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1 be identified by use of our newly developed polygenic risk score.
2 tes family history, and genome-wide diabetes polygenic risk score.
3 gh pathways other than cognition-related and polygenic risk score.
4 h cognition-related pathways not captured by polygenic risk score.
5 artery disease have been leveraged to create polygenic risk scores.
6 anels could be clinically more relevant than polygenic risk scores.
7 l inform the development of subtype-specific polygenic risk scores.
8 the accumulation of AD genetic risk through polygenic risk scores.
9 e genetic risk variants can be combined into polygenic risk scores.
10 tudies, single nucleotide polymorphisms, and polygenic risk scores.
11 an ~57% increase in the predictive power of polygenic risk scores.
12 ions of a key module are associated with the polygenic risk scores.
13 pairment and used these results to construct polygenic risk scores.
14 nic risk score], and high [quintile 5 of the polygenic risk score]).
16 y complex traits, the non-transferability of polygenic risk scores across populations suggests the pr
17 east one copy of the APOE e4 allele and b) a polygenic risk score (AD-PRS) estimated from AD-GWAS.
22 attempt in these independent samples through polygenic risk score analysis (t = 4.02, p = 5.75 x 10(-
26 OPS), as well as the association between the polygenic risk score and coronary artery calcification (
29 much lower but still varied according to the polygenic risk score and the healthy lifestyle score (me
30 absolute risk of CRC varied according to the polygenic risk score and the healthy lifestyle score (me
31 d with an increased PTSD risk and had higher polygenic risk scores and a greater methylation compared
32 risk scores and ED symptoms, and between AN polygenic risk scores and ADHD symptoms, in a genotyped
33 further tested the associations between ADHD polygenic risk scores and ED symptoms, and between AN po
34 regions that were associated with increased polygenic risk scores and enriched risk gene expression
35 ssociation analysis, (v) meta-analysis, (vi) polygenic risk scoring and (vii) replication analysis.
36 genome-wide association testing, followed by polygenic risk scoring and phenome-wide screening, to id
38 Linkage disequilibrium score regression, polygenic risk scoring, and two-sample Mendelian randomi
39 sk score], intermediate [quintile 2-4 of the polygenic risk score], and high [quintile 5 of the polyg
41 e identified multiple disease-associated and polygenic risk score-associated differentially methylate
43 sceptibility to esophageal adenocarcinoma (a polygenic risk score based on 18 recognized genetic vari
45 iet, physical activity, and body fatness), a polygenic risk score (based on 90 single-nucleotide poly
48 by meta-analysis with an independent cohort, polygenic risk score calculation, and cross-phenotype an
49 P-chip heritability estimates of 7.29%, with polygenic risk scoring capturing 4.4% of the variance in
52 esearch should validate our findings using a polygenic risk score constructed from historical data.
53 ared genetic etiology and whether Tourette's polygenic risk scores correlate with worst-ever tic seve
55 formed in FOURIER to determine whether a VTE polygenic risk score could identify high-risk patients w
60 Tests were performed to determine whether polygenic risk scores derived from potentially related t
62 In models including both alcohol and the AF polygenic risk score, each remained associated with AF.
63 as micro-ribonucleic acid (miRNA) genetics, polygenic risk scores, environmental pollutants, and som
66 ur bipolar disorder sample, which shows that polygenic risk scores explain a higher proportion of the
69 (7.05-21.6; P=1 x 10(-4)) with schizophrenia polygenic risk scores explaining up to 0.12% of the vari
70 benign breast disease, mammographic density, polygenic risk score, family history of breast cancer, a
74 men; and as a continuous variable) and an AF polygenic risk score for association with incident AF.
