Katsushi Tokunaga
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Computer Science
Katsushi Tokunaga's Degrees
- PhD Computer Science University of Tokyo
- Masters Computer Science University of Tokyo
- Bachelors Computer Science University of Tokyo
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(Suggest an Edit or Addition)Katsushi Tokunaga's Published Works
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Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- Genome-wide association of IL28B with response to pegylated interferon-α and ribavirin therapy for chronic hepatitis C (2009) (1815)
- An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy (1998) (787)
- Variants in KCNQ1 are associated with susceptibility to type 2 diabetes mellitus (2008) (739)
- Mapping Human Genetic Diversity in Asia (2009) (559)
- Mapping the human genetic architecture of COVID-19 (2021) (455)
- Transcriptional regulation of endochondral ossification by HIF-2α during skeletal growth and osteoarthritis development (2010) (454)
- Hepatic ISG expression is associated with genetic variation in interleukin 28B and the outcome of IFN therapy for chronic hepatitis C. (2010) (438)
- Fcgamma receptor gene polymorphisms in Japanese patients with systemic lupus erythematosus: contribution of FCGR2B to genetic susceptibility. (2002) (333)
- Meta-analysis identifies nine new loci associated with rheumatoid arthritis in the Japanese population (2012) (299)
- HLA-haplotype banking and iPS cells (2008) (285)
- Genome-wide association study identifies TNFSF15 and POU2AF1 as susceptibility loci for primary biliary cirrhosis in the Japanese population. (2012) (244)
- A SNP in the ABCC11 gene is the determinant of human earwax type (2006) (238)
- Narcolepsy is strongly associated with the TCR alpha locus (2009) (219)
- A scan for genetic determinants of human hair morphology: EDAR is associated with Asian hair thickness. (2008) (215)
- Common variants in P2RY11 are associated with narcolepsy (2010) (213)
- FcγRIIB Ile232Thr transmembrane polymorphism associated with human systemic lupus erythematosus decreases affinity to lipid rafts and attenuates inhibitory effects on B cell receptor signaling (2005) (212)
- Sequence-based association analysis of HLA class I and II alleles in Japanese supports conservation of common haplotypes (1997) (194)
- A Practical Genome Scan for Population-Specific Strong Selective Sweeps That Have Reached Fixation (2007) (190)
- The GenomeAsia 100K Project enables genetic discoveries across Asia (2019) (189)
- Association of the oxytocin receptor (OXTR) gene polymorphisms with autism spectrum disorder (ASD) in the Japanese population (2010) (184)
- Erratum: Narcolepsy is strongly associated with the T-cell receptor alpha locus (2009) (181)
- BAFF/BLyS can potentiate B-cell selection with the B-cell coreceptor complex. (2004) (170)
- Association of Fcgamma receptor IIb and IIIb polymorphisms with susceptibility to systemic lupus erythematosus in Thais. (2003) (169)
- Association of eNOS Glu298Asp Polymorphism With End-Stage Renal Disease (2002) (167)
- TRAIL expression by activated human CD4(+)V alpha 24NKT cells induces in vitro and in vivo apoptosis of human acute myeloid leukemia cells. (2001) (167)
- SORL1 Is Genetically Associated with Late-Onset Alzheimer’s Disease in Japanese, Koreans and Caucasians (2013) (161)
- Human Leukocyte Antigen Matching Estimations in a Hypothetical Bank of Human Embryonic Stem Cell Lines in the Japanese Population for Use in Cell Transplantation Therapy (2007) (152)
- Association of Fcgamma receptor IIb polymorphism with susceptibility to systemic lupus erythematosus in Chinese: a common susceptibility gene in the Asian populations. (2004) (146)
- FTO polymorphisms in oceanic populations (2007) (146)
- Replication of genome-wide association studies of type 2 diabetes susceptibility in Japan. (2008) (143)
- Effect of genetic polymorphism of OATP-C (SLCO1B1) on lipid-lowering response to HMG-CoA reductase inhibitors. (2004) (141)
- Genome-Wide Association Study Confirming Association of HLA-DP with Protection against Chronic Hepatitis B and Viral Clearance in Japanese and Korean (2012) (135)
- Association of tumor necrosis factor receptor 2 (TNFR2) polymorphism with susceptibility to systemic lupus erythematosus. (1999) (133)
- Extended linkage disequilibrium surrounding the hemoglobin E variant due to malarial selection. (2004) (133)
- Natural selection and population history in the human angiotensinogen gene (AGT): 736 complete AGT sequences in chromosomes from around the world. (2004) (133)
- Small RNA class transition from siRNA/piRNA to miRNA during pre-implantation mouse development (2010) (132)
- A genome-wide association study identifies two novel susceptibility loci and trans population polygenicity associated with bipolar disorder (2017) (129)
- Genetic origins of the Ainu inferred from combined DNA analyses of maternal and paternal lineages (2004) (129)
- Killer Cell Immunoglobulin Receptors and T Cell Receptors Bind Peptide-Major Histocompatibility Complex Class I with Distinct Thermodynamic and Kinetic Properties* (1999) (128)
- Association of HLA-B39 with HLA-B27-negative ankylosing spondylitis and pauciarticular juvenile rheumatoid arthritis in Japanese patients. Evidence for a role of the peptide-anchoring B pocket. (1995) (127)
- Variant between CPT1B and CHKB associated with susceptibility to narcolepsy (2008) (127)
- Differential association of HLA with three subtypes of type 1 diabetes: fulminant, slowly progressive and acute-onset (2009) (124)
- DISCRIMINATION OF HUMAN HLA‐DRB1 ALLELES BY PCR‐SSCP (SINGLE‐STRAND CONFORMATION POLYMORPHISM) METHOD (1994) (123)
- C/EBPβ and RUNX2 cooperate to degrade cartilage with MMP-13 as the target and HIF-2α as the inducer in chondrocytes. (2012) (122)
- Pre-treatment prediction of response to pegylated-interferon plus ribavirin for chronic hepatitis C using genetic polymorphism in IL28B and viral factors. (2011) (122)
- Comparison of statistical power between 2 * 2 allele frequency and allele positivity tables in case-control studies of complex disease genes. (2001) (115)
- Association of Fcγ receptor IIIB, but not of Fcγ receptor IIA and IIIA, polymorphisms with systemic lupus erythematosus in Japanese (1999) (115)
- Association of IRF5 polymorphisms with systemic lupus erythematosus in a Japanese population: support for a crucial role of intron 1 polymorphisms. (2008) (113)
- Analysis on the association of human BLYS (BAFF, TNFSF13B) polymorphisms with systemic lupus erythematosus and rheumatoid arthritis (2002) (112)
- Spermatogenic ability is different among males in different Y chromosome lineage (1999) (111)
- Genome-wide association studies of tuberculosis in Asians identify distinct at-risk locus for young tuberculosis (2012) (110)
- Rapid Evolution of Major Histocompatibility Complex Class I Genes in Primates Generates New Disease Alleles in Humans via Hitchhiking Diversity (2006) (109)
- Association of human leukocyte antigen class II alleles with severe acute respiratory syndrome in the Vietnamese population (2009) (108)
- Strong association of insulin autoimmune syndrome with HLA-DR4 (1992) (107)
- Common Variants in the ATP2B1 Gene Are Associated With Susceptibility to Hypertension: The Japanese Millennium Genome Project (2010) (105)
- The history of human populations in the Japanese Archipelago inferred from genome-wide SNP data with a special reference to the Ainu and the Ryukyuan populations (2012) (105)
- FcgammaRIIB Ile232Thr transmembrane polymorphism associated with human systemic lupus erythematosus decreases affinity to lipid rafts and attenuates inhibitory effects on B cell receptor signaling. (2005) (104)
- Genome-wide association study of panic disorder in the Japanese population (2009) (104)
- Significant association of the arylalkylamine N-acetyltransferase (AA-NAT) gene with delayed sleep phase syndrome (2003) (99)
- HLA antigens in Japanese patients with myasthenia gravis. (1990) (99)
- Putative amino acid sequence of HLA-DRB chain contributing to rheumatoid arthritis susceptibility (1989) (99)
- Exon-trapping mediated by the human retrotransposon SVA. (2009) (99)
- Significant association of a single nucleotide polymorphism in the tumor necrosis factor-alpha (TNF-alpha) gene promoter with human narcolepsy. (1999) (98)
- Allele-specific binding of the ubiquitous transcription factor OCT-1 to the functional single nucleotide polymorphism (SNP) sites in the tumor necrosis factor-alpha gene (TNFA) promoter (2001) (97)
- CD36 polymorphism is associated with protection from cerebral malaria. (2003) (97)
- Molecular genetic analysis of variant phenotypes of the ABO blood group system (1996) (96)
- Meta-analysis of genome-wide association scans for genetic susceptibility to endometriosis in Japanese population (2010) (94)
- Association of TCF7L2 polymorphisms with susceptibility to type 2 diabetes in 4,087 Japanese subjects (2008) (92)
- The origin of Minnan and Hakka, the so-called "Taiwanese", inferred by HLA study. (2001) (91)
- Genetic variants of human β-defensin-1 and chronic obstructive pulmonary disease (2002) (90)
- Long‐lasting RNAi activity in mammalian neurons (2004) (90)
- Genome-Wide Association Study Identifies TLL1 Variant Associated With Development of Hepatocellular Carcinoma After Eradication of Hepatitis C Virus Infection. (2017) (89)
- Extensive polymorphism of ABO blood group gene: three major lineages of the alleles for the common ABO phenotypes (1996) (88)
- A replication study confirmed the EDAR gene to be a major contributor to population differentiation regarding head hair thickness in Asia (2008) (84)
- Recombination and gene conversion-like events may contribute to ABO gene diversity causing various phenotypes (2001) (83)
- Common variation in GPC5 is associated with acquired nephrotic syndrome (2011) (83)
- MIC-A polymorphism in Japanese and a MIC-A-MIC-B null haplotype (1999) (83)
- Soluble MICA and a MICA Variation as Possible Prognostic Biomarkers for HBV-Induced Hepatocellular Carcinoma (2012) (83)
- Genome-wide association study identified ITPA/DDRGK1 variants reflecting thrombocytopenia in pegylated interferon and ribavirin therapy for chronic hepatitis C. (2011) (82)
- The power of genome-wide association studies of complex disease genes: statistical limitations of indirect approaches using SNP markers (2001) (82)
- Association of complement C4 and HLA-DR alleles with systemic lupus erythematosus in Koreans. (1994) (80)
- Positional identification of an asthma susceptibility gene on human chromosome 5q33. (2005) (80)
- Genetic background of Japanese patients with antineutrophil cytoplasmic antibody-associated vasculitis: association of HLA-DRB1*0901 with microscopic polyangiitis. (2003) (79)
- Independent strong association of HLA-A*02:06 and HLA-B*44:03 with cold medicine-related Stevens-Johnson syndrome with severe mucosal involvement (2014) (79)
- Association of a functional CD19 polymorphism with susceptibility to systemic sclerosis. (2004) (79)
- Extensive deletions and insertions in different MHC supratypes detected by pusled field gel electrophoresis (1988) (78)
- Genome‐wide Association Study of Autism Spectrum Disorder in the East Asian Populations (2016) (78)
- Fcgamma receptor IIA and IIIB polymorphisms are associated with susceptibility to cerebral malaria. (2002) (77)
- Extensive polymorphisms of LILRB1 (ILT2, LIR1) and their association with HLA-DRB1 shared epitope negative rheumatoid arthritis. (2005) (77)
- Construction of a prediction model for type 2 diabetes mellitus in the Japanese population based on 11 genes with strong evidence of the association (2009) (76)
- Molecular genetic analyses of human NKG2C (KLRC2) gene deletion. (2004) (76)
- Narcolepsy is strongly associated with the T-cell receptor alpha locus (vol 41, pg 708, 2009) (2014) (76)
- Genetic link between Asians and native Americans: evidence from HLA genes and haplotypes. (2001) (76)
- Crucial Role of Inhibitor of DNA Binding/Differentiation in the Vascular Endothelial Growth Factor-Induced Activation and Angiogenic Processes of Human Endothelial Cells1 (2004) (75)
- Strong association between HLA-A*0206 and Stevens-Johnson syndrome in the Japanese. (2007) (75)
- Specific nucleotide sequence of HLA-C is strongly associated with psoriasis vulgaris. (1991) (74)
- HLA-A, -B, -C, -DRB1 and -DQB1 alleles and haplotypes in the Kinh population in Vietnam. (2007) (73)
- ITPA gene variant protects against anemia induced by pegylated interferon‐α and ribavirin therapy for Japanese patients with chronic hepatitis C (2010) (73)
- Molecular genetic analysis of variant phenotypes of the ABO blood group system. (1996) (72)
- Further development of multiplex single nucleotide polymorphism typing method, the DigiTag2 assay. (2007) (72)
- Three major lineages of Asian Y chromosomes: implications for the peopling of east and southeast Asia (2001) (72)
- Promoter analysis and aberrant expression of the MUC5B gene in diffuse panbronchiolitis. (2005) (72)
- Analysis of the association of HLA-DRB1, TNFα promoter and TNFR2 (TNFRSF1B) polymorphisms with SLE using transmission disequilibrium test (2001) (72)
- Studies on the association of Fcγ receptor IIA, IIB, IIIA and IIIB polymorphisms with rheumatoid arthritis in the Japanese: evidence for a genetic interaction between HLA-DRB1 and FCGR3A (2002) (71)
- Replication and meta-analysis of TMEM132D gene variants in panic disorder (2012) (71)
- Worldwide differences in the incidence of insulin autoimmune syndrome (Hirata disease) with respect to the evolution of HLA-DR4 alleles. (2000) (70)
- FLT3 is fused to ETV6 in a myeloproliferative disorder with hypereosinophilia and a t(12;13)(p13;q12) translocation (2006) (70)
- Candidate genes in panic disorder: meta-analyses of 23 common variants in major anxiogenic pathways (2016) (70)
- A Genome-Wide Association Study for Diabetic Retinopathy in a Japanese Population: Potential Association with a Long Intergenic Non-Coding RNA (2014) (69)
- Lack of a strong association of CTLA-4 exon 1 polymorphism with the susceptibility to rheumatoid arthritis and systemic lupus erythematosus in Japanese: an association study using a novel variation screening method. (1999) (68)
- Activation and suppression of renin-angiotensin system in human dendritic cells. (2002) (68)
