Toshihiro Tanaka
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Computer Science
Toshihiro Tanaka's Degrees
- PhD Computer Science University of Tokyo
- Masters Computer Science University of Tokyo
- Bachelors Computer Science University of Tokyo
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(Suggest an Edit or Addition)Toshihiro Tanaka's Published Works
Number of citations in a given year to any of this author's works
Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- The International HapMap Project (2003) (5160)
- A second generation human haplotype map of over 3.1 million SNPs (2007) (4567)
- Genetic studies of body mass index yield new insights for obesity biology (2015) (3549)
- Sequencing of Aspergillus nidulans and comparative analysis with A. fumigatus and A. oryzae (2005) (1321)
- Genome sequencing and analysis of Aspergillus oryzae (2005) (1134)
- Complete sequencing and characterization of 21,243 full-length human cDNAs (2004) (879)
- Functional SNPs in the lymphotoxin-α gene that are associated with susceptibility to myocardial infarction (2002) (730)
- Cohesin's binding to chromosomes depends on a separate complex consisting of Scc2 and Scc4 proteins. (2000) (713)
- Genome-wide association analyses identify 18 new loci associated with serum urate concentrations (2012) (678)
- Identification of a novel non-coding RNA, MIAT, that confers risk of myocardial infarction (2006) (568)
- Meta-analysis identifies six new susceptibility loci for atrial fibrillation (2012) (535)
- A functional polymorphism in the 5′ UTR of GDF5 is associated with susceptibility to osteoarthritis (2007) (486)
- A high-throughput SNP typing system for genome-wide association studies (2001) (433)
- Multi-ethnic genome-wide association study for atrial fibrillation (2018) (425)
- Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function (2016) (388)
- Meta-analysis identifies common variants associated with body mass index in East Asians (2012) (372)
- p53DINP1, a p53-inducible gene, regulates p53-dependent apoptosis. (2001) (353)
- Identification by cDNA microarray of genes involved in ovarian carcinogenesis. (2000) (349)
- Overview of the BioBank Japan Project: Study design and profile (2017) (346)
- Inhibitory effect of citrus nobiletin on phorbol ester-induced skin inflammation, oxidative stress, and tumor promotion in mice. (2000) (345)
- Gene-based SNP discovery as part of the Japanese Millennium Genome Project: identification of 190 562 genetic variations in the human genome (2002) (312)
- Alterations of gene expression during colorectal carcinogenesis revealed by cDNA microarrays after laser-capture microdissection of tumor tissues and normal epithelia. (2001) (304)
- JSNP: a database of common gene variations in the Japanese population (2002) (291)
- Large-scale genome-wide association studies in east Asians identify new genetic loci influencing metabolic traits (2011) (271)
- A genome-wide association study identifies three new risk loci for Kawasaki disease (2012) (268)
- Meta-analysis identifies multiple loci associated with kidney function–related traits in east Asian populations (2012) (264)
- Identification and characterization of the potential promoter regions of 1031 kinds of human genes. (2001) (260)
- Linkage of familial moyamoya disease (spontaneous occlusion of the circle of Willis) to chromosome 17q25. (2000) (253)
- Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation (2017) (243)
- A new method for rapid visualization of defects in leaf cuticle reveals five intrinsic patterns of surface defects in Arabidopsis. (2004) (238)
- Functional variation in LGALS2 confers risk of myocardial infarction and regulates lymphotoxin-α secretion in vitro (2004) (237)
- Ordered recruitment of transcription and chromatin remodeling factors to a cell cycle- and developmentally regulated promoter. (1999) (237)
- A DNA methylation biomarker of alcohol consumption (2016) (236)
- Common variants at CDKAL1 and KLF9 are associated with body mass index in east Asian populations (2012) (226)
- Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption (2014) (224)
- Functional SNPs in the lymphotoxin-α gene that are associated with susceptibility to myocardial infarction (2003) (202)
- The p53 Family Member Genes Are Involved in the Notch Signal Pathway* (2002) (201)
- Prediction of sensitivity of esophageal tumors to adjuvant chemotherapy by cDNA microarray analysis of gene-expression profiles. (2001) (200)
- Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases (2020) (191)
- Inhibition of skin development by targeted expression of a dominant-negative retinoic acid receptor (1995) (182)
- Homocysteine and Coronary Heart Disease: Meta-analysis of MTHFR Case-Control Studies, Avoiding Publication Bias (2012) (180)
- Integrating Genetic, Transcriptional, and Functional Analyses to Identify 5 Novel Genes for Atrial Fibrillation (2014) (177)
- Diverse transcriptional initiation revealed by fine, large‐scale mapping of mRNA start sites (2001) (174)
- Suppression of tumor promoter-induced oxidative stress and inflammatory responses in mouse skin by a superoxide generation inhibitor 1'-acetoxychavicol acetate. (1998) (172)
- Meta-analysis of genome-wide association studies in East Asian-ancestry populations identifies four new loci for body mass index. (2014) (163)
- Identification of the gene responsible for gelatinous drop-like corneal dystrophy (1999) (161)
- Role of connexin (gap junction) genes in cell growth control and carcinogenesis. (1999) (160)
- Selective elimination of acentric double minutes from cancer cells through the extrusion of micronuclei. (2000) (160)
- Osteopenia and male-specific sudden cardiac death in mice lacking a zinc transporter gene, Znt5. (2002) (160)
- Novel Calmodulin Mutations Associated With Congenital Arrhythmia Susceptibility (2014) (159)
- Common variants in DVWA on chromosome 3p24.3 are associated with susceptibility to knee osteoarthritis (2008) (155)
- A functional polymorphism in COL11A1, which encodes the alpha 1 chain of type XI collagen, is associated with susceptibility to lumbar disc herniation. (2007) (140)
- Genomewide linkage and linkage disequilibrium analyses identify COL6A1, on chromosome 21, as the locus for ossification of the posterior longitudinal ligament of the spine. (2003) (138)
- Novel genetic markers associate with atrial fibrillation risk in Europeans and Japanese. (2014) (137)
- A single gene for bovine high molecular weight and low molecular weight kininogens (1983) (137)
- Mutations in the NMMHC-A gene cause autosomal dominant macrothrombocytopenia with leukocyte inclusions (May-Hegglin anomaly/Sebastian syndrome). (2001) (133)
- Common variants in CASP3 confer susceptibility to Kawasaki disease. (2010) (128)
- Four novel KVLQT1 and four novel HERG mutations in familial long-QT syndrome. (1997) (125)
- GWAS for executive function and processing speed suggests involvement of the CADM2 gene (2016) (125)
- Multiple Loci Are Associated with White Blood Cell Phenotypes (2011) (123)
- ACR4, a putative receptor kinase gene of Arabidopsis thaliana, that is expressed in the outer cell layers of embryos and plants, is involved in proper embryogenesis. (2002) (120)
- Genotype-Phenotype Correlation of SCN5A Mutation for the Clinical and Electrocardiographic Characteristics of Probands With Brugada Syndrome: A Japanese Multicenter Registry (2017) (120)
- Up-regulation of the ectodermal-neural cortex 1 (ENC1) gene, a downstream target of the beta-catenin/T-cell factor complex, in colorectal carcinomas. (2001) (119)
- Association analyses of East Asian individuals and trans‐ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels (2017) (119)
- Molecular genetics of coronary artery disease (2015) (117)
- Identification of six new genetic loci associated with atrial fibrillation in the Japanese population (2017) (113)
- Cross-sectional analysis of BioBank Japan clinical data: A large cohort of 200,000 patients with 47 common diseases (2017) (112)
- The Id2 gene is a novel target of transcriptional activation by EWS-ETS fusion proteins in Ewing family tumors (2002) (112)
- The genetic association between personality and major depression or bipolar disorder. A polygenic score analysis using genome-wide association data (2011) (111)
- Suppression by citrus auraptene of phorbol ester-and endotoxin-induced inflammatory responses: role of attenuation of leukocyte activation. (2000) (108)
- A genome-wide association study identifies susceptibility loci for ossification of the posterior longitudinal ligament of the spine (2014) (107)
- A functional polymorphism in THBS2 that affects alternative splicing and MMP binding is associated with lumbar-disc herniation. (2008) (106)
- Novel receptor-like kinase ALE2 controls shoot development by specifying epidermis in Arabidopsis (2007) (106)
- Meta-analysis of genome-wide association studies identifies common variants in CTNNA2 associated with excitement-seeking (2011) (105)
