Anu Bashamboo

4.7k total citations
100 papers, 2.5k citations indexed

About

Anu Bashamboo is a scholar working on Molecular Biology, Genetics and Urology. According to data from OpenAlex, Anu Bashamboo has authored 100 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 70 papers in Molecular Biology, 66 papers in Genetics and 23 papers in Urology. Recurrent topics in Anu Bashamboo's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (54 papers), Sexual Differentiation and Disorders (49 papers) and Urological Disorders and Treatments (22 papers). Anu Bashamboo is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (54 papers), Sexual Differentiation and Disorders (49 papers) and Urological Disorders and Treatments (22 papers). Anu Bashamboo collaborates with scholars based in France, United Kingdom and Morocco. Anu Bashamboo's co-authors include Ken McElreavey, Raja Brauner, Joëlle Bignon‐Topalovic, Diana Lourenço, John C. Achermann, Kenneth McElreavey, Célia Ravel, Lin Lin, Radia Boudjenah and Hassan Rouba and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Anu Bashamboo

97 papers receiving 2.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Anu Bashamboo France 29 1.8k 1.6k 670 470 329 100 2.5k
Carolina J. Jorgez United States 21 1.2k 0.7× 548 0.3× 739 1.1× 112 0.2× 830 2.5× 45 2.1k
Daniel Guerrier France 19 825 0.5× 591 0.4× 432 0.6× 170 0.4× 537 1.6× 46 1.7k
Jennifer Brennan United States 12 1.5k 0.8× 1.3k 0.8× 693 1.0× 112 0.2× 322 1.0× 23 2.7k
P. H. Yen United States 22 1.4k 0.8× 1.3k 0.8× 365 0.5× 117 0.2× 63 0.2× 36 2.0k
Susanne Ledig Germany 18 567 0.3× 546 0.3× 197 0.3× 109 0.2× 200 0.6× 33 1.0k
Pierre S. Tung Canada 25 945 0.5× 501 0.3× 1.2k 1.9× 146 0.3× 411 1.2× 42 2.2k
T F Manganaro United States 12 730 0.4× 485 0.3× 676 1.0× 69 0.1× 622 1.9× 14 1.4k
Kaarel Krjutškov Estonia 23 834 0.5× 361 0.2× 312 0.5× 38 0.1× 182 0.6× 60 1.9k
Juan C. Irwin United States 34 612 0.3× 480 0.3× 1.7k 2.6× 46 0.1× 596 1.8× 64 3.6k
P. Couillin France 23 999 0.6× 328 0.2× 142 0.2× 93 0.2× 100 0.3× 60 1.5k

Countries citing papers authored by Anu Bashamboo

Since Specialization
Citations

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

Fields of papers citing papers by Anu Bashamboo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anu Bashamboo

This figure shows the co-authorship network connecting the top 25 collaborators of Anu Bashamboo. A scholar is included among the top collaborators of Anu Bashamboo 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 Anu Bashamboo. Anu Bashamboo 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.
Askari, Masomeh, Ken McElreavey, Anu Bashamboo, et al.. (2025). A novel candidate missense variant in the catalytic domain of USP26 associated with asthenoteratozoospermia. Gene. 982. 149945–149945.
2.
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
3.
Globa, Evgenia, et al.. (2020). Atypical Clinical Presentation of Persistent Müllerian Duct Syndrome in Siblings. Sexual Development. 14(1-6). 27–32. 2 indexed citations
4.
Eozénou, Caroline, et al.. (2019). Mutations in CBX2 Associated with Gonadal Anomalies in 46,XY and 46,XX Individuals. 92. 1 indexed citations
5.
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
6.
Nagara, Majdi, Gregory Papagregoriou, Zied Landoulsi, et al.. (2017). Distal renal tubular acidosis in a Libyan patient: Evidence for digenic inheritance. European Journal of Medical Genetics. 61(1). 1–7. 7 indexed citations
7.
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
8.
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
9.
Steel, Dora, Vincenzo Salpietro, Rahul Phadke, et al.. (2015). Whole exome sequencing reveals a MLL de novo mutation associated with mild developmental delay and without ‘hairy elbows’: expanding the phenotype of Wiedemann–Steiner syndrome. Journal of Genetics. 94(4). 755–758. 20 indexed citations
10.
Brauner, Raja, et al.. (2014). Predominantly Matrilineal Inheritance of Familial Precocious Puberty Suggests an Underlying Imprint Anomaly. 82. 1 indexed citations
11.
Jaillard, Sylvie, Anu Bashamboo, Laurent Pasquier, et al.. (2014). Gene dosage effects in 46, XY DSD: usefulness of CGH technologies for diagnosis. Journal of Assisted Reproduction and Genetics. 32(2). 287–291. 6 indexed citations
12.
Philibert, Pascal, Anu Bashamboo, Françoise Paris, et al.. (2012). Unilateral Cryptorchidism in Mice Mutant forPtgds. Human Mutation. 34(2). 278–282. 20 indexed citations
13.
Bashamboo, Anu & Ken McElreavey. (2012). Gene Mutations Associated with Anomalies of Human Gonad Formation. Sexual Development. 7(1-3). 126–146. 31 indexed citations
14.
Abidi, Omar, Majida Charif, Brahim El Houate, et al.. (2012). Association of the MTHFR A1298C Variant with Unexplained Severe Male Infertility. PLoS ONE. 7(3). e34111–e34111. 39 indexed citations
15.
Houate, Brahim El, Omar Abidi, Majida Charif, et al.. (2012). Association of Spermatogenic Failure with the b2/b3 Partial AZFc Deletion. PLoS ONE. 7(4). e34902–e34902. 35 indexed citations
16.
Bashamboo, Anu, Célia Ravel, & Ken McElreavey. (2011). De nouveaux modèles de cellules souches embryonnaires pour étudier le développement des cellules germinales dans leur niche. 13(1). 31–39. 1 indexed citations
17.
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
18.
Brauner, Raja, Anu Bashamboo, Sébastien Rouget, et al.. (2010). Clinical, Biological and Genetic Analysis of Prepubertal Isolated Ovarian Cyst in 11 Girls. PLoS ONE. 5(6). e11282–e11282. 7 indexed citations
19.
Rahman, Mohammed Mahidur, et al.. (2004). Organizational Variation of DYZ1 Repeat Sequences on the Human Y Chromosome and Its Diagnostic Potentials. DNA and Cell Biology. 23(9). 561–571. 16 indexed citations
20.
Bashamboo, Anu, et al.. (2003). Molecular characterization of a Y-derived marker chromosome and identification of indels in the DYS1 region in a patient with stigmata of Turner syndrome. Current Science. 84(2). 219–22425. 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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