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1 all 12 SNPs were confirmed in an independent replication study.
2 consideration to whether it is a de novo or replication study.
3 risons between NC1 and the autism group as a replication study.
4 a meta-analysis with a published GWAS and a replication study.
5 spectively) but not to cephalosporins in the replication study.
6 ant predictor of the P-value in a subsequent replication study.
7 hese experiments will then be published in a Replication Study.
8 with the risk of clinical CAD in this large replication study.
9 y identified, and 5 SNPs were later found in replication studies.
10 Two additional cohorts were used for replication studies.
11 the initial GWAS were not associated in the replication studies.
12 tiology of NHL, and should be prioritized in replication studies.
13 that variant and facilitate the planning of replication studies.
14 esting additional variants is commonplace in replication studies.
15 novel risk loci that require confirmation by replication studies.
16 ary in the absence of converging evidence or replication studies.
17 DCYAP1R1 were genotyped in our study and six replication studies.
18 diseases, often with inconsistent results in replication studies.
19 mbined meta-analysis of all 22 discovery and replication studies.
20 associated overall and in 3 of 5 individual replication studies.
21 identify SNPs that can be pursued in future replication studies.
22 (cases) and 3,182 controls), an independent replication study (1,440 cases and 1,316 controls) and a
23 N22 (discovery-study allelic P=6.6 x 10(-4); replication-study allelic P=5.6 x 10(-8)), which encodes
26 sis for the design and interpretation of GWA replication studies and point to the importance of a cle
27 egrative summary, we review various types of replication studies and then discuss the most commonly v
29 such two-stage data is to view stage 2 as a replication study and focus on findings that reach stati
30 rried out a genome-wide association scan and replication study and found an association between SLE a
31 rried out a genome-wide association scan and replication study and found an association between SLE a
34 t GTF2I by heterogeneity mapping followed by replication studies, and pinpointed a possible causal va
35 he presence of real effects in a low-powered replication study, and instances of such association inc
36 al white populations were used for follow-up replication studies: another independent cohort of CAD-
44 only tentative evidence of association, and replication studies are required to establish their vali
48 atio of sample sizes between the initial and replication studies, but not on the underlying effect si
57 alysis of primary results was performed with replication studies containing 12 174 heavy and 11 290 l
60 , we report the results of a discovery and a replication study, each involving a double-blind, placeb
62 tients and 400 controls from the U.S. and in replication studies for 308 POAG patients and 178 contro
63 covalently bonded, and carried out in vitro replication studies for the lesion-bearing substrate wit
65 op prediction intervals for the P-value in a replication study given the P-value observed in an initi
68 e association studies (GWAS) and large-scale replication studies have identified common variants in 7
74 in the Pune Maternal Nutrition Study (PMNS), replication studies in 3418 individuals from other India
75 which was followed by in silico and de novo replication studies in 37,691 and 17,642 additional east
79 -wide genotyping of the European cohorts and replication studies in the Japanese cohort identified co
80 thnically matched controls, and we performed replication studies in two independent European cohorts.
84 subsequent transmission disequilibrium test replication study in an independent cohort confirmed the
87 69 individuals to 293,723 individuals, and a replication study in an independent sample of 111,349 in
91 osis household contact study in France and a replication study in families from South Africa to confi
95 of lipid levels in 8344 subjects followed by replication studies including 14 739 additional individu
96 hypertension in 11 816 subjects followed by replication studies including 69 146 additional individu
97 e rankings were followed up in a three-stage replication study including 4,064 cases and 4,685 contro
98 l associations that can be pursued in future replication studies, including an intergenic SNP, rs4761
104 s further delineated in: (1) a pooling-based replication study involving an additional 500 AN patient
105 orts (n = 13,813) followed by two additional replication studies (n = 2,267) including approximately
108 t a genome-wide association (n = 17,967) and replication study (n = 13,615) to identify genetic loci
110 from 11 studies and followed up 6 SNPs in 3 replication studies of 2,198 cases and 4,918 controls.
113 ction: Genetics and Environment, followed by replication studies of prioritized single nucleotide pol
114 whose bypass adheres to the "A-rule." Recent replication studies of the oxidized abasic lesion, 2-deo
115 ce analysis of HLA-DRB3 exon 2 in a targeted replication study of 281 informative T1D family members
116 lipoprotein(a) level measurements, and in a replication study of 379 patients with echocardiography-
119 a trans-ancestry genome-wide association and replication study of blood pressure phenotypes among up
122 asthma risk loci by performing an extensive replication study of the results from the EVE Consortium
124 enes on metabolic outcomes; however, further replication studies on large samples are needed to confi
125 further genotyped this SNP in two subsequent replication studies (one with 3,750 women and the other
134 he three novel SNPs were followed-up in nine replication studies (Stage 2; N = 11 995), with rs905938
136 ss to raw data and protocols, the conduct of replication studies, systematic integration of evidence
139 lly genotyped in an independent family-based replication study that, after quality control, consisted
143 erestimation of the genetic effect may cause replication studies to fail because the necessary sample
148 wide association analysis and an independent replication study using a total of 1131 bladder cancer c
149 gammaRIIA and FcgammaRIIIA in a case-control replication study, using allele-specific polymerase chai
152 nvestigations, a genome-wide association and replication study was conducted in two smoker cohorts to
166 structural region are likely to affect viral replication, studies were performed to evaluate the effe
168 TES effect, we performed detailed retroviral replication studies with an NSI/R5 (B-92BR021) and SI/X4
169 evated risk of lung cancer from the combined replication studies with an OR of 1.15 (95% CI, 1.04-1.5
170 iral life cycle, we carried out a systematic replication study with entire genomes of human papilloma
171 xposure in conjunction with a-priori planned replication studies would reduce the number of false pos
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