Home/Publications and Projects

Publications and Projects

Home/Publications and Projects

Publications and Projects

Publications

Total publications: 65 (46 peer-reviewed publications +7 divulg+12 book chapters)

  • Total peer-reviewed publications: 46 (12 as 1st author, 14 as last author) (29 as an independent group, 8 as postdoc, 9 as predoc)

  • Publications as an independent group (group created in Nov 2009): 29

  • Publications as last author or co-corresponding author: 14

  • Number of 1st decile publications (D1): 20/41 (48.8%)

  • Number of 1st quartile publications (Q1): 35/46 (76.1%)

  • H-index: 22 (Google Scholar, Oct 2021)

  • i-10 Index: 31 (Google Scholar, Oct 2021)

  • Total citations: 2091 (as of Oct 2022, Google Scholar)

  • Other publications: Book chapters: 12; Informative medical publications: 7

Peer-reviewed publications

2023

  • More to come…

2022

  • More to come…

  • Hernández G*, Romero-Cortadellas L*, Ferrer-Cortès X, Venturi V, Dessy-Rodriguez M, Olivella M, Husami A, Pérez de Soto C, Morales-Camacho R-M, Villegas A, González-Fernández F-A, Morado M, Kalfa T-A, Quintana-Bustamante O, Pérez-Montero S, Tornador C, Segovia J-C, Sánchez M. Mutations in the RACGAP1 gene cause autosomal recessive Congenital Dyserythropoietic Anemia type III. Haematologica. 2022. Accepted. IF in 2021: 11.04, Q1. D1. Category: HEMATOLOGY.

  • Roy NBA, Da Costa L, Russo R, Bianchi P, Del Mar Mañú-Pereira M, Fermo E, Andolfo I, Clark B, Proven M, Sanchez M, van Wijk R, van der Zwaag B, Layton M, Rees D, Iolascon A. The Use of Next-generation Sequencing in the Diagnosis of Rare Inherited Anaemias: A Joint BSH/EHA Good Practice Paper. Hemasphere. 2022 Jun 6;6(6):e739. doi: 10.1097/HS9.0000000000000739.

  • Romero-Cortadellas L,* Hernández G*, Ferrer-Cortès X, Zalba-Jadraque L, Fuster JL, Bermúdez-Cortés M, Galera-Miñarro AM, Pérez-Montero S, Tornador C, Sánchez M. New cases of hypochromic microcytic anemia due to mutations in the SLC11A2 gene and functional characterization of the G75R mutation. Int J Mol Sci. 2022, 23(8), 4406. https://doi.org/10.3390/ijms23084406. IF in 2020 : 5.924. Q1

  • Roy NBA, Da Costa L, Russo R, Bianchi P, Mañú-Pereira MM, Fermo E, Andolfo I, Clark B, Proven M, Sanchez M, van Wijk R, van der Zwaag A, Layton M, Rees D, Iolascon A. The use of next-generation sequencing in the diagnosis of rare inherited anaemias: A Joint BSH/EHA Good Practice Paper. Br J Haematol. 2022 Jun 6. doi: 10.1111/bjh.18191. Impact factor: 6.998 in 2020. (Hematology) Q1.

2021

  • Hernández G, Ferrer-Cortès X, Venturi V, Musri M, Pilquil MF, Torres PMM, Rodríguez IH, Mínguez MÀR, Kelleher NJ, Pelucchi S, Piperno A, Alberca EP, Ricós GG, Giró EC, Pérez-Montero S, Tornador C, Villà-Freixa J, Sánchez M. New Mutations in HFE2 and TFR2 Genes Causing Non HFE-Related Hereditary Hemochromatosis. Genes (Basel). 2021 Dec 13;12(12):1980. doi: 10.3390/genes12121980. PMID: 34946929; PMCID: PMC8702017.

  • Celma-Nos F*, Hernández G*, Ferrer‐Cortès X, Hernandez‐Rodriguez I, Navarro‐Almenzar B, Fuster J.L., Mar Bermúdez-Cortés M 5, Pérez‐Montero S, Tornador C, Sanchez M. Hereditary Hyperferritinemia Cataract Syndrome: Ferritin L Gene and Physiopathology behind the Disease—Report of New Cases. International Journal of Molecular Sciences. Int J Mol Sci. 2021. 22(11), 5451. doi: 10.3390/ijms22115451. PMID: 34064225; PMCID: PMC8196845.

