Author details

Full Name

Ken Yamamoto

Affiliation

ORCID

Career Start Year

2008

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37425910	Genome-wide association study identifies a new susceptibility locus in <i>PLA2G4C</i> for Multiple System Atrophy.	medRxiv	2023
37034649	Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications.	medRxiv	2023
36464274	The E2F6 Transcription Factor is Associated with the Mammalian SUZ12-Containing Polycomb Complex.	Kurume Medical Journal	2023
35148957	Genome-wide meta-analysis between renal overload type and renal underexcretion type of clinically defined gout in Japanese populations.	Molecular Genetics and Metabolism	2022
35551307	Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation.	Nat Genet	2022
34940612	Diethyl Succinate Modulates Microglial Polarization and Activation by Reducing Mitochondrial Fission and Cellular ROS.	Metabolites	2021
34290349	Dynamin-related protein 1 deficiency accelerates lipopolysaccharide-induced acute liver injury and inflammation in mice.	Communications Biology	2021
33497256	E148Q variant is more associated with familial Mediterranean fever when combined with other non-exon 10 variants in Japanese patients with recurrent fever.	Modern Rheumatology	2021
32951339	A novel de novo SLC26A3 mutation causing congenital chloride diarrhea in a Japanese neonate.	Molecular genetics & genomic medicine	2020
32355309	Genome-wide association study identifies zonisamide responsive gene in Parkinson's disease patients.	Journal of Human Genetics	2020
32238385	Subtype-specific gout susceptibility loci and enrichment of selection pressure on <i>ABCG2</i> and <i>ALDH2</i> identified by subtype genome-wide meta-analyses of clinically defined gout patients.	Ann Rheum Dis	2020
31780526	Dysfunctional missense variant of <i>OAT10/SLC22A13</i> decreases gout risk and serum uric acid levels.	Ann Rheum Dis	2020
32341455	Intronic variant in IQGAP3 associated with hereditary neuropathy with proximal lower dominancy, urinary disturbance, and paroxysmal dry cough.	Journal of Human Genetics	2020
33124714	Congenital chloride diarrhea in a Japanese neonate with a novel SLC26A3 mutation.	Pediatrics International	2020
30993211	Genome-wide meta-analysis identifies multiple novel loci associated with serum uric acid levels in Japanese individuals.	Commun Biol	2019
31289104	Genome-wide association study revealed novel loci which aggravate asymptomatic hyperuricaemia into gout.	Ann Rheum Dis	2019
31476763	Genome-wide association studies identify polygenic effects for completed suicide in the Japanese population.		2019
30480742	Genome-Wide Association Study to Identify a New Susceptibility Locus for Central Serous Chorioretinopathy in the Japanese Population.	Invest Ophthalmol Vis Sci	2018
29879923	Common variant of BCAS3 is associated with gout risk in Japanese population: the first replication study after gout GWAS in Han Chinese.	BMC Medical Genetics	2018
30487518	Interethnic analyses of blood pressure loci in populations of East Asian and European descent.	Nat Commun	2018
28098149	Characterising private and shared signatures of positive selection in 37 Asian populations.	Eur J Hum Genet	2017
28506971	Protein-Truncating Variants at the Cholesteryl Ester Transfer Protein Gene and Risk for Coronary Heart Disease.	Circ Res	2017
28499412	Genome-wide DNA methylation analysis reveals hypomethylation in the low-CpG promoter regions in lymphoblastoid cell lines.	Human Genomics	2017
28414759	Significant association of RNF213 p.R4810K, a moyamoya susceptibility variant, with coronary artery disease.	PLoS ONE	2017
28515798	Epigenome-wide association of myocardial infarction with DNA methylation sites at loci related to cardiovascular disease.	Clinical Epigenetics	2017
29225919	Multiple common and rare variants of cause gout.	RMD Open	2017
29091727	The fine-scale genetic structure and evolution of the Japanese population.	PLoS ONE	2017
27899376	GWAS of clinically defined gout and subtypes identifies multiple susceptibility loci that include urate transporter genes.	Ann Rheum Dis	2017
28169272	A substrate-bound structure of cyanobacterial biliverdin reductase identifies stacked substrates as critical for activity.	Nature Communications	2017
26785701	Genome-wide association studies in East Asians identify new loci for waist-hip ratio and waist circumference.	Sci Rep	2016
25646370	Genome-wide association study of clinically defined gout identifies multiple risk loci and its association with clinical subtypes.	Ann Rheum Dis	2016
27181629	Identification of rs671, a common variant of ALDH2, as a gout susceptibility locus.	Scientific Reports	2016
27091392	Understanding of HLA-conferred susceptibility to chronic hepatitis B infection requires HLA genotyping-based association analysis.	Sci Rep	2016
26449183	Effects of HLA-DPB1 genotypes on chronic hepatitis B infection in Japanese individuals.	Tissue Antigens	2015
25740055	Heterogeneous effects of association between blood pressure loci and coronary artery disease in east Asian individuals.	Circulation Journal	2015
25429064	Meta-analysis of genome-wide association studies of adult height in East Asians identifies 17 novel loci.	Hum Mol Genet	2015
26404063	Epigenome-wide association study suggests that SNPs in the promoter region of RETN influence plasma resistin level via effects on DNA methylation at neighbouring sites.	Diabetologia	2015
26648100	Mapping the genetic diversity of HLA haplotypes in the Japanese populations.	Scientific Reports	2015
26390057	Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation.	Nat Genet	2015
24647736	Multiple nonglycemic genomic loci are newly associated with blood level of glycated hemoglobin in East Asians.	Diabetes	2014
24441388	ABCG2 dysfunction causes hyperuricemia due to both renal urate underexcretion and renal urate overload.	Scientific Reports	2014
24105470	A meta-analysis of genome-wide association studies for adiponectin levels in East Asians identifies a novel locus near WDR11-FGFR2.	Hum Mol Genet	2014
23746317	Genome-wide association study of degenerative bony changes of the temporomandibular joint.	Oral Diseases	2014
24861553	Meta-analysis of genome-wide association studies in East Asian-ancestry populations identifies four new loci for body mass index.	Hum Mol Genet	2014
24978468	Systematic fine-mapping of association with BMI and type 2 diabetes at the FTO locus by integrating results from multiple ethnic groups.	PLoS One	2014
25086001	Genome-wide SNP analysis reveals population structure and demographic history of the ryukyu islanders in the southern part of the Japanese archipelago.	Molecular Biology and Evolution	2014
24509480	Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility.	Nat Genet	2014
23364394	A genome-wide association study of a coronary artery disease risk variant.	Journal of Human Genetics	2013
22729816	Estrogen receptor-Î² gene polymorphism and colorectal cancer risk: effect modified by body mass index and isoflavone intake.	International Journal of Cancer	2013
23774753	Common dysfunctional variants in ABCG2 are a major cause of early-onset gout.	Scientific Reports	2013