Manon S. Oud

1.5k total citations
22 papers, 608 citations indexed

About

Manon S. Oud is a scholar working on Molecular Biology, Genetics and Reproductive Medicine. According to data from OpenAlex, Manon S. Oud has authored 22 papers receiving a total of 608 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 13 papers in Genetics and 13 papers in Reproductive Medicine. Recurrent topics in Manon S. Oud's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (13 papers), Sperm and Testicular Function (13 papers) and Sexual Differentiation and Disorders (9 papers). Manon S. Oud is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (13 papers), Sperm and Testicular Function (13 papers) and Sexual Differentiation and Disorders (9 papers). Manon S. Oud collaborates with scholars based in Netherlands, United Kingdom and Germany. Manon S. Oud's co-authors include Joris A. Veltman, Liliana Ramos, Lisenka E.L.M. Vissers, Ludmila Voložonoka, Roos M. Smits, Kenneth I. Aston, Miguel J. Xavier, Albert Salas‐Huetos, Moira K. O’Bryan and Brendan J. Houston and has published in prestigious journals such as New England Journal of Medicine, Journal of Clinical Oncology and The FASEB Journal.

In The Last Decade

Manon S. Oud

20 papers receiving 598 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Manon S. Oud Netherlands 11 352 337 325 228 75 22 608
Chiara Chianese Italy 13 370 1.1× 401 1.2× 363 1.1× 149 0.7× 85 1.1× 16 611
Mingrong Lv China 16 336 1.0× 231 0.7× 239 0.7× 299 1.3× 100 1.3× 37 587
Florina Raicu Romania 9 309 0.9× 326 1.0× 264 0.8× 145 0.6× 48 0.6× 15 555
Elias Elinati United Kingdom 11 237 0.7× 228 0.7× 357 1.1× 261 1.1× 53 0.7× 15 569
Maria Rosa Maduro United States 7 276 0.8× 257 0.8× 286 0.9× 163 0.7× 62 0.8× 24 488
Mariem Ben Khelifa France 7 435 1.2× 347 1.0× 249 0.8× 351 1.5× 68 0.9× 12 626
Roseanne Rosario United Kingdom 15 207 0.6× 129 0.4× 234 0.7× 218 1.0× 42 0.6× 25 484
P.J. Turek United States 14 346 1.0× 181 0.5× 273 0.8× 198 0.9× 79 1.1× 18 579
Sandra Yassine France 7 517 1.5× 291 0.9× 268 0.8× 473 2.1× 54 0.7× 7 728
Özlem Okutman France 8 226 0.6× 207 0.6× 179 0.6× 161 0.7× 44 0.6× 18 353

Countries citing papers authored by Manon S. Oud

Since Specialization
Citations

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

Fields of papers citing papers by Manon S. Oud

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Manon S. Oud. 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 Manon S. Oud. The network helps show where Manon S. Oud may publish in the future.

