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Showing 1 to 17 of 17 for “"pharmacogenomic"”.

  1. Towards implementation of pharmacogenomic-guided medicines optimisation for older patients in secondary care

    This research explores the potential of pharmacogenomic (PGx)-guided care for older patients in secondary care. Using a mixed methods approach, the study demonstrates the efficacy of PGx-guided care for patients aged 65 and above, identifies behaviour change techniques for healthcare professionals …

    bradford Repository record for Towards implementation of pharmacogenomic-guided medicines optimisation for older patients in secondary care (opens in a new tab)

  2. Towards implementation of pharmacogenomic-guided medicines optimisation for older patients in secondary care

    This research explores the potential of pharmacogenomic (PGx)-guided care for older patients in secondary care. Using a mixed methods approach, the study demonstrates the efficacy of PGx-guided care for patients aged 65 and above, identifies behaviour change techniques for healthcare professionals …

    bradford Repository record for Towards implementation of pharmacogenomic-guided medicines optimisation for older patients in secondary care (opens in a new tab)

  3. Exploring Barriers to the Adoption of Pharmacogenomic Technology in the Clinical Setting by Clinical Healthcare Providers

    … Personalized medicine and more specifically, pharmacogenomic technology have offered new tools for healthcare providers to use to increase the efficacy, safety, and cost-effectiveness of care. However, these tools are not being utilized to their predicted extent in the clinical setting. This …

    shu-thes Repository record for Exploring Barriers to the Adoption of Pharmacogenomic Technology in the Clinical Setting by Clinical Healthcare Providers (opens in a new tab)

  4. Conception and Implementation of a Pharmacogenomic Plausibility Check: Integrating Molecular Data to Optimize Established Drug Therapy Safety Workflows

    … expansion in the accessibility of high-quality pharmacogenomic knowledge and research exploring its advantages. The increasing availability of freely accessible information on drug-gene interactions enables the use of such data for a plausibility check during the prescribing process, thereby …

    bielefeld Repository record for Conception and Implementation of a Pharmacogenomic Plausibility Check: Integrating Molecular Data to Optimize Established Drug Therapy Safety Workflows (opens in a new tab)

  5. Facilitating Pharmacogenetic Association Studies Using an Extensible Genotype Information Management System

    … management system that provides storage for pharmacogenomic information including genotypic, phenotypic and resequencing data. The system provides an integrated solution for the acquisition, organization, storage, retrieval and analysis of pharmacogenomic data and offers a platform for genome …

    iupui Repository record for Facilitating Pharmacogenetic Association Studies Using an Extensible Genotype Information Management System (opens in a new tab)

  6. Pharmacogenomic profiling and clarification of the role of the mismatch repair genes in response to the chemotherapeutic agent 5-Fluorouracil in a South African colorectal cancer cohort

    To date, surgery is the mainstay treatment for HNPCC. Adjuvant chemotherapy and radiotherapy are often used to reduce systemic and locoregional recurrence, respectively, after curative surgical resection. The main chemotherapeutic agent is 5-Fluoroucacil (5-FU). Studies have attempted to elucidate …

    cape-town Repository record for Pharmacogenomic profiling and clarification of the role of the mismatch repair genes in response to the chemotherapeutic agent 5-Fluorouracil in a South African colorectal cancer cohort (opens in a new tab)

  7. A molecular approach to precision medicine in South African children with Epilepsy: towards a genetics-based diagnostic service for Epilepsy

    … criteria. All 40 probands were tested with two pharmacogenomic arrays, one generalised array, the Veridose® Core Panel produced by Agena Bioscience (San Diego, USA), and one custom-designed anti-seizure medication-specific SNV array targeting eight SNVs across six different genes. Results: Three …

    cape-town Repository record for A molecular approach to precision medicine in South African children with Epilepsy: towards a genetics-based diagnostic service for Epilepsy (opens in a new tab)

  8. Pharmacogenetics : ethics and public policy

    … be so direct. Moreover, challenges for future pharmacogenomics and its translation into personalized drug development need to be addressed. Pharmacogenetics’ applications include refining and improving the safety and efficacy of medicines by genotype-based prediction of responses. It also …

    malta Repository record for Pharmacogenetics : ethics and public policy (opens in a new tab)

  9. Genetic Predictors of Hyperglycemia Due to Hydrochlorothiazide Therapy

    … of Responses to Antihypertensives (GERA) and Pharmacogenomic Evaluation of Antihypertensive Responses (PEAR) clinical trials. No SNP reached the <em>a priori</em> defined threshold of statistical significance (p<5x10<sup>-8</sup>). We detected 50 SNPs in 9 genomic regions with suggestive …

    uthsc Repository record for Genetic Predictors of Hyperglycemia Due to Hydrochlorothiazide Therapy (opens in a new tab)

