Joëlle Bignon‐Topalovic

1.5k total citations
25 papers, 607 citations indexed

About

Joëlle Bignon‐Topalovic is a scholar working on Genetics, Molecular Biology and Reproductive Medicine. According to data from OpenAlex, Joëlle Bignon‐Topalovic has authored 25 papers receiving a total of 607 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 17 papers in Molecular Biology and 9 papers in Reproductive Medicine. Recurrent topics in Joëlle Bignon‐Topalovic's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (16 papers), Sexual Differentiation and Disorders (12 papers) and Sperm and Testicular Function (5 papers). Joëlle Bignon‐Topalovic is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (16 papers), Sexual Differentiation and Disorders (12 papers) and Sperm and Testicular Function (5 papers). Joëlle Bignon‐Topalovic collaborates with scholars based in France, Morocco and United Kingdom. Joëlle Bignon‐Topalovic's co-authors include Anu Bashamboo, Ken McElreavey, Raja Brauner, Hassan Rouba, John C. Achermann, Jean‐Pierre Siffroi, Célia Ravel, Diana Lourenço, Uppala Radhakrishna and Debbie Montjean and has published in prestigious journals such as Nature Communications, PLoS ONE and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Joëlle Bignon‐Topalovic

25 papers receiving 602 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Joëlle Bignon‐Topalovic France 13 432 427 157 121 111 25 607
Nathália Lisboa Gomes Brazil 13 448 1.0× 333 0.8× 86 0.5× 141 1.2× 154 1.4× 28 534
Radia Boudjenah France 9 324 0.8× 333 0.8× 266 1.7× 79 0.7× 37 0.3× 10 558
K.P. Wolffenbuttel Netherlands 8 384 0.9× 269 0.6× 106 0.7× 98 0.8× 31 0.3× 10 480
Yvonne G. van der Zwan Netherlands 12 314 0.7× 131 0.3× 51 0.3× 108 0.9× 48 0.4× 16 421
Keiko Fukutani Japan 13 226 0.5× 228 0.5× 190 1.2× 69 0.6× 78 0.7× 37 521
F Jaubert France 13 450 1.0× 422 1.0× 172 1.1× 123 1.0× 17 0.2× 23 644
Hidenobu Miura Japan 10 187 0.4× 123 0.3× 251 1.6× 24 0.2× 35 0.3× 18 425
J Teter Poland 13 301 0.7× 265 0.6× 150 1.0× 42 0.3× 31 0.3× 42 480
Nicole Morichon France 9 164 0.4× 149 0.3× 83 0.5× 26 0.2× 12 0.1× 10 367
J.H.C. Meijers Netherlands 9 272 0.6× 164 0.4× 94 0.6× 23 0.2× 12 0.1× 16 495

Countries citing papers authored by Joëlle Bignon‐Topalovic

Since Specialization
Citations

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

Fields of papers citing papers by Joëlle Bignon‐Topalovic

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Joëlle Bignon‐Topalovic. 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 Joëlle Bignon‐Topalovic. The network helps show where Joëlle Bignon‐Topalovic may publish in the future.

