S Cabrol
Impact in
- Genetics top 10%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetic Syndromes and Imprinting
- Congenital Ear and Nasal Anomalies
- Reproductive Medicine top 10%
Papers in
-
- Sexual Differentiation and Disorders 7
- Epigenetics and DNA Methylation 2
- Genetics 10
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 5
- Genetic Syndromes and Imprinting 3
- Co-authors
- Yves Le Bouc (8 shared papers)J. Guillemant (2 shared papers)A Allemandou (2 shared papers)S Guillemant (2 shared papers)H Schneid (3 shared papers)G. Pérès (2 shared papers)M Gourmelen (3 shared papers)Gerald B. Pier (1 shared paper)
- Journals
- Journal of Medical Genetics (2 papers)European Journal of Endocrinology (2 papers)Journal of Bacteriology (1 paper)The Journal of Pediatrics (1 paper)Bone (1 paper)
- Partner nations
- FranceSwitzerlandBrazil
In The Last Decade
S Cabrol
24 papers receiving 665 citations
Peers
Comparison fields: 5 of 72
- Genetics 314
- Reproductive Medicine 63
- Genetics 75
- Molecular Medicine 34
- Orthopedics and Sports Medicine 51
Countries citing papers authored by S Cabrol
This map shows the geographic impact of S Cabrol'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 Cabrol with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites S Cabrol more than expected).
Fields of papers citing papers by S Cabrol
This network shows the impact of papers produced by S Cabrol. 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 Cabrol. The network helps show where S Cabrol may publish in the future.
Co-authors
The 25 scholars most cited alongside S Cabrol, 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 24 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2005 | 108 | |
| 2 | 1995 | 89 | |
| 3 | 2003 | 87 | |
| 4 | 1993 | 61 | |
| 5 | 1993 | 41 | |
| 6 | 1995 | 40 | |
| 7 | 2011 | 39 | |
| 8 | 1997 | 37 | |
| 9 | 2008 | 33 | |
| 10 | 2014 | 30 | |
| 11 | 2006 | 29 | |
| 12 | 1992 | 23 | |
| 13 | 1998 | 16 | |
| 14 | 1996 | 14 | |
| 15 | 2007 | 9 | |
| 16 | 2011 | 7 | |
| 17 | 1995 | 6 | |
| 18 | [Epigenetics, genomic imprinting and developmental disorders]. | 2010 | 5 |
| 19 | [Final height in Turner syndrome treated with growth hormone]. | 1994 | 4 |
| 20 | [True hermaphroditism in a child with a chimeric XX/XY chromosome, a double erythrocyte population and an unusual Lewis (a+ b+) phenotype]. | 1987 | 3 |
About S Cabrol
S Cabrol is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Pulmonary and Respiratory Medicine and Endocrinology, Diabetes and Metabolism, having authored 24 papers that have together received 685 indexed citations. Recurring topics across this work include Sexual Differentiation and Disorders (7 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers), Genetic Syndromes and Imprinting (3 papers), Thyroid Disorders and Treatments (2 papers), Epigenetics and DNA Methylation (2 papers), Vitamin D Research Studies (2 papers), Prenatal Screening and Diagnostics (2 papers) and Gender Studies in Language (2 papers). The work is most often cited by research in Genetics (314 citations), Reproductive Medicine (63 citations), Genetics (75 citations), Molecular Medicine (34 citations) and Orthopedics and Sports Medicine (51 citations). S Cabrol has collaborated with scholars based in France, Switzerland and Brazil. Frequent co-authors include Yves Le Bouc, J. Guillemant, A Allemandou, S Guillemant, H Schneid, G. Pérès, M Gourmelen, Gerald B. Pier, Antoine Andremont and Raymond Ruimy. Their work appears in journals such as Journal of Medical Genetics, European Journal of Endocrinology, Journal of Bacteriology, The Journal of Pediatrics and Bone.
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.