- Genomic organization and mutational analysis of KVLQT1, a gene responsible for familial long QT syndrome (1998) (101)
- COL6A1, the Candidate Gene for Ossification of the Posterior Longitudinal Ligament, Is Associated With Diffuse Idiopathic Skeletal Hyperostosis in Japanese (2005) (101)
- A simple phenolic antioxidant protocatechuic acid enhances tumor promotion and oxidative stress in female ICR mouse skin: dose-and timing-dependent enhancement and involvement of bioactivation by tyrosinase. (2000) (99)
- SNPs in BRAP associated with risk of myocardial infarction in Asian populations (2009) (98)
- A functional SNP in PSMA6 confers risk of myocardial infarction in the Japanese population (2006) (96)
- Identification of 187 single nucleotide polymorphisms (SNPs) among 41 candidate genes for ischemic heart disease in the Japanese population (2000) (96)
- Meta-analysis of genome-wide association studies of adult height in East Asians identifies 17 novel loci. (2015) (95)
- ITPKC and CASP3 polymorphisms and risks for IVIG unresponsiveness and coronary artery lesion formation in Kawasaki disease (2011) (93)
- Isolation of a novel human gene, MARKL1, homologous to MARK3 and its involvement in hepatocellular carcinogenesis. (2001) (92)
- Genome-wide association study for C-reactive protein levels identified pleiotropic associations in the IL6 locus. (2011) (90)
- Growth and gene expression profile analyses of endometrial cancer cells expressing exogenous PTEN. (2001) (88)
- Association between a single-nucleotide polymorphism in the promoter of the human interleukin-3 gene and rheumatoid arthritis in Japanese patients, and maximum-likelihood estimation of combinatorial effect that two genetic loci have on susceptibility to the disease. (2001) (87)
- Identification of Nine Novel Loci Associated with White Blood Cell Subtypes in a Japanese Population (2011) (80)
- Association between single-nucleotide polymorphisms in selectin genes and immunoglobulin A nephropathy. (2002) (77)
- Empirical estimation of genome-wide significance thresholds based on the 1000 Genomes Project data set (2016) (76)
- Discovery and fine mapping of serum protein loci through transethnic meta-analysis. (2012) (75)
- Twenty single nucleotide polymorphisms (SNPs) and their allelic frequencies in four genes that are responsible for familial long QT syndrome in the Japanese population (2000) (70)
- Synchronization in the cell cycle by inhibitors of DNA replication induces histone H2AX phosphorylation: an indication of DNA damage (2006) (68)
- Constitutive histone H2AX phosphorylation and ATM activation are strongly amplified during mitogenic stimulation of lymphocytes (2007) (67)
- Association of single-nucleotide polymorphisms in the polymeric immunoglobulin receptor gene with immunoglobulin A nephropathy (IgAN) in Japanese patients (2003) (66)
- Plasma BDNF concentration, Val66Met genetic variant and depression‐related personality traits (2010) (64)
- ATM activation and histone H2AX phosphorylation as indicators of DNA damage by DNA topoisomerase I inhibitor topotecan and during apoptosis (2006) (63)
- Variation of gene-based SNPs and linkage disequilibrium patterns in the human genome. (2004) (62)
- Induced detachment of acentric chromatin from mitotic chromosomes leads to their cytoplasmic localization at G(1) and the micronucleation by lamin reorganization at S phase. (2000) (61)
- Genome-wide association study to identify SNPs conferring risk of myocardial infarction and their functional analyses (2005) (59)
- Multiple Nonglycemic Genomic Loci Are Newly Associated With Blood Level of Glycated Hemoglobin in East Asians (2014) (55)
- Prediction model for knee osteoarthritis based on genetic and clinical information (2010) (55)
- Genomic organization and mutational analysis of HERG, a gene responsible for familial long QT syndrome (1998) (55)
- A roadmap to build a phenotypic metric of ageing: insights from the Baltimore Longitudinal Study of Aging (2020) (54)
- Mapping of a gene for May-Hegglin anomaly to chromosome 22q (1999) (53)
- Genome Wide Analysis of Drug-Induced Torsades de Pointes: Lack of Common Variants with Large Effect Sizes (2013) (53)
- A genome-wide association study identifies PLCL2 and AP3D1-DOT1L-SF3A2 as new susceptibility loci for myocardial infarction in Japanese (2014) (52)
- Novel gene variants predict serum levels of the cytokines IL-18 and IL-1ra in older adults. (2014) (52)
