Author details

Full Name

Yoichiro Kamatani

Affiliation

ORCID

Career Start Year

2004

Papers

258

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
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
36138222	Genetic footprints of assortative mating in the Japanese population.	Nat Hum Behav	2023
37986915	Genetically proxied HTRA1 protease activity and circulating levels independently predict risk of ischemic stroke and coronary artery disease.		2023
37945903	Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants.	Nat Genet	2023
37903058	A large-scale microRNA transcriptome-wide association study identifies two susceptibility microRNAs, miR-1307-5p and miR-192-3p, for colorectal cancer risk.		2023
37723263	Boosting the power of genome-wide association studies within and across ancestries by using polygenic scores.	Nat Genet	2023
37638535	Genetic risk score of cerebral infarction in atrial fibrillation genome-wide association study.		2023
37612283	Androgen receptor binding sites enabling genetic prediction of mortality due to prostate cancer in cancer-free subjects.	Nat Commun	2023
37543666	Hyperfructosemia in sleep disordered breathing: metabolome analysis of Nagahama study.		2023
37503126	Understanding the genetic complexity of puberty timing across the allele frequency spectrum.	medRxiv	2023
37415668	Evidence of causality of low body mass index on risk of adolescent idiopathic scoliosis: a Mendelian randomization study.		2023
37388916	Detection of trait-associated structural variations using short-read sequencing.		2023
37315111	Increased PDGFRB and NF-ÎºB signaling caused by highly prevalent somatic mutations in intracranial aneurysms.	Sci Transl Med	2023
37309008	Improved genetic prediction of the risk of knee osteoarthritis using the risk factor-based polygenic score.	Arthritis Res Ther	2023
37236969	Genome-wide association study of lung adenocarcinoma in East Asia and comparison with a European population.	Nat Commun	2023
37169872	Mobile element variation contributes to population-specific genome diversification, gene regulation and disease risk.	Nat Genet	2023
37151119	Genome-wide Association Studies Categorized by Class of Antihypertensive Drugs Reveal Complex Pathogenesis of Hypertension with Drug Resistance.		2023
36988593	<i>Helicobacter pylori</i>, Homologous-Recombination Genes, and Gastric Cancer.	N Engl J Med	2023
36655558	Genetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical Heterogeneity.		2023
36576811	Predictive Utility of a Coronary Artery Disease Polygenic Risk Score in Primary Prevention.	JAMA Cardiol	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
36411359	Prediction of the cell-type-specific transcription of non-coding RNAs from genome sequences via machine learning.	Nat Biomed Eng	2023
36322930	Germ line DDX41 mutations define a unique subtype of myeloid neoplasms.	Blood	2023
36240095	Contribution of Common Genetic Variants to Risk of Early-Onset Ischemic Stroke.	Neurology	2022
36093724	Prevalence and risk estimation of cancer-predisposing genes for upper urinary tract urothelial carcinoma in Japanese.	Jpn J Clin Oncol	2022
36065483	Association between germline pathogenic variants in cancer-predisposing genes and lymphoma risk.	Cancer Sci	2022
35915156	Large-scale genome-wide association study of coronary artery disease in genetically diverse populations.	Nat Med	2022
35841947	Genetic Architectures Underlie Onset Age of Atopic Dermatitis.		2022
35764097	Different risk genes contribute to clear cell and non-clear cell renal cell carcinoma in 1532 Japanese patients and 5996 controls.	Hum Mol Genet	2022
35753705	Multi-trait and cross-population genome-wide association studies across autoimmune and allergic diseases identify shared and distinct genetic component.	Ann Rheum Dis	2022
35697829	Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals.	Commun Biol	2022
33309985	Population-based Screening for Hereditary Colorectal Cancer Variants in Japan.	Clin Gastroenterol Hepatol	2022
35637176	Author Correction: Genetic variants of calcium and vitamin D metabolism in kidney stone disease.	Nature Communications	2022
35590097	SARS-CoV-2 ORF6 disrupts nucleocytoplasmic trafficking to advance viral replication.	Communications Biology	2022
35551307	Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation.	Nat Genet	2022
35495141	Editorial: Current Status and Future Challenges of Biobank Data Analysis.	Frontiers in Genetics	2022
35420638	Expansion of Cancer Risk Profile for BRCA1 and BRCA2 Pathogenic Variants.	JAMA Oncol	2022
35396580	Mapping genomic loci implicates genes and synaptic biology in schizophrenia.	Nature	2022
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
35266989	Large-scale Integrated Analysis of Genetics and Metabolomic Data Reveals Potential Links Between Lipids and Colorectal Cancer Risk.	Cancer Epidemiol Biomarkers Prev	2022
35260632	Efficient prediction of a spatial transcriptomics profile better characterizes breast cancer tissue sections without costly experimentation.	Scientific Reports	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
34999880	Trans-ethnic Mendelian-randomization study reveals causal relationships between cardiometabolic factors and chronic kidney disease.	Int J Epidemiol	2022
37118362	Mendelian randomization of genetically independent aging phenotypes identifies LPA and VCAM1 as biological targets for human aging.	Nat Aging	2022
36777335	Decoding the diversity of killer immunoglobulin-like receptors by deep sequencing and a high-resolution imputation method.	Cell Genom	2022
36582826	Genetic influences on human blood metabolites in the Japanese population.	iScience	2022
36477530	Genetic diversity fuels gene discovery for tobacco and alcohol use.	Nature	2022
36344522	Discerning asthma endotypes through comorbidity mapping.	Nat Commun	2022
36333501	Multi-ancestry genome-wide association analyses identify novel genetic mechanisms in rheumatoid arthritis.	Nat Genet	2022