Lista de obras -

A deletion mutation in myosin heavy chain 11 causing familial thoracic aortic dissection in two Japanese pedigrees

artículo científico publicado en 2015

A functional SNP in CILP, encoding cartilage intermediate layer protein, is associated with susceptibility to lumbar disc disease

artículo científico publicado en 2005

A functional SNP in FLT1 increases risk of coronary artery disease in a Japanese population

artículo científico publicado en 2016

A functional SNP in PSMA6 confers risk of myocardial infarction in the Japanese population

artículo científico publicado en 2006

A functional variant in ZNF512B is associated with susceptibility to amyotrophic lateral sclerosis in Japanese

A genome-wide association analysis identifies NMNAT2 and HCP5 as susceptibility loci for Kawasaki disease.

artículo científico

A genome-wide association study identified AFF1 as a susceptibility locus for systemic lupus eyrthematosus in Japanese

scientific journal article

A genome-wide association study identifies 2 susceptibility Loci for Crohn's disease in a Japanese population

scientific journal article

A genome-wide association study identifies PLCL2 and AP3D1-DOT1L-SF3A2 as new susceptibility loci for myocardial infarction in Japanese

scientific journal article

A genome-wide association study identifies common variants near LBX1 associated with adolescent idiopathic scoliosis

artículo científico publicado en 2011

A genome-wide association study identifies four susceptibility loci for keloid in the Japanese population

artículo científico publicado en 2010

A genome-wide association study identifies locus at 10q22 associated with clinical outcomes of adjuvant tamoxifen therapy for breast cancer patients in Japanese

scientific journal article

A genome-wide association study identifies three new risk loci for Kawasaki disease

artículo científico publicado en 2012

A genome-wide association study identifies three new susceptibility loci for ulcerative colitis in the Japanese population

artículo científico publicado en 2009

A genome-wide association study identifies variants in the HLA-DP locus associated with chronic hepatitis B in Asians.

artículo científico publicado en 2009

A genome-wide association study in the Japanese population identifies susceptibility loci for type 2 diabetes at UBE2E2 and C2CD4A-C2CD4B

artículo científico publicado en 2010

A genome-wide association study of chronic hepatitis B identified novel risk locus in a Japanese population

scientific article published on 12 July 2011

A genome-wide association study of nephrolithiasis in the Japanese population identifies novel susceptible Loci at 5q35.3, 7p14.3, and 13q14.1

scientific journal article

A practical method to detect SNVs and indels from whole genome and exome sequencing data

artículo científico publicado en 2013

A regulatory variant in CCR6 is associated with rheumatoid arthritis susceptibility

artículo científico publicado en 2010

A second generation human haplotype map of over 3.1 million SNPs

artículo científico publicado en 2007

A single-nucleotide polymorphism in ANK1 is associated with susceptibility to type 2 diabetes in Japanese populations

artículo científico publicado en 2012

Analyses of non-coding somatic drivers in 2,658 cancer whole genomes

artículo científico publicado en 2020

Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels

artículo científico publicado en 2017

Association of a novel long non-coding RNA in 8q24 with prostate cancer susceptibility

artículo científico publicado en 2010

Association of an IGHV3-66 gene variant with Kawasaki disease

artículo científico publicado en 2020

Association study of COL9A2 with lumbar disc disease in the Japanese population

artículo científico publicado en 2006

CYP2D6 genotyping for functional-gene dosage analysis by allele copy number detection

artículo científico publicado en 2009

Circulating Tumor DNA Analysis for Liver Cancers and Its Usefulness as a Liquid Biopsy

artículo científico publicado en 2015

Common variants at CDKAL1 and KLF9 are associated with body mass index in east Asian populations

artículo científico publicado en 2012

Common variants on 14q32 and 13q12 are associated with DLBCL susceptibility

scientific journal article

DeepInsight: A methodology to transform a non-image data to an image for convolution neural network architecture

artículo científico publicado en 2019

Erratum: Whole-genome mutational landscape and characterization of noncoding and structural mutations in liver cancer

artículo científico publicado en 2016

Exome Analyses of Long QT Syndrome Reveal Candidate Pathogenic Mutations in Calmodulin-Interacting Genes

artículo científico publicado en 2015

Exploring predictive biomarkers from clinical genome-wide association studies via multidimensional hierarchical mixture models

artículo científico publicado en 2018

Functional SNPs in CD244 increase the risk of rheumatoid arthritis in a Japanese population.

