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1 i for fiber-quality-related traits through a genome-wide association study.
2 -nucleotide polymorphisms were identified by genome-wide association study.
3 oaches that can be used to test for GxE in a genome-wide association study.
4 ffect estimates (odds ratios) extracted from genome-wide association studies.
5 n content (PC) using single- and multi-locus genome-wide association studies.
6 netic variants is a promising alternative to genome-wide association studies.
7 el locus missed by conventional single-trait genome-wide association studies.
8 on in complex human diseases, especially via genome-wide association studies.
9 P (rs964184) for triglycerides identified by genome-wide association studies.
10 were associated with 100 genetic loci using genome-wide association studies.
11 AAA risk loci using data from all available genome-wide association studies.
12 case-control status have been replicated by genome-wide association studies.
13 tives to the standard univariate analysis in genome-wide association studies.
14 ntial heritability not explained by previous genome-wide association studies.
16 Omics data included those from historical genome-wide association studies (23,000 children) and DN
17 nducting a meta-analysis of worldwide asthma genome-wide association studies (23,948 asthma cases, 11
20 genetics to CKD progression, we performed a genome-wide association study among participants in the
22 te at Bonferroni significance in an external genome-wide association study analysis of 37,930 individ
25 etic predictors of inflammatory markers from genome-wide association studies and applied them to a la
27 proved mmLD method will be useful for future genome-wide association studies and genetic association
28 ivariate methods has often been neglected in genome-wide association studies and if used, replication
29 ted in autoimmune diseases in humans through genome-wide association studies and in mice using cell t
30 th the continued emergence of risk loci from Genome-Wide Association studies and variants of uncertai
31 with genes near loci identified by psoriasis genome-wide association studies and were enriched for ge
33 ETATION: Despite the small sample size for a genome-wide association study, and acknowledging the pot
34 proximately 4200 common variants reported in genome-wide association studies, approximately 1000 de n
36 s (SNPs), the most common genetic markers in genome-wide association studies, are usually in linkage
37 polymorphisms previously identified through genome-wide association studies as robustly associated w
38 gene implicated in human type 2 diabetes by genome-wide association studies but without a clear conn
39 mputation can enhance the discovery power of genome-wide association studies by assessing previously
40 NPs) on the panel from previous studies, and genome-wide association studies by using FarmCPU R packa
41 QT interval at baseline, identified through genome-wide association studies, can predict individual
42 d from these sequences into new and existing genome-wide association study cohorts and tested for ass
43 erived from summary statistics of 2 separate genome-wide association studies conducted from 2007 to 2
44 ata set consisting of summary results from 4 genome-wide association studies conducted from 2007 to 2
45 ythematosus (SLE) susceptibility by a recent genome-wide association study conducted in Europeans.
46 lymorphisms for schizophrenia in the largest genome-wide association study conducted to date suggeste
47 tionship between ALS and schizophrenia using genome-wide association study data from over 100,000 uni
49 Finally, integrating our data with human genome-wide association study data implicates two previo
53 METHODS AND Through a meta-analysis of 6 genome-wide association study data sets and a validation
55 -sample MR approach and publically available genome-wide association study data.MR results indicated
59 el and colleagues perform a meta-analysis of genome-wide association studies for whole body lean body
66 d then validated significant SNPs in another genome-wide association study from Harvard University.
68 disease-associated genetic variants through genome wide association studies (GWAS), genetic risk pre
76 ingle-nucleotide polymorphisms identified by genome-wide association studies (GWAS) are in noncoding
77 trafficking receptor that was identified by genome-wide association studies (GWAS) as a novel regula
80 Applying this approach, we mined Caucasian genome-wide association studies (GWAS) data from two of
84 We conducted the largest meta-analysis of genome-wide association studies (GWAS) for psoriasis to
103 vances in genome sequencing technologies and genome-wide association studies (GWAS) have provided unp
111 We developed a Bayesian-based method for genome-wide association studies (GWAS) in which RNA-seq-
113 loci from the largest body mass index (BMI) genome-wide association studies (GWAS) meta-analysis wit
114 risk by using summary data of six published genome-wide association studies (GWAS) of 12,160 cases a
115 orts and the underlying trait heterogeneity, genome-wide association studies (GWAS) of chronic period
116 bility variants have been identified through genome-wide association studies (GWAS) of predominantly
123 tic loci that are identified using data from Genome-Wide Association Studies (GWAS) provide insights
124 functional variants responsible for observed genome-wide association studies (GWAS) signals is one of
125 y marker arrays and Immunochips have powered genome-wide association studies (GWAS) that have mapped
126 among loci previously linked to IBD through genome-wide association studies (GWAS) using functional
127 quantitative trait locus (QTL) analysis and genome-wide association studies (GWAS) using the MAGIC p
131 g single nucleotide polymorphism (SNP)-based genome-wide association studies (GWAS) would identify gr
139 ombined with existing data for an aggregated genome-wide association study (GWAS) analysis of lung ca
144 ed in conjunction with data from a recent CF genome-wide association study (GWAS) meta-analysis to de
146 s of hippocampal structure here we perform a genome-wide association study (GWAS) of 33,536 individua
147 on and biology underlying AF, we undertook a genome-wide association study (GWAS) of 6,337 AF individ
150 Biobank sample (N=108 976), we carried out a genome-wide association study (GWAS) of responses to the
152 er requiring transplantation, we conducted a genome-wide association study (GWAS) on 1,404 FECD cases
154 enetics of Alcoholism (COGA), we performed a genome-wide association study (GWAS) on resting-state fa
155 nt of this vasculitis we performed the first genome-wide association study (GWAS) on this condition.