- Significant Association of KIR2DL3-HLA-C1 Combination with Cerebral Malaria and Implications for Co-evolution of KIR and HLA (2012) (67)
- Different Alleles Cause an Imbalance in A2 and A2B Phenotypes of the ABO Blood Group (1998) (66)
- Differential Immunogenetic Determinants of Polyclonal Insulin Autoimmune Syndrome (Hirata's Disease) and Monoclonal Insulin Autoimmune Syndrome (1995) (66)
- Evaluating the performance of Affymetrix SNP Array 6.0 platform with 400 Japanese individuals (2008) (66)
- Association study of the DISC1/TRAX locus with schizophrenia in a Japanese population (2005) (65)
- Common Variants on Chromosome 9p21 Are Associated with Normal Tension Glaucoma (2012) (64)
- Anti-Tribbles homolog 2 autoantibodies in Japanese patients with narcolepsy. (2010) (64)
- Polymorphic Microsatellite Markers for the Diagnosis of Graft-versus-Host Disease (1994) (64)
- HLA class II allele and haplotype frequencies in Koreans based on 107 families. (2002) (63)
- Protein binding of a DRPLA family through arginine-glutamic acid dipeptide repeats is enhanced by extended polyglutamine. (2000) (63)
- Heterogeneity of Taiwan's indigenous population: possible relation to prehistoric Mongoloid dispersals. (2000) (63)
- Donor killer immunoglobulin-like receptor (KIR) genotype-patient cognate KIR ligand combination and antithymocyte globulin preadministration are critical factors in outcome of HLA-C-KIR ligand-mismatched T cell-replete unrelated bone marrow transplantation. (2008) (63)
- Identification of Hypertension-Susceptibility Genes and Pathways by a Systemic Multiple Candidate Gene Approach: The Millennium Genome Project for Hypertension (2008) (63)
- GA4GH: International policies and standards for data sharing across genomic research and healthcare (2021) (62)
- Genome-wide SNP-based linkage analysis of tuberculosis in Thais (2009) (62)
- HLA class I and II gene polymorphisms in Stevens-Johnson syndrome with ocular complications in Japanese (2008) (62)
- Meta-analysis of genome-wide association studies for panic disorder in the Japanese population (2012) (62)
- Fine localization of a major disease-susceptibility locus for diffuse panbronchiolitis. (2000) (61)
- Identification of the gene variations in human CD22 (1999) (60)
- Associations of human leukocyte antigens with autoimmune diseases: challenges in identifying the mechanism (2015) (60)
- Analysis by the polymerase chain reaction of histocompatibility leucocyte antigen-DR9-linked susceptibility to insulin-dependent diabetes mellitus. (1992) (60)
- Human histocompatibility leukocyte antigen (HLA) haplotype frequencies estimated from the data on HLA class I, II, and III antigens in 111 Japanese narcoleptics. (1985) (60)
- Patients with Graves' disease who developed insulin autoimmune syndrome (Hirata disease) possess HLA-Bw62/Cw4/DR4 carrying DRB1*0406. (1993) (59)
- Diversity of HLA among Taiwan's indigenous tribes and the Ivatans in the Philippines. (2001) (59)
- Genomewide association analysis of human narcolepsy and a new resistance gene. (2006) (58)
- ADAM33 polymorphisms are associated with asthma susceptibility in a Japanese population (2006) (58)
- Splice acceptor site mutation of the transporter associated with antigen processing-1 gene in human bare lymphocyte syndrome. (1999) (57)
- 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 (2014) (57)
- Cell-surface MHC density profiling reveals instability of autoimmunity-associated HLA. (2015) (57)
- Polymorphisms of tumour necrosis factors A and B in breast cancer. (2002) (55)
- Genome-wide profiling of DNA methylation in human cancer cells. (2011) (55)
- Variations of human killer cell lectin-like receptors: common occurrence of NKG2-C deletion in the general population (2003) (55)
- Targeting Id1 and Id3 inhibits peritoneal metastasis of gastric cancer (2005) (55)
- Linkage-disequilibrium mapping narrows the Fukuyama-type congenital muscular dystrophy (FCMD) candidate region to <100 kb. (1996) (55)
- A subject with a novel type I bare lymphocyte syndrome has tapasin deficiency due to deletion of 4 exons by Alu-mediated recombination. (2002) (55)
- Evidence for Shared Genetic Risk Between Methamphetamine-Induced Psychosis and Schizophrenia (2013) (54)
- IKZF1, a new susceptibility gene for cold medicine-related Stevens-Johnson syndrome/toxic epidermal necrolysis with severe mucosal involvement. (2015) (54)
- SNP-SNP Interactions Discovered by Logic Regression Explain Crohn's Disease Genetics (2012) (54)
- Genetic variants of human beta-defensin-1 and chronic obstructive pulmonary disease. (2002) (54)
- Significant association of longer forms of CCTTT Microsatellite repeat in the inducible nitric oxide synthase promoter with severe malaria in Thailand. (2002) (54)
- Differential association of HLA-DRB1 alleles in Japanese patients with early rheumatoid arthritis in relationship to autoantibodies to cyclic citrullinated peptide. (2007) (54)
- ROUTINE LOW AND HIGH RESOLUTION TYPING OF THE HLA‐DRB GENE USING THE PCR‐MPH (MICROTITRE PLATE HYBRIDIZATION) METHOD (1996) (54)
- Genetic variations on the Y chromosome in the Japanese population and implications for modern human Y chromosome lineage (1999) (53)
- Tumor necrosis factor α 5'-flanking region, tumor necrosis factor receptor II, and HLA-DRB1 polymorphisms in Japanese patients with rheumatoid arthritis (2000) (53)
- Independent contribution of HLA-DRB1 and TNFα promoter polymorphisms to the susceptibility to Crohn’s disease (2000) (53)
- Recognition of human insulin in the context of HLA-DRB1*0406 products by T cells of insulin autoimmune syndrome patients and healthy donors. (1993) (53)
- Identification of KCNJ15 as a susceptibility gene in Asian patients with type 2 diabetes mellitus. (2010) (52)
- Gene flow and natural selection in oceanic human populations inferred from genome-wide SNP typing. (2008) (52)
- Enhancement of Allele Discrimination by Introduction of Nucleotide Mismatches into siRNA in Allele-Specific Gene Silencing by RNAi (2008) (52)
- Molecular cloning of two novel mucin-like genes in the disease-susceptibility locus for diffuse panbronchiolitis (2011) (52)
- HLA and Human Mate Choice: Tests on Japanese Couples (2000) (52)
- Appropriate data cleaning methods for genome-wide association study (2008) (51)
- MICA allele typing of HLA-B27 positive Japanese patients with seronegative spondylarthropathies and healthy individuals: differential linkage disequilibrium with HLA-B27 subtypes. (1998) (51)
- HLA class II alleles in Ainu living in Hidaka District, Hokkaido, northern Japan. (1996) (50)
- 14-3-3zeta is indispensable for aggregate formation of polyglutamine-expanded huntingtin protein (2008) (50)
- Contribution of HLA genes to genetic predisposition in diffuse panbronchiolitis. (1998) (50)
- Significant association of the tumor necrosis factor receptor 2 (TNFR2) gene with human narcolepsy. (2000) (49)
- Association of TLR polymorphisms with development of tuberculosis in Indonesian females. (2012) (49)
- Association of IL28B variants with response to pegylated‐interferon alpha plus ribavirin combination therapy reveals intersubgenotypic differences between genotypes 2a and 2b (2011) (49)
- Determination of HLA class II alleles by genotyping in a Manchu population in the northern part of China and its relationship with Han and Japanese populations. (1995) (49)
- A polymorphism in the AMPKalpha2 subunit gene is associated with insulin resistance and type 2 diabetes in the Japanese population. (2006) (49)
- Association of HLA-DRB1*0901-DQB1*0303 haplotype with microscopic polyangiitis in Japanese (2006) (48)
- Variations in immune response genes and their associations with multifactorial immune disorders (2002) (48)
- Immunogenetic features in 120 Japanese patients with idiopathic inflammatory myopathy. (2004) (48)
- HLA haplotypes in Koreans based on 107 families. (2008) (48)
- Schizophrenia and the HLA-DRB1 gene in the Japanese population. (1999) (47)
- A functional single-nucleotide polymorphism in the CR1 promoter region contributes to protection against cerebral malaria. (2008) (47)
- Evidence for natural selection on leukocyte immunoglobulin-like receptors for HLA class I in Northeast Asians. (2008) (46)
- Genome-wide association study identified ITPA / DDRGK 1 variants reflecting thrombocytopenia in pegylated interferon and ribavirin therapy for chronic hepatitis C (2011) (46)
- Association of Fc gamma receptor IIIB, but not of Fc gamma receptor IIA and IIIA polymorphisms with systemic lupus erythematosus in Japanese. (1999) (46)
- Functional polymorphisms in the vascular endothelial growth factor gene are associated with development of end-stage renal disease in males. (2006) (46)
- Discerning the Origins of the Negritos, First Sundaland People: Deep Divergence and Archaic Admixture (2017) (46)
- Polymorphisms of HLA genes in Western Javanese (Indonesia): close affinities to Southeast Asian populations. (2009) (46)
- HLA-A, HLA-B, and HLA-DRB1 alleles and haplotypes in Naxi and Han populations in southwestern China (Yunnan province). (2006) (45)
- Sequence Variation of Human Platelet Membrane Glycoprotein IIIa Associated with the Yuka/Yukb Alloantigen System. (1991) (45)
- Genome‐wide association studies identify PRKCB as a novel genetic susceptibility locus for primary biliary cholangitis in the Japanese population (2017) (45)
- A single-nucleotide substitution from C to T at position −1055 in the IL-13 promoter is associated with protection from severe malaria in Thailand (2003) (45)
- Distribution of HLA-A, -B, -Cw, and -DRB1 alleles and haplotypes in an isolated Han population in Southwest China. (2009) (45)
- λ‐Interferons and the single nucleotide polymorphisms: A milestone to tailor‐made therapy for chronic hepatitis C (2010) (44)
- HLA-A*11:01:01:01, HLA-C*12:02:02:01-HLA-B*52:01:02:02, Age and Sex Are Associated With Severity of Japanese COVID-19 With Respiratory Failure (2021) (44)
- FGFR2 is associated with hair thickness in Asian populations (2009) (44)
- Genetic features of Mongolian ethnic groups revealed by Y-chromosomal analysis. (2005) (43)
- Effects of Oral L-Carnitine Administration in Narcolepsy Patients: A Randomized, Double-Blind, Cross-Over and Placebo-Controlled Trial (2013) (43)
- Significant association between TNF-alpha (TNF) promoter allele (-1031C, -863C, and -857C) and cerebral malaria in Thailand. (2007) (43)
- Analysis of HLA genes and haplotypes in Ainu (from Hokkaido, northern Japan) supports the premise that they descent from Upper Paleolithic populations of East Asia. (2000) (43)
- Pathogen lineage-based genome-wide association study identified CD53 as susceptible locus in tuberculosis (2017) (43)
- Wide distribution of the MICA-MICB null haplotype in East Asians. (2001) (43)
- Epigenome-wide association study of DNA methylation in panic disorder (2017) (43)
- Replication of a genome-wide association study of panic disorder in a Japanese population (2010) (43)
- Association of Fcgamma receptor IIA, but not IIB and IIIA, polymorphisms with systemic lupus erythematosus: A family-based association study in Caucasians. (2004) (43)
- Absence of an association between the polymorphisms in the genes encoding adiponectin receptors and type 2 diabetes (2005) (43)
- New polymorphisms of human CD80 and CD86: lack of association with rheumatoid arthritis and systemic lupus erythematosus (2000) (43)
- No association for Chinese HBV-related hepatocellular carcinoma susceptibility SNP in other East Asian populations (2012) (42)
- Family study on HLA-DPB1 polymorphism: linkage analysis with HLA-DR/DQ and two "new" alleles. (1992) (42)
- HLA-DR4 genotype and insulin-processing in insulin autoimmune syndrome (1992) (42)
- Allele typing of human TNFA 5'-flanking region using polymerase chain reaction-preferential homoduplex formation assay (PCR-PHFA): linkage disequilibrium with HLA class I and class II genes in Japanese. (1999) (42)
- siRNA-mediated inhibition of endogenous Huntington disease gene expression induces an aberrant configuration of the ER network in vitro. (2005) (42)
- Polymorphisms of promoter and coding regions of the arylamine N-acetyltransferase 2 (NAT2) gene in the Indonesian population: proposal for a new nomenclature (2008) (42)
- Association of HLA-A, -B, and -DRB1 with pulmonary tuberculosis in western Javanese Indonesia. (2010) (42)
- Chromosomal localization of the human natural killer cell class I receptor family genes to 19q13.4 by fluorescence in situ hybridization. (1996) (42)
- Founder SVA retrotransposal insertion in Fukuyama‐type congenital muscular dystrophy and its origin in Japanese and Northeast Asian populations (2005) (42)
- Association study of the dysbindin (DTNBP1) gene in schizophrenia from the Japanese population (2006) (41)
- Tumor necrosis factor-alpha mRNA expression in lipopolysaccharide-stimulated rat kidney. Chronological analysis of localization. (1994) (41)
- Power of genome-wide linkage disequilibrium testing by using microsatellite markers (2003) (41)
- Lack of gene deletion for complement C4A deficiency in Japanese patients with systemic lupus erythematosus. (1990) (41)
- NAT2 variants are associated with drug-induced liver injury caused by anti-tuberculosis drugs in Indonesian patients with tuberculosis (2016) (41)
- CD72 polymorphisms associated with alternative splicing modify susceptibility to human systemic lupus erythematosus through epistatic interaction with FCGR2B. (2004) (41)
- Do specific pockets of HLA-C molecules predispose Jewish patients to psoriasis vulgaris? (1994) (40)
- A 12-kb structural variation in progressive myoclonic epilepsy was newly identified by long-read whole-genome sequencing (2019) (40)
- Human leukocyte antigen and season of birth in Japanese patients with schizophrenia. (2000) (40)
- Relationship between Polymorphisms of the Inosine Triphosphatase Gene and Anaemia or Outcome after Treatment with Pegylated Interferon and Ribavirin (2011) (40)
- Single-nucleotide-polymorphism genotyping for whole-genome-amplified samples using automated fluorescence correlation spectroscopy. (2004) (40)
- Analysis of Human Leukocyte Antigen‐G Polymorphism Including Intron 4 in Japanese Couples with Habitual Abortion (1999) (40)
- NAT2 slow acetylator associated with anti-tuberculosis drug-induced liver injury in Thai patients. (2016) (40)
