Marcel M. A. M. Mannens

13.3k citations

129 papers · 7.5k indexed · h-index 46

Molecular Biology top 1%
Cardiology and Cardiovascular Medicine top 0.5%
Genetics top 1%
Pediatrics, Perinatology and Child Health top 1%
Physiology top 5%

Co-authors: Arthur A.M. Wilde Connie R. Bezzina Jet Bliek Alex V. Postma Mariëlle Alders Zahurul A. Bhuiyan Irene M. van Langen Denis Escande
Topics: Epigenetics and DNA Methylation (31 papers)Genetic Syndromes and Imprinting (21 papers)Prenatal Screening and Diagnostics (21 papers)
Cited by: Cardiology and Cardiovascular Medicine Molecular Biology Genetics
Journals: Journal of Biological Chemistry Circulation Nature Genetics
Partner nations: Netherlands United States United Kingdom

In The Last Decade

Marcel M. A. M. Mannens

123 papers receiving 7.4k citations

Peers

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

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20 of 20 papers shown

#	Work	Indexed citations
1	Distinct saliva DNA methylation profiles in relation to treatment outcome in youth with posttraumatic stress disorder 2024 ·Translational Psychiatry ·Judith Ensink,Peter Henneman,Andrea Venema,Jasper B. Zantvoord,(unknown),Marcel M. A. M. Mannens,Ramón Lindauer	4
2	The utility of obesity polygenic risk scores from research to clinical practice: A review 2024 ·Obesity Reviews ·Philip R. Jansen,Niels Vos,(unknown),Ilona A. Dekkers,(unknown),Marcel M. A. M. Mannens,Mieke M. van Haelst	7
3	Functional Insight into and Refinement of the Genomic Boundaries of the JARID2-Neurodevelopmental Disorder Episignature 2023 ·International Journal of Molecular Sciences ·(unknown),Kathleen Rooney,Sadegheh Haghshenas,(unknown),Haley McConkey,Raissa Relator,(unknown),Irene Valenzuela,(unknown),(unknown),Berta Campos,(unknown),(unknown),Saskia M. Maas,Mariëlle Alders,Marcel M. A. M. Mannens,Mieke M. van Haelst,Bekim Sadiković,Peter Henneman	3
4	Prenatal Neun+ Neurons of Down Syndrome Display Aberrant Integrative DNA Methylation and Gene Expression Profiles 2022 ·Epigenomics ·Peter Henneman,Adri N. Mul,(unknown),(unknown),Mariëlle Alders,(unknown),Mark R. Mizee,Marcel M. A. M. Mannens	0
5	DNA methylation episignatures: insight into copy number variation 2022 ·Epigenomics ·(unknown),Kathleen Rooney,(unknown),Marcel M. A. M. Mannens,Bekim Sadiković,Peter Henneman	12
6	Genome-wide DNA methylation analysis on C-reactive protein among Ghanaians suggests molecular links to the emerging risk of cardiovascular diseases 2021 ·npj Genomic Medicine ·Felix P. Chilunga,Peter Henneman,Andrea Venema,Karlijn Meeks,Ana Requena‐Méndez,Erik Beune,Frank P. Mockenhaupt,Liam Smeeth,Silver Bahendeka,Ina Danquah,Kerstin Klipstein‐Grobusch,Adebowale Adeyemo,Marcel M. A. M. Mannens,Charles Agyemang	3
7	Screening for inborn errors of metabolism in psychotic patients using Next Generation Sequencing 2021 ·Journal of Psychiatric Research ·(unknown),Silvana van Koningsbruggen,(unknown),Nicole Leibold,Pilar Martínez‐Martínez,Marcel M. A. M. Mannens,Thérèse van Amelsvoort	2
8	DNA Methylation as the Link between Migration and the Major Noncommunicable Diseases: the RODAM Study 2021 ·Epigenomics ·Felix P. Chilunga,Peter Henneman,Andrea Venema,Karlijn Meeks,(unknown),Carlos Ruiz-Arenas,Ana Requena‐Méndez,Erik Beune,Joachim Spranger,Liam Smeeth,Silver Bahendeka,Ellis Owusu‐Dabo,Kerstin Klipstein‐Grobusch,Adebowale Adeyemo,Marcel M. A. M. Mannens,(unknown)	7
9	Comparing genome-scale DNA methylation and CNV marks between adult human cultured ITGA6+ testicular cells and seminomas to assess in vitro genomic stability 2020 ·PLoS ONE ·(unknown),Lambert C. J. Dorssers,Peter Henneman,Martin A. Rijlaarsdam,Andrea Venema,Aldo Jongejan,Marcel M. A. M. Mannens,Leendert H. J. Looijenga,Sjoerd Repping,Ans M. M. van Pelt	11
10	Epigenome-wide association study for perceived discrimination among sub-Saharan African migrants in Europe - the RODAM study 2020 ·Scientific Reports ·(unknown),Karlijn Meeks,Felix P. Chilunga,Charles Agyemang,Andrea Venema,Marcel M. A. M. Mannens,Mohammad Hadi Zafarmand,Kerstin Klipstein‐Grobusch,Liam Smeeth,Adebowale Adeyemo,Peter Henneman	10
