What is he best known for?
The fields of study he is best known for:
- Gene
- Mutation
- Internal medicine
The scientist’s investigation covers issues in Genetics, Pathology, Mutation, Parkinsonism and Parkinson's disease.
His work on Genetics is being expanded to include thematically relevant topics such as Ataxia.
His Mutation research is multidisciplinary, relying on both Cotton wool plaques, Presenilin and Cell biology.
His research investigates the connection with Parkinsonism and areas like Dystonia which intersect with concerns in Infantile neuroaxonal dystrophy and Exome sequencing.
As a part of the same scientific family, he mostly works in the field of Parkinson's disease, focusing on Genome-wide association study and, on occasion, Meta-analysis, LRRK2 and Allele frequency.
His research integrates issues of Molecular biology and Frontotemporal dementia and parkinsonism linked to chromosome 17 in his study of Exon.
His most cited work include:
- Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17 (2839 citations)
- Genome-wide association study reveals genetic risk underlying Parkinson's disease (1433 citations)
- A pathogenic mutation for probable Alzheimer's disease in the APP gene at the N-terminus of beta-amyloid. (1308 citations)
What are the main themes of his work throughout his whole career to date?
His primary scientific interests are in Genetics, Pathology, Mutation, Disease and Neuroscience.
His works in Gene, Phenotype, Missense mutation, Exome sequencing and Genetic heterogeneity are all subjects of inquiry into Genetics.
His study in Atrophy, Parkinsonism, Dementia, Neurodegeneration with brain iron accumulation and Frontotemporal dementia is carried out as part of his studies in Pathology.
His work in Mutation is not limited to one particular discipline; it also encompasses Exon.
Henry Houlden is involved in the study of Disease that focuses on Parkinson's disease in particular.
Henry Houlden integrates many fields, such as Neuroscience and Clinical neurology, in his works.
He most often published in these fields:
- Genetics (38.17%)
- Pathology (19.76%)
- Mutation (13.44%)
What were the highlights of his more recent work (between 2019-2021)?
- Genetics (38.17%)
- Disease (13.17%)
- Internal medicine (10.35%)
In recent papers he was focusing on the following fields of study:
His scientific interests lie mostly in Genetics, Disease, Internal medicine, Exome sequencing and Phenotype.
Genetics is represented through his Missense mutation, Allele, Gene, Sanger sequencing and Exome research.
His Disease research includes themes of Computational biology, Intellectual disability, Bioinformatics and Genetic architecture.
The study incorporates disciplines such as Gastroenterology and Endocrinology in addition to Internal medicine.
Atrophy is a subfield of Pathology that Henry Houlden explores.
His Pathology research focuses on Cerebellar ataxia and how it relates to Pediatrics and Hypotonia.
Between 2019 and 2021, his most popular works were:
- Cerebellar ataxia, neuropathy, vestibular areflexia syndrome due to RFC1 repeat expansion. (35 citations)
- Diagnosis Across the Spectrum of Progressive Supranuclear Palsy and Corticobasal Syndrome. (23 citations)
- Diagnosis Across the Spectrum of Progressive Supranuclear Palsy and Corticobasal Syndrome. (23 citations)
In his most recent research, the most cited papers focused on:
- Gene
- Mutation
- Internal medicine
Henry Houlden focuses on Genetics, Internal medicine, Cerebellar ataxia, Pathology and Allele.
Phenotype, Missense mutation, Haplotype, Microcephaly and Intron are the primary areas of interest in his Genetics study.
While the research belongs to areas of Internal medicine, Henry Houlden spends his time largely on the problem of Endocrinology, intersecting his research to questions surrounding Hypotonia, Congenital myasthenic syndrome, Neuromuscular junction and Weakness.
His Cerebellar ataxia study incorporates themes from Cerebellum, Molecular biology and Trinucleotide repeat expansion.
His work on Atrophy, Cognitive decline and Calcification as part of general Pathology research is frequently linked to Fragile X-associated tremor/ataxia syndrome, bridging the gap between disciplines.
His Allele study integrates concerns from other disciplines, such as Odds ratio, Hyperintensity, Genetic predisposition, Gastroenterology and Genetic association.
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