- Association of HLA class I and class II alleles with myositis in Japanese patients. (1998) (40)
- Association of HLA-DRB1*1502-DQB1*0501 haplotype with susceptibility to systemic lupus erythematosus in Thais. (2002) (40)
- Association of Cw11 in Japanese patients with psoriasis vulgaris. (1990) (40)
- Overlapping peptide-binding specificities of HLA-B27 and B39: evidence for a role of peptide supermotif in the pathogenesis of spondylarthropathies. (1999) (40)
- Evolutionary Analysis of Classical HLA Class I and II Genes Suggests That Recent Positive Selection Acted on DPB1*04∶01 in Japanese Population (2012) (39)
- Deletion of entire HLA-A gene accompanied by an insertion of a retrotransposon. (2007) (39)
- Association of HLA-DR with progressive systemic sclerosis in Japanese. (1994) (39)
- Further molecular diversity in the HLA-B15 group. (1996) (39)
- Association of killer cell immunoglobulin-like receptor genotypes with microscopic polyangiitis. (2006) (39)
- Polymorphisms of human CD19 gene: possible association with susceptibility to systemic lupus erythematosus in Japanese (2002) (38)
- A simple method of HLA-DRB typing using enzymatically amplified DNA and immobilized probes on microtiter plate. (1994) (38)
- Understanding of HLA-conferred susceptibility to chronic hepatitis B infection requires HLA genotyping-based association analysis (2016) (38)
- Founder-haplotype analysis in Fukuyama-type congenital muscular dystrophy (FCMD) (1998) (38)
- A simple method for detecting single base substitutions and its application to HLA-DPB1 typing. (1994) (38)
- Possible association of human leucocyte antigen DR1 with delayed sleep phase syndrome (1999) (38)
- An approach based on a genome-wide association study reveals candidate loci for narcolepsy (2010) (37)
- Evidence for natural selection in the HAVCR1 gene: high degree of amino-acid variability in the mucin domain of human HAVCR1 protein (2005) (37)
- DBTSS/DBKERO for integrated analysis of transcriptional regulation (2017) (37)
- Haplotype analysis with 14 Y-STR loci using 2 multiplex amplification and typing systems in 2 regional populations in Japan (2003) (37)
- Association of CD22 gene polymorphism with susceptibility to limited cutaneous systemic sclerosis. (2007) (37)
- Id1/Id3 knockdown inhibits metastatic potential of pancreatic cancer. (2010) (37)
- The human histocompatibility leukocyte antigen (HLA) haplotype is associated with the onset of postherpetic neuralgia after herpes zoster (2004) (37)
- Hepatocyte Nuclear Factor-4α P2 Promoter Haplotypes Are Associated With Type 2 Diabetes in the Japanese Population (2006) (37)
- An HLA-B null allele (B*1526N) with a stop codon in exon 3 generated by a point mutation. (1997) (36)
- Strong Association of the HLA-DR/DQ Locus with Childhood Steroid-Sensitive Nephrotic Syndrome in the Japanese Population. (2018) (36)
- Key HLA‐DRB1‐DQB1 haplotypes and role of the BTNL2 gene for response to a hepatitis B vaccine (2018) (36)
- Polymorphisms of the HLA-B and HLA-DRB1 genes in Thai malaria patients. (2005) (36)
- Lack of primary association between transporter associated with antigen processing genes and atopic dermatitis. (1995) (36)
- Abnormally low serum acylcarnitine levels in narcolepsy patients. (2011) (36)
- Evidence for Host-Bacterial Co-evolution via Genome Sequence Analysis of 480 Thai Mycobacterium tuberculosis Lineage 1 Isolates (2018) (36)
- Association of HLA-A*3303-B*4403-DRB1*1302 haplotype, but not of TNFA promoter and NKp30 polymorphism, with postherpetic neuralgia (PHN) in the Japanese population (2002) (35)
- HLA-A*0206 with TLR3 Polymorphisms Exerts More than Additive Effects in Stevens-Johnson Syndrome with Severe Ocular Surface Complications (2012) (35)
- Expression of renin-angiotensin system genes in immature and mature dendritic cells identified using human cDNA microarray. (2001) (35)
- Association of IL-10 receptor 2 (IL10RB) SNP with systemic sclerosis. (2008) (35)
- HLA genes and haplotypes in Ryukyuans suggest recent gene flow to the Okinawa Islands. (1999) (35)
- Profiling of genes expressed in human monocytes and monocyte‐derived dendritic cells using cDNA expression array (2001) (34)
- Single nucleotide polymorphisms in the coding regions of human CXC-chemokine receptors CXCR1, CXCR2 and CXCR3 (2000) (34)
- A polymorphism in CCR1/CCR3 is associated with narcolepsy (2015) (34)
- Study of HLA class I, class II and complement genes (C2, C4A, C4B and BF) in Japanese psoriatics and analysis of a newly-found high-risk haplotype by pulsed field gel electrophoresis (2004) (34)
- Association and interaction analyses of NRG1 and ERBB4 genes with schizophrenia in a Japanese population (2008) (33)
- Distribution of HLA alleles and haplotypes in Jinuo and Wa populations in Southwest China. (2008) (33)
- New Susceptibility and Resistance HLA-DP Alleles to HBV-Related Diseases Identified by a Trans-Ethnic Association Study in Asia (2014) (33)
- Analysis of disease-associated amino acid epitopes on HLA class II molecules in atopic dermatitis. (1995) (33)
- Crucial Role of Inhibitor of DNA Binding/Differentiation in the Vascular Endothelial Growth Factor-Induced Activation and Angiogenic Processes of Human Endothelial Cells. (2005) (32)
- Structural and functional analysis of 3' untranslated region of mouse Period1 mRNA. (2003) (32)
- Case-control study with narcoleptic patients and healthy controls who, like the patients, possess both HLA-DRB1*1501 and -DQB1*0602. (2001) (32)
- Inhibition of Glucose-Stimulated Insulin Secretion by KCNJ15, a Newly Identified Susceptibility Gene for Type 2 Diabetes (2012) (32)
- The expected power of genome‐wide linkage disequilibrium testing using single nucleotide polymorphism markers for detecting a low‐frequency disease variant (2002) (32)
- HLA-B27 subtypes in Japanese with seronegative spondyloarthropathies and healthy controls. (1996) (31)
- Expression of ID family genes in the synovia from patients with rheumatoid arthritis. (2001) (31)
- Polymorphisms of transporter associated with antigen processing genes in atopic dermatitis. (1994) (31)
- Association of eNOS Glu 298 Asp Polymorphism With End-Stage Renal Disease (2002) (31)
- Narcolepsy and HLA in the Japanese (1988) (31)
- Monozygotic twins incompletely concordant for narcolepsy (2001) (30)
- Large-scale comparative mapping of the MHC class I region of predominant haplotypes in Japanese (1997) (30)
- A novel Ancestral Beijing sublineage of Mycobacterium tuberculosis suggests the transition site to Modern Beijing sublineages (2019) (30)
- Association of a particular amino acid sequence of the HLA‐DR β1 chain with HTLV‐I‐associated myelopathy (1990) (30)
- Large‐scale DNA typing for human platelet alloantigens by PCR‐PHFA (preferential homoduplex formation assay) (1996) (30)
- A genome-wide CNV association study on panic disorder in a Japanese population (2011) (30)
- High-density Association Mapping and Interaction Analysis of PLA2R1 and HLA Regions with Idiopathic Membranous Nephropathy in Japanese (2016) (29)
- Systemic and local expression levels of TNF‐like ligand 1A and its decoy receptor 3 are increased in primary biliary cirrhosis (2014) (29)
- High‐throughput single nucleotide polymorphism typing by fluorescent single‐strand conformation polymorphism analysis with capillary electrophoresis (2004) (29)
- Human Leukocyte Antigen Class I Genes Associated With Stevens-Johnson Syndrome and Severe Ocular Complications Following Use of Cold Medicine in a Brazilian Population (2017) (29)
- Phylogenetic relationship of the populations within and around Japan using 105 short tandem repeat polymorphic loci (2006) (29)
- Sequence-based typing of HLA-A2 alleles using a primer with an extra base mismatch. (1995) (29)
- Mutations in rrs, rpsL and gidB in streptomycin-resistant Mycobacterium tuberculosis isolates from Thailand. (2016) (29)
- Development of a prediction system for anti-tuberculosis drug-induced liver injury in Japanese patients (2016) (29)
- Brief communication: mitochondrial DNA variation suggests extensive gene flow from Polynesian ancestors to indigenous Melanesians in the northwestern Bismarck Archipelago. (2006) (29)
- Epistatic interaction between Toll-like receptor 3 (TLR3) and prostaglandin E receptor 3 (PTGER3) genes. (2012) (29)
- New single nucleotide polymorphisms in the coding region of human TNFR2: association with systemic lupus erythematosus (2000) (29)
- Genome‐wide association study of HPV‐associated cervical cancer in Japanese women (2014) (28)
- The HLA system in the population of Mongolia. (1997) (28)
- Polymorphism of Human Leukocyte Antigen‐E Gene in the Japanese Population with or without Recurrent Abortion (2001) (28)
- Genome-wide association study identified new susceptible genetic variants in HLA class I region for hepatitis B virus-related hepatocellular carcinoma (2018) (28)
- New susceptibility variants to narcolepsy identified in HLA class II region. (2015) (28)
- HLA-G gene polymorphism in a Japanese population (1996) (28)
- Comparative mapping of the human major histocompatibility complex in different racial groups by pulsed field gel electrophoresis. (1989) (27)
- A functional SNP in the NKX2.5-binding site of ITPR3 promoter is associated with susceptibility to systemic lupus erythematosus in Japanese population (2008) (27)
- Digenic mutations in ALDH2 and ADH5 impair formaldehyde clearance and cause a multisystem disorder, AMeD syndrome. (2020) (27)
- Polymorphism Located between CPT1B and CHKB, and HLA-DRB1*1501-DQB1*0602 Haplotype Confer Susceptibility to CNS Hypersomnias (Essential Hypersomnia) (2009) (27)
- Genome‐wide association study of atypical psychosis (2013) (27)
- Genome‐Wide Association Study Identifies Risk Variants for Lichen Planus in Patients With Hepatitis C Virus Infection (2017) (27)
- Nomenclature of Granulocyte Alloantigens (1999) (27)
- Genetics of narcolepsy (2019) (27)
- Polymorphisms of human leucocyte antigen genes in Maonan people in China (2007) (27)
- Reference Typing Report for Complement Components C6, C7 and C9 Including Mutations Leading to Deficiencies (1999) (27)
- The First Pilot Genome-Wide Gene-Environment Study of Depression in the Japanese Population (2016) (26)
- Unique characteristics of the Ainu population in Northern Japan (2015) (26)
- Association study between the TNXB locus and schizophrenia in a Japanese population (2007) (26)
- Long-term persistence of both functional and non-functional alleles at the leukocyte immunoglobulin-like receptor A3 (LILRA3) locus suggests balancing selection (2006) (26)
- Breakpoints at 1p36.3 in three MDS/AML(M4) patients with t(1;3)(p36;q21) occur in the first intron and in the 5′ region of MEL1 (2003) (26)
- New variations of human CC-chemokine receptors CCR3 and CCR4 (1999) (26)
- An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs (2021) (26)
- Presence of four major haplotypes in human BCMA gene: lack of association with systemic lupus erythematosus and rheumatoid arthritis (2001) (26)
- Variations in the human CC chemokine eotaxin gene (2001) (26)
- Study of aspartate at residue 9 of HLA-C molecules in Japanese patients with psoriasis vulgaris. (1996) (26)
- Proposal for the Nomenclature of Human Plasminogen (PLG) Polymorphism (1986) (26)
- Human leukocyte antigen variants and risk of hepatocellular carcinoma modified by hepatitis C virus genotypes: A genome‐wide association study (2018) (26)
- Support for an association between HLA-DR1 and schizophrenia in the Japanese population. (2000) (25)
- Association of diffuse panbronchiolitis with microsatellite polymorphism of the human interleukin 8 (IL-8) gene (1999) (25)
- Genome-wide association study of self-reported food reactions in Japanese identifies shrimp and peach specific loci in the HLA-DR/DQ gene region (2018) (25)
- Family study on the polymorphisms of the sixth and seventh components (C6 and C7) of human complement: linkage and haplotype analyses. (1986) (25)
- Comparative analysis of copy number variation detection methods and database construction (2011) (25)
- HLA‐class II and class I genotypes among Japanese children with Type 1A diabetes and their families (2012) (25)
- RNAi induction and activation in mammalian muscle cells where Dicer and eIF2C translation initiation factors are barely expressed. (2004) (25)
- The CD1d natural killer T-cell antigen presentation pathway is highly conserved between humans and rhesus macaques (2003) (25)
- Genetic link among Hani, Bulang and other Southeast Asian populations: evidence from HLA ‐A, ‐B, ‐C, ‐DRB1 genes and haplotypes distribution (2010) (25)
- Role of APRIL (TNFSF13) polymorphisms in the susceptibility to systemic lupus erythematosus in Japanese. (2007) (25)
- Analysis of whole Y-chromosome sequences reveals the Japanese population history in the Jomon period (2019) (24)
- Association of LILRA2 (ILT1, LIR7) splice site polymorphism with systemic lupus erythematosus and microscopic polyangiitis (2008) (24)
- Association of IFNGR2 gene polymorphisms with pulmonary tuberculosis among the Vietnamese (2011) (24)
- The human natural killer gene complex (NKC) is located on chromosome 12p13.1-p13.2 (1997) (24)
- Genetic Diversity and Dynamic Distribution of Mycobacterium tuberculosis Isolates Causing Pulmonary and Extrapulmonary Tuberculosis in Thailand (2014) (24)
- Association of CD209 polymorphisms with tuberculosis in an Indonesian population. (2011) (24)
- Utility of fingernail DNA for evaluation of chimerism after bone marrow transplantation and for diagnostic testing for transfusion-associated graft-versus-host disease. (1996) (24)
- Absence of association between the allele coding methionine at position 29 in the N-terminal domain of ICAM-1 (ICAM-1(Kilifi)) and severe malaria in the northwest of Thailand. (2001) (24)
- Common variants in P 2 RY 11 are associated with narcolepsy (2010) (24)
- Pulmonary Mycobacterium avium complex infection associated with the IVS8-T5 allele of the CFTR gene. (2007) (24)
- Common risk variants in NPHS1 and TNFSF15 are associated with childhood steroid-sensitive nephrotic syndrome. (2020) (24)
- Identification of Novel Schizophrenia Loci by Homozygosity Mapping Using DNA Microarray Analysis (2011) (24)
- HLA-B40, B18, B27, and B37 allele discrimination using group-specific amplification and SSCP method. (1996) (24)
- Genome-wide association database developed in the Japanese Integrated Database Project (2009) (23)
