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Javier Santoyo-Lopez
Javier Santoyo-Lopez
Edinburgh Genomics
Verified email at ed.ac.uk - Homepage
Title
Cited by
Cited by
Year
Initial sequencing and analysis of the human genome
US DOE Joint Genome Institute: Hawkins Trevor 4 Branscomb Elbert 4 Predki ...
Nature 409 (6822), 860-921, 2001
242642001
Finishing the euchromatic sequence of the human genome
International Human Genome Sequencing Consortium
Nature 431 (7011), 931-945, 2004
52412004
A comprehensive assessment of RNA-seq accuracy, reproducibility and information content by the Sequencing Quality Control Consortium
Nature biotechnology 32 (9), 903-914, 2014
8502014
Statistical methods for analysis of high-throughput RNA interference screens
A Birmingham, LM Selfors, T Forster, D Wrobel, CJ Kennedy, E Shanks, ...
Nature methods 6 (8), 569-575, 2009
6812009
Promoting coherent minimum reporting guidelines for biological and biomedical investigations: the MIBBI project
CF Taylor, D Field, SA Sansone, J Aerts, R Apweiler, M Ashburner, ...
Nature biotechnology 26 (8), 889-896, 2008
6192008
Initial genomics of the human nucleolus
A Németh, A Conesa, J Santoyo-Lopez, I Medina, D Montaner, B Péterfia, ...
PLoS genetics 6 (3), e1000889, 2010
4402010
The eIF‐2α kinases and the control of protein synthesis1
C De Haro, R Méndez, J Santoyo
The FASEB journal 10 (12), 1378-1387, 1996
3871996
Babelomics: an integrative platform for the analysis of transcriptomics, proteomics and genomic data with advanced functional profiling
I Medina, J Carbonell, L Pulido, SC Madeira, S Goetz, A Conesa, ...
Nucleic acids research 38 (suppl_2), W210-W213, 2010
3662010
Characterization of a mammalian homolog of the GCN2 eukaryotic initiation factor 2α kinase
JJ Berlanga, J Santoyo, C de Haro
European journal of biochemistry 265 (2), 754-762, 1999
3481999
GEPAS: A web-based resource for microarray gene expression data analysis
J Herrero, F Al-Shahrour, R Diaz-Uriarte, A Mateos, JM Vaquerizas, ...
Nucleic acids research 31 (13), 3461-3467, 2003
2322003
Integrated analysis of whole-exome sequencing and transcriptome profiling in males with autism spectrum disorders
M Codina-Solà, B Rodríguez-Santiago, A Homs, J Santoyo, M Rigau, ...
Molecular autism 6, 1-16, 2015
1442015
Mutational landscape of a chemically-induced mouse model of liver cancer
F Connor, TF Rayner, SJ Aitken, C Feig, M Lukk, J Santoyo-Lopez, ...
Journal of hepatology 69 (4), 840-850, 2018
1282018
Assessing technical performance in differential gene expression experiments with external spike-in RNA control ratio mixtures
SA Munro, SP Lund, PS Pine, H Binder, DA Clevert, A Conesa, J Dopazo, ...
Nature communications 5 (1), 5125, 2014
1272014
PupaSNP Finder: a web tool for finding SNPs with putative effect at transcriptional level
L Conde, JM Vaquerizas, J Santoyo, F Al-Shahrour, S Ruiz-Llorente, ...
Nucleic acids research 32 (suppl_2), W242-W248, 2004
1182004
poRe: an R package for the visualization and analysis of nanopore sequencing data
M Watson, M Thomson, J Risse, R Talbot, J Santoyo-Lopez, K Gharbi, ...
Bioinformatics 31 (1), 114-115, 2015
1062015
Discrete clusters of virus-encoded micrornas are associated with complementary strands of the genome and the 7.2-kilobase stable intron in murine cytomegalovirus
AH Buck, J Santoyo-Lopez, KA Robertson, DS Kumar, M Reczko, ...
Journal of virology 81 (24), 13761-13770, 2007
1022007
Cloning and Characterization of a CDNA Encoding a Protein Synthesis Initiation Factor-2α (EIF-2α) Kinase FromDrosophila Melanogaster: HOMOLOGY TO YEAST GCN2 PROTEIN KINASE
J Santoyo, J Alcalde, R Méndez, D Pulido, C de Haro
Journal of Biological Chemistry 272 (19), 12544-12550, 1997
951997
Mutation spectrum of EYS in Spanish patients with autosomal recessive retinitis pigmentosa
I Barragán, S Borrego, JI Pieras, MG Pozo, J Santoyo, C Ayuso, M Baiget, ...
Human mutation 31 (11), E1772-E1800, 2010
912010
DNA polymerase epsilon deficiency causes IMAGe syndrome with variable immunodeficiency
CV Logan, JE Murray, DA Parry, A Robertson, R Bellelli, Ž Tarnauskaitė, ...
The American Journal of Human Genetics 103 (6), 1038-1044, 2018
852018
A dominantly inherited 5′ UTR variant causing methylation-associated silencing of BRCA1 as a cause of breast and ovarian cancer
DGR Evans, EM van Veen, HJ Byers, AJ Wallace, JM Ellingford, ...
The American Journal of Human Genetics 103 (2), 213-220, 2018
852018
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