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CORDIS - Forschungsergebnisse der EU
CORDIS

Ubiquitous Pharmacogenomics (U-PGx): Making actionable pharmacogenomic data and effective treatment optimization accessible to every European citizen

CORDIS bietet Links zu öffentlichen Ergebnissen und Veröffentlichungen von HORIZONT-Projekten.

Links zu Ergebnissen und Veröffentlichungen von RP7-Projekten sowie Links zu einigen Typen spezifischer Ergebnisse wie Datensätzen und Software werden dynamisch von OpenAIRE abgerufen.

Leistungen

Therapeutic recommendations in Dutch, Greek, German, Italian, Slovene and Spanish (öffnet in neuem Fenster)

Therapeutic recommendations in Dutch Greek German Italian Slovene and Spanish

Report on ELSI education needs (öffnet in neuem Fenster)
Report on design of future study employing one promising model (öffnet in neuem Fenster)
Overall report on ELSI aspects of U-PGx (öffnet in neuem Fenster)

Overall report on ELSI aspects of UPGx

Survey to evaluate the state of PGx knowledge in the 7 participating countries (öffnet in neuem Fenster)
Report on ethical issues, guidelines, governance model and principals for patients included in U-PGx (öffnet in neuem Fenster)

Report on ethical issues guidelines governance model and principals for patients included in UPGx

Establishment of PK models for prediction of DDI and genetic polymorphisms on drug exposure for candidate genes included in the U-PGx trial (öffnet in neuem Fenster)

Establishment of PK models for prediction of DDI and genetic polymorphisms on drug exposure for candidate genes included in the UPGx trial

Detection, assessment and evaluation of clinically relevant DDI in the U-PGx trial (öffnet in neuem Fenster)

Detection assessment and evaluation of clinically relevant DDI in the UPGx trial

Report on detailed analysis of existing information infrastructures and requirements of implementation sites (öffnet in neuem Fenster)
Report on predictions from first model (öffnet in neuem Fenster)
Analysis of European regulatory requirements (öffnet in neuem Fenster)
Report on models identified to be developed (öffnet in neuem Fenster)
Policy recommendations on the pre-emptive use of U-PGx testing in routine clinical practice and uptake by health care systems (öffnet in neuem Fenster)

Policy recommendations on the preemptive use of UPGx testing in routine clinical practice and uptake by health care systems

Report on comparison of model predictions and observed data from WP4 (öffnet in neuem Fenster)
Critical re-evaluation and first implementation of revised DPWG guidelines by consideration of relevant DDI (öffnet in neuem Fenster)

Critical reevaluation and first implementation of revised DPWG guidelines by consideration of relevant DDI

Report on predictions from further models (öffnet in neuem Fenster)
List of relevant genetic variants for pre-emptive PGx testing (öffnet in neuem Fenster)

List of relevant genetic variants for preemptive PGx testing

Report on the association of novel genomic variants and extreme phenotypes (öffnet in neuem Fenster)
Report on finalization endpoint data extraction from clinical database into NONMEM dataset (öffnet in neuem Fenster)
Report on public events and societal activities in relation with U-PGx (öffnet in neuem Fenster)

Report on public events and societal activities in relation with UPGx

PGx-guidelines therapeutic recommendations and risk-assessments in English (öffnet in neuem Fenster)

PGxguidelines therapeutic recommendations and riskassessments in English

Published review paper based upon the current scientific and grey literature on ethics of PGx (öffnet in neuem Fenster)
Midterm Review (öffnet in neuem Fenster)
Report on interoperability and development of a shared semantic model (öffnet in neuem Fenster)
Translated patient surveys for the web-based intensive monitoring system (öffnet in neuem Fenster)

Translated patient surveys for the webbased intensive monitoring system

Final report on decision support solutions at implementation sites (öffnet in neuem Fenster)
Organization of a U-PGx Personalized Medicine Day in France (öffnet in neuem Fenster)

Organization of a UPGx Personalized Medicine Day in France

Organization of the 1st patient/general public oriented PGx information events (öffnet in neuem Fenster)

Organization of the 1st patientgeneral public oriented PGx information events

Education programme for non-participants (öffnet in neuem Fenster)

