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C. Beldjord | Researchclopedia

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C. Beldjord

Délégation Paris 5

89

Works

3,747

Citations

25

h-index

46

i10-index

Research Topics

Genetics and Neurodevelopmental Disorders Hemoglobinopathies and Related Disorders Cystic Fibrosis Research Advances

Affiliations

Délégation Paris 52005–2018

Hôpital américain de paris1998–1998

Hôpital Necker-Enfants Malades1999–1999

Centre National de la Recherche Scientifique2005–2014

Albert Einstein College of Medicine1981–1984

Top Works

Uniparental paternal disomy in a genetic cancer-predisposing syndrome

Isabelle Henry,Catherine Bonaïti‐Pellié,et al.

1991422 citations

Epigenetics and DNA Methylation

Iron Metabolism and Disorders

X‐chromosome inactivation in female patients with Fabry disease

Lucía Echevarría,Karelle Bénistan,et al.

2015411 citations

Evidence for the multicentric origin of the sickle cell hemoglobin gene in Africa.

J. Pagnier,J. Gregory Mears,et al.

1984410 citations

A new member of the IL-1 receptor family highly expressed in hippocampus and involved in X-linked mental retardation

Alain Carrié,Jun Li,et al.

1999296 citations

Doublecortin Is the Major Gene Causing X-Linked Subcortical Laminar Heterotopia (SCLH)

V. des Portes,Fiona Francis,et al.

1998262 citations

Common haplotype dependency of high G gamma-globin gene expression and high Hb F levels in beta-thalassemia and sickle cell anemia patients.

Dominique Labie,J. Pagnier,et al.

1985231 citations

Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity

Fédérica Piccolo,Steven L. Roberds,et al.

1995191 citations

Somatic Mosaicism for Partial Paternal Isodisomy in Wiedemann-Beckwith Syndrome: A Post-Fertilization Event

Isabelle Henry,Anne Puech,et al.

1993140 citations

Mutational diversity and hot spots in the alpha-sarcoglycan gene in autosomal recessive muscular dystrophy (LGMD2D).

Alain Carrié,Fédérica Piccolo,et al.

1997116 citations