Delphine Zénaty

2.0k total citations
34 papers, 1000 citations indexed

About

Delphine Zénaty is a scholar working on Endocrinology, Diabetes and Metabolism, Genetics and Molecular Biology. According to data from OpenAlex, Delphine Zénaty has authored 34 papers receiving a total of 1000 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Endocrinology, Diabetes and Metabolism, 14 papers in Genetics and 11 papers in Molecular Biology. Recurrent topics in Delphine Zénaty's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (12 papers), Sexual Differentiation and Disorders (7 papers) and Thyroid Disorders and Treatments (6 papers). Delphine Zénaty is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (12 papers), Sexual Differentiation and Disorders (7 papers) and Thyroid Disorders and Treatments (6 papers). Delphine Zénaty collaborates with scholars based in France, United States and Italy. Delphine Zénaty's co-authors include Juliane Léger, Jean‐Claude Carel, Jérôme Bertherat, Olivier Chabre, Bernard Goichot, Françoise Audran, Pascal Philibert, Nicolás de Roux, S. Soskin and Juliane Léger and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Human Molecular Genetics and Diabetologia.

In The Last Decade

Delphine Zénaty

34 papers receiving 965 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Delphine Zénaty France 18 522 438 306 222 168 34 1000
Nurçin Saka Türkiye 18 265 0.5× 307 0.7× 441 1.4× 103 0.5× 187 1.1× 63 961
S. F. Ahmed United Kingdom 19 324 0.6× 460 1.1× 357 1.2× 76 0.3× 198 1.2× 32 1.1k
Laura Audí Spain 22 533 1.0× 702 1.6× 412 1.3× 125 0.6× 117 0.7× 54 1.2k
Juliane Léger France 15 357 0.7× 320 0.7× 564 1.8× 109 0.5× 315 1.9× 26 1.1k
S L S Drop Netherlands 16 323 0.6× 437 1.0× 367 1.2× 146 0.7× 415 2.5× 25 1.1k
S. L. S. Drop Netherlands 22 409 0.8× 674 1.5× 537 1.8× 321 1.4× 224 1.3× 45 1.2k
Rachel Reynaud France 24 495 0.9× 538 1.2× 899 2.9× 184 0.8× 147 0.9× 99 1.6k
Sofia Helena Valente de Lemos‐Marini Brazil 16 440 0.8× 526 1.2× 357 1.2× 79 0.4× 66 0.4× 99 880
Agnethe Berglund Denmark 15 415 0.8× 348 0.8× 160 0.5× 72 0.3× 99 0.6× 44 734
Roelof J. Odink Netherlands 21 317 0.6× 334 0.8× 514 1.7× 295 1.3× 268 1.6× 40 1.0k