Education programme for nonparticipants

Organization of a U-PGx Personalized Medicine Day in Greece (öffnet in neuem Fenster)

Organization of a UPGx Personalized Medicine Day in Greece

Organization of a U-PGx Personalized Medicine Day in the UK (öffnet in neuem Fenster)

Organization of a UPGx Personalized Medicine Day in the UK

Organization of the 3rd patient/general public-oriented PGx information event (öffnet in neuem Fenster)

Organization of a UPGx Personalized Medicine Day in Germany

Organization of a major 4-day U-PGx Personalized Medicine Symposium in Leiden, Netherlands (öffnet in neuem Fenster)

Organization of a major 4day UPGx Personalized Medicine Symposium in Leiden Netherlands

Summer school including ELSI topics (prepared by WP8) for medical and pharmacy students (öffnet in neuem Fenster)

Summer school including ELSI topics prepared by WP8 for medical and pharmacy students

Organization of the 2nd patient/general public oriented PGx information events (öffnet in neuem Fenster)

Organization of the 2nd patientgeneral public oriented PGx information events

Organization of a U-PGx Personalized Medicine Day in Slovenia (öffnet in neuem Fenster)

Organization of a UPGx Personalized Medicine Day in Slovenia

Organization of a U-PGx Personalized Medicine Day in Sweden (öffnet in neuem Fenster)

Organization of a UPGx Personalized Medicine Day in Sweden

Organization of a U-PGx Personalized Medicine Day in Spain (öffnet in neuem Fenster)

Organization of a UPGx Personalized Medicine Day in Spain

Promotional video will be produced that visualises and promotes the idea of the idea of personalised medicine and pre-emptive PGx testing (öffnet in neuem Fenster)

Promotional video will be produced that visualises and promotes the idea of the idea of personalised medicine and preemptive PGx testing

Workshop for participating healthcare professionals (öffnet in neuem Fenster)
Organization of a U-PGx Personalized Medicine Day in Austria (öffnet in neuem Fenster)

Organization of a UPGx Personalized Medicine Day in Austria

1st version of the public-domain web-based U-PGx information portal (öffnet in neuem Fenster)

1st version of the publicdomain webbased UPGx information portal

Delivery of decision support solutions including framework for digital infrastructure including secure cloud solutions (öffnet in neuem Fenster)
Dedicated webpage with secured login access for investigators and study staff (öffnet in neuem Fenster)
3rd version of the public-domain web-based PGx information portal (öffnet in neuem Fenster)

3rd version of the publicdomain webbased PGx information portal

Standardized Electronic Case Record Form (eCRF) (öffnet in neuem Fenster)

Standardized Electronic Case Record Form eCRF

A new model of cost-effectiveness analysis, taking into account the restriction of budget (öffnet in neuem Fenster)

A new model of costeffectiveness analysis taking into account the restriction of budget

Validated bioinformatics tool (öffnet in neuem Fenster)
2nd version of the public-domain web-based PGx information portal (öffnet in neuem Fenster)

2nd version of the publicdomain webbased PGx information portal

A standard cost-effectiveness model to assess cost-effectiveness of PGx testing in each implementation site (öffnet in neuem Fenster)

A standard costeffectiveness model to assess costeffectiveness of PGx testing in each implementation site

Release of open-source software artefacts for decision support solutions (öffnet in neuem Fenster)

Release of opensource software artefacts for decision support solutions

eLearning program for the train the trainers concept (öffnet in neuem Fenster)

Veröffentlichungen

Population pharmacogenomics: an update on ethnogeographic differences and opportunities for precision public health. (öffnet in neuem Fenster)

Autoren: Zhou Y, Lauschke VM.
Veröffentlicht in: Human genetics, 2021, ISSN 0340-6717
Herausgeber: Springer Verlag
DOI: 10.1007/s00439-021-02385-x

Tri-Allelic Haplotypes Determine and Differentiate Functionally Normal Allele CYP2D6*2 and Impaired Allele CYP2D6*41. (öffnet in neuem Fenster)

Autoren: Zanger UM, Momoi K, Hofmann U, Schwab M, Klein K.
Veröffentlicht in: Clinical pharmacology and therapeutics, 2021, ISSN 0009-9236
Herausgeber: Nature Publishing Group
DOI: 10.1002/cpt.2078

