Wouter W. Wiegant

3.5k total citations
31 papers, 2.3k citations indexed

About

Wouter W. Wiegant is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Wouter W. Wiegant has authored 31 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Molecular Biology, 12 papers in Genetics and 11 papers in Oncology. Recurrent topics in Wouter W. Wiegant's work include DNA Repair Mechanisms (27 papers), Genomics and Chromatin Dynamics (10 papers) and PARP inhibition in cancer therapy (9 papers). Wouter W. Wiegant is often cited by papers focused on DNA Repair Mechanisms (27 papers), Genomics and Chromatin Dynamics (10 papers) and PARP inhibition in cancer therapy (9 papers). Wouter W. Wiegant collaborates with scholars based in Netherlands, United States and Poland. Wouter W. Wiegant's co-authors include Haico van Attikum, Martijn S. Luijsterburg, Małgorzata Z. Zdzienicka, Godelieve Smeenk, Albert Pastink, Alfred C.O. Vertegaal, Barbara C. Godthelp, Hans Vrolijk, Aldo Solari and Fré Arwert and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Wouter W. Wiegant

31 papers receiving 2.3k citations

Peers

Countries citing papers authored by Wouter W. Wiegant

Since Specialization

Citations

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

Fields of papers citing papers by Wouter W. Wiegant

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Wouter W. Wiegant. 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 Wouter W. Wiegant. The network helps show where Wouter W. Wiegant may publish in the future.

