論文 / Publications
20262 papers
Mixed-model and transcriptome-wide association analyses identify transcription factors and genes associated with colorectal cancer susceptibility.
Nature communications, 17(1), 1377, Jan 15, 2026, doi: 10.1038/s41467-025-68127-z
Genetic risk impacts stroke mortality and pathogenesis in patients with ischemic stroke: a cohort study of BioBank Japan.
Frontiers in neurology, 17, 1664594, 2026, doi: 10.3389/fneur.2026.1664594
20259 papers
Pan-cancer prevalence, risk, and clinical and demographic characteristics of Lynch Syndrome-associated variants in BioBank Japan.
Communications medicine, 5(1), 522, Nov 13, 2025, doi: 10.1038/s43856-025-01231-9
Whole-genome sequencing of 3135 individuals representing the genetic diversity of the Japanese population.
Journal of human genetics, Nov 8, 2025, doi: 10.1038/s10038-025-01430-1
Case-Control Study for 23 Cancer Types With Functional Analysis of CHEK2: Risk Estimation and Clinical Recommendations in East Asia.
JCO precision oncology, 9, e2400945, Sep, 2025, doi: 10.1200/PO-24-00945
Identification and replication of sex-dimorphic protein quantitative trait loci across multiple ancestries and their associations with diseases
Scientific Reports, 15(1), Aug 28, 2025, doi: 10.1038/s41598-025-10031-z
Multi-ancestry polygenic risk scores for the prediction of type 2 diabetes and complications in diverse ancestries.
medRxiv : the preprint server for health sciences, Jul 23, 2025, doi: 10.1101/2025.07.21.25331778
Increased somatic mosaicism in autosomal and X chromosomes for suicide death.
Molecular psychiatry, 30(3), 881-888, Mar, 2025, doi: 10.1038/s41380-024-02718-y
A variant in HMMR/HMMR-AS1 is associated with serum alanine aminotransferase levels in the Ryukyu population
Scientific Reports, 15(1), Feb 22, 2025, doi: 10.1038/s41598-025-90195-w
Mosaic loss of chromosome Y characterises late-onset rheumatoid arthritis and contrasting associations of polygenic risk score based on age at onset
Annals of the Rheumatic Diseases, Feb, 2025, doi: 10.1016/j.ard.2025.01.034
Genomics yields biological and phenotypic insights into bipolar disorder.
Nature, Jan 22, 2025, doi: 10.1038/s41586-024-08468-9
202420 papers
Population-specific reference panel improves imputation quality for genome-wide association studies conducted on the Japanese population.
Communications biology, 7(1), 1665, Dec 19, 2024, doi: 10.1038/s42003-024-07338-4
Cancer and disease profiles for PTEN pathogenic variants in Japanese population.
Journal of human genetics, Dec 12, 2024, doi: 10.1038/s10038-024-01311-z
Common and rare genetic variants predisposing females to unexplained recurrent pregnancy loss
Nature Communications, 15(1), Dec, 2024, doi: 10.1038/s41467-024-49993-5
Polygenic risk score and lung adenocarcinoma risk among never-smokers by EGFR mutation status-a brief report.
Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer, Nov 22, 2024, doi: 10.1016/j.jtho.2024.11.019
Genome-wide analysis of heart failure yields insights into disease heterogeneity and enables prognostic prediction in the Japanese population
Nov 15, 2024, doi: 10.1101/2024.11.14.24317249
Stratifying Lung Adenocarcinoma Risk with Multi-ancestry Polygenic Risk Scores in East Asian Never-Smokers.
medRxiv : the preprint server for health sciences, Nov 6, 2024, doi: 10.1101/2024.06.26.24309127
Genome-wide association studies for pelvic organ prolapse in the Japanese population
Communications Biology, 7(1), Sep 30, 2024, doi: 10.1038/s42003-024-06875-2
Causal relevance of different blood pressure traits on risk of cardiovascular diseases: GWAS and Mendelian randomisation in 100,000 Chinese adults
Nature Communications, 15(1), Jul 24, 2024, doi: 10.1038/s41467-024-50297-x
Genetic Risk Stratification of Primary Open-Angle Glaucoma in Japanese Individuals.
Ophthalmology, Jul 17, 2024, doi: 10.1016/j.ophtha.2024.05.026
Identification of epistatic SNP combinations in rheumatoid arthritis using LAMPLINK and Japanese cohorts.
Journal of human genetics, Jul 16, 2024, doi: 10.1038/s10038-024-01269-y
Proteogenomics in cerebrospinal fluid and plasma reveals new biological fingerprint of cerebral small vessel disease
Jul 2, 2024, doi: 10.21203/rs.3.rs-4535534/v1
RNF213 Variants, Vasospastic Angina, and Risk of Fatal Myocardial Infarction.
JAMA cardiology, Jun 18, 2024, doi: 10.1001/jamacardio.2024.1483
Body mass index stratification optimizes polygenic prediction of type 2 diabetes in cross-biobank analyses
Nature Genetics, Jun 11, 2024, doi: 10.1038/s41588-024-01782-y
Genome-Wide Association Study with Three Control Cohorts of Japanese Patients with Esotropia and Exotropia of Comitant Strabismus and Idiopathic Superior Oblique Muscle Palsy
International Journal of Molecular Sciences, 25(6986), 1-25, Jun, 2024, doi: 10.3390/ijms25136986
Protocol for genome-wide association study of human blood metabolites
STAR Protocols, 5(2), 103052, Jun, 2024, doi: 10.1016/j.xpro.2024.103052
Genetically proxied HTRA1 protease activity and circulating levels independently predict risk of ischemic stroke and coronary artery disease
Nature Cardiovascular Research, 3, 701-713, May 20, 2024
Genetic variants for head size share genes and pathways with cancer.
Cell reports. Medicine, 101529, May 3, 2024, doi: 10.1016/j.xcrm.2024.101529
Decoding triancestral origins, archaic introgression, and natural selection in the Japanese population by whole-genome sequencing.
Science advances, 10(16), eadi8419, Apr 19, 2024, doi: 10.1126/sciadv.adi8419
Poor accuracy and sustainability of the first‐step FIB4 EASL pathway for stratifying steatotic liver disease risk in the general population
Alimentary Pharmacology & Therapeutics, Mar 18, 2024, doi: 10.1111/apt.17953
X-chromosome and kidney function: evidence from a multi-trait genetic analysis of 908,697 individuals reveals sex-specific and sex-differential findings in genes regulated by androgen response elements
Nature Communications, 15(1), Jan 18, 2024, doi: 10.1038/s41467-024-44709-1
202330 papers
Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants
Nature Genetics, 55(12), 2065-2074, Dec, 2023, doi: 10.1038/s41588-023-01534-4
Pan-cancer and cross-population genome-wide association studies dissect shared genetic backgrounds underlying carcinogenesis
Nature Communications, 14(1), Dec, 2023, doi: 10.1038/s41467-023-39136-7
East Asian-specific and cross-ancestry genome-wide meta-analyses provide mechanistic insights into peptic ulcer disease
Nature Genetics, 55(12), 2129-2138, Nov 30, 2023, doi: 10.1038/s41588-023-01569-7
A large-scale microRNA transcriptome-wide association study identifies two susceptibility microRNAs, miR-1307-5p and miR-192-3p, for colorectal cancer risk.
Human molecular genetics, Oct 30, 2023, doi: 10.1093/hmg/ddad185
Identification of telomere maintenance gene variations related to lung adenocarcinoma risk by genome‐wide association and whole genome sequencing analyses
Cancer Communications, Oct 26, 2023, doi: 10.1002/cac2.12498
Boosting the power of genome-wide association studies within and across ancestries by using polygenic scores
Nature Genetics, 55(10), 1769-1776, Sep 18, 2023, doi: 10.1038/s41588-023-01500-0
GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture
Nature Genetics, Aug 31, 2023, doi: 10.1038/s41588-023-01485-w
Genetic risk score of cerebral infarction in atrial fibrillation genome-wide association study.
European journal of clinical investigation, e14084, Aug 28, 2023, doi: 10.1111/eci.14084
Androgen receptor binding sites enabling genetic prediction of mortality due to prostate cancer in cancer-free subjects.
Nature communications, 14(1), 4863, Aug 23, 2023, doi: 10.1038/s41467-023-39858-8
Hyperfructosemia in sleep disordered breathing: metabolome analysis of Nagahama study.
Scientific reports, 13(1), 12735, Aug 5, 2023, doi: 10.1038/s41598-023-40002-1
Genome-wide association study identifies risk loci within the major histocompatibility complex region for Hunner-type interstitial cystitis
Cell Reports Medicine, 4(7), Jul 18, 2023, doi: 10.1016/j.xcrm.2023.101114
Evidence of causality of low body mass index on risk of adolescent idiopathic scoliosis: a Mendelian randomization study
Frontiers in Endocrinology, 14, Jun 20, 2023, doi: 10.3389/fendo.2023.1089414
Detection of trait-associated structural variations using short-read sequencing.
Cell genomics, 3(6), 100328, Jun 14, 2023, doi: 10.1016/j.xgen.2023.100328
Increased PDGFRB and NF-κB signaling caused by highly prevalent somatic mutations in intracranial aneurysms
Science Translational Medicine, 15(700), Jun 14, 2023, doi: 10.1126/scitranslmed.abq7721
Improved genetic prediction of the risk of knee osteoarthritis using the risk factor-based polygenic score.