Pharmacogenetics Guidelines: Overview and Comparison of the DPWG, CPIC, CPNDS, and RNPGx Guidelines. (öffnet in neuem Fenster)

Autoren: Abdullah-Koolmees H, van Keulen AM, Nijenhuis M, Deneer VHM.
Veröffentlicht in: Frontiers in pharmacology, 2020, ISSN 1663-9812
Herausgeber: Frontiers Media S.A.
DOI: 10.3389/fphar.2020.595219

Genomewide Association Study of Platelet Reactivity and Cardiovascular Response in Patients Treated With Clopidogrel: A Study by the International Clopidogrel Pharmacogenomics Consortium (öffnet in neuem Fenster)

Autoren: Shefali Setia Verma, Thomas O. Bergmeijer, Li Gong, Jean‐Luc Reny, Joshua P. Lewis, Braxton D. Mitchell, Dimitrios Alexopoulos, Daniel Aradi, Russ B. Altman, Kevin Bliden, Yuki Bradford, Gianluca Campo, Kiyuk Chang, John H. Cleator, Jean‐Pierre Déry, Nadia P. Dridi, Israel Fernandez‐Cadenas, Pierre Fontana, Meinrad Gawaz, Tobias Geisler, Gian Franco Gensini, Betti Giusti, Paul A. Gurbel, Wi
Veröffentlicht in: Clinical Pharmacology & Therapeutics, Ausgabe 108/5, 2020, Seite(n) 1067-1077, ISSN 0009-9236
Herausgeber: Nature Publishing Group
DOI: 10.1002/cpt.1911

Substrate specificity of CYP2D6 genetic variants. (öffnet in neuem Fenster)

Autoren: van der Lee M, Guchelaar HJ, Swen JJ.
Veröffentlicht in: Pharmacogenomics, 2021, ISSN 1462-2416
Herausgeber: Ashley Publications Ltd.
DOI: 10.2217/pgs-2021-0093

Clinically Relevant Cytochrome P450 3A4 Induction Mechanisms and Drug Screening in Three‐Dimensional Spheroid Cultures of Primary Human Hepatocytes (öffnet in neuem Fenster)

Autoren: Delilah F.G. Hendriks, Sabine U. Vorrink, Tomas Smutny, Sarah C. Sim, Åsa Nordling, Shahid Ullah, Masaki Kumondai, Barry C. Jones, Inger Johansson, Tommy B. Andersson, Volker M. Lauschke, Magnus Ingelman‐Sundberg
Veröffentlicht in: Clinical Pharmacology & Therapeutics, Ausgabe 108/4, 2020, Seite(n) 844-855, ISSN 0009-9236
Herausgeber: Nature Publishing Group
DOI: 10.1002/cpt.1860

Toward predicting CYP2D6-mediated variable drug response from CYP2D6 gene sequencing data (öffnet in neuem Fenster)

Autoren: Maaike van der Lee; William G. Allard; Rolf H. A. M. Vossen; Renee Baak-Pablo; Roberta Menafra; Birgit A. L. M. Deiman; Maarten J. Deenen; Patrick Neven; Inger Johansson; Stefano Gastaldello; Magnus Ingelman-Sundberg; Henk-Jan Guchelaar; Jesse J. Swen; Seyed Yahya Anvar
Veröffentlicht in: VOLUME=13;ISSUE=603;TITLE=Science Translational Medicine, Ausgabe 6, 2021, ISSN 1946-6234
Herausgeber: American Association for the Advancement of Science
DOI: 10.1126/scitranslmed.abf3637

Can CYP Inhibition Overcome Chemotherapy Resistance? (öffnet in neuem Fenster)

Autoren: Magnus Ingelman-Sundberg, Volker M. Lauschke
Veröffentlicht in: Trends in Pharmacological Sciences, Ausgabe 41/8, 2020, Seite(n) 503-506, ISSN 0165-6147
Herausgeber: Elsevier BV
DOI: 10.1016/j.tips.2020.05.007

Economic evaluation in psychiatric pharmacogenomics: a systematic review. (öffnet in neuem Fenster)