artículo científico publicado en 2008

Functional variants in ADH1B and ALDH2 coupled with alcohol and smoking synergistically enhance esophageal cancer risk

artículo científico publicado en 2009

Functional variants in NFKBIE and RTKN2 involved in activation of the NF-κB pathway are associated with rheumatoid arthritis in Japanese

scientific journal article

Gene expression dataset for whole cochlea of Macaca fascicularis

artículo científico publicado en 2018

Genetic Variation in the SLC8A1 Calcium Signaling Pathway Is Associated With Susceptibility to Kawasaki Disease and Coronary Artery Abnormalities

artículo científico publicado en 2016

Genetic differences in the two main groups of the Japanese population based on autosomal SNPs and haplotypes

artículo científico publicado en 2012

Genetic variants in GPR126 are associated with adolescent idiopathic scoliosis

artículo científico publicado en 2013

Genome-Wide Association Study of Peripheral Arterial Disease in a Japanese Population

artículo científico publicado en 2015

Genome-wide association study for C-reactive protein levels identified pleiotropic associations in the IL6 locus

Genome-wide association study identifies eight new susceptibility loci for atopic dermatitis in the Japanese population

scientific journal article

Genome-wide association study identifies five new susceptibility loci for prostate cancer in the Japanese population

scientific journal article

Genome-wide association study identifies three new susceptibility loci for adult asthma in the Japanese population

scientific journal article

Genome-wide association study identifies three novel loci for type 2 diabetes

artículo científico publicado en 2013

Genome-wide association study suggests four variants influencing outcomes with ranibizumab therapy in exudative age-related macular degeneration

artículo científico publicado en 2018

Genome-wide detection and characterization of positive selection in human populations

artículo científico publicado en 2007

Growth Hormone-Dependent Pathogenesis of Human Hepatic Steatosis in a Novel Mouse Model Bearing a Human Hepatocyte-Repopulated Liver ⬇️

artículo científico publicado el 8 de febrero de 2011

HLA-DQB1*03 confers susceptibility to chronic hepatitis C in Japanese: a genome-wide association study

artículo científico publicado en 2013

Hierarchical Maximum Likelihood Clustering Approach

artículo científico publicado en 2017

IL-28B predicts response to chronic hepatitis C therapy--fine-mapping and replication study in Asian populations.

artículo científico publicado en 2011

IMSindel: An accurate intermediate-size indel detection tool incorporating de novo assembly and gapped global-local alignment with split read analysis.

artículo científico publicado en 2018

IRX4 at 5p15 suppresses prostate cancer growth through the interaction with vitamin D receptor, conferring prostate cancer susceptibility

artículo científico publicado en 2012

Identification of a susceptibility locus for severe adolescent idiopathic scoliosis on chromosome 17q24.3.

artículo científico publicado en 2013

Identification of independent risk loci for Graves' disease within the MHC in the Japanese population

artículo científico publicado en 2011

Identification of nine novel loci associated with white blood cell subtypes in a Japanese population

artículo científico publicado en 2011

Immune subtypes and neoantigen-related immune evasion in advanced colorectal cancer

artículo científico publicado en 2022

Integrated analysis of human genetic association study and mouse transcriptome suggests LBH and SHF genes as novel susceptible genes for amyloid-β accumulation in Alzheimer's disease

scientific article published on 13 July 2018

Integrated analysis of whole genome and transcriptome sequencing reveals diverse transcriptomic aberrations driven by somatic genomic changes in liver cancers

artículo científico publicado en 2014

Integrating genetic, transcriptional, and functional analyses to identify 5 novel genes for atrial fibrillation

artículo científico publicado en 2014

International network of cancer genome projects

artículo científico publicado en 2010

Lessons for pharmacogenomics studies: association study between CYP2D6 genotype and tamoxifen response

artículo científico publicado en 2010

Lumbar disc degeneration is linked to a carbohydrate sulfotransferase 3 variant.