Arthritis research & therapy, 25(1), 103, Jun 12, 2023, doi: 10.1186/s13075-023-03082-y
Genotype imputation accuracy and the quality metrics of the minor ancestry in multi-ancestry reference panels
May 30, 2023, doi: 10.1101/2023.05.30.542466
POS0354 IDENTIFICATION OF SOMATIC MUTATIONS IN PATIENTS WITH ANCA-ASSOCIATED VASCULITIS
Annals of the Rheumatic Diseases, 82(Suppl 1), 427.2-427, May 30, 2023, doi: 10.1136/annrheumdis-2023-eular.243
Author Correction: The power of genetic diversity in genome-wide association studies of lipids
Nature, 618(7965), E19-E20, May 26, 2023, doi: 10.1038/s41586-023-06194-2
Genome-wide association study of lung adenocarcinoma in East Asia and comparison with a European population
Nature Communications, 14(1), May 26, 2023, doi: 10.1038/s41467-023-38196-z
Genome‐wide Association Studies Categorized by Class of Antihypertensive Drugs Reveal Complex Pathogenesis of Hypertension with Drug Resistance
Clinical Pharmacology & Therapeutics, 114(2), 393-403, May 25, 2023, doi: 10.1002/cpt.2934
Mobile element variation contributes to population-specific genome diversification, gene regulation and disease risk.
Nature genetics, 55(6), 939-951, May 11, 2023, doi: 10.1038/s41588-023-01390-2
The high-dimensional space of human diseases built from diagnosis records and mapped to genetic loci.
Nature computational science, 3(5), 403-417, May, 2023, doi: 10.1038/s43588-023-00453-y
Helicobacter pylori, Homologous-Recombination Genes, and Gastric Cancer.
The New England journal of medicine, 388(13), 1181-1190, Mar 30, 2023, doi: 10.1056/NEJMoa2211807
The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions.
Nature genetics, 55(3), 423-436, Mar, 2023, doi: 10.1038/s41588-023-01323-z
Genome-wide association study reveals BET1L associated with survival time in the 137,693 Japanese individuals
Communications Biology, 6(1), Feb 3, 2023, doi: 10.1038/s42003-023-04491-0
Germ line DDX41 mutations define a unique subtype of myeloid neoplasms.
Blood, 141(5), 534-549, Feb 2, 2023, doi: 10.1182/blood.2022018221
Cross-ancestry genome-wide analysis of atrial fibrillation unveils disease biology and enables cardioembolic risk prediction.
Nature genetics, 55(2), 187-197, Jan 19, 2023, doi: 10.1038/s41588-022-01284-9
Genetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical Heterogeneity.
Stroke, Jan 19, 2023, doi: 10.1161/STROKEAHA.122.040715
Identification of serum metabolome signatures associated with retinal and renal complications of type 2 diabetes
Communications Medicine, 3(1), Jan 9, 2023, doi: 10.1038/s43856-022-00231-3
Genetic influences on human blood metabolites in the Japanese population
iScience, 26(1), 105738, Jan, 2023, doi: 10.1016/j.isci.2022.105738
202241 papers
Predictive Utility of a Coronary Artery Disease Polygenic Risk Score in Primary Prevention.
JAMA cardiology, Dec 28, 2022, doi: 10.1001/jamacardio.2022.4466
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis.
Genome biology, 23(1), 268, Dec 27, 2022, doi: 10.1186/s13059-022-02837-1
Prevalence and risk estimation of cancer-predisposing genes for upper urinary tract urothelial carcinoma in Japanese.
Japanese journal of clinical oncology, 52(12), 1441-1445, Dec 5, 2022, doi: 10.1093/jjco/hyac141
Genetic diversity fuels gene discovery for tobacco and alcohol use.
Nature, 612(7941), 720-724, Dec, 2022, doi: 10.1038/s41586-022-05477-4
Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants.
Nature genetics, 54(12), 1803-1815, Dec, 2022, doi: 10.1038/s41588-022-01233-6
Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals
Communications Biology, 5(1), Dec, 2022, doi: 10.1038/s42003-022-03448-z
Genome-Wide Association Study of Age-Related Macular Degeneration Reveals 2 New Loci Implying Shared Genetic Components with Central Serous Chorioretinopathy.
Ophthalmology, 130(4), 361-372, Nov 22, 2022, doi: 10.1016/j.ophtha.2022.10.034
Prediction of the cell-type-specific transcription of non-coding RNAs from genome sequences via machine learning
Nature Biomedical Engineering, Nov 21, 2022, doi: 10.1038/s41551-022-00961-8
Detailed Analysis of the Impact of Clonal Hematopoiesis on the Risk of Severe COVID-19 Infection
Blood, 140(Supplement 1), 5747-5748, Nov 15, 2022, doi: 10.1182/blood-2022-160436
Multi-ancestry genome-wide association analyses identify novel genetic mechanisms in rheumatoid arthritis.
Nature genetics, 54(11), 1640-1651, Nov, 2022, doi: 10.1038/s41588-022-01213-w
Genetic footprints of assortative mating in the Japanese population.
Nature human behaviour, Sep 22, 2022, doi: 10.1038/s41562-022-01438-z
Association between germline pathogenic variants in cancer-predisposing genes and lymphoma risk.
Cancer science, 113(11), 3972-3979, Sep 5, 2022, doi: 10.1111/cas.15522
Inframe insertion and splice site variants in MFGE8 associate with protection against coronary atherosclerosis
Communications Biology, 5(1), Aug 17, 2022, doi: 10.1038/s42003-022-03552-0
A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids.
American journal of human genetics, 109(8), 1366-1387, Aug 4, 2022, doi: 10.1016/j.ajhg.2022.06.012
Large-scale genome-wide association study of coronary artery disease in genetically diverse populations.
Nature medicine, 28(8), 1679-1692, Aug, 2022, doi: 10.1038/s41591-022-01891-3
Genetic architectures underlie onset age of atopic dermatitis.
The Journal of investigative dermatology, 142(12), 3337-3341, Jul 13, 2022, doi: 10.1016/j.jid.2022.06.010
Trans-ancestry meta-analysis improves performance of genetic scores for multiple adiposity-related traits in East Asian populations
Jul 7, 2022, doi: 10.1101/2022.07.05.22277254
Multi-trait and cross-population genome-wide association studies across autoimmune and allergic diseases identify shared and distinct genetic component
Annals of the Rheumatic Diseases, 81(9), annrheumdis-2022, Jun 26, 2022, doi: 10.1136/annrheumdis-2022-222460
Different risk genes contribute to clear cell and non-clear cell renal cell carcinoma in 1532 Japanese patients and 5996 controls.
Human molecular genetics, 31(12), 1962-1969, Jun 22, 2022, doi: 10.1093/hmg/ddab345
Multi‐phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations
Journal of Thrombosis and Haemostasis, 20(6), 1331-1349, Jun, 2022, doi: 10.1111/jth.15698
Genetic analysis of right heart structure and function in 40,000 people.
Nature genetics, 54(6), 792-803, Jun, 2022, doi: 10.1038/s41588-022-01090-3
Large-scale Integrated Analysis of Genetics and Metabolomic Data Reveals Potential Links Between Lipids and Colorectal Cancer Risk.
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 31(6), 1216-1226, Jun 1, 2022, doi: 10.1158/1055-9965.EPI-21-1008
Author Correction: Genetic variants of calcium and vitamin D metabolism in kidney stone disease.
Nature communications, 13(1), 3115, May 30, 2022, doi: 10.1038/s41467-022-30920-5
SARS-CoV-2 ORF6 disrupts nucleocytoplasmic trafficking to advance viral replication.
Communications biology, 5(1), 483, May 19, 2022, doi: 10.1038/s42003-022-03427-4
A polygenic risk score improves risk stratification of coronary artery disease: a large-scale prospective Chinese cohort study.
European heart journal, 43(18), 1702-1711, May 7, 2022, doi: 10.1093/eurheartj/ehac093
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation.
Nature genetics, 54(5), 560-572, May, 2022, doi: 10.1038/s41588-022-01058-3
Genetic risk score for intracranial aneurysms to predict aneurysmal subarachnoid hemorrhage and identify associations with patient characteristics
Apr 29, 2022, doi: 10.1101/2022.04.29.22274404
Expansion of Cancer Risk Profile for BRCA1 and BRCA2 Pathogenic Variants.
JAMA oncology, 8(6), 871-878, Apr 14, 2022, doi: 10.1001/jamaoncol.2022.0476
Response to Comment on Dawed et al. Genome-Wide Meta-analysis Identifies Genetic Variants Associated With Glycemic Response to Sulfonylureas. Diabetes Care 2021;44:2673-2682.
Diabetes care, 45(4), e82-e83, Apr 1, 2022, doi: 10.2337/dci21-0066
Leveraging fine-mapping and multipopulation training data to improve cross-population polygenic risk scores
Nature Genetics, 54(4), 450-458, Apr, 2022, doi: 10.1038/s41588-022-01036-9
Mapping genomic loci implicates genes and synaptic biology in schizophrenia.
Nature, 604(7906), 502-508, Apr, 2022, doi: 10.1038/s41586-022-04434-5
Mobile elements in human population-specific genome and phenotype divergence
Mar 27, 2022, doi: 10.1101/2022.03.25.485726
Efficient prediction of a spatial transcriptomics profile better characterizes breast cancer tissue sections without costly experimentation.
Scientific reports, 12(1), 4133, Mar 8, 2022, doi: 10.1038/s41598-022-07685-4
Whole exome analysis of patients in Japan with hearing loss reveals high heterogeneity among responsible and novel candidate genes.
