C. Beldjord
Délégation Paris 5(FR)Université Paris Cité(FR)Sorbonne Paris Cité(FR)
Publications by Year
Research Areas
Genetics and Neurodevelopmental Disorders, Hemoglobinopathies and Related Disorders, Cystic Fibrosis Research Advances, Epigenetics and DNA Methylation, Iron Metabolism and Disorders
Most-Cited Works
- → Uniparental paternal disomy in a genetic cancer-predisposing syndrome(1991)422 cited
- → X‐chromosome inactivation in female patients with Fabry disease(2015)410 cited
- → Evidence for the multicentric origin of the sickle cell hemoglobin gene in Africa.(1984)410 cited
- → A new member of the IL-1 receptor family highly expressed in hippocampus and involved in X-linked mental retardation(1999)296 cited
- → Doublecortin Is the Major Gene Causing X-Linked Subcortical Laminar Heterotopia (SCLH)(1998)262 cited
- → Common haplotype dependency of high G gamma-globin gene expression and high Hb F levels in beta-thalassemia and sickle cell anemia patients.(1985)231 cited