A. Meguro

发表

A Scoring System to Evaluate the Impact of SNPs in a Path Related Context to Study Behçet’s Disease Aetiology in Japanese Population

O. Ozisik, A. Meguro, N. Mizuki, 2018, bioRxiv.

Association of Toll-like receptor 4 gene polymorphisms with normal tension glaucoma.

H. Inoko, T. Nishida, T. Kanamoto, 2008, Investigative ophthalmology & visual science.

Association study of genetic variants on chromosome 7q31 with susceptibility to normal tension glaucoma in a Japanese population

H. Inoko, M. Nakamura, T. Nishida, 2013, Eye.

Analysis of microsatellite polymorphisms within the GLC1F locus in Japanese patients with normal tension glaucoma

H. Inoko, T. Nishida, T. Kanamoto, 2010, Molecular vision.

Association of the toll-like receptor 4 gene polymorphisms with Behçet’s disease

S. Ohno, A. Meguro, N. Mizuki, 2007, Annals of the rheumatic diseases.

Identification of possible pathogenic pathways in Behçet’s disease using genome-wide association study data from two different populations

E. Remmers, D. Kastner, A. Meguro, 2014, European Journal of Human Genetics.

Investigation of the Association of TLR2 and TLR4 Polymorphisms with Susceptibility to Helicobacter pylori-Related Gastrointestinal Diseases

H. Inoko, H. Yuhara, A. Meguro, 2014 .

A single nucleotide polymorphism analysis of the LAMA1 gene in Japanese patients with high myopia

H. Inoko, S. Ohno, A. Meguro, 2007, Clinical ophthalmology.

Association of Major Histocompatibility Complex Class I Chain-Related Gene A and HLA-B Alleles with Behçet's Disease in Turkey

I. Tohnai, S. Ohno, A. Meguro, 2007, Japanese Journal of Ophthalmology.

Genome-wide association study identifies GIMAP as a novel susceptibility locus for Behçet's disease

E. Lee, E. Lee, Yeong-Wook Song, 2012, Annals of the rheumatic diseases.

KIR and HLA Genotypes Implicated in Reduced Killer Lymphocytes Immunity Are Associated with Vogt-Koyanagi-Harada Disease

S. Ohno, A. Meguro, N. Mizuki, 2016, PloS one.

Investigation of the association between the GLC3A locus and normal tension glaucoma in Japanese patients by microsatellite analysis

H. Inoko, M. Nakamura, T. Nishida, 2009, Clinical ophthalmology.

Genome-wide association meta-analysis of corneal curvature identifies novel loci and shared genetic influences across axial length and refractive error

Milly S. Tedja, David M. Evans, C. Sudlow, 2020, Communications Biology.

Clinical manifestations of Behçet’s disease depending on sex and age: results from Japanese nationwide registration

N. Horita, A. Meguro, N. Mizuki, 2017, Rheumatology.

Meta-analysis of gene–environment-wide association scans accounting for education level identifies additional loci for refractive error

Milly S. Tedja, Claire L. Simpson, David M. Evans, 2016, Nature Communications.

New susceptibility locus for high myopia is linked to the uromodulin-like 1 (UMODL1) gene region on chromosome 21q22.3

H. Inoko, S. Ohno, A. Meguro, 2009, Eye.

Association analysis of Toll-like receptor 7 gene polymorphisms and Behçet's disease in Japanese patients.

H. Inoko, S. Ohno, A. Meguro, 2011, Human immunology.

Association of TLR4 polymorphisms with Behcet's disease in a Korean population.

H. Inoko, E. Lee, Yeong-Wook Song, 2009, Rheumatology.

Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error.

Thomas Meitinger, Toomas Haller, Andres Metspalu, 2013, American journal of human genetics.