75 wins with genome-wide data, we constructed a polygenic risk score for BMI (PRSBMI) using almost 1 mil
77 to optimize the predictive performance of a polygenic risk score for CAD based on summary statistics
80 d for sex, age, family socioeconomic status, polygenic risk score for cognitive function, adolescent/
90 any substance use disorder diagnosis and the polygenic risk score for schizophrenia (mega-analysis ps
96 hat could allow selection of those with high polygenic risk scores for clinical trials and precision
97 m (PGC) datasets as a reference, we estimate polygenic risk scores for depression (depression-PRS) in
98 linkage disequilibrium score regression and polygenic risk scores for depressive symptoms, schizophr
99 ed published summary statistics to calculate polygenic risk scores for eight well-studied phenotypes.
101 brain regions and highlights the utility of polygenic risk scores for identifying molecular pathways
107 lso significantly positively correlated with polygenic risk scores for schizophrenia, alcohol use dis
109 t updates to the role of genetic testing and polygenic risk scores for the prediction of stroke and c
111 d in increased trans-ancestry portability of polygenic risk scores from Europeans to East Asians acro
112 in the general population by 1) constructing polygenic risk scores from large genome-wide association
113 low-density lipoprotein cholesterol (LDL-C) polygenic risk score further increased CVD risk in patie
115 monogenic FH and superimposed elevated LDL-C polygenic risk scores have the greatest risk of prematur
118 relationships between gmCBF with APOE and AD polygenic risk score in a young cohort (N = 75; aged: 19
120 (PGx) markers, blood antigen serotyping, and polygenic risk scores in 100 individuals (50 with cardio
121 g by testing the association between partner polygenic risk scores in 34,987 couple pairs from the UK
122 from the meta-analysis, we constructed five polygenic risk scores in a range of thresholds (p=5 x 10
124 ew opportunities for developing and applying polygenic risk scores in the clinic, to systematically e
126 urements of genetic risk (e.g. schizophrenia polygenic risk scores) in causation models to assess the
129 e than a third (2.71%, CI 2.41-3.85%) of the polygenic risk score influence was mediated through cogn
130 disease risk for some disorders by means of polygenic risk scores integrated with classical epidemio
131 fied by genetic risk (low [quintile 1 of the polygenic risk score], intermediate [quintile 2-4 of the
136 ches, including genomics approaches (such as polygenic risk scores), microbiome profiling and, potent
137 ty was measured using a previously described polygenic risk score (N=929 single-nucleotide polymorphi
140 ion paths, exceeding the direct influence of polygenic risk score on schizophrenia risk (1.43%, CI 0.
143 can subjects in either cohort, nor did an AD polygenic risk score or genetic skin pigment score expla
144 s for incident depression were identified by polygenic risk scores or by reported traumatic life even
148 d to evaluate the predictive accuracy of the polygenic risk score, pooled cohort equations, and both
150 r meta-GWAS hit replication rates and poorer polygenic risk score predictive performance in survivor
155 ociation analyses were conducted between MDD polygenic risk score (PRS) and AD case-control status in
156 s interactions between an established 77-SNP polygenic risk score (PRS) and non-genetic risk factors
157 investigate the relationship between an IOP polygenic risk score (PRS) and short-term IOP profile.
