S Thieffry
- Molecular Biology
- Genetics
- Pediatrics, Perinatology and Child Health
- Physiology
- Cellular and Molecular Neuroscience
- Topics
- RNA regulation and disease (5 papers)Genomic variations and chromosomal abnormalities (4 papers)Neurological diseases and metabolism (3 papers)
- Partner nations
- France
In The Last Decade
S Thieffry
49 papers receiving 312 citations
Peers
Comparison fields: 5 of 78
- Molecular Biology 133
- Genetics 101
- Pediatrics, Perinatology and Child Health 52
- Physiology 43
- Cellular and Molecular Neuroscience 35
Countries citing papers authored by S Thieffry
This map shows the geographic impact of S Thieffry'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 Thieffry with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites S Thieffry more than expected).
Fields of papers citing papers by S Thieffry
This network shows the impact of papers produced by S Thieffry. 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 Thieffry. The network helps show where S Thieffry may publish in the future.
Co-authorship network of co-authors of S Thieffry
This figure shows the co-authorship network connecting the top 25 collaborators of S Thieffry. A scholar is included among the top collaborators of S Thieffry 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 S Thieffry. S Thieffry is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | [Deletion of the short arms of chromosome 17-18: complex deformities with oligophrenia]. | 5 |
| 2 | Leucoencphalopathie familiale associe une acidose lactique congnitale@@@Familial leukoencephalopathy associated with congenital lactic acidosis | 1 |
| 3 | 16 | |
| 4 | [Contribution of histoenzymological technics to the study of congenital hypotonias]. | 4 |
| 5 | [The role of intubation and artificial ventilation in the treatment of severe bronchoalveolitis in infants. (Apropos of 7 cases)]. | 2 |
| 6 | Malformations multiples chez un enfant porteur d'une monosomie partielle pour un chromosome 21-22. | 9 |
| 7 | Technique de la ventilation artificielle prolongée du nouveau-né et du prématuré. | 2 |
| 8 | Maturation histoenzymologique du cortex cérébelleux et de la corne d'Ammon chez l'enfant. | 4 |
| 9 | [Subacute necrotizing encephalitis in children. Anatomo-clinical study]. | 8 |
| 10 | [THE CRYING CAT SYNDROME: A FURTHER CASE]. | 7 |
| 11 | ENT'EROVIRUS (POLIOMY'ELITE, COXSACKIE, E.C.H.O.) ET MALADIES DU SYST'EME NERVEUX. R'EVISION CRITIQUE ET EXP'ERIENCE PERSONNELLE. | 1 |
| 12 | [Ataxiatelangiectasis. (7 personal cases)]. | 48 |
| 13 | [Infantile amaurotic idiocy with serious changes of the white matter]. | 5 |
| 14 | [Acute isolated cerebellar ataxia in child, with recovery]. | 2 |
| 15 | Fistules dermiques congénitales communiquant avec le système nerveux central. | 7 |
| 16 | [Pheochromocytoma in children]. | 1 |
| 17 | [Case of essential thrombocythemia]. | 3 |
| 18 | [Familial leukodystrophy and spleno-hepatic determination characterizing a general metabolic disorder]. | 14 |
| 19 | [Incidence of human infections in France by the Coxsackie group (virus C); isolation of the virus]. | 5 |
| 20 | The Presence in France of Human Infections with the Coxsackie Group (Virus C). Isolation of the Virus. | 2 |
About S Thieffry
S Thieffry is a scholar working on Anatomy, Clinical Biochemistry and Neurology, having authored 54 papers that have together received 382 indexed citations. Recurring topics across this work include RNA regulation and disease (5 papers), Genomic variations and chromosomal abnormalities (4 papers) and Neurological diseases and metabolism (3 papers). The work is most often cited by research in Developmental Biology (10 citations), Clinical Biochemistry (29 citations) and Genetics (101 citations). S Thieffry has collaborated with scholars based in France. Frequent co-authors include G Lyon, M Arthuis, Jean Aicardi, T Alajouanine, E. Farkas‐Bargeton, M. Broyer, R Debré, J Lejeune, R Turpin and Ralph Berger. Their work appears in journals such as Acta Neuropathologica, Revue Neurologique and La Presse Médicale.
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.