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Polymorphisms in the Lymphotoxin Alpha Gene and the Risk of Ischemic Stroke in the Japanese Population.
- Published in:
- Cerebrovascular Diseases, 2008, v. 25, n. 5, p. 417, doi. 10.1159/000121342
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- Article
Plasma Homocyst(e)ine Concentrations and the Risk of Subtypes of Cerebral Infarction.
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- Cerebrovascular Diseases, 2002, v. 13, n. 1, p. 9, doi. 10.1159/000047739
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- Publication type:
- Article
Characteristics of Japanese inflammatory bowel disease susceptibility loci.
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- Journal of Gastroenterology, 2014, v. 49, n. 8, p. 1217, doi. 10.1007/s00535-013-0866-2
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- Article
Genome-wide host-pathogen analyses reveal genetic interaction points in tuberculosis disease.
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- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-36282-w
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- Publication type:
- Article
Genome-wide host-pathogen analyses reveal genetic interaction points in tuberculosis disease.
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- Nature Communications, 2023, v. 14, p. 1, doi. 10.1038/s41467-023-36282-w
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- Publication type:
- Article
Discerning asthma endotypes through comorbidity mapping.
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- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-33628-8
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- Article
Discerning asthma endotypes through comorbidity mapping.
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- Nature Communications, 2022, v. 13, p. 1, doi. 10.1038/s41467-022-33628-8
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- Article
Author Correction: Genetic variants of calcium and vitamin D metabolism in kidney stone disease.
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- 2022
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- Correction Notice
Evaluation of a weighted genetic risk score for the prediction of biomarkers of CYP2A6 activity.
- Published in:
- 2020
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- Publication type:
- journal article
Stepwise iterative maximum likelihood clustering approach.
- Published in:
- BMC Bioinformatics, 2016, v. 17, p. 1, doi. 10.1186/s12859-016-1184-5
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- Publication type:
- Article
Variants encoding a restricted carboxy-terminal domain of SLC12A2 cause hereditary hearing loss in humans.
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- PLoS Genetics, 2020, v. 16, n. 4, p. 1, doi. 10.1371/journal.pgen.1008643
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- Article
Inverse association of IL28B genotype and liver mRNA expression of genes promoting or suppressing antiviral state.
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- Journal of Medical Virology, 2011, v. 83, n. 9, p. 1597, doi. 10.1002/jmv.22158
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- Article
Influence of Genetic Variants in EGF and Other Genes on Hematological Traits in Korean Populations by a Genome-Wide Approach.
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- BioMed Research International, 2015, v. 2015, p. 1, doi. 10.1155/2015/914965
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- Article
PKCη deficiency improves lipid metabolism and atherosclerosis in apolipoprotein E-deficient mice.
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- Genes to Cells, 2016, v. 21, n. 10, p. 1030, doi. 10.1111/gtc.12402
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- Article
Disease susceptibility genes shared by primary biliary cirrhosis and Crohn's disease in the Japanese population.
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- Journal of Human Genetics, 2015, v. 60, n. 9, p. 525, doi. 10.1038/jhg.2015.59
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- Publication type:
- Article
A replication study for three nephrolithiasis loci at 5q35.3, 7p14.3 and 13q14.1 in the Japanese population.
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- Journal of Human Genetics, 2013, v. 58, n. 9, p. 588, doi. 10.1038/jhg.2013.59
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- Publication type:
- Article
Special Section on Pharmacogenomics: recent advances and future directions.
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- Journal of Human Genetics, 2013, v. 58, n. 6, p. 305, doi. 10.1038/jhg.2013.53
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- Publication type:
- Article
Impact of polymorphisms in drug pathway genes on disease-free survival in adults with acute myeloid leukemia.
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- Journal of Human Genetics, 2013, v. 58, n. 6, p. 353, doi. 10.1038/jhg.2013.38
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- Article
Impact of four loci on serum tamsulosin hydrochloride concentration.
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- Journal of Human Genetics, 2013, v. 58, n. 1, p. 21, doi. 10.1038/jhg.2012.126
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- Publication type:
- Article
A genome-wide association study identifies a genetic variant in the SIAH2 locus associated with hormonal receptor-positive breast cancer in Japanese.
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- Journal of Human Genetics, 2012, v. 57, n. 12, p. 766, doi. 10.1038/jhg.2012.108
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- Publication type:
- Article
Genome-wide association studies of tuberculosis in Asians identify distinct at-risk locus for young tuberculosis.
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- Journal of Human Genetics, 2012, v. 57, n. 6, p. 363, doi. 10.1038/jhg.2012.35
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- Publication type:
- Article
Genetic differences in the two main groups of the Japanese population based on autosomal SNPs and haplotypes.
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- Journal of Human Genetics, 2012, v. 57, n. 5, p. 326, doi. 10.1038/jhg.2012.26
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- Publication type:
- Article
A genome-wide association study identifies novel susceptibility genetic variation for thyrotoxic hypokalemic periodic paralysis.
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- Journal of Human Genetics, 2012, v. 57, n. 5, p. 301, doi. 10.1038/jhg.2012.20
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- Publication type:
- Article
A genome-wide association study identifies SNP in DCC is associated with gallbladder cancer in the Japanese population.
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- Journal of Human Genetics, 2012, v. 57, n. 4, p. 235, doi. 10.1038/jhg.2012.9
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- Article
Identification of independent risk loci for Graves' disease within the MHC in the Japanese population.
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- Journal of Human Genetics, 2011, v. 56, n. 11, p. 772, doi. 10.1038/jhg.2011.99
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- Article
Common variants on 14q32 and 13q12 are associated with DLBCL susceptibility.
