Cherif Beldjord

Cherif Beldjord publication distribution in Genetics in 2026

The chart shows the distribution of publications by all Research.com ranked scientists in the field of Genetics in 2026. The highlighted bar marks where Cherif Beldjord sits on this spectrum.

Cherif Beldjord D-index placement in Genetics in 2026

The chart shows the D-index (discipline H-index) distribution of Genetics scientists ranked by Research.com in 2026. The highlighted bar marks where Cherif Beldjord sits on this spectrum.

Overview

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

  1366
  Citations

• 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

  855
  Citations

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

  P Billuart;T Bienvenu;N Ronce;des Portes

  609
  Citations

• 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

  549
  Citations

• UNIPARENTAL PATERNAL DISOMY IN A GENETIC CANCER-PREDISPOSING SYNDROME

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

  524
  Citations

• 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

  416
  Citations

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

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

  409
  Citations

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

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

  386
  Citations

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

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

  359
  Citations

• 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

  349
  Citations

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

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

  345
  Citations

• 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

  328
  Citations

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

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

  302
  Citations

• CLONING AND CHARACTERIZATION OF THE HUMAN V3 PITUITARY VASOPRESSIN RECEPTOR

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

  292
  Citations

• 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

  287
  Citations

• 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

  264
  Citations

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

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

  248
  Citations

• Human disorders of cortical development: from past to present

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

  193
  Citations

• 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

  163
  Citations

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

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

  159
  Citations