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Cherif Beldjord

Cherif Beldjord

D-Index & Metrics

Genetics

D-Index
53
Citations
13176
World Ranking
3717
National Ranking
191

Overview

Cherif Beldjord is affiliated with Inserm in France, a notable institution focused on medical and health research. Their professional profile includes involvement in scientific activities within the field of research, although specific details concerning research areas, topics, and publications remain unspecified.

Their scholarly output does not show recorded recent papers, publications in recognized venues, or collaboration with frequent co-authors based on the data currently available.

No records indicate book publications or notable awards associated with Cherif Beldjord, and their main fields or subfields of study are not documented in the given data.

This absence of detailed publication and research topic information limits the ability to identify specific scientific contributions, thematic focus, or research impact in academic arenas.

Best Publications

  • SOMATIC MUTATIONS OF THE BETA -CATENIN GENE ARE FREQUENT IN MOUSE AND HUMAN HEPATOCELLULAR CARCINOMAS

    Alix de La Coste;Béatrice Romagnolo;Pierre Billuart;Claire-Angélique Renard

  • A Novel CNS Gene Required for Neuronal Migration and Involved in X-Linked Subcortical Laminar Heterotopia and Lissencephaly Syndrome

    Vincent des Portes;Jean Marc Pinard;Pierre Billuart;Marie Claude Vinet

  • Oligophrenin-1 encodes a rhoGAP protein involved in X-linked mental retardation

    P Billuart;T Bienvenu;N Ronce;des Portes

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

    J Pagnier;J G Mears;O Dunda-Belkhodja;K E Schaefer-Rego

  • UNIPARENTAL PATERNAL DISOMY IN A GENETIC CANCER-PREDISPOSING SYNDROME

    I. Henry;C. Bonaiti-Pellié;V. Chehensse;C. Beldjord

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

    A. Carrie;L. Jun;T. Bienvenu;M.C. Vinet

  • Mutations in the [beta]-tubulin gene TUBB2B result in asymmetrical polymicrogyria

    Xavier Hubert Jaglin;Karine Poirier;Karine Poirier;Yoann Saillour;Yoann Saillour;Emmanuelle Buhler

  • Diversity of RET proto-oncogene mutations in familial and sporadic Hirschsprung disease

    Tania Attié;Anna Pelet;Patrick Edery;Charis Eng;Charis Eng

  • MECP2 mutations account for most cases of typical forms of Rett syndrome

    Thierry Bienvenu;Alain Carrié;Nicolas de Roux;Marie-Claude Vinet

  • ARX, a novel Prd-class-homeobox gene highly expressed in the telencephalon, is mutated in X-linked mental retardation

    Thierry Bienvenu;Karine Poirier;Gaelle Friocourt;Nadia Bahi

  • The Wide Spectrum of Tubulinopathies: What Are the Key Features for the Diagnosis?

    Nadia Bahi-Buisson;Karine Poirier;Franck Fourniol;Yoann Saillour;Yoann Saillour

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

    D Labie;J Pagnier;C Lapoumeroulie;F Rouabhi

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

    Vincent Des Portes;Fiona Francis;Jean Marc Pinard;Isabelle Desguerre

  • CLONING AND CHARACTERIZATION OF THE HUMAN V3 PITUITARY VASOPRESSIN RECEPTOR

    Yves de Keyzer;Colette Auzan;Frédéric Lenne;Chérif Beldjord

  • A new gene involved in X-linked mental retardation identified by analysis of an X;2 balanced translocation

    R Zemni;T Bienvenu;M C Vinet;A Sefiani

  • Large spectrum of lissencephaly and pachygyria phenotypes resulting from de novo missense mutations in tubulin alpha 1A (TUBA1A).

    Karine Poirier;Karine Poirier;David A. Keays;Fiona Francis;Fiona Francis;Yoann Saillour;Yoann Saillour

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

    F. Piccolo;S.L. Roberds;M. Jeanpierre;F. Leturcq

  • Human disorders of cortical development: from past to present

    Fiona Francis;Gundela Meyer;Catherine Fallet-Bianco;Sarah Moreno

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

    A. Carrie;F. Piccolo;F. Leturcq;C. De Toma

  • Missense mutation in PAK3, R67C, causes X-linked nonspecific mental retardation.

    T. Bienvenu;V. des Portes;N. McDonell;A. Carrie

Frequent Co-Authors

Jamel Chelly
Jamel Chelly Institute of Genetics and Molecular and Cellular Biology
Thierry Bienvenu
Thierry Bienvenu Université Paris Cité
Jean-Claude Kaplan
Jean-Claude Kaplan Université Paris Cité
Nathalie Boddaert
Nathalie Boddaert Université Paris Cité
Jamel Chelly
Jamel Chelly University of Strasbourg
Jacques Young
Jacques Young University of Paris-Saclay
Hans-Hilger Ropers
Hans-Hilger Ropers Max Planck Society

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