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Author Details
Full Name
Toshihiro Tanaka
Affiliation
Bioresourse Research Center, Tokyo Medical and Dental University (TMDU)
ORCID
Career Start Year
1994
Papers
177
H Index
66
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37904028
JHG Young Scientist Award 2023.
J Hum Genet
2024
37824462
Risk stratification of atrial fibrillation and stroke using single nucleotide polymorphism and circulating biomarkers.
PLoS One
2023
34873306
Correction to: Identification of OPN3 as associated with non-syndromic oligodontia in a Japanese population.
J Hum Genet
2022
36480497
Targeted deep sequencing analyses of long QT syndrome in a Japanese population.
PLoS One
2022
33106546
Association of an IGHV3-66 gene variant with Kawasaki disease.
J Hum Genet
2021
33611338
Identification of OPN3 as associated with non-syndromic oligodontia in a Japanese population.
J Hum Genet
2021
34770175
Association between Smoking during Pregnancy and Short Root Anomaly in Offspring.
Int J Environ Res Public Health
2021
32125007
Coordinated demethylation of H3K9 and H3K27 is required for rapid inflammatory responses of endothelial cells.
EMBO J
2020
32514122
Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases.
Nat Genet
2020
30758498
Association of Genetic and Clinical Aspects of Congenital Long QT Syndrome With Life-Threatening Arrhythmias in Japanese Patients.
JAMA Cardiol
2019
30237584
Genome-wide association analysis of common genetic variants of resistant hypertension.
Pharmacogenomics J
2019
31321287
Pathway analysis with genome-wide association study (GWAS) data detected the association of atrial fibrillation with the mTOR signaling pathway.
Int J Cardiol Heart Vasc
2019
31122742
HLA-C variants associated with amino acid substitutions in the peptide binding groove influence susceptibility to Kawasaki disease.
Hum Immunol
2019
31096184
miRNA299 involvement in CYP11B2 expression in aldosterone-producing adenoma.
Eur J Endocrinol
2019
27670767
Genome-wide association study identifies pharmacogenomic loci linked with specific antihypertensive drug treatment and new-onset diabetes.
Pharmacogenomics J
2018
29892015
Multi-ethnic genome-wide association study for atrial fibrillation.
Nat Genet
2018
29335448
Regional evaluation of childhood acute lymphoblastic leukemia genetic susceptibility loci among Japanese.
Sci Rep
2018
29031612
Variants at HLA-A, HLA-C, and HLA-DQB1 Confer Risk of Psoriasis Vulgaris in Japanese.
J Invest Dermatol
2018
28682159
Association of NOD2 Mutations with Aggressive Periodontitis.
J Dent Res
2017
28087289
Clinical utility and functional analysis of variants in atrial fibrillation-associated locus 4q25.
J Cardiol
2017
28334899
Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels.
Hum Mol Genet
2017
28190660
Overview of BioBank Japan follow-up data in 32 diseases.
J Epidemiol
2017
28190657
Cross-sectional analysis of BioBank Japan clinical data: A large cohort of 200,000 patients with 47 common diseases.
J Epidemiol
2017
28129963
Genetic Variants Associated With Susceptibility to Atrial Fibrillation in a Japanese Population.
Can J Cardiol
2017
28189464
Overview of the BioBank Japan Project: Study design and profile.
J Epidemiol
2017
28416822
Identification of six new genetic loci associated with atrial fibrillation in the Japanese population.
Nat Genet
2017
28416818
Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation.
Nat Genet
2017
28341781
Genotype-Phenotype Correlation of <i>SCN5A</i> Mutation for the Clinical and Electrocardiographic Characteristics of Probands With Brugada Syndrome: A Japanese Multicenter Registry.
Circulation
2017
29097388
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.
J Am Heart Assoc
2017
28747752
Erratum: Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation.
Nat Genet
2017
26134515
Molecular genetics of coronary artery disease.
J Hum Genet
2016
28173122
RpA1 ameliorates symptoms of mutant ataxin-1 knock-in mice and enhances DNA damage repair.
Hum Mol Genet
2016
27879314
Genetic Variation in the SLC8A1 Calcium Signaling Pathway Is Associated With Susceptibility to Kawasaki Disease and Coronary Artery Abnormalities.
Circ Cardiovasc Genet
2016
27784853
Phenotypic Variability of ANK2 Mutations in Patients With Inherited Primary Arrhythmia Syndromes.
Circ J
2016
27803108
Association between maternal education and malocclusion in Mongolian adolescents: a cross-sectional study.
BMJ Open
2016
27625342
Variants in the SCN5A Promoter Associated With Various Arrhythmia Phenotypes.
J Am Heart Assoc
2016
27305981
Empirical estimation of genome-wide significance thresholds based on the 1000 Genomes Project data set.
J Hum Genet
2016
27534188
[Molecular genetics of coronary artery diseases].
Nihon Rinsho
2016
26806401
Cardiovascular genetics.
J Hum Genet
2016
26927695
Significant impact of miRNA-target gene networks on genetics of human complex traits.
Sci Rep
2016
26791355
A functional SNP in FLT1 increases risk of coronary artery disease in a Japanese population.
J Hum Genet
2016
26789410
Variations in ORAI1 Gene Associated with Kawasaki Disease.
PLoS One
2016
24916648
A genome-wide association study identifies PLCL2 and AP3D1-DOT1L-SF3A2 as new susceptibility loci for myocardial infarction in Japanese.
Eur J Hum Genet
2015
26488411
Genome-Wide Association Study of Peripheral Arterial Disease in a Japanese Population.
PLoS One
2015
26425837
PTPRD gene associated with blood pressure response to atenolol and resistant hypertension.
J Hypertens
2015
26132555
Exome Analyses of Long QT Syndrome Reveal Candidate Pathogenic Mutations in Calmodulin-Interacting Genes.
PLoS One
2015
25673413
Genetic studies of body mass index yield new insights for obesity biology.
Nature
2015
25772937
Submicroscopic deletions at 13q32.1 cause congenital microcoria.
Am J Hum Genet
2015
25429064
Meta-analysis of genome-wide association studies of adult height in East Asians identifies 17 novel loci.
Hum Mol Genet
2015
24486271
Novel genetic markers associate with atrial fibrillation risk in Europeans and Japanese.
J Am Coll Cardiol
2014
1 - 50 of 177
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