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Cherif Beldjord

Affiliation : Université Paris Descartes

• 8Publications (affiliation in France)
• 181Total publications
• 11111Citations
• 46h-index

OpenAlex

Research profile

Cherif Beldjord has 8 indexed publications (1988–2015). Their work appears mainly in “Nature Genetics”, “European Journal of Human Genetics” and “Revue Neurologique”. Their most cited article, “A new gene involved in X-linked mental retardation identified by analysis of an X;2 balanced translocation” (2000), has been cited 239 times. 2 of these publications date from the last three years of activity. Their work is co-authored with at least 12 researchers, including institutions in Algeria, United States.

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Research areas

• Genetics and Neurodevelopmental Disorders
• Genomics and Rare Diseases
• Fetal and Pediatric Neurological Disorders
• Hemoglobinopathies and Related Disorders
• Cystic Fibrosis Research Advances

Publications (8)

• Mosaic parental germline mutations causing recurrent forms of malformations of cortical development
  2015 · European Journal of Human Genetics · cited 41 times
• Exploration moléculaire des lissencéphalies : à propos de quatre cas
  2014 · Revue Neurologique
• Molecular Heterogeneity of β-Thalassemia in Algeria: How to Face Up to a Major Health Problem
  2009 · Hemoglobin · cited 21 times
• A new gene involved in X-linked mental retardation identified by analysis of an X;2 balanced translocation
  2000 · Nature Genetics · cited 239 times
• Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity
  1995 · Nature Genetics · cited 188 times
• The spectrum of β‐thalassaemia in Algeria: possible origins of the molecular heterogeneity and a tentative diagnostic strategy
  1993 · British Journal of Haematology · cited 22 times
• A novelβthalassemia gene with a single base mutation in the conserved polypyrimidine sequence at the 3′ end of IVS 2
  1988 · Nucleic Acids Research · cited 33 times
• DNA haplotype distribution in Algerian ? thalassaemia patients
  1988 · Human Genetics · cited 20 times

Publication venues

• Nature Genetics × 2
• European Journal of Human Genetics × 1
• Revue Neurologique × 1
• Hemoglobin × 1
• British Journal of Haematology × 1
• Nucleic Acids Research × 1

Publications per year

• 20151
• 20141
• 20091
• 20001
• 19951
• 19931
• 19882

Collaborations

Partner institutions : Inserm · Hôpital Cochin · Centre National de la Recherche Scientifique · Institut Cochin · Hôpital Mustapha Pacha

Co-authors’ countries : Algeria · United States

Co-authors

• Dominique Labie
• Alain Carrié
• Claudine Lapouméroulie
• Jamel Chelly
• Nathalie Carion
• Kaplan Jc
• Bettina Bessières
• Axel Kahn
• Josée Pagnier
• Marie Claude Vinet
• Nicole Philip
• Michel Fardeau

Bibliographic data from OpenAlex (open database).