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- Journal of Human Genetics, 2011, v. 56, n. 6, p. 436, doi. 10.1038/jhg.2011.35
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- Publication type:
- Article
Impact of LIMK1, MMP2 and TNF-α variations for intracranial aneurysm in Japanese population.
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- Journal of Human Genetics, 2011, v. 56, n. 3, p. 211, doi. 10.1038/jhg.2010.169
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- Article
SNPs on chromosome 5p15.3 associated with myocardial infarction in Japanese population.
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- Journal of Human Genetics, 2011, v. 56, n. 1, p. 47, doi. 10.1038/jhg.2010.141
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- Article
Making a haplotype catalog with estimated frequencies based on SNP homozygotes.
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- Journal of Human Genetics, 2010, v. 55, n. 8, p. 500, doi. 10.1038/jhg.2010.56
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- Article
Establishment of a standardized system to perform population structure analyses with limited sample size or with different sets of SNP genotypes.
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- Journal of Human Genetics, 2010, v. 55, n. 8, p. 525, doi. 10.1038/jhg.2010.63
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- Publication type:
- Article
Association study of the polymorphisms on chromosome 12p13 with atherothrombotic stroke in the Japanese population.
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- Journal of Human Genetics, 2010, v. 55, n. 7, p. 473, doi. 10.1038/jhg.2010.45
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- Publication type:
- Article
A genome-wide association study identifies ITGA9 conferring risk of nasopharyngeal carcinoma.
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- Journal of Human Genetics, 2009, v. 54, n. 7, p. 392, doi. 10.1038/jhg.2009.49
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- Article
Case–control association study of 59 candidate genes reveals the DRD2 SNP rs6277 (C957T) as the only susceptibility factor for schizophrenia in the Bulgarian population.
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- Journal of Human Genetics, 2009, v. 54, n. 2, p. 98, doi. 10.1038/jhg.2008.14
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- Article
Identification of a significant association of a single nucleotide polymorphism in TNXB with systemic lupus erythematosus in a Japanese population.
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- Journal of Human Genetics, 2008, v. 53, n. 1, p. 64, doi. 10.1007/s10038-007-0219-1
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- Article
Association analysis of genetic variants in IL23R, ATG16L1 and 5p13.1 loci with Crohn’s disease in Japanese patients.
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- Journal of Human Genetics, 2007, v. 52, n. 7, p. 575, doi. 10.1007/s10038-007-0156-z
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- Article
Prediction of inflammatory bowel diseases by genetic risk score in Asian general populations.
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- Turkish Journal of Gastroenterology, 2019, v. 30, p. S141, doi. 10.5152/tjg.2019.050919
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- Article
Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations.
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- Nature Genetics, 2015, v. 47, n. 9, p. 979, doi. 10.1038/ng.3359
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- Article
Construction of a population-specific HLA imputation reference panel and its application to Graves' disease risk in Japanese.
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- Nature Genetics, 2015, v. 47, n. 7, p. 798, doi. 10.1038/ng.3310
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- Article
High-density genotyping study identifies four new susceptibility loci for atopic dermatitis.
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- Nature Genetics, 2013, v. 45, n. 7, p. 808, doi. 10.1038/ng.2642
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- Article
Genome-wide association study identifies eight new susceptibility loci for atopic dermatitis in the Japanese population.
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- Nature Genetics, 2012, v. 44, n. 11, p. 1222, doi. 10.1038/ng.2438
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- Article
A genome-wide association study identifies two new susceptibility loci for lung adenocarcinoma in the Japanese population.
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- Nature Genetics, 2012, v. 44, n. 8, p. 900, doi. 10.1038/ng.2353
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- Article
Whole-genome sequencing of liver cancers identifies etiological influences on mutation patterns and recurrent mutations in chromatin regulators.
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- Nature Genetics, 2012, v. 44, n. 7, p. 760, doi. 10.1038/ng.2291
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- Article
Common variants at 11q12, 10q26 and 3p11.2 are associated with prostate cancer susceptibility in Japanese.
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- Nature Genetics, 2012, v. 44, n. 4, p. 426, doi. 10.1038/ng.1104
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- Publication type:
- Article
A genome-wide association study identifies two susceptibility loci for duodenal ulcer in the Japanese population.
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- Nature Genetics, 2012, v. 44, n. 4, p. 430, doi. 10.1038/ng.1109
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- Publication type:
- Article
Common variants at CDKAL1 and KLF9 are associated with body mass index in east Asian populations.
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- Nature Genetics, 2012, v. 44, n. 3, p. 302, doi. 10.1038/ng.1086
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- Publication type:
- Article
Large-scale genome-wide association studies in east Asians identify new genetic loci influencing metabolic traits.
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- Nature Genetics, 2011, v. 43, n. 10, p. 990, doi. 10.1038/ng.939
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- Publication type:
- Article
Genome-wide association study identifies two susceptibility loci for exudative age-related macular degeneration in the Japanese population.
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- Nature Genetics, 2011, v. 43, n. 10, p. 1001, doi. 10.1038/ng.938
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- Article
Genome-wide association study identifies three new susceptibility loci for adult asthma in the Japanese population.
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- Nature Genetics, 2011, v. 43, n. 9, p. 893, doi. 10.1038/ng.887
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- Article
Variation in the DEPDC5 locus is associated with progression to hepatocellular carcinoma in chronic hepatitis C virus carriers.
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- Nature Genetics, 2011, v. 43, n. 8, p. 797, doi. 10.1038/ng.876
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- Publication type:
- Article
A genome-wide association study identifies three loci associated with susceptibility to uterine fibroids.
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- Nature Genetics, 2011, v. 43, n. 5, p. 447, doi. 10.1038/ng.805
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- Publication type:
- Article