Edwin Mientjes

3.2k citations

37 papers · 1.9k indexed · h-index 23

Impact in

Genetics top 2%
- Genetics and Neurodevelopmental Disorders
- Genetic Syndromes and Imprinting
Molecular Biology top 5%
- Epigenetics and DNA Methylation
- RNA Research and Splicing
- RNA modifications and cancer
- Ubiquitin and proteasome pathways
- Nuclear Structure and Function

Papers in ⓘ

Genetics 22
- Genetics and Neurodevelopmental Disorders 13
- Genetic Syndromes and Imprinting 8
Molecular Biology 32
- Epigenetics and DNA Methylation 7
- DNA Repair Mechanisms 6
- Ubiquitin and proteasome pathways 4
- RNA Research and Splicing 3

Co-authors: Gerard C. Grosveld (4 shared papers)Ype Elgersma (13 shared papers)Rob Willemsen (7 shared papers)Rekha Iyengar (1 shared paper)Craig J. McPherson (1 shared paper)Andrew D. Hollenbach (1 shared paper)Ben A. Oostra (4 shared papers)Geeske M. van Woerden (6 shared papers)
Journals: Molecular Autism (3 papers)Environmental and Molecular Mutagenesis (3 papers)Molecular Psychiatry (2 papers)Scientific Reports (1 paper)European Journal of Human Genetics (1 paper)
Partner nations: Netherlands United States Switzerland