artículo científico publicado en 2013

Making a haplotype catalog with estimated frequencies based on SNP homozygotes

artículo científico publicado en 2010

Meta-analysis identifies common variants associated with body mass index in east Asians

artículo científico publicado en 2012

Meta-analysis identifies multiple loci associated with kidney function-related traits in east Asian populations

artículo científico publicado en 2012

Meta-analysis identifies six new susceptibility loci for atrial fibrillation

artículo científico publicado en 2012

Meta-analysis of genome-wide association studies in East Asian-ancestry populations identifies four new loci for body mass index

artículo científico publicado en 2014

Meta-analysis of genome-wide association studies of adult height in East Asians identifies 17 novel loci

artículo científico publicado en 2014

Microarray Analysis of Gene‐expression Profiles in Diffuse Large B‐cell Lymphoma: Identification of Genes Related to Disease Progression ⬇️

artículo científico publicado el 1 de agosto de 2002

Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks.

artículo científico publicado en 2017

Multiple loci are associated with white blood cell phenotypes

artículo científico publicado en 2011

New sequence variants in HLA class II/III region associated with susceptibility to knee osteoarthritis identified by genome-wide association study

artículo científico publicado en 2010

Novel calmodulin mutations associated with congenital arrhythmia susceptibility

artículo científico publicado en 2014

Novel genetic markers associate with atrial fibrillation risk in Europeans and Japanese

artículo científico publicado en 2014

Pathway analysis of genome-wide data improves warfarin dose prediction

artículo científico publicado en 2013

Performance comparison of four commercial human whole-exome capture platforms

artículo científico publicado en 2015

PhoglyStruct: Prediction of phosphoglycerylated lysine residues using structural properties of amino acids

artículo científico publicado en 2018

Polygenic burdens on cell-specific pathways underlie the risk of rheumatoid arthritis

artículo científico publicado en 2017

Prepublication data sharing

artículo científico publicado en 2009

Profiling the inhibitory receptors LAG-3, TIM-3, and TIGIT in renal cell carcinoma reveals malignancy

artículo científico publicado en 2021

Publisher Correction: IMSindel: An accurate intermediate-size indel detection tool incorporating de novo assembly and gapped global-local alignment with split read analysis

artículo científico publicado en 2018

Quantification of multicellular colonization in tumor metastasis using exome-sequencing data

scientific article published on 15 February 2020

RAM-PGK: Prediction of Lysine Phosphoglycerylation Based on Residue Adjacency Matrix

artículo científico publicado en 2020

Reproducibility, performance, and clinical utility of a genetic risk prediction model for prostate cancer in Japanese

artículo científico publicado en 2012

Risk prediction models for dementia constructed by supervised principal component analysis using miRNA expression data

artículo científico publicado en 2019

SNPs in KCNQ1 are associated with susceptibility to type 2 diabetes in East Asian and European populations

article

SNPs on chromosome 5p15.3 associated with myocardial infarction in Japanese population

artículo científico publicado en 2010

Significant effect of polymorphisms in CYP2D6 and ABCC2 on clinical outcomes of adjuvant tamoxifen therapy for breast cancer patients

artículo científico publicado en 2010

Stepwise iterative maximum likelihood clustering approach

artículo científico publicado en 2016

The construction of risk prediction models using GWAS data and its application to a type 2 diabetes prospective cohort

artículo científico publicado en 2014

The prediction models for postoperative overall survival and disease-free survival in patients with breast cancer

artículo científico publicado en 2017

Variants encoding a restricted carboxy-terminal domain of SLC12A2 cause hereditary hearing loss in humans

scientific article published on 15 April 2020

Variants in the SCN5A Promoter Associated With Various Arrhythmia Phenotypes

artículo científico publicado en 2016

Variation in TP63 is associated with lung adenocarcinoma susceptibility in Japanese and Korean populations

scientific article published on 26 September 2010

Variation in the DEPDC5 locus is associated with progression to hepatocellular carcinoma in chronic hepatitis C virus carriers

scientific journal article

Whole genome sequencing discriminates hepatocellular carcinoma with intrahepatic metastasis from multi-centric tumors

artículo científico publicado en 2016

Whole-genome mutational landscape and characterization of noncoding and structural mutations in liver cancer.

