What is she best known for?
The fields of study she is best known for:
Sarah Lincoln mainly investigates Genetics, Parkinsonism, Mutation, Missense mutation and Haplotype.
Her Genetics study combines topics from a wide range of disciplines, such as Frontotemporal lobar degeneration, Parkinson's disease and Pathology.
Alpha-synuclein is the focus of her Parkinson's disease research.
Her Parkinsonism research is multidisciplinary, relying on both Lewy body, Dementia, Proband, Autosomal dominant trait and LRRK2.
Her biological study spans a wide range of topics, including Splice site mutation and Synucleinopathies.
Her work deals with themes such as Candidate gene and Exon, which intersect with Mutation.
Her most cited work include:
- α-Synuclein Locus Triplication Causes Parkinson's Disease (3413 citations)
- Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17 (2839 citations)
- Mutations in LRRK2 Cause Autosomal-Dominant Parkinsonism with Pleomorphic Pathology (2198 citations)
What are the main themes of her work throughout her whole career to date?
Her scientific interests lie mostly in Genetics, Disease, Parkinsonism, Gene and Parkinson's disease.
Many of her studies involve connections with topics such as Parkin and Genetics.
Sarah Lincoln usually deals with Disease and limits it to topics linked to Transcriptome and Cell type.
Sarah Lincoln has researched Parkinsonism in several fields, including Lewy body, Missense mutation, Proband, Substantia nigra and LRRK2.
Her Parkinson's disease research integrates issues from Genetic variation, Polymorphism and Degenerative disease.
Her work in Alpha-synuclein tackles topics such as Synuclein which are related to areas like Beta-synuclein.
She most often published in these fields:
- Genetics (56.67%)
- Disease (27.33%)
- Parkinsonism (22.00%)
What were the highlights of her more recent work (between 2015-2021)?
- Disease (27.33%)
- Genetics (56.67%)
- Transcriptome (4.67%)
In recent papers she was focusing on the following fields of study:
Her primary areas of study are Disease, Genetics, Transcriptome, Gene and Computational biology.
Sarah Lincoln has included themes like Neurology, Immunology and Genotype in her Disease study.
Her Neurology study integrates concerns from other disciplines, such as Gastroenterology, Missense mutation and Autopsy.
Her Genetics research incorporates elements of Temporal cortex and Disease risk.
Her Transcriptome study also includes fields such as
- Cell type which is related to area like Cell biology and Tauopathy,
- Alzheimer's disease, which have a strong connection to Frontotemporal dementia, Posterior cortical atrophy and Exome sequencing.
Her Computational biology study combines topics from a wide range of disciplines, such as Vascular risk, Exome and Genomic profiling.
Between 2015 and 2021, her most popular works were:
- Human whole genome genotype and transcriptome data for Alzheimer’s and other neurodegenerative diseases (167 citations)
- Conserved brain myelination networks are altered in Alzheimer's and other neurodegenerative diseases (68 citations)
- ABI3 and PLCG2 missense variants as risk factors for neurodegenerative diseases in Caucasians and African Americans. (33 citations)
In her most recent research, the most cited papers focused on:
Alzheimer's disease, Temporal cortex, Genetics, Transcriptome and Neuropathology are her primary areas of study.
She has included themes like Exome sequencing, Genetic association and Exon in her Alzheimer's disease study.
Her biological study spans a wide range of topics, including Progressive supranuclear palsy, Reduced representation bisulfite sequencing, Single-nucleotide polymorphism, Epigenetics and CpG site.
Her work often combines Genetics and Hypersensitive site studies.
Her work in Transcriptome covers topics such as Cell type which are related to areas like Tauopathy and Cerebellum.
She combines subjects such as Posterior cortical atrophy, Dementia, Frontotemporal dementia, Bioinformatics and Exome with her study of Neuropathology.
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