What is he best known for?
The fields of study he is best known for:
- Gene
- Internal medicine
- Disease
The scientist’s investigation covers issues in Pathology, Genetics, Amyotrophic lateral sclerosis, Frontotemporal dementia and Frontotemporal lobar degeneration.
His Pathology study typically links adjacent topics like Frontal lobe.
Vivianna M. Van Deerlin regularly ties together related areas like Late onset in his Genetics studies.
His Amyotrophic lateral sclerosis research incorporates elements of Exome sequencing, Missense mutation, RNA-Binding Protein FUS and Neurodegeneration.
The various areas that Vivianna M. Van Deerlin examines in his Frontotemporal dementia study include Progressive supranuclear palsy, Haplotype and Degenerative disease.
He combines subjects such as Primary progressive aphasia, Neuropathology and Spinal cord with his study of Frontotemporal lobar degeneration.
His most cited work include:
- Common variants at MS4A4/MS4A6E , CD2AP , CD33 and EPHA1 are associated with late-onset Alzheimer's disease (1385 citations)
- Exome Sequencing Reveals VCP Mutations as a Cause of Familial ALS (917 citations)
- Ataxin-2 intermediate-length polyglutamine expansions are associated with increased risk for ALS (829 citations)
What are the main themes of his work throughout his whole career to date?
Vivianna M. Van Deerlin mainly focuses on Pathology, Disease, Frontotemporal lobar degeneration, Genetics and Internal medicine.
Vivianna M. Van Deerlin focuses mostly in the field of Pathology, narrowing it down to topics relating to White matter and, in certain cases, Tauopathy.
The Disease study combines topics in areas such as Genetic counseling and Cerebrospinal fluid.
His Frontotemporal lobar degeneration study is concerned with the field of Frontotemporal dementia as a whole.
His Internal medicine study combines topics from a wide range of disciplines, such as Oncology and Genotype.
His Amyotrophic lateral sclerosis research focuses on C9orf72 and how it relates to C9orf72 Protein.
He most often published in these fields:
- Pathology (33.80%)
- Disease (26.76%)
- Frontotemporal lobar degeneration (22.54%)
What were the highlights of his more recent work (between 2017-2021)?
- Disease (26.76%)
- Internal medicine (22.18%)
- Frontotemporal dementia (20.77%)
In recent papers he was focusing on the following fields of study:
Vivianna M. Van Deerlin mostly deals with Disease, Internal medicine, Frontotemporal dementia, Genetics and Pathology.
His Disease research incorporates themes from Odds ratio and Genome-wide association study.
His Internal medicine research is multidisciplinary, relying on both Oncology and Hepatitis C virus.
His Frontotemporal dementia study incorporates themes from Alzheimer's disease and Age of onset.
His study in Genetics is interdisciplinary in nature, drawing from both Published Erratum and Amyotrophic lateral sclerosis.
In his study, Neuropathology, Olivopontocerebellar atrophy, Cortex and Lentiform nucleus is strongly linked to White matter, which falls under the umbrella field of Pathology.
Between 2017 and 2021, his most popular works were:
- Analysis of shared heritability in common disorders of the brain (726 citations)
- Genome-wide Analyses Identify KIF5A as a Novel ALS Gene (215 citations)
- Neurodegenerative disease concomitant proteinopathies are prevalent, age-related and APOE4-associated (183 citations)
In his most recent research, the most cited papers focused on:
- Gene
- Internal medicine
- Disease
His primary areas of investigation include Frontotemporal dementia, Disease, Internal medicine, C9orf72 and Amyotrophic lateral sclerosis.
He combines subjects such as White matter, Molecular pathology, Neurodegeneration, Lateralization of brain function and Alzheimer's disease with his study of Frontotemporal dementia.
He has included themes like Odds ratio and Genome-wide association study in his Disease study.
The study incorporates disciplines such as Oncology and Hepatitis C virus in addition to Internal medicine.
His C9orf72 study is concerned with the larger field of Genetics.
The Amyotrophic lateral sclerosis study which covers Single-nucleotide polymorphism that intersects with Genetic analysis and Missense mutation.
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