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.
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.
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.
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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Germline mutations in HRAS proto-oncogene cause Costello syndrome
Yoko Aoki;Tetsuya Niihori;Hiroshi Kawame;Kenji Kurosawa.
Nature Genetics (2005)
A genome-wide association study identifies RNF213 as the first Moyamoya disease gene
Fumiaki Kamada;Yoko Aoki;Ayumi Narisawa;Yu Abe.
Journal of Human Genetics (2011)
A genome-wide association study identifies three new risk loci for Kawasaki disease
Yoshihiro Onouchi;Kouichi Ozaki;Jane C Burns;Jane C Burns;Chisato Shimizu;Chisato Shimizu.
Nature Genetics (2012)
Type 1 Phosphatase, a Negative Regulator of Cardiac Function
Andrew N. Carr;Albrecht G. Schmidt;Yoichi Suzuki;Federica Del Monte.
Molecular and Cellular Biology (2002)
Thymic Stromal Lymphopoietin Gene Promoter Polymorphisms Are Associated with Susceptibility to Bronchial Asthma
Michishige Harada;Tomomitsu Hirota;Aya I. Jodo;Yuki Hitomi.
American Journal of Respiratory Cell and Molecular Biology (2011)
Associations of functional NLRP3 polymorphisms with susceptibility to food-induced anaphylaxis and aspirin-induced asthma.
Yuki Hitomi;Motohiro Ebisawa;Morimitsu Tomikawa;Takanori Imai.
The Journal of Allergy and Clinical Immunology (2009)
Transgenic expression of a dominant-negative connexin26 causes degeneration of the organ of Corti and non-syndromic deafness
Takayuki Kudo;Shigeo Kure;Katsuhisa Ikeda;An Ping Xia.
Human Molecular Genetics (2003)
Insulin control of glycogen metabolism in knockout mice lacking the muscle-specific protein phosphatase PP1G/RGL.
Yoichi Suzuki;Carita Lanner;Jong-Hwa Kim;Pier Giuseppe Vilardo.
Molecular and Cellular Biology (2001)
The Tohoku Medical Megabank Project: Design and Mission
Shinichi Kuriyama;Nobuo Yaegashi;Fuji Nagami;Tomohiko Arai.
Journal of Epidemiology (2016)
Isolation and characterization of mutations in the human holocarboxylase synthetase cDNA
Yoichi Suzuki;Yoko Aoki;Yoshinori Ishida;Yasushi Chiba.
Nature Genetics (1994)
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