Countries citing papers authored by Delphine Zénaty

Since Specialization
Citations

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

Fields of papers citing papers by Delphine Zénaty

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Delphine Zénaty

This figure shows the co-authorship network connecting the top 25 collaborators of Delphine Zénaty. A scholar is included among the top collaborators of Delphine Zénaty 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 Delphine Zénaty. Delphine Zénaty 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.
Buffet, Alexandre, J. Abeillon, D. Drui, et al.. (2020). Screening of a Large Cohort of Asymptomatic SDHx Mutation Carriers in Routine Practice. The Journal of Clinical Endocrinology & Metabolism. 106(3). e1301–e1315. 8 indexed citations
2.
Reznik, Yves, Pascal Barat, Jérôme Bertherat, et al.. (2018). SFE/SFEDP adrenal insufficiency French consensus: Introduction and handbook. Annales d Endocrinologie. 79(1). 1–22. 27 indexed citations
3.
Cortet, Christine, Pascal Barat, Delphine Zénaty, Laurence Guignat, & Philippe Chanson. (2017). Group 5: Acute adrenal insufficiency in adults and pediatric patients. Annales d Endocrinologie. 78(6). 535–543. 15 indexed citations
4.
Bois, E., et al.. (2017). Otologic disorders in Turner syndrome. European Annals of Otorhinolaryngology Head and Neck Diseases. 135(1). 21–24. 12 indexed citations
5.
Léger, Juliane, Damir Mohamed, Delphine Zénaty, et al.. (2017). Impact of the underlying etiology of growth hormone deficiency on serum IGF-I SDS levels during GH treatment in children. European Journal of Endocrinology. 177(3). 267–276. 5 indexed citations
6.
Carré, Aurore, Athanasia Stoupa, Dulanjalee Kariyawasam, et al.. (2016). Mutations in BOREALIN cause thyroid dysgenesis. Human Molecular Genetics. 26(3). ddw419–ddw419. 36 indexed citations
7.
Zénaty, Delphine, et al.. (2016). X-chromosome gene dosage as a determinant of impaired pre and postnatal growth and adult height in Turner syndrome. European Journal of Endocrinology. 175(3). X1–X1. 13 indexed citations
8.
Bernard, Valérie, Bruno Donadille, Delphine Zénaty, et al.. (2016). Spontaneous fertility and pregnancy outcomes amongst 480 women with Turner syndrome. Human Reproduction. 31(4). 782–788. 146 indexed citations
9.
10.
Zénaty, Delphine, et al.. (2015). X-chromosome gene dosage as a determinant of impaired pre and postnatal growth and adult height in Turner syndrome. European Journal of Endocrinology. 174(3). 281–288. 21 indexed citations
11.
Simon, Dominique, Emmanuel Écosse, Anne Paulsen, et al.. (2015). Mutations in the maternally imprinted gene MKRN3 are common in familial central precocious puberty. European Journal of Endocrinology. 174(1). 1–8. 76 indexed citations
12.
Simon, Dominique, Anne Paulsen, Delphine Zénaty, et al.. (2014). Mutations in the Maternally Imprinted Gene MKRN3 are a Frequent Cause of Familial Central Precocious Puberty. 1 indexed citations
13.
Philibert, Pascal, Françoise Paris, Françoise Audran, et al.. (2011). Phenotypic Variation of SF1 Gene Mutations. Advances in experimental medicine and biology. 707. 67–72. 11 indexed citations
14.
Bailleul‐Forestier, Isabelle, et al.. (2010). Dental agenesis in Kallmann syndrome individuals with FGFR1 mutations. International Journal of Paediatric Dentistry. 20(4). 305–312. 21 indexed citations
15.
Zénaty, Delphine, et al.. (2010). Genetic evidence of the programming of beta cell mass and function by glucocorticoids in mice. Diabetologia. 54(2). 350–359. 44 indexed citations
16.
Philibert, Pascal, Delphine Zénaty, E Thibaud, et al.. (2010). Steroidogenic factor-1 (SF-1) gene mutation as a frequent cause of primary amenorrhea in 46,XY female adolescents with low testosterone concentration. Reproductive Biology and Endocrinology. 8(1). 28–28. 61 indexed citations
17.
Zénaty, Delphine, Y Aigrain, M. Peuchmaur, et al.. (2009). Medullary thyroid carcinoma identified within the first year of life in children with hereditary multiple endocrine neoplasia type 2A (codon 634) and 2B. European Journal of Endocrinology. 160(5). 807–813. 31 indexed citations
18.
Philibert, Pascal, Delphine Zénaty, Lin Lin, et al.. (2007). Mutational analysis of steroidogenic factor 1 (NR5a1) in 24 boys with bilateral anorchia: a French collaborative study. Human Reproduction. 22(12). 3255–3261. 94 indexed citations
19.
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
20.
Zénaty, Delphine, et al.. (2000). Azathioprine-Induced Lung Toxicity and Efficacy of Cyclosporin A in a Young Girl With Type 2 Autoimmune Hepatitis. Journal of Pediatric Gastroenterology and Nutrition. 31(2). 190–192. 7 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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