Autoren: Karamperis K, Koromina M, Papantoniou P, Skokou M, Kanellakis F, Mitropoulos K, Vozikis A, Müller DJ, Patrinos GP, Mitropoulou C.
Veröffentlicht in: The pharmacogenomics journal, 2021, ISSN 1470-269X
Herausgeber: Nature Publishing Group
DOI: 10.1038/s41397-021-00249-1

IL15RA and SMAD3 Genetic Variants Predict Overall Survival in Metastatic Colorectal Cancer Patients Treated with FOLFIRI Therapy: A New Paradigm. (öffnet in neuem Fenster)

Autoren: De Mattia E, Polesel J, Roncato R, Labriet A, Bignucolo A, Gagno S, Buonadonna A, D'Andrea M, Lévesque E, Jonker D, Couture F, Guillemette C, Cecchin E, Toffoli G.
Veröffentlicht in: Cancers, 2021, ISSN 2072-6694
Herausgeber: Multidisciplinary Digital Publishing Institute (MDPI)
DOI: 10.3390/cancers13071705

Impact of antipsychotic polypharmacy on nonadherence of oral antipsychotic drugs – A study based on blood sample analyses from 24,239 patients (öffnet in neuem Fenster)

Autoren: Robert L Smith, Marit Tveito, Lennart Kyllesø, Marin M Jukic, Magnus Ingelman-Sundberg, Ole A Andreassen, Espen Molden
Veröffentlicht in: European Neuropsychopharmacology, Ausgabe 37, 2020, Seite(n) 64-69, ISSN 0924-977X
Herausgeber: Elsevier BV
DOI: 10.1016/j.euroneuro.2020.06.007

Dutch Pharmacogenetics Working Group (DPWG) guideline for the gene-drug interaction between CYP2D6 and opioids (codeine, tramadol and oxycodone). (öffnet in neuem Fenster)

Autoren: Matic M, Nijenhuis M, Soree B, de Boer-Veger NJ, Buunk AM, Houwink EJF, Mulder H, Rongen GAPJM, Weide JV, Wilffert B, Swen JJ, Guchelaar HJ, Deneer VHM, van Schaik RHN.
Veröffentlicht in: European journal of human genetics : EJHG, 2021, ISSN 1018-4813
Herausgeber: Natue Publishing Group
DOI: 10.1038/s41431-021-00920-y

Rare genetic variability in human drug target genes modulates drug response and can guide precision medicine. (öffnet in neuem Fenster)

Autoren: Zhou Y, Arribas GH, Turku A, Jürgenson T, Mkrtchian S, Krebs K, Wang Y, Svobodova B, Milani L, Schulte G, Korabecny J, Gastaldello S, Lauschke VM.
Veröffentlicht in: Science advances, 2021, ISSN 2375-2548
Herausgeber: American Association for the Advancement of Science
DOI: 10.1126/sciadv.abi6856

Global Frequencies of Clinically Important HLA Alleles and Their Implications For the Cost‐Effectiveness of Preemptive Pharmacogenetic Testing (öffnet in neuem Fenster)

Autoren: Yitian Zhou, Kristi Krebs, Lili Milani, Volker M. Lauschke
Veröffentlicht in: Clinical Pharmacology & Therapeutics, 2020, ISSN 0009-9236
Herausgeber: Nature Publishing Group
DOI: 10.1002/cpt.1944

Clinical Pharmacogenetics Implementation Consortium (CPIC) Guideline for CYP2C19 and Proton Pump Inhibitor Dosing. (öffnet in neuem Fenster)

Autoren: Lima JJ, Thomas CD, Barbarino J, Desta Z, Van Driest SL, El Rouby N, Johnson JA, Cavallari LH, Shakhnovich V, Thacker DL, Scott SA, Schwab M, Uppugunduri CRS, Formea CM, Franciosi JP, Sangkuhl K, Gaedigk A, Klein TE, Gammal RS, Furuta T.
Veröffentlicht in: Clinical pharmacology and therapeutics, 2021, ISSN 0009-9236
Herausgeber: Nature Publishing Group
DOI: 10.1002/cpt.2015

CYP2B6 Functional Variability in Drug Metabolism and Exposure Across Populations-Implication for Drug Safety, Dosing, and Individualized Therapy. (öffnet in neuem Fenster)

