What is he best known for?
The fields of study he is best known for:
- Gene
- Internal medicine
- Disease
Zbigniew K. Wszolek focuses on Genetics, Parkinsonism, Pathology, Disease and Mutation.
Zbigniew K. Wszolek usually deals with Genetics and limits it to topics linked to Frontotemporal lobar degeneration and Allele and Charged multivesicular body protein 2B.
His Parkinsonism research is multidisciplinary, relying on both Frontotemporal dementia and parkinsonism linked to chromosome 17, Parkinson's disease, LRRK2 and Haplotype.
Zbigniew K. Wszolek regularly links together related areas like Dopaminergic in his Pathology studies.
His research in Disease tackles topics such as Central nervous system disease which are related to areas like Pediatrics.
The various areas that he examines in his Mutation study include Splice site mutation and Genetic linkage.
His most cited work include:
- Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS (3097 citations)
- Mutations in LRRK2 Cause Autosomal-Dominant Parkinsonism with Pleomorphic Pathology (2198 citations)
- Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease (1387 citations)
What are the main themes of his work throughout his whole career to date?
His primary areas of study are Genetics, Parkinsonism, Pathology, Disease and Parkinson's disease.
His study in Genetics concentrates on Mutation, Gene, Haplotype, Locus and Allele.
His Parkinsonism study incorporates themes from Dementia, Frontotemporal dementia, Neurology, Neuroscience and Pediatrics.
His study in Frontotemporal dementia is interdisciplinary in nature, drawing from both Amyotrophic lateral sclerosis and Tau protein.
Zbigniew K. Wszolek interconnects Phenotype, Allele frequency, Pathological and Bioinformatics in the investigation of issues within Disease.
His work in LRRK2 and Alpha-synuclein is related to Parkinson's disease.
He most often published in these fields:
- Genetics (30.42%)
- Parkinsonism (26.81%)
- Pathology (25.75%)
What were the highlights of his more recent work (between 2016-2021)?
- Disease (21.99%)
- Pathology (25.75%)
- Frontotemporal dementia (12.65%)
In recent papers he was focusing on the following fields of study:
Disease, Pathology, Frontotemporal dementia, Genetics and Internal medicine are his primary areas of study.
His Disease research is multidisciplinary, relying on both Odds ratio and Bioinformatics.
His biological study deals with issues like Mutation, which deal with fields such as Asymptomatic.
His research investigates the connection with Frontotemporal dementia and areas like Tau protein which intersect with concerns in Haplotype.
Genetics and Ataxia are frequently intertwined in his study.
Zbigniew K. Wszolek has included themes like Apathy and Age of onset in his Parkinsonism study.
Between 2016 and 2021, his most popular works were:
- TIA1 Mutations in Amyotrophic Lateral Sclerosis and Frontotemporal Dementia Promote Phase Separation and Alter Stress Granule Dynamics (285 citations)
- Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis. (102 citations)
- Heterozygous PINK1 p.G411S increases risk of Parkinson's disease via a dominant-negative mechanism. (80 citations)
In his most recent research, the most cited papers focused on:
- Gene
- Internal medicine
- Disease
His primary areas of investigation include Pathology, Frontotemporal dementia, Disease, Progressive supranuclear palsy and Genetics.
His study in Parkinsonism, Dementia with Lewy bodies, Atrophy and Neuropathology falls within the category of Pathology.
His study in Age of onset extends to Parkinsonism with its themes.
His studies in Frontotemporal dementia integrate themes in fields like Tau protein and Likely pathogenic.
Zbigniew K. Wszolek studies Disease, namely Parkinson's disease.
His study in Mutation, Genome-wide association study, Sanger sequencing, Genetic association and Missense mutation are all subfields of Genetics.
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