Yap W, Cengnata A, Saw W, Abdul Rahman T, Teo Y, Lim R
Hum Genome Var. 2025; 12(1):4.
PMID: 39774017
PMC: 11707147.
DOI: 10.1038/s41439-024-00308-6.
Alqasrawi M, Al-Mahayri Z, Alblooshi H, AlSafar H, Ali B
Curr Vasc Pharmacol. 2024; 22(3):218-229.
PMID: 38284696
DOI: 10.2174/0115701611283841231227064343.
Tafazoli A, Mikros J, Khaghani F, Alimardani M, Rafigh M, Hemmati M
Hum Genomics. 2023; 17(1):62.
PMID: 37452347
PMC: 10347842.
DOI: 10.1186/s40246-023-00508-1.
Athanasopoulou K, Daneva G, Boti M, Dimitroulis G, Adamopoulos P, Scorilas A
Life (Basel). 2022; 12(12).
PMID: 36556377
PMC: 9785810.
DOI: 10.3390/life12122010.
Tian J, Zhang J, Yang Z, Feng S, Li S, Ren S
Front Pharmacol. 2022; 12:790832.
PMID: 35280256
PMC: 8906509.
DOI: 10.3389/fphar.2021.790832.
Controlling my genome with my smartphone: first clinical experiences of the PROMISE system.
Amr A, Hinderer M, Griebel L, Deuber D, Egger C, Sedaghat-Hamedani F
Clin Res Cardiol. 2021; 111(6):638-650.
PMID: 34694434
PMC: 9151530.
DOI: 10.1007/s00392-021-01942-8.
Early Cost Effectiveness of Whole-Genome Sequencing as a Clinical Diagnostic Test for Patients with Inoperable Stage IIIB,C/IV Non-squamous Non-small-Cell Lung Cancer.
Simons M, Retel V, Ramaekers B, Butter R, Mankor J, Paats M
Pharmacoeconomics. 2021; 39(12):1429-1442.
PMID: 34405371
PMC: 8599348.
DOI: 10.1007/s40273-021-01073-y.
A novel machine learning-based approach for the computational functional assessment of pharmacogenomic variants.
Pandi M, Koromina M, Tsafaridis I, Patsilinakos S, Christoforou E, van der Spek P
Hum Genomics. 2021; 15(1):51.
PMID: 34372920
PMC: 8351412.
DOI: 10.1186/s40246-021-00352-1.
Strategies to Improve the Clinical Outcomes for Direct-to-Consumer Pharmacogenomic Tests.
Tafazoli A, Guggilla R, Kamel-Koleti Z, Miltyk W
Genes (Basel). 2021; 12(3).
PMID: 33802585
PMC: 7999840.
DOI: 10.3390/genes12030361.
Pharmacogenomics, How to Deal with Different Types of Variants in Next Generation Sequencing Data in the Personalized Medicine Area.
Tafazoli A, Wawrusiewicz-Kurylonek N, Posmyk R, Miltyk W
J Clin Med. 2020; 10(1).
PMID: 33374421
PMC: 7796098.
DOI: 10.3390/jcm10010034.
Variation in 100 relevant pharmacogenes among emiratis with insights from understudied populations.
Al-Mahayri Z, Patrinos G, Wattanapokayakit S, Iemwimangsa N, Fukunaga K, Mushiroda T
Sci Rep. 2020; 10(1):21310.
PMID: 33277594
PMC: 7718919.
DOI: 10.1038/s41598-020-78231-3.
Variation in Actionable Pharmacogenetic Markers in Natives and Mestizos From Mexico.
Gonzalez-Covarrubias V, Morales-Franco M, Cruz-Correa O, Martinez-Hernandez A, Garcia-Ortiz H, Barajas-Olmos F
Front Pharmacol. 2019; 10:1169.
PMID: 31649539
PMC: 6796793.
DOI: 10.3389/fphar.2019.01169.
Laying Anchor: Inserting Precision Health into a Public Health Genetics Policy Course.
Modell S, Citrin T, Kardia S
Healthcare (Basel). 2018; 6(3).
PMID: 30081448
PMC: 6163426.
DOI: 10.3390/healthcare6030093.
The New Age of -omics in Urothelial Cancer - Re-wording Its Diagnosis and Treatment.
Katsila T, Liontos M, Patrinos G, Bamias A, Kardamakis D
EBioMedicine. 2018; 28:43-50.
PMID: 29428524
PMC: 5835572.
DOI: 10.1016/j.ebiom.2018.01.044.
Rational confederation of genes and diseases: NGS interpretation via GeneCards, MalaCards and VarElect.
Rappaport N, Fishilevich S, Nudel R, Twik M, Belinky F, Plaschkes I
Biomed Eng Online. 2017; 16(Suppl 1):72.
PMID: 28830434
PMC: 5568599.
DOI: 10.1186/s12938-017-0359-2.
Exploring public genomics data for population pharmacogenomics.
Lakiotaki K, Kanterakis A, Kartsaki E, Katsila T, Patrinos G, Potamias G
PLoS One. 2017; 12(8):e0182138.
PMID: 28771511
PMC: 5542428.
DOI: 10.1371/journal.pone.0182138.
The global spectrum of protein-coding pharmacogenomic diversity.
Wright G, Carleton B, Hayden M, Ross C
Pharmacogenomics J. 2016; 18(1):187-195.
PMID: 27779249
PMC: 5817389.
DOI: 10.1038/tpj.2016.77.
ePGA: A Web-Based Information System for Translational Pharmacogenomics.
Lakiotaki K, Kartsaki E, Kanterakis A, Katsila T, Patrinos G, Potamias G
PLoS One. 2016; 11(9):e0162801.
PMID: 27631363
PMC: 5025168.
DOI: 10.1371/journal.pone.0162801.
Pharmacogenetics and anaesthetic drugs: Implications for perioperative practice.
Behrooz A
Ann Med Surg (Lond). 2016; 4(4):470-4.
PMID: 26779337
PMC: 4685230.
DOI: 10.1016/j.amsu.2015.11.001.
Cracking the Code of Human Diseases Using Next-Generation Sequencing: Applications, Challenges, and Perspectives.
Precone V, Del Monaco V, Esposito M, De Palma F, Ruocco A, Salvatore F
Biomed Res Int. 2015; 2015:161648.
PMID: 26665001
PMC: 4668301.
DOI: 10.1155/2015/161648.