C. Beldjord

3.7k total citations
54 papers, 2.5k citations indexed

About

C. Beldjord is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, C. Beldjord has authored 54 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Genetics, 19 papers in Molecular Biology and 17 papers in Genetics. Recurrent topics in C. Beldjord's work include Genetics and Neurodevelopmental Disorders (15 papers), Hemoglobinopathies and Related Disorders (15 papers) and Iron Metabolism and Disorders (6 papers). C. Beldjord is often cited by papers focused on Genetics and Neurodevelopmental Disorders (15 papers), Hemoglobinopathies and Related Disorders (15 papers) and Iron Metabolism and Disorders (6 papers). C. Beldjord collaborates with scholars based in France, United States and Algeria. C. Beldjord's co-authors include Dominique Labie, R L Nagel, J. Pagnier, Isabelle Henry, Claudine Junien, J. Gregory Mears, Catherine Bonaïti‐Pellié, Charles E. Schwartz, K Schaefer-Rego and Gerd Utermann and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Blood.

In The Last Decade

C. Beldjord

54 papers receiving 2.4k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
C. Beldjord France 22 1.0k 887 690 574 495 54 2.5k
T. Grimm Germany 28 1.6k 1.5× 618 0.7× 441 0.6× 142 0.2× 120 0.2× 100 2.3k
John Tolmie United Kingdom 32 2.1k 2.0× 1.7k 1.9× 213 0.3× 402 0.7× 102 0.2× 108 3.5k
Michael B. Petersen Greece 34 1.7k 1.6× 1.9k 2.1× 232 0.3× 1.1k 2.0× 200 0.4× 172 4.1k
Susan Kenwrick United Kingdom 24 1.6k 1.5× 770 0.9× 263 0.4× 307 0.5× 177 0.4× 48 2.9k
Ruth Newbury‐Ecob United Kingdom 25 2.0k 1.9× 1.3k 1.4× 222 0.3× 238 0.4× 123 0.2× 64 3.2k
Norio Sakuragawa Japan 29 1.2k 1.1× 360 0.4× 949 1.4× 186 0.3× 58 0.1× 122 2.7k
Lina Basel‐Vanagaite Israel 32 1.9k 1.8× 1.4k 1.6× 182 0.3× 497 0.9× 82 0.2× 111 3.6k
Susan Moore United Kingdom 20 873 0.8× 716 0.8× 113 0.2× 297 0.5× 317 0.6× 30 2.0k
Maria Anvret Sweden 39 2.5k 2.4× 1.3k 1.5× 191 0.3× 354 0.6× 390 0.8× 125 4.7k
F. Dagna Bricarelli Italy 19 2.1k 2.0× 1.8k 2.1× 216 0.3× 271 0.5× 77 0.2× 51 4.4k

Countries citing papers authored by C. Beldjord

Since Specialization
Citations

This map shows the geographic impact of C. Beldjord's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by C. Beldjord with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites C. Beldjord more than expected).

Fields of papers citing papers by C. Beldjord

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by C. Beldjord. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by C. Beldjord. The network helps show where C. Beldjord may publish in the future.