  • Ducamp S*, Luscieti S*, Ferrer-Cortès X, Nicolas G, Manceau H, Peoc’h K, Yien YY, Kannengiesser C, Gouya L, Puy H** and Sanchez M**. A mutation in the Iron-Responsive Element of ALAS2 is a modifier of disease severity in a patient suffering from CLPX associated Erythropoietic Protoporphyria. Haematologica. 2021 Feb 18. doi: 10.3324/haematol.2020.272450. Epub ahead of print. PMID: 33596641.

  • Girelli D, Busti F, Brissot P, Cabantchik I, Muckenthaler MU, Porto G. Hemochromatosis classification: update and recommendations by the BIOIRON Society. Blood. 2021 Oct 3:blood.2021011338. doi: 10.1182/blood.2021011338. Epub ahead of print. PMID: 34601591.

    All listed Authors: Members of the Nomenclature Committee of the International Society for the Study of Iron in Biology and Medicine – BIOIRON Society (alphabetical order): Paul C Adams , Edouard Bardou-Jacquet , Patricia Bignell , Pierre Brissot , Fabiana Busti , Barbara Butzeck , Ioav Cabantchik , Clara Camaschella , Robert Evans , Robert Fleming, Tomas Ganz, Domenico Girelli , Olivier Loréal , Giacomo Marchi , Martina U. Muckenthaler, Elizabeta Nemeth, Antonello Pietrangelo , Alberto Piperno, Graça Porto, Dianne Prince , John D. Ryan , Mayka Sanchez , Paulo Santos , Dorine W. Swinkels, Heinz Zoller.

2020

  • Tybl E, Gunshin H, Gupta S, Barrientos T, Bonadonna M, Celma Nos F, Palais G, Karim Z, Sanchez M, Andrews NC, Galy B. Control of Systemic Iron Homeostasis by the 3′ Iron-Responsive Element of Divalent Metal Transporter 1 in Mice. Hemasphere. 2020 Sep 23;4(5):e459. doi: 10.1097/HS9.0000000000000459. PMID: 33062942; PMCID: PMC7523796.

  • Vila Cuenca M, Marchi G, Barqué A, Esteban-Jurado C, Marchetto A, Giorgetti A, Chelban V, Houlden H, Wood NW, Piubelli C, Dorigatti Borges M, Martins de Albuquerque D, Yotsumoto Fertrin K, Jové-Buxeda E, Sanchez-Delgado J, Baena-Díez N, Burnyte B, Utkus A, Busti F, Kaubrys G, Suku E, Kowalczyk K, Karaszewski B, Porter JB, Pollard S, Eleftheriou P, Bignell P, Girelli D, Sanchez M. Genetic and Clinical Heterogeneity in Thirteen New Cases with Aceruloplasminemia. Atypical Anemia as a Clue for an Early Diagnosis. Int J Mol Sci. 2020 Mar 30;21(7):2374. doi: 10.3390/ijms21072374. PMID: 32235485; PMCID: PMC7178074.

2019

  • Cadenas B, Fita-Torró J, Bermúdez-Cortés M, Hernandez-Rodriguez I, Fuster JL, Llinares ME, Galera AM, Romero JL, Pérez-Montero S, Tornador C, Sanchez M. L-Ferritin: One Gene, Five Diseases; from Hereditary Hyperferritinemia to Hypoferritinemia-Report of New Cases. Pharmaceuticals (Basel). 2019 Jan 23;12(1):17. doi: 10.3390/ph12010017. PMID: 30678075; PMCID: PMC6469184.

  • Tornador C, Sánchez-Prados E, Cadenas B, Russo R, Venturi V, Andolfo I, Hernández-Rodriguez I, Iolascon A, Sánchez M. CoDysAn: A Telemedicine Tool to Improve Awareness and Diagnosis for Patients With Congenital Dyserythropoietic Anemia. Front Physiol. 2019 Sep 13;10:1063. doi: 10.3389/fphys.2019.01063. PMID: 31572203; PMCID: PMC6753183.