166 d with risk for BE or EAC, and constructed a polygenic risk score (PRS) for cases and controls by sum
169 measure of total susceptibility burden, the polygenic risk score (PRS) for each individual was defin
170 e combined Magnetic Resonance Imaging with a polygenic risk score (PRS) for five psychiatric patholog
173 ease risk we test the extent to which higher polygenic risk score (PRS) identifies the affected sibli
177 ized sequence kernel association testing and polygenic risk score (PRS) methods to examine rare and c
178 sk by using summarized GWAS results to build polygenic risk score (PRS) models in three PTC study gro
182 , we examined gene-diet interactions using a polygenic risk score (PRS) that combined the effects of
183 iac arterial beds, and derived a genome-wide polygenic risk score (PRS) to identify a subset of the p
185 schizophrenia risk alleles, as indexed by a polygenic risk score (PRS), carried by 139,679 participa
189 (GWAS) on delta age, combined into distinct polygenic risk scores (PRS(cis-eQTL) and PRS(GWAS)), and
190 ne-out analyses generated highly significant polygenic risk scores (PRS) (explained variance of up to
191 014 FWE corrected), as were their respective polygenic risk scores (PRS) (r = 0.17, n = 874, p = 6.5
193 as to evaluate the associations between ADHD polygenic risk scores (PRS) and a broad range of childho
194 study, we explore the association between MS polygenic risk scores (PRS) and brain imaging outcomes f
198 We used data from the UK Biobank to combine polygenic risk scores (PRS) for 13 diseases and 12 morta
204 Psychiatric risk alleles were indexed by polygenic risk scores (PRS) for schizophrenia using geno
208 ifferent approaches to generating predictive polygenic risk scores (PRS) from genome-wide association
213 opulations, which limits the use of existing polygenic risk scores (PRS) to identify subpopulations a
215 ts at the 99th risk percentile of underlying polygenic risk scores (PRS), compared to average risk, r
220 stimate associations between 135 SNPs (and a polygenic risk score, PRS) and LCADs among 6345 individu
221 orts showed evidence for interaction between polygenic risk scores (PRSs) and CT, albeit in opposing
222 tologies, for association with schizophrenia polygenic risk scores (PRSs) and with diagnosis, and als
225 e we developed an alternative approach using polygenic risk scores (PRSs) based on genome-wide associ
229 ding to their risk of breast cancer based on polygenic risk scores (PRSs) could improve screening and
235 n The Netherlands (2002-2006), we calculated polygenic risk scores (PRSs) for ASD and attention-defic
236 Psychiatric genetic risk was indexed by polygenic risk scores (PRSs) for attention deficit hyper
237 SUA in 6,881 Korean individuals, calculated polygenic risk scores (PRSs) for common variants, and va
247 To facilitate scientific collaboration on polygenic risk scores (PRSs) research, we created an ext
249 ividual risk prediction based on genome-wide polygenic risk scores (PRSs) using millions of genetic v
250 o, high psoriasis, and low atopic dermatitis polygenic risk scores (PRSs) were associated with longer
259 Models without using hazard weights, i.e. polygenic risk scores, showed lower predictive power tha
260 EO-IBD patients have, on average, higher IBD polygenic risk scores than population controls (99 patie
261 summarizes clinical CKD risk factors, and a polygenic risk score that summarizes genetic information
263 y lifestyle factors and family history and a polygenic risk score, the model identified women at high
264 and, although it generates highly predictive polygenic risk scores, the predictive power can be expla
265 In clinical research, the application of polygenic risk scores-the cumulative sum of associated a
266 anding of EoE and provides a framework for a polygenic risk score to be validated in future studies.
267 ng a risk threshold of 7.5%, addition of the polygenic risk score to pooled cohort equations resulted
269 risk threshold of 7.5%, the addition of the polygenic risk score to the pooled cohort equations did
271 riking ability of genetics, in the form of a polygenic risk score, to identify those individuals at h
273 those at high genetic risk (top quintile of polygenic risk score) versus all others (WOSCOPS), as we
274 among participants at the 95th percentile of polygenic risk score was 88.2% (95% CI, 71.8-95.7).
276 redictive accuracy of a previously validated polygenic risk score was assessed among 4847 adults of w
280 this analysis of 2 cohorts of US adults, the polygenic risk score was associated with incident corona
282 10-5), while the estrogen receptor-negative polygenic risk score was much higher in blacks than in w
284 2DS and population-based cohorts showed that polygenic risk score was significantly greater in indivi
288 depressive symptoms, we found that higher RA polygenic risk scores were associated with increased str
295 Project, we found that higher schizophrenia polygenic risk scores were significantly correlated with
297 These have been combined into a vitiligo polygenic risk score, which has allowed various aspects
300 We show a significant interaction of the polygenic risk scores with personal life events (0.12% o