Maëva Elzaïat

647 total citations
14 papers, 379 citations indexed

About

Maëva Elzaïat is a scholar working on Molecular Biology, Genetics and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Maëva Elzaïat has authored 14 papers receiving a total of 379 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 9 papers in Genetics and 3 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Maëva Elzaïat's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (9 papers), Sexual Differentiation and Disorders (4 papers) and Reproductive Biology and Fertility (3 papers). Maëva Elzaïat is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (9 papers), Sexual Differentiation and Disorders (4 papers) and Reproductive Biology and Fertility (3 papers). Maëva Elzaïat collaborates with scholars based in France, Morocco and United Kingdom. Maëva Elzaïat's co-authors include Maëlle Pannetier, Éric Pailhoux, Reiner A. Veitia, Aurélie Allais‐Bonnet, Laurent Boulanger, Christophe Richard, Daniel Le Bourhis, Corinne Cotinot, Nathalie Daniel and Anne‐Laure Todeschini and has published in prestigious journals such as Nature Communications, Current Biology and Scientific Reports.

In The Last Decade

Maëva Elzaïat

14 papers receiving 377 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Maëva Elzaïat France	9	274	217	114	91	29	14	379
Lisa Haig‐Ladewig United States	7	186 0.7×	174 0.8×	293 2.6×	242 2.7×	11 0.4×	9	447
Jake D. Lehle United States	4	129 0.5×	280 1.3×	212 1.9×	172 1.9×	38 1.3×	6	436
Frédéric Leduc Canada	9	125 0.5×	262 1.2×	186 1.6×	151 1.7×	32 1.1×	17	477
Kerry D. Fulcher United States	7	229 0.8×	225 1.0×	383 3.4×	315 3.5×	13 0.4×	9	582
Suming Yang China	7	146 0.5×	348 1.6×	103 0.9×	87 1.0×	52 1.8×	8	436
Shangying Liao China	13	224 0.8×	449 2.1×	231 2.0×	165 1.8×	129 4.4×	17	653
Sylvie Ruffini France	12	119 0.4×	224 1.0×	171 1.5×	363 4.0×	12 0.4×	21	465
Ida Björkgren Finland	11	87 0.3×	195 0.9×	213 1.9×	153 1.7×	88 3.0×	18	435
Ellen K. Velte United States	9	234 0.9×	438 2.0×	430 3.8×	349 3.8×	57 2.0×	9	722
Stephan Awe Germany	8	195 0.7×	425 2.0×	179 1.6×	125 1.4×	36 1.2×	10	583

Countries citing papers authored by Maëva Elzaïat

Since Specialization

Citations

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

Fields of papers citing papers by Maëva Elzaïat

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Maëva Elzaïat

This figure shows the co-authorship network connecting the top 25 collaborators of Maëva Elzaïat. A scholar is included among the top collaborators of Maëva Elzaïat 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 Maëva Elzaïat. Maëva Elzaïat is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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14 of 14 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.

França, Mônica M., Maëva Elzaïat, Natalia Felipe‐Medina, et al.. (2022). A truncating variant of RAD51B associated with primary ovarian insufficiency provides insights into its meiotic and somatic functions. Cell Death and Differentiation. 29(12). 2347–2361. 5 indexed citations

4.

Elzaïat, Maëva, Ken McElreavey, & Anu Bashamboo. (2022). Genetics of 46,XY gonadal dysgenesis. Best Practice & Research Clinical Endocrinology & Metabolism. 36(1). 101633–101633. 28 indexed citations

5.

Elzaïat, Maëva, et al.. (2020). DHH pathogenic variants involved in 46,XY disorders of sex development differentially impact protein self-cleavage and structural conformation. Human Genetics. 139(11). 1455–1470. 4 indexed citations

6.

Elzaïat, Maëva, Nicolas Meunier, Eli Sellem, et al.. (2019). Dual role of DMXL2 in olfactory information transmission and the first wave of spermatogenesis. PLoS Genetics. 15(2). e1007909–e1007909. 11 indexed citations

7.

Elzaïat, Maëva, et al.. (2019). High-throughput Exploration of the Network Dependent on AKT1 in Mouse Ovarian Granulosa Cells. Molecular & Cellular Proteomics. 18(7). 1307–1319. 8 indexed citations

8.

Elzaïat, Maëva, et al.. (2019). High-throughput Exploration of the Network Dependent on AKT1 in Mouse Ovarian Granulosa Cells. Molecular & Cellular Proteomics. 18(7). 1307–1319. 9 indexed citations

9.

Elzaïat, Maëva, et al.. (2017). A homozygous donor splice-site mutation in the meiotic gene MSH4 causes primary ovarian insufficiency. Human Molecular Genetics. 26(16). 3161–3166. 61 indexed citations

10.

Elzaïat, Maëva, Anne‐Laure Todeschini, Sandrine Caburet, & Reiner A. Veitia. (2016). The genetic make‐up of ovarian development and function: the focus on the transcription factor FOXL2. Clinical Genetics. 91(2). 173–182. 41 indexed citations

11.

Allais‐Bonnet, Aurélie, Johan Castille, Maëlle Pannetier, et al.. (2015). A specific role for PRND in goat foetal Leydig cells is suggested by prion family gene expression during gonad development in goats and mice. FEBS Open Bio. 6(1). 4–15. 3 indexed citations

12.

Boulanger, Laurent, Maëlle Pannetier, Aurélie Allais‐Bonnet, et al.. (2014). FOXL2 Is a Female Sex-Determining Gene in the Goat. Current Biology. 24(4). 404–408. 140 indexed citations

13.

Elzaïat, Maëva, Luc Jouneau, Dominique Thépot, et al.. (2014). High-Throughput Sequencing Analyses of XX Genital Ridges Lacking FOXL2 Reveal DMRT1 Up-Regulation Before SOX9 Expression During the Sex-Reversal Process in Goats1. Biology of Reproduction. 91(6). 153–153. 31 indexed citations

14.

Pannetier, Maëlle, Maëva Elzaïat, Dominique Thépot, & Éric Pailhoux. (2011). Telling the Story of XX Sex Reversal in the Goat: Highlighting the Sex-Crossroad in Domestic Mammals. Sexual Development. 6(1-3). 33–45. 34 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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