Autoren: Langmia IM, Just KS, Yamoune S, Brockmöller J, Masimirembwa C, Stingl JC.
Veröffentlicht in: Frontiers in genetics, 2021, ISSN 1664-8021
Herausgeber: Frontiers Media
DOI: 10.3389/fgene.2021.692234

Dutch Pharmacogenetics Working Group (DPWG) guideline for the gene-drug interaction between CYP2C19 and CYP2D6 and SSRIs. (öffnet in neuem Fenster)

Autoren: Brouwer JMJL, Nijenhuis M, Soree B, Guchelaar HJ, Swen JJ, van Schaik RHN, Weide JV, Rongen GAPJM, Buunk AM, de Boer-Veger NJ, Houwink EJF, van Westrhenen R, Wilffert B, Deneer VHM, Mulder H.
Veröffentlicht in: European journal of human genetics : EJHG, 2021, ISSN 1018-4813
Herausgeber: Natue Publishing Group
DOI: 10.1038/s41431-021-01004-7

Population-scale predictions of DPD and TPMT phenotypes using a quantitative pharmacogene-specific ensemble classifier (öffnet in neuem Fenster)

Autoren: Yitian Zhou, Carolina Dagli Hernandez, Volker M. Lauschke
Veröffentlicht in: British Journal of Cancer, 2020, ISSN 0007-0920
Herausgeber: Nature Publishing Group
DOI: 10.1038/s41416-020-01084-0

CYP2D6 in the Brain: Potential Impact on Adverse Drug Reactions in the Central Nervous System-Results From the ADRED Study. (öffnet in neuem Fenster)

Autoren: Katja S. Just; Harald Dormann; Mathias Freitag; Marlen Schurig; Miriam Böhme; Michael Steffens; Catharina Scholl; Thomas Seufferlein; Ingo Graeff; Matthias Schwab; Matthias Schwab; Matthias Schwab; Julia C. Stingl
Veröffentlicht in: Frontiers in Pharmacology, Ausgabe 9, 2021, ISSN 1663-9812
Herausgeber: Frontiers Media S.A.
DOI: 10.3389/fphar.2021.624104

Application of long-read sequencing to elucidate complex pharmacogenomic regions: a proof of principle. (öffnet in neuem Fenster)

Autoren: van der Lee M, Rowell WJ, Menafra R, Guchelaar HJ, Swen JJ, Anvar SY.
Veröffentlicht in: The pharmacogenomics journal, 2022, ISSN 1470-269X
Herausgeber: Nature Publishing Group
DOI: 10.1038/s41397-021-00259-z

Generating evidence for precision medicine: considerations made by the Ubiquitous Pharmacogenomics Consortium when designing and operationalizing the PREPARE study (öffnet in neuem Fenster)

Autoren: Cathelijne H. van der Wouden, Stefan Böhringer, Erika Cecchin, Ka-Chun Cheung, Cristina Lucía Dávila-Fajardo, Vera H.M. Deneer, Vita Dolžan, Magnus Ingelman-Sundberg, Siv Jönsson, Mats O. Karlsson, Marjolein Kriek, Christina Mitropoulou, George P. Patrinos, Munir Pirmohamed, Emmanuelle Rial-Sebbag, Matthias Samwald, Matthias Schwab, Daniela Steinberger, Julia Stingl, Gere Sunder-Plassmann, Gi
Veröffentlicht in: Pharmacogenetics and Genomics, Ausgabe 30/6, 2020, Seite(n) 131-144, ISSN 1744-6872
Herausgeber: Lippincott Williams & Wilkins Ltd.
DOI: 10.1097/fpc.0000000000000405

Evaluation of the CYP2D6 Haplotype Activity Scores Based on Metabolic Ratios of 4,700 Patients Treated With Three Different CYP2D6 Substrates. (öffnet in neuem Fenster)

Autoren: Jukić MM, Smith RL, Molden E, Ingelman-Sundberg M.
Veröffentlicht in: Clinical pharmacology and therapeutics, 2021, ISSN 0009-9236
Herausgeber: Nature Publishing Group
DOI: 10.1002/cpt.2246

