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Alicia Vela Boza
Alicia Vela Boza
Roche Diagnostics
Verified email at roche.com
Title
Cited by
Cited by
Year
A comprehensive assessment of RNA-seq accuracy, reproducibility and information content by the Sequencing Quality Control Consortium
Nature biotechnology 32 (9), 903-914, 2014
8382014
267 Spanish exomes reveal population-specific differences in disease-related genetic variation
J Dopazo, A Amadoz, M Bleda, L Garcia-Alonso, A Alemán, ...
Molecular biology and evolution 33 (5), 1205-1218, 2016
822016
Extension of human lncRNA transcripts by RACE coupled with long-read high-throughput sequencing (RACE-Seq)
J Lagarde, B Uszczynska-Ratajczak, J Santoyo-Lopez, JM Gonzalez, ...
Nature communications 7 (1), 12339, 2016
772016
A map of human microRNA variation uncovers unexpectedly high levels of variability
J Carbonell, E Alloza, P Arce, S Borrego, J Santoyo, M Ruiz-Ferrer, ...
Genome medicine 4, 1-17, 2012
462012
The role of the interactome in the maintenance of deleterious variability in human populations
L Garcia‐Alonso, J Jiménez‐Almazán, J Carbonell‐Caballero, ...
Molecular systems biology 10 (9), 752, 2014
392014
Whole-exome sequencing identifies novel compound heterozygous mutations in USH2A in Spanish patients with autosomal recessive retinitis pigmentosa
C Méndez-Vidal, M González-del Pozo, A Vela-Boza, J Santoyo-López, ...
Molecular vision 19, 2187, 2013
292013
Novel RP1 mutations and a recurrent BBS1variant explain the co-existence of two distinct retinal phenotypes in the same pedigree
C Méndez-Vidal, N Bravo-Gil, M González-del Pozo, A Vela-Boza, ...
BMC genetics 15, 1-11, 2014
212014
Deciphering intrafamilial phenotypic variability by exome sequencing in a Bardet–Biedl family
M González‐del Pozo, C Méndez‐Vidal, J Santoyo‐Lopez, A Vela‐Boza, ...
Molecular genetics & genomic medicine 2 (2), 124-133, 2014
182014
Exome sequencing reveals novel and recurrent mutations with clinical significance in inherited retinal dystrophies
MG Pozo, C Méndez-Vidal, N Bravo-Gil, A Vela-Boza, J Dopazo, ...
PLoS One 9 (12), e116176, 2014
172014
GB virus C: lack of association with transaminases levels, CD4 and HIV viral load in aids patients
A Vela, A Castro, A Cid, A Aguilera, P Vega, M Hermida, BJ Regueiro, ...
Anales de Medicina Interna (Madrid, Spain: 1984) 20 (4), 175-178, 2003
72003
Construction and characterization of a minimized version of the HIV-1 pNL4-3 plasmid and its application for pseudotyping HIV-1 vectors
ML Abad, T Verdura, A Vela, MJ Iglesias, D Gutiérrez, M Veiga, A Aguilera, ...
Molecular biotechnology 28, 87-95, 2004
42004
Obtaining unacceptable results in assays for quantitation of Human Immunodeficiency Virus type 1 RNA in plasma samples
A Aguilera, A Vela, M Treviño, E Varela, R Seoane, BJ Regueiro
Journal of Clinical Microbiology 38 (1), 472-473, 2000
12000
Exome Sequencing Reveals Novel and Recurrent Mutations with Clinical Significance in Inherited Retinal Dystrophies (vol 9, e116176, 2014)
PM Gonzalez-del, C Mendez-Vidal, N Bravo-Gil, A Vela-Boza, J Dopazo, ...
PLOS ONE 10 (3), 2015
2015
GBPA: una plataforma de investigación en el ámbito de la genómica y la bioinformática en Andalucía
JP Florido, FJL Domingo, A Rueda, A Vela, JS López
Biosaia: Revista de los másteres de Biotecnología Sanitaria y Biotecnología …, 2014
2014
Whole exome sequencing analysis pipeline for the discovery of mutations causative of human rare diseases.
FJL Domingo, AR Martin, JP Florido, AV Boza, PA Garcia, LMC Renedo, ...
IWBBIO, 253-254, 2013
2013
GB virus C: lack of association with aminotransferase levels, CD4 and HIV viral load in AIDS patients.
S López Calvo, A Vela, A Castro, A Cid, A Aguilera, P Vega, M Hermida, ...
2003
Virus GB-C: ausencia de asociación con niveles de transaminasas, CD4 y carga vírica en pacientes con sida
S López Calvo, A Vela, A Castro, A Cid, A Aguilera, P Vega, M Hermida, ...
Anales de medicina interna 20 (4), 17-20, 2003
2003
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