Adri N. Mul

773 total citations
16 papers, 563 citations indexed

About

Adri N. Mul is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Genetics. According to data from OpenAlex, Adri N. Mul has authored 16 papers receiving a total of 563 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 5 papers in Pediatrics, Perinatology and Child Health and 5 papers in Genetics. Recurrent topics in Adri N. Mul's work include Epigenetics and DNA Methylation (5 papers), Prenatal Substance Exposure Effects (3 papers) and Down syndrome and intellectual disability research (2 papers). Adri N. Mul is often cited by papers focused on Epigenetics and DNA Methylation (5 papers), Prenatal Substance Exposure Effects (3 papers) and Down syndrome and intellectual disability research (2 papers). Adri N. Mul collaborates with scholars based in Netherlands, United Kingdom and United States. Adri N. Mul's co-authors include Marcel M. A. M. Mannens, Peter Henneman, Marian J.A. Groot Koerkamp, Raoul C. M. Hennekam, Martijn Rep, Henk F. Tabak, Cristina Al‐Khalili Szigyarto, Harmen J. Bussemaker, Guy Hardy and Rutger Meinsma and has published in prestigious journals such as PLoS ONE, Cancer Research and FEBS Letters.

In The Last Decade

Adri N. Mul

14 papers receiving 559 citations

Peers

Countries citing papers authored by Adri N. Mul

Since Specialization

Citations

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

Fields of papers citing papers by Adri N. Mul

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Adri N. Mul. 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 Adri N. Mul. The network helps show where Adri N. Mul may publish in the future.

