What is he best known for?
The fields of study he is best known for:
- Gene
- Internal medicine
- Genetics
Yoichi Suzuki mainly investigates Genetics, Single-nucleotide polymorphism, Molecular biology, Immunology and Haplotype.
Hearing loss and Caenorhabditis elegans is closely connected to Cell biology in his research, which is encompassed under the umbrella topic of Genetics.
His Single-nucleotide polymorphism study combines topics from a wide range of disciplines, such as Kawasaki disease and Allele.
His Molecular biology research is multidisciplinary, incorporating perspectives in Complementary DNA, Multiple carboxylase deficiency and Mutant, Point mutation.
His research in Immunology intersects with topics in Phenotype and Genetic association.
Many of his research projects under Haplotype are closely connected to Eosinophil activation with Eosinophil activation, tying the diverse disciplines of science together.
His most cited work include:
- Germline mutations in HRAS proto-oncogene cause Costello syndrome (524 citations)
- A genome-wide association study identifies RNF213 as the first Moyamoya disease gene (354 citations)
- Type 1 Phosphatase, a Negative Regulator of Cardiac Function (232 citations)
What are the main themes of his work throughout his whole career to date?
Yoichi Suzuki spends much of his time researching Genetics, Immunology, Single-nucleotide polymorphism, Molecular biology and Internal medicine.
His work is connected to Gene, Mutation, Allele, Exon and Missense mutation, as a part of Genetics.
His Immunology research is multidisciplinary, incorporating elements of Allele frequency and Genotype.
Yoichi Suzuki has researched Single-nucleotide polymorphism in several fields, including Case-control study and Haplotype.
His Molecular biology research incorporates themes from Complementary DNA, Biochemistry, Point mutation and Holocarboxylase synthetase deficiency.
His studies link Endocrinology with Internal medicine.
He most often published in these fields:
- Genetics (25.37%)
- Immunology (23.88%)
- Single-nucleotide polymorphism (15.42%)
What were the highlights of his more recent work (between 2016-2021)?
- Cohort study (4.48%)
- Genetics (25.37%)
- Internal medicine (13.93%)
In recent papers he was focusing on the following fields of study:
His main research concerns Cohort study, Genetics, Internal medicine, Cohort and Amyotrophic lateral sclerosis.
His Cohort study study incorporates themes from Biobank, Prospective cohort study, Personalized medicine and Incidence.
His study involves Genome-wide association study, Gene and Genome, a branch of Genetics.
The subject of his Genome-wide association study research is within the realm of Single-nucleotide polymorphism.
Yoichi Suzuki works in the field of Single-nucleotide polymorphism, focusing on Genetic association in particular.
His work on Peripheral blood, Respiratory system, Obesity and Quiet breathing is typically connected to Forced Oscillation Technique as part of general Internal medicine study, connecting several disciplines of science.
Between 2016 and 2021, his most popular works were:
- Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma (47 citations)
- Cohort Profile: Tohoku Medical Megabank Project Birth and Three-Generation Cohort Study (TMM BirThree Cohort Study): rationale, progress and perspective. (23 citations)
- Genome analyses for the Tohoku Medical Megabank Project towards establishment of personalized healthcare. (23 citations)
In his most recent research, the most cited papers focused on:
- Gene
- Internal medicine
- Mutation
Yoichi Suzuki focuses on Genomics, Cohort study, Cohort, Atopic dermatitis and Food allergy.
In his study, which falls under the umbrella issue of Cohort study, Omics and Prospective cohort study is strongly linked to Family medicine.
His Atopic dermatitis research is multidisciplinary, relying on both Mutation and Allergy.
The study incorporates disciplines such as Psychological intervention and Outcome assessment in addition to Immunology.
His Allele study contributes to a more complete understanding of Genetics.
His study in Single-nucleotide polymorphism and Candidate gene are all subfields of Genetics.
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