S Cabrol

999 total citations
24 papers, 685 citations indexed

About

S Cabrol is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, S Cabrol has authored 24 papers receiving a total of 685 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 10 papers in Genetics and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in S Cabrol's work include Sexual Differentiation and Disorders (7 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers) and Genetic Syndromes and Imprinting (3 papers). S Cabrol is often cited by papers focused on Sexual Differentiation and Disorders (7 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers) and Genetic Syndromes and Imprinting (3 papers). S Cabrol collaborates with scholars based in France, Switzerland and Brazil. S Cabrol's co-authors include Yves Le Bouc, H Schneid, G. Pérès, S Guillemant, J. Guillemant, A Allemandou, M Gourmelen, Raymond Ruimy, Gerald B. Pier and Antoine Andremont and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Journal of Bacteriology and The Journal of Pediatrics.

In The Last Decade

S Cabrol

24 papers receiving 665 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
S Cabrol France 14 380 314 111 98 97 24 685
P. Barbet France 13 250 0.7× 194 0.6× 67 0.6× 63 0.6× 47 0.5× 31 604
Maria Betânia Pereira Toralles Brazil 15 261 0.7× 207 0.7× 46 0.4× 18 0.2× 81 0.8× 67 609
M.M. Grumbach United States 13 231 0.6× 124 0.4× 298 2.7× 76 0.8× 356 3.7× 18 909
B. W. Brown Australia 10 78 0.2× 98 0.3× 59 0.5× 46 0.5× 29 0.3× 30 616
Laurence Loubière United Kingdom 13 152 0.4× 167 0.5× 273 2.5× 37 0.4× 64 0.7× 14 747
Rebecca P. Green United States 9 619 1.6× 424 1.4× 39 0.4× 118 1.2× 39 0.4× 9 919
H. Welter Germany 19 226 0.6× 153 0.5× 26 0.2× 51 0.5× 82 0.8× 48 771
Belgin Selam Türkiye 20 203 0.5× 196 0.6× 169 1.5× 27 0.3× 70 0.7× 50 1.2k
Lluís Bassas Spain 16 556 1.5× 364 1.2× 208 1.9× 616 6.3× 24 0.2× 21 1.5k
Philip D. Pallister United States 12 302 0.8× 313 1.0× 167 1.5× 32 0.3× 17 0.2× 19 655

Countries citing papers authored by S Cabrol

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of S Cabrol

This figure shows the co-authorship network connecting the top 25 collaborators of S Cabrol. A scholar is included among the top collaborators of S Cabrol 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 Cabrol. S Cabrol is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Ramos, Helton Estrela, Aurore Carré, L. Chevrier, et al.. (2014). Extreme phenotypic variability of thyroid dysgenesis in six new cases of congenital hypothyroidism due to PAX8 gene loss-of-function mutations. European Journal of Endocrinology. 171(4). 499–507. 30 indexed citations
2.
Linglart, Agnès, S Cabrol, P. Berlier, et al.. (2011). Growth hormone treatment before the age of 4 years prevents short stature in young girls with Turner syndrome. European Journal of Endocrinology. 164(6). 891–897. 39 indexed citations
3.
Cabrol, S, Laurence Périn, M Colle, et al.. (2011). Evolution of IGF-1 in Children Born Small for Gestational Age and with Growth Retardation, Treated by Growth Hormone Adapted to IGF-1 Levels after 1 Year. Hormone Research in Paediatrics. 76(6). 419–427. 7 indexed citations
4.
Cabrol, S, et al.. (2010). Existe-t-il un risque de déficit corticotrope au décours du traitement d’induction d’une leucémie aiguë lymphoblastique ?. Archives de Pédiatrie. 17(12). 1637–1644. 1 indexed citations
5.
Cavarzere, Paolo, Mireille Castanet, Michel Polak, et al.. (2008). SFRP-08 – Recherche clinique – Hypothyroïdie congénitale avec trouble de l’organification de l’iode : description phénotypique précise d’une cohorte d’enfants. Archives de Pédiatrie. 15(5). 1033–1033. 1 indexed citations
6.
Cabrol, S. (2007). Le syndrome de Turner. Annales d Endocrinologie. 68(1). 2–9. 9 indexed citations
7.
Zénaty, Delphine, Frédérique Dijoud, Yves Morel, et al.. (2006). Bilateral anorchia in infancy: Occurence of micropenis and the effect of testosterone treatment. The Journal of Pediatrics. 149(5). 687–691. 29 indexed citations
8.
Pinto, Graziella, Véronique Abadie, Robin Mesnage, et al.. (2005). CHARGE Syndrome Includes Hypogonadotropic Hypogonadism and Abnormal Olfactory Bulb Development. The Journal of Clinical Endocrinology & Metabolism. 90(10). 5621–5626. 108 indexed citations
9.
Cabrol, S, et al.. (2003). Transcription of Quorum-Sensing System Genes inClinical and Environmental Isolates of Pseudomonasaeruginosa. Journal of Bacteriology. 185(24). 7222–7230. 87 indexed citations
10.
Guillemant, J., A Allemandou, S Cabrol, G. Pérès, & S Guillemant. (1998). Statut vitaminique D de l’adolescent: variations saisonnières et effets d’une supplémentation hivernale par la vitamine D3. Archives de Pédiatrie. 5(11). 1211–1215. 16 indexed citations
11.
Schneid, H, M.-P. Vazquez, C. Vacher, et al.. (1997). The Beckwith-Wiedemann syndrome phenotype and the risk of cancer. Medical and Pediatric Oncology. 28(6). 411–415. 37 indexed citations
12.
Cabrol, S, et al.. (1996). Syndrome de Turner: croissance staturopondérale et maturation osseuse spontanées. Archives de Pédiatrie. 3(4). 313–318. 14 indexed citations
13.
Cabrol, S, et al.. (1995). Hyponatrémie sévère associée à une anorexie mentale: rôle d'une sécrétion inappropriée d'hormone antidiurétique?. Archives de Pédiatrie. 2(10). 977–979. 6 indexed citations
14.
Guillemant, J., S Cabrol, A Allemandou, G. Pérès, & S Guillemant. (1995). Vitamin D-dependent seasonal variation of PTH in growing male adolescents. Bone. 17(6). 513–516. 89 indexed citations
15.
Rochiccioli, P, J Battin, A.-M. Bertrand, et al.. (1995). Final Height in Turner Syndrome Patients Treated with Growth Hormone. Hormone Research. 44(4). 172–176. 40 indexed citations
16.
Rocchiccioli, Paul, J Battin, M Bost, et al.. (1994). [Final height in Turner syndrome treated with growth hormone].. PubMed. 1(4). 359–62. 4 indexed citations
17.
Schneid, H, Danielle Seurin, M.-P. Vazquez, et al.. (1993). Parental allele specific methylation of the human insulin-like growth factor II gene and Beckwith-Wiedemann syndrome.. Journal of Medical Genetics. 30(5). 353–362. 61 indexed citations
18.
19.
Gicquel, Christine, S Cabrol, H Schneid, F Girard, & Yves Le Bouc. (1992). Molecular diagnosis of Turner's syndrome.. Journal of Medical Genetics. 29(8). 547–551. 23 indexed citations
20.
Cabrol, S, et al.. (1985). [Hydrocholecystis, unrecognized cause of painful abdominal crises in patients with sickle cell anemia].. PubMed. 42(10). 859–61. 1 indexed citations

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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