List of works - Toshihiro Tanaka

A second generation human haplotype map of over 3.1 million SNPs

scientific article

Genetic studies of body mass index yield new insights for obesity biology

scientific article

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

scientific article

Complete sequencing and characterization of 21,243 full-length human cDNAs

scientific article

Functional SNPs in the lymphotoxin-alpha gene that are associated with susceptibility to myocardial infarction

scientific article published on 11 November 2002

Genome-wide association analyses identify 18 new loci associated with serum urate concentrations

scientific article published in February 2013

A high-throughput SNP typing system for genome-wide association studies

Meta-analysis identifies six new susceptibility loci for atrial fibrillation

scientific article published on 29 April 2012

Identification of a novel non-coding RNA, MIAT, that confers risk of myocardial infarction

scientific article

A functional polymorphism in the 5' UTR of GDF5 is associated with susceptibility to osteoarthritis

scientific article published on 25 March 2007

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

scientific article published on 19 February 2012

p53DINP1, a p53-inducible gene, regulates p53-dependent apoptosis

scientific journal article

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

scientific article published on 15 July 2012

Large-scale genome-wide association studies in East Asians identify new genetic loci influencing metabolic traits

scientific article published on 11 September 2011

Gene-based SNP discovery as part of the Japanese Millennium Genome Project: identification of 190,562 genetic variations in the human genome. Single-nucleotide polymorphism

scientific article published on January 2002

JSNP: a database of common gene variations in the Japanese population

scientific article published on January 2002

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

scientific article published on 25 March 2012

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

scientific article published on 19 February 2012

Diverse transcriptional initiation revealed by fine, large-scale mapping of mRNA start sites

scientific article

Functional variation in LGALS2 confers risk of myocardial infarction and regulates lymphotoxin-alpha secretion in vitro

scientific article

Linkage of Familial Moyamoya Disease (Spontaneous Occlusion of the Circle of Willis) to Chromosome 17q25

scientific article published on 01 April 2000

The p53 family member genes are involved in the Notch signal pathway

scientific article

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

scientific article published on 14 August 2014

Identification and characterization of the potential promoter regions of 1031 kinds of human genes

scientific article

Osteopenia and male-specific sudden cardiac death in mice lacking a zinc transporter gene, Znt5.

scientific article

Identification of the gene responsible for gelatinous drop-like corneal dystrophy

scientific article

Common variants in CASP3 confer susceptibility to Kawasaki disease

scientific article

Multiple loci are associated with white blood cell phenotypes

scientific article

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

scientific article

Homocysteine and Coronary Heart Disease: Meta-analysis of MTHFR Case-Control Studies, Avoiding Publication Bias

scientific article (publication date: February 2012)

Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation.

scientific article

Common variants in DVWA on chromosome 3p24.3 are associated with susceptibility to knee osteoarthritis

scientific article

Alterations of gene expression during colorectal carcinogenesis revealed by cDNA microarrays after laser-capture microdissection of tumor tissues and normal epithelia.

scientific article

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

scientific article published on 30 January 2014

A functional polymorphism in THBS2 that affects alternative splicing and MMP binding is associated with lumbar-disc herniation

scientific article

Identification by cDNA microarray of genes involved in ovarian carcinogenesis

article

Small intestinal stem cell identity is maintained with functional Paneth cells in heterotopically grafted epithelium onto the colon

scientific article published on August 2014

Novel calmodulin mutations associated with congenital arrhythmia susceptibility

scientific article published on 10 June 2014

Multi-ethnic genome-wide association study for atrial fibrillation

article

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

scientific article

ITPKC and CASP3 polymorphisms and risks for IVIG unresponsiveness and coronary artery lesion formation in Kawasaki disease

Mutations in the NMMHC-A gene cause autosomal dominant macrothrombocytopenia with leukocyte inclusions (May-Hegglin anomaly/Sebastian syndrome).

scientific article

Discovery and fine mapping of serum protein loci through transethnic meta-analysis

scientific article

SNPs in BRAP associated with risk of myocardial infarction in Asian populations.

