Item Type | Name |
Concept
|
Chromosomes, Human, Pair 11
|
Concept
|
Chromosomes, Human, Pair 2
|
Concept
|
Chromosomes, Human, Pair 6
|
Concept
|
Chromosomes, Human, Pair 8
|
Concept
|
Chromosomes, Human, Pair 1
|
Concept
|
Chromosomes, Human, Pair 15
|
Concept
|
Chromosomes, Human, Pair 21
|
Concept
|
Chromosomes, Human, Pair 3
|
Concept
|
Chromosomes, Human, Pair 12
|
Concept
|
Chromosomes, Human, Pair 14
|
Concept
|
Chromosomes, Human, Pair 13
|
Concept
|
Chromosomes, Human, Pair 22
|
Concept
|
Chromosomes, Human, Pair 4
|
Concept
|
Chromosomes, Human, Pair 5
|
Concept
|
Chromosomes, Human, Pair 7
|
Concept
|
Chromosomes, Human, Pair 20
|
Concept
|
Chromosomes, Human, Pair 10
|
Concept
|
Chromosomes, Human, Pair 17
|
Concept
|
Chromosomes, Human, Pair 19
|
Concept
|
Chromosomes, Human, Pair 9
|
Concept
|
Chromosomes, Human
|
Concept
|
Chromosomes, Human, Pair 16
|
Concept
|
Chromosomes, Human, Pair 18
|
Concept
|
Chromosomes, Human, X
|
Academic Article
|
A physical and genetic linkage map of the distal long arm of human chromosome 5.
|
Academic Article
|
Association analysis of genetic variants in IL23R, ATG16L1 and 5p13.1 loci with Crohn's disease in Japanese patients.
|
Academic Article
|
Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21.
|
Academic Article
|
A genome-wide association study identifies four susceptibility loci for keloid in the Japanese population.
|
Academic Article
|
Association of a novel long non-coding RNA in 8q24 with prostate cancer susceptibility.
|
Academic Article
|
A genome-wide association study reveals susceptibility variants for non-small cell lung cancer in the Korean population.
|
Academic Article
|
Genome-wide associations and functional genomic studies of musculoskeletal adverse events in women receiving aromatase inhibitors.
|
Academic Article
|
Common variants on 14q32 and 13q12 are associated with DLBCL susceptibility.
|
Academic Article
|
SNPs on chromosome 5p15.3 associated with myocardial infarction in Japanese population.
|
Academic Article
|
Common variants at 11q12, 10q26 and 3p11.2 are associated with prostate cancer susceptibility in Japanese.
|
Academic Article
|
A genome-wide association study identifies three loci associated with susceptibility to uterine fibroids.
|
Academic Article
|
Genome-wide association meta-analysis identifies new endometriosis risk loci.
|
Academic Article
|
Genome-wide association study identifies two susceptibility loci for exudative age-related macular degeneration in the Japanese population.
|
Academic Article
|
A genome-wide association study of nephrolithiasis in the Japanese population identifies novel susceptible Loci at 5q35.3, 7p14.3, and 13q14.1.
|
Academic Article
|
Functional SNPs in CD244 increase the risk of rheumatoid arthritis in a Japanese population.
|
Academic Article
|
Variation in the DEPDC5 locus is associated with progression to hepatocellular carcinoma in chronic hepatitis C virus carriers.
|
Academic Article
|
Physical localization of 70 polymorphic markers to human chromosome 5 by fluorescence in situ hybridization.
|
Academic Article
|
A genome-wide association study identifies novel susceptibility genetic variation for thyrotoxic hypokalemic periodic paralysis.
|
Academic Article
|
A genome-wide association study in the Japanese population identifies susceptibility loci for type 2 diabetes at UBE2E2 and C2CD4A-C2CD4B.
|
Academic Article
|
Replication analysis of SNPs on 9p21.2 and 19p13.3 with amyotrophic lateral sclerosis in East Asians.
|
Academic Article
|
Common variants in a novel gene, FONG on chromosome 2q33.1 confer risk of osteoporosis in Japanese.
|
Academic Article
|
Common variant near the endothelin receptor type A (EDNRA) gene is associated with intracranial aneurysm risk.
