F Despert

530 total citations
22 papers, 264 citations indexed

About

F Despert is a scholar working on Molecular Biology, Endocrinology, Diabetes and Metabolism and Genetics. According to data from OpenAlex, F Despert has authored 22 papers receiving a total of 264 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 8 papers in Endocrinology, Diabetes and Metabolism and 7 papers in Genetics. Recurrent topics in F Despert's work include Sexual Differentiation and Disorders (4 papers), Genetic Syndromes and Imprinting (3 papers) and Metabolism and Genetic Disorders (3 papers). F Despert is often cited by papers focused on Sexual Differentiation and Disorders (4 papers), Genetic Syndromes and Imprinting (3 papers) and Metabolism and Genetic Disorders (3 papers). F Despert collaborates with scholars based in France. F Despert's co-authors include R. Coutant, Blandine Esteva, Danielle Naville, Stéphanie Rouleau, Céline Jaillard, Laure Barjhoux, Damien Faury, D. Loisel, Jean‐Marie Limal and Martine Bégeot and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, European Journal of Endocrinology and European Journal of Pediatrics.

In The Last Decade

F Despert

22 papers receiving 255 citations

Peers

F Despert

EDM

GENET

EAS

SURGE

M. Hernández Spain

R Wolter Belgium

Alma Toromanović Bosnia and Herzegovina

Cyril A. L. Abrams United States

Mirta Miras Argentina

Francesca Teofoli Italy

V. Beauloye Belgium

Annemarie M. Simonis-Bik Netherlands

Noriyuki Takubo Japan

Tiina Lappalainen Finland

M. Hernández Spain

F Despert

118 ×0.9

183 ×1.3

EDM

52 ×0.9

GENET

39 ×1.0

EAS

30 ×1.2

SURGE

Citations per year, relative to F Despert F Despert (= 1×) peers M. Hernández

Countries citing papers authored by F Despert

Since Specialization

Citations

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

Fields of papers citing papers by F Despert

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of F Despert

This figure shows the co-authorship network connecting the top 25 collaborators of F Despert. A scholar is included among the top collaborators of F Despert 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 F Despert. F Despert 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

Pierre, P., F Despert, François Tranquart, et al.. (2012). Adrenal rest tissue in gonads of patients with classical congenital adrenal hyperplasia: Multicenter study of 45 French male patients. Annales d Endocrinologie. 73(6). 515–522. 17 indexed citations

Al‐Salameh, Abdallah, F Despert, Marie‐Laure Kottler, et al.. (2010). Resistance to epinephrine and hypersensitivity (hyperresponsiveness) to CB1 antagonists in a patient with pseudohypoparathyroidism type Ic. European Journal of Endocrinology. 162(4). 819–824. 7 indexed citations

Menassa, Rita, et al.. (2008). p.H62L, a Rare Mutation of the CYP21 Gene Identified in Two Forms of 21-Hydroxylase Deficiency. The Journal of Clinical Endocrinology & Metabolism. 93(5). 1901–1908. 29 indexed citations

Despert, F, et al.. (2007). Adrenal rest tissue in gonads in 70 French patients with classical congenital adrenal hyperplasia (21 hydroxylase deficiency). 14. 2 indexed citations

Lorette, G, D. Sirinelli, C. Bonnard, et al.. (2006). Complications de la neurofibromatose de type 1 chez l'enfant : à propos d'une série de 100 cas. Archives de Pédiatrie. 13(7). 1009–1014. 8 indexed citations

Lorette, G. & F Despert. (2006). Dactylite à HLA B27 chez un enfant. La Presse Médicale. 35(2). 249–249. 1 indexed citations

Labarthe, François, Jean François Benoist, M. Brivet, et al.. (2006). Partial hypoparathyroidism associated with mitochondrial trifunctional protein deficiency. European Journal of Pediatrics. 165(6). 389–391. 14 indexed citations

Coutant, R., et al.. (2001). Growth and Adult Height in GH-Treated Children with Nonacquired GH Deficiency and Idiopathic Short Stature: The Influence of Pituitary Magnetic Resonance Imaging Findings. The Journal of Clinical Endocrinology & Metabolism. 86(10). 4649–4654. 56 indexed citations

Bureau, Jean‐François, et al.. (1999). L'enfant adopté d'origine étrangère en France. Analyse de 68 observations sur 12 ans au CHU de Tours. Archives de Pédiatrie. 6(10). 1053–1058. 20 indexed citations

10.

Chantepie, A, et al.. (1999). [Evolution of ventricular septal defects. Relation to echocardiographic anatomy].. PubMed. 92(5). 623–8. 2 indexed citations

11.

Cuisset, Laurence, Catherine Le Stunff, Jean‐Michel Dupont, et al.. (1997). PEG1 expression in maternal uniparental disomy 7.. PubMed. 40(4). 211–5. 5 indexed citations

12.

Naville, Danielle, Laure Barjhoux, Céline Jaillard, et al.. (1996). Demonstration by transfection studies that mutations in the adrenocorticotropin receptor gene are one cause of the hereditary syndrome of glucocorticoid deficiency.. The Journal of Clinical Endocrinology & Metabolism. 81(4). 1442–1448. 69 indexed citations

13.

Naville, Danielle, Laure Barjhoux, Céline Jaillard, et al.. (1996). [Mutations of ACTH receptor gene and familial syndrome of glucocorticoid deficiency].. PubMed. 57(2). 101–6. 9 indexed citations

14.

Dieckmann, K.‐P., et al.. (1995). Hyperplasie congénitale des surrénales et hypertrophie testiculaire. Archives de Pédiatrie. 2(12). 1167–1172. 4 indexed citations

15.

Despert, F, et al.. (1993). [Hypopituitarism caused by pituitary stalk transsection syndrome. Pathogenic hypotheses apropos of 7 cases].. PubMed. 48(9). 639–44. 5 indexed citations

16.

Despert, F, et al.. (1991). [Early onset of hypopituitarism with pituitary stalk transection syndrome].. PubMed. 48(4). 271–4. 2 indexed citations

17.

Mougenot, J. F., et al.. (1981). Maladie des chaînes lourdes alpha. Rémission complète d'un cas traité au stade de sarcome immunoblastique.. 38(6). 1 indexed citations

18.

Despert, F, et al.. (1981). [Alpha chain disease. Complete remission in one child treated at the stage of immunoblastic sarcoma (author's transl)].. PubMed. 38(6). 431–4. 2 indexed citations

19.

Morand, Pierre, et al.. (1979). Myopathie lipidique avec cardiomyopathie sévère par déficit généralisé en carnitine. Evolution favorable sous un traitement par chlorhydrate de carnitine.. Archives Des Maladies Du Coeur Et Des Vaisseaux. 72(5). 3 indexed citations

20.

Despert, F, et al.. (1979). [Lipidic myopathy with severe cardiomyopathy caused by a generalized carnitine deficiency. Favourable course during carnitine hydrochloride treatment].. PubMed. 72(5). 536–44. 3 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