Co-authorship network of co-authors of Joëlle Bignon‐Topalovic

This figure shows the co-authorship network connecting the top 25 collaborators of Joëlle Bignon‐Topalovic. A scholar is included among the top collaborators of Joëlle Bignon‐Topalovic 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 Joëlle Bignon‐Topalovic. Joëlle Bignon‐Topalovic 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.
Houzelstein, Denis, Caroline Eozénou, Carlos F. Lagos, et al.. (2024). A conserved NR5A1-responsive enhancer regulates SRY in testis-determination. Nature Communications. 15(1). 2796–2796. 1 indexed citations
2.
Bignon‐Topalovic, Joëlle, Denis Houzelstein, Nassim Nouri, et al.. (2024). Evidence for NR2F2/COUP-TFII involvement in human testis development. Scientific Reports. 14(1). 17869–17869. 3 indexed citations
3.
Brauner, Raja, Joëlle Bignon‐Topalovic, Anu Bashamboo, & Ken McElreavey. (2023). Exome sequencing in 16 patients with pituitary stalk interruption syndrome: A monocentric study. PLoS ONE. 18(12). e0292664–e0292664. 3 indexed citations
4.
5.
Globa, Evgenia, et al.. (2022). Disorders of Sex Development in a Large Ukrainian Cohort: Clinical Diversity and Genetic Findings. Frontiers in Endocrinology. 13. 810782–810782. 26 indexed citations
6.
Brauner, Raja, Joëlle Bignon‐Topalovic, Anu Bashamboo, & Ken McElreavey. (2021). Peripheral Precocious Puberty of Ovarian Origin in a Series of 18 Girls: Exome Study Finds Variants in Genes Responsible for Hypogonadotropic Hypogonadism. Frontiers in Pediatrics. 9. 641397–641397. 4 indexed citations
7.
Brauner, Raja, Joëlle Bignon‐Topalovic, Anu Bashamboo, & Ken McElreavey. (2020). Pituitary stalk interruption syndrome is characterized by genetic heterogeneity. PLoS ONE. 15(12). e0242358–e0242358. 29 indexed citations
8.
Eozénou, Caroline, Anu Bashamboo, Joëlle Bignon‐Topalovic, et al.. (2019). The TALE homeodomain of PBX1 is involved in human primary testis‐determination. Human Mutation. 40(8). 1071–1076. 13 indexed citations
9.
Bashamboo, Anu, Caroline Eozénou, Anne Jørgensen, et al.. (2018). Loss of Function of the Nuclear Receptor NR2F2, Encoding COUP-TF2, Causes Testis Development and Cardiac Defects in 46,XX Children. The American Journal of Human Genetics. 102(3). 487–493. 65 indexed citations
10.
Bashamboo, Anu, et al.. (2017). Mutations in the Human ROBO1 Gene in Pituitary Stalk Interruption Syndrome. The Journal of Clinical Endocrinology & Metabolism. 102(7). 2401–2406. 33 indexed citations
11.
Charoute, Hicham, Joëlle Bignon‐Topalovic, Abderrahim Malki, et al.. (2017). A Novel Homozygous Missense Mutation in the FU-CRD2 Domain of the<b><i> R-spondin1 </i></b>Gene Associated with Familial 46,XX DSD. Sexual Development. 11(5-6). 269–274. 14 indexed citations
12.
Brauner, Raja, H. Lottmann, Sébastien Rouget, et al.. (2016). Familial forms of disorders of sex development may be common if infertility is considered a comorbidity. BMC Pediatrics. 16(1). 195–195. 7 indexed citations
13.
Mazen, Inas, Mohamed S. Abdel‐Hamid, Mona K. Mekkawy, et al.. (2016). Identification of <b><i>NR5A1</i></b> Mutations and Possible Digenic Inheritance in 46,XY Gonadal Dysgenesis. Sexual Development. 10(3). 147–151. 32 indexed citations
14.
Mougou-Zerelli, Soumaya, Sarra Dimassi, Molka Kammoun, et al.. (2016). Novel homozygous nonsense mutations in the luteinizing hormone receptor (LHCGR) gene associated with 46,XY primary amenorrhea. Fertility and Sterility. 106(1). 225–229.e11. 11 indexed citations
15.
Lortat‐Jacob, Stephen, Claire Nihoul‐Feketé, Joëlle Bignon‐Topalovic, et al.. (2015). Genetic mutations and somatic anomalies in association with 46,XY gonadal dysgenesis. Fertility and Sterility. 103(5). 1297–1304. 17 indexed citations
16.
Bashamboo, Anu, Joëlle Bignon‐Topalovic, Hassan Rouba, Ken McElreavey, & Raja Brauner. (2015). A Nonsense Mutation in the Hedgehog Receptor CDON Associated With Pituitary Stalk Interruption Syndrome. The Journal of Clinical Endocrinology & Metabolism. 101(1). 12–15. 38 indexed citations
17.
Bashamboo, Anu, Raja Brauner, Joëlle Bignon‐Topalovic, et al.. (2014). Mutations in the FOG2/ZFPM2 gene are associated with anomalies of human testis determination. Human Molecular Genetics. 23(14). 3657–3665. 63 indexed citations
18.
19.
Ravel, Célia, Anu Bashamboo, Joëlle Bignon‐Topalovic, et al.. (2012). Polymorphisms in DLGH1 and LAMC1 in Mayer–Rokitansky–Kuster–Hauser syndrome. Reproductive BioMedicine Online. 24(4). 462–465. 14 indexed citations
20.
Bashamboo, Anu, Bruno Ferraz‐de‐Souza, Diana Lourenço, et al.. (2010). Human Male Infertility Associated with Mutations in NR5A1Encoding Steroidogenic Factor 1. The American Journal of Human Genetics. 87(5). 736–736. 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.

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