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María Del Mar Mañú Pereira

Observed names: Mar Mañú‐Pereira, Maria Del Mar Mañú Pereira, Maria Pereira, Maria del Mar Manu Pereira, Maria del Mar Mañu Pereira, Maria del Mar Mañú Pereira, María del Mar Mañú Pereira, María del Mar Mañú-Pereira, María del Mar Mañú‐Pereira
Observed institutions: Vall d'Hebron Institut de Recerca, Hospital Clínic de Barcelona, Vall d'Hebron Hospital Universitari, Gecko Biomedical (France), Consorci Institut D'Investigacions Biomediques August Pi I Sunyer, ERN EuroBloodNet, Universitat de Barcelona
ORCID: 0000-0003-4770-7460
Observed ORCID: 0000-0003-4770-7460
OpenAlex ID: A5103190649
Haemoglobinopathies in Europe: health & migration policy perspectives
2014 · Patricia Aguilar Martinez, Michael Angastiniotis, et al. · Orphanet Journal of Rare Diseases · 110
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The variable manifestations of disease in pyruvate kinase deficiency and their management
2020 · Hanny Al-Samkari, Eduard J. Van Beers, et al. · Haematologica · 56
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Sickle cell disease landscape and challenges in the EU: the ERN-EuroBloodNet perspective
2023 · María del Mar Mañú Pereira, Raffaella Colombatti, et al. · The Lancet Haematology · 40
Challenges in IBD Research: Novel Technologies
2019 · Manish Dhyani, Nitin Joshi, et al. · Inflammatory Bowel Diseases · 26
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Diagnosis and management of pyruvate kinase deficiency: international expert guidelines
2024 · Hanny Al-Samkari, Nadine Shehata, et al. · The Lancet Haematology · 24
First description of phosphofructokinase deficiency in spain: identification of a novel homozygous missense mutation in the PFKM gene
2013 · Joan-Lluis Vives-Corrons, Pavla Koralkova, et al. · Frontiers in Physiology · 19
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Cribado neonatal de hemoglobinopatías y déficit de glucosa-6-fosfato deshidrogenasa (G6PD) en Cataluña. Estudio molecular de la anemia falciforme asociada a alfatalasemia y déficit de G6PD
2007 · María del Mar Mañú Pereira, Anna Cabot, et al. · Medicina Clínica · 18
Molecular Heterogeneity of β-Thalassemia Alleles in Spain and its Importance in the Diagnosis and Prevention of β-Thalassemia Major and Sickle Cell Disorders
2009 · Maria del Mar Mañú Pereira, Anna Cabot Dalmau, et al. · Hemoglobin · 17
Recommendations for Centres of Expertise in Rare Anaemias. The ENERCA White Book
2014 · Joan-Lluis Vives Corrons, María del Mar Mañú Pereira, et al. · Thalassemia Reports · 12
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HELIOS Action: Advancing research, education, and equity in hemoglobinopathies across Europe and beyond
2025 · Sotiroula Chatzimatthaiou, Fedele Bonifazi, et al. · HemaSphere · 9
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Newborn Screening for Sickle Cell Disease in Catalonia between 2015 and 2022—Epidemiology and Impact on Clinical Events
2024 · José Manuel González de Aledo-Castillo, Ana Argudo-Ramírez, et al. · International Journal of Neonatal Screening · 8
Limited access to transcranial Doppler screening and stroke prevention for children with sickle cell disease in Europe: Results of a multinational EuroBloodNet survey
2024 · Vincenzo Voi, Victoria Gutierrez‐Valle, et al. · Pediatric Blood & Cancer · 8
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Low affinity hemoglobinopathy ( H b V igo) due to a new mutation of beta globin gene (c200 A > T ; L ys> I le). A cause of rare anemia misdiagnosis
2017 · María del Mar Mañú Pereira, Paloma Ropero, et al. · American Journal of Hematology · 6
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Sickle cell disease: embedding patient participation into an international conference can transform the role of lived experience
2023 · Mariangela Pellegrini, Subarna Chakravorty, et al. · Orphanet Journal of Rare Diseases · 5
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COVID- 19 in patients affected by red blood cell disorders, results from the European registry ERN-EuroBloodNet
2025 · Pablo Velasco Puyo, Soteroula Christou, et al. · Orphanet Journal of Rare Diseases · 4
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Limited Access to Transcranial Doppler Screening and Stroke Prevention for Children with Sickle Cell Disease in Europe: Results of a Multinational Eurobloodnet Survey
2021 · Daniela Cuzzubbo, Victoria Gutierrez-Valle, et al. · Blood · 4
Anemias raras y fallos medulares hereditarios
2018 · Joan Lluis Vives Corrons, Maria del Mar Mañú Pereira, et al. · Arbor · 4
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Rethinking Trust in Synthetic Health Data: Lessons From 7 European Research Initiatives
2026 · Jens Declerck, Dipak Kalra, et al. · Journal of Medical Internet Research · 3
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. · Blood · 3
Pathophysiology of Anemia in HIV-Infected Children Exposed to Malaria
2021 · Cinta Moraleda, Ruth Aguilar, et al. · American Journal of Tropical Medicine and Hygiene · 3
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Undetectable Hydroxyurea Levels in the Majority of Sickle Cell Disease Patients, Especially in Young Children
2026 · Sigrid van der Veen, Bart J. Biemond, et al. · American Journal of Hematology · 2
ERN-EuroBloodNet European Registry of Patients Affected by Red Blood Cell Disorders and COVID-19
2021 · Pablo Velasco, Filomena Longo, et al. · Blood · 2
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European Reference Networks as core health structures where referring genetic newborn screening positive infants: an innovative operational research framework
2026 · Fernanda Fortunato, Rita Selvatici, et al. · Frontiers in Public Health · 1
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Pb2518: Optimizing the Detection of 2,3- Diphosphoglycerate in Dried Blood Spots of Patients With Sickle Cell Disease: Untargeted Metabolomics Within the Genomed4all Project
2023 · Sigrid van der Veen, Myrthe van Dijk, et al. · HemaSphere · 1
ERN-EurobloodNet: A European Reference Network for Rare Blood Diseases and a Model for Emulation
2019 · Pierre Fenaux, Béatrice Gulbis, et al. · Hemoglobin · 1
Works count: 38
Citation count: 388
H-index: 9
I10-index: 9
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