- Influence of assembly of siRNA elements into RNA-induced silencing complex by fork-siRNA duplex carrying nucleotide mismatches at the 3'- or 5'-end of the sense-stranded siRNA element. (2005) (23)
- Sequences of four splits of HLA-A10 group. Implications for serologic cross-reactivities and their evolution. (1994) (23)
- Human primary biliary cirrhosis-susceptible allele of rs4979462 enhances TNFSF15 expression by binding NF-1 (2015) (23)
- Association analysis of susceptibility candidate region on chromosome 5q31 for tuberculosis (2010) (23)
- Phenome-wide association study maps new diseases to the human major histocompatibility complex region (2016) (23)
- Genome-Wide Association Study Confirming a Strong Effect of HLA and Identifying Variants in CSAD/lnc-ITGB7-1 on Chromosome 12q13.13 Associated With Susceptibility to Fulminant Type 1 Diabetes (2018) (23)
- A nested PCR-RFLP method for high-resolution typing of HLA-A alleles. (1998) (23)
- Quality control project of NGS HLA genotyping for the 17th International HLA and Immunogenetics Workshop. (2019) (22)
- Identification of HLA-C alleles using PCR-single-strand-conformation polymorphism and direct sequencing. (1997) (22)
- Founder effect of the C9 R95X mutation in Orientals (2003) (22)
- Strain‐based HLA association analysis identified HLA‐DRB1*09:01 associated with modern strain tuberculosis (2017) (22)
- High-resolution HLA-DQB1 typing by combination of group-specific amplification and restriction fragment length polymorphism. (1995) (22)
- Identification of a haplotype block in the 5q31 cytokine gene cluster associated with the susceptibility to severe malaria (2009) (22)
- Follistatin-related protein gene (FRP) is expressed in the synovial tissues of rheumatoid arthritis, but its polymorphisms are not associated with genetic susceptibility. (2004) (22)
- A novel HLA-B27 allele (B*2711) encoding an antigen reacting with both B27- and B40-specific antisera. (1997) (22)
- Five HLA-B22 group alleles in Japanese. (1997) (22)
- Polymorphism located in TCRA locus confers susceptibility to essential hypersomnia with HLA-DRB1*1501-DQB1*0602 haplotype (2010) (22)
- An association analysis of HLA-DQB1 with narcolepsy without cataplexy and idiopathic hypersomnia with/without long sleep time in a Japanese population (2015) (22)
- Comparative FISH mapping of the ancestral fusion point of human chromosome 2 (2004) (21)
- Genome-wide association study of HLA-DQB1*06:02 negative essential hypersomnia (2013) (21)
- Identification of the functional variant driving ORMDL3 and GSDMB expression in human chromosome 17q12-21 in primary biliary cholangitis (2017) (21)
- Comparison of statistical power between 2×2 allele frequency and allele positivity tables in case‐control studies of complex disease genes (2001) (21)
- Transformation of Ba/F3 cells and Rat-1 cells by ETV6/ARG (2002) (21)
- Haplotype analysis of NAD(P)H oxidase p22 phox polymorphisms in end-stage renal disease (2005) (21)
- Genome-wide association study using the ethnicity-specific Japonica array: identification of new susceptibility loci for cold medicine-related Stevens–Johnson syndrome with severe ocular complications (2017) (21)
- HLA alleles and haplotypes distribution in Dai population in Yunnan province, Southwest China. (2010) (21)
- HLA-A null allele with a stop codon, HLA-A*0215N, identified in a homozygous state in a healthy adult (2004) (21)
- Establishment of human cell lines showing circadian rhythms of bioluminescence (2008) (21)
- HLA and atopic dermatitis with high serum IgE levels. (1994) (20)
- NAT2 ultra-slow acetylator and risk of anti-tuberculosis drug-induced liver injury: a genotype-based meta-analysis (2018) (20)
- Active role of small non-coding RNAs derived from SINE/B1 retrotransposon during early mouse development (2012) (20)
- Antibody to a specific HLA-DR beta 1 sequence in Japanese patients with rheumatoid arthritis. (1990) (20)
- DOCK2 is involved in the host genetics and biology of severe COVID-19 (2022) (20)
- Lack of association of -308A/G TNFA promoter and 196R/M TNFR2 polymorphisms with disease severity in Thai adult malaria patients. (2001) (20)
- Dendritic cells rapidly undergo apoptosis in vitro following culture with activated CD4+ Vα24 natural killer T cells expressing CD40L (2001) (20)
- POGLUT1, the putative effector gene driven by rs2293370 in primary biliary cholangitis susceptibility locus chromosome 3q13.33 (2019) (20)
- Distribution of HLA antigens and haplotypes in the Buryat population of Siberia. (1995) (20)
- Evaluation of polygenic risks for narcolepsy and essential hypersomnia (2016) (20)
- Principal contribution of HLA-DQ alleles, DQB1*06:04 and DQB1*03:01, to disease resistance against primary biliary cholangitis in a Japanese population (2017) (20)
- A functional polymorphism in the IL1B gene promoter, IL1B -31C>T, is not associated with cerebral malaria in Thailand (2005) (20)
- Disease susceptibility genes shared by primary biliary cirrhosis and Crohn’s disease in the Japanese population (2015) (20)
- NFKB1 and MANBA Confer Disease Susceptibility to Primary Biliary Cholangitis via Independent Putative Primary Functional Variants (2018) (20)
- Tumor necrosis factor alpha 5'-flanking region, tumor necrosis factor receptor II, and HLA-DRB1 polymorphisms in Japanese patients with rheumatoid arthritis. (2000) (19)
- Analysis of human leukocyte antigen HLA-DR beta amino acid sequence in Vogt-Koyanagi-Harada syndrome. (1991) (19)
- Practical guide for managing large-scale human genome data in research (2020) (19)
- Significant Association Between TIM1 Promoter Polymorphisms and Protection Against Cerebral Malaria in Thailand (2008) (19)
- Cell surface expression of HLA-E molecules on PBMC from a TAP1-deficient patient. (1999) (19)
- HLA-A26 subtype A pockets accommodate acidic N-termini of ligands (1998) (19)
- Polymorphisms in the ABO blood group gene in three populations in the New Georgia group of the Solomon Islands (2006) (19)
- Molecular polymorphism of ABO blood group gene in Austronesian and non-Austronesian populations in Oceania. (2004) (19)
- Polymorphism of human minor histocompatibility antigens: T cell recognition of human minor histocompatibility peptides presented by HLA- B35 subtype molecules (1995) (19)
- Association of SLC11A1 (NRAMP1) polymorphisms with pulmonary Mycobacterium avium complex infection. (2012) (19)
- Assessment of allele-specific gene silencing by RNA interference with mutant and wild-type reporter alleles (2006) (19)
- HLA-A*02:06 and PTGER3 polymorphism exert additive effects in cold medicine-related Stevens–Johnson syndrome with severe ocular complications (2015) (19)
- YAC and cosmid contigs encompassing the Fukuyama-type congenital muscular dystrophy (FCMD) candidate region on 9q31. (1997) (19)
- HLA antigens in Behçet's disease with refractory ocular attacks. (2008) (18)
- Role of HLA‐DP and HLA‐DQ on the clearance of hepatitis B virus and the risk of chronic infection in a multiethnic population (2017) (18)
- Human leukocyte antigen-A specificities and its relation with season of birth in Japanese patients with schizophrenia (2002) (18)
- A powerful, novel, multiplex typing system for six short tandem repeat loci and the allele frequency distributions in two Japanese regional populations (2002) (18)
- Human leucocyte antigen association of patients with Stevens-Johnson syndrome/toxic epidermal necrolysis with severe ocular complications in Han Chinese (2021) (18)
- MHC (Major Histocompatibility Complex)-DRB Genes and Polymorphisms in Common Marmoset (2000) (18)
- Sequence Analysis of Fibroblast Growth Factor Receptor 2 (FGFR2) in Japanese Patients with Craniosynostosis (2001) (18)
- HLA-DR types in Japanese schizophrenics: analysis by group-specific PCR amplification (1994) (18)
- Role of B cell inhibitory receptor polymorphisms in systemic lupus erythematosus: a negative times a negative makes a positive (2006) (18)
- A recurrent duodenal gastrointestinal stromal tumor with a frameshift mutation resulting in a stop codon in KIT exon 13 (2005) (18)
- Variations of the CFTR gene in the Hanoi‐Vietnamese (2005) (18)
- Coexistence of an MHC chromosomal segment marked by HLA B17,BfS,C4A6,B1,DR7, and DQw9 in different ethnic groups. (1988) (18)
- Association study between the Down syndrome cell adhesion molecule (DSCAM) gene and bipolar disorder (2008) (18)
- Self-sustained circadian rhythm in cultured human mononuclear cells isolated from peripheral blood (2010) (17)
- De novo polyalanine expansion of PHOX2B in congenital central hypoventilation syndrome: unequal sister chromatid exchange during paternal gametogenesis (2007) (17)
- Genotyping and association analysis of HLA-B61 in Japanese. (1993) (17)
- Specific HLA genotypes confer susceptibility to acute necrotizing encephalopathy (2016) (17)
- Correction: A Genome-Wide Association Study for Diabetic Retinopathy in a Japanese Population: Potential Association with a Long Intergenic Non-Coding RNA (2014) (17)
- DNA‐Based Typing of Human Platelet Antigen Systems by Polymerase Chain Reaction‐Single‐Strand Conformation Polymorphism Method (1995) (17)
- HLA-G gene polymorphism in a Japanese population (2007) (17)
- Association of six polymorphisms of the NOTCH4 gene with schizophrenia in the Japanese population (2004) (17)
- Sequence analysis of serological HLA-A11 split antigens, A11.1 and A11.2. (1994) (17)
- Glypican-5 Increases Susceptibility to Nephrotic Damage in Diabetic Kidney. (2015) (17)
- Immune-related pathways including HLA-DRB1∗13:02 are associated with panic disorder (2015) (16)
- Genetic polymorphisms in HLA-A, -B, -C and -DR antigens in Japanese patients with palmoplantar pustulosis. (1994) (16)
- HLA-DRB1 frequencies of non-Austronesian-speaking Gidra in south New Guinea and their genetic affinities with Oceanian populations. (1995) (16)
- X chromosome contribution to the genetic architecture of primary biliary cholangitis. (2021) (16)
- Large‐scale genome‐wide association study identifies HLA class II variants associated with chronic HBV infection: a study from Taiwan Biobank (2020) (16)
- Determination of Granulocyte–Specific Antigens on Neutrophil FcÁ Receptor IIIb by PCR–Preferential Homoduplex Formation Assay, and Gene Frequencies in the Japanese Population (1999) (16)
- Major Histocompatibility Complex Haplotype Is Associated with Postherpetic Pain in Mice (2006) (16)
- A new HLA-A9 subtype lacking the Bw4 epitope. Ancestral or revertant allele? (1995) (16)
- Whole-exome sequencing and gene-based rare variant association tests suggest that PLA2G4E might be a risk gene for panic disorder (2018) (16)
- The first genome-wide association study identifying new susceptibility loci for obstetric antiphospholipid syndrome (2017) (16)
- Association of Human Leukocyte Antigen Class 1 genes with Stevens Johnson Syndrome with severe ocular complications in an Indian population (2017) (16)
- Visual demonstration of the organization of the human complement C4 and 21-hydroxylase genes by high-resolution fluorescence in situ hybridization. (1996) (16)
- IFNGR1 polymorphisms in Thai malaria patients. (2009) (15)
- In Silico Risk Assessment of HLA-A*02:06-Associated Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis Caused by Cold Medicine Ingredients (2013) (15)
- Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative (2022) (15)
- Genomewide Association Study Confirming the Association of NAT2 with Susceptibility to Antituberculosis Drug-Induced Liver Injury in Thai Patients (2019) (15)
- Haplotype analyses with the human leucocyte antigen and tumour necrosis factor‐alpha genes in narcolepsy families (2001) (15)
- A common Japanese haplotype HLA-A26-Cw3-B61-DR9-DQ3 carries HLA-B*4002. (1992) (15)
- Homoplastic single nucleotide polymorphisms contributed to phenotypic diversity in Mycobacterium tuberculosis (2020) (15)
- New variations of human SHP-1 (1999) (15)
- POLYMORPHISM OF THE COMPLEMENT COMPONENT C6 IN JAPANESE (1983) (15)
- Identification and DNA typing of two Cw7 alleles (Cw*0702 and Cw*0704) in Japanese, with the corrected sequence of Cw*0702. (1996) (15)
- Fine-mapping analysis revealed complex pleiotropic effect and tissue-specific regulatory mechanism of TNFSF15 in primary biliary cholangitis, Crohn’s disease and leprosy (2016) (15)
- Lack of Association of the HbE Variant with Protection from Cerebral Malaria in Thailand (2008) (15)
- A Genome-wide Association Study Identifying RAP1A as a Novel Susceptibility Gene for Crohn’s Disease in Japanese Individuals (2018) (15)
- Evaluation of microsatellite markers in association studies: a search for an immune-related susceptibility gene in sarcoidosis (2005) (15)
- HLA Class I analysis provides insight into the genetic and epigenetic background of immune evasion in colorectal cancer with high microsatellite instability. (2021) (15)
- Association of TNFRSF4 gene polymorphisms with essential hypertension (2008) (14)
- Absence of association between the Fc gamma receptor IIIA-176F/V polymorphism and the severity of malaria in Thai. (2002) (14)
- Polymorphisms of CD36 in Thai malaria patients. (2002) (14)
- Diversity of HLA-B61 alleles and haplotypes in East Asians and Spanish Gypsies. (2008) (14)
- Epigenome-wide association study of DNA methylation in narcolepsy: an integrated genetic and epigenetic approach (2018) (14)
- Novel mutations of the HOXD13 gene in hand and foot malformations. (2007) (14)
- Genetic polymorphism of the second component of human complement (C2) in Japanese (1980) (14)
- HLA Class I DNA typing using sequence specific oligonucleotide probes (SSOP) (1997) (14)
- A high-resolution genotyping method for HLA-C alleles and possible shared HLA-C-B haplotypes between Japanese and Caucasians. (1997) (14)
- Amino acid position 37 of HLA‐DR&bgr;1 affects susceptibility to Crohn's disease in Asians (2018) (14)
- Identification of novel single nucleotide substitutions in the NKp30 gene expressed in human natural killer cells. (2001) (14)
- The association and differentiation of MHC class I polymorphic Alu insertions and HLA-B/Cw alleles in seven Chinese populations. (2010) (14)
- A high-resolution HLA imputation system for the Taiwanese population: a study of the Taiwan Biobank (2020) (14)
- Role of anchor residues in peptide binding to three HLA-A26 molecules. (1999) (14)