  10. Application of Informatics Tools to Facilitate the Practice of Precision Medicine with Genomic Testing and Clinical Data

    … pertaining to the gene selection practices of pharmacogenomic (PGx) tests effectively communicated large amounts of information into concise heatmaps. After a thorough search identifying potential PGx tests, their detection rates were assessed based on their gene targets and the genomic …

    chapman Repository record for Application of Informatics Tools to Facilitate the Practice of Precision Medicine with Genomic Testing and Clinical Data (opens in a new tab)

  11. Making augmented human intelligence in medicine practical: A case study of treating major depressive disorder

    … depression severity assessments augmented with pharmacogenomic measures can accurately predict remission of depressive symptoms using supervised learning. Finally, probabilistic graphs provide early and easily interpretable prognoses at the “right time” to a psychiatrist by accounting for …

    uiuc Repository record for Making augmented human intelligence in medicine practical: A case study of treating major depressive disorder (opens in a new tab)

  12. Genetic Predictors of Metabolic Side Effects of Diuretic Therapy

    … to HCTZ from two different clinical trials: the Pharmacogenomic Evaluation of Antihypertensive Responses (PEAR) and the Genetic Epidemiology of Responses to Antihypertensive (GERA) studies. Two SNPs (rs12279250 and rs4319515 (r2=0.73)), located at 11p15.1 in the NELL1 gene, achieved genome-wide …

    uthsc Repository record for Genetic Predictors of Metabolic Side Effects of Diuretic Therapy (opens in a new tab)

  13. Clinical Drug-Gene and Drug-Drug-Gene Interactions for the Most Commonly Used Chronic Drugs in the UK

    … the value of using large population datasets for pharmacogenomic discovery and has identified novel findings that may impact on clinical care.

    dundee Repository record for Clinical Drug-Gene and Drug-Drug-Gene Interactions for the Most Commonly Used Chronic Drugs in the UK (opens in a new tab)

  14. Associations of genetic variants in ABCB1, ABCG2, CYP3A4, CYP3A5, and SLCO1B1 with statin-associated muscle symptom (SAMS) in South African populations

    … knowledge of SAMS in a population with limited pharmacogenomic data, potentially informing personalized statin therapy. Key Words: dyslipidaemia, SAMS, pharmacogenetics, ABCB1, ABCG2, SLCO1B1, South African

    cape-town Repository record for Associations of genetic variants in ABCB1, ABCG2, CYP3A4, CYP3A5, and SLCO1B1 with statin-associated muscle symptom (SAMS) in South African populations (opens in a new tab)

  15. Συγκριτική μελέτη και αξιολόγηση της υιοθέτησης της γενετικής και της φαρμακογονιδιωματικής στην ελληνική κοινωνία

    Η υπηρεσία γενετικής και φαρμακογονιδιωματικής ανάλυσης έχει τη δυνατότητα να εξασφαλίσει τη βέλτιστη θεραπεία και την καλύτερη χρήση φαρμακευτικής αγωγής σε έναν αυξανόμενο αριθμό ασθενειών, ενώ η εξατομικευμένη και η γονιδιωματική ιατρική θα γίνουν όλο και πιο χρήσιμες με αποτέλεσμα τη σταδιακή …

    patras-thes Repository record for Συγκριτική μελέτη και αξιολόγηση της υιοθέτησης της γενετικής και της φαρμακογονιδιωματικής στην ελληνική κοινωνία (opens in a new tab)

  16. Advancing precision medicine: harnessing data from diverse sources and individuals to predict medication efficacy and safety.

    … East Asian subgroup, revealed unique pharmacogenomic (PGx) traits impacting their warfarin dosing. Analyzing data from two Hmong cohorts (n=236 and n=198), we found significantly higher CYP2C9*3 allele frequencies (18.9% vs. 3.0%) and lower predicted warfarin maintenance doses (19.8 …

    umn Repository record for Advancing precision medicine: harnessing data from diverse sources and individuals to predict medication efficacy and safety. (opens in a new tab)

  17. Sensibilidad a la Heparina, reversión y sangrado en revascularización miocárdica: estudio de cohorte, Fundación Cardioinfantil, 2019

    Introducción: La revascularización miocárdica es la cirugía cardíaca más frecuente, la sensibilidad a heparina y los efectos anticoagulantes de la protamina están relacionados con el sangrado peri-operatorio. Objetivo: Establecer la relación protamina-heparina y el sangrado postoperatorio según la …

    rosario Repository record for Sensibilidad a la Heparina, reversión y sangrado en revascularización miocárdica: estudio de cohorte, Fundación Cardioinfantil, 2019 (opens in a new tab)