B. Wieringa

2.4k total citations
43 papers, 2.0k citations indexed

About

B. Wieringa is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Cell Biology. According to data from OpenAlex, B. Wieringa has authored 43 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Molecular Biology, 11 papers in Cellular and Molecular Neuroscience and 7 papers in Cell Biology. Recurrent topics in B. Wieringa's work include Genetic Neurodegenerative Diseases (9 papers), RNA Research and Splicing (5 papers) and DNA Repair Mechanisms (4 papers). B. Wieringa is often cited by papers focused on Genetic Neurodegenerative Diseases (9 papers), RNA Research and Splicing (5 papers) and DNA Repair Mechanisms (4 papers). B. Wieringa collaborates with scholars based in Netherlands, United States and Germany. B. Wieringa's co-authors include Charles Weissmann, Erhard Hofer, P. H. K. Jap, H.-H. Ropers, Frank Oerlemans, Jakob Reiser, Thomas D. Kühne, Marten H. Hofker, Joost Schalkwijk and H.O.F. Molhuizen and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

B. Wieringa

43 papers receiving 1.9k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
B. Wieringa Netherlands 24 1.5k 451 304 299 277 43 2.0k
Gregory L. Bennett United States 17 943 0.6× 494 1.1× 149 0.5× 242 0.8× 448 1.6× 21 2.3k
Karl‐Heinz Grzeschik Germany 17 1.4k 0.9× 388 0.9× 542 1.8× 233 0.8× 268 1.0× 25 1.9k
Julie M. Rochelle United States 23 924 0.6× 470 1.0× 207 0.7× 232 0.8× 105 0.4× 38 1.7k
Yanmin Yang United States 20 1.2k 0.8× 478 1.1× 156 0.5× 1.0k 3.4× 125 0.5× 31 2.1k
Fabrizio G. Mastronardi Canada 21 1.3k 0.9× 223 0.5× 310 1.0× 172 0.6× 160 0.6× 32 3.0k
David Goudie United Kingdom 25 1.2k 0.8× 441 1.0× 663 2.2× 325 1.1× 69 0.2× 69 2.6k
Martin C. Wapenaar Netherlands 24 1.4k 0.9× 208 0.5× 724 2.4× 151 0.5× 254 0.9× 45 2.2k
Vittorio Enrico Avvedimento Italy 25 1.1k 0.7× 179 0.4× 352 1.2× 130 0.4× 67 0.2× 53 1.9k
Richard C. Stahl United States 29 842 0.6× 428 0.9× 229 0.8× 579 1.9× 121 0.4× 42 1.7k
C. Jimenez‐Mallebrera Spain 25 1.5k 0.9× 256 0.6× 177 0.6× 303 1.0× 273 1.0× 78 1.9k