Impact of Perioperative Dry Eye Treatment with Rebamipide Versus Artificial Tears on Visual Outcomes After Cataract Surgery in Japanese Population

A. Meguro, N. Mizuki, Takeshi Teshigawara, 2022, Ophthalmology and Therapy.

Genetic determinants and an epistasis of LILRA3 and HLA-B*52 in Takayasu arteritis

Y. Okada, T. Kawaguchi, I. Komuro, 2018, Proceedings of the National Academy of Sciences.

Correction: Investigation of Susceptibility Genes Triggering Lachrymal/Salivary Gland Lesion Complications in Japanese Patients with Type 1 Autoimmune Pancreatitis

A. Meguro, S. Kawa, M. Ota, 2015, PloS one.

Genetic control of CCL24, POR, and IL23R contributes to the pathogenesis of sarcoidosis

N. Horita, H. Inoko, E. Remmers, 2020, Communications Biology.

Effects of Rebamipide on Differences in Power and Axis of Corneal Astigmatism Between Two Intra-patient Keratometric Measurements in Dry Eyes

A. Meguro, N. Mizuki, Takeshi Teshigawara, 2021, Ophthalmology and Therapy.

A Comparison Between Monofocal and Multifocal Intraocular Lenses in the Influence of Pupil Dilation on Target Postoperative Refraction

A. Meguro, N. Mizuki, Takeshi Teshigawara, 2020, Asia-Pacific journal of ophthalmology.

Investigation of the Association Between Toll-like Receptor 9 Gene Polymorphisms and Sarcoidosis in Japanese Patients

H. Inoko, S. Ohno, A. Meguro, 2013, Ocular immunology and inflammation.

Confirmation of TBK1 duplication in normal tension glaucoma.

R. Ritch, A. Robin, A. Meguro, 2012, Experimental eye research.

Common Variants in the COL4A4 Gene Confer Susceptibility to Lattice Degeneration of the Retina

H. Ideta, H. Inoko, A. Meguro, 2012, PloS one.

Dogs and Humans Share a Common Susceptibility Gene SRBD1 for Glaucoma Risk

A. Meguro, N. Mizuki, M. Sakaguchi, 2013, PloS one.

Interleukin 1 beta promoter polymorphism is associated with keratoconus in a Japanese population

T. Nishida, A. Meguro, N. Mizuki, 2013, Molecular vision.

HLA-B51 Carriers are Susceptible to Ocular Symptoms of Behçet Disease and the Association between the Two Becomes Stronger towards the East along the Silk Road: A Literature Survey

H. Inoko, E. Lee, S. Ohno, 2017, Ocular immunology and inflammation.

Four-digit allele genotyping of the HLA-A and HLA-B genes in Japanese patients with Behcet's disease by a PCR-SSOP-Luminex method.

H. Inoko, S. Ohno, J. Kulski, 2006, Tissue antigens.

On the genetics of the Silk Route: association analysis of HLA, IL10, and IL23R-IL12RB2 regions with Behçet’s disease in an Iranian population

H. Inoko, F. Shahram, A. Meguro, 2015, Immunogenetics.

Genome-wide association studies identify IL23R-IL12RB2 and IL10 as Behçet's disease susceptibility loci

H. Inoko, M. Mochizuki, Yeong-Wook Song, 2010, Nature Genetics.

Variants in IL23R-C1orf141 and ADO-ZNF365-EGR2 are associated with susceptibility to Vogt-Koyanagi-Harada disease in Japanese population

N. Horita, S. Ohno, A. Meguro, 2020, PloS one.

Investigation of Association between TLR9 Gene Polymorphisms and VKH in Japanese Patients

H. Inoko, S. Ohno, A. Meguro, 2011, Ocular immunology and inflammation.

Tuberculosis Exposure With Risk of Behçet Disease Among Patients With Uveitis.

X. Zuo, S. Ohno, A. Meguro, 2021, JAMA ophthalmology.

Dense genotyping of immune-related loci implicates host responses to microbial exposure in Behçet’s disease susceptibility

Akira Meguro, Massimo Gadina, Nobuhisa Mizuki, 2017, Nature Genetics.

Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B*51 and ERAP1

Akira Meguro, Nobuhisa Mizuki, Hidetoshi Inoko, 2013, Nature Genetics.

A Major Review: Current Aspects of Ocular Behçet's Disease in Japan

S. Ohno, A. Meguro, N. Mizuki, 2015, Ocular immunology and inflammation.

Alpha-Arbutin Promotes Wound Healing by Lowering ROS and Upregulating Insulin/IGF-1 Pathway in Human Dermal Fibroblast

Natalia Polouliakh, A. Meguro, N. Mizuki, 2020, Frontiers in Physiology.

Genetics of Behçet disease inside and outside the MHC

H. Inoko, S. Ohno, A. Meguro, 2009, Annals of the rheumatic diseases.

Toll-like receptor 2 (TLR2) gene polymorphisms are not associated with sarcoidosis in the Japanese population

H. Inoko, S. Ohno, A. Meguro, 2011, Molecular vision.

Genetic characterization and susceptibility for sarcoidosis in Japanese patients: risk factors of BTNL2 gene polymorphisms and HLA class II alleles.

H. Inoko, S. Ohno, A. Meguro, 2012, Investigative ophthalmology & visual science.

The ocular involvement did not accompany with the genital ulcer or the gastrointestinal symptoms at the early stage of Behçet’s disease

T. Fukumoto, N. Horita, A. Meguro, 2019, Modern rheumatology.

Targeted resequencing implicates the familial Mediterranean fever gene MEFV and the toll-like receptor 4 gene TLR4 in Behçet disease

Alexander F. Wilson, A. F. Wilson, J. Mullikin, 2013, Proceedings of the National Academy of Sciences.

Association of toll-like receptor 2 gene polymorphisms with normal tension glaucoma

H. Inoko, T. Nishida, T. Kanamoto, 2009, Molecular vision.

Association study of fibroblast growth factor 10 (FGF10) polymorphisms with susceptibility to extreme myopia in a Japanese population

A. Meguro, N. Mizuki, N. Nomura, 2013, Molecular vision.

Behçet’s Syndrome According to Classical and Population Genetics

S. Ohno, A. Meguro, N. Mizuki, 2014 .

Genome-wide association study of normal tension glaucoma: common variants in SRBD1 and ELOVL5 contribute to disease susceptibility.

H. Inoko, A. Meguro, N. Mizuki, 2010, Ophthalmology.

Association Study of ARMC9 Gene Variants with Vogt-Koyanagi-Harada Disease in Japanese Patients

S. Ohno, A. Meguro, N. Mizuki, 2018, Ocular immunology and inflammation.

Keratoconus-susceptibility gene identification by corneal thickness genome-wide association study and artificial intelligence IBM Watson

T. Kawaguchi, S. Saw, Ching-Yu Cheng, 2020, Communications Biology.

Childhood gene-environment interactions and age-dependent effects of genetic variants associated with refractive error and myopia: The CREAM Consortium

Claire L. Simpson, David M. Evans, C. Gieger, 2016, Scientific Reports.

A comprehensive overview on the genetics of Behçet's disease

F. Shahram, A. Meguro, N. Mizuki, 2020, International reviews of immunology.

O 02-P 039 A comparative study about ERAP 1 polymorphisms in Behçet syndrome and ankylosing spondylitis Italian patients

N. Horita, A. Meguro, N. Mizuki, 2018 .

The association analysis between HLA-A*26 and Behçet’s disease

A. Meguro, N. Mizuki, T. Mihara, 2019, Scientific Reports.

TRIM39 and RNF39 are associated with Behçet's disease independently of HLA-B∗51 and -A∗26.