2018

  • Riley LG, Heeney MM, Rudinger-Thirion J, Frugier M, Campagna DR, Zhou R, Hale GA, Hilliard LM, Kaplan JA, Kwiatkowski JL, Sieff CA, Steensma DP, Rennings A, Simons A, Schaap M, Richard Roodenburg R, Kleefstra T, Arenillas L, Fita-Torró J, Ahmed R, Abboud M, Bechara E, Farah R, Tamminga RYJ, Bottomley SS, Sanchez M, Swinkels DW, Christodoulou J, Fleming MD. The phenotypic spectrum of germline YARS2 variants: from isolated sideroblastic anemia to mitochondrila myopathy, lactic acidosis and sideroblastic anemia. Haematologica 2018. IF in 2017: 9.090, Q1. D1. Category: HEMATOLOGY. Cites: 1 (Google Scholar Nov 2018).

  • Adams P, Altes A, Brissot P, Butzeck B, Cabantchik I, Cançado R, Distante S, Evans P, Evans R, Ganz T, Girelli D, Hultcrantz R, McLaren G, Marris B, Milman N, Nemeth E, Nielsen P, Pineau B, Piperno A, Porto G, Prince D, Ryan J, Sanchez M, Santos P, Swinkels D, Teixeira E, Toska K, Vanclooster A, White D; Contributors and Hemochromatosis International Taskforce. Therapeutic recommendations in HFE hemochromatosis for p.Cys282Tyr (C282Y/C282Y) homozygous genotype. Hepatol Int. 2018 Mar;12(2):83-86. doi: 10.1007/s12072-018-9855-0. Epub 2018 Mar 27. PubMed PMID: 29589198. Authors in alphabetical order. IF 2017: 4.117, Q2. Category: GASTROENTEROLOGY & HEPATOLOGY. Cites: 1 (Google Scholar Nov 2018).

2017

  • Van de Sompele S, Pécheux L, Couso J, Meunier A, Sanchez M*, De Baere E*. 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 Report 2017 Dec 21;7(1):18025. *Last co-corresponding author. Q1. IF: 4.122. Category: MULTIDISCIPLINARY SCIENCES. Cites: 0 (Google Scholar Nov 2018).

  • Luscieti S, Galy B, Gutierrez L, Reinke M, Couso J, Shvartsman M, Di Pascale A, Witke W, Hentze M.W., Pilo Boyl P, Sanchez M. The actin binding protein profilin 2 is a novel regulator of iron homeostasis. Blood, 2017 Oct 26;130(17):1934-1945. doi: 10.1182/blood-2016-11-754382. Epub 2017 Aug 3. IF: 15.132, D1. Cites: 5 (Google Scholar Nov 2018).

2016

  • Andreas Engert, Carlo Balduini, Anneke Brand, Bertrand Coiffier, Catherine Cordonnier, Hartmut Döhner, Thom Duyvené de Wit, Sabine Eichinger, Willem Fibbe, Tony Green, Fleur de Haas, Achille Iolascon, Thierry Jaffredo, Francesco Rodeghiero, Gilles Salles, Jan Jacob Schuringa, Carin Smand, and remaining EHA Roadmap for European Hematology Research authors. The European Hematology Association Roadmap for European Hematology Research. A Consensus Document. Haematologica 2016. Feb;101(2):115-208. doi: 10.3324/haematol.2015.136739. Epub 2016 Jan 27. IF: 7,702, Q1. D1. Cites: 28 (Google Scholar Nov 2018).

2015

  • Joshi R*, Shvartsman M*, Morán E, Lois S, Aranda J, Barqué A, de la Cruz X, Bruguera M, Vagace JM, Gervasini G, Sanz C, Sánchez M. Functional consequences of transferrin receptor-2 mutations causing Hereditary Hemochromatosis type 3. Molecular Genetics & Genomic Medicine 2015 May;3(3):221-32. doi: 10.1002/mgg3.136. Epub 2015 Mar 6. IF: 2.622. Q2. Category: GENETICS & HEREDITY, Cites: 9 (Google Scholar Nov 2018).

