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María del Mar Mañú‐Pereira

Observed names: M. M. Mañú‐Pereira, M.M. Mañú-Pereira, Mar Mañú-Pereira, Maria Del Mar Mañú-Pereira, Maria Mañú-Pereira, Maria del Mar Mañu‐Pereira, Maria del Mar Mañú-Pereira, Maria del Mar Mañú‐Pereira, María Del Mar Mañú‐Pereira, María del Mar Mañu-Pereira, María del Mar Mañú-Pereira, Mañú-Pereira, Maria, Mañú-Pereira, María del Mar
Observed institutions: Universitat Autònoma de Barcelona, Josep Carreras Leukaemia Research Institute, Vall d'Hebron Institut de Recerca, Hospital Clínic de Barcelona, Vall d'Hebron Hospital Universitari, Consorci Institut D'Investigacions Biomediques August Pi I Sunyer, Universitat de Barcelona
OpenAlex ID: A5110781653
Addressing the diagnostic gaps in pyruvate kinase deficiency: Consensus recommendations on the diagnosis of pyruvate kinase deficiency
2018 · Paola Bianchi, Elisa Fermo, et al. · American Journal of Hematology · 100
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Osmotic gradient ektacytometry: A valuable screening test for hereditary spherocytosis and other red blood cell membrane disorders
2017 · E. Llaudet‐Planas, J. L. Vives‐Corrons, et al. · International Journal of Laboratory Hematology · 90
Red Cell Properties after Different Modes of Blood Transportation
2016 · Asya Makhro, Rick Huisjes, et al. · Frontiers in Physiology · 78
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Is Increased Intracellular Calcium in Red Blood Cells a Common Component in the Molecular Mechanism Causing Anemia?
2017 · Laura Hertz, Rick Huisjes, et al. · Frontiers in Physiology · 68
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Combining microfluidics with machine learning algorithms for RBC classification in rare hereditary hemolytic anemia
2021 · Valeria Rizzuto, Arianna Mencattini, et al. · Scientific Reports · 65
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Safe and Efficient Gene Therapy for Pyruvate Kinase Deficiency
2016 · Maria Garcia-Gomez, Andrea Calabria, et al. · Molecular Therapy · 64
Density, heterogeneity and deformability of red cells as markers of clinical severity in hereditary spherocytosis
2019 · Rick Huisjes, Asya Makhro, et al. · Haematologica · 55
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The International Hemoglobinopathy Research Network ( INHERENT ): An international initiative to study the role of genetic modifiers in hemoglobinopathies
2021 · Petros Kountouris, Coralea Stephanou, et al. · American Journal of Hematology · 42
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The Use of Next-generation Sequencing in the Diagnosis of Rare Inherited Anaemias: A Joint BSH/EHA Good Practice Paper
2022 · Noémi B. A. Roy, Lydie Da Costa, et al. · HemaSphere · 28
Heterogeneity of G6PD deficiency prevalence in Mozambique: a school-based cross-sectional survey in three different regions
2017 · Beatriz Galatas, Lurdes Mabote, et al. · Malaria Journal · 28
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Machine learning microfluidic based platform: Integration of Lab-on-Chip devices and data analysis algorithms for red blood cell plasticity evaluation in Pyruvate Kinase Disease monitoring
2023 · A. Mencattini, V. Rizzuto, et al. · Sensors and Actuators A Physical · 27
Usefulness of NGS for Diagnosis of Dominant Beta-Thalassemia and Unstable Hemoglobinopathies in Five Clinical Cases
2021 · Valeria Rizzuto, Tamara T. Koopmann, et al. · Frontiers in Physiology · 25
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The use of next‐generation sequencing in the diagnosis of rare inherited anaemias: A Joint BSH/EHA Good Practice Paper*
2022 · Noémi B. A. Roy, Lydie Da Costa, et al. · British Journal of Haematology · 15
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Red Blood Cell Membrane Conductance in Hereditary Haemolytic Anaemias
2019 · Polina Petkova-Kirova, Laura Hertz, et al. · Frontiers in Physiology · 15
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Challenges and Opportunities of Precision Medicine in Sickle Cell Disease: Novel European Approach by GenoMed4All Consortium and ERN-EuroBloodNet
2023 · Anna Collado, Maria Paola Boaro, et al. · HemaSphere · 13
Red cell pyruvate kinase deficiency in Spain: A study of 15 cases
2017 · Laura Montllor, María del Mar Mañú-Pereira, et al. · Medicina Clínica (English Edition) · 10
Déficit de piruvato cinasa eritrocitaria en España: estudio de 15 casos
2016 · Laura Montllor, María del Mar Mañú-Pereira, et al. · Medicina Clínica · 10
Cribado neonatal de hemoglobinopatías y déficit de glucosa-6-fosfato deshidrogenasa en Cataluña. Estudio piloto en población anónima no relacionada
2006 · Maria del Mar Mañú-Pereira, Antonio Maya, et al. · Medicina Clínica · 9
An Artificial Intelligence-Based Federated Learning Platform to Boost Precision Medicine in Rare Hematological Diseases: An Initiative By GenoMed4all and Synthema Consortia
2024 · Gianluca Asti, Saverio D'Amico, et al. · Blood · 8
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A Previously Unrecognized Ca2+‐inhibited Nonselective Cation Channel in Red Blood Cells
2018 · Polina Petkova‐Kirova, Laura Hertz, et al. · HemaSphere · 8
Pyruvate kinase deficiency and severe congenital hemolytic anemia in a double heterozygous patient with paternal transmission of an early germ‐line de novo mutation
2015 · María Del Mar Mañú‐Pereira, Eva Gonzalez‐Roca, et al. · American Journal of Hematology · 6
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Southeast Asian ovalocytosis detected in a critical patient with COVID‐19 pneumonia
2022 · Ana Belén Moreno‐Castaño, Maribel Diaz‐Ricart, et al. · International Journal of Laboratory Hematology · 3
Cell counter-based parameters and formulas in detection of beta-thalassemia trait.
2008 · Jordi Juncà, Mar Mañú-Pereira, et al. · PubMed · 2
Cryopreservation of Red Blood Cells From Sickle Cell Disease Patients for Comparison of Oxygen Gradient Ektacytometry Parameters Between Laboratories to Enable Data Harmonization
2026 · Marissa J. M. Traets, Amira Idrizovic, et al. · International Journal of Laboratory Hematology · 1
Metabolic dysregulation linked to sickling tendency in sickle cell anemia independent of HbF
2026 · Sigrid van der Veen, Amira Idrizovic, et al. · Blood Cells Molecules and Diseases
Works count: 35
Citation count: 770
H-index: 14
I10-index: 17
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