H. Inoko, T. Shiina, I. Inoue, 2010, Biochemical and Biophysical Research Communications - BBRC.

Comprehensive analysis of the association between UBAC2 polymorphisms and Behçet’s disease in a Japanese population

S. Ohno, A. Meguro, N. Mizuki, 2017, Scientific Reports.

Correction: Investigation of Susceptibility Genes Triggering Lachrymal/Salivary Gland Lesion Complications in Japanese Patients with Type 1 Autoimmune Pancreatitis

A. Meguro, S. Kawa, M. Ota, 2015, PloS one.

Replication Study of the Association of GAS6 and PROS1 Polymorphisms with Behçet's Disease in a Japanese Population.

S. Ohno, A. Meguro, N. Mizuki, 2023, Ocular immunology and inflammation.

Investigation of the association between Toll-like receptor 2 gene polymorphisms and Behçet's disease in Japanese patients.

H. Inoko, S. Ohno, A. Meguro, 2009, Human immunology.

Replication of a microsatellite genome-wide association study of Behcet's disease in a Korean population.

H. Inoko, E. Lee, S. Ohno, 2012, Rheumatology.

Interleukin‐17A gene polymorphism with the susceptibility of intestinal symptoms in patients with Behçet's disease

Koichiro Nakamura, A. Meguro, N. Mizuki, 2016, The Journal of dermatology.

Ocular Behçet's disease is less complicated with allergic disorders. A nationwide survey in Japan.

M. Mochizuki, S. Ohno, A. Meguro, 2016, Clinical and experimental rheumatology.

Genetic Variants on Chromosome 1q41 Influence Ocular Axial Length and High Myopia

Xiaoping Zhou, Y. Teo, T. Wong, 2012, PLoS genetics.

Chum salmon egg extracts induce upregulation of collagen type I and exert antioxidative effects on human dermal fibroblast cultures

Natalia Polouliakh, A. Meguro, N. Mizuki, 2016, Clinical interventions in aging.

Trabeculotomy ab interno with internal limiting membrane forceps for open-angle glaucoma

A. Meguro, N. Mizuki, R. Uemoto, 2014, Graefe's Archive for Clinical and Experimental Ophthalmology.

Investigation of the association between SLC1A3 gene polymorphisms and normal tension glaucoma

H. Inoko, T. Nishida, T. Kanamoto, 2011, Molecular vision.

Genome-wide association analyses identify two susceptibility loci for pachychoroid disease central serous chorioretinopathy

T. Wong, C. Khor, R. Yamada, 2019, Communications Biology.

Genome-wide association study in Asians identifies novel loci for high myopia and highlights a nervous system role in its pathogenesis.

H. Inoko, S. Saw, Ching-Yu Cheng, 2020, Ophthalmology.

Keratoconus-susceptibility gene identification by corneal thickness genome-wide association study and artificial intelligence IBM Watson

T. Kawaguchi, C. Khor, F. Matsuda, 2020, Communications Biology.

Edinburgh Research Explorer Identification of myopia-associated WNT7B polymorphisms provides insights into the mechanism underlying the development of myopia

A. Sekine, T. Wong, E. Tai, 2022 .

The advantages of femtosecond laser-assisted cataract surgery for zonulopathy

A. Meguro, N. Mizuki, S. Hata, 2019, International medical case reports journal.

Common variants in the COL2A1 gene are associated with lattice degeneration of the retina in a Japanese population

H. Ideta, A. Meguro, N. Mizuki, 2019, Molecular vision.

Genotyping HLA-DRB1 and HLA-DQB1 alleles in Japanese patients with normal tension glaucoma

H. Inoko, T. Nishida, T. Kanamoto, 2010, Molecular vision.

Association of microsatellite polymorphisms of the GPDS1 locus with normal tension glaucoma in the Japanese population

H. Inoko, T. Nishida, T. Kanamoto, 2009, Clinical ophthalmology.

Rare variant analyses across multiethnic cohorts identify novel genes for refractive error

Adriana I. Iglesias, T. Lehtimäki, J. Jonas, 2021, Communications Biology.

