Restores Dystrophin Function in hiPSC-Derived Muscle Cells (198 citations)
- Effect of Genetic Diagnosis on Patients with Previously Undiagnosed Disease (103 citations)
- Joint mouse–human phenome-wide association to test gene function and disease risk (84 citations)
In his most recent research, the most cited papers focused on:
His scientific interests lie mostly in Genetics, Exome sequencing, Phenotype, Missense mutation and Pediatrics.
His Gene, Microcephaly, Genome-wide association study, Duchenne muscular dystrophy and Genomics study are his primary interests in Genetics.
The Genomics study combines topics in areas such as Domestication, Bioinformatics and Candidate gene.
In his work, Human genome, Mendelian inheritance, Rare disease and Genomic Structural Variation is strongly intertwined with DNA sequencing, which is a subfield of Exome sequencing.
His Phenotype research is multidisciplinary, incorporating elements of Mutation and Exon.
His Missense mutation research includes elements of Intellectual disability, Atrophy, Pathology, Neurodevelopmental disorder and Pontocerebellar hypoplasia.
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