George P. Patrinos

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Theodora KatsilaResearch Assistant Professor-Head of Lab at National Hellenic Research FoundationPatvirtintas el. paštas eie.gr
David N. CooperProfessor of Human Molecular Genetics, Cardiff University, UKPatvirtintas el. paštas cardiff.ac.uk
Bassam R AliProfessor of Molecular Genetics, College of Medicine, United Arab Emirates UniversityPatvirtintas el. paštas uaeu.ac.ae
Alessio SquassinaUniversity of CagliariPatvirtintas el. paštas unica.it
Kollia PanagoulaNational and Kapodistrian University of Athens, Biology, Dept. Genetics and BiotechnologyPatvirtintas el. paštas biol.uoa.gr
Athanassios VozikisProfessor, Laboratory of Health Economics and Management (LabHEM), University of PiraeusPatvirtintas el. paštas unipi.gr
Giannis TzimasProfessor, Department of Electrical & Computer Engineering, University of PeloponnesePatvirtintas el. paštas tzimas.info
Ross C. HardisonProfessor Emeritus of Biochemistry and Molecular Biology, The Pennsylvania State UniversityPatvirtintas el. paštas psu.edu
Ron van SchaikProfessor Pharmacogenetics, ErasmusPatvirtintas el. paštas erasmusmc.nl
Belinda Giardinecomputer programmer, Penn State UniversityPatvirtintas el. paštas bx.psu.edu
Peter van der SpekErasmus University Medical CenterPatvirtintas el. paštas erasmusmc.nl
Emmanouil ViennasUniversity of PatrasPatvirtintas el. paštas ceid.upatras.gr
Webb MillerPenn State University, UC Santa Barbara, ArizonaPatvirtintas el. paštas bx.psu.edu
George A. GarinisProfessor of Genetics, University of Crete and affiliated group leader at the IMBB-FORTH.Patvirtintas el. paštas imbb.forth.gr
Velegraki AristeaAsst. Professor in Mycology, National and Kapodistrian University of AthensPatvirtintas el. paštas med.uoa.gr
Petros PapadopoulosUniversity of Helsinki, Faculty of MedicinePatvirtintas el. paštas helsinki.fi
Jian-Min Chen, MD, PhD, Directeur de...EFS, Univ Brest, Inserm, UMR 1078, GGB, F-29200 Brest, FrancePatvirtintas el. paštas univ-brest.fr
Claude FerecMD-PhD, Pharm, Professor of Genetics, INSERM and University of BrestPatvirtintas el. paštas univ-brest.fr
Marc S. WilliamsProfessor and Director Emeritus, Genomic Medicine Institute, GeisingerPatvirtintas el. paštas geisinger.edu
Ming Ta Michael LeeGalatea BioPatvirtintas el. paštas galatea.bio

Stebėti

George P. Patrinos

University of Patras, Department of Pharmacy

Patvirtintas el. paštas upatras.gr - Pagrindinis puslapis

Pharmacogenomics Genome Informatics Public Health Genomics


Pavadinimas Rūšiuoti pagal šaltinius Rūšiuoti pagal metus Rūšiuoti pagal pavadinimą	Cituota Cituota	Metai
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	734	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	648	2013
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	571	2021
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	510	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	449	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	438	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	430	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	337	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	265	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	261	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	223	2004
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	182	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	179	2011
DNA hypermethylation: when tumour suppressor genes go silent GA Garinis, GP Patrinos, NE Spanakis, PG Menounos Human genetics 111 (2), 115-127, 2002	179	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	175	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	167	2010
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), 1-8, 2020	160	2020
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	156	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	147	2016
Molecular diagnosis of inherited disorders: lessons from hemoglobinopathies GP Patrinos, P Kollia, MN Papadakis Human mutation 26 (5), 399-412, 2005	117	2005

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