Pharmacogenomics in the UK National Health Service: opportunities and challenges. (öffnet in neuem Fenster)

Autoren: Turner RM, Newman WG, Bramon E, McNamee CJ, Wong WL, Misbah S, Hill S, Caulfield M, Pirmohamed M.
Veröffentlicht in: Pharmacogenomics, 2020, ISSN 1462-2416
Herausgeber: Ashley Publications Ltd.
DOI: 10.2217/pgs-2020-0091

Pharmacogenomics for Primary Care: An Overview. (öffnet in neuem Fenster)

Autoren: Rollinson V, Turner R, Pirmohamed M.
Veröffentlicht in: Genes, 2020, ISSN 2073-4425
Herausgeber: Multidisciplinary Digital Publishing Institute (MDPI)
DOI: 10.3390/genes11111337

The ethnogeographic variability of genetic factors underlying G6PD deficiency (öffnet in neuem Fenster)

Autoren: iamoglou S, Koromina M, Hishinuma E, Yamazaki S, Tsermpini EE, Kordou Z, Fukunaga K, Chantratita W, Zhou Y, Lauschke VM, Mushiroda T, Hiratsuka M, Patrinos GP.
Veröffentlicht in: Pharmacological research, 2021, ISSN 1043-6618
Herausgeber: Academic Press
DOI: 10.1016/j.phrs.2021.105904

Diagnostic Test Criteria for HLA Genotyping to Prevent Drug Hypersensitivity Reactions: A Systematic Review of Actionable HLA Recommendations in CPIC and DPWG Guidelines (öffnet in neuem Fenster)

Autoren: Lisanne E. N. Manson, Jesse J. Swen, Henk-Jan Guchelaar
Veröffentlicht in: Frontiers in Pharmacology, Ausgabe 11, 2020, ISSN 1663-9812
Herausgeber: Frontiers Media S.A.
DOI: 10.3389/fphar.2020.567048

Characterization of Genetic Heterogeneity in Recurrent Metastases of Renal Cell Carcinoma. (öffnet in neuem Fenster)

Autoren: Sauter-Meyerhoff C, Bohnert R, Mazzola P, Stühler V, Kandabarau S, Büttner FA, Winter S, Herrmann L, Rausch S, Hennenlotter J, Fend F, Scharpf M, Stenzl A, Ossowski S, Bedke J, Schwab M, Schaeffeler E.
Veröffentlicht in: Cancers, 2021, ISSN 2072-6694
Herausgeber: Multidisciplinary Digital Publishing Institute (MDPI)
DOI: 10.3390/cancers13246221

A Novel CYP2C-Haplotype Associated With Ultrarapid Metabolism of Escitalopram. (öffnet in neuem Fenster)

Autoren: Line Skute Bråten; Tore Haslemo; Marin M. Jukic; Marin M. Jukic; Maxim Ivanov; Magnus Ingelman-Sundberg; Espen Molden; Marianne Kristiansen Kringen
Veröffentlicht in: Clinical Pharmacology & Therapeutics, Ausgabe 13, 2021, ISSN 0009-9236
Herausgeber: Nature Publishing Group
DOI: 10.1002/cpt.2233

A Review of the Important Role of CYP2D6 in Pharmacogenomics. (öffnet in neuem Fenster)

Autoren: Taylor C, Crosby I, Yip V, Maguire P, Pirmohamed M, Turner RM.
Veröffentlicht in: Genes, 2020, ISSN 2073-4425
Herausgeber: Multidisciplinary Digital Publishing Institute (MDPI)
DOI: 10.3390/genes11111295

Data-driven personalization of a physiologically based pharmacokinetic model for caffeine: A systematic assessment. (öffnet in neuem Fenster)

Autoren: Fendt R, Hofmann U, Schneider ARP, Schaeffeler E, Burghaus R, Yilmaz A, Blank LM, Kerb R, Lippert J, Schlender JF, Schwab M, Kuepfer L.
Veröffentlicht in: CPT: pharmacometrics & systems pharmacology, 2021, ISSN 2163-8306
Herausgeber: Nature Publishing Group
DOI: 10.1002/psp4.12646

