Mayka Sanchez-Fernandez

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Professor and Group leader

Universitat Internacional de Catalunya

Spain

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Recent Grants

Grant: Close

ARETHA: Advances in diagnostic and therapy for rare hereditary haematological diseases (ARETHA, Advances in Rare hErediTary Hematological diseAses)

Open Date: 2022-09-01

Close Date: 2025-09-01

Grant: Close

NANOANEMIA: Nanobiosensores multiplexados para el diagnóstico instantáneo y clasificación de la anemia en el punto de atención.

Open Date: 2021-12-01

Close Date: 2024-12-01

Grant: Close

Advances in the Diagnosis and Gene Therapy of Congenital dyserythropoietic Anemia

Open Date: 2020-09-01

Close Date: 2023-09-01

Grant: Close

PhD Program from Generalitat de Catalunya. Ref- 2020FI-B00038

Open Date: 2020-04-01

Close Date: 2023-04-01

Grant: Close

Mejoras en el diagnóstico y desarrollo de herramientas moleculares para terapia génica en Anemia diseritropoyética congénita

Open Date: 2020-01-01

Close Date: 2021-12-01

Articles (14)

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2024

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2023

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2022

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2022

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2022

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2022

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2022

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2021

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2021

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2021

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2020

Collaborators (4)

Roberta Russo

Assistant Professor

Università degli Studi di Napoli Federico II

ITALY

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Mate Maus

Vall d´Hebron Institut d´Oncologia

SPAIN

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Eloi Cañamero Giró

Institut Català d'Oncologia

SPAIN

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Immacolata Andolfo

ITALY

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Mayka Sanchez-Fernandez

Research Interests

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Contact this professor

Recent Grants

Articles (14)

Novel transferrin gene mutations in four new cases of congenital Atransferrinaemia: Functional and diagnostic pathogenicity despite negative bioinformatics

New Cases and Mutations in <i>SEC23B</i> Gene Causing Congenital Dyserythropoietic Anemia Type II

Iron accumulation drives fibrosis, senescence and the senescence-associated secretory phenotype

Haemochromatosis patients' research priorities: Towards an improved quality of life

The use of next‐generation sequencing in the diagnosis of rare inherited anaemias: A Joint BSH/EHA Good Practice Paper*

Mutations in the <i>RACGAP1</i> gene cause autosomal recessive congenital dyserythropoietic anemia type III.

The Use of Next-generation Sequencing in the Diagnosis of Rare Inherited Anaemias: A Joint BSH/EHA Good Practice Paper

Hemochromatosis classification: update and recommendations by the BIOIRON Society

New Cases of Hypochromic Microcytic Anemia Due to Mutations in the <i>SLC11A2</i> Gene and Functional Characterization of the G75R Mutation

The Use of Next-generation Sequencing in the Diagnosis of Rare Inherited Anaemias: A Joint BSH/EHA Good Practice Paper

New Mutations in <i>HFE2</i> and <i>TFR2</i> Genes Causing Non <i>HFE</i>-Related Hereditary Hemochromatosis

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

A mutation in the iron-responsive element of ALAS2 is a modifier of disease severity in a patient suffering from CLPX associated erythropoietic protoporphyria

Control of Systemic Iron Homeostasis by the 3' Iron-Responsive Element of Divalent Metal Transporter 1 in Mice.

Collaborators (4)

Roberta Russo

Mate Maus

Eloi Cañamero Giró

Immacolata Andolfo

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