2014

  • De FalcoL, Silvestri L, Kannengiesser C, Morán E, Oudin C, Rausa M, Bruno M, Aranda J, Argiles B, Yenicesu I, Falcon-Rodriguez M, Yilmaz-Keskin E, Kocak U, Beaumont C, Camaschella C, Iolascon A, Grandchamp B, Sanchez M. Functional and clinical impact of novel TMPRSS6 mutations in Iron-Refractory Iron-Deficiency Anaemia patients and genotype-phenotype studies. Hum Mutat. 2014 35(11):1321-9 doi: 10.1002/humu.22632. IF: 5.340, Q1. 26/164 Category: Genetics and Heredity. Cites: 29 (Google Scholar Nov 2018)

  • Teixeira E, Borlido-Santos J, Brissot P, Butzeck B, Courtois F, Evans RW, Fernau J, Nunes JA, Mullett M, Paneque M, Pineau B, Porto G, Sorrill R, Sanchez M, Swinkels DW, Toska K, Varkonyi J; the EFAPH, the European Federation of Associations of Patients with Haemochromatosis. The importance of the general practitioner as an information source for patients with hereditary haemochromatosis. Patient Educ Couns. 2014; 96 (1), 86-92. IF: 2,598 (2013 JCR), Q1. D1. 8/98 Category: SOCIAL SCIENCES, INTERDISCIPLINARY. Cites: 5 (Google Scholar Nov 2018)

  • Tzou W-S, Chu Y, Lin T-Y, Hu C-H, Pai T-W, Liu H-F, Lin H-J, Cases I, Rojas A, Sanchez M, You Z-Y, Hsu M-W. Molecular Evolution of Multiple-Level Control of Heme Biosynthesis Pathway in Animal Kingdom. PLoS ONE 2014 9(1): e86718. IF: 3.234. Q1 8/55 Multidisciplinary Sciences. Cites: 1 (Google Scholar Nov 2018)

  • Altés A, Pérez-Lucena MJ, Bruguera M en representación de la Comisión de Hiperferritinemia del Grupo Ibérico de Ferropatología* (Componentes de la Comisión de Hiperferritinemia del Grupo Ibérico de Ferropatología, co-autores de este trabajo: Rosario López R, Ruiz MA, Torres M, Sanchez M, Félez J, Beneitez D, Matute MF, Remacha A, Sanz C). Systematic approach to the diagnosis of hyperferritinemia. Medicina Clinica (Barc) 2014 May 6;142(9):412-7. doi: 10.1016/j.medcli.2013.06.010. IF: 1.417. Category: MEDICINE, GENERAL & INTERNAL Q2. Cites: 14 (Google Scholar Nov 2018).

2013

  • Athiyarath R, Arora N, Fuster F, Schwarzenbacher R, Ahmed R, George B, Chandy M, Srivastava A, Rojas AM, Sánchez M, Edison ES. Two Novel Missense Mutations in Iron Transport Protein Transferrin Causing Hypochromic Microcytic Anaemia and Haemosiderosis: molecular characterisation and structural implications. Brit J Haematol 2013 Nov;163(3):404-407. IF: 4.959. Q1. 11/68 Category: HEMATOLOGY . Cites: 9 (Google Scholar Nov 2018)

  • De Falco L*, Sánchez M*, Silvestri L, Kannengiesser C, Muckenthaler MU, Iolascon A, Gouya L, Camaschella C, Beaumont C. Iron Refractory Iron Deficiency Anemia. Haematologica 2013 Jun;98(6):845-53. doi: 10.3324/haematol.2012.075515. IF: 5.868. *equal contributor authors.Q1. D1 5/68 Category: HEMATOLOGY. Cites: 108 (Google Scholar Nov 2018)

  • Luscieti S, Tolle G, Aranda J, Benet-Campos C, Risse F, Morán E, Muckenthaler MU, Sánchez M. Novel mutations in the Ferritin-L iron-responsive element that only mildly impair IRP binding cause Hereditary Hyperferritinaemia Cataract Syndrome. Orphanet Journal of Rare Diseases 2013. Feb 19;8(1):30. IF: 3.958. Q1. 25/122 Category: MEDICINE, RESEARCH & EXPERIMENTAL. Cites: 24 (Google Scholar Nov 2018)

