Mayka Sanchez (Mayka Sánchez)

ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 16

Top Venues

International journal of molecular sciences

Nature metabolism

Scientific reports

Pharmaceuticals (Basel, Switzerland)

Universitat Internacional de Catalunya

University of Barcelona (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Universitat Internacional de Catalunya Sep 01 2018

Spain

Professor and Group leader :: Faculty of Medicine and Health Sciences. Department of Basic Sciences

BLOOGENETICS S.L. Nov 02 2016

Spain

Promoter and co-founder

Josep Carreras Leukaemia Research Institute (IJC) Mar 01 2015 - May 22 2018

Spain

Principal Investigator: Iron Metabolism: Regulation and Diseases & Head of Diagnostics in Iron Metabolism Disease (D•IRON)

Institute of Predictive and Personalized Medicine of Cancer (IMPPC) Nov 01 2009 - Feb 28 2015

Spain

Group leader: Iron and Cancer Group

European Molecular Biology Laboratory Jun 03 2002 - Oct 31 2009

Germany

Postdoctoral researcher

Education History

University of Barcelona Sep 02 1996 - May 31 2002

Spain

PHD

Publications

Lídia Romero-Cortadellas, Xènia Ferrer-Cortès, Laura Calvo-López, Mireia Olivella, Anna Barqué, Christina Diaz de Heredia, Katja Moser, Ilona Kleine Budde, Mayka Sanchez
Novel transferrin gene mutations in four new cases of congenital Atransferrinaemia: Functional and diagnostic pathogenicity despite negative bioinformatics. British journal of haematology (2024)
Melina Mara Musri, Veronica Venturi, Xènia Ferrer-Cortès, Lídia Romero-Cortadellas, Gonzalo Hernandez, Pilar Leoz, María Pilar Ricard Andrés, Marta Morado, María Del Carmen Fernández Valle, David Beneitez Pastor, Ana Ortuño Cabrero, Maite Moreno Gamiz, Leonor Senent Peris, Amanda Isabel Perez-Valencia, Santiago Pérez-Montero, Cristian Tornador, Mayka Sanchez
New Cases and Mutations in SEC23B Gene Causing Congenital Dyserythropoietic Anemia Type II. International journal of molecular sciences 24 (12) (2023)
Mate Maus, Vanessa López-Polo, Lidia Mateo, Miguel Lafarga, Mònica Aguilera, Eugenia De Lama, Kathleen Meyer, Dolors Serra, Cecilia Lopez-Martinez, Ines López-Alonso, Marc Guasch-Piqueras, Fernanda Hernandez-Gonzalez, Selim Chaib, Miguel Rovira, Mayka Sanchez, Rosa Faner, Alvar Agustí, Rodrigo Diéguez-Hurtado, Sagrario Ortega, Anna Manonelles, Stefan Engelhardt, Freddy Monteiro, Camille Stephan-Otto Attolini, Neus Prats, Guillermo M Albaiceta, Josep M Cruzado, Manuel Serrano
Iron accumulation drives fibrosis, senescence and the senescence-associated secretory phenotype. Nature metabolism 5 (12) (2023)
Melina Mara Musri, Veronica Venturi, Xènia Ferrer-Cortès, Lídia Romero-Cortadellas, Gonzalo Hernandez, Pilar Leoz, María Pilar Ricard Andrés, Marta Morado, María Del Carmen Fernández Valle, David Beneitez Pastor, Ana Ortuño Cabrero, Maite Moreno Gamiz, Leonor Senent Peris, Amanda Isabel Perez-Valencia, Santiago Pérez-Montero, Cristian Tornador, Mayka Sanchez
New Cases and Mutations in SEC23B Gene Causing Congenital Dyserythropoietic Anemia Type II. International journal of molecular sciences 24 (12) (2023)
