Sylvie Cabrol

7.0k total citations · 1 hit paper
36 papers, 3.6k citations indexed

About

Sylvie Cabrol is a scholar working on Molecular Biology, Endocrinology, Diabetes and Metabolism and Genetics. According to data from OpenAlex, Sylvie Cabrol has authored 36 papers receiving a total of 3.6k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 15 papers in Endocrinology, Diabetes and Metabolism and 15 papers in Genetics. Recurrent topics in Sylvie Cabrol's work include Sexual Differentiation and Disorders (10 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8 papers) and Growth Hormone and Insulin-like Growth Factors (7 papers). Sylvie Cabrol is often cited by papers focused on Sexual Differentiation and Disorders (10 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8 papers) and Growth Hormone and Insulin-like Growth Factors (7 papers). Sylvie Cabrol collaborates with scholars based in France, Australia and United States. Sylvie Cabrol's co-authors include Yves Le Bouc, Najiba Lahlou, M Gourmelen, Christian Vaisse, Philippe Froguel, Pierre Bougnères, Jean Chambaz, B Guy-Grand, Jean‐Marc Lacorte and Christian Dina and has published in prestigious journals such as Nature, Nature Genetics and Endocrine Reviews.

In The Last Decade

Sylvie Cabrol

36 papers receiving 3.5k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

A mutation in the human leptin receptor gene causes obesity and pituitary dysfunction

1998 1.7k citations Karine Clément, Christian Vaisse et al. Nature profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Sylvie Cabrol France	22	1.4k	1.4k	1.3k	921	695	36	3.6k
Najiba Lahlou France	36	1.5k 1.1×	1.5k 1.1×	1.5k 1.2×	947 1.0×	839 1.2×	91	5.4k
M Gourmelen France	23	878 0.6×	594 0.4×	1.3k 1.0×	902 1.0×	720 1.0×	59	3.3k
Allen W. Root United States	35	998 0.7×	732 0.5×	239 0.2×	313 0.3×	244 0.4×	170	3.7k
Veronica Sanna Italy	13	390 0.3×	334 0.2×	2.0k 1.6×	1.2k 1.3×	982 1.4×	20	3.4k
Gabriel Ángel Martos‐Moreno Spain	26	523 0.4×	290 0.2×	339 0.3×	434 0.5×	191 0.3×	118	1.9k
R. G. Hoskins	1	783 0.6×	613 0.5×	245 0.2×	318 0.3×	136 0.2×	2	3.0k
Robert A. McKnight United States	30	1.6k 1.1×	861 0.6×	146 0.1×	485 0.5×	336 0.5×	74	3.4k
Shehla Mohammed United Kingdom	7	409 0.3×	279 0.2×	1.6k 1.3×	1.2k 1.3×	890 1.3×	7	2.4k
Jacques Weill France	25	470 0.3×	630 0.5×	427 0.3×	479 0.5×	210 0.3×	55	1.8k
I. Caroline McMillen Australia	41	556 0.4×	213 0.2×	436 0.3×	1.0k 1.1×	480 0.7×	114	4.4k

Countries citing papers authored by Sylvie Cabrol

Since Specialization

Citations

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

Fields of papers citing papers by Sylvie Cabrol

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sylvie Cabrol

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Legendre, Marie, Florence Dastot, Nathalie Collot, et al.. (2016). Contribution of GHR and IGFALS Mutations to Growth Hormone Resistance - Identification of New Variants and Impact on the Inheritance Pattern. 86. 1 indexed citations

Bachelot, Anne, Jean Louis Golmard, Jérôme Dulon, et al.. (2015). Determining clinical and biological indicators for health outcomes in adult patients with childhood onset of congenital adrenal hyperplasia. European Journal of Endocrinology. 173(2). 175–184. 28 indexed citations

Portnoï, Marie‐France, Sandra Chantot‐Bastaraud, Sophie Christin‐Maître, et al.. (2012). Familial Turner syndrome with an X;Y translocation mosaicism: Implications for genetic counseling. European Journal of Medical Genetics. 55(11). 635–640. 35 indexed citations

Martinerie, Laëtitia, Yves Morel, Claire-Lise Gay, et al.. (2012). Impaired puberty, fertility, and final stature in 45,X/46,XY mixed gonadal dysgenetic patients raised as boys. European Journal of Endocrinology. 166(4). 687–694. 56 indexed citations

Afenjar, Alexandra, et al.. (2011). Floating-Harbor Syndrome. Clinical Dysmorphology. 21(1). 11–14. 9 indexed citations