- Association of HLA class I and II gene polymorphisms with acetaminophen-related Stevens–Johnson syndrome with severe ocular complications in Japanese individuals (2019) (14)
- Narcolepsy risk loci are enriched in immune cells and suggest autoimmune modulation of the T cell receptor repertoire (2018) (14)
- The Origin and Composition of Korean Ethnicity Analyzed by Ancient and Present-Day Genome Sequences (2020) (14)
- Identification of ITPA on chromosome 20 as a susceptibility gene for young-onset tuberculosis (2016) (13)
- Haplotype study on C4 polymorphism in Japanese. Associations with MIHC Alleles, complotypes, and HLA-complement haplotypes (2004) (13)
- Sensitivity to gene dosage and gene expression affects genes with copy number variants observed among neuropsychiatric diseases (2020) (13)
- Molecular cloning and characterization of decay-accelerating factor deficiency in Cromer blood group Inab phenotype. (1998) (13)
- DigiTag assay for multiplex single nucleotide polymorphism typing with high success rate. (2005) (13)
- Brief report: polymorphic microsatellite markers for the diagnosis of graft-versus-host disease. (1994) (13)
- Establishment of a method of anonymization of DNA samples in genetic research (2003) (13)
- Mucocutaneous inflammation in the Ikaros Family Zinc Finger 1‐keratin 5–specific transgenic mice (2018) (13)
- Association of LILRA2 (ILT1, LIR7) splice site polymorphism with systemic lupus erythematosus and microscopic polyangiitis (2008) (13)
- An epigenome-wide methylation study of healthy individuals with or without depressive symptoms (2018) (13)
- Novel allele containing a 190C>T nonsynonymous substitution in the N‐acetyltransferase (NAT2) gene (2000) (13)
- Determination of Granulocyte‐Specific Antigens on Neutrophil Fcγ Receptor IIIb by PCR‐Preferential Homoduplex Formation Assay, and Gene Frequencies in the Japanese Population (1999) (13)
- C4A and C4B null alleles are genetic markers of different types of systemic sclerosis in Japanese patients. (1998) (12)
- Model incorporating the ITPA genotype identifies patients at high risk of anemia and treatment failure with pegylated‐interferon plus ribavirin therapy for chronic hepatitis C (2013) (12)
- Negative association of the HLA-DRB1*1502-DQB1*0601 haplotype with human narcolepsy (2000) (12)
- Consequences of Nucleic Acid Amplification Testing for Blood Transfusion Centres (1998) (12)
- A Case of a Japanese Patient with Cleidocranial Dysplasia Possessing a Mutation of CBFA1 Gene (2002) (12)
- TNFR2 position 196 polymorphism in Japanese patients with rheumatoid arthritis: comment on the article by Dieudé et al. (2003) (12)
- Human CD72 splicing isoform responsible for resistance to systemic lupus erythematosus regulates serum immunoglobulin level and is localized in endoplasmic reticulum (2012) (12)
- Japan COVID-19 Task Force: a nation-wide consortium to elucidate host genetics of COVID-19 pandemic in Japan (2021) (12)
- MULTIPLEX ARMS‐PCR‐RFLP METHOD FOR HIGH‐RESOLUTION TYPING OF HLA‐DRB1 (1995) (12)
- Molecular cloning and characterization of decay-accelerating factor deficiency in Cromer blood group Inab phenotype (1998) (12)
- Highly Parallel and Short-Acting Amplification with Locus-Specific Primers to Detect Single Nucleotide Polymorphisms by the DigiTag2 Assay (2012) (12)
- Allele typing of HLA-A10 group by nested-PCR-low ionic strength single stranded conformation polymorphism and a novel A26 allele (A26KY, A*2605). (1996) (12)
- Functional Polymorphism of the Myeloperoxidase Gene in Hypertensive Nephrosclerosis Dialysis Patients (2007) (12)
- Recent divergence of the HLA-DRB1*04 allelic lineage from the DRB1*0701 lineage after the separation of the human and chimpanzee species (2003) (12)
- Analysis of HLA-DRB1 polymorphism in the Gidra of Papua New Guinea. (2000) (12)
- Association study of schizophrenia with D11s35 and dopamine D2 receptor gene loci using dinucleotide repeat polymorphisms (1993) (12)
- A replication study of the association between the IL12B promoter allele CTCTAA and susceptibility to cerebral malaria in Thai population (2009) (12)
- A novel method for isolation of endothelial cells and macrophages from murine tumors based on Ac-LDL uptake and CD16 expression. (2004) (12)
- Identification of HLA-A*02:06:01 as the primary disease susceptibility HLA allele in cold medicine-related Stevens-Johnson syndrome with severe ocular complications by high-resolution NGS-based HLA typing (2019) (12)
- Association study of PDE4B with panic disorder in the Japanese population (2011) (12)
- Human genetic research, race, ethnicity and the labeling of populations: recommendations based on an interdisciplinary workshop in Japan (2014) (12)
- Identification of HLA-DRB1*04:10 allele as risk allele for Japanese moyamoya disease and its association with autoimmune thyroid disease: A case-control study (2019) (11)
- Genetic influences on prefrontal activation during a verbal fluency task in adults: A twin study based on multichannel near-infrared spectroscopy (2014) (11)
- A missense variant in PER2 is associated with delayed sleep–wake phase disorder in a Japanese population (2019) (11)
- A new HLA-C allele, Cw*1403, associated with HLA-B44 in Japanese. (1995) (11)
- Contribution of TAP genes to genetic predisposition for diffuse panbronchiolitis. (1999) (11)
- An immunoblotting technique for complement C6 typing: Three new variants (1984) (11)
- Typing for human platelet alloantigens. (1999) (11)
- Novel rare variations of the oxytocin receptor (OXTR) gene in autism spectrum disorder individuals (2015) (11)
- Genome-wide association study identifies a PSMD3 variant associated with neutropenia in interferon-based therapy for chronic hepatitis C (2015) (11)
- Polymorphism of properdin factor B in Japanese. Description of a rare variant and data of association with HLA and C2 (2004) (11)
- Effects of HLA-DPB1 genotypes on chronic hepatitis B infection in Japanese individuals. (2015) (11)
- Detection of Hereditary 1,25-Hydroxyvitamin D-Resistant Rickets Caused by Uniparental Disomy of Chromosome 12 Using Genome-Wide Single Nucleotide Polymorphism Array (2015) (11)
- A new member of the HLA-B40 family of alleles, B*4007, coding for B'FU' serological specificity. (1995) (11)
- HLA polymorphism of the Zhuang population reflects the common HLA characteristics among Zhuang-Dong language-speaking populations (2011) (11)
- Polymorphisms in the TMEM132D region are associated with panic disorder in HLA-DRB1*13:02-negative individuals of a Japanese population (2016) (11)
- Both HLA-B*1301 and B*1302 exist in Asian populations and are associated with different haplotypes. (1995) (11)
- Integrative genome analysis identified the KANNO blood group antigen as prion protein (2019) (11)
- Glucose-6-phosphate dehydrogenase deficiency among three national minorities in Hainan Island, China. (1988) (11)
- Population Genetic Study in Hainan Island, China I. Distribution of Blood Genetic Markers (1993) (11)
- SUSCEPTIBILITY EPITOPE ON HLA‐DR β CHAIN FOR RHEUMATOID ARTHRITIS AND THE EFFECT OF THE POSITIVITY ON THE CLINICAL FEATURES (1989) (11)
- Establishment of a T‐Cell Line from Lymphocytes Presumably Implicated in Posttransfusion Graft‐versus‐Host Disease (1995) (10)
- A new HLA-DR11 DRB1 allele found in a Korean. (1994) (10)
- DNA polymorphism in the FKBP5 gene affects impulsivity in intertemporal choice (2013) (10)
- A new B18 sequence (B*1802) from Asian individuals. (1995) (10)
- Bf and C2 polymorphism in Japanese patients with juvenile onset diabetes mellitus: existence of a variant Bf allele. (1981) (10)
- Coexistence of Philadelphia chromosome positive cells with and without der(9) deletion in a patient with chronic myelogenous leukemia. (2006) (10)
- Direct determination of MUC5B promoter haplotypes based on the method of single-strand conformation polymorphism and their statistical estimation. (2004) (10)
- Genetic Overlap Between Antipsychotic Response and Susceptibility to Schizophrenia (2015) (10)
- Identification and characterization of HIV-1-specific CD8+ T cell epitopes presented by HLA-A*2601. (2005) (10)
- NAT2 slow acetylator is associated with anti-tuberculosis drug-induced liver injury severity in indonesian population. (2019) (10)
- Restricted use of T‐cell receptor V beta genes in posttransfusion graft‐ versus‐host disease (1997) (10)
- Clinical Characteristics of Patients with Coronavirus Disease (COVID-19): Preliminary Baseline Report of Japan COVID-19 Task Force, a Nationwide Consortium to Investigate Host Genetics of COVID-19 (2021) (10)
- Identification of a telomeric boundary of the HLA region with potential for predisposition to human narcolepsy (2000) (10)
- Genes highly expressed in the early phase of murine graft-versus-host reaction. (2001) (10)
- Evidence of involvement of cytotoxic antibodies directed against patient’s HLA class II produced by transfused donor‐derived B cells in post‐transfusion graft‐versus‐host disease (1996) (10)
- Diversity of HLA-B17 alleles and haplotypes in East Asians and a novel Cw6 allele (Cw*0604) associated with B*5701. (1999) (10)
- Lack of association between interleukin-10 gene promoter polymorphism, -1082G/A, and severe malaria in Thailand. (2002) (10)
- Genome study of kidney disease in the age of post genome-sequencing. (2008) (10)
- Association of complement alleles C4AQ0 and C4B5 with rheumatoid arthritis in Japanese patients. (1989) (10)
- New variations in human OX40 ligand (CD134L) gene (2000) (10)
- Fc g RIIB Ile232Thr transmembrane polymorphism associated with human systemic lupus erythematosus decreases affinity to lipid rafts and attenuates inhibitory effects on B cell receptor signaling (2005) (9)
- DNA Typing for HLA-DR Using Polymerase Chain Reaction: Application to Frozen Blood (1990) (9)
- Human Lymphocytes Obtained from Decidual Tissue Express Killer Activatory Receptors as Well as Killer Inhibitory Receptors: Analysis Using a Single Strand Conformation Polymorphism Method (1998) (9)
- The juxtamembrane domain in ETV6/FLT3 is critical for PIM-1 up-regulation and cell proliferation. (2009) (9)
- HLA class I distribution in Japanese patients with schizophrenia. (2002) (9)
- Significant association of HLA-B and HLA-DRB1 alleles with cleft lip with or without cleft palate. (1999) (9)
- Correction: SORL1 Is Genetically Associated with Late-Onset Alzheimer’s Disease in Japanese, Koreans and Caucasians (2013) (9)
- Gene Expression Analysis in Human Monocytes, Monocyte-Derived Dendritic Cells, and α-Galactosylceramide-Pulsed Monocyte- Derived Dendritic Cells (2001) (9)
- Association study of the chemokine, CXC motif, ligand 1 (CXCL1) gene with sporadic Alzheimer's disease in a Japanese population (2005) (9)
- DNA single-strand conformation polymorphism method to distinguish DR4 alleles (1993) (9)
- Identification of the gene encoding a novel HLA-B39 subtype. Two amino acid substitutions on the beta-sheet out of the peptide-binding floor form a novel serological epitope. (1994) (9)
- Genome-Wide Association Study Identifies ZNF354C Variants Associated with Depression from Interferon-Based Therapy for Chronic Hepatitis C (2016) (9)
- The genomic structure of two ancestral haplotypes carrying C4A duplications (2004) (9)
- Genetic Background of Mesalamine-induced Fever and Diarrhea in Japanese Patients with Inflammatory Bowel Disease. (2021) (9)
- Genome-wide association study in patients with pulmonary Mycobacterium avium complex disease (2019) (9)
- Genome‐Wide Association Study of Lean Nonalcoholic Fatty Liver Disease Suggests Human Leukocyte Antigen as a Novel Candidate Locus (2020) (9)
- HLA-VBSeq v2: improved HLA calling accuracy with full-length Japanese class-I panel (2019) (8)
- New polymorphisms within human TAP2 in the ATP-binding domain and profiles of TAP polymorphism in Japanese. (1996) (8)
- HLA genotyping of 5,000- and 6,000-year-old ancient bones in Japan. (1999) (8)
- Lessons from Genome-Wide Search for Disease-Related Genes with Special Reference to HLA-Disease Associations (2014) (8)
- DNA typing of Cw*14 alleles in Japanese and the corrected sequence of Cw*1402. (1996) (8)
- NELFCD and CTSZ loci are associated with jaundice-stage progression in primary biliary cholangitis in the Japanese population (2018) (8)
- Identification of genes upregulated in the inflamed colonic lesions of Crohn's disease. (2001) (8)
- Identification of a two-SNP PLA2R1 Haplotype and HLA-DRB1 Alleles as Primary Risk Associations in Idiopathic Membranous Nephropathy (2018) (8)
- A novel apolipoprotein E5 variant with a 24-bp insertion causing hyperlipidemia (2001) (8)
- Establishment and characterization of a novel Philadelphia-chromosome positive chronic myeloid leukemia cell line, TCC-S, expressing P210 and P190 BCR/ABL transcripts but missing normal ABL gene (2008) (8)
- [A controlled study of AO-90, a methionine-free intravenous amino acid solution, in combination with 5-fluorouracil and mitomycin C in advanced gastric cancer patients (internal medicine group evaluation)]. (1995) (8)
- Novel DNA Chip Based on a Modified DigiTag2 Assay for High-Throughput Species Identification and Genotyping of Mycobacterium tuberculosis Complex Isolates (2014) (8)
- Association of Functional Polymorphisms in Interferon Regulatory Factor 2 (IRF2) with Susceptibility to Systemic Lupus Erythematosus: A Case-Control Association Study (2014) (8)
- Monocyte chemoattractant protein 1 (MCP-1) gene polymorphism is not associated with severe and cerebral malaria in Thailand. (2006) (8)
- Sequence of a new HLA-A allele (A*0218) encoding a serological variant, HLA-A2K, observed in Japanese. (1996) (8)
- Human C7 polymorphism: Classification and association analysis with C6 (1986) (8)
- HLA in Japanese Insulin‐Dependent Diabetes Mellitus (1984) (8)
- Isolation, Migration and Health: Genetic affinities of human populations (1992) (8)
- Association between fatty acid binding protein 3 gene variants and essential hypertension in humans. (2008) (8)
- Polymorphism of TAPASIN and its linkage disequilibria with HLA class II genes in the Japanese population. (1998) (8)
- Direct sequencing of a HLA-DRB gene by polymerase chain reaction: Sequence variation in DRw8 specificity (1990) (8)
- Genetic polymorphisms of complement C6 and C7 in two Chinese populations (1986) (8)
- Genome-wide SNP data of Izumo and Makurazaki populations support inner-dual structure model for origin of Yamato people (2021) (7)
