Cristian Tornador, Tornador C
机构: PhD in Biomedicine - Bioinformatic, Universitat Pompeu Fabra
主页: wholegenix.com
每年引用次数
引用次数
引用: 3,029
H-指数: 15
I10-指数 : 16
出版物: 41
Further development of OpenJade.
Javier Farreres , Cristian Tornador
Extreme Markup Languages®
2002
Modelling Congenital Dyserythropoietic Anemia Type II through Gene Editing in Hematopoietic Stem and Progenitor Cells
José C Segovia , Veronica Venturi , Mercedes Dessy-Rodriguez , Gonzalo Hernandez
Blood 136 27 -27
1
2020
Hereditary Hyperferritinemia Cataract Syndrome: Ferritin L Gene and Physiopathology behind the Disease-Report of New Cases.
Cristian Tornador , José Luis Fuster , Mayka Sanchez , Ines Hernandez-Rodriguez
International Journal of Molecular Sciences 22 ( 11) 5451
2021
L-Ferritin: One Gene, Five Diseases; from Hereditary Hyperferritinemia to Hypoferritinemia-Report of New Cases.
Beatriz Cadenas , Josep Fita-Torró , Mar Bermúdez-Cortés , Inés Hernandez-Rodriguez
Pharmaceuticals 12 ( 1) 17
6
2019
Evolutionary Dynamics of the Ty3/Gypsy LTR Retrotransposons in the Genome of Anopheles gambiae
Jose Manuel C. Tubio , Marta Tojo , Laia Bassaganyas , Georgia Escaramis
PLoS ONE 6 ( 1) e16328
8
2011
Altered resting-state whole-brain functional networks of neonates with intrauterine growth restriction
Dafnis Batalle , Emma Muñoz-Moreno , Cristian Tornador , Nuria Bargallo
Cortex 77 119 -131
12
2016
PeSV-Fisher: Identification of Somatic and Non-Somatic Structural Variants Using Next Generation Sequencing Data
Geòrgia Escaramís , Cristian Tornador , Laia Bassaganyas , Raquel Rabionet
PLOS ONE 8 ( 5)
19
2013
Whole-genome sequencing identifies recurrent mutations in chronic lymphocytic leukaemia
Xose S Puente , Magda Pinyol , Víctor Quesada , Laura Conde
Nature 475 ( 7354) 101 -105
1,754
2011
Altered amygdalar resting‐state connectivity in depression is explained by both genes and environment
Aldo Córdova‐Palomera , Cristian Tornador , Carles Falcon , Nuria Bargallo
Human Brain Mapping 36 ( 10) 3761 -3776
7
2015
Dynamic functional connectivity reveals altered variability in functional connectivity among patients with major depressive disorder
Murat Demirtaş , Cristian Tornador , Carles Falcón , Marina López‐Solà
Human Brain Mapping 37 ( 8) 2918 -2930
182
2016
Accurate molecular diagnosis of phenylketonuria and tetrahydrobiopterin-deficient hyperphenylalaninemias using high-throughput targeted sequencing
Georgia Escaramis , Stephan Ossowski , Lluís Armengol , Verónica Cornejo
European Journal of Human Genetics 22 ( 4) 528 -534
32
2014
Environmental factors linked to depression vulnerability are associated with altered cerebellar resting-state synchronization
Aldo Córdova-Palomera , Cristian Tornador , Carles Falcón , Nuria Bargalló
Scientific Reports 6 ( 1) 37384 -37384
15
2016
Increased methylation at an unexplored glucocorticoid responsive element within exon 1D of NR3C1 gene is related to anxious-depressive disorders and decreased hippocampal connectivity.
Helena Palma-Gudiel , Aldo Córdova-Palomera , Cristian Tornador , Carles Falcón
European Neuropsychopharmacology 28 ( 5) 579 -588
33
2018
Genomic insights into the Ixodes scapularis tick vector of Lyme disease
Monika Gulia-Nuss , Andrew B Nuss , Jason M Meyer , Daniel E Sonenshine
Nature Communications 7 ( 1) 10507 -10507
439
2016
CoDysAn: A Telemedicine Tool to Improve Awareness and Diagnosis for Patients With Congenital Dyserythropoietic Anemia
Cristian Tornador , Edgar Sánchez-Prados , Beatriz Cadenas , Roberta Russo
Frontiers in Physiology 10 1063
3
2019
Activating Mutations Cluster in the “Molecular Brake” Regions of Protein Kinases and Do Not Associate with Conserved or Catalytic Residues
Miguel A. Molina-Vila , Nuria Nabau-Moretó , Cristian Tornador , Amit J. Sabnis
Human Mutation 35 ( 3) 318 -328
21
2014
BID expression determines the apoptotic fate of cancer cells after abrogation of the spindle assembly checkpoint by AURKB or TTK inhibitors
Jordi Bertran-Alamillo , Ana Giménez-Capitán , Ruth Román , Sara Talbot
Molecular Cancer 22 ( 1) 110 -110
3
2023
New mutations in HFE2 and TFR2 genes causing non HFE-related hereditary hemochromatosis
Gonzalo Hernández , Xenia Ferrer-Cortès , Veronica Venturi , Melina Musri
Genes 12 ( 12) 1980 -1980
10
2021
New cases and mutations in SEC23B gene causing congenital dyserythropoietic anemia type II
Melina Mara Musri , Veronica Venturi , Xènia Ferrer-Cortès , Lídia Romero-Cortadellas
International Journal of Molecular Sciences 24 ( 12) 9935 -9935
4
2023
Mutations in the RACGAP1 gene cause autosomal recessive congenital dyserythropoietic anemia type III
Gonzalo Hernández , Lídia Romero-Cortadellas , Xènia Ferrer-Cortès , Veronica Venturi
Haematologica 108 ( 2) 581 -581
5
2023