11	Whole-Genome DNA Methylation Profiling of CD14+ Monocytes Reveals Disease Status and Activity Differences in Crohn’s Disease Patients 2020 ·Journal of Clinical Medicine ·Andrew Y. F. Li Yim,(unknown),Mohammed Ghiboub,Catriona Sharp,Enrico Ferrero,Marcel M. A. M. Mannens,Geert D’Haens,Wouter J. de Jonge,Anje A. te Velde,Peter Henneman	16
12	Perceived discrimination and stressful life events are associated with cardiovascular risk score in migrant and non-migrant populations: The RODAM study 2018 ·International Journal of Cardiology ·Felix P. Chilunga,Daniel Boateng,Peter Henneman,Erik Beune,Ana Requena‐Méndez,Karlijn Meeks,Liam Smeeth,Juliet Addo,Silver Bahendeka,Ina Danquah,Matthias B. Schulze,Kerstin Klipstein‐Grobusch,Marcel M. A. M. Mannens,Charles Agyemang	21
13	A distinct epigenetic profile distinguishes stenotic from non-inflamed fibroblasts in the ileal mucosa of Crohn’s disease patients 2018 ·PLoS ONE ·Andrew Y. F. Li Yim,Jessica R. de Bruyn,(unknown),Catriona Sharp,Enrico Ferrero,Wouter J. de Jonge,Manon E. Wildenberg,Marcel M. A. M. Mannens,Christianne J. Buskens,Geert D’Haens,Peter Henneman,Anje A. te Velde	14
14	Epigenome-wide association study in whole blood on type 2 diabetes among sub-Saharan African individuals: findings from the RODAM study 2018 ·International Journal of Epidemiology ·Karlijn Meeks,Peter Henneman,Andrea Venema,Juliet Addo,Silver Bahendeka,Tom Burr,Ina Danquah,Cecilia Galbete,Marcel M. A. M. Mannens,Frank P. Mockenhaupt,Ellis Owusu‐Dabo,Charles N. Rotimi,Matthias B. Schulze,Liam Smeeth,Joachim Spranger,Mohammad Hadi Zafarmand,Adebowale Adeyemo,Charles Agyemang	58
15	Truncating Titin Mutations are Associated with a Mild and Treatable form of Dilated Cardiomyopathy 2016 ·European Journal of Heart Failure ·Joeri A. Jansweijer,(unknown),Francesco Paolo Russo,Edgar T. Hoorntje,Jan D.H. Jongbloed,Ronald H. Lekanne Deprez,Alex V. Postma,Marieke Bronk,Ingrid A.W. van Rijsingen,Simone de Haij,Elena Biagini,Paul L. van Haelst,Jan van Wijngaarden,Maarten P. van den Berg,Arthur A.M. Wilde,Marcel M. A. M. Mannens,Rudolf A. de Boer,Karin Y. van Spaendonck‐Zwarts,J. Peter van Tintelen,Yigal M. Pinto	108
16	Genetic susceptibility for cow’s milk allergy in Dutch children: the start of the allergic march? 2015 ·Clinical and Translational Allergy ·Peter Henneman,(unknown),Andrea Venema,(unknown),K. Lip,Raoul C. M. Hennekam,Marcel M. A. M. Mannens,A. B. Sprikkelman	11
17	Methylation analysis in tongue tissue of BWS patients identifies the (EPI)genetic cause in 3 patients with normal methylation levels in blood 2014 ·European Journal of Medical Genetics ·Mariëlle Alders,Saskia M. Maas,D.J. Kadouch,K. Lip,Jet Bliek,Chantal M.A.M. van der Horst,Marcel M. A. M. Mannens	20
18	High rate of mosaicism in individuals with Cornelia de Lange syndrome 2013 ·Journal of Medical Genetics ·Sylvia Huisman,E. Redeker,Saskia M. Maas,Marcel M. A. M. Mannens,Raoul C. M. Hennekam	81
19	Molecular Genetic Testing for Familial Hypercholesterolemia in The Netherlands: A Stepwise Screening Strategy Enhances the Mutation Detection Rate 2006 ·Genetic Testing ·Maria Lombardi,E. Redeker,David H. Gent,(unknown),(unknown),Marcel M. A. M. Mannens	13
20	[Sudden death at young age and the importance of molecular-pathologic investigation]. 2005 ·PubMed ·Arthur A.M. Wilde,Irene M. van Langen,Marcel M. A. M. Mannens,Reinier A. Waalewijn,Alfons Maes	2

About Marcel M. A. M. Mannens

Marcel M. A. M. Mannens is a scholar working on Cardiology and Cardiovascular Medicine, Genetics and Pediatrics, Perinatology and Child Health, having authored 129 papers that have together received 7.5k indexed citations. Recurring topics across this work include Epigenetics and DNA Methylation (31 papers), Genetic Syndromes and Imprinting (21 papers) and Prenatal Screening and Diagnostics (21 papers). The work is most often cited by research in Cardiology and Cardiovascular Medicine (3.5k citations), Molecular Biology (4.8k citations) and Genetics (1.4k citations). Marcel M. A. M. Mannens has collaborated with scholars based in Netherlands, United States and United Kingdom. Frequent 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. Their work appears in journals such as Journal of Biological Chemistry, Circulation and Nature Genetics.

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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