Jérôme Dulon

1.2k total citations
28 papers, 737 citations indexed

About

Jérôme Dulon is a scholar working on Molecular Biology, Endocrinology, Diabetes and Metabolism and Genetics. According to data from OpenAlex, Jérôme Dulon has authored 28 papers receiving a total of 737 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 13 papers in Endocrinology, Diabetes and Metabolism and 9 papers in Genetics. Recurrent topics in Jérôme Dulon's work include Sexual Differentiation and Disorders (13 papers), Reproductive Biology and Fertility (8 papers) and Hormonal and reproductive studies (7 papers). Jérôme Dulon is often cited by papers focused on Sexual Differentiation and Disorders (13 papers), Reproductive Biology and Fertility (8 papers) and Hormonal and reproductive studies (7 papers). Jérôme Dulon collaborates with scholars based in France, Australia and United States. Jérôme Dulon's co-authors include Philippe Touraine, Anne Bachelot, Jean Louis Golmard, Yasmina Badachi, Maud Bidet, Christiane Coussieu, Michel Polak, Zeina Chakhtoura, Monique Leban and A. Rouxel and has published in prestigious journals such as PLoS ONE, The Journal of Clinical Endocrinology & Metabolism and Journal of Hypertension.

In The Last Decade

Jérôme Dulon

26 papers receiving 715 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jérôme Dulon France 14 385 271 258 257 214 28 737
Mary M. Lee United States 8 260 0.7× 67 0.2× 251 1.0× 337 1.3× 200 0.9× 16 601
Nora Saraco Argentina 14 339 0.9× 205 0.8× 92 0.4× 241 0.9× 383 1.8× 25 661
María Sonia Baquedano Argentina 11 244 0.6× 200 0.7× 43 0.2× 142 0.6× 224 1.0× 19 462
D. Levy United States 5 501 1.3× 472 1.7× 94 0.4× 248 1.0× 132 0.6× 7 738
Ioanna Bouba Greece 13 147 0.4× 83 0.3× 90 0.3× 209 0.8× 202 0.9× 31 561
Felix Schreiner Germany 13 215 0.6× 89 0.3× 60 0.2× 44 0.2× 215 1.0× 35 546
F Lorenzen Germany 12 791 2.1× 721 2.7× 112 0.4× 345 1.3× 179 0.8× 17 1.1k
Akira Tohda Japan 13 292 0.8× 61 0.2× 399 1.5× 573 2.2× 271 1.3× 37 881
Lea Langhoff Thuesen Denmark 12 202 0.5× 97 0.4× 293 1.1× 358 1.4× 100 0.5× 17 687
Véronique Tardy France 17 975 2.5× 776 2.9× 52 0.2× 116 0.5× 421 2.0× 34 1.1k