Longitudinal analysis of 5-year refractive changes in a large Japanese population

A. Meguro, N. Mizuki, E. Okada, 2022, Scientific Reports.

ERAP1 polymorphisms interactions and their association with Behçet’s disease susceptibly: Application of Model-Based Multifactor Dimension Reduction Algorithm (MB-MDR)

F. Shahram, A. Kazemnejad, A. Meguro, 2020, PloS one.

Genome-wide association analyses identify two susceptibility loci for pachychoroid disease central serous chorioretinopathy

T. Wong, C. Khor, R. Yamada, 2019, Communications Biology.

Lack of association between IL10 polymorphisms and sarcoidosis in Japanese patients

H. Inoko, S. Ohno, A. Meguro, 2012, Molecular vision.

HLA-A26 is a risk factor for Behçet’s disease ocular lesions

T. Fukumoto, N. Horita, A. Meguro, 2019, Modern rheumatology.

A new polygenic score for refractive error improves detection of children at risk of high myopia but not the prediction of those at risk of myopic macular degeneration

Jonathan H. Morgan, Adriana I. Iglesias, Kristina L. H. Lee, 2023, EBioMedicine.

Associations between CRYBA4 gene variants and high myopia in a Japanese population

A. Meguro, N. Mizuki, M. Ota, 2017, Clinical ophthalmology.

Association study of IGF1 polymorphisms with susceptibility to high myopia in a Japanese population

A. Meguro, N. Mizuki, N. Nomura, 2013, Clinical ophthalmology.

A polymorphism in CCR1/CCR3 is associated with narcolepsy

K. Hirata, E. Remmers, A. Koike, 2015, Brain, Behavior, and Immunity.

A polymorphism in CCR 1 / CCR

K. Hirata, E. Remmers, A. Koike, 2015 .

Genetic analysis of the aquaporin-4 gene for anti-AQP4 antibody-positive neuromyelitis optica in a Japanese population

K. Fujihara, A. Meguro, N. Mizuki, 2016, Japanese Journal of Ophthalmology.

Clinical features of early-stage possible Behçet’s disease patients with a variant-type major organ involvement in Japan

T. Fukumoto, N. Horita, A. Meguro, 2018, Modern rheumatology.

Epistatic Interaction of ERAP1 and HLA-B*51 in Iranian Patients with Behçet’s Disease

F. Shahram, A. Meguro, N. Mizuki, 2018, Scientific Reports.

Study of association of PAX6 polymorphisms with susceptibility to high myopia in a Japanese population

A. Meguro, N. Mizuki, E. Okada, 2015, Clinical ophthalmology.

Clinical Ophthalmology Dovepress Dovepress Analysis of the Association between the Lum Rs3759223 Variant and High Myopia in a Japanese Population

A. Meguro, N. Mizuki, E. Okada, 2022 .

Comparison of tendency and accuracy in predicted post-operative refraction and recommended IOL power between IOL Master and VERION before and after optimizing IOL-constant in the VERION

A. Meguro, N. Mizuki, Takeshi Teshigawara, 2020 .

Visual performance of the intraindividual implantation of a trifocal intraocular lens in the bag and a +4.0 D bifocal intraocular lens in the sulcus with optic capture created by femtosecond laser-assisted cataract surgery

A. Meguro, N. Mizuki, Kazuro Yabuki, 2018, International medical case reports journal.

Lack of association between toll-like receptor 4 gene polymorphisms and sarcoidosis-related uveitis in Japan

H. Inoko, S. Ohno, A. Meguro, 2009, Molecular vision.

On the genetics of the Silk Route: association analysis of HLA, IL10, and IL23R-IL12RB2 regions with Behçet’s disease in an Iranian population

H. Inoko, F. Shahram, A. Meguro, 2015, Immunogenetics.

Comprehensive analysis of the association between UBAC2 polymorphisms and Behçet’s disease in a Japanese population

S. Ohno, A. Meguro, N. Mizuki, 2017, Scientific Reports.

The Effect of Age, Postoperative Refraction, and Pre- and Postoperative Pupil Size on Halo Size and Intensity in Eyes Implanted with a Trifocal or Extended Depth-of-Focus Lens

A. Meguro, N. Mizuki, Takeshi Teshigawara, 2021, Clinical ophthalmology.

Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error

Jonathan H. Morgan, M. P. Concas, Adriana I. Iglesias, 2018, Nature Genetics.