Orphanet journal of rare diseases, 17(1), 114, Mar 5, 2022, doi: 10.1186/s13023-022-02262-4
Genome-wide association study of colorectal polyps identified highly overlapping polygenic architecture with colorectal cancer
Journal of Human Genetics, 67(3), 149-156, Mar, 2022, doi: 10.1038/s10038-021-00980-4
Decoding the diversity of killer immunoglobulin-like receptors by deep sequencing and a high-resolution imputation method
Cell Genomics, 2(3), 100101, Mar, 2022, doi: 10.1016/j.xgen.2022.100101
Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors
Biological Psychiatry, 91(3), 313-327, Feb, 2022, doi: 10.1016/j.biopsych.2021.05.029
Trans-ethnic Mendelian-randomization study reveals causal relationships between cardiometabolic factors and chronic kidney disease.
International journal of epidemiology, 50(6), 1995-2010, Jan 6, 2022, doi: 10.1093/ije/dyab203
Stroke genetics informs drug discovery and risk prediction across ancestries
Jan 4, 2022, doi: 10.21203/rs.3.rs-1175817/v1
日本人を対象としたX染色体ワイドメタ解析による尿酸関連SNP rs3020789の同定
日本痛風・尿酸核酸学会総会プログラム・抄録集, 55回, 67, Jan, 2022
Mendelian randomization of genetically independent aging phenotypes identifies LPA and VCAM1 as biological targets for human aging
Nature Aging, Jan, 2022, doi: 10.1038/s43587-021-00159-8
202134 papers
Trans-ancestry genome-wide association study identifies novel genetic mechanisms in rheumatoid arthritis
Dec 5, 2021, doi: 10.1101/2021.12.01.21267132
Model-based assessment of replicability for genome-wide association meta-analysis
Nature Communications, 12(1), Dec 1, 2021, doi: 10.1038/s41467-021-21226-z
ゲノムワイド関連解析による病型特異的な痛風関連遺伝子の同定と日本人の適応進化
痛風と尿酸・核酸, 45(2), 196, Dec, 2021
腎がんの組織型に寄与する遺伝子が異なることを示した大規模ゲノム解析
日本泌尿器科学会総会, 109回, AOP03-05, Dec, 2021
Genome-Wide Meta-analysis Identifies Genetic Variants Associated With Glycemic Response to Sulfonylureas.
Diabetes care, 44(12), 2673-2682, Dec, 2021, doi: 10.2337/dc21-1152
The power of genetic diversity in genome-wide association studies of lipids.
Nature, 600(7890), 675-679, Dec, 2021, doi: 10.1038/s41586-021-04064-3
Genetic susceptibility to hepatocellular carcinoma in chromosome 22q13.31, findings of a genome-wide association study.
JGH open : an open access journal of gastroenterology and hepatology, 5(12), 1363-1372, Dec, 2021, doi: 10.1002/jgh3.12682
A genome-wide association study identifies a novel candidate locus at the DLGAP1 gene with susceptibility to resistant hypertension in the Japanese population
Scientific Reports, 11(1), 19497, Dec, 2021, doi: 10.1038/s41598-021-98144-z
Leveraging supervised learning for functionally informed fine-mapping of cis-eQTLs identifies an additional 20,913 putative causal eQTLs
Nature Communications, 12(1), Dec, 2021, doi: 10.1038/s41467-021-23134-8
A deep learning method for HLA imputation and trans-ethnic MHC fine-mapping of type 1 diabetes
Nature Communications, 12(1), 1639, Dec, 2021, doi: 10.1038/s41467-021-21975-x
Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries
Nature Communications, 12(1), 1258, Dec, 2021, doi: 10.1038/s41467-020-20851-4
Genetic Contributions to Early and Late Onset Ischemic Stroke
Nov 8, 2021, doi: 10.1101/2021.11.06.21265795
Trans-ethnic Mendelian-randomization study reveals causal relationships between cardiometabolic factors and chronic kidney disease.
International journal of epidemiology, Oct 20, 2021, doi: 10.1093/ije/dyab203
A cross-population atlas of genetic associations for 220 human phenotypes
Nature Genetics, 53(10), 1415-1424, Oct, 2021, doi: 10.1038/s41588-021-00931-x
Trans-ancestry genome-wide analysis of atrial fibrillation provides new insights into disease biology and enables polygenic prediction of cardioembolic risk
Sep 12, 2021, doi: 10.1101/2021.09.06.21263189
「研究利活用のための脳卒中病態解明に資するゲノムデータベースの構築」一次調査結果
臨床神経学, 61(Suppl.), S337, Sep, 2021
Polygenic Risk Score of Adolescent Idiopathic Scoliosis for Potential Clinical Use.
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, 36(8), 1481-1491, Aug, 2021, doi: 10.1002/jbmr.4324
Combined landscape of single-nucleotide variants and copy number alterations in clonal hematopoiesis.
Nature medicine, 27(7), 1239-1249, Jul, 2021, doi: 10.1038/s41591-021-01411-9
Eight novel susceptibility loci and putative causal variants in atopic dermatitis.
The Journal of allergy and clinical immunology, 148(5), 1293-1306, Jun 2, 2021, doi: 10.1016/j.jaci.2021.04.019
Hematopoietic mosaic chromosomal alterations increase the risk for diverse types of infection.
Nature medicine, 27(6), 1012-1024, Jun, 2021, doi: 10.1038/s41591-021-01371-0
Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology.
Nature genetics, 53(6), 817-829, Jun, 2021, doi: 10.1038/s41588-021-00857-4
An X chromosome-wide meta-analysis based on Japanese cohorts revealed that non-autosomal variations are associated with serum urate.
Rheumatology (Oxford, England), 60(9), 4430-4432, May 4, 2021, doi: 10.1093/rheumatology/keab404
Publisher Correction: Clinical use of current polygenic risk scores may exacerbate health disparities (Nature Genetics, (2019), 51, 4, (584-591), 10.1038/s41588-019-0379-x)
Nature Genetics, 53(5), 763, May 1, 2021, doi: 10.1038/s41588-021-00797-z
Whole genome sequencing of 45 Japanese patients with intellectual disability.
American journal of medical genetics. Part A, 185(5), 1468-1480, May, 2021, doi: 10.1002/ajmg.a.62138
Regional differences in genes and variants causing retinitis pigmentosa in Japan.
Japanese journal of ophthalmology, 65(3), 338-343, May, 2021, doi: 10.1007/s10384-021-00824-w
Genome‐wide association study of epilepsy in a Japanese population identified an associated region at chromosome 12q24
Epilepsia, 62(6), 1391-1400, Apr 29, 2021, doi: 10.1111/epi.16911
Genome-wide analysis identifies novel susceptibility loci for myocardial infarction.
European heart journal, 42(9), 919-933, Mar 1, 2021, doi: 10.1093/eurheartj/ehaa1040
Author Correction: Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors (Nature Genetics, (2020), 52, 12, (1303-1313), 10.1038/s41588-020-00725-7)
Nature Genetics, 53(2), 254, Feb 1, 2021, doi: 10.1038/s41588-020-00760-4
Impact of sleep-disordered breathing on glucose metabolism among individuals with a family history of diabetes: the Nagahama study.
Journal of clinical sleep medicine : JCSM : official publication of the American Academy of Sleep Medicine, 17(2), 129-140, Feb 1, 2021, doi: 10.5664/jcsm.8796
Tractor uses local ancestry to enable the inclusion of admixed individuals in GWAS and to boost power
Nature Genetics, 53(2), 195-204, Feb, 2021, doi: 10.1038/s41588-020-00766-y
Genome-wide SNP data of Izumo and Makurazaki populations support inner-dual structure model for origin of Yamato people.
Journal of human genetics, Jan 25, 2021, doi: 10.1038/s10038-020-00898-3
Genetic variations in medical research in the past, at present and in the future.
Proceedings of the Japan Academy. Series B, Physical and biological sciences, 97(6), 324-335, 2021, doi: 10.2183/pjab.97.018
Two decades after Human Genome Project: do large-genetic studies lead to path of the genomic medicine of complex diseases?
Journal of Human Genetics, 66(1), 1, Jan, 2021, doi: 10.1038/s10038-020-00828-3
Whole genome sequence analyses of eGFR in 23,732 people representing multiple ancestries in the NHLBI trans-omics for precision medicine (TOPMed) consortium.
EBioMedicine, 63, 103157, Jan, 2021, doi: 10.1016/j.ebiom.2020.103157
202037 papers
Population-based Screening for Hereditary Colorectal Cancer Variants in Japan.
Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association, 20(9), 2132-2141, Dec 11, 2020, doi: 10.1016/j.cgh.2020.12.007
Cerebral small vessel disease genomics and its implications across the lifespan
Nature Communications, 11(1), Dec, 2020, doi: 10.1038/s41467-020-19111-2
Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors.
Nature genetics, 52(12), 1303-1313, Dec, 2020, doi: 10.1038/s41588-020-00725-7
A Mendelian randomization study identified obesity as a causal risk factor of uterine endometrial cancer in Japanese.
Cancer science, 111(12), 4646-4651, Dec, 2020, doi: 10.1111/cas.14667
Identification of a novel uterine leiomyoma GWAS locus in a Japanese population
Scientific Reports, 10(1), Dec, 2020, doi: 10.1038/s41598-020-58066-8
Dimensionality reduction reveals fine-scale structure in the Japanese population with consequences for polygenic risk prediction
Nature Communications, 11(1), Dec 1, 2020, doi: 10.1038/s41467-020-15194-z
Genetic and phenotypic landscape of the mitochondrial genome in the Japanese population
Communications Biology, 3(1), Dec 1, 2020, doi: 10.1038/s42003-020-0812-9
Prevalence and Spectrum of Pathogenic Germline Variants in Japanese Patients With Early-Onset Colorectal, Breast, and Prostate Cancer.