scientific article published on 8 February 2009

Identification of AXUD1, a novel human gene induced by AXIN1 and its reduced expression in human carcinomas of the lung, liver, colon and kidney

scientific article

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

scientific article

The Id2 gene is a novel target of transcriptional activation by EWS-ETS fusion proteins in Ewing family tumors.

scientific article

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

Four novel KVLQT1 and four novel HERG mutations in familial long-QT syndrome

scientific article published on February 1997

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

scientific article

List of works by Toshihiro Tanaka

A second generation human haplotype map of over 3.1 million SNPs

Genetic studies of body mass index yield new insights for obesity biology

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

Complete sequencing and characterization of 21,243 full-length human cDNAs

Functional SNPs in the lymphotoxin-alpha gene that are associated with susceptibility to myocardial infarction

Genome-wide association analyses identify 18 new loci associated with serum urate concentrations

A high-throughput SNP typing system for genome-wide association studies

Meta-analysis identifies six new susceptibility loci for atrial fibrillation

Identification of a novel non-coding RNA, MIAT, that confers risk of myocardial infarction

A functional polymorphism in the 5' UTR of GDF5 is associated with susceptibility to osteoarthritis

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

p53DINP1, a p53-inducible gene, regulates p53-dependent apoptosis

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

Large-scale genome-wide association studies in East Asians identify new genetic loci influencing metabolic traits

Gene-based SNP discovery as part of the Japanese Millennium Genome Project: identification of 190,562 genetic variations in the human genome. Single-nucleotide polymorphism

JSNP: a database of common gene variations in the Japanese population

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

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

Diverse transcriptional initiation revealed by fine, large-scale mapping of mRNA start sites

Functional variation in LGALS2 confers risk of myocardial infarction and regulates lymphotoxin-alpha secretion in vitro

Linkage of Familial Moyamoya Disease (Spontaneous Occlusion of the Circle of Willis) to Chromosome 17q25

The p53 family member genes are involved in the Notch signal pathway

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

Identification and characterization of the potential promoter regions of 1031 kinds of human genes

Osteopenia and male-specific sudden cardiac death in mice lacking a zinc transporter gene, Znt5.

Identification of the gene responsible for gelatinous drop-like corneal dystrophy

Common variants in CASP3 confer susceptibility to Kawasaki disease

Multiple loci are associated with white blood cell phenotypes

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

Homocysteine and Coronary Heart Disease: Meta-analysis of MTHFR Case-Control Studies, Avoiding Publication Bias

Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation.

Common variants in DVWA on chromosome 3p24.3 are associated with susceptibility to knee osteoarthritis

Alterations of gene expression during colorectal carcinogenesis revealed by cDNA microarrays after laser-capture microdissection of tumor tissues and normal epithelia.

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

A functional polymorphism in THBS2 that affects alternative splicing and MMP binding is associated with lumbar-disc herniation

Identification by cDNA microarray of genes involved in ovarian carcinogenesis

Small intestinal stem cell identity is maintained with functional Paneth cells in heterotopically grafted epithelium onto the colon

Novel calmodulin mutations associated with congenital arrhythmia susceptibility

Multi-ethnic genome-wide association study for atrial fibrillation

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

ITPKC and CASP3 polymorphisms and risks for IVIG unresponsiveness and coronary artery lesion formation in Kawasaki disease

Mutations in the NMMHC-A gene cause autosomal dominant macrothrombocytopenia with leukocyte inclusions (May-Hegglin anomaly/Sebastian syndrome).

Discovery and fine mapping of serum protein loci through transethnic meta-analysis

SNPs in BRAP associated with risk of myocardial infarction in Asian populations.

Identification of AXUD1, a novel human gene induced by AXIN1 and its reduced expression in human carcinomas of the lung, liver, colon and kidney

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

The Id2 gene is a novel target of transcriptional activation by EWS-ETS fusion proteins in Ewing family tumors.

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

Four novel KVLQT1 and four novel HERG mutations in familial long-QT syndrome

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