- A functional variant in ZNF512B is associated with susceptibility to amyotrophic lateral sclerosis in Japanese. (2011) (51)
- A functional SNP in EDG2 increases susceptibility to knee osteoarthritis in Japanese. (2008) (51)
- Antiangiogenic activity of BAI1 in vivo: implications for gene therapy of human glioblastomas (2006) (50)
- Identification of AXUD1, a novel human gene induced by AXIN1 and its reduced expression in human carcinomas of the lung, liver, colon and kidney (2001) (49)
- Planning the Human Variome Project: The Spain report (2009) (48)
- Genomic structure and multiple single-nucleotide polymorphisms (SNPs) of the thiopurine S-methyltransferase (TPMT) gene (2000) (48)
- Haplotypes with Copy Number and Single Nucleotide Polymorphisms in CYP2A6 Locus Are Associated with Smoking Quantity in a Japanese Population (2012) (47)
- Overview of BioBank Japan follow-up data in 32 diseases (2017) (46)
- Identification of AF17 as a downstream gene of the beta-catenin/T-cell factor pathway and its involvement in colorectal carcinogenesis. (2001) (45)
- Expression profiling to predict postoperative prognosis for estrogen receptor‐negative breast cancers by analysis of 25,344 genes on a cDNA microarray (2004) (44)
- Induction of tenascin‐C by tumor‐specific EWS‐ETS fusion genes (2003) (43)
- Significant impact of miRNA–target gene networks on genetics of human complex traits (2016) (43)
- Isolation and chromosomal mapping of the human homolog of perilipin (PLIN), a rat adipose tissue-specific gene, by differential display method. (1998) (39)
- Regulatory polymorphism in transcription factor KLF5 at the MEF2 element alters the response to angiotensin II and is associated with human hypertension (2010) (38)
- Genetic Variation in the SLC8A1 Calcium Signaling Pathway Is Associated With Susceptibility to Kawasaki Disease and Coronary Artery Abnormalities (2016) (38)
- Inhibition of Experimental Intimal Thickening in Mice Lacking a Novel G-Protein–Coupled Receptor (2003) (38)
- BRAP Activates Inflammatory Cascades and Increases the Risk for Carotid Atherosclerosis (2011) (37)
- Identification of 142 single nucleotide polymorphisms in 41 candidate genes for rheumatoid arthritis in the Japanese population (2000) (37)
- PTPRD gene associated with blood pressure response to atenolol and resistant hypertension (2015) (36)
- Variants at HLA-A, HLA-C, and HLA-DQB1 Confer Risk of Psoriasis Vulgaris in Japanese. (2017) (35)
- Common Variants in a Novel Gene, FONG on Chromosome 2q33.1 Confer Risk of Osteoporosis in Japanese (2011) (35)
- Isolation of HELAD1, a novel human helicase gene up-regulated in colorectal carcinomas (2002) (34)
- Variations in ORAI1 Gene Associated with Kawasaki Disease (2016) (34)
- Genome-Wide Association Study of Peripheral Arterial Disease in a Japanese Population (2015) (33)
- SNPs on chromosome 5p15.3 associated with myocardial infarction in Japanese population (2011) (33)
- Single-nucleotide polymorphisms in the class II region of the major histocompatibility complex in Japanese patients with immunoglobulin A nephropathy (2002) (32)
- Identification of the interleukin 4 receptor alpha gene as a direct target for p73. (2003) (32)
- Coordinated demethylation of H3K9 and H3K27 is required for rapid inflammatory responses of endothelial cells (2018) (30)
- Multiple single-nucleotide polymorphisms (SNPs) in the Japanese population in six candidate genes for long QT syndrome (2001) (30)
- Inflammation as a risk factor for myocardial infarction (2006) (30)
- Impact of atherosclerosis-related gene polymorphisms on mortality and recurrent events after myocardial infarction. (2006) (29)
- Association of a single-nucleotide polymorphism in the immunoglobulin μ-binding protein 2 gene with immunoglobulin A nephropathy (2005) (29)
- Atrial fibrillation genetic risk differentiates cardioembolic stroke from other stroke subtypes (2018) (29)
- Common genetic variation near the connexin-43 gene is associated with resting heart rate in African Americans: a genome-wide association study of 13,372 participants. (2013) (28)
- Construction of a normalized directionally cloned cDNA library from adult heart and analysis of 3040 clones by partial sequencing. (1996) (28)
- Localization of the gene responsible for Peutz-Jeghers syndrome within a 6-cM region of chromosome 19p13.3 (1998) (28)
- Exome Analyses of Long QT Syndrome Reveal Candidate Pathogenic Mutations in Calmodulin-Interacting Genes (2015) (27)
- A functional SNP in ITIH3 is associated with susceptibility to myocardial infarction (2007) (26)