JCO precision oncology, 4, 183-191, Nov, 2020, doi: 10.1200/PO.19.00224
Population-specific and trans-ancestry genome-wide analyses identify distinct and shared genetic risk loci for coronary artery disease.
Nature genetics, 52(11), 1169-1177, Nov, 2020, doi: 10.1038/s41588-020-0705-3
A global atlas of genetic associations of 220 deep phenotypes
Oct 27, 2020, doi: 10.1101/2020.10.23.20213652
Genetic characterization of pancreatic cancer patients and prediction of carrier status of germline pathogenic variants in cancer-predisposing genes.
EBioMedicine, 60, 103033, Oct, 2020, doi: 10.1016/j.ebiom.2020.103033
Association of the RPA3-UMAD1 locus with interstitial lung diseases complicated with rheumatoid arthritis in Japanese.
Annals of the rheumatic diseases, 79(10), 1305-1309, Oct, 2020, doi: 10.1136/annrheumdis-2020-217256
A multi-ethnic meta-analysis identifies novel genes, including ACSL5, associated with amyotrophic lateral sclerosis.
Communications biology, 3(1), 526, Sep 23, 2020, doi: 10.1038/s42003-020-01251-2
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations
Cell, 182(5), 1198-1213.e14, Sep 3, 2020, doi: 10.1016/j.cell.2020.06.045
The Polygenic and Monogenic Basis of Blood Traits and Diseases
Cell, 182(5), 1214-1231.e11, Sep, 2020, doi: 10.1016/j.cell.2020.08.008
Endogenization and excision of human herpesvirus 6 in human genomes
PLOS Genetics, 16(8), e1008915, Aug 10, 2020, doi: 10.1371/journal.pgen.1008915
Chromosomal alterations among age-related haematopoietic clones in Japan.
Nature, 584(7819), 130-135, Aug, 2020, doi: 10.1038/s41586-020-2426-2
Evidence of Polygenic Adaptation in Sardinia at Height-Associated Loci Ascertained from the Biobank Japan.
American journal of human genetics, 107(1), 60-71, Jul 2, 2020, doi: 10.1016/j.ajhg.2020.05.014
LDL receptor gene familyのひとつであるLRP2遺伝子の一塩基多型rs2544390は痛風発症と関連する 日本人男性におけるメタ解析
痛風と尿酸・核酸, 44(1), 87, Jul, 2020
LDL receptor gene familyのひとつであるLRP2遺伝子の一塩基多型rs2544390は痛風発症と関連する 日本人男性におけるメタ解析
痛風と尿酸・核酸, 44(1), 87, Jul, 2020
Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases.
Nature genetics, 52(7), 669-679, Jul, 2020, doi: 10.1038/s41588-020-0640-3
Genome-wide association meta-analysis identifies GP2 gene risk variants for pancreatic cancer.
Nature communications, 11(1), 3175, Jun 24, 2020, doi: 10.1038/s41467-020-16711-w
Identification of type 2 diabetes loci in 433,540 East Asian individuals
Nature, 582(7811), 240-245, Jun, 2020, doi: 10.1038/s41586-020-2263-3
Transethnic Meta-Analysis of Genome-Wide Association Studies Identifies Three New Loci and Characterizes Population-Specific Differences for Coronary Artery Disease.
Circulation. Genomic and precision medicine, 13(3), e002670, Jun, 2020, doi: 10.1161/CIRCGEN.119.002670
Genome-Wide Natural Selection Signatures Are Linked to Genetic Risk of Modern Phenotypes in the Japanese Population
Molecular Biology and Evolution, 37(5), 1306-1316, May 1, 2020, doi: 10.1093/molbev/msaa005
Subtype-specific gout susceptibility loci and enrichment of selection pressure on ABCG2 and ALDH2 identified by subtype genome-wide meta-analyses of clinically defined gout patients.
Annals of the rheumatic diseases, 79(5), 657-665, May, 2020, doi: 10.1136/annrheumdis-2019-216644
A common variant of LDL receptor related protein 2 (LRP2) gene is associated with gout susceptibility: a meta-analysis in a Japanese population.
Human cell, 33(2), 303-307, Apr, 2020, doi: 10.1007/s13577-019-00318-5
Variants encoding a restricted carboxy-terminal domain of SLC12A2 cause hereditary hearing loss in humans.
PLoS genetics, 16(4), e1008643, Apr, 2020, doi: 10.1371/journal.pgen.1008643
Predicting cell-type-specific non-coding RNA transcription from genome sequence
Mar 30, 2020, doi: 10.1101/2020.03.29.011205
Claudin-2 deficiency associates with hypercalciuria in mice and human kidney stone disease
Journal of Clinical Investigation, 130(4), 1948-1960, Mar 9, 2020, doi: 10.1172/jci127750
GWAS of 165,084 Japanese individuals identified nine loci associated with dietary habits.
Nature human behaviour, 4(3), 308-316, Mar, 2020, doi: 10.1038/s41562-019-0805-1
Functional variants in ADH1B and ALDH2 are non-additively associated with all-cause mortality in Japanese population.
European journal of human genetics : EJHG, 28(3), 378-382, Mar, 2020, doi: 10.1038/s41431-019-0518-y
The Natural Metabolite 4-Cresol Improves Glucose Homeostasis and Enhances β-Cell Function.
Cell reports, 30(7), 2306-2320, Feb 18, 2020, doi: 10.1016/j.celrep.2020.01.066
Identification of Novel Loci and New Risk Variant in Known Loci for Colorectal Cancer Risk in East Asians
Cancer Epidemiology Biomarkers & Prevention, 29(2), 477-486, Feb, 2020, doi: 10.1158/1055-9965.epi-19-0755
LDL receptor gene familyのひとつであるLRP2遺伝子の一塩基多型rs2544390は痛風発症と関連する 日本人男性におけるメタ解析
日本痛風・核酸代謝学会総会プログラム抄録集, 53回, 67, Jan, 2020
Legacy Data Confound Genomics Studies.
Molecular biology and evolution, 37(1), 2-10, Jan 1, 2020, doi: 10.1093/molbev/msz201
GWAS of five gynecologic diseases and cross-trait analysis in Japanese.
European journal of human genetics : EJHG, 28(1), 95-107, Jan, 2020, doi: 10.1038/s41431-019-0495-1
201964 papers
Associations of autozygosity with a broad range of human phenotypes
Nature Communications, 10(1), Dec, 2019, doi: 10.1038/s41467-019-12283-6
Comparative genetic architectures of schizophrenia in East Asian and European populations.
Nature genetics, 51(12), 1670-1678, Dec, 2019, doi: 10.1038/s41588-019-0512-x
A novel PAK3 pathogenic variant identified in two siblings from a Japanese family with X-linked intellectual disability: case report and review of the literature.
Cold Spring Harbor molecular case studies, 5(6), Dec, 2019, doi: 10.1101/mcs.a003988
Genetic predisposition to mosaic Y chromosome loss in blood.
Nature, 575(7784), 652-657, Nov, 2019, doi: 10.1038/s41586-019-1765-3
日本人のアテローム血栓性脳梗塞の強力な遺伝子多型RNF213 p.4810K
臨床神経学, 59(Suppl.), S233, Nov, 2019
Polygenic burden in focal and generalized epilepsies
Brain, 142(11), 3473-3481, Nov 1, 2019, doi: 10.1093/brain/awz292
日本人のアテローム血栓性脳梗塞の強力な遺伝子多型RNF213 p.4810K
臨床神経学, 59(Suppl.), S233, Nov, 2019
Genome-wide association studies identify polygenic effects for completed suicide in the Japanese population.
Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 44(12), 2119-2124, Nov, 2019, doi: 10.1038/s41386-019-0506-5
Identification of two novel breast cancer loci through large-scale genome-wide association study in the Japanese population.
Scientific reports, 9(1), 17332, Nov, 2019, doi: 10.1038/s41598-019-53654-9
HLA-DQ and RBFOX1 as susceptibility genes for an outbreak of hydrolyzed wheat allergy.
The Journal of allergy and clinical immunology, 144(5), 1354-1363, Nov, 2019, doi: 10.1016/j.jaci.2019.06.034
Genetic variants of calcium and vitamin D metabolism in kidney stone disease.
Nature communications, 10(1), 5175, Nov, 2019, doi: 10.1038/s41467-019-13145-x
Large scale genome-wide association study in a Japanese population identified 45 novel susceptibility loci for 22 diseases
Oct 8, 2019, doi: 10.1101/795948
Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels
Nature Genetics, 51(10), 1459-1474, Oct, 2019, doi: 10.1038/s41588-019-0504-x
Comparison of effects of UGT1A1*6 and UGT1A1*28 on irinotecan-induced adverse reactions in the Japanese population: analysis of the Biobank Japan Project.
Journal of human genetics, 64(12), 1195-1202, Oct, 2019, doi: 10.1038/s10038-019-0677-2
HLA-B*51:01 and CYP2C9*3 are risk factors for phenytoin-induced eruption in the Japanese population: analysis of data from the Biobank Japan Project.
