Author details

Full Name

Michiaki Kubo

Affiliation

ORCID

Career Start Year

1982

Papers

628

H Index

107

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37881853	Genome-wide assessment of genetic risk loci for childhood acute lymphoblastic leukemia in Japanese patients.	Haematologica	2024
37882647	Identification of telomere maintenance gene variations related to lung adenocarcinoma risk by genome-wide association and whole genome sequencing analyses.	Cancer Commun (Lond)	2024
34421081	Population-Based Impact of Smoking, Drinking, and Genetic Factors on HDL-cholesterol Levels in J-MICC Study Participants.	Journal of Epidemiology	2023
36322930	Germ line DDX41 mutations define a unique subtype of myeloid neoplasms.	Blood	2023
36423732	Genome-Wide Association Study of Age-Related Macular Degeneration Reveals 2 New Loci Implying Shared Genetic Components with Central Serous Chorioretinopathy.	Ophthalmology	2023
37945903	Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants.	Nat Genet	2023
37556544	A whole-genome reference panel of 14,393 individuals for East Asian populations accelerates discovery of rare functional variants.	Sci Adv	2023
37612283	Androgen receptor binding sites enabling genetic prediction of mortality due to prostate cancer in cancer-free subjects.	Nat Commun	2023
37415668	Evidence of causality of low body mass index on risk of adolescent idiopathic scoliosis: a Mendelian randomization study.		2023
36753494	Effects of gene-lifestyle interactions on obesity based on a multi-locus risk score: A cross-sectional analysis.		2023
37236969	Genome-wide association study of lung adenocarcinoma in East Asia and comparison with a European population.	Nat Commun	2023
36725857	Genome-wide host-pathogen analyses reveal genetic interaction points in tuberculosis disease.	Nat Commun	2023
35349657	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	2022
35396580	Mapping genomic loci implicates genes and synaptic biology in schizophrenia.	Nature	2022
36240095	Contribution of Common Genetic Variants to Risk of Early-Onset Ischemic Stroke.	Neurology	2022
36356581	Genome- and transcriptome-wide association studies of 386,000 Asian and European-ancestry women provide new insights into breast cancer genetics.	Am J Hum Genet	2022
35383711	Two polymorphic gene loci associated with treprostinil dose in pulmonary arterial hypertension.	Pharmacogenet Genomics	2022
35574023	Glucagon Test Is a Useful Predictor of Withdrawal From Insulin Therapy in Subjects With Type 2 Diabetes Mellitus.	Frontiers in Endocrinology	2022
35637176	Author Correction: Genetic variants of calcium and vitamin D metabolism in kidney stone disease.	Nature Communications	2022
36344522	Discerning asthma endotypes through comorbidity mapping.	Nat Commun	2022
35377938	ABO O blood group as a risk factor for platelet reactivity in heparin-induced thrombocytopenia.	Blood	2022
35740506	Genome-Wide Meta-Analysis Identifies Variants in <i>DSCAM</i> and <i>PDLIM3</i> That Correlate with Efficacy Outcomes in Metastatic Renal Cell Carcinoma Patients Treated with Sunitinib.	Cancers (Basel)	2022
35420638	Expansion of Cancer Risk Profile for BRCA1 and BRCA2 Pathogenic Variants.	JAMA Oncol	2022
35666837	Associations of Genome-Wide Polygenic Risk Score and Risk Factors With Hypertension in a Japanese Population.	Circulation. Genomic and precision medicine	2022
35533259	Genome-wide association study of platelet factor 4/heparin antibodies in heparin-induced thrombocytopenia.	Blood Adv	2022
33612706	Assessing the Relationship Between High-sensitivity C-reactive Protein and Kidney Function Employing Mendelian Randomization in the Japanese Community-based J-MICC Study.	Journal of Epidemiology	2022
33309985	Population-based Screening for Hereditary Colorectal Cancer Variants in Japan.	Clin Gastroenterol Hepatol	2022
35248088	Whole exome analysis of patients in Japan with hearing loss reveals high heterogeneity among responsible and novel candidate genes.	Orphanet Journal of Rare Diseases	2022
35195259	A polygenic risk score improves risk stratification of coronary artery disease: a large-scale prospective Chinese cohort study.	Eur Heart J	2022
35190513	Accuracy and applications of sequencing and genotyping approaches for CYP2A6 and homologous genes.	Pharmacogenet Genomics	2022
35132194	A genome-wide association study on adherence to low-carbohydrate diets in Japanese.	European Journal of Clinical Nutrition	2022
34476898	Functional characterization of novel rare CYP2A6 variants and potential implications for clinical outcomes.	Clinical and Translational Science	2022
34593835	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	2021
31839644	Impact of PSCA Polymorphisms on the Risk of Duodenal Ulcer.	Journal of Epidemiology	2021
32147644	Differential Effect of Polymorphisms on Body Mass Index Across the Life Course of Japanese: The Japan Multi-Institutional Collaborative Cohort Study.	Journal of Epidemiology	2021
33913524	Genome-wide association study of epilepsy in a Japanese population identified an associated region at chromosome 12q24.	Epilepsia	2021
34239136	Combined landscape of single-nucleotide variants and copy number alterations in clonal hematopoiesis.	Nat Med	2021
33632354	A genome-wide association study on confection consumption in a Japanese population: the Japan Multi-Institutional Collaborative Cohort Study.	British Journal of Nutrition	2021
33739539	Incorporating European GWAS findings improve polygenic risk prediction accuracy of breast cancer among East Asians.	Genetic Epidemiology	2021
33629268	Regional differences in genes and variants causing retinitis pigmentosa in Japan.	Japanese Journal of Ophthalmology	2021
33627673	Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries.	Nat Commun	2021
33624935	Whole genome sequencing of 45 Japanese patients with intellectual disability.	American Journal of Medical Genetics, Part A	2021
34159637	Polygenic Risk Score of Adolescent Idiopathic Scoliosis for Potential Clinical Use.	Journal of Bone and Mineral Research	2021
34002096	Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology.	Nat Genet	2021
33727749	Genome-wide association study of serum prostate-specific antigen levels based on 1000 Genomes imputed data in Japanese: the Japan Multi-Institutional Collaborative Cohort Study.	Nagoya Journal of Medical Science	2021
34198553	Comprehensive Analysis of Risk Factors for Periodontitis Focusing on the Saliva Microbiome and Polymorphism.	International Journal of Environmental Research and Public Health	2021
33555323	Transethnic analysis of the human leukocyte antigen region for ulcerative colitis reveals not only shared but also ethnicity-specific disease associations.	Hum Mol Genet	2021
33650309	Relationship of hemoglobin level and plasma coproporphyrin-I concentrations as an endogenous probe for phenotyping OATP1B.	Clinical and Translational Science	2021
33300144	Transferability of Ancestry-Specific and Cross-Ancestry CYP2A6 Activity Genetic Risk Scores in African and European Populations.	Clin Pharmacol Ther	2021
32958699	Genomic Analysis of Germline Variation Associated with Survival of Patients with Colorectal Cancer Treated with Chemotherapy Plus Biologics in CALGB/SWOG 80405 (Alliance).	Clin Cancer Res	2021