P.M. Grootscholten

2.1k total citations
15 papers, 1.4k citations indexed

About

P.M. Grootscholten is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, P.M. Grootscholten has authored 15 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 7 papers in Genetics and 2 papers in Surgery. Recurrent topics in P.M. Grootscholten's work include Muscle Physiology and Disorders (8 papers), Neurogenetic and Muscular Disorders Research (7 papers) and RNA modifications and cancer (5 papers). P.M. Grootscholten is often cited by papers focused on Muscle Physiology and Disorders (8 papers), Neurogenetic and Muscular Disorders Research (7 papers) and RNA modifications and cancer (5 papers). P.M. Grootscholten collaborates with scholars based in Netherlands, United Kingdom and United States. P.M. Grootscholten's co-authors include Johan T. den Dunnen, Egbert Bakker, P. Pearson, G J van Ommen, Christine Van Broeckhoven, Martin C. Wapenaar, Lau A.J. Blonden, H.B. Ginjaar, C.H.C.M. Buys and Hans Scheffer and has published in prestigious journals such as Nucleic Acids Research, Neurology and International Journal of Molecular Sciences.

In The Last Decade

P.M. Grootscholten

15 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
P.M. Grootscholten Netherlands	13	1.2k	517	272	268	222	15	1.4k
Bruce M. Wentworth United States	19	1.4k 1.1×	265 0.5×	236 0.9×	407 1.5×	255 1.1×	24	1.9k
Barbara C. Byth Canada	9	1.1k 0.9×	287 0.6×	167 0.6×	190 0.7×	131 0.6×	14	1.2k
Toshifumi Yokota Canada	21	1.2k 1.0×	304 0.6×	160 0.6×	294 1.1×	150 0.7×	47	1.3k
Lau A.J. Blonden Netherlands	12	727 0.6×	157 0.3×	172 0.6×	219 0.8×	54 0.2×	15	861
Anne E. Deconinck United States	12	1.7k 1.4×	125 0.2×	246 0.9×	289 1.1×	166 0.7×	12	1.8k
P N Ray Canada	13	643 0.5×	136 0.3×	102 0.4×	225 0.8×	83 0.4×	17	783
Terry Partridge United Kingdom	9	964 0.8×	304 0.6×	87 0.3×	203 0.8×	313 1.4×	15	1.2k
J. Rohwedel Germany	14	1.2k 1.0×	219 0.4×	177 0.7×	123 0.5×	635 2.9×	25	1.7k
Joseph X. DiMario United States	18	1.2k 0.9×	156 0.3×	170 0.6×	156 0.6×	206 0.9×	41	1.3k
David A. Hutcheson United States	10	1.5k 1.2×	359 0.7×	101 0.4×	179 0.7×	438 2.0×	15	1.7k

Countries citing papers authored by P.M. Grootscholten

Since Specialization

Citations

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

Fields of papers citing papers by P.M. Grootscholten

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of P.M. Grootscholten

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

All Works

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15 of 15 papers shown

Boer, Eddy N. de, Dennis Hendriksen, Bart Charbon, et al.. (2025). Nanopore Long-Read Sequencing as a First-Tier Diagnostic Test to Detect Repeat Expansions in Neurological Disorders. International Journal of Molecular Sciences. 26(7). 2850–2850. 1 indexed citations

Rump, Patrick, P.M. Grootscholten, Johanna M. Fock, et al.. (2005). A novel 3-bp deletion in the PANK2 gene of Dutch patients with pantothenate kinase-associated neurodegeneration: evidence for a founder effect. Neurogenetics. 6(4). 201–207. 14 indexed citations

Scheffer, Hans, Marjolein Visser, Gerrit van der Steege, et al.. (1996). Prenatal Prediction of SpinalMuscular Atrophy. European Journal of Human Genetics. 4(4). 231–236. 9 indexed citations

Grootscholten, P.M., J. M. Cobben, Stefania Zappata, et al.. (1996). Apparent gene conversions involving the SMN gene in the region of the spinal muscular atrophy locus on chromosome 5.. PubMed. 59(4). 834–8. 86 indexed citations

Grootscholten, P.M., et al.. (1995). A Provisional Transcript Map ofthe Spinal Muscular Atrophy(SMA) Critical Region. European Journal of Human Genetics. 3(2). 87–95. 25 indexed citations

Pasini, Barbara, Robert M.W. Hofstra, Ling Yin, et al.. (1995). The physical map of the human RET proto-oncogene.. PubMed. 11(9). 1737–43. 76 indexed citations

Cobben, J. M., Gerrit van der Steege, P.M. Grootscholten, et al.. (1995). Deletions of the survival motor neuron gene in unaffected siblings of patients with spinal muscular atrophy.. PubMed. 57(4). 805–8. 174 indexed citations

Dunnen, Johan T. den, P.M. Grootscholten, J.G. Dauwerse, et al.. (1992). Reconstruction of the 204 Mb human DMD-gene bhy homologous YAC recombination. Human Molecular Genetics. 1(1). 19–28. 66 indexed citations

Rapaport, Debora, Doron Lederfein, Johan T. den Dunnen, et al.. (1992). Characterization and cell type distribution of a novel, major transcript of the Duchenne Muscular Dystrophy gene. Differentiation. 49(3). 187–193. 62 indexed citations

10.

Bakker, Egbert, H Veenema, Johan T. den Dunnen, et al.. (1989). Prenatal diagnosis of Duchenne muscular dystrophy: A three‐year experience in a rapidly evolving field. Journal of Inherited Metabolic Disease. 12(S1). 174–190. 16 indexed citations

11.

Blonden, Lau A.J., Johan T. den Dunnen, Martin C. Wapenaar, et al.. (1989). High resoluation deletion breakpoint mapping in the DMD gene by whole cosmid hybridization. Nucleic Acids Research. 17(14). 5611–5621. 52 indexed citations

12.

Gospe, Sídney M., Reynaldo P. Lazaro, Neil Lava, et al.. (1989). Familial X‐linked myalgia and cramps. Neurology. 39(10). 1277–1277. 115 indexed citations

13.

Dunnen, Johan T. den, P.M. Grootscholten, Egbert Bakker, et al.. (1989). Topography of the Duchenne muscular dystrophy (DMD) gene: FIGE and cDNA analysis of 194 cases reveals 115 deletions and 13 duplications.. PubMed. 45(6). 835–47. 438 indexed citations

14.

Bakker, Egbert, H Veenema, Johan T. den Dunnen, et al.. (1989). Germinal mosaicism increases the recurrence risk for 'new' Duchenne muscular dystrophy mutations.. Journal of Medical Genetics. 26(9). 553–559. 153 indexed citations

15.

Wapenaar, Martin C., Tim Kievits, K Hart, et al.. (1988). A deletion hot spot in the Duchenne muscular dystrophy gene. Genomics. 2(2). 101–108. 99 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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