Clinical pharmacology and therapeutics, 107(5), 1170-1178, Oct, 2019, doi: 10.1002/cpt.1706
Genome-wide association study revealed novel loci which aggravate asymptomatic hyperuricaemia into gout.
Annals of the rheumatic diseases, 78(10), 1430-1437, Oct, 2019, doi: 10.1136/annrheumdis-2019-215521
GWAS of mosaic loss of chromosome Y highlights genetic effects on blood cell differentiation.
Nature communications, 10(1), 4719, Oct, 2019, doi: 10.1038/s41467-019-12705-5
Association of Birth Weight With Type 2 Diabetes and Glycemic Traits: A Mendelian Randomization Study.
JAMA network open, 2(9), e1910915, Sep 4, 2019, doi: 10.1001/jamanetworkopen.2019.10915
バイオバンキングが切り拓く新しいがん研究 わが国における骨髄性腫瘍およびクローン性造血に関するプレディスポジションの研究(Innovative cancer research based on biobanking Germline predisposition to myeloid neoplasms and clonal hematopoiesis of indeterminate potential in Japan)
日本癌学会総会記事, 78回, S11-5, Sep, 2019
IgG4-related disease in the Japanese population: a genome-wide association study
The Lancet Rheumatology, 1(1), e14-e22, Sep, 2019, doi: 10.1016/S2665-9913(19)30006-2
12 new susceptibility loci for prostate cancer identified by genome-wide association study in Japanese population.
Nature communications, 10(1), 4422, Sep, 2019, doi: 10.1038/s41467-019-12267-6
Characterizing rare and low-frequency height-associated variants in the Japanese population.
Nature communications, 10(1), 4393, Sep, 2019, doi: 10.1038/s41467-019-12276-5
Polygenic risk scores in schizophrenia with clinically significant copy number variants.
Psychiatry and clinical neurosciences, 74(1), 35-39, Aug, 2019, doi: 10.1111/pcn.12926
The schizophrenia genetics knowledgebase: a comprehensive update of findings from candidate gene studies.
Translational psychiatry, 9(1), 205, Aug, 2019, doi: 10.1038/s41398-019-0532-4
Genome-wide association study identifies 14 previously unreported susceptibility loci for adolescent idiopathic scoliosis in Japanese.
Nature communications, 10(1), 3685, Aug, 2019, doi: 10.1038/s41467-019-11596-w
Publisher Correction: Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes
Nature Genetics, 51(7), 1192-1193, Jul, 2019, doi: 10.1038/s41588-019-0449-0
無症候性高尿酸血症群と痛風症例群のゲノムワイド関連解析により痛風発症に関連する新規遺伝子座を同定した
痛風と尿酸・核酸, 43(1), 29-30, Jul, 2019
日本人121,745人を対象としたゲノムワイドメタ解析により血清尿酸値と関連する8つの新規遺伝子座を同定した
痛風と尿酸・核酸, 43(1), 31, Jul, 2019
National platform for Rare Diseases Data Registry of Japan
LEARNING HEALTH SYSTEMS, 3(3), Jul, 2019, doi: 10.1002/lrh2.10080
Genome-wide analysis of dental caries and periodontitis combining clinical and self-reported data.
Nature communications, 10(1), 2773, Jun 24, 2019, doi: 10.1038/s41467-019-10630-1
Genome-Wide Association Study Detected Novel Susceptibility Genes for Schizophrenia and Shared Trans-Populations/Diseases Genetic Effect.
Schizophrenia bulletin, 45(4), 824-834, Jun 18, 2019, doi: 10.1093/schbul/sby140
Germline pathogenic variants in 7,636 Japanese patients with prostate cancer and 12,366 controls.
Journal of the National Cancer Institute, 112(4), 369-376, Jun, 2019, doi: 10.1093/jnci/djz124
Genetic characteristics of retinitis pigmentosa in 1204 Japanese patients.
Journal of medical genetics, 56(10), 662-670, Jun, 2019, doi: 10.1136/jmedgenet-2018-105691
A frequent variant in the Japanese population determines quasi-Mendelian inheritance of rare retinal ciliopathy.
Nat Commun., 10(1), 2884, Jun, 2019, doi: 10.1038/s41467-019-10746-4
Multiancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions.
American journal of epidemiology, 188(6), 1033-1054, Jun, 2019, doi: 10.1093/aje/kwz005
A catalog of genetic loci associated with kidney function from analyses of a million individuals.
Nature genetics, 51(6), 957-972, Jun, 2019, doi: 10.1038/s41588-019-0407-x
Comprehensive evaluation of structural variation detection algorithms for whole genome sequencing.
Genome biology, 20(1), 117, Jun, 2019, doi: 10.1186/s13059-019-1720-5
Novel Risk Loci Identified in a Genome-Wide Association Study of Urolithiasis in a Japanese Population.
Journal of the American Society of Nephrology : JASN, 30(5), 855-864, May, 2019, doi: 10.1681/ASN.2018090942
GWAS of smoking behaviour in 165,436 Japanese people reveals seven new loci and shared genetic architecture.
Nature human behaviour, 3(5), 471-477, May, 2019, doi: 10.1038/s41562-019-0557-y
大規模ゲノム解析による28の新規2型糖尿病感受性領域および日本人と欧米人に特徴的な2型糖尿病の生物学的パスウェイの同定
日本臨床分子医学会学術総会プログラム・抄録集, 56回, 46, Apr, 2019
大規模ゲノム解析による28の新規2型糖尿病感受性領域および日本人と欧米人に特徴的な2型糖尿病の生物学的パスウェイの同定
糖尿病, 62(Suppl.1), S-108, Apr, 2019
Large-Scale Genome-Wide Association Study of East Asians Identifies Loci Associated With Risk for Colorectal Cancer.
Gastroenterology, 156(5), 1455-1466, Apr, 2019, doi: 10.1053/j.gastro.2018.11.066
PLD4 is a genetic determinant to systemic lupus erythematosus and involved in murine autoimmune phenotypes.
Annals of the rheumatic diseases, 78(4), 509-518, Apr, 2019, doi: 10.1136/annrheumdis-2018-214116
Clinical use of current polygenic risk scores may exacerbate health disparities.
Nature genetics, 51(4), 584-591, Apr, 2019, doi: 10.1038/s41588-019-0379-x
Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids.
Nature genetics, 51(4), 636-648, Apr, 2019, doi: 10.1038/s41588-019-0378-y
A multi-ancestry genome-wide study incorporating gene-smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure.
Human molecular genetics, 28(15), 2615-2633, Apr, 2019, doi: 10.1093/hmg/ddz070
Genetic and phenotypic landscape of the major histocompatibilty complex region in the Japanese population.
Nature genetics, 51(3), 470-480, Mar, 2019, doi: 10.1038/s41588-018-0336-0
Identification of 28 new susceptibility loci for type 2 diabetes in the Japanese population.
Nature genetics, 51(3), 379-386, Mar, 2019, doi: 10.1038/s41588-018-0332-4
Association between genetic risk and development of type 2 diabetes in a general Japanese population: The Hisayama Study.
The Journal of clinical endocrinology and metabolism, 104(8), 3213-3222, Mar, 2019, doi: 10.1210/jc.2018-01782
Genome-Wide Association and Functional Studies Reveal Novel Pharmacological Mechanisms for Allopurinol.
Clinical pharmacology and therapeutics, Mar, 2019, doi: 10.1002/cpt.1439
Diabetes and cancer risk: A Mendelian randomization study.
International journal of cancer, 146(3), 712-719, Mar, 2019, doi: 10.1002/ijc.32310
Hidden 'risk' in polygenic scores: clinical use today could exacerbate health disparities.
Nature genetics, In Press, Feb, 2019
Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use.
Nature genetics, 51(2), 237-244, Feb, 2019, doi: 10.1038/s41588-018-0307-5
Empirical evaluation of variant calling accuracy using ultra-deep whole-genome sequencing data.
Scientific reports, 9(1), 1784, Feb, 2019, doi: 10.1038/s41598-018-38346-0
Genome-wide association study of cervical cancer suggests a role for ARRDC3 gene in human papillomavirus infection.
Human molecular genetics, 28(2), 341-348, Jan 15, 2019, doi: 10.1093/hmg/ddy390
GWAS identifies nine nephrolithiasis susceptibility loci related with metabolic metabolic and crystallization pathways
Jan 13, 2019, doi: 10.1101/519553
Moyamoya Disease Susceptibility Variant RNF213 p.R4810K Increases the Risk of Ischemic Stroke Attributable to Large-Artery Atherosclerosis.
Circulation, 139(2), 295-298, Jan 8, 2019, doi: 10.1161/CIRCULATIONAHA.118.038439
無症候性高尿酸血症群と痛風症例群のゲノムワイド関連解析により痛風発症に関連する新規遺伝子座を同定した
日本痛風・核酸代謝学会総会プログラム抄録集, 52回, 74, Jan, 2019
日本人121,745人を対象としたゲノムワイドメタ解析により血清尿酸値と関連する8つの新規遺伝子座を同定した
日本痛風・核酸代謝学会総会プログラム抄録集, 52回, 75, Jan, 2019
日本人の臨床検査値に影響する遺伝的背景の解明 58の量的形質における大規模ゲノムワイド関連解析
臨床免疫・アレルギー科, 71(1), 78-85, Jan, 2019
A novel intragenic deletion in OPHN1 in a Japanese patient with Dandy-Walker malformation.
Human genome variation, 6, 1, 2019, doi: 10.1038/s41439-018-0032-8
Genetically Determined Levels of Circulating Cytokines and Risk of Stroke.