2012

  • Liu Z, Lanford R, Mueller S, Gerhard GS, Luscieti S, Sánchez M, Devireddy L. Siderophore-mediated iron trafficking in humans is regulated by iron. Journal of Molecular Medicine 2012 Oct;90(10):1209-21. Epub 2012 Apr 15. IF: 4.768 Q1. Cites: 14 (Google Scholar Nov 2018)

2011

  • Sánchez M, Galy B, Schwanhaeusser B, Blake J, Bähr-Ivacevic T, Benes V, Selbach M, Muckenthaler MU and Hentze MW. Iron regulatory protein-1 and -2: transcriptome-wide definition of binding mRNAs and shaping of the cellular proteome by IRPs. Blood 2011 Nov 24;118(22):e168-79. Epub 2011 Sep22. IF: 9.898. Q1. D1. Cites: 68 (Google Scholar Nov 2018)

  • Rodrigues PN, Gomes SS, Neves JV, Gomes-Pereira S, Correia-Neves M, Nunes-Alves C, Stolte J, Sanchez M, Appelberg R, Muckenthaler MU, Gomes MS. Mycobacteria-induced anaemia revisited: a molecular approach reveals the involvement of NRAMP1 and lipocalin-2, but not of hepcidin. Immunobiology. 2011 Oct;216(10):1127-34. Epub 2011 Apr 20. PubMed PMID: 21601942. IF: 3.205. Q1. Cites: 24 (Google Scholar Nov 2018)

  • Kannengiesser C*, Sanchez M*, Sweeney M*, Hetet G, Kerr B, Moran E, Fuster-Soler JL, Maloum K, Matthes T, Oudot C, Lascaux A, Pondarré C, Sevilla-Navarro J, Vidyatilake S, Beaumont C, Grandchamp B, May A. Missense SLC25A38 gene variations play an important role in autosomal recessive inherited sideroblastic anaemia.*equal contributor authors. Haematologica. 2011 Jun;96 (6):808-13. Epub 2011 Mar 10. PubMed PMID: 21393332. IF: 6.424. Q1. D1. Cites: 38 (Google Scholar Nov 2018). This manuscript led to the Editorial article by Cazzola M. and Invernizzi R. entitled: Ring sideroblasts and sideroblastic anemias in Haematologica. 2011 Jun:96 (6):789-792.

2010

  • Campillos M, Cases I, Hentze MW, Sánchez M. SIREs: Searching for Iron-Responsive Elements. Nucleic Acids Research 2010 Jul 1;38 (Web Server Issue)W360-7. Epub 2010 May 11. PubMed PMID: 20460462. IF: 7.836. Q1. Cites: 52 (Google Scholar Nov 2018).

  • Vainshtein Y, Sánchez M, Brazma A, Hentze MW, Dandekar T, Muckenthaler MU. The IronCip Evaluation Package: A package of Perl modules for robust analyisis of custom microarrays. BMC Bioinformatics 2010, 11:112. IF: 3.028. Q2. Cites: 5 (Google Scholar Nov 2018)

2009

  • Ramsay AJ, Quesada V, Sánchez M, Garabaya C, Sardà MP, Baiget M, Remacha A, Velasco G, López-Otín C. Matriptase-2 mutations in iron-refractory iron deficiency anemia patients provide new insights into protease activation mechanisms. Human Molecular Genetics. 2009 Oct 1;18(19):3673-83. Epub 2009 Jul 10. PubMed PMID: 19592582. IF: 7.386. Q1. D1. Cites: 69 (Google Scholar Nov 2018)

2007

  • Sánchez M, Galy B, Hentze MW., and Muckenthaler MU. Identification of target mRNAs of regulatory RNA binding proteins using mRNP immunopurification and microarrays. Nature Protocols 2007, 2(8):2033-2042. IF: 1.671. Q1. D1. Cites: 14 (Google Scholar Nov 2018)

  • Percy MJ*, Sánchez M*, Swierczek S*, McMullin MF, Mojica-Henshaw MP, Martina U Muckenthaler MU, Prchal JT, and Hentze MW. Is congenital Secondary Erythrocytosis/Polycythemia caused by activating mutations within the HIF-2〈 iron responsive element? Blood 2007; 110(7):2776-2777. * equal contribution authors. PubMed PMID: 17881647. IF : 10.896. Q1. D1. Cites: 4 (Google Scholar Nov 2018)

