about
Genes to diseases (G2D) computational method to identify asthma candidate genesConfounding from cryptic relatedness in case-control association studies.Genotyping DNA pools on microarrays: tackling the QTL problem of large samples and large numbers of SNPsMapping the new frontier: complex genetic disorders.The genetics of inflammatory bowel diseaseA comprehensive review of genetic association studiesProspects for admixture mapping of complex traitsGenomewide scans of complex human diseases: true linkage is hard to findA genomic pathway approach to a complex disease: axon guidance and Parkinson diseaseProgress in genetic studies of pain and analgesiaFunctional genetic polymorphisms and female reproductive disorders: Part I: Polycystic ovary syndrome and ovarian responseGenetic implication of a novel thiamine transporter in human hypertension.Genetic structure, self-identified race/ethnicity, and confounding in case-control association studiesA compelling genetic hypothesis for a complex disease: PRODH2/DGCR6 variation leads to schizophrenia susceptibility.Absolute pitch: an approach for identification of genetic and nongenetic componentsAnalysis of Hemicentin-1, hOgg1, and E-selectin single nucleotide polymorphisms in age-related macular degenerationEvidence for gradients of human genetic diversity within and among continentsLogarithm of odds (lods) for linkage in complex inheritanceThe Promises and Pitfalls of GenoeconomicsVoxelwise genome-wide association study (vGWAS)High-throughput variation detection and genotyping using microarraysCoat variation in the domestic dog is governed by variants in three genesA commonly carried allele of the obesity-related FTO gene is associated with reduced brain volume in the healthy elderlyGenetic design and statistical power of nested association mapping in maizeThe TDT and other family-based tests for linkage disequilibrium and associationPLINK: a tool set for whole-genome association and population-based linkage analysesA polymorphism in the norepinephrine transporter gene alters promoter activity and is associated with attention-deficit hyperactivity disorderThe melanocortin-1 receptor gene mediates female-specific mechanisms of analgesia in mice and humansGenetics and occupational asthmaAn Increased Risk of Osteoporosis during Acquired Immunodeficiency SyndromeFeasibility of identifying families for genetic studies of birth defects using the National Health Interview SurveySNP frequency, haplotype structure and linkage disequilibrium in elite maize inbred linesUsing single nucleotide polymorphisms as a means to understanding the pathophysiology of asthmaStudy of human SP-A, SP-B and SP-D loci: allele frequencies, linkage disequilibrium and heterozygosity in different races and ethnic groupsInteractions between genes and environmental factors in asthma and atopy: new developmentsGenetic markers of osteoarticular disorders: facts and hopesRisk for rheumatic disease in relation to ethnicity and admixture.Genome-wide association mapping in Arabidopsis identifies previously known flowering time and pathogen resistance genes.Improved prediction of complex diseases by common genetic markers: state of the art and further perspectivesSex Differences in Kappa Opioid Receptor Function and Their Potential Impact on Addiction
P2860
Q21092184-8D565D06-2C23-4370-A374-00D39D4C55A9Q21092505-36579974-9D14-408B-87DA-12B64D5C1D6AQ21266602-C362FC9D-00F0-48F6-93DA-C036BB6E2A2AQ22065343-9E692AC6-3629-4BF9-BC65-E1BAC21C92B8Q22242040-ADC0F64A-8C56-4DB7-905B-2CB317CB0BF7Q22337119-CB452EAB-FC56-4453-B178-4637A0C6083DQ22337163-AD577871-BD83-4787-8887-E8DEB972C6DCQ22337170-7D44E6BD-4E85-461C-AFC9-238563392699Q24288779-992531EC-2822-463E-AF77-813AD19A94AFQ24289028-35183CF5-B80D-4BBC-805C-7102B00D2382Q24289192-2C0E1010-9D34-4D51-A621-83B01AD294C5Q24336342-E2A037B0-2E0D-474A-A213-3135474C3AB4Q24530649-76B010C9-D002-407D-9928-010DB9185C24Q24534073-7FB37C59-A761-4355-ACD9-A6A6F8657F98Q24538704-D5357DCC-A2A5-4951-A646-F38CB71BDE82Q24544270-8ADF28F7-4793-4541-816A-2051DD4278E1Q24562683-E3F5839B-C737-41B8-B73A-5F7B3881C9B7Q24567938-45BF1E92-5854-4952-9D6D-565E24394125Q24608580-64144D1B-2CC0-4A38-8DB1-857FE92DF0F5Q24616471-27C2CA96-81CE-4015-B519-70EB4E35B803Q24617968-F252AA0C-F5E2-4C46-9161-3DB1E142D22BQ24619255-415C0026-0CBB-4079-90D5-7DF487A3EBBFQ24631142-CC05F695-F2D7-40DD-9889-39BA7356B642Q24649597-F0C74B67-3DEF-40F5-BE11-34B01C35071AQ24675685-0510E657-0254-4461-8381-D1106F6678DEQ24677407-F908F9DA-DFE9-4038-A63E-FC50FEC727C2Q24677816-311C1A1D-42BC-48EE-8A01-01AB6550A77CQ24681114-991FDEA4-8DD9-43BA-816D-084ACA0104ADQ24707080-76F0F93E-F916-4F2E-86BC-BA16A6804A6FQ24791238-6C90DD1E-C214-436F-B409-11D4C5B69331Q24791263-3D02CF5B-E49E-4CC1-8006-CA9900BDA550Q24791809-CD9842AF-8C5C-4A56-98E8-3600B6D7F4AEQ24791962-62DA9304-C037-4A30-AFC6-51A37E4657C5Q24798092-E43069F2-D601-441F-B53F-AE2087C2251AQ24799143-7A3BCA46-C5C3-4F73-961D-7965965C8227Q24805695-89AE9C8B-DCD7-4D68-A3AC-F7569000E9D5Q24806807-7E531A4A-2424-4E2F-8C2C-1B92F45179CCQ24816825-B09E67CF-75A3-497F-9215-55B38054DEDCQ26770167-FA06F46D-45EE-407E-BA1A-D0A56F1E3C34Q26770785-DB8334AD-1F07-445F-9D02-077EF5E5649E
P2860
description
1994 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
1994 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
article publié dans la revue scientifique Science
@fr
artículu científicu espublizáu en 1994
@ast
im September 1994 veröffentlichter wissenschaftlicher Artikel
@de
scientific article (publication date: 30 September 1994)
@en
wetenschappelijk artikel (gepubliceerd op 1994/09/30)
@nl
наукова стаття, опублікована у вересні 1994
@uk
مقالة علمية (نشرت في 30-9-1994)
@ar
name
Genetic dissection of complex traits
@ast
Genetic dissection of complex traits
@en
type
label
Genetic dissection of complex traits
@ast
Genetic dissection of complex traits
@en
prefLabel
Genetic dissection of complex traits
@ast
Genetic dissection of complex traits
@en
P3181
P356
P1433
P1476
Genetic dissection of complex traits
@en
P2093
P304
P3181
P356
10.1126/SCIENCE.8091226
P407
P50
P577
1994-09-30T00:00:00Z