Didier Theophile
Impact in
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
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- Down syndrome and intellectual disability research
Papers in
-
- Congenital limb and hand anomalies 2
- Genetics 9
- Genomic variations and chromosomal abnormalities 7
- Congenital Ear and Nasal Anomalies 2
- Co-authors
- Zoubida ChettouhPierre‐Marie SinetZohra RahmaniJean Maurice DelabarJean-Louis BlouinBernard NoëlMarguerite PrieurMichel Vekemans
- Journals
- European Journal of Human Genetics (2 papers)Genomics (2 papers)Biomedicine & Pharmacotherapy (1 paper)New England Journal of Medicine (1 paper)Acta Obstetricia Et Gynecologica Scandinavica (1 paper)
- Partner nations
- FranceLebanonUnited States
In The Last Decade
Didier Theophile
15 papers receiving 689 citations
Peers
Comparison fields: 5 of 59
- Genetics 413
- Public Health, Environmental and Occupational Health 338
- Reproductive Medicine 55
- Pediatrics, Perinatology and Child Health 127
- Molecular Biology 310
Countries citing papers authored by Didier Theophile
This map shows the geographic impact of Didier Theophile'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 Didier Theophile with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Didier Theophile more than expected).
Fields of papers citing papers by Didier Theophile
This network shows the impact of papers produced by Didier Theophile. 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 Didier Theophile. The network helps show where Didier Theophile may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Didier Theophile, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | Incidence of sex chromosome abnormalities in spermatozoa from patients entering an IVF or ICSI protocol. | 1998 | 51 |
| 2 | 1998 | 23 | |
| 3 | 1997 | 16 | |
| 4 | Trisomy for the distal segment of the short arm of chromosome 17 in a boy with mild mental retardation and some dysmorphic features. | 1997 | 1 |
| 5 | 1995 | 12 | |
| 6 | 1995 | 21 | |
| 7 | 1995 | 65 | |
| 8 | 1994 | 28 | |
| 9 | 1994 | 51 | |
| 10 | 1993 | 24 | |
| 11 | 1993 | 352 | |
| 12 | Molecular mapping of the Down syndrome phenotype on chromosome 21. | 1993 | 4 |
| 13 | 1992 | 5 | |
| 14 | 1992 | 10 | |
| 15 | No significant effect of monosomy for distal 21q22.3 on the Down syndrome phenotype in "mirror" duplications of chromosome 21. | 1992 | 40 |
About Didier Theophile
Didier Theophile is a scholar working on Developmental Biology, Genetics, Reproductive Medicine, Genetics and Public Health, Environmental and Occupational Health, having authored 15 papers that have together received 703 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (7 papers), Down syndrome and intellectual disability research (4 papers), Immunodeficiency and Autoimmune Disorders (3 papers), Prenatal Screening and Diagnostics (3 papers), Congenital limb and hand anomalies (2 papers), Chromosomal and Genetic Variations (2 papers), Congenital heart defects research (2 papers) and Congenital Ear and Nasal Anomalies (2 papers). The work is most often cited by research in Genetics (413 citations), Public Health, Environmental and Occupational Health (338 citations), Reproductive Medicine (55 citations), Pediatrics, Perinatology and Child Health (127 citations) and Molecular Biology (310 citations). Didier Theophile has collaborated with scholars based in France, Lebanon and United States. Frequent co-authors include Zoubida Chettouh, Pierre‐Marie Sinet, Zohra Rahmani, Jean Maurice Delabar, Jean-Louis Blouin, Bernard Noël, Marguerite Prieur, Michel Vekemans, M Prieur and Jean‐Maurice Delabar. Their work appears in journals such as European Journal of Human Genetics, Genomics, Biomedicine & Pharmacotherapy, New England Journal of Medicine and Acta Obstetricia Et Gynecologica Scandinavica.
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.