S. Odent

1.0k citations
22 papers · 215 · h-index 7

Impact in

Papers in

    • Connective tissue disorders research 3
    • Craniofacial Disorders and Treatments 2
    • Genetic Syndromes and Imprinting 2
    • Pancreatic and Hepatic Oncology Research 2

S. Odent

22 papers receiving 209 citations

Peers

S. Odent
Comparison fields: 5 of 40
  • Cell Biology 52
  • Physiology 73
  • Genetics 68
  • Pediatrics, Perinatology and Child Health 40
  • Developmental Biology 5
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Citations per year

Countries citing papers authored by S. Odent

Since Specialization
Citations

This map shows the geographic impact of S. Odent'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 S. Odent with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites S. Odent more than expected).

Fields of papers citing papers by S. Odent

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by S. Odent. 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 S. Odent. The network helps show where S. Odent may publish in the future.

Co-authors

The 25 scholars most cited alongside S. Odent, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with S. Odent Line = papers co-authored together S. Odent links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 22 papers — load more, or switch the sort, to bring in the rest.

#Work
1 200375
2
Prenatal detection of a congenital pancreatic cyst and Beckwith-Wiedemann syndrome.
199728
3 199724
4 201420
5
A case of Larsen syndrome with severe cervical malformations.
199410
6 20077
7
[Oto-palato-digital type I syndrome in five generations. Relationship to the type II form].
19887
8 19956
9
[Hair dysplasia in oculo-dento-digital syndrome. Apropos of a mother-daughter case].
19946
10 19885
11
Triphalangeal thumb and split foot in the same family.
19904
12
[Diffuse subcortical heterotopias of the gray matter].
19934
13
A new syndrome with ptosis, coloboma and mental retardation.
19924
14
[Reflections on 10 years of medically induced abortions in Ille-et-Vilaine].
19943
15 19993
16
[Autopsy in neonatal death].
19893
17 19941
18
[Indications for therapeutic interruption of pregnancy in Ille-et-Villaine from 1982 to 1986. Apropos of 222 cases].
19891
19
[Percutaneous catheterization of the axillary vein in the newborn infant].
19841
20
[Therapeutic termination of pregnancy. Diagnosis and protocols. 54 cases].
19921

About S. Odent

S. Odent is a scholar working on Genetics, Oncology, Pediatrics, Perinatology and Child Health, Molecular Biology and Public Health, Environmental and Occupational Health, having authored 22 papers that have together received 215 indexed citations. Recurring topics across this work include Connective tissue disorders research (3 papers), Biomedical Research and Pathophysiology (2 papers), Craniofacial Disorders and Treatments (2 papers), Pancreatic and Hepatic Oncology Research (2 papers), Genetic Syndromes and Imprinting (2 papers), Prenatal Screening and Diagnostics (2 papers), Congenital limb and hand anomalies (2 papers) and Assisted Reproductive Technology and Twin Pregnancy (2 papers). The work is most often cited by research in Cell Biology (52 citations), Physiology (73 citations), Genetics (68 citations), Pediatrics, Perinatology and Child Health (40 citations) and Developmental Biology (5 citations). S. Odent has collaborated with scholars based in France. Frequent co-authors include Catherine Tréguier, Patrice Poulain, B. Frémond, B. Le Marec, Cyril Mignot, I Maire, B. Bessières, F. Daffos, Patrice Josset and J. Roume. Their work appears in journals such as Prenatal Diagnosis, Journal of Medical Genetics, Clinical Genetics, American Journal of Medical Genetics Part A and Molecular Syndromology.

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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