Rowdy Meijer

1.5k total citations
17 papers, 612 citations indexed

About

Rowdy Meijer is a scholar working on Molecular Biology, Cell Biology and Genetics. According to data from OpenAlex, Rowdy Meijer has authored 17 papers receiving a total of 612 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 7 papers in Cell Biology and 7 papers in Genetics. Recurrent topics in Rowdy Meijer's work include Skin and Cellular Biology Research (7 papers), Genetic Neurodegenerative Diseases (5 papers) and Autoimmune Bullous Skin Diseases (4 papers). Rowdy Meijer is often cited by papers focused on Skin and Cellular Biology Research (7 papers), Genetic Neurodegenerative Diseases (5 papers) and Autoimmune Bullous Skin Diseases (4 papers). Rowdy Meijer collaborates with scholars based in Netherlands, United States and United Kingdom. Rowdy Meijer's co-authors include Hans Scheffer, Sascha Vermeer, Bart P.C. van de Warrenburg, Erik‐Jan Kamsteeg, Christian Gilissen, Marcel F. Jonkman, Peter C. van den Akker, B. Kremer, Nine Knoers and Helenius J. Schelhaas and has published in prestigious journals such as Human Molecular Genetics, Journal of Investigative Dermatology and British Journal of Dermatology.

In The Last Decade

Rowdy Meijer

17 papers receiving 602 citations

Peers

Countries citing papers authored by Rowdy Meijer

Since Specialization

Citations

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

Fields of papers citing papers by Rowdy Meijer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rowdy Meijer