|
Academic Article
|
A genome-wide association study identifies locus at 10q22 associated with clinical outcomes of adjuvant tamoxifen therapy for breast cancer patients in Japanese.
|
Academic Article
|
Prostate cancer genomics, biology, and risk assessment through genome-wide association studies.
|
Academic Article
|
Common variants at CDKAL1 and KLF9 are associated with body mass index in east Asian populations.
|
Academic Article
|
Genome-wide association study identifies five new susceptibility loci for prostate cancer in the Japanese population.
|
Academic Article
|
Genome-wide association study identifies variations in 6p21.3 associated with nevirapine-induced rash.
|
Academic Article
|
Genome-wide association study for intracranial aneurysm in the Japanese population identifies three candidate susceptible loci and a functional genetic variant at EDNRA.
|
Academic Article
|
IRX4 at 5p15 suppresses prostate cancer growth through the interaction with vitamin D receptor, conferring prostate cancer susceptibility.
|
Academic Article
|
Physical and genetic map of 5q31: use of fluorescence in situ hybridization data to identify errors in the CEPH database. Centre d'Etude de Polymorphisme Humain.
|
Academic Article
|
Replication study for the association between four Loci identified by a genome-wide association study on European American subjects with type 1 diabetes and susceptibility to diabetic nephropathy in Japanese subjects with type 2 diabetes.
|
Academic Article
|
Genome-wide association study of white blood cell count in 16,388 African Americans: the continental origins and genetic epidemiology network (COGENT).
|
Academic Article
|
Genome-wide association study identifies three new susceptibility loci for adult asthma in the Japanese population.
|
Academic Article
|
Identification of a significant association of a single nucleotide polymorphism in TNXB with systemic lupus erythematosus in a Japanese population.
|
Academic Article
|
A genome-wide association study identifies three new susceptibility loci for ulcerative colitis in the Japanese population.
|
Academic Article
|
Association study of the polymorphisms on chromosome 12p13 with atherothrombotic stroke in the Japanese population.
|
Academic Article
|
Polymorphic human insulin-responsive glucose-transporter gene on chromosome 17p13.
|
Academic Article
|
A genome-wide association study in the Japanese population confirms 9p21 and 14q23 as susceptibility loci for primary open angle glaucoma.
|
Academic Article
|
Association of allelic loss at 8p22 with poor prognosis among breast cancer cases treated with high-dose adjuvant chemotherapy.
|
Academic Article
|
Correlation of allelic losses and clinicopathological factors in 504 primary breast cancers.
|
Academic Article
|
Single-nucleotide polymorphisms in the class II region of the major histocompatibility complex in Japanese patients with immunoglobulin A nephropathy.
|
Academic Article
|
Identification of 46 novel SNPs in the 130-kb region containing a myocardial infarction susceptibility gene on chromosomal band 6p21.
|
Academic Article
|
Identification of a novel non-coding RNA, MIAT, that confers risk of myocardial infarction.
|
Academic Article
|
Functional SNPs in the lymphotoxin-alpha gene that are associated with susceptibility to myocardial infarction.
|
Academic Article
|
Fine-scale SNP map of an 11-kb genomic region at 22q13.1 containing the galectin-1 gene.
|
Academic Article
|
Association of single-nucleotide polymorphisms in the polymeric immunoglobulin receptor gene with immunoglobulin A nephropathy (IgAN) in Japanese patients.
|
Academic Article
|
Functional haplotypes of PADI4, encoding citrullinating enzyme peptidylarginine deiminase 4, are associated with rheumatoid arthritis.
|
Academic Article
|
A functional single nucleotide polymorphism in mucin 1, at chromosome 1q22, determines susceptibility to diffuse-type gastric cancer.
|
Academic Article
|
An intronic SNP in a RUNX1 binding site of SLC22A4, encoding an organic cation transporter, is associated with rheumatoid arthritis.
|
Academic Article
|
Identification of 45 novel SNPs in the 83-kb region containing peptidylarginine deiminase types 1 and 3 loci on chromosomal band 1p36.13.
|
Academic Article
|
Association of a single-nucleotide polymorphism in the immunoglobulin mu-binding protein 2 gene with immunoglobulin A nephropathy.
