George P. Patrinos
George P. Patrinos
University of Patras, Department of Pharmacy
Verified email at - Homepage
Cited by
Cited by
Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology
N Mullins, AJ Forstner, KS O’Connell, B Coombes, JRI Coleman, Z Qiao, ...
Nature genetics 53 (6), 817-829, 2021
Gene conversion: mechanisms, evolution and human disease
JM Chen, DN Cooper, N Chuzhanova, C Férec, GP Patrinos
Nature Reviews Genetics 8 (10), 762-775, 2007
Defining the disease liability of variants in the cystic fibrosis transmembrane conductance regulator gene
PR Sosnay, KR Siklosi, F Van Goor, K Kaniecki, H Yu, N Sharma, ...
Nature genetics 45 (10), 1160-1167, 2013
HbVar: A relational database of human hemoglobin variants and thalassemia mutations at the globin gene server
RC Hardison, DHK Chui, B Giardine, C Riemer, GP Patrinos, N Anagnou, ...
Human mutation 19 (3), 225-233, 2002
Haploinsufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobin
J Borg, P Papadopoulos, M Georgitsi, L Gutiérrez, G Grech, P Fanis, ...
Nature genetics 42 (9), 801-805, 2010
Improvements in the HbVar database of human hemoglobin variants and thalassemia mutations for population and sequence variation studies
GP Patrinos, B Giardine, C Riemer, W Miller, DHK Chui, NP Anagnou, ...
Nucleic acids research 32 (suppl_1), D537-D541, 2004
Updates of the HbVar database of human hemoglobin variants and thalassemia mutations
B Giardine, J Borg, E Viennas, C Pavlidis, K Moradkhani, P Joly, ...
Nucleic acids research 42 (D1), D1063-D1069, 2014
Computational approaches in target identification and drug discovery
T Katsila, GA Spyroulias, GP Patrinos, MT Matsoukas
Computational and structural biotechnology journal 14, 177-184, 2016
Implementing pharmacogenomics in Europe: design and implementation strategy of the ubiquitous pharmacogenomics consortium
CH van der Wouden, A Cambon‐Thomsen, E Cecchin, KC Cheung, ...
Clinical Pharmacology & Therapeutics 101 (3), 341-358, 2017
HbVar database of human hemoglobin variants and thalassemia mutations: 2007 update
B Giardine, S van Baal, P Kaimakis, C Riemer, W Miller, M Samara, ...
Human mutation 28 (2), 206-206, 2007
Multiple interactions between regulatory regions are required to stabilize an active chromatin hub
GP Patrinos, M de Krom, E de Boer, A Langeveld, AMA Imam, ...
Genes & development 18 (12), 1495-1509, 2004
A 12-gene pharmacogenetic panel to prevent adverse drug reactions: an open-label, multicentre, controlled, cluster-randomised crossover implementation study
JJ Swen, CH van der Wouden, LEN Manson, H Abdullah-Koolmees, ...
The Lancet 401 (10374), 347-356, 2023
RD-Connect: an integrated platform connecting databases, registries, biobanks and clinical bioinformatics for rare disease research
R Thompson, L Johnston, D Taruscio, L Monaco, C Béroud, IG Gut, ...
Journal of general internal medicine 29, 780-787, 2014
Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach
B Giardine, J Borg, DR Higgs, KR Peterson, S Philipsen, D Maglott, ...
Nature genetics 43 (4), 295-301, 2011
Human genetic factors associated with susceptibility to SARS-CoV-2 infection and COVID-19 disease severity
C Anastassopoulou, Z Gkizarioti, GP Patrinos, A Tsakris
Human genomics 14 (1), 40, 2020
DNA hypermethylation: when tumour suppressor genes go silent
GA Garinis, GP Patrinos, NE Spanakis, PG Menounos
Human genetics 111 (2), 115-127, 2002
Genomic rearrangements in inherited disease and cancer
JM Chen, DN Cooper, C Férec, H Kehrer-Sawatzki, GP Patrinos
Seminars in cancer biology 20 (4), 222-233, 2010
Realities and expectations of pharmacogenomics and personalized medicine: impact of translating genetic knowledge into clinical practice
A Squassina, M Manchia, VG Manolopoulos, M Artac, C Lappa-Manakou, ...
Pharmacogenomics 11 (8), 1149-1167, 2010
Global implementation of genomic medicine: we are not alone
TA Manolio, M Abramowicz, F Al-Mulla, W Anderson, R Balling, ...
Science translational medicine 7 (290), 290ps13-290ps13, 2015
Krüppeling erythropoiesis: an unexpected broad spectrum of human red blood cell disorders due to KLF1 variants
A Perkins, X Xu, DR Higgs, GP Patrinos, L Arnaud, JJ Bieker, S Philipsen, ...
Blood, The Journal of the American Society of Hematology 127 (15), 1856-1862, 2016
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