Countries citing papers authored by Jérôme Dulon

Since Specialization
Citations

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

Fields of papers citing papers by Jérôme Dulon

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jérôme Dulon

This figure shows the co-authorship network connecting the top 25 collaborators of Jérôme Dulon. A scholar is included among the top collaborators of Jérôme Dulon 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 Jérôme Dulon. Jérôme Dulon 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.
Tucker, Elena J., Michael F. Sharp, Katrina M. Bell, et al.. (2024). Biallelic FANCA variants detected in sisters with isolated premature ovarian insufficiency. Clinical Genetics. 106(3). 321–335. 2 indexed citations
2.
Dulon, Jérôme, et al.. (2023). Family building after diagnosis of premature ovarian insufficiency: a cross-sectional survey in 324 women. European Journal of Endocrinology. 188(3). 282–289. 3 indexed citations
3.
Sreenivasan, Rajini, Katrina M. Bell, Jocelyn van den Bergen, et al.. (2022). Whole exome sequencing reveals copy number variants in individuals with disorders of sex development. Molecular and Cellular Endocrinology. 546. 111570–111570. 7 indexed citations
4.
Dulon, Jérôme, et al.. (2022). Classical and non-classical congenital adrenal hyperplasia: What is the difference in subsequent fertility?. Annales d Endocrinologie. 83(3). 181–185. 1 indexed citations
5.
Tucker, Elena J., Katrina M. Bell, Gorjana Robevska, et al.. (2021). Meiotic genes in premature ovarian insufficiency: variants in HROB and REC8 as likely genetic causes. European Journal of Human Genetics. 30(2). 219–228. 23 indexed citations
6.
Tucker, Elena J., Sylvie Jaillard, Sonia Grover, et al.. (2019). TP63‐truncating variants cause isolated premature ovarian insufficiency. Human Mutation. 40(7). 886–892. 36 indexed citations
7.
Rosenbaum, David, Antonio Gallo, Éric Bruckert, et al.. (2018). Early central blood pressure elevation in adult patients with 21-hydroxylase deficiency. Journal of Hypertension. 37(1). 175–181. 12 indexed citations
8.
Salem, Joe‐Elie, Lee S. Nguyen, Nadjib Hammoudi, et al.. (2017). Complex Association of Sex Hormones on Left Ventricular Systolic Function: Insight into Sexual Dimorphism. Journal of the American Society of Echocardiography. 31(2). 231–240.e1. 13 indexed citations
9.
Desai, Swapna S., Michelle A. Wood, Huaiyang Jiang, et al.. (2016). MCM8 and MCM9 Nucleotide Variants in Women with Primary Ovarian Insufficiency. The Journal of Clinical Endocrinology & Metabolism. 102(2). jc.2016–2565. 70 indexed citations
10.
Bachelot, Anne, et al.. (2016). Poor Compliance to Hormone Therapy and Decreased Bone Mineral Density in Women with Premature Ovarian Insufficiency. PLoS ONE. 11(12). e0164638–e0164638. 22 indexed citations
11.
Bachelot, Anne, Caroline Nicolas, Jérôme Dulon, et al.. (2016). Devenir à long terme de la reprise de la fonction ovarienne chez les patientes ayant une insuffisance ovarienne précoce. Annales d Endocrinologie. 77(4). 252–252.
12.
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
13.
Bachelot, Anne, Zeina Chakhtoura, Geneviève Plu‐Bureau, et al.. (2012). Influence of hormonal control on LH pulsatility and secretion in women with classical congenital adrenal hyperplasia. European Journal of Endocrinology. 167(4). 499–505. 31 indexed citations
14.
Bidet, Maud, Anne Bachelot, Jean Louis Golmard, et al.. (2011). Resumption of Ovarian Function and Pregnancies in 358 Patients with Premature Ovarian Failure. The Journal of Clinical Endocrinology & Metabolism. 96(12). 3864–3872. 133 indexed citations
15.
Bachelot, Anne, Zeina Chakhtoura, Dinane Samara‐Boustani, et al.. (2010). Bone Health Should Be an Important Concern in the Care of Patients Affected by 21 Hydroxylase Deficiency. International Journal of Pediatric Endocrinology. 2010. 1–7. 16 indexed citations
16.
Bachelot, Anne, Zeina Chakhtoura, Dinane Samara‐Boustani, et al.. (2010). Bone Health Should Be an Important Concern in the Care of Patients Affected by 21 Hydroxylase Deficiency. International Journal of Pediatric Endocrinology. 2010(1). 326275–326275. 6 indexed citations
17.
Bachelot, Anne, A. Rouxel, Nathalie Massin, et al.. (2009). Phenotyping and genetic studies of 357 consecutive patients presenting with premature ovarian failure. European Journal of Endocrinology. 161(1). 179–187. 99 indexed citations
18.
Bachelot, Anne, et al.. (2008). Classical Forms of Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency in Adults. Hormone Research in Paediatrics. 69(4). 203–211. 28 indexed citations
19.
Chakhtoura, Zeina, Anne Bachelot, Dinane Samara‐Boustani, et al.. (2008). Impact of total cumulative glucocorticoid dose on bone mineral density in patients with 21-hydroxylase deficiency.. European Journal of Endocrinology. 158(6). 879–887. 75 indexed citations
20.
Bachelot, Anne, Zeina Chakhtoura, A. Rouxel, Jérôme Dulon, & Philippe Touraine. (2007). Hormonal treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Annales d Endocrinologie. 68(4). 274–280. 12 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

Breakdown of academic impact, for papers by Mary M. Lee Breakdown of academic impact, for papers by Nora Saraco Breakdown of academic impact, for papers by María Sonia Baquedano Breakdown of academic impact, for papers by D. Levy Breakdown of academic impact, for papers by Ioanna Bouba Breakdown of academic impact, for papers by Felix Schreiner Breakdown of academic impact, for papers by F Lorenzen Breakdown of academic impact, for papers by Akira Tohda Breakdown of academic impact, for papers by Lea Langhoff Thuesen Breakdown of academic impact, for papers by Véronique Tardy
Rankless by CCL
2026