What is he best known for?
The fields of study he is best known for:
His scientific interests lie mostly in Genetics, Human genome, Chromosome, Gene duplication and Segmental duplication.
All of his Genetics and Angelman syndrome, Chromosome 15, Germline, Gene rearrangement and Recombination investigations are sub-components of the entire Genetics study.
The various areas that Stuart Schwartz examines in his Angelman syndrome study include Imprinting, Happy puppet syndrome and Genomic imprinting.
His research integrates issues of Centromere, Molecular evolution, Homologous recombination and Euchromatin in his study of Human genome.
His Chromosome study combines topics in areas such as Mutation, Gene mutation, Microsatellite instability and Genomic organization.
His Gene duplication research incorporates themes from Chromosome breakage and Copy-number variation.
His most cited work include:
- Recent Segmental Duplications in the Human Genome (1139 citations)
- Segmental Duplications and Copy-Number Variation in the Human Genome (812 citations)
- Prader-Willi syndrome (803 citations)
What are the main themes of his work throughout his whole career to date?
Stuart Schwartz mostly deals with Genetics, Molecular biology, Chromosome, Cytogenetics and Fluorescence in situ hybridization.
His study in Karyotype, Gene duplication, Phenotype, Chromosome 15 and Centromere are all subfields of Genetics.
His Gene duplication research incorporates elements of Gene dosage, Comparative genomic hybridization and Human genome.
Stuart Schwartz focuses mostly in the field of Chromosome 15, narrowing it down to topics relating to Angelman syndrome and, in certain cases, Happy puppet syndrome, Genomic imprinting and Imprinting.
His Chromosome research is multidisciplinary, incorporating elements of Y chromosome and Short stature.
His work deals with themes such as Meiosis and Interphase, which intersect with Fluorescence in situ hybridization.
He most often published in these fields:
- Genetics (65.61%)
- Molecular biology (27.60%)
- Chromosome (25.79%)
What were the highlights of his more recent work (between 2008-2021)?
- Genetics (65.61%)
- SNP array (4.52%)
- Molecular biology (27.60%)
In recent papers he was focusing on the following fields of study:
Genetics, SNP array, Molecular biology, Bioinformatics and Single-nucleotide polymorphism are his primary areas of study.
His study in Genetics concentrates on Chromosome, Copy-number variation, Haploinsufficiency, Uniparental disomy and Gene dosage.
His research in Chromosome is mostly concerned with Karyotype.
His Gene dosage research includes elements of Angelman syndrome, Chromosome 15, Gene duplication, Penetrance and Host factor.
Stuart Schwartz interconnects Neocentromere, Microarray, Gene, Fluorescence in situ hybridization and Interphase in the investigation of issues within Molecular biology.
His Intellectual disability research includes themes of Germline, DNA methylation, Genomic imprinting and Microcephaly.
Between 2008 and 2021, his most popular works were:
- Prader-Willi syndrome (803 citations)
- Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: a susceptibility region for neurological dysfunction including developmental and language delay (173 citations)
- Assessment of 2q23.1 Microdeletion Syndrome Implicates MBD5 as a Single Causal Locus of Intellectual Disability, Epilepsy, and Autism Spectrum Disorder (158 citations)
In his most recent research, the most cited papers focused on:
Stuart Schwartz mostly deals with Genetics, Gene duplication, Bioinformatics, Gene dosage and Copy-number variation.
In his papers, Stuart Schwartz integrates diverse fields, such as Genetics and Autism spectrum disorder.
His studies in Gene duplication integrate themes in fields like MYC Gene Rearrangement, Comparative genomic hybridization, Medical physics and Clinical significance.
His Bioinformatics research is multidisciplinary, relying on both Failure to thrive, Intellectual disability, Locus and Genomic imprinting.
The Gene dosage study combines topics in areas such as Immune system and Virology.
The various areas that Stuart Schwartz examines in his Copy-number variation study include Non-coding RNA and Host factor.
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