Seuraa
Gonzalo R. Ordóñez
Gonzalo R. Ordóñez
Director de MP y Laboratorios NASERTIC
Vahvistettu sähköpostiosoite verkkotunnuksessa nasertic.es
Nimike
Viittaukset
Viittaukset
Vuosi
A comprehensive catalogue of somatic mutations from a human cancer genome
ED Pleasance, RK Cheetham, PJ Stephens, DJ McBride, SJ Humphray, ...
Nature 463 (7278), 191-196, 2010
20762010
Whole-genome sequencing identifies recurrent mutations in chronic lymphocytic leukaemia
XS Puente, M Pinyol, V Quesada, L Conde, GR Ordóñez, N Villamor, ...
Nature 475 (7354), 101-105, 2011
19642011
A small-cell lung cancer genome with complex signatures of tobacco exposure
ED Pleasance, PJ Stephens, S O’Meara, DJ McBride, A Meynert, D Jones, ...
Nature 463 (7278), 184-190, 2010
13182010
Exome sequencing identifies recurrent mutations of the splicing factor SF3B1 gene in chronic lymphocytic leukemia
V Quesada, L Conde, N Villamor, GR Ordóñez, P Jares, L Bassaganyas, ...
Nature genetics 44 (1), 47-52, 2012
12952012
Genome analysis of the platypus reveals unique signatures of evolution
Nature 453 (7192), 175-183, 2008
7812008
Comparative and demographic analysis of orang-utan genomes
DP Locke, LDW Hillier, WC Warren, KC Worley, LV Nazareth, DM Muzny, ...
Nature 469 (7331), 529-533, 2011
7142011
Exome sequencing and functional analysis identifies BANF1 mutation as the cause of a hereditary progeroid syndrome
XS Puente, V Quesada, FG Osorio, R Cabanillas, J Cadiñanos, JM Fraile, ...
The American Journal of Human Genetics 88 (5), 650-656, 2011
2542011
The Degradome database: mammalian proteases and diseases of proteolysis
V Quesada, GR Ordonez, LM Sanchez, XS Puente, C López-Otín
Nucleic acids research 37 (suppl_1), D239-D243, 2009
2202009
Integrating genomic alterations in diffuse large B-cell lymphoma identifies new relevant pathways and potential therapeutic targets
K Karube, A Enjuanes, I Dlouhy, P Jares, D Martín-García, F Nadeu, ...
Leukemia 32 (3), 675-684, 2018
1962018
Comprehensive genomic diagnosis of non-syndromic and syndromic hereditary hearing loss in Spanish patients
R Cabanillas, M Diñeiro, GA Cifuentes, D Castillo, PC Pruneda, R Álvarez, ...
BMC medical genomics 11, 1-17, 2018
1052018
Comparative genomic analysis of human and chimpanzee proteases
XS Puente, A Gutiérrez-Fernández, GR Ordóñez, LDW Hillier, ...
Genomics 86 (6), 638-647, 2005
1042005
Loss of genes implicated in gastric function during platypus evolution
GR Ordoñez, LDW Hillier, WC Warren, F Grützner, C López-Otín, ...
Genome biology 9, 1-11, 2008
632008
Metalloproteases and the degradome
AP Ugalde, GR Ordóñez, PM Quirós, XS Puente, C López-Otín
Matrix metalloproteinase protocols, 3-29, 2010
592010
Application of a molecular diagnostic algorithm for haemophilia A and B using next-generation sequencing of entire F8, F9 and VWF genes
JM Bastida, JR González-Porras, C Jiménez, R Benito, GR Ordoñez, ...
Thrombosis and haemostasis 26 (01), 66-74, 2017
492017
From Waldenström’s macroglobulinemia to aggressive diffuse large B-cell lymphoma: a whole-exome analysis of abnormalities leading to transformation
C Jiménez, S Alonso-Álvarez, M Alcoceba, GR Ordóñez, ...
Blood cancer journal 7 (8), e591-e591, 2017
462017
A next-generation sequencing strategy for evaluating the most common genetic abnormalities in multiple myeloma
C Jiménez, M Jara-Acevedo, LA Corchete, D Castillo, GR Ordóñez, ...
The Journal of Molecular Diagnostics 19 (1), 99-106, 2017
362017
New chondrosarcoma cell lines with preserved stem cell properties to study the genomic drift during in vitro/in vivo growth
V Rey, ST Menendez, O Estupiñan, A Rodriguez, L Santos, J Tornin, ...
Journal of Clinical Medicine 8 (4), 455, 2019
272019
Selectivity of lipases and esterases towards phenol esters
UT Bornscheuer, GR Ordoñez, A Hidalgo, A Gollin, J Lyon, TS Hitchman, ...
Journal of molecular catalysis B: enzymatic 36 (1-6), 8-13, 2005
222005
Proteolytic systems: constructing degradomes
GR Ordóñez, XS Puente, V Quesada, C López-Otín
Proteases and Cancer: Methods and Protocols, 33-47, 2009
202009
Comprehensive genomic diagnosis of inherited retinal and optical nerve disorders reveals hidden syndromes and personalized therapeutic options
M Diñeiro, R Capín, GÁ Cifuentes, B Fernández‐Vega, E Villota, A Otero, ...
Acta Ophthalmologica 98 (8), e1034-e1048, 2020
182020
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Artikkelit 1–20