Cristian Tornador

Esplugues De Llobregat, CT 08950, Spain

Last Updated: 09/26/2026

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Found 22 publications

The role of genetic testing in accurate diagnosis of X-linked sideroblastic anemia: novel ALAS2 mutations and the impact of X-chromosome inactivation.

The role of genetic testing in accurate diagnosis of X-linked sideroblastic anemia: novel ALAS2 mutations and the impact of X-chromosome inactivation.

Journal: Scientific reports

Published: January 07, 2025

New Cases and Mutations in SEC23B Gene Causing Congenital Dyserythropoietic Anemia Type II.

New Cases and Mutations in SEC23B Gene Causing Congenital Dyserythropoietic Anemia Type II.

Journal: International journal of molecular sciences

Published: April 20, 2023

BID expression determines the apoptotic fate of cancer cells after abrogation of the spindle assembly checkpoint by AURKB or TTK inhibitors.

BID expression determines the apoptotic fate of cancer cells after abrogation of the spindle assembly checkpoint by AURKB or TTK inhibitors.

Journal: Molecular cancer

Published: February 27, 2023

Mutations in the RACGAP1 gene cause autosomal recessive congenital dyserythropoietic anemia type III.

Mutations in the RACGAP1 gene cause autosomal recessive congenital dyserythropoietic anemia type III.

Journal: Haematologica

Published: April 29, 2022

New Cases of Hypochromic Microcytic Anemia Due to Mutations in the SLC11A2 Gene and Functional Characterization of the G75R Mutation.

New Cases of Hypochromic Microcytic Anemia Due to Mutations in the SLC11A2 Gene and Functional Characterization of the G75R Mutation.

Journal: International journal of molecular sciences

Published: March 16, 2022

New Mutations in HFE2 and TFR2 Genes Causing Non HFE-Related Hereditary Hemochromatosis.

New Mutations in HFE2 and TFR2 Genes Causing Non HFE-Related Hereditary Hemochromatosis.

Journal: Genes

Published: October 25, 2021

Hereditary Hyperferritinemia Cataract Syndrome: Ferritin L Gene and Physiopathology behind the Disease-Report of New Cases.

Hereditary Hyperferritinemia Cataract Syndrome: Ferritin L Gene and Physiopathology behind the Disease-Report of New Cases.

Journal: International journal of molecular sciences

Published: April 27, 2021

CoDysAn: A Telemedicine Tool to Improve Awareness and Diagnosis for Patients With Congenital Dyserythropoietic Anemia.

CoDysAn: A Telemedicine Tool to Improve Awareness and Diagnosis for Patients With Congenital Dyserythropoietic Anemia.

Journal: Frontiers in physiology

Published: March 28, 2019

L-Ferritin: One Gene, Five Diseases; from Hereditary Hyperferritinemia to Hypoferritinemia-Report of New Cases.

L-Ferritin: One Gene, Five Diseases; from Hereditary Hyperferritinemia to Hypoferritinemia-Report of New Cases.

Journal: Pharmaceuticals (Basel, Switzerland)

Published: December 23, 2018

Increased methylation at an unexplored glucocorticoid responsive element within exon 1D of NR3C1 gene is related to anxious-depressive disorders and decreased hippocampal connectivity.

Increased methylation at an unexplored glucocorticoid responsive element within exon 1D of NR3C1 gene is related to anxious-depressive disorders and decreased hippocampal connectivity.

Journal: European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology

Published: October 31, 2017

Environmental factors linked to depression vulnerability are associated with altered cerebellar resting-state synchronization.

Environmental factors linked to depression vulnerability are associated with altered cerebellar resting-state synchronization.

Journal: Scientific reports

Published: March 31, 2016

Dynamic functional connectivity reveals altered variability in functional connectivity among patients with major depressive disorder.

Dynamic functional connectivity reveals altered variability in functional connectivity among patients with major depressive disorder.

Journal: Human brain mapping

Published: July 08, 2015

Showing 1-12 of 22

Last Updated: 09/26/2026