Interpretation of association signals and identification of causal variants from genome-wide association studies
about
Five years of GWAS discoveryThe contribution of genomic research to explaining racial disparities in cardiovascular disease: a systematic reviewClinical review: Genome-wide association studies of skeletal phenotypes: what we have learned and where we are headedDetecting low frequent loss-of-function alleles in genome wide association studies with red hair color as examplePrediction of gene-phenotype associations in humans, mice, and plants using phenologsRisk loci for chronic obstructive pulmonary disease: a genome-wide association study and meta-analysis.Insights into kidney diseases from genome-wide association studies.Ion channels and schizophrenia: a gene set-based analytic approach to GWAS data for biological hypothesis testing.A genome-wide association study of autism incorporating autism diagnostic interview-revised, autism diagnostic observation schedule, and social responsiveness scale.Transcriptome profiling of human ulcerative colitis mucosa reveals altered expression of pathways enriched in genetic susceptibility lociConsistent association of type 2 diabetes risk variants found in europeans in diverse racial and ethnic groups.Gene Set Enrichment Analyses: lessons learned from the heart failure phenotype.Investigation of a genome wide association signal for obesity: synthetic association and haplotype analyses at the melanocortin 4 receptor gene locus.Genome-wide association study SNPs in the human genome diversity project populations: does selection affect unlinked SNPs with shared trait associations?Synthetic associations created by rare variants do not explain most GWAS results.Synthetic associations are unlikely to account for many common disease genome-wide association signalsGenetic variants associated with breast cancer risk for Ashkenazi Jewish women with strong family histories but no identifiable BRCA1/2 mutationPrioritizing candidate disease genes by network-based boosting of genome-wide association data.Comparative linkage meta-analysis reveals regionally-distinct, disparate genetic architectures: application to bipolar disorder and schizophrenia.A hidden two-locus disease association pattern in genome-wide association studiesHaplotype kernel association test as a powerful method to identify chromosomal regions harboring uncommon causal variants.Haplotype analysis improved evidence for candidate genes for intramuscular fat percentage from a genome wide association study of cattle.New loci associated with central cornea thickness include COL5A1, AKAP13 and AVGR8.Principal component analysis characterizes shared pathogenetics from genome-wide association studies.The population genetics of chronic kidney disease: insights from the MYH9-APOL1 locus.Predicting signatures of "synthetic associations" and "natural associations" from empirical patterns of human genetic variation.Simultaneous SNP identification and assessment of allele-specific bias from ChIP-seq dataAssociation of single nucleotide polymorphisms in TCF2 with type 2 diabetes susceptibility in a Han Chinese population.Properties and modeling of GWAS when complex disease risk is due to non-complementing, deleterious mutations in genes of large effect.Resequencing of nicotinic acetylcholine receptor genes and association of common and rare variants with the Fagerström test for nicotine dependence.The use of genomic information to optimize cancer chemotherapyCombined admixture mapping and association analysis identifies a novel blood pressure genetic locus on 5p13: contributions from the CARe consortiumConvergent mechanisms of somatic mutations in polycythemia vera.A robust GWSS method to simultaneously detect rare and common variants for complex disease.The contribution of genetic variants to disease depends on the rulerMapping of the UGT1A locus identifies an uncommon coding variant that affects mRNA expression and protects from bladder cancer.Characterizing linkage disequilibrium and evaluating imputation power of human genomic insertion-deletion polymorphisms.Common and Low Frequency Variants in MERTK Are Independently Associated with Multiple Sclerosis Susceptibility with Discordant Association Dependent upon HLA-DRB1*15:01 Status.Role of cytokines in systemic lupus erythematosus: recent progress from GWAS and sequencing.The impact of genomics on pediatric research and medicine.