Bouc, Yves Le, Sylvie Rossignol, Salah Azzi, et al.. (2010). Anomalies épigénétiques et de l’empreinte parentale dans les maladies du développement humain. Bulletin de l Académie Nationale de Médecine. 194(2). 287–300. 3 indexed citations

Demars, Julie, Sylvie Rossignol, Jun Okabe, et al.. (2009). Analysis of the IGF2/H19 imprinting control region uncovers new genetic defects, including mutations of OCT-binding sequences, in patients with 11p15 fetal growth disorders. Human Molecular Genetics. 19(5). 803–814. 92 indexed citations

Azzi, Salah, Sylvie Rossignol, Virginie Steunou, et al.. (2009). Multilocus methylation analysis in a large cohort of 11p15-related foetal growth disorders (Russell Silver and Beckwith Wiedemann syndromes) reveals simultaneous loss of methylation at paternal and maternal imprinted loci. Human Molecular Genetics. 18(24). 4724–4733. 179 indexed citations

Cavarzere, Paolo, Mireille Castanet, Michel Polak, et al.. (2008). Clinical Description of Infants with Congenital Hypothyroidism and Iodide Organification Defects. Hormone Research in Paediatrics. 70(4). 240–248. 26 indexed citations

10.

Bellanné‐Chantelot, Christine, et al.. (2006). Characterization of novel missense mutations in CYP21 causing congenital adrenal hyperplasia. Journal of Molecular Medicine. 85(3). 247–255. 25 indexed citations

11.

Soriano-Guillén, Leandro, Joël Coste, Emmanuel Écosse, et al.. (2005). Adult Height and Pubertal Growth in Turner Syndrome after Treatment with Recombinant Growth Hormone. The Journal of Clinical Endocrinology & Metabolism. 90(9). 5197–5204. 100 indexed citations

12.

Gicquel, Christine, Sylvie Rossignol, Sylvie Cabrol, et al.. (2005). Epimutation of the telomeric imprinting center region on chromosome 11p15 in Silver-Russell syndrome. Nature Genetics. 37(9). 1003–1007. 379 indexed citations

13.

Donadieu, Jean, Caroline Thomas, Laurence Brugières, et al.. (2004). Endocrine involvement in pediatric-onset langerhans' cell histiocytosis: a population-based study. The Journal of Pediatrics. 144(3). 344–350. 117 indexed citations

14.

Donadieu, Jean, Caroline Thomas, François Doz, et al.. (2004). Incidence of Growth Hormone Deficiency in Pediatric-Onset Langerhans Cell Histiocytosis: Efficacy and Safety of Growth Hormone Treatment. The Journal of Clinical Endocrinology & Metabolism. 89(2). 604–609. 55 indexed citations

15.

Baudon, Jean‐Jacques, et al.. (2004). Diagnosing Celiac Disease. Archives of Pediatrics and Adolescent Medicine. 158(6). 584–584. 36 indexed citations

16.

Méas, T., Didier Chevenne, E Thibaud, et al.. (2002). Endocrine consequences of premature pubarche in post‐pubertal Caucasian girls. Clinical Endocrinology. 57(1). 101–106. 55 indexed citations

17.

Ducos, Bertrand, Sylvie Cabrol, Muriel Houang, et al.. (2001). IGF Type 1 Receptor Ligand Binding Characteristics Are Altered in a Subgroup of Children with Intrauterine Growth Retardation. The Journal of Clinical Endocrinology & Metabolism. 86(11). 5516–5524. 16 indexed citations

18.

Houang, Muriel, Sylvie Cabrol, Laurence Périn, et al.. (2000). Insulin-like growth factor-I (IGF-I), insulin-like growth factor binding proteins (IGFBP) and insulin-like growth factor type I receptor in children with various status of chronic renal failure. Growth Hormone & IGF Research. 10(6). 332–341. 17 indexed citations

19.

Clément, Karine, Christian Vaisse, Najiba Lahlou, et al.. (1998). A mutation in the human leptin receptor gene causes obesity and pituitary dysfunction. Nature. 392(6674). 398–401. 1692 indexed citations breakdown →

20.

Schneid, H, Yves Le Bouc, Danielle Seurin, et al.. (1990). Insulin-Like Growth Factor-I Gene Analysis in Subjects with Constitutionally Variant Stature. Pediatric Research. 27(5). 488–491. 16 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.

Explore authors with similar magnitude of impact