  • Sánchez M, Galy B, Muckenthaler MU, and Hentze MW. Iron-regulatory proteins limit hypoxia-inducible factor 2α expression in iron deficiency. Nature Structural & Molecular Biology. 2007 ;14(5):420-426. PubMed PMID: 17417656. IF : 11.085. Q1. D1. Cites: 228 (Google Scholar Nov 2018)

2006

  • Sánchez M, Galy B, Dandekar T, Bengert P, Vainshtein Y, Stolte J, Muckenthaler MU, and Hentze MW. Iron regulation and the cell cycle: Identification of an Iron-Responsive Element in the 3’ unstranslated region of human CDC14A mRNA by a refined microarray-based screening strategy. Journal of Biological Chemistry 2006; 281(32):22865-74. PubMed PMID: 16760464. IF : 5.808. Q1. Cites: 94 (Google Scholar Nov 2018)

2004

  • Roy CN, Custodio AO, de Graaf J, Schneider S, Akpan I, Montross LK, Sánchez M, Gaudino A, Hentze MW, Andrews NC and Muckenthaler M. An Hfe-dependent pathway mediates hyposideremia in response to lipopolysaccharide-induced inflammation in mice. Nature Genetics 2004 ;36(5):481-5. IF: 24.695. Q1. D1. Cites: 133 (Google Scholar Nov 2018)

  • Oliva R, Novials A, Sánchez M, Villa M, Ingelmo M, Recasens M, Ascaso C, Bruguera M, Gomis R. The HFE gene is associated to an earlier age of onset and to the presence of diabetic nephropathy in diabetes mellitus type 2. Endocrine 2004 ;24(2):111-4. IF: 1.515. Q4. Cites: 10 (Google Scholar Nov 2018)

2003

  • Sánchez M, Villa M, Ingelmo M, Sanz C, Bruguera M, Ascaso C, Oliva R. Population screening for hemochromatosis: a study in 5370 Spanish blood donors. Journal of Hepatology 2003; 38(6):745-50. IF : 5.283. Q1D1. Cites: 60 (Google Scholar Nov 2018)

2001

  • Sánchez M, Bruguera M, Rodés J, Oliva R. Complete characterization of the 3’ region of the human and mouse hereditary hemochromatosis HFE gene and dectection of novel splicing forms. Blood Cells, Molecules and Diseases 2001; 27 (1): 35-43. IF : 1.703. Q2. Cites: 25 (Google Scholar Nov 2018).

2000

  • Sánchez M, Bruguera M, Quintero E, Barrio Y, Mazzara R, Rodés J, Oliva R. Hereditary Hemochromatosis in Spain. Genetic Testing 2000; 4 (2):171-6. IF : 1.893. Q3. Cites: 20 (Google Scholar Nov 2018)

  • Oliva R, Bruguera M, Sánchez M, and Rodés J. Utilidad clínica de la detección de mutaciones del gen HFE en la hemocromatosis. Gastroenterol Hepatol 2000; 23: 433-435. Q4.

1998

  • Sánchez M, Bruguera M, Bosch J, Rodés J, Ballesta F and Oliva R. Prevalence of the Cys282Tyr and His63Asp HFE gene mutations in Spanish patients with hereditary hemochromatosis and in controls. Journal of Hepatology 1998; 29: 725-728. IF: 3.189. Q1. D1. Cites: 119 (Google Scholar Nov 2018)

  • Sánchez M, Queralt R, Bruguera M, Bosch J, Rodés J, and Oliva R. Cloning, sequencing and characterization of the rat HFE promoter. Comparison of the human, mouse and rat hemochromatosis HFE promoter regions. Gene 1998; 225: 77-87. IF: 2.007. Q3 Cites: 28 (Google Scholar Nov 2018).

  • Margarit E, Guillem A, Rebordosa C, Vidal-Taboada JM, Sánchez M, and Oliva R. Identification of conserved potentially regulatory sequences of the SRY gene from different species of mammals. Biochemical and Biophysical Research Communication 1998; 245: 370-377. IF: 2.780. Q2. Cites: 60 (Google Scholar Nov 2018).

