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1 ic basis of disease and drug response (i.e., pharmacogenomics).
2 functional approaches and model systems, and pharmacogenomics.
3 l applications in both genetic screening and pharmacogenomics.
4 genetic profiling studies), and host-related pharmacogenomics.
5 ll molecules and have clear implications for pharmacogenomics.
6 ic gene variants for medical diagnostics and pharmacogenomics.
7 genetic information, an application known as pharmacogenomics.
8 odules, with direct implications to clinical pharmacogenomics.
9 ing the realization of the full potential of pharmacogenomics.
10 impact and evolving evidence for clopidogrel pharmacogenomics.
11 at remain for the clinical implementation of pharmacogenomics.
12 o be important in disease susceptibility and pharmacogenomics.
13 atabase with direct implications in clinical pharmacogenomics.
14  interventions and assessing cancer risk and pharmacogenomics.
15                                              Pharmacogenomics addresses this issue by seeking to iden
16 an application of functional neuroimaging in pharmacogenomics and extend basic evidence of an inverte
17                                  A review of pharmacogenomics and how it affects the response to anal
18  developments in the field of cardiovascular pharmacogenomics and personalized medicine.
19                               In the future, pharmacogenomics and point-of-care testing will likely p
20                                Data from the Pharmacogenomics and Risk of Cardiovascular Disease (PAR
21              We discuss the implications for pharmacogenomics and the uncharted complexity in genotyp
22 is review will focus on pharmacogenetics and pharmacogenomics and their role in reducing ADRs, especi
23  level, the relationship between transporter pharmacogenomics and therapeutics in the age of individu
24 sed test to a sequencing study in anticancer pharmacogenomics and uncovered mechanistic insights into
25 fficiency may have important consequences in pharmacogenomics and variable drug toxicity observed in
26 ociation between genetics and drug response (pharmacogenomics) and the association of sequence variat
27 tion based on patients' pharmacodynamics and pharmacogenomics, and improved supportive care.
28 with experimental medications in humans; the pharmacogenomics applied to these medications and disord
29                     Systems pharmacology and pharmacogenomics are emerging to exploit the available d
30                                 Genomics and pharmacogenomics are signalling the start of a new era f
31                                              Pharmacogenomics attempts to elucidate the inherited bas
32 ic strategies, particularly patient-specific pharmacogenomics-based therapy, with monitoring of thera
33 ts leading mostly to monogenic disorders and pharmacogenomics biomarkers.
34 ut microenvironment, gut-brain interactions, pharmacogenomics, biopsychosocial, gender and cross cult
35       We cover the practical applications of pharmacogenomics both in the pharmaceutical industry and
36                           In drug discovery, pharmacogenomics can be used to aid lead identification,
37 namic properties of pharmacological systems, pharmacogenomics can now provide an objective measure of
38  as a foundation for further research on how pharmacogenomics can reduce the incidence of adverse rea
39 e publicly available International Tamoxifen Pharmacogenomics Consortium (ITPC) dataset.
40 URPOSE To explore whether population-related pharmacogenomics contribute to differences in patient ou
41 a (CCLE) study as the benchmark dataset, all pharmacogenomics data exhibited their roles in inferring
42  based on integration of the heterogeneously pharmacogenomics data from both cell and drug sides.
43             Computational analysis of cancer pharmacogenomics data has resulted in biomarkers predict
44                        By analyzing existing pharmacogenomics data, we propose the potential design o
45              We demonstrate how to integrate pharmacogenomics databases through integration of the bi
46 ried disease-specific mutation databases and pharmacogenomics databases to identify genes and mutatio
47                         Samples collected in pharmacogenomics databases typically belong to various c
48 mation is currently distributed over several pharmacogenomics databases.
49 ients is very challenging; thus, most cancer pharmacogenomics discovery is conducted in preclinical s
50 to review the state of research on metformin pharmacogenomics, discuss the scientific and clinical hu
51 ses, dermatology, clinical pharmacology, and pharmacogenomics discussed the current state of drug all
52 t for therapies based on molecular genetics (pharmacogenomics, DNA microarrays, etc.) drives pharmace
53             RECENT FINDINGS: As the field of pharmacogenomics expands, more and more candidate genes
54  is of immediate use for prioritizing cancer pharmacogenomics experiments, and recovers known clinica
55               The rapidly expanding field of pharmacogenomics focuses on the genetic contributions to
56                               In the case of pharmacogenomics, for instance, variants of consequence
57 understanding of cellular protein complexes, pharmacogenomics, genetic diagnosis and gene therapies.
