C. Beldjord
Impact in
- Genetics top 1%
- Hemoglobinopathies and Related Disorders
- Genetic Syndromes and Imprinting
- Genetics and Neurodevelopmental Disorders
- Hematology top 2%
- Iron Metabolism and Disorders
- Blood groups and transfusion
Papers in
- Genetics 24
- Hemoglobinopathies and Related Disorders 15
- Genetics and Neurodevelopmental Disorders 15
- Genomic variations and chromosomal abnormalities 4
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- RNA modifications and cancer 5
- Epigenetics and DNA Methylation 5
- Co-authors
- Dominique Labie (12 shared papers)R L Nagel (4 shared papers)J. Pagnier (2 shared papers)Isabelle Henry (3 shared papers)Claudine Junien (2 shared papers)J. Gregory Mears (2 shared papers)Gerd Utermann (1 shared paper)Catherine Bonaïti‐Pellié (1 shared paper)
- Journals
- Human Genetics (4 papers)Neuromuscular Disorders (3 papers)Journal of Medical Genetics (3 papers)Proceedings of the National Academy of Sciences (2 papers)Blood (2 papers)
- Partner nations
- FranceAlgeriaUnited States
In The Last Decade
C. Beldjord
54 papers receiving 2.4k citations
Peers
Comparison fields: 5 of 103
- Genetics 690
- Hematology 495
- Genetics 887
- Developmental Neuroscience 125
- Pediatrics, Perinatology and Child Health 574
Countries citing papers authored by C. Beldjord
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
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-authors
The 25 scholars most cited alongside C. Beldjord, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 54 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1984 | 332 | |
| 2 | 1991 | 331 | |
| 3 | 2015 | 291 | |
| 4 | 1998 | 209 | |
| 5 | 1985 | 199 | |
| 6 | 1993 | 114 | |
| 7 | 1997 | 97 | |
| 8 | 2008 | 85 | |
| 9 | 2005 | 67 | |
| 10 | 1998 | 66 | |
| 11 | 1995 | 52 | |
| 12 | 1997 | 45 | |
| 13 | Anthropological approach to the heterogeneity of beta-thalassemia mutations in northern Africa. | 1994 | 39 |
| 14 | Biological and clinical significance of concurrent p53 gene alterations, MDR1 gene expression, and S-phase fraction analyses in breast cancer patients treated with primary chemotherapy or radiotherapy. | 1997 | 37 |
| 15 | Oligophrenin 1 encodes a rho-GAP protein involved in X-linked mental retardation. | 1998 | 33 |
| 16 | 2005 | 32 | |
| 17 | 1992 | 32 | |
| 18 | Mapping of the X-breakpoint involved in a balanced X;12 translocation in a female with mild mental retardation. | 1997 | 32 |
| 19 | 1999 | 30 | |
| 20 | 2014 | 25 |
About C. Beldjord
C. Beldjord is a scholar working on Genetics, Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health and Hematology, having authored 54 papers that have together received 2.5k indexed citations. Recurring topics across this work include Hemoglobinopathies and Related Disorders (15 papers), Genetics and Neurodevelopmental Disorders (15 papers), Iron Metabolism and Disorders (6 papers), Fetal and Pediatric Neurological Disorders (6 papers), RNA modifications and cancer (5 papers), Cystic Fibrosis Research Advances (5 papers), Epigenetics and DNA Methylation (5 papers) and Genomic variations and chromosomal abnormalities (4 papers). The work is most often cited by research in Genetics (690 citations), Hematology (495 citations), Genetics (887 citations), Developmental Neuroscience (125 citations) and Pediatrics, Perinatology and Child Health (574 citations). C. Beldjord has collaborated with scholars based in France, Algeria and United States. Frequent co-authors include Dominique Labie, R L Nagel, J. Pagnier, Isabelle Henry, Claudine Junien, J. Gregory Mears, Gerd Utermann, Catherine Bonaïti‐Pellié, K Schaefer-Rego and Charles E. Schwartz. Their work appears in journals such as Human Genetics, Neuromuscular Disorders, Journal of Medical Genetics, Proceedings of the National Academy of Sciences and Blood.
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.