Evaluation of Shared Genetic Susceptibility to High and Low Myopia and Hyperopia.

Jonathan H. Morgan, Adriana I. Iglesias, Kristina L. H. Lee, 2021, JAMA ophthalmology.

Genome-wide association meta-analysis of corneal curvature identifies novel loci and shared genetic influences across axial length and refractive error

Jonathan H. Morgan, Adriana I. Iglesias, C. Sudlow, 2020, Communications Biology.

Interleukin 1 receptor type 1 gene variants associate with disease susceptibility to IgG4-related periaortitis/periarteritis in IgG4-related disease

A. Meguro, S. Kawa, M. Ota, 2020 .

Lack of association with high myopia and the MYP2 locus in the Japanese population by high resolution microsatellite analysis on chromosome 18

H. Inoko, S. Ohno, J. Kulski, 2007, Clinical ophthalmology.

Identification of myopia-associated WNT7B polymorphisms provides insights into the mechanism underlying the development of myopia

D. Mackey, C. Hayward, V. Vitart, 2022 .

Behçet's disease and activities of daily living.

T. Fukumoto, N. Horita, A. Meguro, 2021, Rheumatology.

Identification of Novel Risk Loci for Behçet's Disease–Related Uveitis in a Chinese Population in a Genome‐Wide Association Study

X. Zuo, S. Ohno, A. Meguro, 2022 .

The association analysis between HLA-A*26 and Behçet’s disease

A. Meguro, N. Mizuki, T. Mihara, 2019, Scientific Reports.

IL1R1 gene variants associate with disease susceptibility to IgG4-related periaortitis/periarteritis in IgG4-related disease.

A. Meguro, S. Kawa, M. Ota, 2022, Gene.

[Four-digit allele genotyping of HLA-A and HLA-B genes in Japanese patients with Behçet's disease (BD) by a PCR-SSOP-luminex method and stratification analysis according to each major symptom of BD].

H. Inoko, S. Ohno, A. Meguro, 2008, Nippon Ganka Gakkai zasshi.

study of association of PAX6 polymorphisms with susceptibility to high myopia in a Japanese population

A. Meguro, N. Mizuki, E. Okada, 2015 .

SLC1A1 Gene Variants and Normal Tension Glaucoma: An Association Study

H. Inoko, T. Nishida, T. Kanamoto, 2016, Ophthalmic genetics.

Staining internal limiting membrane with a mixture of BBG and sodium hyaluronate

A. Meguro, N. Mizuki, R. Uemoto, 2012, British Journal of Ophthalmology.

Reply to Stoimenis et al

E. Remmers, D. Kastner, A. Meguro, 2015, European Journal of Human Genetics.

Investigation of Susceptibility Genes Triggering Lachrymal/Salivary Gland Lesion Complications in Japanese Patients with Type 1 Autoimmune Pancreatitis

A. Meguro, S. Kawa, M. Ota, 2015, PloS one.

Association of PDGFRA polymorphisms with the risk of corneal astigmatism in a Japanese population

A. Meguro, N. Mizuki, M. Takeuchi, 2023, Scientific reports.

Epistatic Interaction of ERAP1 and HLA-B*51 in Iranian Patients with Behçet’s Disease

F. Shahram, A. Meguro, N. Mizuki, 2018, Scientific Reports.

Association Study of ARMC9 Gene Variants with Vogt-Koyanagi-Harada Disease in Japanese Patients

S. Ohno, A. Meguro, N. Mizuki, 2018, Ocular immunology and inflammation.

Genome-wide association study of normal tension glaucoma: common variants in SRBD1 and ELOVL5 contribute to disease susceptibility.

H. Inoko, A. Meguro, N. Mizuki, 2010, Ophthalmology.

HLA-B51 Carriers are Susceptible to Ocular Symptoms of Behçet Disease and the Association between the Two Becomes Stronger towards the East along the Silk Road: A Literature Survey

H. Inoko, E. Lee, S. Ohno, 2017, Ocular immunology and inflammation.

A polymorphism in CCR1/CCR3 is associated with narcolepsy

K. Hirata, E. Remmers, A. Koike, 2015, Brain, Behavior, and Immunity.

Rare variant analyses across multiethnic cohorts identify novel genes for refractive error

Adriana I. Iglesias, Claire L. Simpson, T. Lehtimäki, 2023, Communications Biology.

Multiple linear regression model for improving accuracy of capsulorhexis size calculation in femtosecond laser-assisted cataract surgery for adults: a retrospective single-center study

A. Meguro, N. Mizuki, S. Hata, 2023, BMC Ophthalmology.

Modified Technique of Setting Capsulotomy Thickness in Reducing Capsulotomy-Related Complications During Femtosecond Laser-Assisted Cataract Surgery: A Prospective, Comparative Cohort Study

A. Meguro, N. Mizuki, S. Hata, 2023, Ophthalmology and Therapy.

Relationship Between Postoperative Intraocular Lens Shift and Postoperative Refraction Change in Cataract Surgery Using Three Different Types of Intraocular Lenses

A. Meguro, N. Mizuki, Takeshi Teshigawara, 2021, Ophthalmology and Therapy.

Suction Break During Femtosecond Laser-Assisted Cataract Surgery and Misplaced Laser Beam Delivery to the Corneal Layers

A. Meguro, N. Mizuki, Takeshi Teshigawara, 2020, International medical case reports journal.

The Effect of Rebamipide on Refractive Accuracy of Cataract Surgery in Patients with Dry Eye

A. Meguro, N. Mizuki, Takeshi Teshigawara, 2022, Ophthalmology and Therapy.

SLC1A1 Gene Variants and Normal Tension Glaucoma: An Association Study

H. Inoko, T. Nishida, T. Kanamoto, 2016, Ophthalmic genetics.

IL1B promoter polymorphisms are associated with keratoconus in a Japanese population

A. Meguro, N. Mizuki, K. Fukagawa, 2013 .

Usefulness of Combined Measurement of Serum Soluble IL-2R and Angiotensin-Converting Enzyme in the Detection of Uveitis Associated with Japanese Sarcoidosis

A. Meguro, N. Mizuki, E. Shibuya, 2020, Clinical ophthalmology.

Clinical Ophthalmology Dovepress Dovepress Association Study of Igf1 Polymorphisms with Susceptibility to High Myopia in a Japanese Population

A. Meguro, N. Mizuki, N. Nomura, 2022 .

Investigation of the association between Toll-like receptor 2 gene polymorphisms and Behçet's disease in Japanese patients.

H. Inoko, S. Ohno, A. Meguro, 2009, Human immunology.

Effect of Long-Acting Diquafosol Sodium on Astigmatism Measurement Repeatability in Preoperative Cataract Cases with Dry Eyes: A Multicenter Prospective Study

A. Meguro, N. Mizuki, M. Takeuchi, 2024, Ophthalmology and therapy.

Genome-wide association analysis reveals the associations of NPHP4, TYW1-AUTS2 and SEMA6D for Behçet's disease and HLA-B*46:01 for its intestinal involvement.

D. Ellinghaus, F. Degenhardt, A. Meguro, 2023, Digestive and Liver Disease.