- Correlation of genetic etiology with response to β-adrenergic blockade among symptomatic patients with familial long-QT syndrome (2001) (25)
- Transcriptional regulation by p53 and p73. (2005) (24)
- Extent of constitutive histone H2AX phosphorylation on Ser‐139 varies in cells with different TP53 status (2006) (24)
- Complete Genome Sequence of an Aerobic Hyper-thermophilic Crenarchaeon, Aeropyrum pernix K1 (Supplement) (1999) (24)
- Genetic variations in five genes involved in the excitement of cardiomyocytes (2001) (23)
- Gene expression patterns as marker for 5-year postoperative prognosis of primary breast cancers (2004) (22)
- Variants in the SCN5A Promoter Associated With Various Arrhythmia Phenotypes (2016) (22)
- Molecular cloning and mapping of a human cDNA for cytosolic malate dehydrogenase (MDH1). (1996) (22)
- Association of Genetic and Clinical Aspects of Congenital Long QT Syndrome With Life-Threatening Arrhythmias in Japanese Patients (2019) (21)
- Regional evaluation of childhood acute lymphoblastic leukemia genetic susceptibility loci among Japanese (2018) (20)
- Characterization of S818L mutation in HERG C‐terminus in LQT2 (2000) (18)
- Association between maternal education and malocclusion in Mongolian adolescents: a cross-sectional study (2016) (18)
- Phenotypic Variability of ANK2 Mutations in Patients With Inherited Primary Arrhythmia Syndromes. (2016) (17)
- Fine mapping of the Darier's disease locus on chromosome 12q. (1994) (17)
- Identification of a novel gene (ECM2) encoding a putative extracellular matrix protein expressed predominantly in adipose and female-specific tissues and its chromosomal localization to 9q22.3. (1998) (17)
- Association of an IGHV3-66 gene variant with Kawasaki disease (2020) (16)
- Epigenetic regulation of drug transporter expression in human tissues (2017) (16)
- Somatic, positive and negative domains of the Center for Epidemiological Studies Depression (CES-D) scale: a meta-analysis of genome-wide association studies (2016) (16)
- Genetic Variants Associated With Susceptibility to Atrial Fibrillation in a Japanese Population. (2017) (16)
- New findings in the degenerating tissues of the periodontal ligament during experimental tooth movement. (1996) (16)
- Linkage disequilibrium of evolutionarily conserved regions in the human genome (2006) (14)
- Preparation of unfixed and undecalcified frozen sections of adult rat periodontal ligament during experimental tooth movement. (1994) (14)
- Association of NOD2 Mutations with Aggressive Periodontitis (2017) (13)
- Molecular cloning of a human cDNA encoding putative cysteine protease (PRSC1) and its chromosome assignment to 14q32.1. (1996) (13)
- Genome-wide association analysis of common genetic variants of resistant hypertension (2018) (12)
- Fine-scale SNP map of an 11-kb genomic region at 22q13.1 containing the galectin-1 gene (2005) (12)
- Gene transcripts associated with muscle strength: a CHARGE meta-analysis of 7,781 persons (2015) (12)
- Lipoprotein receptor-related protein 1 variants and dietary fatty acids: meta-analysis of European origin and African American studies (2013) (12)
- A genome-wide association study to identify genomic modulators of rate control therapy in patients with atrial fibrillation. (2014) (11)
- Reduced risk of recurrent myocardial infarction in homozygous carriers of the chromosome 9p21 rs1333049 C risk allele in the contemporary percutaneous coronary intervention era: a prospective observational study (2014) (11)
- Genetic Variants Associated With Uncontrolled Blood Pressure on Thiazide Diuretic/β‐Blocker Combination Therapy in the PEAR (Pharmacogenomic Evaluation of Antihypertensive Responses) and INVEST (International Verapamil‐SR Trandolapril Study) Trials (2017) (11)
- Genome-wide association study for C-reactive protein levels identified pleiotropic associations in the IL 6 locus (2011) (10)
- Identification of 46 novel SNPs in the 130-kb region containing a myocardial infarction susceptibility gene on chromosomal band 6p21 (2003) (10)
- Akaike's information criterion for a measure of linkage disequilibrium (2002) (10)
- Submicroscopic deletions at 13q32.1 cause congenital microcoria. (2015) (10)
- Characteristics of Shed Snake Skin Permeability to Indomethacin and Fatty Alcohols (1996) (10)
- Investigation of novel variations of ORAI1 gene and their association with Kawasaki disease (2019) (9)
- Recombination rates of genes expressed in human tissues. (2008) (9)
