George P. Patrinos
George P. Patrinos
University of Patras, Department of Pharmacy
Η διεύθυνση ηλεκτρονικού ταχυδρομείου έχει επαληθευτεί στον τομέα upatras.gr - Αρχική σελίδα
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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
5802007
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
4662013
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
4532002
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
3942004
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
3632010
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
2802014
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
2272007
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
2152004
DNA hypermethylation: when tumour suppressor genes go silent
GA Garinis, GP Patrinos, NE Spanakis, PG Menounos
Human genetics 111 (2), 115-127, 2002
1632002
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
1622010
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
1572016
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, 2011
1402011
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
1382010
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
1292014
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
1182017
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
1102015
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
882007
Molecular diagnosis of inherited disorders: lessons from hemoglobinopathies
GP Patrinos, P Kollia, MN Papadakis
Human mutation 26 (5), 399-412, 2005
872005
Evidence for association of an ACCN1 gene variant with response to lithium treatment in Sardinian patients with bipolar disorder
A Squassina, M Manchia, J Borg, D Congiu, M Costa, M Georgitsi, ...
Pharmacogenomics 12 (11), 1559-1569, 2011
842011
Erythroid phenotypes associated with KLF1 mutations
J Borg, GP Patrinos, AE Felice, S Philipsen
haematologica 96 (5), 635-638, 2011
842011
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