Marcel M. A. M. Mannens

13.3k total citations
129 papers, 7.5k citations indexed

About

Marcel M. A. M. Mannens is a scholar working on Molecular Biology, Genetics and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Marcel M. A. M. Mannens has authored 129 papers receiving a total of 7.5k indexed citations (citations by other indexed papers that have themselves been cited), including 82 papers in Molecular Biology, 40 papers in Genetics and 33 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Marcel M. A. M. Mannens's work include Epigenetics and DNA Methylation (31 papers), Genetic Syndromes and Imprinting (21 papers) and Prenatal Screening and Diagnostics (21 papers). Marcel M. A. M. Mannens is often cited by papers focused on Epigenetics and DNA Methylation (31 papers), Genetic Syndromes and Imprinting (21 papers) and Prenatal Screening and Diagnostics (21 papers). Marcel M. A. M. Mannens collaborates with scholars based in Netherlands, United States and United Kingdom. Marcel M. A. M. Mannens's co-authors include Arthur A.M. Wilde, Connie R. Bezzina, Jet Bliek, Alex V. Postma, Mariëlle Alders, Zahurul A. Bhuiyan, Irene M. van Langen, Denis Escande, Rosalyn Slater and J. Peter van Tintelen and has published in prestigious journals such as Journal of Biological Chemistry, Circulation and Nature Genetics.

In The Last Decade

Marcel M. A. M. Mannens

123 papers receiving 7.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Marcel M. A. M. Mannens Netherlands 46 4.8k 3.5k 1.4k 839 658 129 7.5k
Eliécer Coto Spain 45 3.3k 0.7× 1.1k 0.3× 2.1k 1.5× 482 0.6× 704 1.1× 304 8.1k
Masafumi Matsuo Japan 46 5.2k 1.1× 982 0.3× 1.3k 0.9× 1.1k 1.3× 853 1.3× 395 8.3k
Jean-Marc Lalouel United States 41 2.1k 0.4× 1.9k 0.5× 2.2k 1.6× 558 0.7× 404 0.6× 111 7.2k
Gerald F. Cox United States 42 2.4k 0.5× 2.2k 0.6× 946 0.7× 658 0.8× 2.0k 3.1× 102 6.7k
Daniela Toniolo Italy 47 5.6k 1.2× 844 0.2× 2.4k 1.7× 744 0.9× 315 0.5× 139 8.6k
Mariëlle Alders Netherlands 36 2.1k 0.4× 1.6k 0.4× 1.2k 0.9× 494 0.6× 169 0.3× 114 4.0k
Cheryl R. Greenberg Canada 54 6.3k 1.3× 605 0.2× 1.8k 1.3× 692 0.8× 1.0k 1.6× 218 10.2k
Rafał Płoski Poland 38 2.8k 0.6× 679 0.2× 1.6k 1.1× 207 0.2× 394 0.6× 396 6.6k
Mary Ella Pierpont United States 36 3.9k 0.8× 726 0.2× 1.6k 1.1× 507 0.6× 272 0.4× 98 6.0k
Stephanie M. Ware United States 35 3.1k 0.6× 1.4k 0.4× 1.1k 0.8× 294 0.4× 192 0.3× 141 4.9k

Countries citing papers authored by Marcel M. A. M. Mannens

Since Specialization
Citations

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

Fields of papers citing papers by Marcel M. A. M. Mannens

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marcel M. A. M. Mannens. 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 Marcel M. A. M. Mannens. The network helps show where Marcel M. A. M. Mannens may publish in the future.