In The Last Decade

Edwin Mientjes

35 papers receiving 1.9k citations

Peers

Countries citing papers authored by Edwin Mientjes

Since Specialization

Citations

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

Fields of papers citing papers by Edwin Mientjes

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Edwin Mientjes, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Edwin Mientjes Line = papers co-authored together Edwin Mientjes links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 37 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Daxx and histone deacetylase II associate with chromatin through an interaction with core histones and the chromatin-associated protein Dek Journal of Cell Science ·Andrew D. Hollenbach, Craig J. McPherson, Edwin Mientjes, Rekha Iyengar, Gerard C. Grosveld	2002	224
2	The generation of a conditional Fmr1 knock out mouse model to study Fmrp function in vivo Neurobiology of Disease ·Edwin Mientjes, Ingeborg M. Nieuwenhuizen, Laura Kirkpatrick, Tao Zu, Marianne Hoogeveen‐Westerveld, LA Severijnen, M. Rifé, Rob Willemsen, David L. Nelson, Ben A. Oostra	2005	176
3	Ube3a reinstatement identifies distinct developmental windows in a murine Angelman syndrome model Journal of Clinical Investigation ·Sara Silva-Santos, Geeske M. van Woerden, Caroline F. Bruinsma, Edwin Mientjes, Mehrnoush Aghadavoud Jolfaei, Ben Distel, Steven A. Kushner, Ype Elgersma	2015	174
4	The Acute Myeloid Leukemia-Associated Protein, Dek, Forms a Splicing-Dependent Interaction with Exon-Product Complexes The Journal of Cell Biology ·Tim McGarvey, Emanuel Rosonina, Susan McCracken, Qiyu Li, Ramy Arnaout, Edwin Mientjes, Jeffrey A. Nickerson, Don Awrey, Jack Greenblatt, Gerard C. Grosveld, Benjamin J. Blencowe	2000	112
5	Fxr1 knockout mice show a striated muscle phenotype: implications for Fxr1p function in vivo Human Molecular Genetics ·Edwin Mientjes	2004	107
6	Cognitive decline, neuromotor and behavioural disturbances in a mouse model for fragile-X-associated tremor/ataxia syndrome (FXTAS) Behavioural Brain Research ·Debby Van Dam, V. Errijgers, R. Frank Kooy, Rob Willemsen, Edwin Mientjes, Ben A. Oostra, Peter Paul De Deyn	2005	98
7	Elevated Fmr1 mRNA levels and reduced protein expression in a mouse model with an unmethylated Fragile X full mutation Experimental Cell Research ·Judith R. Brouwer, Edwin Mientjes, C.E. Bakker, Ingeborg M. Nieuwenhuizen, L. A. Severijnen, Herma C. van der Linde, David L. Nelson, Ben A. Oostra, Rob Willemsen	2006	97
8	Synaptic ionotropic glutamate receptors and plasticity are developmentally altered in the CA1 field of Fmr1 knockout mice The Journal of Physiology ·Yair Pilpel, Alexander Kolleker, Sven Berberich, Melanie Ginger, Andreas Frick, Edwin Mientjes, Ben A. Oostra, Peter H. Seeburg	2008	86
9	Loss of nuclear UBE3A causes electrophysiological and behavioral deficits in mice and is associated with Angelman syndrome Nature Neuroscience ·Rossella Avagliano Trezza, Monica Sonzogni, Stijn N. V. Bossuyt, F. Isabella Zampeta, A. Mattijs Punt, Marlene van den Berg, Diana C. Rotaru, Linda M. C. Koene, Shashini T. Munshi, Jeffrey Stedehouder, Johan M. Kros, Mark Williams, Helen Heussler, Femke M.S. de Vrij, Edwin Mientjes, Geeske M. van Woerden, Steven A. Kushner, Ben Distel, Ype Elgersma	2019	71
10	The GABA_Areceptor is an FMRP target with therapeutic potential in fragile X syndrome Cell Cycle ·Sien Braat, Charlotte D’Hulst, Inge Heulens, Silvia De Rubeis, Edwin Mientjes, David L. Nelson, Rob Willemsen, Claudia Bagni, Debby Van Dam, Peter Paul De Deyn, R. Frank Kooy	2015	71
11	DAZL Limits Pluripotency, Differentiation, and Apoptosis in Developing Primordial Germ Cells Stem Cell Reports ·Hsu-Hsin Chen, Maaike Welling, Donald B. Bloch, Javier Muñoz, Edwin Mientjes, Xinjie Chen, Cody Alexander Tramp, Jie Wu, Akiko Yabuuchi, Yu‐Fen Chou, Christa Buecker, Adrian R. Krainer, Rob Willemsen, Albert J. R. Heck, Niels Geijsen	2014	70
12	HCN channels are a novel therapeutic target for cognitive dysfunction in Neurofibromatosis type 1 Molecular Psychiatry ·Azar Omrani, Thijs van der Vaart, Edwin Mientjes, Geeske M. van Woerden, Mohammad Reza Hojjati, Ka Wan Li, David H. Gutmann, Christiaan N. Levelt, August B. Smit, Alcino J. Silva, Steven A. Kushner, Ype Elgersma	2015	69
13	Negative Regulation of the RelA/p65 Transactivation Function by the Product of the DEK Proto-oncogene Journal of Biological Chemistry ·Morgan A. Sammons, Shan Wan, Nancy L. Vogel, Edwin Mientjes, Gerard C. Grosveld, Brian P. Ashburner	2006	49
14	Antisense oligonucleotide treatment rescues UBE3A expression and multiple phenotypes of an Angelman syndrome mouse model JCI Insight ·Claudia Milazzo, Edwin Mientjes, Ilse Wallaard, Søren Rasmussen, Kamille Dumong Erichsen, Tejaswini Kakunuri, A.S. Elise van der Sman, Thomas Kremer, Meghan T. Miller, Marius C. Hoener, Ype Elgersma	2021	49
15	Angelman Syndrome: From Mouse Models to Therapy Neuroscience ·Diana C. Rotaru, Edwin Mientjes, Ype Elgersma	2020	47
16	An improved selection method for λlacZ − phages based on galactose sensitivity Transgenic Research ·Edwin Mientjes, Joost H.M. van Delft, B.M. op 't Hof, Jan A. Gossen, Jan Vijg, P.H.M. Lohman, Robert A. Baan	1994	42
17	DNA adducts, mutant frequencies, and mutation spectra in various organs of lambda lacZ mice exposed to ethylating agents. PubMed ·Edwin Mientjes, Anja Luiten-Schuite, E. Wolf, Yvonne Borsboom, Angela Bergmans, Frits J. Berends, P.H.M. Lohman, Robert A. Baan, Joost HM van Delft	1998	38
18	Reduction in fragile X related 1 protein causes cardiomyopathy and muscular dystrophy in zebrafish Journal of Experimental Biology ·Sandra van’t Padje, Bill Chaudhry, Lies‐Anne Severijnen, Herma C. van der Linde, Edwin Mientjes, Ben A. Oostra, Rob Willemsen	2009	37
19	Improvement of ubiquitylation site detection by Orbitrap mass spectrometry Journal of Proteomics ·Lennart van der Wal, Karel Bezstarosti, Karen A. Sap, Dick H. W. Dekkers, Erikjan Rijkers, Edwin Mientjes, Ype Elgersma, Jeroen Demmers	2017	30
20	Effects of SET and SET-CAN on the differentiation of the human promonocytic cell line U937 Leukemia ·Ayten Kandilci, Edwin Mientjes, Gerard C. Grosveld	2003	30

About Edwin Mientjes

Edwin Mientjes is a scholar working on Genetics, Molecular Biology, Cancer Research, Cell Biology and Cellular and Molecular Neuroscience, having authored 37 papers that have together received 1.9k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (13 papers), Genetic Syndromes and Imprinting (8 papers), Epigenetics and DNA Methylation (7 papers), DNA Repair Mechanisms (6 papers), Ubiquitin and proteasome pathways (4 papers), Carcinogens and Genotoxicity Assessment (4 papers), Prenatal Screening and Diagnostics (3 papers) and RNA Research and Splicing (3 papers). The work is most often cited by research in Genetics (1.1k citations), Molecular Biology (1.4k citations), Cognitive Neuroscience (387 citations), Developmental Neuroscience (51 citations) and Cancer Research (183 citations). Edwin Mientjes has collaborated with scholars based in Netherlands, United States and Switzerland. Frequent co-authors include Gerard C. Grosveld, Ype Elgersma, Rob Willemsen, Rekha Iyengar, Craig J. McPherson, Andrew D. Hollenbach, Ben A. Oostra, Geeske M. van Woerden, David L. Nelson and Steven A. Kushner. Their work appears in journals such as Molecular Autism, Environmental and Molecular Mutagenesis, Molecular Psychiatry, Scientific Reports and European Journal of Human 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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