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1 ied from a GWAS of body mass index, a highly polygenic trait.
2 tion for what is usually considered a highly polygenic trait.
3 the case in H. pylori, Mtz(r) might not be a polygenic trait.
4 adult height, a highly heritable and classic polygenic trait.
5  majority of human obesity is inherited as a polygenic trait.
6  Human height is a highly heritable, classic polygenic trait.
7  into the genetic architecture of this model polygenic trait.
8                      Breast cancer risk is a polygenic trait.
9 o many autoimmune diseases is inherited as a polygenic trait.
10 D. sechellia and D. simulans appears to be a polygenic trait.
11 carcinoma susceptibility in the COP rat is a polygenic trait.
12 nds (USA) deer exhibit smaller body sizes, a polygenic trait.
13  coefficients, and inference of selection on polygenic traits.
14 nderstanding of the genetic basis of complex polygenic traits.
15 es over marker-assisted selection for highly polygenic traits.
16  locus and, more broadly, works best in less polygenic traits.
17  We present a novel way to select for highly polygenic traits.
18 tudies identified>1,000 genetic variants for polygenic traits.
19        Behaviors are often highly heritable, polygenic traits.
20 ltiple loci that function together to encode polygenic traits.
21 on of major gene(s) responsible for complex, polygenic traits.
22 ntly for simplifying the genetic analysis of polygenic traits.
23 be used to sensitize the genetic analysis of polygenic traits.
24 ingle-gene models are quite robust, even for polygenic traits.
25 es and pathways most associated with complex polygenic traits.
26 ct quantitative trait loci associations with polygenic traits.
27 lved cases and the 'missing heritability' of polygenic traits.
28 blood cell counts (WBC) are both complex and polygenic traits.
29 of sheep, focusing on the analysis of eleven polygenic traits.
30                      Human height is a model polygenic trait - additive effects of many individual va
31 ion in GWAS may not always be sufficient for polygenic trait analyses, and (2) that claims of differe
32                             This is a highly polygenic trait and, using quantitative validation studi
33  successful in identifying genes involved in polygenic traits and are valuable for crop improvement.
34 y be applied to GWA studies for other common polygenic traits and diseases, thus providing a new gene
35 e biology underlying genetic associations in polygenic traits and diseases.
36 ution is thought to be less likely in highly polygenic traits and distantly related species, this has
37 the genetic architecture of a set of related polygenic traits and the skeleton of the domestic dog (C
38 table hybrid strain that contains a complex, polygenic trait, and identifies new avenues for metaboli
39 n comorbid with obesity, a common and highly polygenic trait, and it is underdiagnosed in biobank dat
40 , addressing genetic redundancy, engineering polygenic traits, and accelerating trait stacking and de
41 on genetic variants that are associated with polygenic traits, and have typically been performed with
42 ar pathways can be modified in monogenic and polygenic traits, and how the environment may tweak prot
43 ric proteins, indicating their importance to polygenic traits; and 4) the importance of allosteric pr
44                       Through simulations of polygenic trait architecture evolution and GWASs, we sho
45 c evolution of guppies may be facilitated by polygenic trait architectures, but subsequent genetic re
46  that differences in architectures of highly polygenic traits arise mainly from the two scaling param
47 use of Drosophila as a vehicle for analyzing polygenic traits as an aid in human genetics.
48 eds from standing variation and selection on polygenic traits, both of which may leave faint genomic
49 icate that human height is not only a highly polygenic trait, but also has high allelic heterogeneity
50                      Adult height is a model polygenic trait, but there has been limited success in i
51 rmation can favor genetic analysis of highly polygenic traits, but not genome-wide prediction accurac
52 g of monogenic traits, genetic dissection of polygenic traits, construction of genome-wide physical m
53 at variation in the frequency of a heritable polygenic trait depends on spatial variation in two domi
54                    Odor-guided behavior is a polygenic trait determined by the concerted expression o
55                            Pigmentation is a polygenic trait encompassing some of the most visible ph
56  effect, but unlike these other prototypical polygenic traits, genetic influence on anxiety is not we
57 ur results indicate that growth is a complex polygenic trait governed by carbon and energy partitioni
58 tion of the gastrointestinal microbiota is a polygenic trait governed by interactions between host ge
59            Identifying the genes involved in polygenic traits has been difficult.
60 within the Croatian data, and for the highly polygenic traits height and BMI when predicting into the
61                      Validated prediction of polygenic traits improves our understanding of ancient p
62 usarium oxysporum f.sp. matthioli (FOM) is a polygenic trait in Arabidopsis thaliana.