- High-density SNP map of human ITR, a gene associated with vascular remodeling (2003) (9)
- Identification by differential display of eight known genes induced during in vivo intimal hyperplasia (1998) (9)
- Renin-angiotensin-aldosterone system polymorphisms and 5-year mortality in survivors of acute myocardial infarction: a report from the Osaka Acute Coronary Insufficiency Study. (2014) (8)
- High-density single-nucleotide polymorphism (SNP) map in the 96-kb region containing the entire human DiGeorge syndrome critical region 2 (DGCR2) gene at 22q11.2 (2001) (8)
- Relationship between DNA Methylation in the 5′ CpG Island of the SLC47A1 (Multidrug and Toxin Extrusion Protein MATE1) Gene and Interindividual Variability in MATE1 Expression in the Human Liver (2018) (8)
- Nucleotide Sequence of 55-rDNA Intergenic Spacer Region in Angelica acutiloba. (1998) (8)
- The human insulin receptor substrate-1 gene (IRS1) is localized on 2q36. (1994) (8)
- Large scale genome-wide association study in a Japanese population identified 45 novel susceptibility loci for 22 diseases (2019) (7)
- Genome-wide association study to identify single-nucleotide polymorphisms conferring risk of myocardial infarction. (2006) (7)
- A functional SNP in FLT1 increases risk of coronary artery disease in a Japanese population (2016) (7)
- miRNA299 involvement in CYP11B2 expression in aldosterone-producing adenoma. (2019) (7)
- Thiamine pyrophosphatase activity in the Golgi apparatus of calcitonin-treated osteoclasts. (1991) (7)
- Genome-Wide Association Study Identifies Pharmacogenomic Loci Linked with Specific Antihypertensive Drug Treatment and New-Onset Diabetes (2016) (7)
- Cardiovascular genetics (2016) (6)
- Twenty single-nucleotide polymorphisms in four genes encoding cardiac ion channels (2002) (6)
- Association of heat shock proteins with all-cause mortality (2012) (6)
- Buried object detection with Synthetic Aperture Sonar (2004) (5)
- Lymphotoxin-alpha3 mediates monocyte-endothelial interaction by TNFR I/NF-kappaB signaling. (2009) (5)
- Alkaline phosphatase activity in the osteoclasts induced by experimental tooth movement. (1991) (5)
- Decreased mortality associated with statin treatment in patients with acute myocardial infarction and lymphotoxin-alpha C804A polymorphism. (2013) (5)
- Assignment of the human caltractin gene (CALT) to Xq28 by fluorescence in situ hybridization. (1994) (5)
- Pathway analysis with genome-wide association study (GWAS) data detected the association of atrial fibrillation with the mTOR signaling pathway (2019) (5)
- Heterozygosities and allelic frequencies of 358 dinucleotide-repeat marker loci in the Japanese population (1998) (5)
- HLA-C variants associated with amino acid substitutions in the peptide binding groove influence susceptibility to Kawasaki disease. (2019) (5)
- Clinical utility and functional analysis of variants in atrial fibrillation-associated locus 4q25. (2017) (4)
- Environmental factor dependent maximum likelihood method for association study targeted to personalized medicine. (2000) (3)
- Multi-ethnic genome-wide association study for atrial fibrillation (2018) (3)
- Low specificity of cytokeratin 19 mRNA expression in the peripheral blood cells from patients with ovarian tumors. (2000) (3)
- Abstract 13371: CALM2 Mutations Associated With Atypical Juvenile Long QT Syndrome (2013) (3)
- Correction to: Identification of OPN3 as associated with non-syndromic oligodontia in a Japanese population (2021) (3)
- Assignment1 of OVCOV1 (alias CGI-15) to human chromosome 20 band q13.1→q13.2 by fluorescent in situ hybridization (2001) (2)
- [Identification of common disease related genes by means of genome-wide SNP typing]. (2002) (2)
- [Genome-wide SNP association study to identify genes related to myocardial infarction and their functional analyses]. (2004) (2)
- Novel Calmodulin (CALM2) Mutations Associated with Congenital Arrhythmia Susceptibility (2)
- Genetic linkage analyses of Romano-Ward syndrome (RWS) in 13 Japanese families (1994) (2)
- Erratum: Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation (2017) (2)
- Large-scale Rare Variant Burden Testing in Parkinson's Disease Identifies Novel Associations with Genes Involved in Neuro-inflammation (2022) (2)
- Treatment of Coral Reef Aorta by Endovascular VIABAHN VBX Balloon-Expandable Stent-Graft Placement (2021) (2)
- Refined mapping of caltractin in human Xq28 and in the homologous region of the mouse X Chromosome places the gene within the bare patches (Bpa) and striated (Str) critical regions (1995) (2)
