His primary areas of study are Genetics, Genome-wide association study, Single-nucleotide polymorphism, Genetic association and Internal medicine. His Genetics research includes elements of Meta-analysis and Obesity. His Genome-wide association study study incorporates themes from SNP, CDKAL1, Polymorphism, Case-control study and Type 2 diabetes.
His research integrates issues of Hyperuricemia and Allele in his study of Single-nucleotide polymorphism. His Genetic association research integrates issues from Imputation, Hemodynamics and Blood pressure. His study in Internal medicine is interdisciplinary in nature, drawing from both Viral disease and Endocrinology.
Ken Yamamoto spends much of his time researching Genetics, Single-nucleotide polymorphism, Genome-wide association study, Internal medicine and Immunology. His is involved in several facets of Genetics study, as is seen by his studies on Allele, Genetic association, Gene, Polymorphism and Locus. The Single-nucleotide polymorphism study combines topics in areas such as Genotyping and Haplotype.
His work deals with themes such as CDKAL1, Gout, Case-control study, Disease and Type 2 diabetes, which intersect with Genome-wide association study. His studies deal with areas such as Gastroenterology, Endocrinology, Oncology and Cardiology as well as Internal medicine. His research investigates the connection between Immunology and topics such as Hemophagocytic lymphohistiocytosis that intersect with problems in Familial Hemophagocytic Lymphohistiocytosis.
Ken Yamamoto mainly focuses on Genome-wide association study, Genetics, Single-nucleotide polymorphism, Gout and Internal medicine. His Genome-wide association study research is multidisciplinary, relying on both Allele, Linkage disequilibrium, Genetic association and Disease. His Allele study integrates concerns from other disciplines, such as Expression quantitative trait loci, Genotyping and Immunology.
His Genetics research incorporates themes from Body mass index and Natural selection. His work in Single-nucleotide polymorphism addresses issues such as Heritability, which are connected to fields such as Blood pressure and Selective sweep. His Internal medicine study incorporates themes from Gastroenterology, Endocrinology, Oncology and T-cell receptor.
Genetics, Genome-wide association study, Single-nucleotide polymorphism, Gout and Locus are his primary areas of study. His study in Genetics concentrates on Gene, Genotype, Genetic association, CpG site and SNP. His Genome-wide association study research includes elements of Quantitative trait locus, Case-control study and Linkage disequilibrium, Haplotype.
His Single-nucleotide polymorphism study frequently intersects with other fields, such as Epigenetics. He has researched Gout in several fields, including Uric acid, Hyperuricemia and Gene polymorphism. His research investigates the connection with Locus and areas like Allele which intersect with concerns in Expression quantitative trait loci and Meta-analysis.
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Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility.
Anubha Mahajan;Min Jin Go;Weihua Zhang;Jennifer E. Below.
Nature Genetics (2014)
Variants in KCNQ1 are associated with susceptibility to type 2 diabetes mellitus.
Kazuki Yasuda;Kazuaki Miyake;Yukio Horikawa;Kazuo Hara.
Nature Genetics (2008)
Meta-analysis of genome-wide association studies identifies eight new loci for type 2 diabetes in east Asians
Yoon Shin Cho;Chien Hsiun Chen;Chien Hsiun Chen;Cheng Hu;Jirong Long.
Nature Genetics (2012)
The clinical significance of human leukocyte antigen (HLA) allele compatibility in patients receiving a marrow transplant from serologically HLA-A, HLA-B, and HLA-DR matched unrelated donors.
Yasuo Morishima;Takehiko Sasazuki;Hidetoshi Inoko;Takeo Juji.
CCAT2, a novel noncoding RNA mapping to 8q24, underlies metastatic progression and chromosomal instability in colon cancer
Hui Ling;Riccardo Spizzo;Yaser Atlasi;Milena Nicoloso.
Genome Research (2013)
Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians
Norihiro Kato;Fumihiko Takeuchi;Yasuharu Tabara;Tanika N. Kelly.
Nature Genetics (2011)
Nationwide survey of hemophagocytic lymphohistiocytosis in Japan.
Eiichi Ishii;Shouichi Ohga;Shinsaku Imashuku;Masaki Yasukawa.
International Journal of Hematology (2007)
Meta-analysis identifies common variants associated with body mass index in east Asians
Wanqing Wen;Yoon Shin Cho;Wei Zheng;Rajkumar Dorajoo;Rajkumar Dorajoo.
Nature Genetics (2012)
Sexual maturation of Japanese eel and production of eel larvae in the aquarium
K. Yamamoto;K. Yamauchi.
Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation
Norihiro Kato;Marie Loh;Marie Loh;Marie Loh;Fumihiko Takeuchi;Niek Verweij.
Nature Genetics (2015)
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