Co-authorship network of co-authors of Wouter W. Wiegant

This figure shows the co-authorship network connecting the top 25 collaborators of Wouter W. Wiegant. A scholar is included among the top collaborators of Wouter W. Wiegant 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 Wouter W. Wiegant. Wouter W. Wiegant 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	The Fanconi anemia core complex promotes CtIP-dependent end resection to drive homologous recombination at DNA double-strand breaks 2024 ·Nature Communications ·Bert van de Kooij, (unknown), Magdalena B. Rother, Wouter W. Wiegant, Pau Creixell, (unknown), Brian A. Joughin, (unknown), Matthias Altmeyer, Marcel A.T.M. van Vugt, Michael B. Yaffe, Haico van Attikum	8
2	Chaperoning of the histone octamer by the acidic domain of DNA repair factor APLF 2022 ·Science Advances ·(unknown), (unknown), (unknown), Domenico Fasci, Wouter W. Wiegant, Melissa A. Graewert, Kees Vreeken, Hans Wienk, Dmitri I. Svergun, Albert J. R. Heck, Haico van Attikum, Rolf Boelens, Titia K. Sixma, Francesca Mattiroli, Hugo van Ingen	12
3	Functional Analysis Identifies Damaging CHEK2 Missense Variants Associated with Increased Cancer Risk 2021 ·Cancer Research ·Rick A.C.M. Boonen, Wouter W. Wiegant, (unknown), Bas Vroling, (unknown), Zsofia Kote‐Jarai, Martina Mijušković, Simona Cristea, (unknown), Tom van Wezel, Niko Beerenwinkel, Rosalind A. Eeles, Peter Devilee, Maaike P.G. Vreeswijk, Giancarlo Marra, Haico van Attikum	33
4	ERCC1mutations impede DNA damage repair and cause liver and kidney dysfunction in patients 2020 ·The Journal of Experimental Medicine ·Katja Apelt, Susan M. White, (unknown), Jung-Eun Yeo, Angela Kragten, (unknown), Martin A. Rooimans, Román González‐Prieto, Wouter W. Wiegant, Sebastian Lunke, (unknown), (unknown), Catherine Quinlan, Winita Hardikar, Haico van Attikum, Alfred C.O. Vertegaal, Brian T. Wilson, Rob M.F. Wolthuis, Orlando D. Schärer, Martijn S. Luijsterburg	24
5	CHD7 and 53BP1 regulate distinct pathways for the re-ligation of DNA double-strand breaks 2020 ·Nature Communications ·Magdalena B. Rother, Stefania Pellegrino, Rebecca Smith, Marco Gatti, Cornelia Meisenberg, Wouter W. Wiegant, Martijn S. Luijsterburg, Ralph Imhof, Jessica A. Downs, Alfred C.O. Vertegaal, Sébastien Huet, Matthias Altmeyer, Haico van Attikum	34
6	PHF2 regulates homology-directed DNA repair by controlling the resection of DNA double strand breaks 2020 ·Nucleic Acids Research ·(unknown), (unknown), Magdalena B. Rother, Wouter W. Wiegant, (unknown), Juan R. Hernández‐Fernaud, Pablo Huertas, Raimundo Freire, Haico van Attikum, Veronique A. J. Smits	26
7	Functional analysis of genetic variants in the high-risk breast cancer susceptibility gene PALB2 2019 ·Nature Communications ·Rick A.C.M. Boonen, Amélie Rodrigue, Chantal Stoepker, Wouter W. Wiegant, Bas Vroling, (unknown), Magdalena B. Rother, (unknown), Maaike P.G. Vreeswijk, Fergus J. Couch, Jacques Simard, Peter Devilee, Jean‐Yves Masson, Haico van Attikum	40
8	WWP2 ubiquitylates RNA polymerase II for DNA-PK-dependent transcription arrest and repair at DNA breaks 2019 ·Genes & Development ·Pierre Caron, Tibor Pankotai, Wouter W. Wiegant, Maxim A. X. Tollenaere, Audrey Furst, Céline Bonhomme, Angela Helfricht, (unknown), Albert Pastink, Alfred C.O. Vertegaal, Martijn S. Luijsterburg, Evi Soutoglou, Haico van Attikum	72
9	Map of synthetic rescue interactions for the Fanconi anemia DNA repair pathway identifies USP48 2018 ·Nature Communications ·Georgia Velimezi, (unknown), Francisco Muñoz‐Martínez, Wouter W. Wiegant, Joana Ferreira da Silva, (unknown), (unknown), Marc Wiedner, Sara Brin Rosenthal, Kathleen M. Fisch, Jason Moffat, Jörg Menche, Haico van Attikum, Stephen P. Jackson, Joanna I. Loizou	28
10	Ataxin‐3 consolidates the MDC 1‐dependent DNA double‐strand break response by counteracting the SUMO ‐targeted ubiquitin ligase RNF 4 2017 ·The EMBO Journal ·Annika Pfeiffer, Martijn S. Luijsterburg, Klára Ács, Wouter W. Wiegant, Angela Helfricht, (unknown), Melania Minoia, Claudia Böttcher, Florian A. Salomons, Haico van Attikum, Nico P. Dantuma	65
11	ZMYND8 Co-localizes with NuRD on Target Genes and Regulates Poly(ADP-Ribose)-Dependent Recruitment of GATAD2A/NuRD to Sites of DNA Damage 2016 ·Cell Reports ·Cornelia G. Spruijt, Martijn S. Luijsterburg, Roberta Menafra, Rik G.H. Lindeboom, Pascal W.T.C. Jansen, Raghu Ram Edupuganti, Marijke Baltissen, Wouter W. Wiegant, (unknown), Filomena Matarese, Anneloes Mensinga, Ina Poser, Harmjan R. Vos, Hendrik G. Stunnenberg, Haico van Attikum, Michiel Vermeulen	85
12	The de-ubiquitylating enzymes USP26 and USP37 regulate homologous recombination by counteracting RAP80 2015 ·Nucleic Acids Research ·Dimitris Typas, Martijn S. Luijsterburg, Wouter W. Wiegant, (unknown), Angela Helfricht, Peter Thijssen, Bram van den Broek, Leon H.F. Mullenders, Haico van Attikum	63
13	Poly(ADP-ribosyl)ation links the chromatin remodeler SMARCA5/SNF2H to RNF168-dependent DNA damage signaling 2012 ·Journal of Cell Science ·Godelieve Smeenk, Wouter W. Wiegant, Jurgen A. Marteijn, Martijn S. Luijsterburg, (unknown), Thomas Costelloe, Ron Romeijn, Albert Pastink, Niels Mailand, Wim Vermeulen, Haico van Attikum	117
14	A new non‐catalytic role for ubiquitin ligase RNF8 in unfolding higher‐order chromatin structure 2012 ·The EMBO Journal ·Martijn S. Luijsterburg, Klára Ács, Leena Ackermann, Wouter W. Wiegant, Simon Bekker‐Jensen, Dorthe Helena Larsen, Kum Kum Khanna, Haico van Attikum, Niels Mailand, Nico P. Dantuma	91
15	The yeast Fun30 and human SMARCAD1 chromatin remodellers promote DNA end resection 2012 ·Nature ·Thomas Costelloe, (unknown), Nozomi Tomimatsu, Bipasha Mukherjee, Emmanuelle Martini, (unknown), (unknown), Wouter W. Wiegant, Agnès Thierry, Sandeep Burma, Haico van Attikum, Bertrand Llorente	212
16	Artemis splice defects cause atypical SCID and can be restored in vitro by an antisense oligonucleotide 2011 ·Genes and Immunity ·Hanna IJspeert, A Lankester, J. Merlijn van den Berg, Wouter W. Wiegant, Menno C. van Zelm, Corry M.R. Weemaes, Adilia Warris, Qiang Pan‐Hammarström, Albert Pastink, Maarten J. D. van Tol, Jacques J. M. van Dongen, Dik C. van Gent, Mirjam van der Burg	25
17	A novel radiosensitive SCID patient with a pronounced G2/M sensitivity 2010 ·DNA repair ·Wouter W. Wiegant, (unknown), Nicole S. Verkaik, Mirjam van der Burg, F. Darroudi, Ron Romeijn, Ewa Bernatowska, Beata Wolska‐Kuśnierz, Bożena Mikołuć, Nicolaas G.J. Jaspers, (unknown), Hanna IJspeert, (unknown), Anna A. Friedl, Jean‐Pierre de Villartay, Leon H.F. Mullenders, Jacques J. M. van Dongen, Dik C. van Gent, Albert Pastink, Małgorzata Z. Zdzienicka	3
18	A DNA-PKcs mutation in a radiosensitive T–B– SCID patient inhibits Artemis activation and nonhomologous end-joining 2008 ·Journal of Clinical Investigation ·Mirjam van der Burg, Hanna IJspeert, Nicole S. Verkaik, Tuba Turul, Wouter W. Wiegant, Keiko Morotomi‐Yano, Pierre‐Olivier Mari, İlhan Tezcan, David J. Chen, Małgorzata Z. Zdzienicka, Jacques J. M. van Dongen, Dik C. van Gent	200
19	The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J 2005 ·Nature Genetics ·Marieke Levitus, Quinten Waisfisz, Barbara C. Godthelp, Yne de Vries, Shobbir Hussain, Wouter W. Wiegant, (unknown), Jûrgen Steltenpool, Martin A. Rooimans, Gerard Pals, Fré Arwert, Christopher G. Mathew, Małgorzata Z. Zdzienicka, Kevin Hiom, Johan P. de Winter, Hans Joenje	338
20	Oestradiol, a new hapten for detecting nucleic acid sequences by FISH 1997 ·Histochemistry and Cell Biology ·Mariëtte P.C. van de Corput, Roeland W. Dirks, Wouter W. Wiegant, J. Wiegant, Klaus Mühlegger, Anton K. Raap	3

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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