- Genetic polymorphism of the complement C2 in Japanese (2004) (7)
- High-resolution melt analysis enables simple genotyping of complicated polymorphisms of codon 18 rendering the NUDT15 diplotype (2019) (7)
- CD 72 polymorphisms associated with alternative splicing modify susceptibility to human systemic lupus erythematosus through epistatic interaction with FCGR 2 B (2004) (7)
- Haplotype-specific sequence encoding the protein kinase, interferon-inducible double-stranded RNA-dependent activator in the human leukocyte antigen class II region (2000) (7)
- rs1944919 on chromosome 11q23.1 and its effector genes COLCA1/COLCA2 confer susceptibility to primary biliary cholangitis (2021) (7)
- Unique secondary chromosomal abnormalities are frequently found in the chronic phase of chronic myeloid leukemia in southern Vietnam. (2006) (7)
- Selecting a contingency table in a population-based association study: allele frequency or positivity? (1999) (7)
- Genetic polymorphisms of human complement components BF and C2 in Korean: Population and association studies (1985) (7)
- HLA-DRB1 polymorphism on Ha’ano island of the Kingdom of Tonga (2006) (7)
- Protective association of HLA-DRB1*13:02, HLA-DRB1*04:06, and HLA-DQB1*06:04 alleles with cervical cancer in a Korean population. (2019) (7)
- Massive Blood Replacement (1999) (7)
- Genome-wide association study of idiopathic hypersomnia in a Japanese population (2021) (7)
- Integrated GWAS and mRNA Microarray Analysis Identified IFNG and CD40L as the Central Upstream Regulators in Primary Biliary Cholangitis (2020) (7)
- A novel allele, Cw*1702 with serological Cw2 specificity. (1997) (7)
- The association of NAD(P)H oxidase p22phox with diabetic nephropathy is still uncertain: response to Hodgkinson, Millward, and Demaine. (2004) (7)
- Indo-Oceanic Mycobacterium tuberculosis strains from Thailand associated with higher mortality. (2019) (7)
- A new HLA-DR8 subtype showing unusual serological reaction and the confirmatory sequence of DRB1*0809. (1995) (6)
- Genome-Wide Association Study Reveals Host Genetic Factors for Liver Diseases (2013) (6)
- Ethnic differences in allele frequencies of two microsatellite markers closely linked to the locus for polycystic kidney disease 1 (PKD1). (1995) (6)
- Further study on a BF silent allele (2004) (6)
- Impact of a single nucleotide polymorphism upstream of the IL28B gene in patients positive for anti‐HCV antibody in an HCV hyperendemic area in Japan (2014) (6)
- Regional heritability mapping identifies several novel loci (STAT4, ULK4, and KCNH5) for primary biliary cholangitis in the Japanese population (2021) (6)
- Genetic polymorphisms of complement components C6 and C7 in Korean (1988) (6)
- Restriction fragment length polymorphism of complement C4 in Japanese patients with rheumatoid arthritis and normal Japanes (1990) (6)
- THE ANTIGENIC DETERMINANTS, Rg/Ch/WH, EXPRESSED BY JAPANESE C4 ALLOTYPES (1988) (6)
- No evidence for association between the interferon regulatory factor 1 (IRF1) gene and clinical tuberculosis. (2009) (6)
- Questionable expression of unstable DQ heterodimer containing HLA-DQA1*01:07. (2015) (6)
- Epigenome-wide association study of narcolepsy-affected lateral hypothalamic brain and overlapping DNA methylation profiles between narcolepsy and multiple sclerosis. (2020) (6)
- Genome-wide analysis of CNV (copy number variation) and their associations with narcolepsy in a Japanese population (2014) (6)
- A human PSMB11 variant affects thymoproteasome processing and CD8+ T cell production. (2017) (6)
- The association of integration patterns of human papilloma virus and single nucleotide polymorphisms on immune- or DNA repair-related genes in cervical cancer patients (2019) (6)
- C7*N is a hypomorphic allele of the human complement c7 M/N protein polymorphism. (1991) (6)
- Comparative study of the haplotype structure and linkage disequilibrium of chromosome 1p36.2 region in the Korean and Japanese populations (2004) (6)
- Genetic association of IL17 and the importance of ABO blood group antigens in saliva to COVID-19 (2022) (6)
- Verifying nomenclature of DNA variants in submitted manuscripts: Guidance for journals (2020) (6)
- Effects of down-regulating the Id genes in human colorectal cancer cells on early steps of haematogenous metastasis. (2006) (6)
- Sequence analysis of DPB1-like genes in cynomolgus monkeys (Macaca fascicularis) (2004) (6)
- Sojourn times and substitution rate at overdominant and linked neutral loci. (2000) (5)
- Erratum: Common variants in P2RY11 are associated with narcolepsy (2011) (5)
- Increased expression and altered localization of cathepsin Z are associated with progression to jaundice stage in primary biliary cholangitis (2018) (5)
- Linkage disequilibrium structure of the 5q31-33 region in a Thai population (2008) (5)
- Phasing analysis of lung cancer genomes using a long read sequencer (2022) (5)
- Promoter variation of tumour necrosis factor-alpha gene: possible high risk for chronic bronchitis but not diffuse panbronchiolitis. (1999) (5)
- Correction of the HLA-G*01012 genomic sequence. (1997) (5)
- [Polymorphism of HLA-DRB1 in Han population in Yunnan and comparison with 9 Han populations]. (2004) (5)
- Genetic polymorphism of properdin factor B (BF) in a chinese population: Existence of two rare variants (1987) (5)
- Narcolepsy susceptibility gene CCR3 modulates sleep-wake patterns in mice (2017) (5)
- MGeND: an integrated database for Japanese clinical and genomic information (2019) (5)
- New Year’s Greetings (2012) (5)
- Variation in Malaria Endemicity in Relation to Microenvironmental Conditions in the Admiralty Islands, Papua New Guinea (2001) (5)
- GWAS identifies candidate susceptibility loci and microRNA biomarkers for acute encephalopathy with biphasic seizures and late reduced diffusion (2021) (5)
- Properdin Factor B Allotypes in Japanese Patients with Psoriasis (1987) (5)
- A novel C3 allotype C3'F02' has an amino acid substitution that may inhibit IC3b synthesis and cause C3-hypocohplehentehia (1993) (5)
- A polymorphism in CCR 1 / CCR (2015) (5)
- An optimized genomic VCF workflow for precise identification of Mycobacterium tuberculosis cluster from cross-platform whole genome sequencing data. (2019) (5)
- Novel (CA)n marker DXYS241 on the nonrecombinant part of the human Y chromosome. (1999) (5)
- Nucleotide sequence of a novel DPB1 allele, DPB1*4701. (1993) (5)
- Isoelectric focusing pattern of desialyzed C2. (1982) (5)
- Strong linkage disequilibrium of a HbE variant with the (AT)9(T)5 repeat in the BP1 binding site upstream of the β-globin gene in the Thai population (2005) (5)
- Human C7 polymorphism: Quantitative analysis of different phenotypes (1988) (5)
- Metabolome analysis using cerebrospinal fluid from narcolepsy type 1 patients. (2020) (5)
- Significance of functional disease-causal/susceptible variants identified by whole-genome analyses for the understanding of human diseases (2017) (5)
- Computer simulation analysis suggests weak balancing selection operative at the MICA locus. (2000) (5)
- Complement C4A, C4B and BF haplotypes in Koreans. (1996) (5)
- Practical forensic use of kinship determination using high-density SNP profiling based on a microarray platform, focusing on low-quantity DNA. (2022) (5)
- CHARACTERIZATION OF MHC ANCESTRAL HAPLOTYPES ASSOCIATED WITH INSULIN‐DEPENDENT DIABETES MELLITUS: EVIDENCE FOR INVOLVEMENT OF NON‐HLA GENES (1990) (5)
- Identification of the target molecule of cytotoxic T cells presumably responsible for development of transfusion‐associated graft‐versus‐host disease (1996) (5)
- An Association Study of HLA with the Kinetics of SARS-CoV-2 Spike Specific IgG Antibody Responses to BNT162b2 mRNA Vaccine (2022) (4)
- Haplotype Analyses (2006) (4)
- Histamine, cytokine and anaphylatoxin levels in stored platelet concentrates. (1994) (4)
- A variant at 9q34.11 is associated with HLA-DQB1*06:02 negative essential hypersomnia (2018) (4)
- Association of disease severity with toll-like receptor polymorphisms in multidrug-resistant tuberculosis patients (2020) (4)
- Genome-wide haplotype association analysis of primary biliary cholangitis risk in Japanese (2018) (4)
- HLA polymorphisms in a Han Chinese population of Sichuan. (2008) (4)
- An Integrated Genomic and Transcriptomic Analysis Reveals Candidates of Susceptibility Genes for Crohn’s Disease in Japanese Populations (2020) (4)
- Identification of a novel HLA-B allele, HLA-B*5904. (2009) (4)
- Haplotype-specific PCR for NAT2 diplotyping (2020) (4)
- gene with human narcolepsy (2000) (4)
- NARCOLEPSY. AUTHOR'S REPLY (1991) (4)
- HLA-DRB1 alleles encoding the shared epitope associated with rheumatoid arthritis confer additional susceptibility to seronegative spondyloarthropathies in HLA-B27-positive Japanese individuals (1999) (4)
- Novel single nucleotide polymorphisms (SNPs) at positions 497 (T/G) and 829 (T/C) in the human c‐FOS gene and haplotype association (2000) (4)
- Genetic characterization of N-acetyltransferase 2 variants in acquired multidrug-resistant tuberculosis in Indonesia. (2021) (4)
- Association of complement alleles C4AQ0 and C4B5 with rheumatoid arthritis in Koreans. (1996) (4)
- The whole blood transcriptional regulation landscape in 465 COVID-19 infected samples from Japan COVID-19 Task Force (2022) (3)
- 726 GENOME-WIDE ASSOCIATION STUDY IDENTIFIES GENETIC VARIANTS IN THE HLA-DP LOCUS ASSOCIATED WITH CHRONIC HEPATITIS B (2010) (3)
- Discovery of a novel HLA‐B*40 allele, HLA‐B*40:02:01:30 in a Japanese individual (2022) (3)
- Estimation of the species-specific mutation rates at the DRB1 locus in humans and chimpanzee. (2006) (3)
- Haplotype-specific PCR for NAT2 diplotyping. (2020) (3)
- Gene expression analysis in human monocytes, monocyte-derived dendritic cells, and alpha-galactosylceramide-pulsed monocyte-derived dendritic cells. (2001) (3)
- A novel protein polymorphism of human complement C7 detected by a monoclonal antibody (2004) (3)
- Identification of the novel HLA‐DQB1 allele, HLA‐DQB1*05:03:01:04, in a Japanese individual (2019) (3)
- Genetic features of Khoton Mongolians revealed by SNP analysis of the X chromosome. (2005) (3)
- Genomic Heritabilities and Correlations of 17 Traits Related to Obesity and Associated Conditions in the Japanese Population (2020) (3)
- Full genomic sequence of the novel HLA‐C*14:132 allele identified using next‐generation sequencing (2022) (3)
- Detection of the HLA‐B*15:01:74 allele, an HLA‐B*15 variant discovered in a Japanese individual (2022) (3)
- Non-association of VEGF genetic polymorphisms in promoter--5' UTR with end-stage renal disease. (2006) (3)
- Response to COVID‐19 vaccine is reduced in patients with inflammatory bowel disease, but improved with additional dose (2022) (3)
- No evidence for linkage between the loci for coagulation factor XIII-A and HLA (1986) (3)
- Implications of HLA diversity among regions for bone marrow donor searches in Japan (2020) (3)
- Genetic polymorphism of the fourth component of human complement in Japanese (1979) (3)
- [Genetic variants of the complement components and HLA-antigens associated in patients with psoriasis vulgaris in Japanese]. (1989) (3)
- P23 - A new HLA-B27 allele found in a healthy Japanese (1996) (3)
- Identification and in silico functional prediction of lineage-specific SNPs distributed in DosR-related proteins and resuscitation-promoting factor proteins of Mycobacterium tuberculosis (2020) (3)
- Importance of HBsAg recognition by HLA molecules as revealed by responsiveness to different hepatitis B vaccines (2021) (3)
- Combining effects of polymorphism of tumor necrosis factor α 5′-flanking region and HLA-DRB1 on radiological progression in patients with rheumatoid arthritis (2009) (3)
- 1169 GENETIC POLYMORPHISM IN IL28B PREDICTS NULL VIROLOGICAL RESPONSE TO PEGYLATED-INTERFERON PLUS RIBAVIRIN THERAPY FOR CHRONIC HEPATITIS C (2010) (3)
- The genetic studies of familial amyloid polyneuropathy in the Arao district of Japan: II. Studies of genetic markers in blood (1984) (3)
- Detection of the novel HLA‐C*06:02:01:62 allele by next‐generation sequencing in a Japanese individual (2022) (3)
- Allotypes of the fourth component of complement in Korean (1992) (3)
- Composition and Structure of Anodic Oxide Film on Iron in Neutral Phosphate Solution (1982) (3)
- Identification of the novel HLA‐B*40:01:02:40 and HLA‐B*40:01:02:41 alleles in a Japanese individual (2022) (2)
- rs2013278 in the multiple immunological-trait susceptibility locus CD28 regulates the production of non-functional splicing isoforms (2022) (2)
- Association of Fc gamma receptor gene polymorphisms in the Japanese patients with systemic lupus erythematosus: Independent contributions from FCGR2B and FCGR3A. (2001) (2)
- Low carnitine palmitoyltransferase1 activity is a risk factor for narcolepsy type 1 and other hypersomnia. (2022) (2)
- Sequence variation in Japanese HLA-DRw8 specificity. (1992) (2)
- Polymorphism of BF, C2, and GLO in Japanese patients with insulin-dependent diabetes mellitus: Confirmation of an increase of BF*FT (2004) (2)
- HLA association with antipyretic analgesics-induced Stevens-Johnson Syndrome / toxic epidermal necrolysis with severe ocular surface complications in japanese patients (2014) (2)
- Power of association test for detecting minor histocompatibility gene causing graft-versus-host disease following bone barrow transplantation (2003) (2)
- Chromosomal localization of the human natural killer cell class I receptor family genes (1996) (2)
- Cw*0103, a new allele encoding for a novel HLA-Cw1 split in the Japanese population. (1998) (2)
- Characterization of intermediate-sized insertions using whole-genome sequencing data and analysis of their functional impact on gene expression (2021) (2)
- Protective association of HLA-DPB1*04:01:01 with acute encephalopathy with biphasic seizures and late reduced diffusion identified by HLA imputation (2022) (2)
- Polo-like kinase 4 and Stromal antigen 3 are not associated with recurrent pregnancy loss caused by embryonic aneuploidy (2020) (2)
- Antigen Society #14 Report (B40 CREG, BW60, BW61, BW41, BW48, B13) (1989) (2)
- Polymorphisms of HLA-A and -B Genes in the Kyrgyz Population (2000) (2)
- Detection of the novel HLA‐A allele, HLA‐A*02:01:01:58, in a Japanese individual (2019) (2)
- Genetic Analysis of Ulcerative Colitis in Japanese Individuals Using Population-specific SNP Array. (2020) (2)
