Alexandre Moerman

1.4k total citations
11 papers, 378 citations indexed

About

Alexandre Moerman is a scholar working on Reproductive Medicine, Molecular Biology and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Alexandre Moerman has authored 11 papers receiving a total of 378 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Reproductive Medicine, 4 papers in Molecular Biology and 3 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Alexandre Moerman's work include Reproductive Biology and Fertility (3 papers), Sperm and Testicular Function (3 papers) and Hypothalamic control of reproductive hormones (2 papers). Alexandre Moerman is often cited by papers focused on Reproductive Biology and Fertility (3 papers), Sperm and Testicular Function (3 papers) and Hypothalamic control of reproductive hormones (2 papers). Alexandre Moerman collaborates with scholars based in France, Belgium and Poland. Alexandre Moerman's co-authors include Marc Delpech, Jacques Young, Anne Lienhardt-Roussie, Catherine Dodé, Graeme Morgan, Arnaud Murat, Jean-Pierre Hardelin, Sławomir Wołczyński, Jacqueline Levilliers and Marie-Laure Kottler and has published in prestigious journals such as PLoS Genetics, Muscle & Nerve and Orphanet Journal of Rare Diseases.

In The Last Decade

Alexandre Moerman

10 papers receiving 372 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Alexandre Moerman France	5	247	186	152	60	55	11	378
Beatriz R. Versiani Brazil	10	178 0.7×	126 0.7×	149 1.0×	34 0.6×	26 0.5×	16	335
Eeva‐Maria Laitinen Finland	11	353 1.4×	234 1.3×	211 1.4×	64 1.1×	139 2.5×	17	516
Luciana Mattos Barros Oliveira Brazil	7	474 1.9×	296 1.6×	260 1.7×	32 0.5×	74 1.3×	12	584
Johanna Känsäkoski Finland	12	227 0.9×	233 1.3×	189 1.2×	27 0.5×	92 1.7×	21	405
Samuel D. Quaynor United States	6	275 1.1×	160 0.9×	169 1.1×	23 0.4×	58 1.1×	8	406
Milena Beranova United States	7	523 2.1×	325 1.7×	271 1.8×	25 0.4×	80 1.5×	10	643
Cassandra Buck United States	6	203 0.8×	153 0.8×	160 1.1×	52 0.9×	53 1.0×	8	303
Blandine Esteva France	7	65 0.3×	112 0.6×	88 0.6×	20 0.3×	61 1.1×	8	283
Naoko Tsukamoto Japan	13	96 0.4×	200 1.1×	67 0.4×	12 0.2×	98 1.8×	18	405
Jennifer M. Mulvaney United States	8	226 0.9×	250 1.3×	152 1.0×	4 0.1×	76 1.4×	11	475

Countries citing papers authored by Alexandre Moerman

Since Specialization

Citations

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

Fields of papers citing papers by Alexandre Moerman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alexandre Moerman

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

All Works

Sort: Min cites: Since: Top N: Style:

11 of 11 papers shown

Barbotin, Anne‐Laure, Anne‐Sophie Jourdain, Alexandre Moerman, et al.. (2024). Identification of a novel CFAP61 homozygous splicing variant associated with multiple morphological abnormalities of the flagella. Journal of Assisted Reproduction and Genetics. 41(6). 1499–1505. 3 indexed citations

Mitchell, Valérie, Anne Loyens, Nathalie Rives, et al.. (2023). Results and perinatal outcomes from 189 ICSI cycles of couples with asthenozoospermic men and flagellar defects assessed by transmission electron microscopy. Reproductive BioMedicine Online. 47(5). 103328–103328. 4 indexed citations

Espiard, Stéphanie, Christine Do Cao, M. Ladsous, et al.. (2019). Systematic thyroid screening in myotonic dystrophy: link between thyroid volume and insulin resistance. Orphanet Journal of Rare Diseases. 14(1). 42–42. 6 indexed citations

Curt, Marie Joncquel-Chevalier, Monique Fontaine, Guillemette Huet, et al.. (2018). Functional assessment of creatine transporter in control and X-linked SLC6A8-deficient fibroblasts. Molecular Genetics and Metabolism. 123(4). 463–471. 3 indexed citations

Petit, Florence, Jean‐Marie Cuisset, Claude Cancés, et al.. (2010). Insights into genotype–phenotype correlations in spinal muscular atrophy: A retrospective study of 103 patients. Muscle & Nerve. 43(1). 26–30. 21 indexed citations

Mitchell, Valérie, Marie-Claire Peers, Carole Marchetti, et al.. (2008). Altérations morphologiques des spermatozoïdes en microscopie électronique: indications, phénotypes, fécondance, et pronostic de fertilité. Andrologie. 18(1). 35–45.

Dodé, Catherine, Luís Teixeira, Jacqueline Levilliers, et al.. (2006). Kallmann Syndrome: Mutations in the Genes Encoding Prokineticin-2 and Prokineticin Receptor-2. PLoS Genetics. 2(10). e175–e175. 315 indexed citations

Dodé, Catherine, Luís Augusto Teixeira, Jacqueline Levilliers, et al.. (2005). Kallmann Syndrome: Mutations in the Genes Encoding Prokineticin-2 and Prokineticin Receptor-2. PLoS Genetics. preprint(2006). e175–e175. 5 indexed citations

Dieux‐Coëslier, Anne, Alexandre Moerman, Muriel Holder, et al.. (2003). Metaphyseal chondrodysplasia with cone‐shaped epiphyses: A specific form involving the lower limbs. American Journal of Medical Genetics Part A. 124A(1). 60–66. 3 indexed citations

10.

Manouvrier, Sylvie, et al.. (2000). Radioulnar synostosis, radial ray abnormalities, and severe malformations in the male: A new X-linked dominant multiple congenital anomalies syndrome?. American Journal of Medical Genetics. 90(5). 351–355. 4 indexed citations

11.

Walter-Nicolet, E., et al.. (1999). The Richieri-Costa and Pereira form of acrofacial dysostosis: First case in a non-Brazilian infant. American Journal of Medical Genetics. 87(5). 430–433. 14 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