Co-authorship network of co-authors of Adri N. Mul

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

All Works

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16 of 16 papers shown

#	Work	Indexed citations
1	Discovery of a DNA methylation episignature as a molecular biomarker for fetal alcohol syndrome 2025 ·Genetics in Medicine ·(unknown), Raissa Relator, Irene Valenzuela, Adri N. Mul, Mariëlle Alders, Michael A. Levy, Jennifer Kerkhof, (unknown), Anna M. Cueto‐González, (unknown), (unknown), Marcel M. A. M. Mannens, Mieke M. van Haelst, Eduardo F. Tizzano, Bekim Sadiković, Peter Henneman	0
2	Expression Quantitative Trait Methylation Analysis Identifies Whole Blood Molecular Footprint in Fetal Alcohol Spectrum Disorder (FASD) 2023 ·International Journal of Molecular Sciences ·(unknown), (unknown), Adri N. Mul, (unknown), Andrew Y. F. Li Yim, Jan Maarten Cobben, Jacek Nikliński, (unknown), Robert Śmigiel, Marcel M. A. M. Mannens, Peter Henneman	5
3	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
4	Genome-wide methylation profiling of Beckwith-Wiedemann syndrome patients without molecular confirmation after routine diagnostics 2019 ·Clinical Epigenetics ·(unknown), Mariëlle Alders, Saskia M. Maas, Jet Bliek, (unknown), Peter Henneman, Faisal I. Rezwan, K. Lip, Adri N. Mul, Deborah Mackay, Marcel M. A. M. Mannens	18
5	DNA Methylation Abundantly Associates with Fetal Alcohol Spectrum Disorder and its Subphenotypes 2019 ·Epigenomics ·Jan Maarten Cobben, (unknown), Andrea Venema, Adri N. Mul, Abeltje M. Polstra, Alex V. Postma, Robert Śmigiel, Karolina Pesz, Jacek Nikliński, (unknown), Peter Henneman, Marcel M. A. M. Mannens	26
6	Genetic variant in CACNA1C is associated with PTSD in traumatized police officers 2018 ·European Journal of Human Genetics ·(unknown), Judith Ensink, Laura Nawijn, Adri N. Mul, Saskia B.J. Koch, Andrea Venema, (unknown), Jessie L. Frijling, (unknown), Ramón Lindauer, Miranda Olff, Marcel M. A. M. Mannens, Mirjam van Zuiden, Peter Henneman	19
7	Widespread domain-like perturbations of DNA methylation in whole blood of Down syndrome neonates 2018 ·PLoS ONE ·Peter Henneman, Arjan Bouman, Adri N. Mul, (unknown), Anne-Marie Van Der Kevie-Kersemaekers, Nitash Zwaveling‐Soonawala, Hanne Meijers‐Heijboer, A S Paul van Trotsenburg, Marcel M. A. M. Mannens	20
8	Oxytocin receptor gene methylation in male and female PTSD patients and trauma-exposed controls 2018 ·European Neuropsychopharmacology ·Laura Nawijn, (unknown), Mirjam van Zuiden, Peter Henneman, Saskia B.J. Koch, Adri N. Mul, Jessie L. Frijling, Dick J. Veltman, Marcel M. A. M. Mannens, Miranda Olff	25
9	Peripheral blood methylation profiling of female Crohn’s disease patients 2016 ·Clinical Epigenetics ·Andrew Y. F. Li Yim, (unknown), Jing Hua Zhao, Wouter J. de Jonge, Geert D’Haens, Marcel M. A. M. Mannens, Adri N. Mul, Anje A. te Velde, Peter Henneman	37
10	Cow’s milk allergy in Dutch children: an epigenetic pilot survey 2016 ·Clinical and Translational Allergy ·(unknown), Peter Henneman, Andrea Venema, Adri N. Mul, (unknown), Martin A. Haagmans, Olaf R.F. Mook, Raoul C. M. Hennekam, A. B. Sprikkelman, Marcel M. A. M. Mannens	30
11	Radioprotection of IDH1 -Mutated Cancer Cells by the IDH1-Mutant Inhibitor AGI-5198 2015 ·Cancer Research ·Remco J. Molenaar, Dennis Botman, (unknown), Vashendriya V.V. Hira, Sanne A. M. van Lith, Jan Stap, Peter Henneman, Mohammed Khurshed, Krissie Lenting, Adri N. Mul, (unknown), Cornelis M. van Drunen, Ron A. Hoebe, Tomas Radivoyevitch, Johanna W. Wilmink, Jaroslaw P. Maciejewski, W. Peter Vandertop, William P. J. Leenders, Fonnet E. Bleeker, Cornelis J.F. Van Noorden	116
12	Intragenic deletions and a deep intronic mutation affecting pre-mRNA splicing in the dihydropyrimidine dehydrogenase gene as novel mechanisms causing 5-fluorouracil toxicity 2010 ·Human Genetics ·André B. P. Kuilenburg, Judith Meijer, Adri N. Mul, Rutger Meinsma, (unknown), Doreen Dobritzsch, Raoul C. M. Hennekam, Marcel M. A. M. Mannens, Marion Kiechle, Marie-Christine Étienne-Grimaldi, Heinz‐Josef Klümpen, Jan Gerard Maring, (unknown), (unknown), G. Milano, Raymon Vijzelaar, Eva Groß	93
13	Analysis of severely affected patients with dihydropyrimidine dehydrogenase deficiency reveals large intragenic rearrangements of DPYD and a de novo interstitial deletion del(1)(p13.3p21.3) 2009 ·Human Genetics ·André B. P. Kuilenburg, Judith Meijer, Adri N. Mul, Raoul C. M. Hennekam, J.M.N. Hoovers, Christine de Die‐Smulders, Christian Weber, Andrea Mori, Jörgen Bierau, Brian Fowler, (unknown), Jörn Oliver Sass, Rutger Meinsma, Julia B. Hennermann, Peter Miny, Lida Zoetekouw, Raymon Vijzelaar, Joost Nicolai, Bauke Ylstra, M. Estela Rubio‐Gozalbo	39
14	Array comparative genomic hybridization analysis of a familial duplication of chromosome 13q: A recognizable syndrome 2005 ·American Journal of Medical Genetics Part A ·Inge B. Mathijssen, J.M.N. Hoovers, Adri N. Mul, (unknown), (unknown), Raoul C. M. Hennekam	11
15	Dissection of Transient Oxidative Stress Response inSaccharomyces cerevisiaeby Using DNA Microarrays 2002 ·Molecular Biology of the Cell ·Marian J.A. Groot Koerkamp, Martijn Rep, Harmen J. Bussemaker, Guy Hardy, Adri N. Mul, (unknown), Cristina Al‐Khalili Szigyarto, (unknown), Henk F. Tabak	99
16	Changes in mRNA expression profile underlie phenotypic adaptations in creatine kinase‐deficient muscles 2001 ·FEBS Letters ·Ad J.C. de Groof, Bart Smeets, Marian J.A. Groot Koerkamp, Adri N. Mul, Edwin Janssen, (unknown), Bé Wieringa	25

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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