Circulation, 139(2), 256-268, Jan, 2019, doi: 10.1161/CIRCULATIONAHA.118.035905
Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies.
Nature communications, 10(1), 29, Jan, 2019, doi: 10.1038/s41467-018-07867-7
Genome-wide meta-analysis identifies multiple novel loci associated with serum uric acid levels in Japanese individuals.
Communications biology, 2(1), 115, 2019, doi: 10.1038/s42003-019-0339-0
201832 papers
Integration of genetics and miRNA-target gene network identified disease biology implicated in tissue specificity.
Nucleic acids research, 46(22), 11898-11909, Dec 14, 2018, doi: 10.1093/nar/gky1066
GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes
Nature Communications, 9(1), Dec 1, 2018, doi: 10.1038/s41467-018-07340-5
日本人における尿酸値のGWASメタ解析による8個の新規遺伝子座の同定
防衛衛生, 66(別冊), 44, Dec, 2018
Genome-wide association study identifies gastric cancer susceptibility loci at 12q24.11-12 and 20q11.21
CANCER SCIENCE, 109(12), 4015-4024, Dec, 2018, doi: 10.1111/cas.13815
Deep whole-genome sequencing reveals recent selection signatures linked to evolution and disease risk of Japanese
Nature Communications, 9(1), 1631, Dec 1, 2018, doi: 10.1038/s41467-018-03274-0
Elucidating the genetic architecture of reproductive ageing in the Japanese population
Nature Communications, 9(1), 1977, Dec 1, 2018, doi: 10.1038/s41467-018-04398-z
Genome-wide association study identifies gastric cancer susceptibility loci at 12q24.11-12 and 20q11.21.
Cancer science, 109(12), 4015-4024, Dec, 2018, doi: 10.1111/cas.13815
Analysis of Genomic Predispositions to Sporadic Myeloid Neoplasms Mediated By DDX41 in Japan
BLOOD, 132, Nov 29, 2018, doi: 10.1182/blood-2018-99-117664
Interethnic analyses of blood pressure loci in populations of East Asian and European descent.
Nature communications, 9(1), 5052, Nov 28, 2018, doi: 10.1038/s41467-018-07345-0
Amino acid position 37 of HLA-DRβ1 affects susceptibility to Crohn's disease in Asians.
Human molecular genetics, 27(22), 3901-3910, Nov, 2018, doi: 10.1093/hmg/ddy285
Germline pathogenic variants of 11 breast cancer genes in 7,051 Japanese patients and 11,241 controls.
Nature communications, 9(1), 4083, Oct, 2018, doi: 10.1038/s41467-018-06581-8
Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation.
Nature communications, 9(1), 4455, Oct, 2018, doi: 10.1038/s41467-018-06356-1
A locus at 7p14.3 predisposes to refractory celiac disease progression from celiac disease.
European journal of gastroenterology & hepatology, 30(8), 828-837, Aug, 2018, doi: 10.1097/MEG.0000000000001168
Re-evaluating classical body type theories: genetic correlation between psychiatric disorders and body mass index.
Psychological medicine, 48(10), 1745-1748, Jul, 2018, doi: 10.1017/S0033291718000685
Multi-ethnic genome-wide association study for atrial fibrillation
Nature Genetics, 50(9), 1-9, Jun 11, 2018, doi: 10.1038/s41588-018-0133-9
Genome-Wide Association Study of Renal Function Traits: Results from the Japan Multi-Institutional Collaborative Cohort Study
American Journal of Nephrology, 47(5), 304-316, Jun 1, 2018, doi: 10.1159/000488946
Analysis of shared heritability in common disorders of the brain.
Science (New York, N.Y.), 360(6395), Jun, 2018, doi: 10.1126/science.aap8757
Identification of LEF1 as a Susceptibility Locus for Kawasaki Disease in Patients Younger than 6 Months of Age.
Genomics & informatics, 16(2), 36-41, Jun, 2018, doi: 10.5808/GI.2018.16.2.36
GWAS identifies two novel colorectal cancer loci at 16q24.1 and 20q13.12.
Carcinogenesis, 39(5), 652-660, May, 2018, doi: 10.1093/carcin/bgy026
Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma
Human Molecular Genetics, 27(8), 1486-1496, Apr 15, 2018, doi: 10.1093/hmg/ddy053
Re-evaluating classical body type theories: Genetic correlation between psychiatric disorders and body mass index
Psychological Medicine, 1-4, Apr 13, 2018, doi: 10.1017/S0033291718000685
Splicing variant of WDFY4 augments MDA5 signalling and the risk of clinically amyopathic dermatomyositis.
Annals of the rheumatic diseases, 77(4), 602-611, Apr, 2018, doi: 10.1136/annrheumdis-2017-212149
Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes
Nature Genetics, 50(4), 524-537, Apr 1, 2018, doi: 10.1038/s41588-018-0058-3
A genome-wide association study identifies two novel susceptibility loci and trans population polygenicity associated with bipolar disorder
Molecular Psychiatry, 23(3), 639-647, Mar 1, 2018, doi: 10.1038/mp.2016.259
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases
Nature Genetics, 50(3), 390-400, Mar 1, 2018, doi: 10.1038/s41588-018-0047-6
A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure
American Journal of Human Genetics, 102(3), 375-400, Mar 1, 2018, doi: 10.1016/j.ajhg.2018.01.015
Citrullination of RGG Motifs in FET Proteins by PAD4 Regulates Protein Aggregation and ALS Susceptibility.
Cell reports, 22(6), 1473-1483, Feb 6, 2018, doi: 10.1016/j.celrep.2018.01.031
A GWAS identifies gastric cancer susceptibility loci at 12q24.11-12 and 20q11.21.
Cancer Sci., 2018
Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries.
PloS one, 13(6), e0198166, 2018, doi: 10.1371/journal.pone.0198166
Genetics of the thrombomodulin-endothelial cell protein C receptor system and the risk of early-onset ischemic stroke.
PloS one, 13(11), e0206554, 2018, doi: 10.1371/journal.pone.0206554
Genome-wide association study (GWAS) of ovarian cancer in Japanese predicted regulatory variants in 22q13.1.
PloS one, 13(12), e0209096, 2018, doi: 10.1371/journal.pone.0209096
A variant within the FTO confers susceptibility to diabetic nephropathy in Japanese patients with type 2 diabetes.
PloS one, 13(12), e0208654, 2018, doi: 10.1371/journal.pone.0208654
201737 papers
Genetic landscape of interactive effects of HLA-DRB1 alleles on susceptibility to ACPA(+) rheumatoid arthritis and ACPA levels in Japanese population
JOURNAL OF MEDICAL GENETICS, 54(12), 853-858, Dec, 2017, doi: 10.1136/jmedgenet-2017-104779
Common variants at 2q11.2, 8q21.3, and 11q13.2 are associated with major mood disorders
TRANSLATIONAL PSYCHIATRY, 7(12), 1273, Dec, 2017, doi: 10.1038/s41398-017-0019-0
Genome-wide Association Study of Idiopathic Osteonecrosis of the Femoral Head
SCIENTIFIC REPORTS, 7(1), 15035, Nov, 2017, doi: 10.1038/s41598-017-14778-y
Genome-wide association study identifies 112 new loci for body mass index in the Japanese population
NATURE GENETICS, 49(10), 1458-+, Oct, 2017, doi: 10.1038/ng.3951
A functional variant in MIR4300HG, the host gene of microRNA MIR4300 is associated with progression of adolescent idiopathic scoliosis
HUMAN MOLECULAR GENETICS, 26(20), 4086-4092, Oct, 2017, doi: 10.1093/hmg/ddx291
Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation (vol 49, pg 946, 2017)
NATURE GENETICS, 49(8), 1286, Aug, 2017, doi: 10.1038/ng0817-1286c
Erratum to "Characteristics and prognosis of Japanese colorectal cancer patients: The BioBank Japan Project" [J Epidemiol 27(3S) (2017) S36-S42].
Journal of epidemiology, 27(8), 398-399, Aug, 2017, doi: 10.1016/j.je.2017.04.001
Polygenic burdens on cell-specific pathways underlie the risk of rheumatoid arthritis
NATURE GENETICS, 49(7), 1120-+, Jul, 2017, doi: 10.1038/ng.3885
Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation
NATURE GENETICS, 49(6), 946-+, Jun, 2017, doi: 10.1038/ng.3843
Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation (vol 49, pg 946, 2017)
NATURE GENETICS, 49(6), 946-952, Jun, 2017, doi: 10.1038/ng.3843
Identification of six new genetic loci associated with atrial fibrillation in the Japanese population
NATURE GENETICS, 49(6), 953-+, Jun, 2017, doi: 10.1038/ng.3842
Association of variations in HLA-class II and other loci with susceptibility to EGFR-mutated lung adenocarcinoma
CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION, 26(5), May, 2017, doi: 10.1158/1538-7755.CARISK16-B25
GWAS of clinically defined gout and subtypes identifies multiple susceptibility loci that include urate transporter genes.
