Zobrazeno 1 - 10
of 42
pro vyhledávání: '"Maria Koromina"'
Autor:
Stavroula Siamoglou, Ruben Boers, Maria Koromina, Joachim Boers, Anna Tsironi, Theodora Chatzilygeroudi, Vasileios Lazaris, Evgenia Verigou, Alexandra Kourakli, Wilfred F. J. van IJcken, Joost Gribnau, Argiris Symeonidis, George P. Patrinos
Publikováno v:
Human Genomics, Vol 17, Iss 1, Pp 1-12 (2023)
Abstract Myelodysplastic syndromes (MDS) consist of a group of hematological malignancies characterized by ineffective hematopoiesis, cytogenetic abnormalities, and often a high risk of transformation to acute myeloid leukemia (AML). So far, there ha
Externí odkaz:
https://doaj.org/article/7c0c414837a84d989ecf5b115c2b56a9
Autor:
Maria-Theodora Pandi, Maria Koromina, Iordanis Tsafaridis, Sotirios Patsilinakos, Evangelos Christoforou, Peter J. van der Spek, George P. Patrinos
Publikováno v:
Human Genomics, Vol 15, Iss 1, Pp 1-13 (2021)
Abstract Background The field of pharmacogenomics focuses on the way a person’s genome affects his or her response to a certain dose of a specified medication. The main aim is to utilize this information to guide and personalize the treatment in a
Externí odkaz:
https://doaj.org/article/116be51350a64a59aef0c3ac7fd4cf03
Autor:
Kariofyllis Karamperis, Maria T. Tsoumpeli, Fotios Kounelis, Maria Koromina, Christina Mitropoulou, Catia Moutinho, George P. Patrinos
Publikováno v:
Human Genomics, Vol 15, Iss 1, Pp 1-18 (2021)
Abstract For decades, various strategies have been proposed to solve the enigma of hemoglobinopathies, especially severe cases. However, most of them seem to be lagging in terms of effectiveness and safety. So far, the most prevalent and promising tr
Externí odkaz:
https://doaj.org/article/b8036c2e88c743ed9525fd736c3b25c7
Autor:
Chakkaphan Runcharoen, Koya Fukunaga, Insee Sensorn, Nareenart Iemwimangsa, Sommon Klumsathian, Hang Tong, Nam Sy Vo, Ly Le, Tin Maung Hlaing, Myo Thant, Shamsul Mohd Zain, Zahurin Mohamed, Yuh-Fen Pung, Francis Capule, Jose Nevado, Catherine Lynn Silao, Zeina N. Al-Mahayri, Bassam R. Ali, Rika Yuliwulandari, Kinasih Prayuni, Hilyatuz Zahroh, Dzul Azri Mohamed Noor, Phonepadith Xangsayarath, Dalouny Xayavong, Sengchanh Kounnavong, Somphou Sayasone, Zoe Kordou, Ioannis Liopetas, Athina Tsikrika, Evangelia-Eirini Tsermpini, Maria Koromina, Christina Mitropoulou, George P. Patrinos, Aumpika Kesornsit, Angkana Charoenyingwattana, Sukanya Wattanapokayakit, Surakameth Mahasirimongkol, Taisei Mushiroda, Wasun Chantratita
Publikováno v:
Human Genome Variation, Vol 8, Iss 1, Pp 1-6 (2021)
Abstract Pharmacogenomics can enhance the outcome of treatment by adopting pharmacogenomic testing to maximize drug efficacy and lower the risk of serious adverse events. Next-generation sequencing (NGS) is a cost-effective technology for genotyping
Externí odkaz:
https://doaj.org/article/d9ba2428e119486e956cf700ff929c5d
Publikováno v:
Human Genomics, Vol 14, Iss 1, Pp 1-10 (2020)
Abstract Background Genome-wide association studies (GWAS) have significantly contributed to the association of many clinical conditions and phenotypic characteristics with genomic variants. The majority of these genomic findings have been deposited
Externí odkaz:
https://doaj.org/article/b152fb948e8c47d4ab9c3c3fb869f6ae
Publikováno v:
PLoS ONE, Vol 17, Iss 5 (2022)
Motivation The outbreak of coronavirus health issues caused by COVID-19(SARS-CoV-2) creates a global threat to public health. Therefore, there is a need for effective remedial measures using existing and approved therapies with proven safety measures
Externí odkaz:
https://doaj.org/article/bb30d94695e04c1f8a4eed81fac38254
Publikováno v:
Frontiers in Pharmacology, Vol 11 (2020)
Text mining in biomedical literature is an emerging field which has already been shown to have a variety of implementations in many research areas, including genetics, personalized medicine, and pharmacogenomics. In this study, we describe a novel te
Externí odkaz:
https://doaj.org/article/1c1709f544ec41c3895b27be28f379d3
Autor:
James Buchanan, Usa Chaikledkaew, Ian Cromwell, Brett Doble, Morgan Ehman, Patrick Fahr, Vasileios Fragoulakis, Jiraphun Jittikoon, Maria Koromina, Margarita-Ioanna Koufaki, Paula K. Lorgelly, Surakameth Mahasirimongkol, Deborah Marshall, Christopher McCabe, Christina Mitropoulou, George P. Patrinos, Katherine Payne, Kathryn Philips, Samantha Pollard, Kinasih Prayuni, Dean A. Regier, Saowalak Turongkaravee, Athanassios Vozikis, Sukanya Wattanapokayakit, Deirdre Weymann, Sarah Wordsworth, Rika Yuliwulandari, Hilyatuz Zahroh
Publikováno v:
Economic Evaluation in Genomic and Precision Medicine ISBN: 9780128133828
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::319335777613979a8d2a249f58f02b99
https://doi.org/10.1016/b978-0-12-813382-8.09992-4
https://doi.org/10.1016/b978-0-12-813382-8.09992-4
Autor:
Maria Koromina, George P. Patrinos
Publikováno v:
Economic Evaluation in Genomic and Precision Medicine ISBN: 9780128133828
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::27f71ab15aee6a5d3d9112a290150306
https://doi.org/10.1016/b978-0-12-813382-8.00006-9
https://doi.org/10.1016/b978-0-12-813382-8.00006-9
Autor:
Panagiotis Bosganas, Aggeliki Charalampidi, Maria Koromina, Evangelia-Eirini Tsermpini, Wasun Chantratita, Zoe Kordou, Taisei Mushiroda, George P. Patrinos, Koya Fukunaga
Publikováno v:
Pharmacogenomics. 22:749-760
Aim: Regardless of the plethora of next-generation sequencing studies in the field of pharmacogenomics (PGx), the potential effect of covariate variables on PGx response within deeply phenotyped cohorts remains unexplored. Materials & methods: We exp