George P. Patrinos

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Theodora KatsilaResearch Associate Professor-Head of Lab at National Hellenic Research FoundationPotvrđena adresa e-pošte na eie.gr
David N. CooperProfessor of Human Molecular Genetics, Cardiff University, UKPotvrđena adresa e-pošte na cardiff.ac.uk
Bassam R AliProfessor of Molecular Genetics, College of Medicine, United Arab Emirates UniversityPotvrđena adresa e-pošte na uaeu.ac.ae
Alessio SquassinaUniversity of CagliariPotvrđena adresa e-pošte na unica.it
Athanassios VozikisProfessor, Laboratory of Health Economics and Management (LabHEM), University of PiraeusPotvrđena adresa e-pošte na unipi.gr
Kollia PanagoulaNational and Kapodistrian University of Athens, Biology, Dept. Genetics and BiotechnologyPotvrđena adresa e-pošte na biol.uoa.gr
Giannis TzimasProfessor, Department of Electrical & Computer Engineering, University of PeloponnesePotvrđena adresa e-pošte na tzimas.info
Ross C. HardisonProfessor Emeritus of Biochemistry and Molecular Biology, The Pennsylvania State UniversityPotvrđena adresa e-pošte na psu.edu
Belinda Giardinecomputer programmer, Penn State UniversityPotvrđena adresa e-pošte na bx.psu.edu
Ron van SchaikProfessor Pharmacogenetics, ErasmusPotvrđena adresa e-pošte na erasmusmc.nl
Peter van der SpekErasmus University Medical CenterPotvrđena adresa e-pošte na erasmusmc.nl
Emmanouil ViennasUniversity of PatrasPotvrđena adresa e-pošte na ceid.upatras.gr
Webb MillerPenn State University, UC Santa Barbara, ArizonaPotvrđena adresa e-pošte na bx.psu.edu
George A. GarinisProfessor of Genetics, University of Crete and affiliated group leader at the IMBB-FORTH.Potvrđena adresa e-pošte na imbb.forth.gr
Petros PapadopoulosUniversity of Helsinki, Faculty of MedicinePotvrđena adresa e-pošte na helsinki.fi
Jian-Min Chen, MD, PhD, Directeur de...Univ Brest, Inserm, EFS, UMR 1078, GGB, F-29200 Brest, FrancePotvrđena adresa e-pošte na univ-brest.fr
Claude FerecMD-PhD, Pharm, Professor of Genetics, INSERM and University of BrestPotvrđena adresa e-pošte na univ-brest.fr
Marc S. WilliamsProfessor and Director Emeritus, Genomic Medicine Institute, GeisingerPotvrđena adresa e-pošte na geisinger.edu
Nick SpanakisAssistant Professor of Microbiology, NKUAPotvrđena adresa e-pošte na med.uoa.gr
Giovanni SeverinoUniversity of CagliariPotvrđena adresa e-pošte na unica.it

Prati

George P. Patrinos

University of Patras, Department of Pharmacy

Potvrđena adresa e-pošte na upatras.gr - Početna stranica

Pharmacogenomics Genome Informatics Public Health Genomics


Naslov Poredaj po navodima Poredaj po godini Poredaj po naslovu	Citirano Citirano	Godina
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	1115	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	765	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	726	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	526	2002
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	492	2014
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	470	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	467	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	443	2016
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	335	2023
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	326	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	268	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	227	2004
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	203	2020
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	195	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	194	2010
Dissecting the shared genetic architecture of suicide attempt, psychiatric disorders, and known risk factors N Mullins, JE Kang, AI Campos, JRI Coleman, AC Edwards, H Galfalvy, ... Biological psychiatry 91 (3), 313-327, 2022	192	2022
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	192	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	190	2011
DNA hypermethylation: when tumour suppressor genes go silent GA Garinis, GP Patrinos, NE Spanakis, PG Menounos Human genetics 111 (2), 115-127, 2002	185	2002
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	182	2015

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