World's Best Scientists 2026 revealed!

D-Index & Metrics

Biology and Biochemistry

D-Index
56
Citations
12367
World Ranking
14344
National Ranking
554

Overview

Yves Beuzard is affiliated with the University of Paris-Saclay in France and focuses their research primarily within the field of Medicine. Their scholarly work addresses several specific subfields including Genetics, Pediatrics, Perinatology and Child Health, Infectious Diseases, Physiology, and Hematology.

The scientist's primary research topics encompass Hemoglobinopathies and Related Disorders, Prenatal Screening and Diagnostics, Parvovirus B19 Infection Studies, Erythrocyte Function and Pathophysiology, and Blood groups and transfusion.

Recent publications by Yves Beuzard provide insight into their scope of study and contributions to the scientific community. These include:

  • Haemoglobin and haemoglobinopathies at the forefront in the 21st century (2021), published in Hématologie
  • Long-term outcomes of lentiviral gene therapy for the β-hemoglobinopathies: the HGB-205 trial (2022), published in Nature Medicine
  • Sickle cell disease and risk of haematological malignancies (2021), published in Hématologie
  • Dosage de l'hémolyse dans les anémies hémolytiques et le DHTR (2021), published in Transfusion Clinique et Biologique

The publication venues where Yves Beuzard frequently contributes include:

  • Hématologie
  • Nature Medicine
  • Transfusion Clinique et Biologique

Collaborations with other researchers form an integral part of Yves Beuzard's scientific activity. Frequent co-authors include:

  • Nicolas Hebert
  • Laurent Kiger
  • Pablo Bartolucci
  • Elisa Magrin
  • Michaëla Semeraro

Best Publications

  • Transfusion independence and HMGA2 activation after gene therapy of human β-thalassaemia

    Marina Cavazzana-Calvo;Emmanuel Payen;Olivier Negre;Gary Wang

  • Gene Therapy in a Patient with Sickle Cell Disease.

    Jean-Antoine Ribeil;Salima Hacein-Bey-Abina;Emmanuel Payen;Alessandra Magnani

  • Gene Therapy in Patients with Transfusion-Dependent β-Thalassemia

    Alexis A. Thompson;Mark C. Walters;Janet Kwiatkowski;John E.J. Rasko;John E.J. Rasko;John E.J. Rasko

  • Correction of Sickle Cell Disease in Transgenic Mouse Models by Gene Therapy

    Robert Pawliuk;Karen A. Westerman;Mary E. Fabry;Emmanuel Payen

  • Isoelectric focusing of human hemoglobin: its application to screening, to the characterization of 70 variants, and to the study of modified fractions of normal hemoglobins

    P Basset;Y Beuzard;MC Garel;J Rosa

  • Sickle hemoglobin confers tolerance to Plasmodium infection.

    Ana Ferreira;Ivo Marguti;Ingo Bechmann;Ingo Bechmann;Viktória Jeney

  • Hematological Values of 163 Normal Fetuses between 18 and 30 Weeks of Gestation

    François Forestier;Fernand Daffos;Frèdèric Galactèros;Josiane Bardakjian

  • An activin receptor IIA ligand trap corrects ineffective erythropoiesis in β-thalassemia

    Michael Dussiot;Thiago T Maciel;Aurélie Fricot;Céline Chartier

  • Effect of excess alpha-hemoglobin chains on cellular and membrane oxidation in model beta-thalassemic erythrocytes.

    M. D. Scott;J. J. M. Van Den Berg;T. Repka;P. Rouyer-Fessard

  • ICA-17043, a novel Gardos channel blocker, prevents sickled red blood cell dehydration in vitro and in vivo in SAD mice

    Jonathan W. Stocker;Lucia De Franceschi;Grant A. McNaughton-Smith;Roberto Corrocher

  • Permanent and panerythroid correction of murine β thalassemia by multiple lentiviral integration in hematopoietic stem cells

    Suzan Imren;Emmanuel Payen;Karen A. Westerman;Robert Pawliuk

  • Oral magnesium supplements reduce erythrocyte dehydration in patients with sickle cell disease.

    L De Franceschi;D Bachir;F Galacteros;G Tchernia

  • Effect of mutated TP53 on response of advanced breast cancers to high-dose chemotherapy

    P Bertheau;F Plassa;M Espié;E Turpin

  • Exquisite sensitivity of TP53 mutant and basal breast cancers to a dose-dense epirubicin-cyclophosphamide regimen.

    Philippe Bertheau;Elisabeth Turpin;David S Rickman;Marc Espié

  • Gene Therapy of the β-Hemoglobinopathies by Lentiviral Transfer of the βA(T87Q)-Globin Gene

    Olivier Negre;Anne-Virginie Eggimann;Yves Beuzard;Jean-Antoine Ribeil

  • Treatment with oral clotrimazole blocks Ca(2+)-activated K+ transport and reverses erythrocyte dehydration in transgenic SAD mice. A model for therapy of sickle cell disease.

    L De Franceschi;N Saadane;M Trudel;S L Alper

  • The first case of a complete deficiency of diphosphoglycerate mutase in human erythrocytes.

    R Rosa;M O Prehu;Y Beuzard;J Rosa

  • HSP70 sequestration by free α-globin promotes ineffective erythropoiesis in β-thalassaemia

    Jean-Benoît Arlet;Jean-Antoine Ribeil;Flavia Guillem;Olivier Negre

  • Endothelin receptor antagonism prevents hypoxia-induced mortality and morbidity in a mouse model of sickle-cell disease

    Nathalie Sabaa;Lucia de Franceschi;Philippe Bonnin;Yves Castier

  • Covalent binding of glutathione to hemoglobin. I. Inhibition of hemoglobin S polymerization.

    M C Garel;C Domenget;J Caburi-Martin;C Prehu

Frequent Co-Authors

Philippe Leboulch
Philippe Leboulch Brigham and Women's Hospital
Ugo Testa
Ugo Testa Istituto Superiore di Sanità
William Vainchenker
William Vainchenker Institut Gustave Roussy
Carlo Brugnara
Carlo Brugnara Boston Children's Hospital
Anne Janin
Anne Janin Université Paris Cité
Aldo Scarpa
Aldo Scarpa University of Verona
Olivier Hermine
Olivier Hermine Necker-Enfants Malades Hospital
Bénédicte Neven
Bénédicte Neven Université Paris Cité
Stéphane Blanche
Stéphane Blanche Université Paris Cité
Michel Goossens
Michel Goossens Grenoble Alpes University

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