S Thieffry
Impact in
-
- Metabolism and Genetic Disorders
Papers in
-
- RNA regulation and disease 5
- Mitochondrial Function and Pathology 3
- Genetics 7
- Genomic variations and chromosomal abnormalities 4
- Connective tissue disorders research 3
- Dermatological and Skeletal Disorders 2
- Co-authors
- G Lyon (7 shared papers)M Arthuis (12 shared papers)Jean Aicardi (6 shared papers)T Alajouanine (1 shared paper)E. Farkas‐Bargeton (8 shared papers)M. Broyer (2 shared papers)R Debré (3 shared papers)J Lejeune (1 shared paper)
- Journals
- Acta Neuropathologica (2 papers)Revue Neurologique (1 paper)La Presse Médicale (1 paper)PubMed (44 papers)Ann. Inst. Pasteur (1 paper)
- Partner nations
- France
In The Last Decade
S Thieffry
49 papers receiving 312 citations
Peers
Comparison fields: 5 of 78
- Developmental Biology 10
- Clinical Biochemistry 29
- Genetics 101
- Genetics 30
- Pediatrics, Perinatology and Child Health 52
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-authors
The 25 scholars most cited alongside S Thieffry, 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 | [Ataxiatelangiectasis. (7 personal cases)]. | 1961 | 48 |
| 2 | [PARTIAL MONOSOMY FOR A SMALL ACROCENTRIC CHROMOSOME]. | 1964 | 45 |
| 3 | [Comprehensive clinical study of 210 cases of poisoning by organic salts of tin]. | 1958 | 38 |
| 4 | [Diagnosis of a case of metachromatic leucodystrophy (Scholz type) by biopsy of a peripheral nerve]. | 1959 | 29 |
| 5 | [A special form of essential hereditary and familial osteolysis originating in early childhood and stabilizing spontaneously in later years]. | 1958 | 17 |
| 6 | 1971 | 16 | |
| 7 | [Familial leukodystrophy and spleno-hepatic determination characterizing a general metabolic disorder]. | 1954 | 14 |
| 8 | [Multiple malformations in a child with partial monosomy for a 21-22 chromosome]. | 1966 | 13 |
| 9 | [Forty cases of Werdnig-Hoffmann disease with eleven anatomical examinations]. | 1955 | 12 |
| 10 | 1958 | 10 | |
| 11 | Malformations multiples chez un enfant porteur d'une monosomie partielle pour un chromosome 21-22. | 1966 | 9 |
| 12 | Symptomatology and diagnosis of poliomyelitis. | 1955 | 9 |
| 13 | [Subacute necrotizing encephalitis in children. Anatomo-clinical study]. | 1965 | 8 |
| 14 | Fistules dermiques congénitales communiquant avec le système nerveux central. | 1958 | 7 |
| 15 | [Metachromatic leukdystrophy (Sulfatidosis) and mucopolysaccharidosis associated in the same patient]. | 1966 | 7 |
| 16 | [THE CRYING CAT SYNDROME: A FURTHER CASE]. | 1964 | 7 |
| 17 | [Papillomas of the choroid plexus in children]. | 1968 | 6 |
| 18 | [Partial trisomy C by t(Cq-; Dp+) translocation with a C(p- q+) remnant]. | 1967 | 6 |
| 19 | [Incidence of human infections in France by the Coxsackie group (virus C); isolation of the virus]. | 1951 | 5 |
| 20 | [Deletion of the short arms of chromosome 17-18: complex deformities with oligophrenia]. | 1998 | 5 |
About S Thieffry
S Thieffry is a scholar working on Molecular Biology, Genetics, Pulmonary and Respiratory Medicine, Epidemiology and Infectious Diseases, 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), Mitochondrial Function and Pathology (3 papers), Metabolism and Genetic Disorders (3 papers), Connective tissue disorders research (3 papers), Neurological diseases and metabolism (3 papers), Hereditary Neurological Disorders (2 papers) and Dermatological and Skeletal Disorders (2 papers). The work is most often cited by research in Developmental Biology (10 citations), Clinical Biochemistry (29 citations), Genetics (101 citations), Genetics (30 citations) and Pediatrics, Perinatology and Child Health (52 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, H Jérôme and Ralph Berger. Their work appears in journals such as Acta Neuropathologica, Revue Neurologique, La Presse Médicale, PubMed and Ann. Inst. Pasteur.
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.