58                                              Pharmacogenomics has employed candidate gene studies and
59                                     However, pharmacogenomics has made only a few inroads into clinic
60                                 The field of pharmacogenomics has seen some exciting advances in the
61         Pharmacogenetics and, more recently, pharmacogenomics have been applied to the field of ADRs
62                                              Pharmacogenomics holds great promise for the development
63 to leukemogenesis, drug resistance, and host pharmacogenomics, identified novel subtypes of leukemia,
64                    Important associations of pharmacogenomics in cardiovascular medicine include clop
65 olizing enzymes, genetic susceptibility, and pharmacogenomics in determining cardiovascular disease r
66 review will discuss recent investigations of pharmacogenomics in heart failure, and the challenge of
67 udy was conducted to investigate the role of pharmacogenomics in NCPH in HIV patients with prior dida
68  the prospective study of population-related pharmacogenomics in which ethnic differences in antineop
69 d the first steps towards the integration of pharmacogenomics into clinical practice.
70 e polymorphism association studies in muscle pharmacogenomics is a field of expected future growth.
71              Nevertheless, the importance of pharmacogenomics is likely to increase as the cost of dr
72                           The impact of host pharmacogenomics is outlined.
73                               The promise of pharmacogenomics is that it will one day result in targe
74                                              Pharmacogenomics is the study of how human genetic infor
75                                              Pharmacogenomics is the study of the inherited basis of
76                          One of the goals of pharmacogenomics is the use of genetic variants to predi
77                  Because one of the goals of pharmacogenomics is to identify individuals and target p
78       The goal of the emerging discipline of pharmacogenomics is to personalize therapy based on an i
79                    The behavioural impact of pharmacogenomics is untested.
80   Through increased knowledge in the area of pharmacogenomics, it is hoped that that treatment of pai
81  named kinome-wide network module for cancer pharmacogenomics (KNMPx), for identifying actionable mut
82 rs, biomarkers, advanced cardiac imaging and pharmacogenomics may be used to classify patients at ris
83 spective study was performed by the Canadian Pharmacogenomics Network for Drug Safety using patients
84 n's Hospital, Memphis, TN) who discussed the pharmacogenomics of acute lymphoblastic leukemia as a ca
85 elet therapy in individuals (n=565) from the Pharmacogenomics of Anti-Platelet Intervention (PAPI) St
86 sease (epilepsy), genomics of drug response (pharmacogenomics of antiepileptic drugs) and genomics of
87    DESIGN, SETTING, AND PARTICIPANTS: In the Pharmacogenomics of Antiplatelet Intervention (PAPI) Stu
88  last year that address the pathogenesis and pharmacogenomics of asthma.
89 o model basic tumor biology and to study the pharmacogenomics of BCa.
90 gations of minimal residual disease and host pharmacogenomics, offer promising avenues of research.
91 expression), response to treatment, and host pharmacogenomics offers the potential to enhance or supp
92 icacy of ADT, establishing the importance of pharmacogenomics on individual's response to this therap
93 ern the potential role of population-related pharmacogenomics (PG) in outcomes, we conducted a large
94 ccurate local ancestry analysis in genetics, pharmacogenomics, population genetics, and clinical diag
95 ctronic Medical Records and Genomics Network Pharmacogenomics project from 7 US academic medical cent
96 omics, structural genomics, transcriptomics, pharmacogenomics, proteomics and metabolomics, allows fo
97 ere to assess the feasibility of prospective pharmacogenomics research in multicenter international c
98                                          The Pharmacogenomics Research Network and the Clinical Pharm
99      We used a pharmacometabolomics-informed pharmacogenomics research strategy to identify genes ass
100 iew describes some of the recent advances in pharmacogenomics research.
101 rapy in 768 hypertensive participants in the Pharmacogenomics Responses of Antihypertensive Responses
102  enabling resources for the nascent field of pharmacogenomics (see Glossary), which tests the idea th
103                                 The field of pharmacogenomics seeks to identify genetic factors that
104 ega-3 fatty acids), providing a means toward pharmacogenomics stratification of patients and monitori
105                           This comprehensive pharmacogenomics study showed that individuals with the
106               Common and classic features of pharmacogenomics that are related to both antiretroviral
107 utine sample storage and processing has made pharmacogenomics the most widely applied discovery-based
108  colleagues took a different approach: using pharmacogenomics to focus on neural stem cell lineage, t
109 PMT polymorphism illustrate the potential of pharmacogenomics to optimize cancer therapy by avoiding
110      Advances in the clinical application of pharmacogenomics to predict response to oncology therape
111            HIV and cancer medicine have used pharmacogenomics to some extent in clinical care.
112  genotyping may be required to define cancer pharmacogenomics unequivocally.
113                                              Pharmacogenomics will have an increasing role in the tre
114 rogress in the field of pharmacogenetics and pharmacogenomics will help further our understanding of
115                  By resolving these hurdles, pharmacogenomics will yield significant, but incremental
116 germline genetics analysis methods to cancer pharmacogenomics with a focus on the special considerati
117 with a focus on monogenetic traits to become pharmacogenomics, with a genome-wide perspective.

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