Co-authorship network of co-authors of C. Beldjord

This figure shows the co-authorship network connecting the top 25 collaborators of C. Beldjord. A scholar is included among the top collaborators of C. Beldjord based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with C. Beldjord. C. Beldjord is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Deloison, B., P. Sonigo, A. Millischer, et al.. (2018). Prenatally diagnosed periventricular nodular heterotopia: Further delineation of the imaging phenotype and outcome. European Journal of Medical Genetics. 61(12). 773–782. 12 indexed citations
2.
Mâazoul, Faouzi, et al.. (2008). [Molecular diagnosis of fragile X syndrome].. PubMed. 86(11). 973–7. 7 indexed citations
3.
Bahi‐Buisson, Nadia, Nathalie Boddaert, Yoann Saillour, et al.. (2008). Malformations cérébrales et épilepsie : présentations radiocliniques et implications pour le diagnostic génétique. Revue Neurologique. 164(12). 995–1009. 7 indexed citations
4.
Bahi‐Buisson, Nadia, Karine Poirier, Nathalie Boddaert, et al.. (2008). Refinement of cortical dysgeneses spectrum associated with TUBA1A mutations. Journal of Medical Genetics. 45(10). 647–653. 85 indexed citations
5.
Poirier, Karine, Didier Lacombe, Brigitte Gilbert‐Dussardier, et al.. (2005). Screening of ARX in mental retardation families: consequences for the strategy of molecular diagnosis. Neurogenetics. 7(1). 39–46. 32 indexed citations
6.
Poirier, Karine, Isabelle Souville, Cécile Laroche-Raynaud, et al.. (2005). Maternal mosaicism for mutations in the ARX gene in a family with X linked mental retardation. Human Genetics. 118(1). 45–48. 19 indexed citations
7.
Portes, V. des, Jean-Marc Pinard, Fiona Francis, et al.. (2000). Retard mental et troubles de la corticogenèse. Archives de Pédiatrie. 7. 109s–111s. 1 indexed citations
8.
Jemâa, Lamia Ben, Vincent des Portes, Ramzi Zemni, et al.. (1999). Refined 2.7 centimorgan locus in Xp21.3-22.1 for a nonspecific X-linked mental retardation gene (MRX54). American Journal of Medical Genetics. 85(3). 276–282. 7 indexed citations
9.
Billuart, Pierre, T. Bienvenu, Nathalie Ronce, et al.. (1998). Oligophrenin 1 encodes a rho-GAP protein involved in X-linked mental retardation.. PubMed. 46(9). 678–678. 33 indexed citations
10.
Keyzer, Yves de, Patricia René, C. Beldjord, Frédéric Lenne, & Xavier Bertagna. (1998). Overexpression of vasopressin (V3) and corticotrophin‐releasing hormone receptor genes in corticotroph tumours. Clinical Endocrinology. 49(4). 475–482. 66 indexed citations
11.
Steffann, Julie, et al.. (1998). Novel double mutant CF allele identified in a cystic fibrosis patient with meconium ileus.. PubMed. 41(4). 213–5. 1 indexed citations
12.
Portes, V. des, Fiona Francis, J.-M. Pinard, et al.. (1998). Doublecortin Is the Major Gene Causing X-Linked Subcortical Laminar Heterotopia (SCLH). Human Molecular Genetics. 7(7). 1063–1070. 209 indexed citations
13.
Portes, V. des, L Bachner, Thomas Brüls, et al.. (1996). X-linked neurodegenerative syndrome with congenital ataxia, late-onset progressive myoclonic encephalopathy and selective macular degeneration, linked to Xp22.33-pter. American Journal of Medical Genetics. 64(1). 69–72. 7 indexed citations
14.
Jeanpierre, Marc, Alain Carrié, Fédérica Piccolo, et al.. (1996). From adhalinopathies to alpha-sarcoglycanopathies: An overview. Neuromuscular Disorders. 6(6). 463–465. 13 indexed citations
15.
Thiberville, Luc, J. Bourguignon, C. Beldjord, et al.. (1994). Detection by the polymerase chain reaction of two polymorphisms in exon 14 of the human inter-?-trypsin inhibitor heavy chain H1 gene. Human Genetics. 93(1). 91–2. 6 indexed citations
16.
Henry, Isabelle, Anne Puech, A. Riesewijk, et al.. (1993). Somatic Mosaicism for Partial Paternal Isodisomy in Wiedemann-Beckwith Syndrome: A Post-Fertilization Event. European Journal of Human Genetics. 1(1). 19–29. 114 indexed citations
17.
Tamouza, Ryad, F. Rouabhi, M. Benabadji, et al.. (1993). The spectrum of β‐thalassaemia in Algeria: possible origins of the molecular heterogeneity and a tentative diagnostic strategy. British Journal of Haematology. 84(2). 335–337. 18 indexed citations
18.
Sébillon, Pascale, Thierry Bienvenu, Robert Girot, et al.. (1991). Detection of the Most Frequent β-Thalassemic Defect in Southeast Asia by PCR. Hemoglobin. 15(4). 313–315. 5 indexed citations
19.
Henry, Isabelle, Catherine Bonaïti‐Pellié, C. Beldjord, et al.. (1991). Uniparental paternal disomy in a genetic cancer-predisposing syndrome. Nature. 351(6328). 665–667. 331 indexed citations
20.
Labie, Dominique, et al.. (1990). β‐Thalassemia in Algeria. Annals of the New York Academy of Sciences. 612(1). 43–54. 20 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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