Published in J Hum Genet on September 07, 2017
A meta-analysis of 87,040 individuals identifies 23 new susceptibility loci for prostate cancer. Nat Genet (2014) 2.72
Novel genetic markers associate with atrial fibrillation risk in Europeans and Japanese. J Am Coll Cardiol (2014) 1.86
A genome-wide association study for diabetic retinopathy in a Japanese population: potential association with a long intergenic non-coding RNA. PLoS One (2014) 1.49
Overview of the BioBank Japan Project: Study design and profile. J Epidemiol (2017) 1.32
Cross-sectional analysis of BioBank Japan clinical data: A large cohort of 200,000 patients with 47 common diseases. J Epidemiol (2017) 1.21
Overview of BioBank Japan follow-up data in 32 diseases. J Epidemiol (2017) 1.18
High-density genotyping of immune-related loci identifies new SLE risk variants in individuals with Asian ancestry. Nat Genet (2016) 1.09
Construction of a population-specific HLA imputation reference panel and its application to Graves' disease risk in Japanese. Nat Genet (2015) 1.02
Whole-genome mutational landscape and characterization of noncoding and structural mutations in liver cancer. Nat Genet (2016) 1.02
Multiple nonglycemic genomic loci are newly associated with blood level of glycated hemoglobin in East Asians. Diabetes (2014) 0.93
Associations of human leukocyte antigens with autoimmune diseases: challenges in identifying the mechanism. J Hum Genet (2015) 0.91
Performance comparison of four commercial human whole-exome capture platforms. Sci Rep (2015) 0.89
Meta-analysis of genome-wide association studies identifies multiple lung cancer susceptibility loci in never-smoking Asian women. Hum Mol Genet (2016) 0.87
Circulating Tumor DNA Analysis for Liver Cancers and Its Usefulness as a Liquid Biopsy. Cell Mol Gastroenterol Hepatol (2015) 0.86
Genetic diversity and dynamic distribution of Mycobacterium tuberculosis isolates causing pulmonary and extrapulmonary tuberculosis in Thailand. J Clin Microbiol (2014) 0.85
Exome Analyses of Long QT Syndrome Reveal Candidate Pathogenic Mutations in Calmodulin-Interacting Genes. PLoS One (2015) 0.85
Immune-related pathways including HLA-DRB1(∗)13:02 are associated with panic disorder. Brain Behav Immun (2015) 0.84
The construction of risk prediction models using GWAS data and its application to a type 2 diabetes prospective cohort. PLoS One (2014) 0.83
New susceptibility variants to narcolepsy identified in HLA class II region. Hum Mol Genet (2014) 0.83
A deletion mutation in myosin heavy chain 11 causing familial thoracic aortic dissection in two Japanese pedigrees. Int J Cardiol (2015) 0.82
Trans-ethnic study confirmed independent associations of HLA-A*02:06 and HLA-B*44:03 with cold medicine-related Stevens-Johnson syndrome with severe ocular surface complications. Sci Rep (2014) 0.82
Trans-ethnic meta-analysis of white blood cell phenotypes. Hum Mol Genet (2014) 0.82
Genome-Wide Association Study of Peripheral Arterial Disease in a Japanese Population. PLoS One (2015) 0.80
Unique characteristics of the Ainu population in Northern Japan. J Hum Genet (2015) 0.79
Genome-wide association and replication study of anti-tuberculosis drugs-induced liver toxicity. BMC Genomics (2016) 0.79
A genome-wide association study to identify genomic modulators of rate control therapy in patients with atrial fibrillation. Am J Cardiol (2014) 0.79
ABCB1 polymorphism is associated with atorvastatin-induced liver injury in Japanese population. BMC Genet (2016) 0.78
Detection of Hereditary 1,25-Hydroxyvitamin D-Resistant Rickets Caused by Uniparental Disomy of Chromosome 12 Using Genome-Wide Single Nucleotide Polymorphism Array. PLoS One (2015) 0.78
