Author details

Full Name

Masato Akiyama

Affiliation

ORCID

Career Start Year

2008

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
36423732	Genome-Wide Association Study of Age-Related Macular Degeneration Reveals 2 New Loci Implying Shared Genetic Components with Central Serous Chorioretinopathy.	Ophthalmology	2023
37629406	Differences in Central and Peripheral Choroidal Thickness among the Subtypes of Age-Related Macular Degeneration in an Asian Population.		2023
37386247	Large-scale multitrait genome-wide association analyses identify hundreds of glaucoma risk loci.	Nat Genet	2023
37310312	Mapping the genetic architecture of suicide attempt and suicide death using polygenic risk scores for clinically-related psychiatric disorders and traits.	Psychol Med	2023
36685570	Corrigendum: Intraocular human cytomegaloviruses of ocular diseases are distinct from those of viremia and are capable of escaping from innate and adaptive immunity by exploiting HLA-E-mediated peripheral and central tolerance.	Front Immunol	2023
36138192	Japan Ocular Imaging Registry: a national ophthalmology real-world database.	Japanese Journal of Ophthalmology	2022
35710107	Likely pathogenic structural variants in genetically unsolved patients with retinitis pigmentosa revealed by long-read sequencing.	J Med Genet	2022
35697829	Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals.	Commun Biol	2022
35551307	Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation.	Nat Genet	2022
35529318	Circulating inflammatory monocytes oppose microglia and contribute to cone cell death in retinitis pigmentosa.		2022
35103281	TNFRSF10A downregulation induces retinal pigment epithelium degeneration during the pathogenesis of age-related macular degeneration and central serous chorioretinopathy.	Human Molecular Genetics	2022
35038016	One-year efficacy of "rescue photodynamic therapy" for patients with typical age-related macular degeneration, polypoidal choroidal vasculopathy, and pachychoroid neovasculopathy refractory to anti-vascular endothelial growth factor therapy.	Graefe's Archive for Clinical and Experimental Ophthalmology	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
36812514	Regulatory-approved deep learning/machine learning-based medical devices in Japan as of 2020: A systematic review.		2022
34393209	RECURRENCE RATE OF CYSTOID MACULAR EDEMA WITH TOPICAL DORZOLAMIDE TREATMENT AND ITS RISK FACTORS IN RETINITIS PIGMENTOSA.	Retina	2022
34339662	Drainage Retinotomy Confers Risk of Epiretinal Membrane Formation After Vitrectomy for Rhegmatogenous Retinal Detachment Repair.	American Journal of Ophthalmology	2022
36477530	Genetic diversity fuels gene discovery for tobacco and alcohol use.	Nature	2022
36456827	Genetic variants associated with glaucomatous visual field loss in primary open-angle glaucoma.	Sci Rep	2022
36344522	Discerning asthma endotypes through comorbidity mapping.	Nat Commun	2022
34099852	Publisher Correction: Diabetic vascular hyperpermeability: optical coherence tomography angiography and functional loss assessments of relationships among retinal vasculature changes.	Scientific Reports	2021
33636399	Genotype and Long-term Clinical Course of Bietti Crystalline Dystrophy in Korean and Japanese Patients.	Ophthalmology Retina	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
33603034	Diabetic vascular hyperpermeability: optical coherence tomography angiography and functional loss assessments of relationships among retinal vasculature changes.	Scientific Reports	2021
33514863	A hypomorphic variant in EYS detected by genome-wide association study contributes toward retinitis pigmentosa.	Commun Biol	2021
33257802	Risk factors for myopia at 1-year corrected age following laser photocoagulation for retinopathy of prematurity.	Eye	2021
32948838	Multi-omics study for interpretation of genome-wide association study.	Journal of Human Genetics	2021
32924732	Cohort Profile: The <i>Ganka-Ekigaku</i> Network (GEN), a Network of Japanese Ophthalmological Epidemiology Studies.	Ophthalmic Epidemiol	2021
34594039	A cross-population atlas of genetic associations for 220 human phenotypes.	Nat Genet	2021
34314466	Drusen and pigment abnormality predict the development of neovascular age-related macular degeneration in Japanese patients.	PLoS ONE	2021
31488892	GWAS of five gynecologic diseases and cross-trait analysis in Japanese.	Eur J Hum Genet	2020
33112920	Changes in metamorphopsia after the treat-and-extend regimen of anti-VEGF therapy for macular edema associated with branch retinal vein occlusion.	PLoS ONE	2020
33020668	Population-specific and trans-ancestry genome-wide analyses identify distinct and shared genetic risk loci for coronary artery disease.	Nature Genetics	2020
32936303	Changes of Serum Inflammatory Molecules and Their Relationships with Visual Function in Retinitis Pigmentosa.	Investigative Ophthalmology and Visual Science	2020
32888494	The Polygenic and Monogenic Basis of Blood Traits and Diseases.	Cell	2020
32888493	Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.	Cell	2020
32749464	Relationship Between Macular Curvature and Common Causative Genes of Retinitis Pigmentosa in Japanese Patients.	Investigative Ophthalmology and Visual Science	2020
32581364	Chromosomal alterations among age-related haematopoietic clones in Japan.	Nature	2020
32533944	Evidence of Polygenic Adaptation in Sardinia at Height-Associated Loci Ascertained from the Biobank Japan.	Am J Hum Genet	2020
32514122	Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases.	Nat Genet	2020
32469254	Transethnic Meta-Analysis of Genome-Wide Association Studies Identifies Three New Loci and Characterizes Population-Specific Differences for Coronary Artery Disease.	Circ Genom Precis Med	2020
32383070	Mendelian randomization analysis does not support causal associations of birth weight with hypertension risk and blood pressure in adulthood.	Eur J Epidemiol	2020
32251405	Trans-biobank analysis with 676,000 individuals elucidates the association of polygenic risk scores of complex traits with human lifespan.	Nat Med	2020
32218440	Dimensionality reduction reveals fine-scale structure in the Japanese population with consequences for polygenic risk prediction.	Nat Commun	2020
32196539	Neurodevelopmental outcomes following intravitreal bevacizumab injection in Japanese preterm infants with type 1 retinopathy of prematurity.	PLoS ONE	2020
32193659	A founder Alu insertion in RP1 gene in Japanese patients with retinitis pigmentosa.	Japanese Journal of Ophthalmology	2020
32152314	Author Correction: Characterizing rare and low-frequency height-associated variants in the Japanese population.	Nat Commun	2020
32112665	Association of CRX genotypes and retinal phenotypes confounded by variable expressivity and electronegative electroretinogram.	Clinical and Experimental Ophthalmology	2020
31959922	GWAS of 165,084 Japanese individuals identified nine loci associated with dietary habits.	Nat Hum Behav	2020