|
Academic Article
|
Impact of four loci on serum tamsulosin hydrochloride concentration.
|
Academic Article
|
A genome-wide association study identifies a genetic variant in the SIAH2 locus associated with hormonal receptor-positive breast cancer in Japanese.
|
Academic Article
|
A functional variant in FCRL3, encoding Fc receptor-like 3, is associated with rheumatoid arthritis and several autoimmunities.
|
Academic Article
|
A genomewide linkage analysis of Kawasaki disease: evidence for linkage to chromosome 12.
|
Academic Article
|
ITPKC functional polymorphism associated with Kawasaki disease susceptibility and formation of coronary artery aneurysms.
|
Academic Article
|
TSPYL5 SNPs: association with plasma estradiol concentrations and aromatase expression.
|
Academic Article
|
The human AIRE gene at chromosome 21q22 is a genetic determinant for the predisposition to rheumatoid arthritis in Japanese population.
|
Academic Article
|
Whole-genome-wide association study in the Bulgarian population reveals HHAT as schizophrenia susceptibility gene.
|
Academic Article
|
Functional promoter polymorphism in the TBX21 gene associated with aspirin-induced asthma.
|
Academic Article
|
A replication study for three nephrolithiasis loci at 5q35.3, 7p14.3 and 13q14.1 in the Japanese population.
|
Academic Article
|
High-resolution SNP map in the 55-kb region containing the selectin gene family on chromosome 1q24-q25.
|
Academic Article
|
Tumor suppressive role of a 2.4 Mb 9q33-q34 critical region and DEC1 in esophageal squamous cell carcinoma.
|
Academic Article
|
Association analysis of SLC22A4, SLC22A5 and DLG5 in Japanese patients with Crohn disease.
|
Academic Article
|
Genome-wide association analysis in East Asians identifies breast cancer susceptibility loci at 1q32.1, 5q14.3 and 15q26.1.
|
Academic Article
|
Laser capture microdissection and microarray expression analysis of lung adenocarcinoma reveals tobacco smoking- and prognosis-related molecular profiles.
|
Academic Article
|
Genome-wide association study identified SNP on 15q24 associated with bladder cancer risk in Japanese population.
|
Academic Article
|
High-density SNP map of human ITR, a gene associated with vascular remodeling.
|
Academic Article
|
A functional SNP in CILP, encoding cartilage intermediate layer protein, is associated with susceptibility to lumbar disc disease.
|
Academic Article
|
Genome-wide association study of breast cancer in the Japanese population.
|
Academic Article
|
High-resolution SNP map of ASPN, a susceptibility gene for osteoarthritis.
|
Academic Article
|
hzAnalyzer: detection, quantification, and visualization of contiguous homozygosity in high-density genotyping datasets.
|
Academic Article
|
Single-nucleotide polymorphisms in GALNT8 are associated with the response to interferon therapy for chronic hepatitis C.
|
Academic Article
|
Association between single-nucleotide polymorphisms in selectin genes and immunoglobulin A nephropathy.
|
Academic Article
|
A genome-wide association study identifies PLCL2 and AP3D1-DOT1L-SF3A2 as new susceptibility loci for myocardial infarction in Japanese.
|
Academic Article
|
Variation of gene-based SNPs and linkage disequilibrium patterns in the human genome.
|
Academic Article
|
Identification of PDZK4, a novel human gene with PDZ domains, that is upregulated in synovial sarcomas.
|
Academic Article
|
Heterozygous TGFBR2 mutations in Marfan syndrome.
|
Academic Article
|
Common variants in DVWA on chromosome 3p24.3 are associated with susceptibility to knee osteoarthritis.
|
Academic Article
|
An association study of asthma and related phenotypes with polymorphisms in negative regulator molecules of the TLR signaling pathway.
|
Academic Article
|
Inhibition of experimental intimal thickening in mice lacking a novel G-protein-coupled receptor.
|
Academic Article
|
Genome-wide association study identifies gastric cancer susceptibility loci at 12q24.11-12 and 20q11.21.
|
Academic Article
|
Genome-wide association study of epilepsy in a Japanese population identified an associated region at chromosome 12q24.
|