  • Vidal-Taboada JM, Bergoñón S, Sánchez M, López-Acebo C, Groet J, Nizetic D, Egeo A, Scartezzini P, Katsanis N, Fisher EMC, Delabar JM and Oliva R. High resolution mapping and identification of transcribed sequences in the Down Syndrome region-2. Biochemical and Biophysical Research Communication 1998; 243: 572-578. IF: 2.780. Q2. Cites: 11 (Google Scholar Nov 2018).

Home/Publications and Projects

Projects

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

    Proyectos de I+D+i en Generación de Conocimiento 2021. Modalidad: INVESTIGACIÓN ORIENTADA TIPO B.

    REFERENCE: PID2021-122436OB-I00

    01/09/2022 – 31/08/2025

    IP: Sánchez, M.

    Funding: 290.400 euros

    PROYECTOS DE I+D+i en Generación de Conocimiento 2021.

    MINISTERIO DE CIENCIA Y INNOVACION

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

    Prioridad temática: Nanomateriales y nanotecnología para el diagnóstico de enfermedades humanas.

    REFERENCE: PLEC2021-007727

    01/12/2021 – 01/12/2024

    IP-ICN2: A. Merkoçi; IP-UIC: Sánchez, M. IP-BloodGenetics: C. Tornador

    PROYECTOS DE I+D+I EN LÍNEAS ESTRATÉGICAS PROGRAMA ESTATAL DE I+D+I ORIENTADA A LOS RETOS DE LA SOCIEDAD EXTRATEGICAS.

    MINISTERIO DE CIENCIA Y INNOVACION

  • Nuevas aproximaciones para el diagnóstico y tratamiento de la anemia diseritropoyética congénita: Secuenciación masiva y terapia génica. (ADVANCE_CDA)

    REFERENCE: RTC2019-007074-1

    01/01/2020 – 31/12/2023

    IP: Sánchez, M.

    RETOS COLABORACION

    MINISTERIO DE CIENCIA E INNOVACION

  • Advances in the Diagnosis and Gene Therapy of Congenital dyserythropoietic Anemia

    REFERENCE: EU project 894737 – ADGENTHE-CDA-H2020-MSCA-IF-2019

    16/03/2021 – 15/05/2023

    Coordinator: Sánchez, M. Researcher: Musri, M.

    European Union- Marie Curie SME grant

  • Mejoras en el diagnóstico y desarrollo de herramientas moleculares para terapia génica en Anemia diseritropoyética congénita (ADC)

    REFERENCE: SNEO-20191246

    01/01/2020 – 31/12/2021

    IP: Sánchez, M.; Tornador, C.

    Centro para el Desarrollo Tecnológico Industrial: CDTI- NEOTEC. Ministerio de Ciencia e Innovación (MICINN)

  • Advances in new molecular pathways and novel diseases in iron homeostasis (A-IRON)

    REFERENCE: RTI2018-101735-B-I00

    01/01/2019 – 31/12/2021

    IP: Sánchez, M.

    Ministerio de Ciencia, Innovación y Universidades

  • Towards the improvement of diagnosis and treatment in Congenital Dyserythropoyetic Anaemias

    02/03/2017 – 01/03/2020

    IP: Sánchez, M.

    Fundación Ramón Areces

  • Uncovering new molecular and pathophysiological networks in iron metabolism.

    REFERENCE: SAF2015-70412-R

    01/01/2016 – 31/12/2018

    IP: Sánchez, M.

    MINECO. Ministerio de Economía y Competitividad

  • Myelodisplastic syndromes: cause of mitochondrial iron overload in sideroblastic anemia.

    01/01/2015 – 31/12/2017

    IP: Sánchez, M.

    Deutsche Josep Carreras Leukämie-Stiftung

  • Non- Competitive Funds
  • APU_ADISCON_UIC Colaborative agreement

    01/12/2018-01/12-2022

    IP: Sánchez, M.

    ASOCIACIÓN PABLO UGARTE

    ASOCIACION ADISCON

    UNIVERSITAT INTERNACIONAL DE CATALUNYA (UIC)

Home/Publications and Projects