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Fulfilling the promise of personalized medicine? Systematic review and field synopsis of pharmacogenetic studiesMetabolic reconstruction for metagenomic data and its application to the human microbiomeNucleotide discrimination with DNA immobilized in the MspA nanoporeAn Environment-Wide Association Study (EWAS) on type 2 diabetes mellitusThe past and future of tuberculosis researchTrait-associated SNPs are more likely to be eQTLs: annotation to enhance discovery from GWASGenetic testing and common disorders in a public health framework: how to assess relevance and possibilities. Background Document to the ESHG recommendations on genetic testing and common disordersGenome-wide association studies: a primerGenotyping sleep disorders patientsWhen Quality Beats Quantity: Decision Theory, Drug Discovery, and the Reproducibility CrisisPersonalized medicine: hope or hype?TNF receptor 1 genetic risk mirrors outcome of anti-TNF therapy in multiple sclerosisGenetic variation in IL28B and spontaneous clearance of hepatitis C virusJoint influence of small-effect genetic variants on human longevityDifferent differences: the use of 'genetic ancestry' versus race in biomedical human genetic researchA novel computational biostatistics approach implies impaired dephosphorylation of growth factor receptors as associated with severity of autism.Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype scoreBiological, clinical and population relevance of 95 loci for blood lipidsThe PhenX Toolkit: get the most from your measuresHundreds of variants clustered in genomic loci and biological pathways affect human heightGenome-wide searching of rare genetic variants in WTCCC dataA weighted false discovery rate control procedure reveals alleles at FOXA2 that influence fasting glucose levelsSystems psychopharmacology: A network approach to developing novel therapiesA conceptual framework for pharmacodynamic genome-wide association studies in pharmacogenomicsThe genetics of major depressionChild development and molecular genetics: 14 years laterPharmacogenetics and anaesthesia: the value of genetic profilingMechanisms of age-related macular degenerationEpistasis and immunity: the role of genetic interactions in autoimmune diseasesGenetic variants at the IFNL3 locus and their association with hepatitis C virus infections reveal novel insights into host-virus interactionsThe Convergence of Systems and Reductionist Approaches in Complex Trait AnalysisA genome-wide genetic screen for host factors required for hepatitis C virus propagationCommon Genetic Variants Found in HLA and KIR Immune Genes in Autism Spectrum DisorderUnderstanding rare and common diseases in the context of human evolutionEpigenetic Inheritance across the LandscapeEnvironment and Genes: What Is the Interaction?Inherited heart disease - what can we expect from the second decade of human iPS cell research?Mutations in LRPAP1 are associated with severe myopia in humansThe Archon Genomics X PRIZE for whole human genome sequencingGetting personalized cancer genome analysis into the clinic: the challenges in bioinformatics
P2860
Q21091172-07C936B9-0415-45E4-8FBC-DE723D6B17FFQ21092513-3BB93590-A45B-45DD-A4A8-AB3803F5CEB5Q21135005-697C34ED-1537-4BBE-A2C3-A2C86DD073B3Q21136362-ABC7867A-D3D8-4D77-96B1-3CBFC8DE7F62Q21559415-A7E62895-5A26-41D1-B029-AF654932C613Q21563317-594ABEE5-BD3D-47CC-AF59-6060DCB6E25FQ22330767-584DF322-A5D3-4DC5-8230-FAF217472436Q24273247-166B17A0-A0E6-4CAA-B9E5-AE1790DC5560Q24273285-7807EC65-E7A7-414A-9C91-EB2212DD00BEQ24288687-0850E540-941C-41E8-9FBD-043C3DCB6C98Q24289193-D55DBF94-F88B-4058-AFA9-CB8FF6BE326FQ24293476-ACF187A6-82DB-404E-8792-B4E5D00110B4Q24596340-09605DF0-AB06-47A6-99F2-E2C991767684Q24602526-C056E653-907A-4D6B-B815-BA51CEF9C1ABQ24604314-F8042DEE-8240-4F8F-89AA-665BF5EC35A2Q24612710-95528AB5-3FDF-4839-A9E0-6458679C1C87Q24621065-35BFA984-416A-4025-9FEE-4F504AA75A7FQ24622541-DA608ADB-9C7D-40DD-947B-505DF923C700Q24630562-5C1D77F4-C66B-4857-BC32-EEDDEEBAD5CAQ24630979-A5B1F3F8-D407-466E-8AE7-97DA229F08D5Q24631272-405DB75B-ED3E-43D2-90FF-141F9F361074Q24632742-6EAFC343-0B2C-4E78-B01E-0783C031001FQ26750901-2149ED39-D404-45B0-B310-9E25B6BA1A8CQ26827814-843BCB44-9A85-4BEA-81F9-D70B594EA8A3Q26830784-262CB42F-48D7-4930-AB66-25249B42A741Q26853446-D9750749-62EA-4FD0-83E4-2A2ABC2278EAQ26859221-7925D6EB-46A8-4463-84A4-7E30D93A5297Q27000182-E5DD1ACE-6F21-484B-8C30-731832E5CBA0Q27010680-BC230DB9-6D31-43D0-8AB5-1A0569F9FC7AQ27014831-D0B45AFA-7BE6-4ADB-90FF-01DC1D64E4DFQ27025585-13805CC9-1E7E-47F6-A464-E7F41F08101FQ27489773-784A08EE-B736-4036-9424-AA88D5CF03D3Q28066081-B646628B-7F75-47E2-B160-D6BCA2F168C8Q28067740-393DA4B1-8D01-4F4E-9FFE-E47586F2EEC2Q28069953-D8A479A4-8E9A-4522-8177-2501334A1708Q28076689-0D0E73DB-E27C-423D-96CA-9E0C5BEF913AQ28079217-2FC91121-E7C6-42E2-B627-FDBC4E130F91Q28294040-EF82608D-B9D0-48E7-95FA-E92DB86A0BA2Q28296848-4855B70C-2D36-4EE5-80EB-357559F85E03Q28394818-12A8B6C9-1763-4356-BD2B-8F095CBF8FCA
P2860
description
2009 nî lūn-bûn
@nan
2009 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Common genetic variation and human traits
@ast
Common genetic variation and human traits
@en
type
label
Common genetic variation and human traits
@ast
Common genetic variation and human traits
@en
prefLabel
Common genetic variation and human traits
@ast
Common genetic variation and human traits
@en
P3181
P356
P1476
Common genetic variation and human traits
@en
P2093
Goldstein DB
P304
P3181
P356
10.1056/NEJMP0806284
P407
P577
2009-04-23T00:00:00Z