Role of HLA-DP and HLA-DQ on the clearance of hepatitis B virus and the risk of chronic infection in a multiethnic population. Liver Int (2017) 0.78
Mutations in rrs, rpsL and gidB in streptomycin-resistant Mycobacterium tuberculosis isolates from Thailand. J Glob Antimicrob Resist (2015) 0.77
Association of HLA genotypes with phenobarbital hypersensitivity in children. Epilepsia (2016) 0.77
Genome-Wide Association Study Identifies TLL1 Variant Associated With Development of Hepatocellular Carcinoma After Eradication of Hepatitis C Virus Infection. Gastroenterology (2017) 0.77
The First Pilot Genome-Wide Gene-Environment Study of Depression in the Japanese Population. PLoS One (2016) 0.76
Disease susceptibility genes shared by primary biliary cirrhosis and Crohn's disease in the Japanese population. J Hum Genet (2015) 0.76
Evaluation of polygenic risks for narcolepsy and essential hypersomnia. J Hum Genet (2016) 0.76
A Genome Wide Study of Copy Number Variation Associated with Nasopharyngeal Carcinoma in Malaysian Chinese Identifies CNVs at 11q14.3 and 6p21.3 as Candidate Loci. PLoS One (2016) 0.76
A polymorphism in CCR1/CCR3 is associated with narcolepsy. Brain Behav Immun (2015) 0.76
Genetic Variation in the SLC8A1 Calcium Signaling Pathway Is Associated with Susceptibility to Kawasaki Disease and Coronary Artery Abnormalities. Circ Cardiovasc Genet (2016) 0.76
Phenome-wide association study maps new diseases to the human major histocompatibility complex region. J Med Genet (2016) 0.75
High-density Association Mapping and Interaction Analysis of PLA2R1 and HLA Regions with Idiopathic Membranous Nephropathy in Japanese. Sci Rep (2016) 0.75
Glypican-5 Increases Susceptibility to Nephrotic Damage in Diabetic Kidney. Am J Pathol (2015) 0.75
Genome-Wide Association Study Identifies ZNF354C Variants Associated with Depression from Interferon-Based Therapy for Chronic Hepatitis C. PLoS One (2016) 0.75
Polygenic burdens on cell-specific pathways underlie the risk of rheumatoid arthritis. Nat Genet (2017) 0.75
Genome-wide analysis of CNV (copy number variation) and their associations with narcolepsy in a Japanese population. J Hum Genet (2014) 0.75
UGT1A1 polymorphism as a prognostic indicator of stage I ovarian clear cell carcinoma patients treated with irinotecan. Jpn J Clin Oncol (2017) 0.75
A genome-wide association analysis identifies NMNAT2 and HCP5 as susceptibility loci for Kawasaki disease. J Hum Genet (2017) 0.75
Genome-wide association studies identify PRKCB as a novel genetic susceptibility locus for primary biliary cholangitis in the Japanese population. Hum Mol Genet (2017) 0.75
Clinical utility and functional analysis of variants in atrial fibrillation-associated locus 4q25. J Cardiol (2017) 0.75
Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis Standard Reporting and Evaluation Guidelines: Results of a National Institutes of Health Working Group. JAMA Dermatol (2017) 0.75
HLA-DQB1*03:01 as a biomarker for genetic susceptibility to bullous pemphigoid induced by DPP-4 inhibitors. J Invest Dermatol (2017) 0.75
Narcolepsy susceptibility gene CCR3 modulates sleep-wake patterns in mice. PLoS One (2017) 0.75
HLA Class I Analysis Provides Insight Into the Genetic and Epigenetic Background of Immune Evasion in Colorectal Cancer With High Microsatellite Instability. Gastroenterology (2021) 0.75
Genetic landscape of interactive effects of HLA-DRB1 alleles on susceptibility to ACPA(+) rheumatoid arthritis and ACPA levels in Japanese population. J Med Genet (2017) 0.75
Genome-wide association study of neovascular age-related macular degeneration in the Thai population. J Hum Genet (2017) 0.75
The first genome-wide association study identifying new susceptibility loci for obstetric antiphospholipid syndrome. J Hum Genet (2017) 0.75