artículo científico publicado en 2016

Whole-genome mutational landscape of liver cancers displaying biliary phenotype reveals hepatitis impact and molecular diversity

artículo científico publicado en 2015

Whole-genome sequencing and comprehensive variant analysis of a Japanese individual using massively parallel sequencing

article

Whole-genome sequencing of liver cancers identifies etiological influences on mutation patterns and recurrent mutations in chromatin regulators

artículo científico publicado en 2012

Lista de obras de

A deletion mutation in myosin heavy chain 11 causing familial thoracic aortic dissection in two Japanese pedigrees

A functional SNP in CILP, encoding cartilage intermediate layer protein, is associated with susceptibility to lumbar disc disease

A functional SNP in FLT1 increases risk of coronary artery disease in a Japanese population

A functional SNP in PSMA6 confers risk of myocardial infarction in the Japanese population

A functional variant in ZNF512B is associated with susceptibility to amyotrophic lateral sclerosis in Japanese

A genome-wide association analysis identifies NMNAT2 and HCP5 as susceptibility loci for Kawasaki disease.

A genome-wide association study identified AFF1 as a susceptibility locus for systemic lupus eyrthematosus in Japanese

A genome-wide association study identifies 2 susceptibility Loci for Crohn's disease in a Japanese population

A genome-wide association study identifies PLCL2 and AP3D1-DOT1L-SF3A2 as new susceptibility loci for myocardial infarction in Japanese

A genome-wide association study identifies common variants near LBX1 associated with adolescent idiopathic scoliosis

A genome-wide association study identifies four susceptibility loci for keloid in the Japanese population

A genome-wide association study identifies locus at 10q22 associated with clinical outcomes of adjuvant tamoxifen therapy for breast cancer patients in Japanese

A genome-wide association study identifies three new risk loci for Kawasaki disease

A genome-wide association study identifies three new susceptibility loci for ulcerative colitis in the Japanese population

A genome-wide association study identifies variants in the HLA-DP locus associated with chronic hepatitis B in Asians.

A genome-wide association study in the Japanese population identifies susceptibility loci for type 2 diabetes at UBE2E2 and C2CD4A-C2CD4B

A genome-wide association study of chronic hepatitis B identified novel risk locus in a Japanese population

A genome-wide association study of nephrolithiasis in the Japanese population identifies novel susceptible Loci at 5q35.3, 7p14.3, and 13q14.1

A practical method to detect SNVs and indels from whole genome and exome sequencing data

A regulatory variant in CCR6 is associated with rheumatoid arthritis susceptibility

A second generation human haplotype map of over 3.1 million SNPs

A single-nucleotide polymorphism in ANK1 is associated with susceptibility to type 2 diabetes in Japanese populations

Analyses of non-coding somatic drivers in 2,658 cancer whole genomes

Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels

Association of a novel long non-coding RNA in 8q24 with prostate cancer susceptibility

Association of an IGHV3-66 gene variant with Kawasaki disease

Association study of COL9A2 with lumbar disc disease in the Japanese population

CYP2D6 genotyping for functional-gene dosage analysis by allele copy number detection

Circulating Tumor DNA Analysis for Liver Cancers and Its Usefulness as a Liquid Biopsy

Common variants at CDKAL1 and KLF9 are associated with body mass index in east Asian populations

Common variants on 14q32 and 13q12 are associated with DLBCL susceptibility

DeepInsight: A methodology to transform a non-image data to an image for convolution neural network architecture

Erratum: Whole-genome mutational landscape and characterization of noncoding and structural mutations in liver cancer

Exome Analyses of Long QT Syndrome Reveal Candidate Pathogenic Mutations in Calmodulin-Interacting Genes

Exploring predictive biomarkers from clinical genome-wide association studies via multidimensional hierarchical mixture models

Functional SNPs in CD244 increase the risk of rheumatoid arthritis in a Japanese population.