63 er, baseline skin pigmentation is a complex, polygenic trait in the KhoeSan.
64 AHR) is a hallmark of asthma and a heritable polygenic trait in the mouse.
65 del the genetic architecture of quantitative polygenic traits in both the general European and the Fi
66 es to understand the genetic architecture of polygenic traits in many different organisms.
67 iphering the genetic architecture underlying polygenic traits in perennial species can inform molecul
68 alyses on seven public datasets, covering 19 polygenic traits in three plant and three livestock spec
69 emonstrated that abscess susceptibility is a polygenic trait inherited in a sex-dependent manner with
70                        Firmness is a complex polygenic trait involving the coregulation of many genes
71 ntiation among species that have diverged in polygenic traits is genomically widespread and much high
72 ed among many weakly specified loci (as in a polygenic trait) is cheap.
73                                 As with most polygenic traits, it is likely that many genetic determi
74 ts to explore rare variants' contribution to polygenic traits, it is of great importance to character
75 Plant disease resistance is often a complex, polygenic trait, making its genetic dissection with trad
76  alone for moderately complex but not highly polygenic traits measured in the maize nested associatio
77 the possibility remains that this is a truly polygenic trait or that multiple, rare variants contribu
78 data from genome-wide association studies of polygenic traits, producing interpretable findings while
79                          Height is a classic polygenic trait, reflecting the combined influence of mu
80    Understanding the genetic architecture of polygenic traits requires investigating how complex netw
81                 The mechanistic basis of how polygenic traits respond to selection is not well unders
82              We apply the method to 56 human polygenic traits, revealing signals of directional selec
83                                          For polygenic traits such as MDD, aggregate measures of gene
84 in understanding the genetic architecture of polygenic traits such as obesity.
85 nk cell-type-specific regulatory networks to polygenic traits such as osteoarthritis.
86                                 However, for polygenic traits, such as psychiatric disorders, the acc
87  However, the evolutionary paths along which polygenic traits, such as size, evolve are poorly unders
88  traits, it improved the fit for some of the polygenic traits, suggesting that dominance, epistasis a
89 ce, GC tumor susceptibility is an inherited, polygenic trait that appears at a low frequency.
90        Leukocyte telomere length is a highly polygenic trait that has been associated with a complex
91  Skin pigmentation is a classic example of a polygenic trait that has experienced directional selecti
92                            Height is a model polygenic trait that is highly heritable.
93 hat autoantibody production in NZW mice is a polygenic trait that is influenced by contributions from
94  ash dieback resistance in F. excelsior is a polygenic trait that should respond well to both natural
95 resistance in European beech is a moderately polygenic trait that should respond well to natural sele
96                      Locomotor activity is a polygenic trait that varies widely among inbred strains
97 we show that screen behaviors are heritable, polygenic traits that partly share genetic signal with m
98 lelic heterogeneity is a frequent feature of polygenic traits, that comprehensive explorations of alr
99 roblem, we have used pigmentation as a model polygenic trait, three common human polymorphisms though
100 sults of the GWAS were compared with complex polygenic traits through a genetic correlation approach
101 y size variation in vertebrates is a complex polygenic trait, tightly correlated with numerous aspect
102    Out of 35, nine (9) MTAs were controlling polygenic trait (two controlling four traits, one contro
103 n genome-wide association studies (GWAS) for polygenic traits typically increases with sample size.
104               Genetic dissection of complex, polygenic trait variation is a key goal of medical and e
105                By studying height, a classic polygenic trait, we demonstrate the first human signatur
106 experimental model for the analysis of adult polygenic traits, we measured a mouse population for mul
107 ining these data with GWASs from 31 distinct polygenic traits, we show that the heritability of multi
108  mineral density is known to be a heritable, polygenic trait whereas genetic variants contributing to
109         Psychiatric disorders are heritable, polygenic traits, which often share risk alleles and for
110        Height is a highly heritable, classic polygenic trait with approximately 700 common associated
111 ent resistance in schizophrenia emerged as a polygenic trait with detectable heritability (1% to 4%),
112            Each analysis assumes an additive polygenic trait with n diallelic loci under stabilizing
113  of the human brain are heritable and highly polygenic traits, with hundreds of associated genes iden
114 orks can model the nonlinear architecture of polygenic traits, yet the reliability of attribution met

 
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