- Natural history and genetic aspects of the Jervell and Lange-Nielsen syndrome. (2001) (2)
- Genetic insights into ossification of the posterior longitudinal ligament of the spine (2022) (1)
- INTRACORONARY ULTRASOUND ASSESSMENT OF CORONARY STENTS (1993) (1)
- A Novel Algorithm from Personal Genome to the Pathogenic Mutant Causing Mitochondrial Cardiomyopathy (2011) (1)
- Combined Angio-CT Systems: A Roadmap Tool for Precision Therapy in Interventional Oncology. (2021) (1)
- Identification of OPN3 as associated with non-syndromic oligodontia in a Japanese population (2021) (1)
- Abstract 13817: Clinical Significance of Whole Exome Analysis Using Next Generation Sequencing in the Genotype-negative Long-QT Syndrome (2014) (1)
- Abstract 13566: Biophysical Properties of Na Channel in the S5-S6 High Risk LQT3 Mutations of the Long QT Syndrome (2012) (1)
- A case of pseudoxanthoma elasticum complicated by angioid streaks and hypertension. (1982) (1)
- Amplification of Papillomavirus Oncogene Transcripts Assay for Bowenoid Papulosis (2013) (1)
- Ultrasonic Heating Detects Lipiodol Deposition within Liver Tumors after Transarterial Embolization: An In Vivo Approach (2021) (1)
- Abstract 12257: Calmodulin Interacting Genes as a Novel Candidate for Pathogenesis of Long-QT Syndrome (2015) (0)
- Abstract 15465: Precision Medicine Approach to Resistant Hypertension: Genetic Markers of Resistant Hypertension Through a Genome-wide Association Study (GWAS) in the Secondary Prevention of Subcortical Strokes (SPS3) (2015) (0)
- OJ-212 Identification of a Novel non-coding RNA, MIAT, that Confers Risk of Myocardial Infarction(Genetics/Genetically engineered models/Gene therapy-2(H/M), The 71st Annual Scientific Meeting of the Japanese Circulation Society) (2007) (0)
- Identification of myocardial infarction-susceptible genes and their functional analyses (2016) (0)
- Abstract 2764: Clinical Phenotype of Japanese LQT3 Form of Congenital Long QT Syndrome by Location of Mutation from Japanese Multicenter Registry (2008) (0)
- POLY (ADENOSINE DIPHOSPHATE-RIBOSE) SYNTHESIS IN TRANSFORMED MOUSE EPIDERMAL CELLS IN CULTURE (1991) (0)
- Genetic backgrounds of myocardial infarction (2007) (0)
- Investigation of novel variations of ORAI1 gene and their association with Kawasaki disease (2019) (0)
- B31 Enzyme Immunoassay of Human Gastrin (1984) (0)
- Abstract 2824: Clinical Phenotype and Prognosis of Probands With Brugada Syndrome in Relation to SCN5A Mutation. - Japanese Brugada Syndrome Multicenter Registry (2009) (0)
- FRS-004 Large Scale SNPs Association Study to Identify Genes Confer Risk of Myocardial Infarction(FRS1,New Molecules for Cardiovascular Regulation (M),Featured Research Session (English),The 73rd Annual Scientific Meeting of The Japanese Circulation Society) (2009) (0)
- Chapter 7 Mutational Analysis of Familial Long QT Syndrome in Japan (1999) (0)
- Relationship between DNA Methylation in the 59 CpG Island of the SLC47A1 (Multidrug and Toxin Extrusion Protein MATE1) Gene and Interindividual Variability in MATE1 Expression in the Human Liver s (2017) (0)
- [The status for genetics of coronary artery disease]. (2011) (0)
- Targeted deep sequencing analyses of long QT syndrome in a Japanese population (2022) (0)
- Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases (2020) (0)
- Genetic Background of Myocardial Infarction (2011) (0)
- JHG Young Scientist Award (2021) (0)
- Exogenous Lipoid Pneumonia Caused by Gargling With Sesame Oil: A Case Report. (2022) (0)
- A case of coil migration into the colon after embolization of the spleno-renal shunt (2022) (0)
- An Imaging Method for Electrical Conductivity Distribution Using Electrical Impedance Computed Tomography (1990) (0)
- The evolution of continuous contrast resolution (1998) (0)
- Education for drug administration in diabetic outpatients (Continued) (1989) (0)
- Segmental testicular infarction diagnosed using microvascular imaging: a case report (2022) (0)
- EARLY EXPERIENCE WITH THE STRECKER CORONARY STENT (1993) (0)
- Diagnosis System of Drug Sensitivity of Cancer Using cDNA Microarray and Multivariate Statistical Analysis (2000) (0)
- Cancer preventive agents in zingiberaceous plants from Southeast Asian countries. (2007) (0)
- Abstract 10937: What Influences {beta}-Blocker Resistance for Secondary Prevention of Cardiac Events in Patients with Congenital Long QT Syndrome? (2011) (0)
- [Mutational analyses of familial long QT syndrome]. (1998) (0)