Annals of the rheumatic diseases, 76(5), 869-877, May, 2017, doi: 10.1136/annrheumdis-2016-209632
GWAS of clinically defined gout and subtypes identifies multiple susceptibility loci that include urate transporter genes
ANNALS OF THE RHEUMATIC DISEASES, 76(5), 869-877, May, 2017, doi: 10.1136/annrheumdis-2016-209632
Meta-analysis identifies five novel loci associated with endometriosis highlighting key genes involved in hormone metabolism
NATURE COMMUNICATIONS, 8, 15539, May, 2017, doi: 10.1038/ncomms15539
日本人2型糖尿病集団における糖尿病網膜症のゲノムワイド関連解析
糖尿病, 60(Suppl.1), S-281, Apr, 2017
次世代シークエンサーによる加齢黄斑変性症感受性多型の同定
日本眼科学会雑誌, 121(臨増), 241, Mar, 2017
Risk prediction models for mortality in patients with cardiovascular disease: The BioBank Japan project
JOURNAL OF EPIDEMIOLOGY, 27(3), S71-S76, Mar, 2017, doi: 10.1016/j.je.2016.10.007
Serum glucose, cholesterol and blood pressure levels in Japanese type 1 and 2 diabetic patients: BioBank Japan
JOURNAL OF EPIDEMIOLOGY, 27(3), S92-S97, Mar, 2017, doi: 10.1016/j.je.2016.12.013
Overview of the BioBank Japan Project: Study design and profile
JOURNAL OF EPIDEMIOLOGY, 27(3), S2-S8, Mar, 2017, doi: 10.1016/j.je.2016.12.005
Cross-sectional analysis of BioBank Japan clinical data: A large cohort of 200,000 patients with 47 common diseases
JOURNAL OF EPIDEMIOLOGY, 27(3), S9-S21, Mar, 2017, doi: 10.1016/j.je.2016.12.003
Demographic and lifestyle factors and survival among patients with esophageal and gastric cancer: The Biobank Japan Project
JOURNAL OF EPIDEMIOLOGY, 27(3), S29-S35, Mar, 2017, doi: 10.1016/j.je.2016.12.002
Overview of BioBank Japan follow-up data in 32 diseases
JOURNAL OF EPIDEMIOLOGY, 27(3), S22-S28, Mar, 2017, doi: 10.1016/j.je.2016.12.006
Statin use and all-cause and cancer mortality: BioBank Japan cohort
JOURNAL OF EPIDEMIOLOGY, 27(3), S84-S91, Mar, 2017, doi: 10.1016/j.je.2016.12.011
Cholesterol levels of Japanese dyslipidaemic patients with various comorbidities: BioBank Japan
JOURNAL OF EPIDEMIOLOGY, 27(3), S77-S83, Mar, 2017, doi: 10.1016/j.je.2016.12.014
Characteristics and prognosis of Japanese male and female lung cancer patients: The BioBank Japan Project
JOURNAL OF EPIDEMIOLOGY, 27(3), S49-S57, Mar, 2017, doi: 10.1016/j.je.2016.12.010
Survival of macrovascular disease, chronic kidney disease, chronic respiratory disease, cancer and smoking in patients with type 2 diabetes: BioBank Japan cohort
JOURNAL OF EPIDEMIOLOGY, 27(3), S98-S106, Mar, 2017, doi: 10.1016/j.je.2016.12.012
Characteristics of patients with liver cancer in the BioBank Japan project
JOURNAL OF EPIDEMIOLOGY, 27(3), S43-S48, Mar, 2017, doi: 10.1016/j.je.2016.12.007
Characteristics and prognosis of Japanese colorectal cancer patients: The BioBank Japan Project
JOURNAL OF EPIDEMIOLOGY, 27(3), S36-S42, Mar, 2017, doi: 10.1016/j.je.2016.12.004
Clinical and histopathological characteristics of patients with prostate cancer in the BioBank Japan project
JOURNAL OF EPIDEMIOLOGY, 27(3), S65-S70, Mar, 2017, doi: 10.1016/j.je.2016.12.008
Characteristics and prognosis of Japanese female breast cancer patients: The BioBank Japan
JOURNAL OF EPIDEMIOLOGY, 27(3), S58-S64, Mar, 2017, doi: 10.1016/j.je.2016.12.009
Genetic Predisposition to Ischemic Stroke: A Polygenic Risk Score
STROKE, 48(2), 253-258, Feb, 2017, doi: 10.1161/STROKEAHA.116.014506
Using spatio-temporal surveillance data to test the infectious environment of children before type 1 diabetes diagnosis
PLOS ONE, 12(2), e0170658, Feb, 2017, doi: 10.1371/journal.pone.0170658
Association of Variations in HLA-Class II and Other Loci with Susceptibility to EGFR-Mutated Lung Adenocarcinonna
JOURNAL OF THORACIC ONCOLOGY, 12(1), S280-S281, Jan, 2017
Hierarchical Maximum Likelihood Clustering Approach
IEEE TRANSACTIONS ON BIOMEDICAL ENGINEERING, 64(1), 112-122, Jan, 2017, doi: 10.1109/TBME.2016.2542212
Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis
AMERICAN JOURNAL OF HUMAN GENETICS, 100(1), 51-63, Jan, 2017, doi: 10.1016/j.ajhg.2016.11.016
Association between GWAS-identified lung adenocarcinoma susceptibility loci and EGFR mutations in never-smoking Asian women, and comparison with findings from Western populations
HUMAN MOLECULAR GENETICS, 26(2), 454-465, Jan, 2017, doi: 10.1093/hmg/ddw414
201618 papers
Genomewide Association Studies in Pharmacogenomics: Meeting Report of the NIH Pharmacogenomics Research Network-RIKEN (PGRN-RIKEN) Collaboration
CLINICAL PHARMACOLOGY & THERAPEUTICS, 100(5), 423-426, Nov, 2016, doi: 10.1002/cpt.405
Risk factors and clinical characteristics of the depressive state induced by pegylated interferon therapy in patients with hepatitis C virus infection: A prospective study
PSYCHIATRY AND CLINICAL NEUROSCIENCES, 70(11), 489-497, Nov, 2016, doi: 10.1111/pcn.12424
Low-frequency coding variants in CETP and CFB are associated with susceptibility of exudative age-related macular degeneration in the Japanese population
HUMAN MOLECULAR GENETICS, 25(22), 5027-5034, Nov, 2016, doi: 10.1093/hmg/ddw335
Low-frequency coding variants in CETP and CFB are associated with susceptibility of exudative age-related macular degeneration in the Japanese population.
Hum Mol Genet, Oct 3, 2016
バイオバンクジャパン 13悪性腫瘍における追跡調査
日本癌学会総会記事, 75回, E-3078, Oct, 2016
ゲノムワイド関連解析による新規子宮筋腫感受性遺伝子の同定
日本癌学会総会記事, 75回, P-3366, Oct, 2016
Dosage Contribution of a Non-Classical HLA Gene, HLA-Doa, to the Risk of Rheumatoid Arthritis
ARTHRITIS & RHEUMATOLOGY, 68, Oct, 2016, doi: 10.1016/j.ajhg.2016.06.019
Pharmacogenomic Study of Clozapine-Induced Agranulocytosis/Granulocytopenia in a Japanese Population
BIOLOGICAL PSYCHIATRY, 80(8), 636-642, Oct, 2016, doi: 10.1016/j.biopsych.2015.12.006
Trans-ethnic Fine Mapping Highlights Kidney-Function Genes Linked to Salt Sensitivity
AMERICAN JOURNAL OF HUMAN GENETICS, 99(3), 636-646, Sep, 2016, doi: 10.1016/j.ajhg.2016.07.012
Contribution of a Non-classical HLA Gene, HLA-DOA, to the Risk of Rheumatoid Arthritis
AMERICAN JOURNAL OF HUMAN GENETICS, 99(2), 366-374, Aug, 2016, doi: 10.1016/j.ajhg.2016.06.019
Association of variations in HLA class II and other loci with susceptibility to EGFR-mutated lung adenocarcinoma
Nature Communications, 7, 12451, Aug, 2016, doi: 10.1038/ncomms12451
Stepwise iterative maximum likelihood clustering approach
BMC BIOINFORMATICS, 17(1), 319, Aug, 2016, doi: 10.1186/s12859-016-1184-5
Identification of additional risk loci for stroke and small vessel disease: a meta-analysis of genome-wide association studies
LANCET NEUROLOGY, 15(7), 695-707, Jun, 2016, doi: 10.1016/s1474-4422(16)00102-2
Genome-wide imputation study identifies novel HLA locus for pulmonary fibrosis and potential role for auto-immunity in fibrotic idiopathic interstitial pneumonia
BMC GENETICS, 17(1), 74, Jun, 2016, doi: 10.1186/s12863-016-0377-2
Search for new loci and low-frequency variants influencing glioma risk by exome-array analysis
EUROPEAN JOURNAL OF HUMAN GENETICS, 24(5), 717-724, May, 2016, doi: 10.1038/ejhg.2015.170
[Genome Wide Association Study:its theory and methodological review].