Co-authorship network of co-authors of Manon S. Oud

This figure shows the co-authorship network connecting the top 25 collaborators of Manon S. Oud. A scholar is included among the top collaborators of Manon S. Oud 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 Manon S. Oud. Manon S. Oud 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.
Colecchia, Maurizio, Jennifer Gordetsky, John R. Srigley, et al.. (2026). International Society of Urological Pathology (ISUP) Consensus Conference on Precursor Lesions. The American Journal of Surgical Pathology.
2.
Menna, Cecilia, Giuseppe Schepisi, Giorgia Gurioli, et al.. (2026). Impact of Circulating Tumor DNA and Copy-Number Alterations on Clinical Outcome in Relapsed/Refractory Germ Cell Tumors Treated With Salvage High-Dose Chemotherapy. Journal of Clinical Oncology. 44(9). 801–811.
3.
Oud, Manon S., Dominique Smeets, Liliana Ramos, et al.. (2024). Innovative all‐in‐one exome sequencing strategy for diagnostic genetic testing in male infertility: Validation and 10‐month experience. Andrology. 13(5). 1078–1092. 2 indexed citations
4.
Gaikwad, Avinash, Philipp Weber, Sara Di Persio, et al.. (2023). Scrutinizing the human TEX genes in the context of human male infertility. Andrology. 12(3). 570–584. 10 indexed citations
5.
6.
Persio, Sara Di, Sandra Laurentino, Margot J. Wyrwoll, et al.. (2023). WWC2 expression in the testis: Implications for spermatogenesis and male fertility. The FASEB Journal. 37(5). e22912–e22912. 2 indexed citations
7.
Wyrwoll, Margot J., Birgit Stallmeyer, Matthias Meyer, et al.. (2023). Linking human Dead end 1 (DND1) variants to male infertility employing zebrafish embryos. Human Reproduction. 38(4). 655–670. 5 indexed citations
8.
Gaikwad, Avinash, Birgit Stallmeyer, Daniela Fietz, et al.. (2022). Functional assessment of DMRT1 variants and their pathogenicity for isolated male infertility. Fertility and Sterility. 119(2). 219–228. 7 indexed citations
9.
Oud, Manon S., et al.. (2022). Phasing of de novo mutations using a scaled‐up multiple amplicon long‐read sequencing approach. Human Mutation. 43(11). 1545–1556. 5 indexed citations
10.
Xavier, Miguel J., Manon S. Oud, Galuh Astuti, et al.. (2022). De novo mutations in children born after medical assisted reproduction. Human Reproduction. 37(6). 1360–1369. 11 indexed citations
11.
Houston, Brendan J., Antoni Riera‐Escamilla, Margot J. Wyrwoll, et al.. (2021). A systematic review of the validated monogenic causes of human male infertility: 2020 update and a discussion of emerging gene–disease relationships. Human Reproduction Update. 28(1). 15–29. 140 indexed citations
12.
Fernández, Lucia Torres, Sibylle Mitschka, Marius Wöste, et al.. (2021). TRIM71 Deficiency Causes Germ Cell Loss During Mouse Embryogenesis and Is Associated With Human Male Infertility. Frontiers in Cell and Developmental Biology. 9. 658966–658966. 18 indexed citations
13.
Nagirnaja, Liina, Nina Mørup, John Nielsen, et al.. (2021). Variant PNLDC1 , Defective piRNA Processing, and Azoospermia. New England Journal of Medicine. 385(8). 707–719. 60 indexed citations
14.
Xavier, Miguel J., Albert Salas‐Huetos, Manon S. Oud, Kenneth I. Aston, & Joris A. Veltman. (2020). Disease gene discovery in male infertility: past, present and future. Human Genetics. 140(1). 7–19. 53 indexed citations
15.
Houston, Brendan J., Manon S. Oud, D. Jo Merriner, et al.. (2020). Programmed Cell Death 2-Like (Pdcd2l) Is Required for Mouse Embryonic Development. G3 Genes Genomes Genetics. 10(12). 4449–4457. 3 indexed citations
16.
Oud, Manon S., Ludmila Voložonoka, Roos M. Smits, et al.. (2019). A systematic review and standardized clinical validity assessment of male infertility genes. Human Reproduction. 34(5). 932–941. 126 indexed citations
17.
Smits, Roos M., Manon S. Oud, Lisenka E.L.M. Vissers, et al.. (2019). Improved detection of CFTR variants by targeted next-generation sequencing in male infertility: a case series. Reproductive BioMedicine Online. 39(6). 963–968. 2 indexed citations
18.
Oud, Manon S., Özlem Okutman, Petra F. de Vries, et al.. (2019). Exome sequencing reveals novel causes as well as new candidate genes for human globozoospermia. Human Reproduction. 35(1). 240–252. 46 indexed citations
19.
Oud, Manon S., Ludmila Voložonoka, Roos M. Smits, et al.. (2018). A systematic review and standardized clinical validity assessment of male infertility genes. bioRxiv (Cold Spring Harbor Laboratory). 20 indexed citations
20.
Oud, Manon S., Liliana Ramos, Moira K. O’Bryan, et al.. (2017). Validation and application of a novel integrated genetic screening method to a cohort of 1,112 men with idiopathic azoospermia or severe oligozoospermia. Human Mutation. 38(11). 1592–1605. 44 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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