Nuria Lopez-Bigas
Nuria Lopez-Bigas
ICREA Research Professor at the Institute for Research in Biomedicine
Verified email at irbbarcelona.org - Homepage
Title
Cited by
Cited by
Year
Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project
ENCODE Project Consortium
nature 447 (7146), 799, 2007
51692007
The cancer genome atlas pan-cancer analysis project
JN Weinstein, EA Collisson, GB Mills, KRM Shaw, BA Ozenberger, ...
Nature genetics 45 (10), 1113, 2013
33462013
International network of cancer genome projects
International Cancer Genome Consortium
Nature 464 (7291), 993, 2010
16462010
Multiplatform analysis of 12 cancer types reveals molecular classification within and across tissues of origin
KA Hoadley, C Yau, DM Wolf, AD Cherniack, D Tamborero, S Ng, ...
Cell 158 (4), 929-944, 2014
10012014
A landscape of pharmacogenomic interactions in cancer
F Iorio, TA Knijnenburg, DJ Vis, GR Bignell, MP Menden, M Schubert, ...
Cell 166 (3), 740-754, 2016
7262016
Expansion of the BioCyc collection of pathway/genome databases to 160 genomes
PD Karp, CA Ouzounis, C Moore-Kochlacs, L Goldovsky, P Kaipa, ...
Nucleic acids research 33 (19), 6083-6089, 2005
7092005
Comprehensive characterization of cancer driver genes and mutations
MH Bailey, C Tokheim, E Porta-Pardo, S Sengupta, D Bertrand, ...
Cell 173 (2), 371-385. e18, 2018
6942018
Improving the assessment of the outcome of nonsynonymous SNVs with a consensus deleteriousness score, Condel
A González-Pérez, N López-Bigas
The American Journal of Human Genetics 88 (4), 440-449, 2011
6882011
Non-coding recurrent mutations in chronic lymphocytic leukaemia
XS Puente, S Beà, R Valdés-Mas, N Villamor, J Gutiérrez-Abril, ...
Nature 526 (7574), 519-524, 2015
5682015
Pan-cancer network analysis identifies combinations of rare somatic mutations across pathways and protein complexes
MDM Leiserson, F Vandin, HT Wu, JR Dobson, JV Eldridge, JL Thomas, ...
Nature genetics 47 (2), 106-114, 2015
5572015
Whole-genome landscapes of major melanoma subtypes
NK Hayward, JS Wilmott, N Waddell, PA Johansson, MA Field, K Nones, ...
Nature 545 (7653), 175-180, 2017
4702017
Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus
A Grifa, CA Wagner, L D'Ambrosio, S Melchionda, F Bernardi, ...
Nature genetics 23 (1), 16-18, 1999
4501999
Comprehensive identification of mutational cancer driver genes across 12 tumor types
D Tamborero, A Gonzalez-Perez, C Perez-Llamas, J Deu-Pons, ...
Scientific reports 3, 2650, 2013
4122013
IntOGen-mutations identifies cancer drivers across tumor types
A Gonzalez-Perez, C Perez-Llamas, J Deu-Pons, D Tamborero, ...
Nature methods 10 (11), 1081-1082, 2013
3852013
Are splicing mutations the most frequent cause of hereditary disease?
N López-Bigas, B Audit, C Ouzounis, G Parra, R Guigó
FEBS letters 579 (9), 1900-1903, 2005
3812005
Jagged1 is the pathological link between Wnt and Notch pathways in colorectal cancer
V Rodilla, A Villanueva, A Obrador-Hevia, À Robert-Moreno, ...
Proceedings of the National Academy of Sciences 106 (15), 6315-6320, 2009
3462009
Functional impact bias reveals cancer drivers
A Gonzalez-Perez, N Lopez-Bigas
Nucleic acids research 40 (21), e169-e169, 2012
3022012
Genome‐wide identification of genes likely to be involved in human genetic disease
N López‐Bigas, CA Ouzounis
Nucleic acids research 32 (10), 3108-3114, 2004
2872004
Molecular basis of childhood deafness resulting from mutations in the GJB2 (connexin 26) gene
R Rabionet, L Zelante, N López-Bigas, L D'Agruma, S Melchionda, ...
Human genetics 106 (1), 40-44, 2000
2712000
The repertoire of mutational signatures in human cancer
LB Alexandrov, J Kim, NJ Haradhvala, MN Huang, AWT Ng, Y Wu, A Boot, ...
Nature 578 (7793), 94-101, 2020
2622020
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