Mate Maus, Vanessa López-Polo, Lidia Mateo, Miguel Lafarga, Mònica Aguilera, Eugenia De Lama, Kathleen Meyer, Dolors Serra, Cecilia Lopez-Martinez, Ines López-Alonso, Marc Guasch-Piqueras, Fernanda Hernandez-Gonzalez, Selim Chaib, Miguel Rovira, Mayka Sanchez, Rosa Faner, Alvar Agustí, Rodrigo Diéguez-Hurtado, Sagrario Ortega, Anna Manonelles, Stefan Engelhardt, Freddy Monteiro, Camille Stephan-Otto Attolini, Neus Prats, Guillermo M Albaiceta, Josep M Cruzado, Manuel Serrano
Iron accumulation drives fibrosis, senescence and the senescence-associated secretory phenotype. Nature metabolism (2023)
Mate Maus, Vanessa López-Polo, Lidia Mateo, Miguel Lafarga, Mònica Aguilera, Eugenia De Lama, Kathleen Meyer, Dolors Serra, Cecilia Lopez-Martinez, Ines López-Alonso, Marc Guasch-Piqueras, Fernanda Hernandez-Gonzalez, Selim Chaib, Miguel Rovira, Mayka Sanchez, Rosa Faner, Alvar Agustí, Rodrigo Diéguez-Hurtado, Sagrario Ortega, Anna Manonelles, Stefan Engelhardt, Freddy Monteiro, Camille Stephan-Otto Attolini, Neus Prats, Guillermo M Albaiceta, Josep M Cruzado, Manuel Serrano
Iron accumulation drives fibrosis, senescence and the senescence-associated secretory phenotype. Nature metabolism 5 (12) (2023)
Mate Maus, Vanessa López-Polo, Lidia Mateo, Miguel Lafarga, Mònica Aguilera, Eugenia De Lama, Kathleen Meyer, Dolors Serra, Cecilia Lopez-Martinez, Ines López-Alonso, Marc Guasch-Piqueras, Fernanda Hernandez-Gonzalez, Selim Chaib, Miguel Rovira, Mayka Sanchez, Rosa Faner, Alvar Agustí, Rodrigo Diéguez-Hurtado, Sagrario Ortega, Anna Manonelles, Stefan Engelhardt, Freddy Monteiro, Camille Stephan-Otto Attolini, Neus Prats, Guillermo M Albaiceta, Josep M Cruzado, Manuel Serrano
Iron accumulation drives fibrosis, senescence and the senescence-associated secretory phenotype. Nature metabolism 5 (12) (2023)
Melina Mara Musri, Veronica Venturi, Xènia Ferrer-Cortès, Lídia Romero-Cortadellas, Gonzalo Hernandez, Pilar Leoz, María Pilar Ricard Andrés, Marta Morado, María Del Carmen Fernández Valle, David Beneitez Pastor, Ana Ortuño Cabrero, Maite Moreno Gamiz, Leonor Senent Peris, Amanda Isabel Perez-Valencia, Santiago Pérez-Montero, Cristian Tornador, Mayka Sanchez
New Cases and Mutations in SEC23B Gene Causing Congenital Dyserythropoietic Anemia Type II. International journal of molecular sciences 24 (12) (2023)
Mate Maus, Vanessa López-Polo, Lidia Mateo, Miguel Lafarga, Mònica Aguilera, Eugenia De Lama, Kathleen Meyer, Dolors Serra, Cecilia Lopez-Martinez, Ines López-Alonso, Marc Guasch-Piqueras, Fernanda Hernandez-Gonzalez, Selim Chaib, Miguel Rovira, Mayka Sanchez, Rosa Faner, Alvar Agustí, Rodrigo Diéguez-Hurtado, Sagrario Ortega, Anna Manonelles, Stefan Engelhardt, Freddy Monteiro, Camille Stephan-Otto Attolini, Neus Prats, Guillermo M Albaiceta, Josep M Cruzado, Manuel Serrano
Iron accumulation drives fibrosis, senescence and the senescence-associated secretory phenotype. Nature metabolism 5 (12) (2023)