- Expanding the BBMRI-ERIC Directory into a Global Catalogue of COVID-19-Ready Collections: A Joint Initiative of BBMRI-ERIC and ISBER (2020) (0)
- OE-009 Identification of a Locus on Chromosome 5p that Confers Risk of Coronary Artery Disease by Genome Wide Association Study(OE02,ACS/AMI (Basic) (IHD),Oral Presentation (English),The 73rd Annual Scientific Meeting of The Japanese Circulation Society) (2009) (0)
- PJ-152 A functional SNP in the Proteasome Subunit Alpha Type 6 Gene confers Risk of Myocardial Infarction in Japanese Population(Acute myocardial infarction, basic-2, The 71st Annual Scientific Meeting of the Japanese Circulation Society) (2007) (0)
- Genome-wide association analysis of common genetic variants of resistant hypertension (2018) (0)
- PE-103 Clinical Phenotype of Japanese LQT3 Form of Congenital Long QT Syndrome by Location of Mutation from Japanese Multicenter Registry(PE018,Arrhythmia, Others (Clinical/Pathophysiology) (A),Poster Session (English),The 73rd Annual Scientific Meeting of The Japanese Circulation Society) (2009) (0)
- Discrimination of Drug Sensitivity of Cancer Using cDNA Microarray and Multivariate Statistical Analysis (1999) (0)
- Abstract 12933: A Genome-Wide Association Analysis to Identify Genomic Modulators of Rate Control Therapy in Patients with Atrial Fibrillation (2011) (0)
- Yeast Sequencing Report A 38 kb segment containing the cdc 2 gene from the left arm of ® ssion yeast chromosome II : sequence analysis and characterization of the genomic DNA and cDNAs encoded on the segment (1999) (0)
- 178. INVESTIGATION OF RARE VARIATIONS OF ORAI1 GENE AND THEIR ASSOCIATION WITH KAWASAKI DISEASE (2019) (0)
- Complete Genome Sequence of an Aerobic Hyperthermophilic Crenarchaeon , Aeropyrum pernixKl (2007) (0)
- Abstract 14674: Cardiovascular Events Associated with Lymphotoxin Alpha and its Polymorphism After the Onset of Myocardial Infarction (2011) (0)
- Genetic Variants in HLA-C and Class I Pathway Genes Influence Susceptibility to Kawasaki Disease (2017) (0)
- Regional evaluation of childhood acute lymphoblastic leukemia genetic susceptibility loci among Japanese (2018) (0)
- Genetics of Coronary Disease (2019) (0)
- [Molecular genetics of coronary artery diseases]. (2016) (0)
- Correction to: Identification of OPN3 as associated with non-syndromic oligodontia in a Japanese population (2021) (0)
- SNP projects in Japan (2002) (0)
- Epithelia Laser-Capture Microdissection of Tumor Tissues and Normal Carcinogenesis Revealed by cDNA Microarrays after Alterations of Gene Expression during Colorectal Updated (2001) (0)
- Identification of the Interleukin 4 Receptor (cid:1) Gene as a Direct Target for p73 (2003) (0)
- Abstract 12798: Mutation Site-Specific Differences in Arrhythmic Risk in the LQT3 Form of Congenital Long QT Syndrome: Multicenter Study in Japan (2011) (0)
- Gene transcripts associated with muscle strength : a CHARGE meta-analysis of 1 7 , 781 persons 2 3 (2015) (0)
- Edinburgh Research Explorer A DNA methylation biomarker of alcohol consumption (2016) (0)
- Abstract 15186: Clinical Features of Congenital Long QT Syndrome in Pre-elementary-age Children (2010) (0)
- EFFECTS OF INTRAVENOUS ADMINISTRATIONOF A TISSUE-TYPE PLASMINOGEN ACTIVATOR (AK-124) IN ACUTE MYOCARDIAL INFARCTION, INCLUDING CHANGES IN BLOOD COAGULATION AND FIBRINOLYTIC ACTIVITY.- PRELIMINARY REPORT (1987) (0)
- Genome-wide association study to identify genes related to myocardial infarction (2002) (0)
- Relationship between DNA methylation in the 5 ’ CpG island of the SLC 47 A 1 ( MATE 1 ) gene and inter-individual variability in MATE 1 expression in the human liver (2017) (0)
- Meta-analysis of genome-wide association studies identifies common variants in CTNNA2 associated with excitement-seeking Terracciano, A (0)
- Association of heat shock proteins with all-cause mortality (2012) (0)
- Circulating micronutrients and clinical biomarkers of ageing in the context of skeletal muscle performance: a cross-sectional analysis using data from the Baltimore longitudinal study of ageing (2022) (0)
- Systematic Comparison of Machine Learning Methods for Identification of miRNA Species as Disease Biomarkers (2015) (0)
- Role of DNA methylation in SLC47A1 (MATE1) promoter region on the expression levels in the human liver (2015) (0)
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What Schools Are Affiliated With Toshihiro Tanaka?
Toshihiro Tanaka is affiliated with the following schools:
