M. Coerwinkel

820 total citations
12 papers, 651 citations indexed

About

M. Coerwinkel is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, M. Coerwinkel has authored 12 papers receiving a total of 651 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 6 papers in Cellular and Molecular Neuroscience and 2 papers in Genetics. Recurrent topics in M. Coerwinkel's work include Genetic Neurodegenerative Diseases (6 papers), DNA Repair Mechanisms (2 papers) and CRISPR and Genetic Engineering (2 papers). M. Coerwinkel is often cited by papers focused on Genetic Neurodegenerative Diseases (6 papers), DNA Repair Mechanisms (2 papers) and CRISPR and Genetic Engineering (2 papers). M. Coerwinkel collaborates with scholars based in Netherlands, Germany and Canada. M. Coerwinkel's co-authors include Gert Jansen, Bé Wieringa, H. Hameister, Frank Oerlemans, H. Smeets, Cees J. A. van Echteld, Marleen Dekker, Lieve Vits, Anton Berns and Patrick J. Willems and has published in prestigious journals such as Nucleic Acids Research, Nature Genetics and Human Molecular Genetics.

In The Last Decade

M. Coerwinkel

12 papers receiving 640 citations

Peers

Countries citing papers authored by M. Coerwinkel

Since Specialization

Citations

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

Fields of papers citing papers by M. Coerwinkel

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M. Coerwinkel

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

All Works

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12 of 12 papers shown

#	Work	Indexed citations
1	Abnormal myotonic dystrophy protein kinase levels produce only mild myopathy in mice 1996 ·Nature Genetics ·Gert Jansen, Patricia J.T.A. Groenen, Dietmar Bächner, P. H. K. Jap, M. Coerwinkel, Frank Oerlemans, (unknown), Bärbel Gohlsch, Dirk Pette, Jaap J. Plomp, Peter Molenaar, Marcel G.J. Nederhoff, Cees J. A. van Echteld, Marleen Dekker, Anton Berns, H. Hameister, Bé Wieringa	250
2	Structural organization and developmental expression pattern of the mouse WD-repeat gene DMR-N9 immediately upstream of the myotonic dystrophy locus 1995 ·Human Molecular Genetics ·Gert Jansen, D. Bächner, M. Coerwinkel, (unknown), H. Hameister, Bé Wieringa	47
3	Gonosomal mosaicism in myotonic dystrophy patients: involvement of mitotic events in (CTG)n repeat variation and selection against extreme expansion in sperm. 1994 ·PubMed ·Gert Jansen, Patrick J. Willems, M. Coerwinkel, (unknown), H. Smeets, Lieve Vits, C Höweler, (unknown), Bé Wieringa	134
4	Characterization of the myotonic dystrophy region predicts multiple protein isoform–encoding mRNAs 1992 ·Nature Genetics ·Gert Jansen, Mani S. Mahadevan, Chris T. Amemiya, (unknown), Bart Segers, Wiljan Hendriks, Kim O'Hoy, Stephen Baird, Luc A. Sabourin, Greg Lennon, (unknown), David Iles, M. Coerwinkel, Marten H. Hofker, A.V. Carrano, Peter J. de Jong, (unknown), B. Wieringa	121
5	Mspl RFLP at 19q13.3 identified by the anonymous DNA sequence pX75B (D19S112) 1991 ·Nucleic Acids Research ·Rosella Hermens, M. Coerwinkel, (unknown), Hubert J.M. Smeets, Bé Wieringa	6
6	AnMspl RFLP detected by the human glandular kallikrein gene (hGK) on chromosome 19q 1990 ·Nucleic Acids Research ·Rosella Hermens, M. Coerwinkel, Jan Trapman, Peter Riegman, R.J. Vlietstra, Hubert J.M. Smeets, B. Wieringa	3
7	A long-range restriction map of the human chromosome 19q13 region: close physical linkage between CKMM and the ERCC1 and ERCC2 genes. 1990 ·PubMed ·H.J.M. Smeets, Linda L. Bachinski, M. Coerwinkel, Jan Schepens, Jan H.J. Hoeijmakers, Marcel van Duin, Karl‐Heinz Grzeschik, C.A. Weber, Peter J. de Jong, MJ Siciliano	38
8	TaqI RFLP at 19q13.1 identified by the anonymous DNA sequence p5B18 [D19S28] 1989 ·Nucleic Acids Research ·H. Smeets, Jan Schepens, M. Coerwinkel, HG Brunner, (unknown), H.-H. Ropers, Bé Wieringa	3
9	A locus at 19cen-19q13.2 (D19S15) containing three RFLPs linked to myotonic dystrophy (DM) is recognized by probe pJSB6 1987 ·Nucleic Acids Research ·Jan Schepens, Theo J.M. Hulsebos, H. Smeets, M. Coerwinkel, Han G. Brunner, Hans‐Hilger Ropers, Bé Wieringa	5
10	AMP deaminase deficiency: Study of the human skeletal muscle purine metabolism during ischaemic isometric exercise 1987 ·Clinical Science ·(unknown), R. A. Binkhorst, E.M.G. Joosten, Ron A. Wevers, M. Coerwinkel, T. L. Oei	22
11	Ischaemic exercise test in myoadenylate deaminase deficiency and McArdle's disease: measurement of plasma adenosine, inosine and hypoxanthine 1986 ·Clinical Science ·(unknown), E.M.G. Joosten, Ron A. Wevers, R. A. Binkhorst, Frank Oerlemans, Coen A. M. van Bennekom, M. Coerwinkel, T. L. Oei	17
12	pHW60, an anonymous single copy clone from the proximal portion of the long arm of chromosome 19 (HGM8 assignment no. D19S13) 1986 ·Nucleic Acids Research ·Theo J.M. Hulsebos, H Westphal, Richard M. Peek, M. Coerwinkel, B. Wieringa	5

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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