Laia Bassaganyas
Laia Bassaganyas
Postdoctoral Researcher - IGF Montpellier
Verified email at
Cited by
Cited by
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
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
Identification of an immune-specific class of hepatocellular carcinoma, based on molecular features
D Sia, Y Jiao, I Martinez-Quetglas, O Kuchuk, C Villacorta-Martin, ...
Gastroenterology 153 (3), 812-826, 2017
Molecular predictors of prevention of recurrence in HCC with sorafenib as adjuvant treatment and prognostic factors in the phase 3 STORM trial
R Pinyol, R Montal, L Bassaganyas, D Sia, T Takayama, GY Chau, ...
Gut 68 (6), 1065-1075, 2019
Molecular classification and therapeutic targets in extrahepatic cholangiocarcinoma
R Montal, D Sia, C Montironi, WQ Leow, R Esteban-Fabró, R Pinyol, ...
Journal of hepatology 73 (2), 315-327, 2020
The role of exome sequencing in newborn screening for inborn errors of metabolism
AN Adhikari, RC Gallagher, Y Wang, RJ Currier, G Amatuni, ...
Nature medicine 26 (9), 1392-1397, 2020
Trunk mutational events present minimal intra-and inter-tumoral heterogeneity in hepatocellular carcinoma
S Torrecilla, D Sia, AN Harrington, Z Zhang, L Cabellos, H Cornella, ...
Journal of hepatology 67 (6), 1222-1231, 2017
Molecular portrait of high alpha-fetoprotein in hepatocellular carcinoma: implications for biomarker-driven clinical trials
R Montal, C Andreu-Oller, L Bassaganyas, R Esteban-Fabró, S Moran, ...
British journal of cancer 121 (4), 340-343, 2019
Unconventional secretion of FABP4 by endosomes and secretory lysosomes
J Villeneuve, L Bassaganyas, S Lepreux, M Chiritoiu, P Costet, J Ripoche, ...
Journal of Cell Biology 217 (2), 649-665, 2018
CNApp, a tool for the quantification of copy number alterations and integrative analysis revealing clinical implications
S Franch-Expósito, L Bassaganyas, M Vila-Casadesús, ...
elife 9, e50267, 2020
Sporadic and reversible chromothripsis in chronic lymphocytic leukemia revealed by longitudinal genomic analysis
L Bassaganyas, S Beà, G Escaramis, C Tornador, I Salaverria, L Zapata, ...
Leukemia 27 (12), 2376-2379, 2013
Copy-number alteration burden differentially impacts immune profiles and molecular features of hepatocellular carcinoma
L Bassaganyas, R Pinyol, R Esteban-Fabró, L Torrens, S Torrecilla, ...
Clinical Cancer Research 26 (23), 6350-6361, 2020
Whole exome and whole genome sequencing with dried blood spot DNA without whole genome amplification
L Bassaganyas, G Freedman, D Vaka, E Wan, R Lao, F Chen, M Kvale, ...
Human mutation 39 (1), 167-171, 2018
New factors for protein transport identified by a genome-wide CRISPRi screen in mammalian cells
L Bassaganyas, SJ Popa, M Horlbeck, C Puri, SE Stewart, F Campelo, ...
Journal of Cell Biology 218 (11), 3861-3879, 2019
PeSV-Fisher: identification of somatic and non-somatic structural variants using next generation sequencing data
G Escaramís, C Tornador, L Bassaganyas, R Rabionet, JMC Tubio, ...
PLoS One 8 (5), e63377, 2013
Evolutionary dynamics of the Ty3/gypsy LTR retrotransposons in the genome of Anopheles gambiae
JMC Tubio, M Tojo, L Bassaganyas, G Escaramis, IV Sharakhov, ...
PLoS One 6 (1), e16328, 2011
Elongin C (ELOC/TCEB1)-associated von Hippel–Lindau disease
A Andreou, B Yngvadottir, L Bassaganyas, G Clark, E Martin, J Whitworth, ...
Human molecular genetics 31 (16), 2728-2737, 2022
Golgi enzymes do not cycle through the endoplasmic reticulum during protein secretion or mitosis
J Villeneuve, J Duran, M Scarpa, L Bassaganyas, J Van Galen, ...
Molecular biology of the cell 28 (1), 141-151, 2017
Worldwide population distribution of the common LCE3C-LCE3B deletion associated with psoriasis and other autoimmune disorders
L Bassaganyas, E Riveira-Muñoz, M García-Aragonés, JR González, ...
BMC genomics 14, 1-11, 2013
Frequency of pathogenic germline variants in cancer susceptibility genes in 1336 renal cell carcinoma cases
B Yngvadottir, A Andreou, L Bassaganyas, A Larionov, AJ Cornish, ...
Human Molecular Genetics 31 (17), 3001-3011, 2022
The system can't perform the operation now. Try again later.
Articles 1–20