- 1178 GENOME-WIDE ASSOCIATION STUDY IDENTIFIES IL28B ASSOCIATED WITH RESPONSE TO PEGYLATED INTERFERON-ALFA AND RIBAVIRIN THERAPY FOR JAPANESE PATIENTS WITH CHRONIC HEPATITIS C (2010) (2)
- Sequence analysis of two serological variants, HLA-A2K and HLA-A9HH, detected in Japanese (1996) (2)
- Molecular analyses of the possible RNA-binding protein gene located in the human leukocyte antigen (HLA)--DR subregion. (1999) (2)
- Identification of the breakpoints at 1p36.2 and 3p21.3 in an AML(M3) patient who had t(1;3)(p36.2;p21.3) at the third relapse (2002) (2)
- [Association of Fc gamma receptor genes with systemic lupus erythematosus]. (2001) (2)
- Crohn's disease and early exposure to thiopurines are independent risk factors for mosaic chromosomal alterations in patients with inflammatory bowel diseases. (2021) (2)
- Anodic Oxide Thin Films on Iron in Neutral Borate-Boric-Acid Solution with and without Chloride Ion (1982) (2)
- Reply to: "Lack of HIF-2α in limb bud mesenchyme causes a modest and transient delay of endochondral bone development" and "Replication studies in various ethnic populations do not support the association of the HIF-2α SNP rs17039192 with knee osteoarthritis" (2011) (2)
- Family segregation analysis of inheritance of human minor histocompatibility antigen. (1995) (2)
- Impact of accumulative smoking exposure and chronic obstructive pulmonary disease on COVID-19 outcomes: report based on findings from the Japan COVID-19 task force (2022) (2)
- HLA-DRB1 Polymorphism of Balopa Islanders in Papua New Guinea (2003) (2)
- Genome-Wide Association Study Identi fi es TLL 1 Variant Associated With Development of Hepatocellular Carcinoma After Eradication of Hepatitis C Virus Infection (2017) (2)
- Full‐length sequence of a novel HLA‐C*03:03:01 allele, HLA‐C*03:03:01:54 identified in a Japanese individual (2022) (2)
- A rare genetic variant in the cleavage site of prepro-orexin is associated with idiopathic hypersomnia (2022) (2)
- The genotypes of GYPA and GYPB carrying the MNSs antigens are not associated with cerebral malaria (2007) (2)
- Characterization of the novel HLA‐A allele, A*24:02:01:111 in a Japanese individual (2022) (2)
- Y chromosome compound haplotypes with the microsatellite markers DXYS265, DXYS266, and DXYS241 (2001) (2)
- Impact of upper and lower respiratory symptoms on COVID-19 outcomes: a multicenter retrospective cohort study (2022) (2)
- HLA‐B*13:01:01:09, a variant of HLA‐B*13:01:01:01, detected in a Japanese individual (2022) (2)
- Risk factors associated with large clusters of tuberculosis patients determined by whole-genome sequencing in a high-tuberculosis-burden country. (2020) (2)
- Genomic sequencing of the novel HLA‐C*07:02:01:107 allele by next‐generation sequencing in two Japanese individuals (2022) (2)
- Evolution of Catarrhini DPB1 exon 2 under intragenic recombination (2000) (2)
- The HLA‐B*15:02:01:05 allele identified by two next‐generation sequencing methods in a Japanese individual (2022) (2)
- rs9459874 and rs1012656 in CCR6/FGFR1OP confer susceptibility to primary biliary cholangitis (2022) (2)
- Integrated analysis of GWAS and mRNA microarray identified IFN-? and CD40I as the central upstream-regulators in primary biliary cholangitis (2020) (2)
- Identification of the gene variations in human IKKA (1999) (2)
- Discovery of the novel HLA‐B allele, HLA‐B*51:01:01:36 in a Japanese individual (2019) (2)
- Characterization of LILRB3 and LILRA6 allelic variants in the Japanese population (2021) (2)
- Thermal Expansion of the Intermetallic Compound MgNi2 (1974) (1)
- P361 - The linkage disequilibria between TAP1, TAP2 and other HLA loci in japanese. A newly identified mutation of TAP2 and it's association with autoimmune disease (1996) (1)
- DETERMINANTS OF TB RELATED DEATH FROM TUBERCULOSIS PATIENTS IN THE NORTHERN THAILAND (2019) (1)
- Mapping of susceptible variants for cold medicine-related Stevens–Johnson syndrome by whole-genome resequencing (2021) (1)
- HLA-A2 alleles in Northeast-Asian populations (1996) (1)
- Cost-Effectiveness Modeling Study of boceprevir for the treatment of patients with genotype 1 chronic hepatitis C virus infection in Hong Kong (2013) (1)
- Chronic neutropenia associated with C2 and C9 deficiency. (1993) (1)
- A Novel Algorithm from Personal Genome to the Pathogenic Mutant Causing Mitochondrial Cardiomyopathy (2011) (1)
- A new HLA-B27 variant found serologically in a healthy Japanese. (1996) (1)
- National Center Biobank Network (2022) (1)
- Genetic variants of beta-globin gene in Thai malaria patients. (2003) (1)
- In the new year (2011) (1)
- Antigen Society #12 Report (Bw54, Bw55, Bw56 and Bw42) (1989) (1)
- Koreans . and C 4 B 5 with rheumatoid arthritis in Association of complement alleles C 4 AQ 0 (1)
- Independent contribution of HLA-DRB1 and TNFA promoter polymorphisms to the susceptibility to Crohns disease in Japanese (2000) (1)
- 83: The histocompatibility leukocyte antigen (hla) haplotype is associated with the onset of postherpetic neuralgia after herpes zoster (2006) (1)
- Practical guide for managing large-scale human genome data in research (2020) (1)
- Genetic polymorphisms of complement systems in Japanese. (1982) (1)
- P316 - Distribution of HLA-B61 alleles in Northeast-Asian populations and in Spanish Gypsies (1996) (1)
- O761 - Distribution of HLA-A, B, and DRB1 haplotypes in five ethnic groups in northeast asia (1996) (1)
- Two rare MHC haplotypes carrying DR2 in the Japanese population. (1994) (1)
- Genetic polymorphism of properdin factor B (BF) in Chinese patients with two types of diabetes mellitus (1986) (1)
- 1171 IDENTIFICATION OF GENETIC VARIANTS OF THE IL28B ASSOCIATED WITH SPONTANEOUS CLEARANCE OF HEPATITIS C VIRUS IN JAPANESE POPULATION (2010) (1)
- A variant in orexin receptor-2 is associated with self-reported daytime sleepiness in the Japanese population (2022) (1)
- Power of association test for detecting minor histocompatibility gene causing graft-versus-host disease following bone marrow transplantation (2003) (1)
- Strong association between hla-a*02:06 and acetaminophen-related stevens-johnson syndrome with severe mucosal involvements in the Japanese (2014) (1)
- [Gentic study of collagen diseases]. (1999) (1)
- Polymorphisms of HLA-DRB1 and TNF α promorter region in adult patients with severe malaria in Thailand (2000) (1)
- Novel rare variations of the oxytocin receptor (OXTR) gene in autism spectrum disorder individuals (2016) (1)
- Mapping of susceptible variants for cold medicine-related Stevens–Johnson syndrome by whole-genome resequencing (2021) (1)
- MEL1 at 1p36.3 Is Fused to Several Partner Genes Including HOXA9 Located at Different Chromosomal Bands from 3q21.3 in t(1;3)(p36.3;q21.3)-Leukemia. (2007) (1)
- Application of partially double-stranded DNA probes to high-throughput SNPs genotyping. (2008) (1)
- HLA-Linked Complement Markers in Narcolepsy (1988) (1)
- MHC polymorphism and diseases (PP-088) (2010) (1)
- The HLA B17,BfS,C4A6,B1,DR7 and DQw3.2 Supratype Marks an Extensive Chromosomal Segment Shared Between Different Ethnic Group (1989) (1)
- BACTERIAL WGS AND HOST GENOME-WIDE SNP ANALYSIS OF TUBERCULOSIS PATIENTS IN THAILAND (2019) (1)
- Genome-wide copy number variation analysis of hepatitis B infection in a Japanese population (2021) (1)
- HLA-A*02:06 and PTGER3 polymorphism exerts additive effects in cold medicine-related Stevens-Johnson syndrome with severe ocular complications in Japanese and Korean populations (2015) (1)
- Differentiation of N-acetyltransferase 2 (NAT2) rapid and intermediate acetylator based on genotype and urinary assay (2019) (1)
- Looking back, looking forward (2010) (1)
- HLA class I genes associated with Cold Medicine related Stevens-Johnson Syndrome with Severe Ocular Complications in the Brazilian population. (2016) (1)
- Sequence-based typing of HLA-A2 alleles (1994) (1)
- High resolution HLA-DRB1 typing by the combination of group-specific amplification and RFLP (1994) (1)
- Development of an assay system for large scale analysis of HLA class II-binding peptides. (2017) (1)
- CD14 and IL18 gene polymorphisms associated with colorectal cancer subsite risks among atomic bomb survivors (2015) (1)
- 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 (2022) (0)
- HLA-DQB1 and -DPB1 allele typing by PCR-PHFA method (1996) (0)
- HLA-DQ dimer formation pattern and its possible contribution to the sleep disorder narcolepsy (93.23) (2007) (0)
- P315 - HLA genes and haplotypes in Khalha-Mongolians (1996) (0)
- 39-OR: Trans dimer formation of HLA-DQ – combinations of DQA1 and DQB1 alleles that form stable dimers (2008) (0)
- Narcolepsy and Hypersomnia: Immunogenetic Aspects of Narcolepsy—Past, Present, and Future (2006) (0)
- Combining effects of polymorphism of tumor necrosis factor α 5′-flanking region and HLA-DRB1 on radiological progression in patients with rheumatoid arthritis (2009) (0)
- O883 - Relation between transfusion-associated graft-versus-host disease (TA-GVHD) and HLA (1996) (0)
- [Progress of DNA based HLA typing methods]. (1996) (0)
- Letters and Replies (2006) (0)
- Diversity of genome in HLA gene group and ABO blood type gene. (1998) (0)
- Identification of risk factors for HBV-derived HCC using HLA-DPB1 genotype and HBV peptides for genome medicine (2022) (0)
- Measurement of MHC-peptide interaction through cell-surface expression and stability assay improves screening of potential CD4+ T-cell epitopes (2019) (0)
- Association of HLA class I and II gene polymorphisms with acetaminophen-related Stevens–Johnson syndrome with severe ocular complications in Japanese individuals (2019) (0)
- Tu1762 – Genetic Background of Thiopurine-Induced Pancreatitis in Japanese Patients with Inflammatory Bowel Disease (2019) (0)
- P258 Evaluation of high-resolution HLA typing of Japanese samples using NXType™ NGS HLA typing kit (2017) (0)
- Japanese population does not manifest significant association between low NK activity and HLA-B(C) locus homozygosity. (1997) (0)
- POLYMICROBIAL BIOFILM FORMATION AS A POSSIBLE CAUSE OF UNEXPECTED DEFAULTED TREATMENT OF PULMONARY TUBERCULOSIS (2018) (0)
- Analysis of HLA-DR protein and peptide interaction in association to type 1 diabetes in Japanese. (P5071) (2013) (0)
- General Contribution (1991) (0)
- Genome-wide association study of self-reported food reactions in Japanese identifies shrimp and peach specific loci in the HLA-DR/DQ gene region (2018) (0)
- 1 IFNGR 1 polymorphisms in Thai malaria patients (2010) (0)
- Initial Movements of Modern Humans in East Eurasia (2017) (0)
- A Subgroup Analysis of Genome-wide Association Study for Panic Disorder (2017) (0)
- Genome-wide association study identifies a PSMD3 variant associated with neutropenia in interferon-based therapy for chronic hepatitis C (2014) (0)
- An Integrated Genomic and Transcriptomic Analysis Reveals Candidates of Susceptibility Genes for Crohn’s Disease in Japanese Populations (2020) (0)
- Subject Index Vol. 77, 1999 (1999) (0)
- HLA antigen Cw7 in the Japanese population. (1981) (0)
- P421 - HLA heterogeneity in juvenile rheumatoid arthritis (1996) (0)
- A case of hyperphosphatemic familial tumoral calcinosis due to maternal uniparental disomy of a GALNT3 variant (2023) (0)
- Restriction fragment length polymorphism of complement C4 in Japanese patients with rheumatoid arthritis and normal Japanese. (1990) (0)
- Heterogeneity of Taiwan's indigenous (2000) (0)
- HLA-DRB 1 gene polymorphism in the Kyrgyz population (2001) (0)
- Deficiency in Cromer Blood Group Inab Phenotype Molecular Cloning and Characterization of Decay-Accelerating Factor (2010) (0)
- Genome-wide haplotype association analysis of primary biliary cholangitis risk in Japanese (2018) (0)
- A genetic variant in CRAT is associated with HLA-DQB1*06 : 02 negative essential hypersomnia (2017) (0)
- A 12-kb structural variation in progressive myoclonic epilepsy was newly identified by long-read whole-genome sequencing (2019) (0)
- Association ofcomplement alleles C4AQO and C4B5withrheumatoid arthritis inKoreans (1996) (0)
- New year wishes and updates (2013) (0)
- O-301 Genome-wide association study identified meiotic variant associated with aneuploid pregnancy loss (2022) (0)
- A new HLA-AG allele lacking BW4 epitope (1994) (0)
- Farewell Editorial (2020) (0)
- Principal contribution of HLA-DQ alleles, DQB1*06:04 and DQB1*03:01, to disease resistance against primary biliary cholangitis in a Japanese population (2017) (0)
- 4-OR: HLA-DQ trans α/β heterodimer formation and stability for disease association studies (2009) (0)
- Cathepsin Z variants are associated with progression to end-stage hepatic failure in Japanese patients with primary biliary cholangitis (2017) (0)
- THU-025-Pathway-analysis using datasets of GWAS and microarray identified IFNG as the most significant upstream-regulator in primary biliary cholangitis (2019) (0)
- MGeND: an integrated database for Japanese clinical and genomic information (2019) (0)
- A 15-YEAR SPATIOTEMPORAL ANALYSIS OF MYCOBACTERIUM TUBERCULOSIS LINEAGES 1 AND 2 IN CHIANG RAI, THAILAND (2019) (0)
- Haplotype analysis of the linkage group HLA-A:HLA-B:C4 in Japanese: Evidence for the C4 locus being between the HLA-A and HLA-B loci (1980) (0)
- O214 - A nested-PCR-RFLP method for high-resolution typing of HLA-B locus alleles (1996) (0)
- Analysis of HLA genes and haplotypes covering a 3Mb genome region supports the premise that Ainu are descendants of Upper Paleolithic populations of East Asia (2000) (0)
- P545 - New HLA-DRB1 alleles found in Japan (1996) (0)
- Mutation and Polymorphism Report (2000) (0)
- A Proposal of BGWAS (Bigenome-Wide Association Study)-Combined analysis of nuclear GWAS and mitochondrial haplogroup for metabolic syndrome and heart failure- (2013) (0)
- Crystal structure of LIR1.01, one of the alleles of LIR1 (2005) (0)
- Scientific Summaries for Families with ASD (2016) (0)
- Analysis of whole Y-chromosome sequences reveals the Japanese population history in the Jomon period (2019) (0)
- Genome-wide copy number variation analysis of hepatitis B infection in a Japanese population (2021) (0)
- Rheumatoid arthritis susceptibility HLA-DR4 alleles in Koreans (1992) (0)
- Composition and Structure of Corrosion Products Formed on Copper in Phosphate Solution (1982) (0)
- CZ single crystal doped with Ga, and Wafer and process for producing same (2000) (0)