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

All Works

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17 of 17 papers shown

#	Work	Indexed citations
1	Evolution of genome diagnostics in epidermolysis bullosa: Unveiling the power of next‐generation sequencing 2024 ·Journal of the European Academy of Dermatology and Venereology ·(unknown), Henny H. Lemmink, V.K. Yenamandra, (unknown), (unknown), Kevin Kooi, Gilles F.H. Diercks, Rowdy Meijer, Michel van Geel, Hans Scheffer, Richard J. Sinke, Birgit Sikkema‐Raddatz, Maria C. Bolling, Peter C. van den Akker	4
2	Copy number variants from 4800 exomes contribute to ~7% of genetic diagnoses in movement disorders, muscle disorders and neuropathies 2023 ·European Journal of Human Genetics ·Maartje Pennings, Rowdy Meijer, Monique M. Gerrits, (unknown), Rolph Pfundt, Nicole de Leeuw, Christian Gilissen, Thatjana Gardeitchik, Meyke Schouten, Nicol C. Voermans, Bart van de Warrenburg, Erik‐Jan Kamsteeg	12
3	Systematic analysis of short tandem repeats in 38,095 exomes provides an additional diagnostic yield 2021 ·Genetics in Medicine ·(unknown), Jordi Corominas, (unknown), Maartje Pennings, Rowdy Meijer, Nienke E. Verbeek, Bart van de Warrenburg, Meyke Schouten, Helger G. Yntema, Lisenka E.L.M. Vissers, Erik‐Jan Kamsteeg, Christian Gilissen	22
4	Natural Exon Skipping Sets the Stage for Exon Skipping as Therapy for Dystrophic Epidermolysis Bullosa 2019 ·Molecular Therapy — Nucleic Acids ·(unknown), (unknown), (unknown), Rowdy Meijer, Henny H. Lemmink, Hans Scheffer, Richard J. Sinke, Marcel F. Jonkman, Anna M.G. Pasmooij, Peter C. van den Akker	22
5	Clinical exome sequencing for cerebellar ataxia and spastic paraplegia uncovers novel gene–disease associations and unanticipated rare disorders 2016 ·European Journal of Human Genetics ·Bart P.C. van de Warrenburg, Meyke Schouten, Susanne T. de Bot, Sascha Vermeer, Rowdy Meijer, Maartje Pennings, Christian Gilissen, (unknown), Hans Scheffer, Erik‐Jan Kamsteeg	76
6	RYR1‐related myopathies: a wide spectrum of phenotypes throughout life 2015 ·European Journal of Neurology ·Marc Snoeck, Baziel G.M. van Engelen, Benno Küsters, Martin Lammens, Rowdy Meijer, J. Molenaar, Joost Raaphorst, (unknown), C.S.M. Straathof, L.T.L. Sie, I.F.M. de Coo, W. Ludo van der Pol, Marjolein Visser, Hans Scheffer, Susan Treves, Heinz Jungbluth, Nicol C. Voermans, Erik‐Jan Kamsteeg	94
7	Mechanisms of Natural Gene Therapy in Dystrophic Epidermolysis Bullosa 2014 ·Journal of Investigative Dermatology ·Dimitra Kiritsi, Marta García, (unknown), Cristina Has, Rowdy Meijer, M.J. Escámez, J. Kohlhase, Peter C. van den Akker, Hans Scheffer, Marcel F. Jonkman, Marcela Del Río, Leena Bruckner‐Tuderman, Anna M.G. Pasmooij	34
8	Somatic mosaicism for theCOL7A1mutation p.Gly2034Arg in the unaffected mother of a patient with dystrophic epidermolysis bullosa pruriginosa 2014 ·British Journal of Dermatology ·Peter C. van den Akker, Anna M.G. Pasmooij, Rowdy Meijer, Hans Scheffer, Marcel F. Jonkman	8
9	The EEC syndrome and SHFM: report of two cases and mutation analysis of p63 gene. 2011 ·PubMed ·Hacer Ergin, (unknown), (unknown), Hans Scheffer, (unknown), (unknown), Rowdy Meijer, N. Lale Şatıroğlu-Tufan	3
10	Massively parallel sequencing of ataxia genes after array-based enrichment 2010 ·Human Mutation ·Alexander Hoischen, Christian Gilissen, Peer Arts, Nienke Wieskamp, Walter van der Vliet, Sascha Vermeer, Marloes Steehouwer, Petra de Vries, Rowdy Meijer, (unknown), Nine V.A.M. Knoers, Michael F. Buckley, Hans Scheffer, Joris A. Veltman	63
11	The inversa type of recessive dystrophic epidermolysis bullosa is caused by specific arginine and glycine substitutions in type VII collagen 2010 ·Journal of Medical Genetics ·Peter C. van den Akker, Jemima E. Mellerio, Anna E. Martinez, (unknown), Rowdy Meijer, (unknown), A.J. van Essen, Hans Scheffer, Robert M.W. Hofstra, John A. McGrath, Marcel F. Jonkman	26
12	Design and Validation of a Conformation-Sensitive Capillary Electrophoresis System for Mutation Identification of the COL7A1 Gene with Automated Peak Comparison 2009 ·Genetic Testing and Molecular Biomarkers ·Peter C. van den Akker, (unknown), Rowdy Meijer, Marcel F. Jonkman, Robert M.W. Hofstra, Hans Scheffer	3
13	Long-term follow-up of patients with recessive dystrophic epidermolysis bullosa in the Netherlands: Expansion of the mutation database and unusual phenotype–genotype correlations 2009 ·Journal of Dermatological Science ·Peter C. van den Akker, Anthonie J. van Essen, (unknown), Rowdy Meijer, Miranda Nijenhuis, (unknown), Robert M.W. Hofstra, Hendri H. Pas, Hans Scheffer, Marcel F. Jonkman	28
14	Design and Validation of a Conformation Sensitive Capillary Electrophoresis-Based Mutation Scanning System and Automated Data Analysis of the More than 15 kbp-Spanning Coding Sequence of the SACS Gene 2009 ·Journal of Molecular Diagnostics ·Sascha Vermeer, Rowdy Meijer, Tom Hofste, Daniëlle Bodmer, Ermanno Bosgoed, Frans P.M. Cremers, B. Kremer, Nine V.A.M. Knoers, Hans Scheffer	6
15	ARSACS in the Dutch population: a frequent cause of early-onset cerebellar ataxia 2008 ·Neurogenetics ·Sascha Vermeer, Rowdy Meijer, (unknown), Janneke Timmermans, J.R.M. Cruysberg, (unknown), Helenius J. Schelhaas, Bart P.C. van de Warrenburg, Nine Knoers, Hans Scheffer, B. Kremer	105
16	Genotype-phenotype correlations in MYCN-related Feingold syndrome 2008 ·Human Mutation ·Carlo Marcelis, Frans A. Hol, Gail E. Graham, Paul N.M.A. Rieu, Richárd Kellermayer, Rowdy Meijer, Dorien Lugtenberg, Hans Scheffer, Hans van Bokhoven, Han G. Brunner, Arjan P.M. de Brouwer	60
17	A novel translation re-initiation mechanism for the p63 gene revealed by amino-terminal truncating mutations in Rapp-Hodgkin/Hay-Wells-like syndromes 2008 ·Human Molecular Genetics ·Tuula Rinne, (unknown), Evert N. Lamme, Pascal H. G. Duijf, Emine Bolat, Rowdy Meijer, Hans Scheffer, Elisabeth Rosser, Tiong Yang Tan, John A. McGrath, Joost Schalkwijk, H.G. Brunner, Huiqing Zhou, Hans van Bokhoven	46

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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