Manon Engels

467 total citations
9 papers, 271 citations indexed

About

Manon Engels is a scholar working on Molecular Biology, Endocrinology, Diabetes and Metabolism and Genetics. According to data from OpenAlex, Manon Engels has authored 9 papers receiving a total of 271 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 6 papers in Endocrinology, Diabetes and Metabolism and 3 papers in Genetics. Recurrent topics in Manon Engels's work include Sexual Differentiation and Disorders (7 papers), Hormonal and reproductive studies (6 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers). Manon Engels is often cited by papers focused on Sexual Differentiation and Disorders (7 papers), Hormonal and reproductive studies (6 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers). Manon Engels collaborates with scholars based in Netherlands, United Kingdom and United States. Manon Engels's co-authors include Matti Annala, Wei Zhang, Hedi L. Claahsen‐van der Grinten, Fred C.G.J. Sweep, Antonius E. van Herwaarden, Paul N. Span, Nike Stikkelbroeck, Agustini Utari, Sultana MH Faradz and Nils Krone and has published in prestigious journals such as Endocrine Reviews, The Journal of Clinical Endocrinology & Metabolism and Endocrinology.

In The Last Decade

Manon Engels

8 papers receiving 266 citations

Peers

Manon Engels

MB

EDM

SURGE

GENET

PRM

Shouyue Sun China

Arístides López‐Márquez Spain

Attje S. Hoekstra Netherlands

Lívia M. Mermejo Brazil

Meshael Alswailem Saudi Arabia

John A. Phillips United States

Nizar Ben Halim Tunisia

Ashish Singh India

Andreína Cattani Chile

Ebtesam Qasem Saudi Arabia

Shouyue Sun China

Manon Engels

257 ×1.2

MB

230 ×1.7

EDM

69 ×1.1

SURGE

133 ×3.6

GENET

11 ×0.3

PRM

Citations per year, relative to Manon Engels Manon Engels (= 1×) peers Shouyue Sun

Countries citing papers authored by Manon Engels

Since Specialization

Citations

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

Fields of papers citing papers by Manon Engels

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Manon Engels

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

All Works

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9 of 9 papers shown

1.

Engels, Manon, et al.. (2025). The European Reference Network on Genetic Tumour Risk Syndromes (ERN GENTURIS): benefits for patients, families, and health care providers. Familial Cancer. 24(2). 33–33.

2.

Engels, Manon, Paul N. Span, Fred C.G.J. Sweep, et al.. (2021). Quality of Life in Men With Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency. Frontiers in Endocrinology. 12. 626646–626646. 10 indexed citations

3.

Engels, Manon, Claire Bouvattier, Henrik Falhammar, et al.. (2019). Sexuality in Males With Congenital Adrenal Hyperplasia Resulting From 21-Hydroxylase Deficiency. Journal of the Endocrine Society. 3(8). 1445–1456. 6 indexed citations

4.

Engels, Manon, Agustini Utari, Sultana MH Faradz, et al.. (2019). Glucocorticoid Activity of Adrenal Steroid Precursors in Untreated Patients With Congenital Adrenal Hyperplasia. The Journal of Clinical Endocrinology & Metabolism. 104(11). 5065–5072. 27 indexed citations

5.

Engels, Manon, Paul N. Span, Antonius E. van Herwaarden, et al.. (2019). Testicular Adrenal Rest Tumors: Current Insights on Prevalence, Characteristics, Origin, and Treatment. Endocrine Reviews. 40(4). 973–987. 79 indexed citations

6.

Engels, Manon, Paul N. Span, Rod T. Mitchell, et al.. (2017). GATA transcription factors in testicular adrenal rest tumours. Endocrine Connections. 6(8). 866–875. 11 indexed citations

7.

Puar, Troy, Manon Engels, Antonius E. van Herwaarden, et al.. (2016). Bilateral Testicular Tumors Resulting in Recurrent Cushing Disease After Bilateral Adrenalectomy. The Journal of Clinical Endocrinology & Metabolism. 102(2). 339–344. 16 indexed citations

8.

Engels, Manon, Christiaan F. Mooij, Aliesha Griffin, et al.. (2015). Adrenal Steroid Metabolites Accumulating in Congenital Adrenal Hyperplasia Lead to Transactivation of the Glucocorticoid Receptor. Endocrinology. 156(10). 3504–3510. 20 indexed citations

9.

Engels, Manon, et al.. (2013). Emergence of FGFR family gene fusions as therapeutic targets in a wide spectrum of solid tumours. The Journal of Pathology. 232(1). 4–15. 102 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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