Association of CYP2C19 and CYP2D6 Poor and Intermediate Metabolizer Status With Antidepressant and Antipsychotic Exposure: A Systematic Review and Meta-analysis. (öffnet in neuem Fenster)

Autoren: Milosavljevic F, Bukvic N, Pavlovic Z, Miljevic C, Pešic V, Molden E, Ingelman-Sundberg M, Leucht S, Jukic MM.
Veröffentlicht in: JAMA psychiatry, 2021, ISSN 2168-622X
Herausgeber: American Medical Association
DOI: 10.1001/jamapsychiatry.2020.3643

Individualized versus Standardized Risk Assessment in Patients at High Risk for Adverse Drug Reactions (The IDrug Randomized Controlled Trial)-Never Change a Running System? (öffnet in neuem Fenster)

Autoren: Just KS, Scholl C, Boehme M, Kastenmüller K, Just JM, Bleckwenn M, Holdenrieder S, Meier F, Weckbecker K, Stingl JC.
Veröffentlicht in: Pharmaceuticals (Basel, Switzerland), 2021, ISSN 1424-8247
Herausgeber: Multidisciplinary Digital Publishing Institute (MDPI)
DOI: 10.3390/ph14101056

OpenBioLink: a benchmarking framework for large-scale biomedical link prediction (öffnet in neuem Fenster)

Autoren: Anna Breit, Simon Ott, Asan Agibetov, Matthias Samwald
Veröffentlicht in: Bioinformatics, Ausgabe 36/13, 2020, Seite(n) 4097-4098, ISSN 1367-4803
Herausgeber: Oxford University Press
DOI: 10.1093/bioinformatics/btaa274

Pharmacometrics-Based Considerations for the Design of a Pharmacogenomic Clinical Trial Assessing Irinotecan Safety. (öffnet in neuem Fenster)

Autoren: Minichmayr IK, Karlsson MO, Jönsson S.
Veröffentlicht in: Pharmaceutical research, 2021, ISSN 0724-8741
Herausgeber: Kluwer Academic/Plenum Publishers
DOI: 10.1007/s11095-021-03024-w

Rates of complete nonadherence among atypical antipsychotic drugs: A study using blood samples from 13,217 outpatients with psychotic disorders. (öffnet in neuem Fenster)

Autoren: Smith RL, Tveito M, Kyllesø L, Jukic MM, Ingelman-Sundberg M, Andreassen OA, Molden E.
Veröffentlicht in: Schizophrenia research, 2021, ISSN 0920-9964
Herausgeber: Elsevier BV
DOI: 10.1016/j.schres.2020.11.025

Genotyping for HLA Risk Alleles to Prevent Drug Hypersensitivity Reactions: Impact Analysis. (öffnet in neuem Fenster)

Autoren: Manson LEN, van den Hout WB, Guchelaar HJ.
Veröffentlicht in: Pharmaceuticals (Basel, Switzerland), 2021, ISSN 1424-8247
Herausgeber: Multidisciplinary Digital Publishing Institute (MDPI)
DOI: 10.3390/ph15010004

Pharmacogenomics of anticancer drugs: Personalising the choice and dose to manage drug response. (öffnet in neuem Fenster)

Autoren: Carr DF, Turner RM, Pirmohamed M.
Veröffentlicht in: British journal of clinical pharmacology, 2021, ISSN 0306-5251
Herausgeber: Blackwell Publishing Inc.
DOI: 10.1111/bcp.14407

Technologies for Pharmacogenomics: A Review. (öffnet in neuem Fenster)

Autoren: van der Lee M, Kriek M, Guchelaar HJ, Swen JJ.
Veröffentlicht in: Genes, 2020, ISSN 2073-4425
Herausgeber: Multidisciplinary Digital Publishing Institute (MDPI)
DOI: 10.3390/genes11121456

Physiologically Based Precision Dosing Approach for Drug-Drug-Gene Interactions: A Simvastatin Network Analysis. (öffnet in neuem Fenster)

Autoren: Wojtyniak JG, Selzer D, Schwab M, Lehr T.
Veröffentlicht in: Clinical pharmacology and therapeutics, 2021, ISSN 0009-9236
Herausgeber: Nature Publishing Group
DOI: 10.1002/cpt.2111

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