Lídia Romero-Cortadellas, Gonzalo Hernandez, Xènia Ferrer-Cortès, Laura Zalba-Jadraque, Jose-Luis Fuster, Mar Bermúdez-Cortés, Ana María Galera, Santiago Pérez-Montero, Cristian Tornador, Mayka Sanchez
New Cases of Hypochromic Microcytic Anemia Due to Mutations in the SLC11A2 Gene and Functional Characterization of the G75R Mutation. International journal of molecular sciences 23 (8) (2022)
Ferran Celma Nos, Gonzalo Hernández, Xènia Ferrer-Cortès, Ines Hernandez-Rodriguez, Begoña Navarro-Almenzar, Jose-Luis Fuster, Mar Bermúdez Cortés, Santiago Pérez-Montero, Cristian Tornador, Mayka Sanchez
Hereditary Hyperferritinemia Cataract Syndrome: Ferritin L Gene and Physiopathology behind the Disease-Report of New Cases. International journal of molecular sciences 22 (11) (2021)
Gonzalo Hernandez, Xenia Ferrer-Cortès, Veronica Venturi, Melina Musri, Martin Floor Pilquil, Pau Marc Muñoz Torres, Ines Hernandez Rodríguez, Maria Àngels Ruiz Mínguez, Nicholas J Kelleher, Sara Pelucchi, Alberto Piperno, Esther Plensa Alberca, Georgina Gener Ricós, Eloi Cañamero Giró, Santiago Pérez-Montero, Cristian Tornador, Jordi Villà-Freixa, Mayka Sanchez
New Mutations in HFE2 and TFR2 Genes Causing Non HFE -Related Hereditary Hemochromatosis. Genes 12 (12) (2021)
Marc Vila Cuenca, Giacomo Marchi, Anna Barqué, Clara Esteban-Jurado, Alessandro Marchetto, Alejandro Giorgetti, Viorica Chelban, Henry Houlden, Nicholas W Wood, Chiara Piubelli, Marina Dorigatti Borges, Dulcinéia Martins de Albuquerque, Kleber Yotsumoto Fertrin, Ester Jové-Buxeda, Jordi Sánchez-Delgado, Neus Baena-Díez, Birute Burnyte, Algirdas Utkus, Fabiana Busti, Gintaras Kaubrys, Eda Suku, Kamil Kowalczyk, Bartosz Karaszewski, John B Porter, Sally Pollard, Perla Eleftheriou, Patricia Bignell, Domenico Girelli, Mayka Sanchez
Genetic and Clinical Heterogeneity in Thirteen New Cases with Aceruloplasminemia. Atypical Anemia as a Clue for an Early Diagnosis. International journal of molecular sciences 21 (7) (2020)
Beatriz Cadenas, Josep Fita-Torró, Mar Bermúdez-Cortés, Inés Hernandez-Rodriguez, Jose-Luis Fuster, María Esther Llinares, Ana María Galera, Julia Lee Romero, Santiago Pérez-Montero, Cristian Tornador, Mayka Sanchez
L-Ferritin: One Gene, Five Diseases; from Hereditary Hyperferritinemia to Hypoferritinemia-Report of New Cases. Pharmaceuticals (Basel, Switzerland) 12 (1) (2019)
Sara Luscieti, Bruno Galy, Lucia Gutiérrez, Michael Reinke, Jorge Couso, Maya Shvartsman, Antonio Di Pascale, Walter Witke, Matthias W Hentze, Pietro Pilo Boyl, Mayka Sanchez
The actin-binding protein profilin 2 is a novel regulator of iron homeostasis. Blood 130 (17) (2017)
Stijn Van de Sompele, Lucie Pécheux, Jorge Couso, Audrey Meunier, Mayka Sanchez, Elfriede De Baere
Functional characterization of a novel non-coding mutation "Ghent +49A > G" in the iron-responsive element of L-ferritin causing hereditary hyperferritinaemia-cataract syndrome. Scientific reports 7 (1) (2017)

Mayka Sanchez.css-eqlu8i{font-size:small;padding-left:4px;} (Mayka Sánchez)

Publication Activity (10 Years)

Top Topics

Top Venues

Mayka Sanchez (Mayka Sánchez)