George P. Patrinos

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Theodora KatsilaAssociate Researcher-Head of Lab at National Hellenic Research FoundationVerified email at eie.gr
David N. CooperProfessor of Human Molecular Genetics, Cardiff University, UKVerified email at cardiff.ac.uk
Alessio SquassinaUniversity of CagliariVerified email at unica.it
Kollia PanagoulaNational and Kapodistrian University of Athens, Biology, Dept. Genetics and BiotechnologyVerified email at biol.uoa.gr
Giannis TzimasAssociate Professor, Department of Electrical & Computer Engineering, University of PeloponneseVerified email at tzimas.info
Bassam R AliProfessor of Molecular Genetics, College of Medicine, United Arab Emirates UniversityVerified email at uaeu.ac.ae
Athanassios VozikisAssociate Professor, Laboratory of Health Economics and Management (LabHEM), University of PiraeusVerified email at unipi.gr
Ross C. HardisonProfessor of Biochemistry and Molecular Biology, The Pennsylvania State UniversityVerified email at psu.edu
Emmanouil ViennasUniversity of PatrasVerified email at ceid.upatras.gr
Ron van SchaikProfessor Pharmacogenetics, ErasmusVerified email at erasmusmc.nl
Belinda Giardinecomputer programmer, Penn State UniversityVerified email at bx.psu.edu
Webb MillerPenn State University, UC Santa Barbara, ArizonaVerified email at bx.psu.edu
Peter van der SpekErasmus University Medical CenterVerified email at erasmusmc.nl
George A. GarinisProfessor of Genetics, University of Crete and affiliated group leader at the IMBB-FORTH.Verified email at imbb.forth.gr
Petros PapadopoulosHospital Clinico San CarlosVerified email at salud.madrid.org
Jian-Min Chen, MD, PhD, Directeur de...EFS, Univ Brest, Inserm, UMR 1078, GGB, F-29200 Brest, FranceVerified email at univ-brest.fr
Claude FerecMD-PhD, Pharm, Professor of Genetics, INSERM and University of BrestVerified email at univ-brest.fr
Nick SpanakisAssistant Professor of Microbiology, NKUAVerified email at med.uoa.gr
Nadia ChuzhanovaProfessor of Biomedical Mathematics, Nottingham Trent University, UKVerified email at ntu.ac.uk
Marc S. WilliamsProfessor and Director Emeritus, Genomic Medicine Institute, GeisingerVerified email at geisinger.edu

George P. Patrinos

University of Patras, Department of Pharmacy

Verified email at upatras.gr - Homepage

Pharmacogenomics Genome Informatics Public Health Genomics


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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	615	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	501	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	466	2002
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	407	2004
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	392	2010
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	315	2014
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	235	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	222	2004
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	191	2016
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	165	2010
DNA hypermethylation: when tumour suppressor genes go silent GA Garinis, GP Patrinos, NE Spanakis, PG Menounos Human genetics 111 (2), 115-127, 2002	165	2002
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	153	2017
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	149	2011
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	146	2010
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 (3), 780-787, 2014	143	2014
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	120	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	94	2016
PhenCode: connecting ENCODE data with mutations and phenotype B Giardine, C Riemer, T Hefferon, D Thomas, F Hsu, J Zielenski, Y Sang, ... Human mutation 28 (6), 554-562, 2007	91	2007
Erythroid phenotypes associated with KLF1 mutations J Borg, GP Patrinos, AE Felice, S Philipsen haematologica 96 (5), 635, 2011	90	2011
Molecular diagnosis of inherited disorders: lessons from hemoglobinopathies GP Patrinos, P Kollia, MN Papadakis Human mutation 26 (5), 399-412, 2005	90	2005

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