Functional variants in ADH1B and ALDH2 coupled with alcohol and smoking synergistically enhance esophageal cancer risk

Functional variants in NFKBIE and RTKN2 involved in activation of the NF-κB pathway are associated with rheumatoid arthritis in Japanese

Gene expression dataset for whole cochlea of Macaca fascicularis

Genetic Variation in the SLC8A1 Calcium Signaling Pathway Is Associated With Susceptibility to Kawasaki Disease and Coronary Artery Abnormalities

Genetic differences in the two main groups of the Japanese population based on autosomal SNPs and haplotypes

Genetic variants in GPR126 are associated with adolescent idiopathic scoliosis

Genome-Wide Association Study of Peripheral Arterial Disease in a Japanese Population

Genome-wide association study for C-reactive protein levels identified pleiotropic associations in the IL6 locus

Genome-wide association study identifies eight new susceptibility loci for atopic dermatitis in the Japanese population

Genome-wide association study identifies five new susceptibility loci for prostate cancer in the Japanese population

Genome-wide association study identifies three new susceptibility loci for adult asthma in the Japanese population

Genome-wide association study identifies three novel loci for type 2 diabetes

Genome-wide association study suggests four variants influencing outcomes with ranibizumab therapy in exudative age-related macular degeneration

Genome-wide detection and characterization of positive selection in human populations

Growth Hormone-Dependent Pathogenesis of Human Hepatic Steatosis in a Novel Mouse Model Bearing a Human Hepatocyte-Repopulated Liver ⬇️

HLA-DQB1*03 confers susceptibility to chronic hepatitis C in Japanese: a genome-wide association study

Hierarchical Maximum Likelihood Clustering Approach

IL-28B predicts response to chronic hepatitis C therapy--fine-mapping and replication study in Asian populations.

IMSindel: An accurate intermediate-size indel detection tool incorporating de novo assembly and gapped global-local alignment with split read analysis.

IRX4 at 5p15 suppresses prostate cancer growth through the interaction with vitamin D receptor, conferring prostate cancer susceptibility

Identification of a susceptibility locus for severe adolescent idiopathic scoliosis on chromosome 17q24.3.

Identification of independent risk loci for Graves' disease within the MHC in the Japanese population

Identification of nine novel loci associated with white blood cell subtypes in a Japanese population

Immune subtypes and neoantigen-related immune evasion in advanced colorectal cancer

Integrated analysis of human genetic association study and mouse transcriptome suggests LBH and SHF genes as novel susceptible genes for amyloid-β accumulation in Alzheimer's disease

Integrated analysis of whole genome and transcriptome sequencing reveals diverse transcriptomic aberrations driven by somatic genomic changes in liver cancers

Integrating genetic, transcriptional, and functional analyses to identify 5 novel genes for atrial fibrillation

International network of cancer genome projects

Lessons for pharmacogenomics studies: association study between CYP2D6 genotype and tamoxifen response

Lumbar disc degeneration is linked to a carbohydrate sulfotransferase 3 variant.

Making a haplotype catalog with estimated frequencies based on SNP homozygotes

Meta-analysis identifies common variants associated with body mass index in east Asians

Meta-analysis identifies multiple loci associated with kidney function-related traits in east Asian populations

Meta-analysis identifies six new susceptibility loci for atrial fibrillation

Meta-analysis of genome-wide association studies in East Asian-ancestry populations identifies four new loci for body mass index

Meta-analysis of genome-wide association studies of adult height in East Asians identifies 17 novel loci

Microarray Analysis of Gene‐expression Profiles in Diffuse Large B‐cell Lymphoma: Identification of Genes Related to Disease Progression ⬇️

Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks.

Multiple loci are associated with white blood cell phenotypes

New sequence variants in HLA class II/III region associated with susceptibility to knee osteoarthritis identified by genome-wide association study

Novel calmodulin mutations associated with congenital arrhythmia susceptibility

Novel genetic markers associate with atrial fibrillation risk in Europeans and Japanese

Pathway analysis of genome-wide data improves warfarin dose prediction