159 t cell types by looking for an enrichment of genome-wide association study (GWAS) signal within funct
161 n in the Japanese population, we performed a genome-wide association study (GWAS) that included 8,180
162 sceptibility loci for MacTel, we performed a genome-wide association study (GWAS) with 476 cases and
165 luded a single nucleotide polymorphism (SNP) genome-wide association study (GWAS), the selection of r
169 dentify shared risk variants, we performed a genome-wide association study (GWAS; n = 360,838) of a b
172 associated polygenic variation identified by genome-wide association studies (GWASs) and specific env
181 oid cancer (DTC) were identified by previous genome-wide association studies (GWASs) in Europeans onl
182 Application of the experimental design of genome-wide association studies (GWASs) is now 10 years
185 by using the summary data from six published genome-wide association studies (GWASs) of Transdiscipli
188 In recent years, as a secondary analysis in genome-wide association studies (GWASs), conditional and
189 trait-associated DNA variants discovered in genome-wide association studies (GWASs), is to estimate
212 The identity of this locus is unknown, but genome-wide association studies identified potentially c
219 particularly on genetic approaches including genome-wide association studies in humans and mice, -omi
220 and provide a behavioral paradigm for future genome-wide association studies in populations with incr
225 NPs) related to fetuin-A concentrations by a genome-wide association study in six population-based st
227 es with the DR3-DQ2.5 haplotype and a recent genome-wide association study indicating that B*08 and B
228 support analyses involving complexity beyond genome-wide association studies is not standardized or c
229 and trait-associated variants identified in genome-wide association studies largely cluster at regul
230 tes that genetic variants identified through genome-wide association studies may contribute significa
234 riants that have been identified in previous genome-wide association studies of 25(OH)D concentration
236 193 CpGs with an enrichment of signals from genome-wide association studies of lipid levels (PTC=0.0
237 r Consortium (TECAC) combined five published genome-wide association studies of testicular germ cell
246 In this study, we performed a two-stage genome-wide association study of executive inhibition in
248 ci underlying LBM, we performed a gene-based genome-wide association study of lean mass index (LMI) i
255 g a polygenic score derived from a published genome-wide association study of subjective well-being.
256 f 43 SCZ risk genes identified by the recent genome-wide association study of the Schizophrenia Worki
258 om a case and control sample, we conducted a genome-wide association study of usual daily methadone d
260 ined a search for protein quantity loci with genome-wide association studies on the abundance of 7S a
261 DNA markers in these regions, we conducted a genome-wide association study on a set of 185 U.S. winte
262 diastolic blood pressure measurements for a genome-wide association study on long-term average systo
263 2, Tyrobp) defined as risk factors for AD by genome-wide association study or identified as genetic n
264 omal K(+) channel, is centered under a major genome-wide association studies peak for PD, making it a
266 f P-wave morphology through meta-analysis of genome-wide association study results for P-wave duratio
267 We also conducted meta-analyses using the genome-wide association study results from the CTD cohor
268 lation of polygenic risk scores was based on genome-wide association study results generated by the P
270 ntified 14,059 segregating polymorphisms and genome-wide association studies revealed 28 GWAS hits in
271 hrenia risk, including several schizophrenia genome-wide association study risk genes (e.g., calcium
273 a subset of these polymorphisms is linked to genome-wide association study signals of complex traits
275 methylation is associated in cis with known genome-wide association study single nucleotide polymorp
278 s applied to two large Caucasian and Chinese genome-wide association study summary datasets of bone m
280 genetics of depression has been explored in genome-wide association studies that focused on either m
282 entifying response-associated genes in large genome-wide association studies, the results have been f
283 ingle-nucleotide polymorphisms identified by genome-wide association studies to be associated with BM
287 tide polymorphisms (SNPs) were analyzed in a genome-wide association study to identify susceptibility
288 For the same maize data, we also conducted genome-wide association study, transcriptome-wide associ
290 ymorphisms associated with BMI from previous genome-wide association studies was constructed, and the
291 mmary association results from 7 large-scale genome-wide association studies, we examined the effect
295 ng information for any diagnostic criterion, genome-wide association studies were performed on 2 samp
297 METHODS AND Summary statistics from several genome-wide association studies were used in a 2-sample
300 In the first step (n = 979), we performed a genome-wide association study with a predefined suggesti
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