Co-authorship network of co-authors of Marcel M. A. M. Mannens

This figure shows the co-authorship network connecting the top 25 collaborators of Marcel M. A. M. Mannens. A scholar is included among the top collaborators of Marcel M. A. M. Mannens 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 Marcel M. A. M. Mannens. Marcel M. A. M. Mannens 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.
Jansen, Philip R., et al.. (2024). The utility of obesity polygenic risk scores from research to clinical practice: A review. Obesity Reviews. 25(11). e13810–e13810. 7 indexed citations
2.
Ensink, Judith, Peter Henneman, Andrea Venema, et al.. (2024). Distinct saliva DNA methylation profiles in relation to treatment outcome in youth with posttraumatic stress disorder. Translational Psychiatry. 14(1). 309–309. 4 indexed citations
3.
Rooney, Kathleen, Sadegheh Haghshenas, Haley McConkey, et al.. (2023). Functional Insight into and Refinement of the Genomic Boundaries of the JARID2-Neurodevelopmental Disorder Episignature. International Journal of Molecular Sciences. 24(18). 14240–14240. 3 indexed citations
4.
Rooney, Kathleen, et al.. (2022). DNA methylation episignatures: insight into copy number variation. Epigenomics. 14(21). 1373–1388. 12 indexed citations
5.
Chilunga, Felix P., Peter Henneman, Andrea Venema, et al.. (2021). Genome-wide DNA methylation analysis on C-reactive protein among Ghanaians suggests molecular links to the emerging risk of cardiovascular diseases. npj Genomic Medicine. 6(1). 46–46. 3 indexed citations
6.
Chilunga, Felix P., Peter Henneman, Andrea Venema, et al.. (2021). DNA Methylation as the Link between Migration and the Major Noncommunicable Diseases: the RODAM Study. Epigenomics. 13(9). 653–666. 7 indexed citations
7.
Koningsbruggen, Silvana van, et al.. (2021). Screening for inborn errors of metabolism in psychotic patients using Next Generation Sequencing. Journal of Psychiatric Research. 138. 125–129. 2 indexed citations
8.
Dorssers, Lambert C. J., Peter Henneman, Martin A. Rijlaarsdam, et al.. (2020). Comparing genome-scale DNA methylation and CNV marks between adult human cultured ITGA6+ testicular cells and seminomas to assess in vitro genomic stability. PLoS ONE. 15(3). e0230253–e0230253. 11 indexed citations
9.
Meeks, Karlijn, Felix P. Chilunga, Charles Agyemang, et al.. (2020). Epigenome-wide association study for perceived discrimination among sub-Saharan African migrants in Europe - the RODAM study. Scientific Reports. 10(1). 4919–4919. 10 indexed citations
10.
Chilunga, Felix P., Daniel Boateng, Peter Henneman, et al.. (2018). Perceived discrimination and stressful life events are associated with cardiovascular risk score in migrant and non-migrant populations: The RODAM study. International Journal of Cardiology. 286. 169–174. 21 indexed citations
11.
Yim, Andrew Y. F. Li, Jessica R. de Bruyn, Catriona Sharp, et al.. (2018). A distinct epigenetic profile distinguishes stenotic from non-inflamed fibroblasts in the ileal mucosa of Crohn’s disease patients. PLoS ONE. 13(12). e0209656–e0209656. 14 indexed citations
12.
Chatzispyrou, Iliana A., Mariëlle Alders, Sergio Guerrero‐Castillo, et al.. (2017). A homozygous missense mutation in ERAL1, encoding a mitochondrial rRNA chaperone, causes Perrault syndrome. Human Molecular Genetics. 26(13). 2541–2550. 56 indexed citations
13.
Maas, Saskia M., Fleur Vansenne, D.J. Kadouch, et al.. (2016). Phenotype, cancer risk, and surveillance in Beckwith–Wiedemann syndrome depending on molecular genetic subgroups. American Journal of Medical Genetics Part A. 170(9). 2248–2260. 124 indexed citations
14.
Henneman, Peter, Andrea Venema, K. Lip, et al.. (2015). Genetic susceptibility for cow’s milk allergy in Dutch children: the start of the allergic march?. Clinical and Translational Allergy. 6(1). 7–7. 11 indexed citations
15.
Alders, Mariëlle, Saskia M. Maas, D.J. Kadouch, et al.. (2014). Methylation analysis in tongue tissue of BWS patients identifies the (EPI)genetic cause in 3 patients with normal methylation levels in blood. European Journal of Medical Genetics. 57(6). 293–297. 20 indexed citations
16.
Huisman, Sylvia, E. Redeker, Saskia M. Maas, Marcel M. A. M. Mannens, & Raoul C. M. Hennekam. (2013). High rate of mosaicism in individuals with Cornelia de Lange syndrome. Journal of Medical Genetics. 50(5). 339–344. 81 indexed citations
17.
Rijsingen, Ingrid A.W. van, Astrid S. Plomp, A. H. Zwinderman, et al.. (2013). A novel lamin A/C mutation in a Dutch family with premature atherosclerosis. Atherosclerosis. 229(1). 169–173. 6 indexed citations
18.
Christiaans, Imke, Phil Barnett, Ronald H. Lekanne Deprez, et al.. (2012). A novel alpha-tropomyosin mutation associates with dilated and non-compaction cardiomyopathy and diminishes actin binding. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1833(4). 833–839. 15 indexed citations
19.
20.
Fijen, C. A. P., et al.. (2000). Molecular characterisation of 10 Dutch properdin type I deficient families: mutation analysis and X-inactivation studies. European Journal of Human Genetics. 8(7). 513–518. 23 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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