- The NBDC-DDBJ imputation server facilitates the use of controlled access reference panel datasets in Japan (2022) (0)
- HLA class II (HLA-DQ) protein stability profile and disease association (100.23) (2011) (0)
- A magneto-optical recording medium (1992) (0)
- Applications of HLA gene polymorphisms (2014) (0)
- Development of a novel microarray data analysis tool without normalization for genotyping degraded forensic DNA. (2023) (0)
- FLT3 Is Fused to ETV6 in a Myeloproliferative Disorder with a t(12;13)(p13;q12) Translocation. (2004) (0)
- A common variant rs2054564 in ADAMST17 is associated with susceptibility to lumbar spondylosis (2023) (0)
- Risk for Prison-to-Community Tuberculosis Transmission, Thailand, 2017–2020 (2023) (0)
- Corrosion Products on Copper in Borate-Boric-Acid Solution (1982) (0)
- Antiferromagnetism of CuF 2 .2H 2 O (1958) (0)
- Urinary L-Type Fatty Acid-Binding Protein Predicts Oxygen Demand of COVID-19 in Initially Mild Cases (2023) (0)
- Exploring the genetic diversity of the Japanese Population: Insights from a Large-Scale Whole Genome Sequencing Analysis (2023) (0)
- Thin Oxide Film on Stainless Steel in 30% Nitric Acid Solution (1983) (0)
- Genome-Wide Association Study and Transcriptome of Japanese Patients with Developmental Dysplasia of the Hip Demonstrates an Association with the Ferroptosis Signaling Pathway (2023) (0)
- The genetic polymorphism of complement component C81 (alpha-gamma) in two Chinese populations. (1988) (0)
- Evidence for Host-Bacterial Co-evolution via Genome Sequence Analysis of 480 Thai Mycobacterium tuberculosis Lineage 1 Isolates (2018) (0)
- Human genetic research, race, ethnicity and the labeling of populations: recommendations based on an interdisciplinary workshop in Japan (2014) (0)
- A variant at 9q34.11 is associated with HLA-DQB1*06:02 negative essential hypersomnia (2018) (0)
- A process for producing a magnetic recording medium (1995) (0)
- The KANNO blood group system (2022) (0)
- Host Genetic Analysis of Pulmonary NTM Disease and Non-CF Bronchietasis (2020) (0)
- Corrigendum to ‘An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs’ [J Hepatol 2021;75(3):572–581] (2021) (0)
- Infectious Diseases and Humans: From Human Genomics Viewpoints (2021) (0)
- Diagnostic significance of secondary bacteremia in patients with COVID-19 (2023) (0)
- Sensitivity to gene dosage and gene expression affects genes with copy number variants observed among neuropsychiatric diseases (2020) (0)
- Use of the neutrophil-to-lymphocyte ratio and an oxygen requirement to predict disease severity in patients with COVID-19 (2023) (0)
- Fe7C3-containing particles and processes for their preparation. (1987) (0)
- Impact of respiratory bacterial infections on mortality in Japanese patients with COVID-19: a retrospective cohort study (2023) (0)
- Design and implementation of a hybrid cloud system for large-scale human genomic research (2023) (0)
- Comparing direct-to-consumer genetic testing services in English, Japanese, and Chinese websites (2023) (0)
- POGLUT1, the putative effector gene driven by rs2293370 in primary biliary cholangitis susceptibility locus chromosome 3q13.33 (2019) (0)
- The Genetic Basis of Sleep and Sleep Disorders: HLA and narcolepsy (2013) (0)
- Large-scale routine HLA-DRB1 allele typing using PCR-MPH and PCR-SSCP methods (1996) (0)
- Increased expression and altered localization of cathepsin Z are associated with progression to jaundice stage in primary biliary cholangitis (2018) (0)
- NELFCD and CTSZ loci are associated with jaundice-stage progression in primary biliary cholangitis in the Japanese population (2018) (0)
- Corrigendum to: "An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs" [J Hepatol 75 (2021) 572-581]. (2023) (0)
- HLA-VBSeq v2: improved HLA calling accuracy with full-length Japanese class-I panel (2019) (0)
- Multi-population genome-wide association study implicates immune and non-immune factors in pediatric steroid-sensitive nephrotic syndrome (2023) (0)
- [Human genome research and bioethics]. (2005) (0)
- Session I: Allergy and Genes Lack of primary association between transporter associated with antigen processing genes and atopic dermatitis (1995) (0)
- Letter from the new Editor-in-Chief (2007) (0)
- A new sister journal to the Journal of Human Genetics—for the interest and benefit of the global community of human genome researchers (2014) (0)
- Brief Genetics Report A Polymorphism in the AMPK (cid:1) 2 Subunit Gene Is Associated With Insulin Resistance and Type 2 Diabetes in the Japanese Population (2006) (0)
- The histocompatibility leukocyte antigen (hla) haplotype is associated with the onset of postherpetic neuralgia after herpes zoster: 83. (2006) (0)
- O07 - Two new alleles of HLA-B22 group in Japaneses (1996) (0)
- O07 - Two new alleles of HLA-B22 group in Japaneses (1996) (0)
- HLA class II (HLA-DQ) protein stability profile and disease association (2011) (0)
- [Analysis of susceptibility genes to rheumatic diseases]. (1999) (0)
- Contents Vol. 77, 1999 (1999) (0)
- EVALUATION OF CELL SURFACE EXPRESSION OF THE SEROLOGICALLY UNDETECTABLE HLA-DQA1*"LA" (HLA-DQA1*0107) (2009) (0)
- HLA class II antigens and complement C4 allotypes in korean patients with rheumatoid arthritis (1991) (0)
- Correction to: High-resolution melt analysis enables simple genotyping of complicated polymorphisms of codon 18 rendering the NUDT15 diplotype (2019) (0)
- A variant in orexin receptor-2 is associated with self-reported daytime sleepiness in the Japanese population (2022) (0)
- P15 Analysis of HLA class II, TAP and HLA-DM genes in Japanese patients with atopic dermatitis (1996) (0)
- A new HLA-DR14 allele, DRB1*1427, identified in the Mongolian population. (1997) (0)
- Response: Multifactorial Disease: Glu298asp of Endothelial Nitric Oxide Synthase (2003) (0)
- LBP18: HLA-PEPTIDE BINDING ANALYSIS BY THE CELL-SURFACE EXPRESSINO ASSAY (2015) (0)
- Association of HLA genes with hepatitis B infection in the Japanese population (2016) (0)
- P864 - Analysis of HLA class II, TAP and HLA-DM genes in Japanese patients with atopic dermatitis (1996) (0)
- Prediction Model with HLA-A*33:03 Reveals Number of Days to Develop Liver Cancer from Blood Test (2023) (0)
- The interaction of a single‐nucleotide polymorphism with age on response to interferon‐α and ribavirin therapy in female patients with hepatitis C infection (2014) (0)
- Active role of small non-coding RNAs derived from SINE/B1 retrotransposon during early mouse development (2011) (0)
- 469 ITPA GENE VARIANT PROTECTS AGAINST TREATMENT-INDUCED ANEMIA AND IMPROVES VIRAL CLEARANCE BY PEGYLATED INTERFERON-ALFA AND RIBAVIRIN THERAPY IN CHRONIC HEPATITIS C PATIENTS (2011) (0)
- Molecular genetic analyses of human NKG2C gene deletion. (2003) (0)
- Nomenclature for human complement component C2 (1993) (0)
- A splice acceptor site mutation of the TAP1 gene in HLA class Ideficient patient (1998) (0)
- Analyses on the association of Fcγreceptor family and TNFR2 (TNFRSF1B) polymorphisms with susceptibility to rheumatoid arthritis in Japanese (2002) (0)
- The expected power of genome-wide linkage disequilibrium testing using single nucleotide polymorphism markers for detecting a low-frequency disease variant. (2002) (0)
- The prevalence of 25(OH)D3 in the patients of South China with chronic HBV infection and high 25(OH)D3 related with low HBV DNA viral load (2014) (0)
- P066 Identification of susceptibility gene loci for cold medicine-related stevens-johnson syndrome with severe ocular complications by whole-genome resequencing (2019) (0)
- Human Diversity as Viewed from Human Genome (2014) (0)
- Nucleotide analysis of an HLA-A null allele (1994) (0)
- Farewell: retirement as Editor-in-Chief of the Journal of Human Genetics and launching Human Genome Variation (2014) (0)
- Genetics of narcolepsy (2019) (0)
- A single-nucleotide-polymorphism in the 5′-flanking region of MSX1 gene as a predictive marker candidate for platinum-based therapy of esophageal carcinoma (2022) (0)
- Su1804 GENETIC ANALYSIS OF ULCERATIVE COLITIS IN JAPANESE INDIVIDUALS USING POPULATION-SPECIFIC SNP ARRAY (2020) (0)
- A large scale screening of HLA-class II-binding peptides from HBs and HBc peptide libraries (2016) (0)
- Lack of association of interleukin-10 gene promother polymorphism, -1082g/a, with severe malaria in Thailand (2016) (0)
- Genome-wide pro fi ling of DNA methylation in human cancer cells (2011) (0)
- Study of HLA-B39 alleles in Japanese and the description of a novel B39 allele, B∗3094 (1994) (0)
- Contents Vol. 15, 1998 (1999) (0)
- Genetic Polymorphisms in the Fourth Component of Complement (C4) and in Properdin Factor B (BF) in Japanese Patients with Palmoplantar Pustulosis (1992) (0)
- Human CD72 splicing isoform responsible for resistance to systemic lupus erythematosus regulates serum immunoglobulin level and is localized in endoplasmic reticulum (2012) (0)
- [Analysis of HLA-DR antigens and complement polymorphism in diffuse panbronchiolitis]. (1987) (0)
- Clinical significance of lupus anticoagulant and genome-wide association study in obstetric antiphospholipid syndrome (2016) (0)
- Subject Index Vol. 15, 1998 (1999) (0)
- Genetics of Infectious Diseases (2019) (0)
- MIC-A polymorphism and a MIC-A-MIC-B null haplotype with ~ 100-kb deletion (2000) (0)
- Genetic Polymorphisms of Compleement Systems in Japanese (血液の遺伝標識 ) (1982) (0)
- Blood group antigens and its genetic analysis.3 HLA A trend of the HLA gene polymorphic analysis of HLA genes. (1994) (0)
- Genome-wide association study identified new susceptible genetic variants in HLA class I region for hepatitis B virus-related hepatocellular carcinoma (2018) (0)
- Genome-wide host-pathogen analyses reveal genetic interaction points in tuberculosis disease (2023) (0)
- Correlation between an amino acid sequence of HLA-DRB and the environmental antigens in Japanese rheumatoid arthritis (1992) (0)
- Association of Human Leukocyte Antigen Class 1 genes with Stevens Johnson Syndrome with severe ocular complications in an Indian population (2017) (0)
- DiscerningtheOriginsof theNegritos , FirstSundalandPeople : Deep Divergence and Archaic Admixture (2017) (0)
- Identification of the Genomic Breakpoints at 1p36.3 and 3q21.3 in Five MDS/AML(M4) Patients with t(1;3)(p36;q21) Translocation. GATA2 Mutation May Be Involved in Leukemogenesis. (2004) (0)
- P061 Association of HLA class II genes with response to hepatitis B vaccine in Japanese (2017) (0)
- 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 (2023) (0)
- P33 - The diversity of HLA-C alleles in Japanese and their associations with HLA-B alleles (1996) (0)
- [Development of genome-wide association database]. (2008) (0)
- Farewell Editorial (2020) (0)
- P1167 : Shared disease-susceptibility genes between primary biliary cirrhosis and crohn's disease in the Japanese population (2015) (0)
- Histamine and anaphylatoxin(C3a) levels in concentrated red cells(CRC) and red cell concentrates with MAP solution(RC-MAP). (1994) (0)
- Identification of the functional variant driving ORMDL3 and GSDMB expression in human chromosome 17q12-21 in primary biliary cholangitis (2017) (0)
- P052 A novel algorithm for KIR copy number imputation by KIBAG and consolidation of population specific KIR references in HKimpNet (HLA & KIR imputation network) (2019) (0)
- Genome-Wide Association Study for Chronic Hepatitis B Infection in the Thai Population (2022) (0)
- Association of HLA-DPB1 alleles with chronic hepatitis B infection in the Japanese population (2015) (0)
- [Anthropological genetics of HLA]. (1996) (0)
- Activation of Nuclear Factor KappaB in ETV6/FLT3-Transformed Ba/F3 Cells Depends on the FLT3 Tyrosine 591. (2007) (0)
- Polo-like kinase 4 and Stromal antigen 3 are not associated with recurrent pregnancy loss caused by embryonic aneuploidy (2020) (0)
- Molecular Genetic Analysis of Variant Phenotypes of the A B 0 Blood Group System (2002) (0)
- P561 - A comprehensive study on HLA class I and class II alleles in Japanese (1996) (0)
- Human genetics of HLA. (1996) (0)
- Crystal structure of LIR1.02, one of the alleles of LIR1 (2004) (0)
- P157 THE ASSOCIATION STUDY BETWEEN HLA GENOTYPE AND MUCOSAL MICROBIAL COMPOSITION IN PATIENTS WITH INFLAMMATORY BOWEL DISEASES (2019) (0)
- 018 HIF2A/NF-kB SIGNAL IN CHONDROCYTES CONTROLS EXTENSIVE STEPS OF OSTEOARTHRITIS DEVELOPMENT IN MICE AND HUMANS (2010) (0)
- A rare genetic variant in the cleavage site of prepro-orexin is associated with idiopathic hypersomnia (2022) (0)
- Human primary biliary cirrhosis-susceptible allele of rs4979462 enhances TNFSF15 expression by binding NF-1 (2015) (0)
- Association of IFNGR2 gene polymorphisms with pulmonary tuberculosis among the Vietnamese (2011) (0)
- Epigenome-wide association study of DNA methylation in panic disorder (2017) (0)
- Evolution of HLA class II through diversification in protein stability levels (P5009) (2013) (0)
- Genome-wide association study of idiopathic hypersomnia in a Japanese population (2021) (0)
- PS-050-Integrated analyses of both human and HBV genome to predict HCC Development (2019) (0)
- Identification of a two-SNP PLA2R1 Haplotype and HLA-DRB1 Alleles as Primary Risk Associations in Idiopathic Membranous Nephropathy (2018) (0)
- PREDICTION OF RESPONSE TO PEGYLATED-INTERFERON FOR CHRONIC HEPATITIS C: IMPACT OF SNPS NEAR THE IL28B GENE AND MUTATIONS IN THE ISDR OF HCV REVEALED BY DATA MINING ANALYSIS (2010) (0)
- Polymorphisms of HLA Genes in Western Javanese (Indonesia) and Their Association to Tuberculosis (2010) (0)
- [Progress in the study of allergy and collagen disease in the last 100 years: Major histocompatibility complex]. (2002) (0)
- Letter to the Editors (2004) (0)
- An epigenome-wide methylation study of healthy individuals with or without depressive symptoms (2018) (0)
- HLA-DQ trans heterodimer association to type 1 diabetes in East Asian population (123.15) (2012) (0)
- High resolution DNA typing of HLA-DRB1 gene using PCR-microtiter-plate hybridization (PCR-MPH) and PCR-preferential homoduplex formation assay (PCR-PHFA) (1994) (0)
- MHC Gene Arrangements on Disease Associated Supratypes Revealed by Pulsed Field Gel Electrophoresis (1989) (0)
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What Schools Are Affiliated With Katsushi Tokunaga?
Katsushi Tokunaga is affiliated with the following schools:
