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Epigenetic aberration of the human REELIN gene in psychiatric disorders

Molecular psychiatry, 2007-06, Vol.12 (6), p.593-600

2007

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The impact of natural selection on an ABCC11 SNP determining earwax type

Molecular biology and evolution, 2011-01, Vol.28 (1), p.849-857

2011

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Is rs34861192 or rs1862513 a more promising variant for determining plasma resistin in an aged Japanese population

Diabetologia, 2010-04, Vol.53 (4), p.795-797

2010

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Gene Flow and Natural Selection in Oceanic Human Populations Inferred from Genome-Wide SNP Typing

Molecular biology and evolution, 2008-08, Vol.25 (8), p.1750-1761

2008

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A genomic analysis of adult T-cell leukemia

Oncogene, 2007-02, Vol.26 (8), p.1245-1255

2007

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The power of genome-wide association studies of complex disease genes: statistical limitations of indirect approaches using SNP markers

Journal of human genetics, 2001-08, Vol.46 (8), p.478-482

2001

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A functional SNP upstream of the beta-2 adrenergic receptor gene (ADRB2) is associated with obesity in Oceanic populations

International Journal of Obesity, 2013-09, Vol.37 (9), p.1204-1210

2013

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The possible association between epigenetic aberration in DNA methylation in RELN and psychiatric disorders

Molecular psychiatry, 2007-06, Vol.12 (6), p.519-519

2007

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Association analysis of susceptibility candidate region on chromosome 5q31 for tuberculosis

Genes and immunity, 2010-07, Vol.11 (5), p.416-422

2010

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Genome-wide SNP-based linkage analysis of tuberculosis in Thais

Genes and immunity, 2009-01, Vol.10 (1), p.77-83

2009

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Absence of an association between the polymorphisms in the genes encoding adiponectin receptors and type 2 diabetes

Diabetologia, 2005-07, Vol.48 (7), p.1307-1314

2005

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Role of APRIL (TNFSF13) polymorphisms in the susceptibility to systemic lupus erythematosus in Japanese

Rheumatology (Oxford, England), 2007-05, Vol.46 (5), p.776-782

2007

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Comparison of statistical power between 2×2 allele frequency and allele positivity tables in case-control studies of complex disease genes

Annals of human genetics, 2001-03, Vol.65 (2), p.197-206, Article S000348000100851X

2001

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Significant Association Between TIM1 Promoter Polymorphisms and Protection Against Cerebral Malaria in Thailand

Annals of human genetics, 2008-05, Vol.72 (3), p.327-336

2008

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Association of Fc gamma receptor IIIB, but not of Fc gamma receptor IIA and IIIA polymorphisms with systemic lupus erythematosus in Japanese

Genes and immunity, 1999-09, Vol.1 (1), p.53-60

1999

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The expected power of genome‐wide linkage disequilibrium testing using single nucleotide polymorphism markers for detecting a low‐frequency disease variant

Annals of human genetics, 2002-07, Vol.66 (4), p.297-306

2002

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The expected power of genome-wide linkage disequilibrium testing using single nucleotide polymorphism markers for detecting a low-frequency disease variant

Annals of human genetics, 2002-07, Vol.66 (4), p.297-306

2002

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Application of the Stepwise Focusing Method to Optimize the Cost‐effectiveness of Genome‐wide Association Studies with Limited Research Budgets for Genotyping and Phenotyping

Annals of human genetics, 2005-05, Vol.69 (3), p.323-328

2005

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The Relation between Contact Lens Oxygen Transmissibility and Binding of Pseudomonas aeruginosa to the Cornea after Overnight Wear

Ophthalmology (Rochester, Minn.), 1994-02, Vol.101 (2), p.371-388

1994

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Rapid selection of sulphadoxine-resistant Plasmodium falciparum and its effect on within-population genetic diversity in Papua New Guinea

Scientific reports, 2018-04, Vol.8 (1), p.5565-12, Article 5565

2018

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Thanking and Politeness in Japanese: Balancing Acts in Interaction

Ohashi, J

1, 2013

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Little Polymorphism at the K13 Propeller Locus in Worldwide Plasmodium falciparum Populations Prior to the Introduction of Artemisinin Combination Therapies

Antimicrobial agents and chemotherapy, 2016-06, Vol.60 (6), p.3340-3347

2016

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Association of IL1B - 31C/T and IL1RA Variable Number of an 86-bp Tandem Repeat With Dengue Shock Syndrome in Thailand

The Journal of infectious diseases, 2014-07, Vol.210 (1), p.138-145

2014

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The G/G Genotype of a Resistin Single-Nucleotide Polymorphism at −420 Increases Type 2 Diabetes Mellitus Susceptibility by Inducing Promoter Activity through Specific Binding of Sp1/3

American journal of human genetics, 2004-10, Vol.75 (4), p.678-686

2004

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Epigenetic aberration of the human REELIN gene in psychiatric disorders

The impact of natural selection on an ABCC11 SNP determining earwax type

Is rs34861192 or rs1862513 a more promising variant for determining plasma resistin in an aged Japanese population

Gene Flow and Natural Selection in Oceanic Human Populations Inferred from Genome-Wide SNP Typing

A genomic analysis of adult T-cell leukemia

The power of genome-wide association studies of complex disease genes: statistical limitations of indirect approaches using SNP markers

A functional SNP upstream of the beta-2 adrenergic receptor gene (ADRB2) is associated with obesity in Oceanic populations

The possible association between epigenetic aberration in DNA methylation in RELN and psychiatric disorders

Association analysis of susceptibility candidate region on chromosome 5q31 for tuberculosis

Genome-wide SNP-based linkage analysis of tuberculosis in Thais

Absence of an association between the polymorphisms in the genes encoding adiponectin receptors and type 2 diabetes

Role of APRIL (TNFSF13) polymorphisms in the susceptibility to systemic lupus erythematosus in Japanese

Comparison of statistical power between 2×2 allele frequency and allele positivity tables in case-control studies of complex disease genes

Significant Association Between TIM1 Promoter Polymorphisms and Protection Against Cerebral Malaria in Thailand

Association of Fc gamma receptor IIIB, but not of Fc gamma receptor IIA and IIIA polymorphisms with systemic lupus erythematosus in Japanese

The expected power of genome‐wide linkage disequilibrium testing using single nucleotide polymorphism markers for detecting a low‐frequency disease variant

The expected power of genome-wide linkage disequilibrium testing using single nucleotide polymorphism markers for detecting a low-frequency disease variant

Application of the Stepwise Focusing Method to Optimize the Cost‐effectiveness of Genome‐wide Association Studies with Limited Research Budgets for Genotyping and Phenotyping

The Relation between Contact Lens Oxygen Transmissibility and Binding of Pseudomonas aeruginosa to the Cornea after Overnight Wear

Rapid selection of sulphadoxine-resistant Plasmodium falciparum and its effect on within-population genetic diversity in Papua New Guinea

Thanking and Politeness in Japanese: Balancing Acts in Interaction

Little Polymorphism at the K13 Propeller Locus in Worldwide Plasmodium falciparum Populations Prior to the Introduction of Artemisinin Combination Therapies

Association of IL1B - 31C/T and IL1RA Variable Number of an 86-bp Tandem Repeat With Dengue Shock Syndrome in Thailand

The G/G Genotype of a Resistin Single-Nucleotide Polymorphism at −420 Increases Type 2 Diabetes Mellitus Susceptibility by Inducing Promoter Activity through Specific Binding of Sp1/3

Clinical impacts of additive use of olmesartan in hypertensive patients with chronic heart failure: the supplemental benefit of an angiotensin receptor blocker in hypertensive patients with stable heart failure using olmesartan (SUPPORT) trial

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