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Anna Collado Gimbert

I am a medical specialist in pediatric hematology, with a focus on the care of patients with rare anemia disorders and other red blood cel disorders. I carry out my clinical work in the hospital setting, where I am responsible for the diagnosis, treatment, and comprehensive follow-up of children and adolescents with rare hematological diseases. I combine clinical activity with translational research, with a particular interest in the use of real-world data (Real World Data), the integration of national and European clinical registries, and the application of emerging technologies such as artificial intelligence in the field of rare hematological diseases. In this context, I participate as a researcher in various European (Genomed4ALL, Synthema, and ERDERA) and international (HELIOS) projects focused on personalized medicine and improving health outcomes.

Institutions of which they are part

Predoctoral researcher
Childhood Cancer and Blood Disorders
Vall Hebron Institut de Recerca
Doctor
Paediatric Oncology and Haematology
Children's Hospital and Woman's Hospital

Anna Collado Gimbert

Institutions of which they are part

Predoctoral researcher
Childhood Cancer and Blood Disorders
Vall Hebron Institut de Recerca
Doctor
Paediatric Oncology and Haematology
Children's Hospital and Woman's Hospital

I am a medical specialist in pediatric hematology, with a focus on the care of patients with rare anemia disorders and other red blood cel disorders. I carry out my clinical work in the hospital setting, where I am responsible for the diagnosis, treatment, and comprehensive follow-up of children and adolescents with rare hematological diseases. I combine clinical activity with translational research, with a particular interest in the use of real-world data (Real World Data), the integration of national and European clinical registries, and the application of emerging technologies such as artificial intelligence in the field of rare hematological diseases. In this context, I participate as a researcher in various European (Genomed4ALL, Synthema, and ERDERA) and international (HELIOS) projects focused on personalized medicine and improving health outcomes.

Graduated in Medicine from the Autonomous University of Barcelona (2014), I completed my MIR residency in Pediatrics at the Vall d'Hebron University Hospital (2015–2019), followed by a Fellowship in Pediatric Oncology, Hematology, and Hematopoietic Stem Cell Transplantation at the same center (2019–2021).

Since 2021, I have worked as a Specialist in the Pediatric Oncology and Hematology Service at Vall d'Hebron University Hospital. In parallel, I work as a clinical reseracher in the Rare Anemias Laboratory, within the Childhood Cancer and Hematological Diseases Research Group at Vall d'Hebron Institute of Research (VHIR).

I have actively participated in the accreditation processes as a Center, Service, and Reference Unit (CSUR) for hereditary erythropathology at the national level, as well as in the accreditation of the Clinical Expertise Units Network (XUEC) in non-oncological hematological diseases.

I am a member of several scientific societies and working groups specialized in pediatric hematology including:
- Erythropathy Group of the Spanish Society of Pediatric Hematology and Oncology (SEHOP)
- Pediatric Hematology Working Group of the Catalan Society of Pediatrics
- Scientific Committee of the Spanish Registry of Hemoglobinopathies and Rare Anemias (REHem-AR SEHOP)
- European Hematology Association (EHA)

Projects

Integración de datos del mundo real, de salud y de investigación para la mejora de los protocolos clínicos en la enfermedad falciforme y otras anemias raras

IP: M Mar Mañu Pereira
Collaborators: Sara Isabel Reidel , David Beneitez Pastor, Maria Cristina Díaz de Heredia Rubio, Adoración Blanco Alvarez, Anna Collado Gimbert
Funding agency: Instituto de Salud Carlos III
Funding: 152500
Reference: PI24/00477
Duration: 01/01/2025 - 31/12/2027

ERDERA: European Rare Disease Research Alliance

IP: M Mar Mañu Pereira
Collaborators: Sara Isabel Reidel , Sara Isabel Reidel , Miguel Chillon Rodriguez, Esther García Pagès, Raquel Mosull del Campo, Raquel Mosull del Campo, Simon Schwartz Navarro, Agustín Arasanz Duque, Sandra Mancilla Zamora, Anna Collado Gimbert, Marc Miquel Moltó Abad, Ángela Menárguez López, Ángela Menárguez López, Ángela Menárguez López, Claire Diot
Funding agency: EUROPEAN COMMISSION
Funding: 771525
Reference: ERDERA_MAÑU_EC_HLTH2023-DISEASE-07-01/2023
Duration: 01/09/2024 - 31/08/2031

SYNTHEMA: Synthetic generation of hematological data over federated computing frameworks

IP: M Mar Mañu Pereira
Collaborators: Sara Isabel Reidel , Anna Collado Gimbert, Ángela Menárguez López, Claire Diot, Amira Idrizovic
Funding agency: EUROPEAN COMMISSION
Funding: 435937.5
Reference: SYNTHEMA_M.MAÑU_HE_2022
Duration: 01/12/2022 - 30/11/2026

GENOMED4ALL - Genomics and Personalized Medicine for all though Artificial Intelligence in Haematological Diseases

IP: M Mar Mañu Pereira
Collaborators: Sara Isabel Reidel , Esther García Pagès, Anna Collado Gimbert, Ángela Menárguez López, Amira Idrizovic
Funding agency: EUROPEAN COMMISSION
Funding: 434000
Reference: GENOMED4ALL_H2020-SC1-FA-DTS-2018-20_2020
Duration: 01/01/2021 - 30/06/2025

Related news

The project’s 4th annual meeting was recently held as part of the Fortalece–Salud programme of the Carlos III Health Institute.

Vall d'Hebron is one of the centers that coordinate this network, which so far has enabled the detection of high-risk genetic alterations and the provision of personalized treatments that have already achieved remission in cases with very few therapeutic alternatives.

The projects, selected under the 2026 Health Research and CaixaImpulse Health Innovation calls, address topics ranging from new therapies for childhood neurological disorders and Parkinson’s disease to the treatment of mitochondrial diseases and cancer.

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