P2860
Q24610574-4FC73E8A-33B4-4319-BA7E-FDFB75BE15EBQ26829341-6BBEF05D-A450-4FAC-B4A6-EAFD07D5E4B5Q27014915-4FF8B1A9-BD57-4F7A-A554-5EC19EF3F8AFQ28478185-5DCE92C8-33D2-4572-81B0-C1B1213DE064Q28679989-8D6234AA-C68F-4CF5-9580-652A8624D3A4Q29416987-4131DB58-206A-465E-94C1-B42D559A4DE9Q30248678-C1FFB9C7-FB32-4F89-B081-820F7B602F17Q30457731-CB950E56-BA52-4D61-A3C7-737826A1BBFEQ33161703-B3E2D669-9C8E-411C-B173-66C33CFAC0A3Q33553350-4DB50ADF-00C3-4009-8F13-45B26920AC41Q33701819-268BD05C-F21E-4A0A-8BE3-A17CB8821607Q33733871-570F7961-AB34-4701-9119-8A1C7C6852A8Q33750073-67DEE1E4-DE19-476D-B3E2-24CD6FDE10E6Q33799136-BF256692-B1DD-432B-85A7-08C0EE9193B5Q33803707-5508BAD0-3CF7-41DB-853E-1B8929054561Q33803713-55970498-08FB-4B44-B641-128593719F68Q33811527-8A9D0506-F972-42FA-86AC-7826BE4E7628Q33887815-C972CAA4-3DFF-4816-B377-BD0F6F25A488Q33895253-05E1AF91-FCC1-4CED-BD8C-006901D5208EQ33899172-AEC9D92B-5AEF-486F-BF6E-2AD4FA5424BCQ33976828-EB2E6C44-10A8-408A-9565-A599F1387B87Q34117780-30F8DD6A-2176-4A5A-B877-B3564D035BDAQ34131948-8D08C382-76BC-47DE-9EF7-C6E84F57524EQ34165673-3CB6B6A9-E10A-45B3-8651-95F44FBFBF11Q34182007-CF3E58EE-5ED1-47F1-ABC7-AB13B5F8B6A2Q34335490-F341D675-92DB-4A1C-BD04-B7257D5317BDQ34403959-7AF63CBF-A7B5-44B1-ABEB-B1F0F2C30B97Q34541436-DCADC3D4-BF33-41C6-ADBE-E168F90078B7Q34597952-FF3C9087-ECC5-4DDD-AD03-22A42AA96A5CQ34660514-7CF55A5D-DF1D-4F8F-86B1-D9CC4CFA7B66Q34791981-6FE775F3-E206-4175-927B-1B55B69C0648Q34955495-C3AB466C-6B0D-4826-B475-35F9CDF29277Q35141810-B209D52E-272F-447B-9B88-5C3B28D1F289Q35447555-6E5DE725-3EA0-4F8B-B8F6-AACB61776BF6Q35547325-9F1CA01D-2286-4EB3-9598-A059FC9508CFQ35856276-F500C8F3-A4DF-4EB1-8B9A-9C34FF325FCAQ35907582-B97DA3AA-9954-4CC5-8137-74B1FC724C12Q35962257-43CF3B5B-2E1E-4A6C-804D-D466C1719F6DQ35986928-B1F9F31D-F1BE-4A86-9632-E8B1693D349FQ35996805-0852F6EB-6E09-4C95-BCDC-8345856221A2
P2860
Interpretation of association signals and identification of causal variants from genome-wide association studies
description
2010 nî lūn-bûn
@nan
2010 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Interpretation of association ...... enome-wide association studies
@ast
Interpretation of association ...... enome-wide association studies
@en
type
label
Interpretation of association ...... enome-wide association studies
@ast
Interpretation of association ...... enome-wide association studies
@en
prefLabel
Interpretation of association ...... enome-wide association studies
@ast
Interpretation of association ...... enome-wide association studies
@en
P2093
P2860
P1476
Interpretation of association ...... enome-wide association studies
@en
P2093
Catherine A Stolle
David B Goldstein
Ian D Krantz
Samuel P Dickson
P2860
P304
P356
10.1016/J.AJHG.2010.04.003
P407
P577
2010-04-29T00:00:00Z