Genome-wide association studies for common diseases and complex traits
about
The diploid genome sequence of an individual humanHippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's diseaseGenomic hotspots for adaptation: the population genetics of Müllerian mimicry in the Heliconius melpomene cladeGenome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart StudyGene-disease network analysis reveals functional modules in mendelian, complex and environmental diseasesAn Environment-Wide Association Study (EWAS) on type 2 diabetes mellitusForty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysisGenetic variation in an individual human exomeChapter 11: Genome-wide association studiesGenetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham StudyMapping the new frontier: complex genetic disorders.Workgroup report: implementing a national occupational reproductive research agenda--decade one and beyondAssociation claims in the sequencing eraFine mapping versus replication in whole-genome association studiesA Bayesian measure of the probability of false discovery in genetic epidemiology studiesHigh-resolution whole-genome association study of Parkinson disease.Handling marker-marker linkage disequilibrium: pedigree analysis with clustered markersIdentification of four gene variants associated with myocardial infarction.Replication of putative candidate-gene associations with rheumatoid arthritis in >4,000 samples from North America and Sweden: association of susceptibility with PTPN22, CTLA4, and PADI4Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controlsMalaCards: an integrated compendium for diseases and their annotationLarge-scale candidate gene analysis of spontaneous clearance of hepatitis C virusBreast cancer in the personal genomics eraGenome-wide association study of antibody response to smallpox vaccineA large-scale replication study identifies TNIP1, PRDM1, JAZF1, UHRF1BP1 and IL10 as risk loci for systemic lupus erythematosusIdentification of Cd101 as a susceptibility gene for Novosphingobium aromaticivorans-induced liver autoimmunityMaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypesKEGG for representation and analysis of molecular networks involving diseases and drugsIL23R variation determines susceptibility but not disease phenotype in inflammatory bowel diseaseFine mapping of new glaucoma locus GLC1M and exclusion of neuregulin 2 as the causative geneThe human GIMAP5 gene has a common polyadenylation polymorphism increasing risk to systemic lupus erythematosusAfrican Americans with asthma: genetic insightsGenetic design and statistical power of nested association mapping in maizeRevealing the architecture of gene regulation: the promise of eQTL studiesGlobal variation in copy number in the human genomePLINK: a tool set for whole-genome association and population-based linkage analysesThe human disease networkA large-scale genetic association study confirms IL12B and leads to the identification of IL23R as psoriasis-risk genesRapid evolution of major histocompatibility complex class I genes in primates generates new disease alleles in humans via hitchhiking diversityPerspectives on human genetic variation from the HapMap Project.
P2860
Q21090194-BAB86750-28D8-48CF-8AF6-2D8896819D96Q21091189-7C693D2E-2B8B-4ED4-BCE6-2B987BAF19F2Q21092449-05E1A4CE-1804-46E5-824B-3E61EF7D16C2Q21093317-A43D8882-DB0D-47DC-9224-6A65D88F502DQ21135363-4E39D374-1949-4DF8-BFE8-FE4CCEEEACAFQ21136362-E4C5A4CE-E159-4A56-8CC8-0E403484FBBDQ21144992-E1ACFDEC-535C-4046-9C0B-B90DE5A604F4Q21145035-190A5BAC-ADAE-45D5-836B-A8E7C0B83AC2Q21145310-1B956BE2-A82E-4674-85AE-98583F7D7388Q21261434-017D2530-8DFD-44BA-A51B-B57BC8A7C1FBQ22065343-F35362F5-BB3A-4E22-82EA-20CA9860040EQ23911095-7999B712-EA24-442F-85C4-067CA981D25BQ24273315-2E336EE2-514A-4EA3-90DC-A2F9A9358178Q24289225-0562CF8E-BE61-4F74-9A72-76F90E802D2EQ24289227-A653F641-12FA-4797-B0B4-080CFBB8757BQ24535861-D351A93D-2685-4623-9864-2F5850B343CBQ24535870-C5D7FA28-3FBA-4F6D-85CF-82164A287343Q24536320-832E68F4-26CE-425A-A9F6-FA3DF0425D4FQ24538382-3CA0A3B9-D188-4DB7-9F39-7FD9507707F6Q24550675-96CB3F5F-71A4-421C-A833-4AFD2EE0C53EQ24570119-19452189-5B5A-47F0-B23E-8D881B194257Q24596652-F3AA45FF-21AA-4969-978C-99A4E85ED375Q24602679-113A6101-BFC5-40F3-BFAB-FCDAB39CF2F2Q24612100-1F2ED0EF-584E-47FD-B417-75276F3AC0BBQ24629130-29C51863-C478-4E98-9A62-3BF6D4E2EA7DQ24633643-F2E949DC-D674-4B68-AB10-D3943734CCC6Q24635938-B34E02D2-9148-4102-8817-DA9E671B9FE4Q24644514-7F9C8672-71EE-4E93-8DAF-AD5D8C8F5A72Q24645890-D5DF7FB6-1031-4D07-A544-8F4B93F98888Q24647614-EB637DD4-FA5F-4382-8024-C3C33F7FE2B4Q24648171-7B13F573-94F8-4C96-9BEF-D972F940696CQ24648561-CF124C42-8729-4D5C-9CCA-4A69C4834536Q24649597-BDF3D552-46CA-4110-8429-00F53A0F6EC1Q24657564-33CFF765-E671-4842-AF0E-5158DB6DDD67Q24658083-3DD68B66-50A8-4ACC-9BD0-2A2F25D73214Q24677407-CEEACA0B-67ED-48B4-B09B-5A48334C87DEQ24678240-BC5589A7-265D-4373-B83E-3A5399FC01A1Q24680489-602A13B4-C35E-4D68-A504-C3F64069530DQ24684291-A0956111-7E63-497A-B666-3650C0BBBFE3Q24810962-6FC13C62-9331-4946-BF8A-EB62A5E7B891
P2860
Genome-wide association studies for common diseases and complex traits
description
2005 nî lūn-bûn
@nan
2005 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
Genome-wide association studies for common diseases and complex traits
@ast
Genome-wide association studies for common diseases and complex traits
@en
type
label
Genome-wide association studies for common diseases and complex traits
@ast
Genome-wide association studies for common diseases and complex traits
@en
prefLabel
Genome-wide association studies for common diseases and complex traits
@ast
Genome-wide association studies for common diseases and complex traits
@en
P2860
P3181
P356
P1476
Genome-wide association studies for common diseases and complex traits
@en
P2093
Hirschhorn JN
P2860
P2888
P304
P3181
P356
10.1038/NRG1521
P407
P577
2005-02-01T00:00:00Z
P5875
P6179
1022754728