Cristian Tornador, Tornador C
Cristian Tornador, Tornador C
PhD in Biomedicine - Bioinformatic, Universitat Pompeu Fabra
Verified email at - Homepage
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
Genomic insights into the Ixodes scapularis tick vector of Lyme disease
M Gulia-Nuss, AB Nuss, JM Meyer, DE Sonenshine, RM Roe, ...
Nature communications 7 (1), 10507, 2016
Dynamic functional connectivity reveals altered variability in functional connectivity among patients with major depressive disorder
DG Demirtaş M, Tornador C, Falcón C, López-Solà M, Hernández-Ribas R, Pujol ...
Hum Brain Mapping, 2016
Next generation diagnostics of cystic fibrosis and CFTR-related disorders by targeted multiplex high-coverage resequencing of CFTR
D Trujillano, MD Ramos, J González, C Tornador, F Sotillo, G Escaramis, ...
Journal of Medical Genetics 50 (7), 455-462, 2013
Accurate molecular diagnosis of phenylketonuria and tetrahydrobiopterin-deficient hyperphenylalaninemias using high-throughput targeted sequencing
D Trujillano, B Perez, J González, C Tornador, R Navarrete, G Escaramis, ...
European Journal of Human Genetics 22 (4), 528-534, 2014
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
Increased methylation at an unexplored glucocorticoid responsive element within exon 1D of NR3C1 gene is related to anxious-depressive disorders and decreased hippocampal …
H Palma-Gudiel, A Córdova-Palomera, C Tornador, C Falcón, N Bargalló, ...
European Neuropsychopharmacology 28 (5), 579-588, 2018
L-Ferritin: One Gene, Five Diseases; from Hereditary Hyperferritinemia to Hypoferritinemia—Report of New Cases
B Cadenas, J Fita-Torró, M Bermúdez-Cortés, I Hernandez-Rodriguez, ...
Pharmaceuticals 12 (1), 17, 2019
Environmental factors linked to depression vulnerability are associated with altered cerebellar resting-state synchronization
A Cordova Palomera, C Tornador, C Falcon, N Bargallo, P Brambilla, ...
Scientific Reports, 2016
Kin-Driver: a database of driver mutations in protein kinases
FL Simonetti, C Tornador, N Nabau-Moreto, MA Molina-Vila, ...
Database 2014, bau104, 2014
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
Altered resting-state whole-brain functional networks of neonates with intrauterine growth restriction
D Batalle, E Muñoz-Moreno, C Tornador, N Bargallo, G Deco, E Eixarch, ...
Cortex 77, 119-131, 2016
Activating mutations cluster in the “molecular brake” regions of protein kinases and do not associate with conserved or catalytic residues
MA Molina‐Vila, N Nabau‐Moretó, C Tornador, AJ Sabnis, R Rosell, ...
Human mutation 35 (3), 318-328, 2014
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
Hereditary hyperferritinemia cataract syndrome: ferritin L gene and physiopathology behind the disease—report of new cases
F Celma Nos, G Hernández, X Ferrer-Cortès, I Hernandez-Rodriguez, ...
International Journal of Molecular Sciences 22 (11), 5451, 2021
Altered amygdalar resting‐state connectivity in depression is explained by both genes and environment
A Córdova‐Palomera, C Tornador, C Falcon, N Bargallo, I Nenadic, ...
Human brain mapping 36 (10), 3761-3776, 2015
New Mutations in HFE2 and TFR2 Genes Causing Non HFE-Related Hereditary Hemochromatosis
G Hernández, X Ferrer-Cortès, V Venturi, M Musri, MF Pilquil, PMM Torres, ...
Genes 12 (12), 1980, 2021
CoDysAn: a telemedicine tool to improve awareness and diagnosis for patients with congenital dyserythropoietic anemia
C Tornador, E Sánchez-Prados, B Cadenas, R Russo, V Venturi, I Andolfo, ...
Frontiers in Physiology 10, 1063, 2019
Mutations in the RACGAP1 gene cause autosomal recessive congenital dyserythropoietic anemia type III
G Hernández, L Romero-Cortadellas, X Ferrer-Cortès, V Venturi, ...
Haematologica 108 (2), 581, 2023
New Cases of Hypochromic Microcytic Anemia Due to Mutations in the SLC11A2 Gene and Functional Characterization of the G75R Mutation
L Romero-Cortadellas, G Hernández, X Ferrer-Cortès, L Zalba-Jadraque, ...
International journal of molecular sciences 23 (8), 4406, 2022
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