Clinical calcium, 26(4), 525-535, Apr, 2016
Genome-Wide Association Analysis of Young-Onset Stroke Identifies a Locus on Chromosome 10q25 Near HABP2
STROKE, 47(2), 307-+, Feb, 2016, doi: 10.1161/STROKEAHA.115.011328
A novel Alzheimer disease locus located near the gene encoding tau protein
MOLECULAR PSYCHIATRY, 21(1), 108-117, Jan, 2016, doi: 10.1038/mp.2015.23
20158 papers
バイオバンクジャパンコホートプロファイル 47疾患20万人の大規模コホートデータ
日本癌学会総会記事, 74回, J-1342, Oct, 2015
Imputation of KIR Types from SNP Variation Data
AMERICAN JOURNAL OF HUMAN GENETICS, 97(4), 593-607, Oct, 2015, doi: 10.1016/j.ajhg.2015.09.005
A Functional SNP in BNC2 Is Associated with Adolescent Idiopathic Scoliosis
AMERICAN JOURNAL OF HUMAN GENETICS, 97(2), 337-342, Aug, 2015, doi: 10.1016/j.ajhg.2015.06.012
Construction of a population-specific HLA imputation reference panel and its application to Graves' disease risk in Japanese
NATURE GENETICS, 47(7), 798-+, Jul, 2015, doi: 10.1038/ng.3310
Directional dominance on stature and cognition in diverse human populations
NATURE, 523(7561), 459-U176, Jul, 2015, doi: 10.1038/nature14618
Convergent genetic and expression data implicate immunity in Alzheimer's disease
ALZHEIMERS & DEMENTIA, 11(6), 658-671, Jun, 2015, doi: 10.1016/j.jalz.2014.05.1757
Circulating lipid levels and risk of coronary artery disease in a large group of patients undergoing coronary angiography
JOURNAL OF THROMBOSIS AND THROMBOLYSIS, 39(1), 15-22, Jan, 2015, doi: 10.1007/s11239-014-1069-2
Common variation in PHACTR1 is associated with susceptibility to cervical artery dissection
NATURE GENETICS, 47(1), 78-+, Jan, 2015, doi: 10.1038/ng.3154
20146 papers
Trans-ethnic meta-analysis of white blood cell phenotypes
HUMAN MOLECULAR GENETICS, 23(25), 6944-6960, Dec, 2014, doi: 10.1093/hmg/ddu401
Rare and common variants in extracellular matrix gene Fibrillin 2 (FBN2) are associated with macular degeneration
HUMAN MOLECULAR GENETICS, 23(21), 5827-5837, Nov, 2014, doi: 10.1093/hmg/ddu276
Genome-wide association meta-analysis of human longevity identifies a novel locus conferring survival beyond 90 years of age
HUMAN MOLECULAR GENETICS, 23(16), 4420-4432, Aug, 2014, doi: 10.1093/hmg/ddu139
Gene-Wide Analysis Detects Two New Susceptibility Genes for Alzheimer's Disease
PLOS ONE, 9(6), e94661, Jun, 2014, doi: 10.1371/journal.pone.0094661
Genetics of rheumatoid arthritis contributes to biology and drug discovery
NATURE, 506(7488), 376-+, Feb, 2014, doi: 10.1038/nature12873
Integration of Sequence Data from a Consanguineous Family with Genetic Data from an Outbred Population Identifies PLB1 as a Candidate Rheumatoid Arthritis Risk Gene
PLOS ONE, 9(2), e87645, Feb, 2014, doi: 10.1371/journal.pone.0087645
20136 papers
Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease
NATURE GENETICS, 45(12), 1452-U206, Dec, 2013, doi: 10.1038/ng.2802
A genome-wide association study of atopic dermatitis identifies loci with overlapping effects on asthma and psoriasis
HUMAN MOLECULAR GENETICS, 22(23), 4841-4856, Dec, 2013, doi: 10.1093/hmg/ddt317
Genome-wide association study in breast cancer survivors reveals SNPs associated with gene expression of genes belonging to MHC class I and II
GENOMICS, 102(4), 278-287, Oct, 2013, doi: 10.1016/j.ygeno.2013.07.006
Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis.
Nature genetics, 45(6), 613-620, Jun, 2013, doi: 10.1038/ng.2609
Genome-wide haplotype association study identifies the FRMD4A gene as a risk locus for Alzheimer's disease
MOLECULAR PSYCHIATRY, 18(4), 461-470, Apr, 2013, doi: 10.1038/mp.2012.14
Seven new loci associated with age-related macular degeneration
NATURE GENETICS, 45(4), 433-439, Apr, 2013, doi: 10.1038/ng.2578
20127 papers
TFAP2B Influences the Effect of Dietary Fat on Weight Loss under Energy Restriction
PLOS ONE, 7(8), e43212, Aug, 2012, doi: 10.1371/journal.pone.0043212
Genome-Wide Association Study in a Lebanese Cohort Confirms PHACTR1 as a Major Determinant of Coronary Artery Stenosis
PLOS ONE, 7(6), e38663, Jun, 2012, doi: 10.1371/journal.pone.0038663
Genetic and environmental influences on total plasma homocysteine and its role in coronary artery disease risk
ATHEROSCLEROSIS, 222(1), 180-186, May, 2012, doi: 10.1016/j.atherosclerosis.2012.02.035
Association of Common Variants in TNFRSF13B, TNFSF13, and ANXA3 with Serum Levels of Non-Albumin Protein and Immunoglobulin Isotypes in Japanese
PLOS ONE, 7(4), e32683, Apr, 2012, doi: 10.1371/journal.pone.0032683
Common genetic factors for hematological traits in Humans
JOURNAL OF HUMAN GENETICS, 57(3), 161-169, Mar, 2012, doi: 10.1038/jhg.2012.2
Genome-Wide Association Study of Classical Hodgkin Lymphoma and Epstein-Barr Virus Status-Defined Subgroups
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 104(3), 240-253, Feb, 2012, doi: 10.1093/jnci/djr516
Functional Variants in NFKBIE and RTKN2 Involved in Activation of the NF-κB Pathway Are Associated with Rheumatoid Arthritis in Japanese
PLoS Genetics, 8(9), 2012, doi: 10.1371/journal.pgen.1002949
20118 papers
Large Scale Association Analysis Identifies Three Susceptibility Loci for Coronary Artery Disease
PLOS ONE, 6(12), e29427, Dec, 2011, doi: 10.1371/journal.pone.0029427
Genome-wide association study on bipolar disorder in the Bulgarian population
GENES BRAIN AND BEHAVIOR, 10(7), 789-797, Oct, 2011, doi: 10.1111/j.1601-183X.2011.00721.x
A genome-wide association study of chronic hepatitis B identified novel risk locus in a Japanese population
HUMAN MOLECULAR GENETICS, 20(19), 3884-3892, Oct, 2011, doi: 10.1093/hmg/ddr301
Family-based designs for genome-wide association studies
NATURE REVIEWS GENETICS, 12(7), 465-474, Jul, 2011, doi: 10.1038/nrg2989
Common variant in 6q26-q27 is associated with distal colon cancer in an Asian population
Gut, 60(6), 799-805, Jun, 2011, doi: 10.1136/gut.2010.215947
Identification of Nine Novel Loci Associated with White Blood Cell Subtypes in a Japanese Population
PLOS GENETICS, 7(6), e1002067, Jun, 2011, doi: 10.1371/journal.pgen.1002067
Multiple Loci Are Associated with White Blood Cell Phenotypes
PLOS GENETICS, 7(6), e1002113, Jun, 2011, doi: 10.1371/journal.pgen.1002113
Genome-wide association study for C-reactive protein levels identified pleiotropic associations in the IL6 locus
HUMAN MOLECULAR GENETICS, 20(6), 1224-1231, Mar, 2011, doi: 10.1093/hmg/ddq551
20104 papers
A Large-Scale, Consortium-Based Genomewide Association Study of Asthma
NEW ENGLAND JOURNAL OF MEDICINE, 363(13), 1211-1221, Sep, 2010
A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci
HUMAN MOLECULAR GENETICS, 19(11), 2303-2312, Jun, 2010, doi: 10.1093/hmg/ddq091
Common variations in PSMD3-CSF3 and PLCB4 are associated with neutrophil count
HUMAN MOLECULAR GENETICS, 19(10), 2079-2085, May, 2010, doi: 10.1093/hmg/ddq080
Genome-wide association study of hematological and biochemical traits in a Japanese population
NATURE GENETICS, 42(3), 210-U25, Mar, 2010, doi: 10.1038/ng.531
20093 papers
Functional Variants in ADH1B and ALDH2 Coupled With Alcohol and Smoking Synergistically Enhance Esophageal Cancer Risk
GASTROENTEROLOGY, 137(5), 1768-1775, Nov, 2009, doi: 10.1053/j.gastro.2009.07.070
A genome-wide association study identifies variants in the HLA-DP locus associated with chronic hepatitis B in Asians
NATURE GENETICS, 41(5), 591-595, May, 2009, doi: 10.1038/ng.348
Evaluation of imputation-based association in and around the integrin-alpha-M (ITGAM) gene and replication of robust association between a non-synonymous functional variant within ITGAM and systemic lupus erythematosus (SLE)
HUMAN MOLECULAR GENETICS, 18(6), 1171-1180, Mar, 2009, doi: 10.1093/hmg/ddp007
20083 papers
Functional SNPs in CD244 increase the risk of rheumatoid arthritis in a Japanese population
NATURE GENETICS, 40(10), 1224-1229, Oct, 2008, doi: 10.1038/ng.205
A functional SNP in the NKX2.5-binding site of ITPR3 promoter is associated with susceptibility to systemic lupus erythematosus in Japanese population
JOURNAL OF HUMAN GENETICS, 53(2), 151-162, Feb, 2008, doi: 10.1007/s10038-007-0233-3
Identification of a significant association of a single nucleotide polymorphism in TNXB with systemic lupus erythematosus in a Japanese population
JOURNAL OF HUMAN GENETICS, 53(1), 64-73, Jan, 2008, doi: 10.1007/s10038-007-0219-1
20041 papers
[Clinical management of metabolic syndrome: discussion].
Nihon Naika Gakkai zasshi. The Journal of the Japanese Society of Internal Medicine, 93(4), 740-755, Apr, 2004
Publications synced from researchmap (Prof. Yoichiro Kamatani).