Countries citing papers authored by B. Wieringa

Since Specialization
Citations

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

Fields of papers citing papers by B. Wieringa

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of B. Wieringa

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

All Works

20 of 20 papers shown
1.
Düfer, Martina, et al.. (2007). An adenylate kinase is involved in KATP channel regulation of mouse pancreatic beta cells. Diabetologia. 50(10). 2126–2134. 23 indexed citations
2.
Katz, Abram, Daniel Andersson, Barbara Norman, et al.. (2003). Contraction‐mediated glycogenolysis in mouse skeletal muscle lacking creatine kinase: the role of phosphorylase b activation. The Journal of Physiology. 553(2). 523–531. 16 indexed citations
3.
Wansink, Derick G. & B. Wieringa. (2003). Transgenic mouse models for myotonic dystrophy type 1 (DM1). Cytogenetic and Genome Research. 100(1-4). 230–242. 25 indexed citations
4.
Zandt, René in ‘t, Frank Oerlemans, B. Wieringa, & Arend Heerschap. (1999). Effects of ischemia on skeletal muscle energy metabolism in mice lacking creatine kinase monitored byin vivo31P nuclear magnetic resonance spectroscopy. NMR in Biomedicine. 12(6). 327–334. 31 indexed citations
5.
Braber, Anouk den, Jan Schepens, Marga Schepens, et al.. (1999). Assignment<footref rid="foot01"><sup>1</sup></footref> of the PTP-SL/PTPBR7 gene (<i>Ptprr</i>/PTPRR) to mouse chromosome region 8A2 by in situ hybridization. Cytogenetic and Genome Research. 84(3-4). 243–244. 6 indexed citations
6.
Steeghs, Karen, A. Heerschap, A. de Haan, et al.. (1997). Use of gene targeting for compromising energy homeostasis in neuro-muscular tissues: The role of sarcomeric mitochondrial creatine kinase. Journal of Neuroscience Methods. 71(1). 29–41. 44 indexed citations
7.
Maagdenberg, Arn M. J. M. van den, D. Olde Weghuis, J.P.L. Rijss, et al.. (1996). The gene (PTPN13) encoding the protein tyrosine phosphatase PTP-BL/PTP-BAS is located in mouse chromosome region 5E/F and human chromosome region 4q21. Cytogenetic and Genome Research. 74(1-2). 153–155. 8 indexed citations
8.
9.
Sistermans, Erik A., et al.. (1995). Tissue- and cell-specific distribution of creatine kinase B: A new and highly specific monoclonal antibody for use in immunohistochemistry. Cell and Tissue Research. 280(2). 435–446. 53 indexed citations
10.
Kok, Yvette J.M. de, M.P.A. Geurds, Erik A. Sistermans, et al.. (1995). Production of native creatine kinase B in insect cells using a baculovirus expression vector. Molecular and Cellular Biochemistry. 143(1). 59–65. 6 indexed citations
11.
Deen, Peter M.T., D. Olde Weghuis, Ad Geurts van Kessel, B. Wieringa, & C.H. van Os. (1994). The human gene for water channel aquaporin 1 (AQP1) is localized on chromosome 7p15→p14. Cytogenetic and Genome Research. 65(4). 243–246. 16 indexed citations
12.
13.
Wieringa, B.. (1994). COMMENTARY: Myotonic dystrophy reviewed: back to the future?. Human Molecular Genetics. 3(1). 1–7. 70 indexed citations
14.
Deursen, Jan van, P. H. K. Jap, A. Heerschap, et al.. (1994). Effects of the creatine analogue β-guanidinopropionic acid on skeletal muscles of mice deficient in muscle creatine kinase. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1185(3). 327–335. 35 indexed citations
15.
Jansen, Gert, Mani S. Mahadevan, Chris T. Amemiya, et al.. (1992). Characterization of the myotonic dystrophy region predicts multiple protein isoform–encoding mRNAs. Nature Genetics. 1(4). 261–266. 121 indexed citations
16.
Smeets, H.J.M., Rosella Hermens, Han G. Brunner, Hans‐Hilger Ropers, & B. Wieringa. (1991). Identification of variable simple sequence motifs in 19q13.2-qter: Markers for the myotonic dystrophy locus. Genomics. 9(2). 257–263. 30 indexed citations
17.
Brunner, Han G., et al.. (1989). A multipoint linkage map around the locus for myotonic dystrophy on chromosome 19. Genomics. 5(3). 589–595. 45 indexed citations
18.
Dijk, Peter R. van, et al.. (1989). Regional localization of the gene encoding pregnancy specific beta-1-glycoprotein 1 (PSBG1) to human chromosome 19q13.1. Cytogenetic and Genome Research. 52(1-2). 95–97. 8 indexed citations
19.
Cremers, Frans P.M., Frank Brunsmann, T.J.R. van de Pol, et al.. (1987). Deletion of the DXS165 locus in patients with classical Choroideremia. Clinical Genetics. 32(6). 421–423. 28 indexed citations
20.
Hulsebos, Theo J.M., B. Wieringa, Ron Hochstenbach, et al.. (1986). Toward early diagnosis of myotonic dystrophy:construction and characterization of a somatic cell hybrid with a single human der(19) chromosome. Cytogenetic and Genome Research. 43(1-2). 47–56. 30 indexed citations

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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