H.B. Ginjaar

2.3k total citations
37 papers, 1.6k citations indexed

About

H.B. Ginjaar is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, H.B. Ginjaar has authored 37 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Molecular Biology, 11 papers in Cellular and Molecular Neuroscience and 10 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in H.B. Ginjaar's work include Muscle Physiology and Disorders (28 papers), Genetic Neurodegenerative Diseases (11 papers) and Cardiomyopathy and Myosin Studies (10 papers). H.B. Ginjaar is often cited by papers focused on Muscle Physiology and Disorders (28 papers), Genetic Neurodegenerative Diseases (11 papers) and Cardiomyopathy and Myosin Studies (10 papers). H.B. Ginjaar collaborates with scholars based in Netherlands, United Kingdom and United States. H.B. Ginjaar's co-authors include Johan T. den Dunnen, Egbert Bakker, P. Pearson, Martin C. Wapenaar, P.M. Grootscholten, Lau A.J. Blonden, Annemieke Aartsma‐Rus, Christine Van Broeckhoven, G J van Ommen and G.J.B. van Ommen and has published in prestigious journals such as Nucleic Acids Research, Brain and Neurology.

In The Last Decade

H.B. Ginjaar

36 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
H.B. Ginjaar Netherlands	20	1.4k	468	397	286	272	37	1.6k
K. Bushby United Kingdom	20	1.4k 1.0×	371 0.8×	303 0.8×	265 0.9×	170 0.6×	49	1.6k
Sylvie Tuffery‐Giraud France	26	1.2k 0.9×	221 0.5×	432 1.1×	269 0.9×	307 1.1×	72	2.0k
Giuliana Galluzzi Italy	19	1.4k 1.0×	411 0.9×	331 0.8×	306 1.1×	153 0.6×	26	1.6k
Rita C.M. Pavanello Brazil	18	899 0.6×	254 0.5×	303 0.8×	210 0.7×	154 0.6×	50	1.0k
Glen B. Banks United States	21	1.0k 0.7×	163 0.3×	235 0.6×	127 0.4×	207 0.8×	28	1.2k
Karine Nguyen France	19	954 0.7×	243 0.5×	337 0.8×	235 0.8×	178 0.7×	59	1.3k
C.S.M. Straathof Netherlands	18	728 0.5×	213 0.5×	154 0.4×	250 0.9×	78 0.3×	35	1.1k
Maria Luisa Mostacciuolo Italy	22	764 0.5×	240 0.5×	521 1.3×	184 0.6×	125 0.5×	48	1.2k
Jill A. Rafael United States	21	2.7k 1.9×	572 1.2×	475 1.2×	240 0.8×	491 1.8×	25	2.9k
Andrew Weir United Kingdom	6	886 0.6×	156 0.3×	159 0.4×	75 0.3×	110 0.4×	8	1.1k

Countries citing papers authored by H.B. Ginjaar

Since Specialization

Citations

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

Fields of papers citing papers by H.B. Ginjaar

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of H.B. Ginjaar

This figure shows the co-authorship network connecting the top 25 collaborators of H.B. Ginjaar. A scholar is included among the top collaborators of H.B. Ginjaar 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 H.B. Ginjaar. H.B. Ginjaar 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

Stunnenberg, Bas C., Joost Raaphorst, Johanna C.W. Deenen, et al.. (2018). Prevalence and mutation spectrum of skeletal muscle channelopathies in the Netherlands. Neuromuscular Disorders. 28(5). 402–407. 40 indexed citations

Bergen, J.C. van den, H.B. Ginjaar, E. Niks, Annemieke Aartsma‐Rus, & Jan J.G.M. Verschuuren. (2014). Prolonged Ambulation in Duchenne Patients with a Mutation Amenable to Exon 44 Skipping. Journal of Neuromuscular Diseases. 1(1). 91–94. 38 indexed citations

Bergen, J.C. van den, H.B. Ginjaar, A.J. van Essen, et al.. (2014). Forty-Five Years of Duchenne Muscular Dystrophy in The Netherlands. Journal of Neuromuscular Diseases. 1(1). 99–109. 41 indexed citations

Bergen, J.C. van den, Beatrijs Wokke, Annika Janson, et al.. (2013). Dystrophin levels and clinical severity in Becker muscular dystrophy patients. Journal of Neurology Neurosurgery & Psychiatry. 85(7). 747–753. 94 indexed citations

Bergen, J.C. van den, Lukas Dekker, Anneke J. van der Kooi, et al.. (2013). Clinical characterisation of Becker muscular dystrophy patients predicts favourable outcome in exon-skipping therapy. Journal of Neurology Neurosurgery & Psychiatry. 85(1). 92–98. 27 indexed citations

Wokke, Beatrijs, Sjoerd G. van Duinen, H.B. Ginjaar, et al.. (2012). G.P.76 Dystrophin levels do not influence disease progression in Becker muscular dystrophy patients with an exon 45–47 deletion. Neuromuscular Disorders. 22(9-10). 834–835. 2 indexed citations

Straathof, C.S.M., Annemieke Aartsma‐Rus, Johan T. den Dunnen, et al.. (2010). Becker muscular dystrophy patients with deletions around exon 51; a promising outlook for exon skipping therapy in Duchenne patients. Neuromuscular Disorders. 20(4). 251–254. 52 indexed citations

Trip, J., Gea Drost, H.B. Ginjaar, et al.. (2009). Redefining the clinical phenotypes of non-dystrophic myotonic syndromes. Journal of Neurology Neurosurgery & Psychiatry. 80(6). 647–652. 73 indexed citations

Stunnenberg, Bas C., H.B. Ginjaar, J. Trip, et al.. (2009). Isolated eyelid closure myotonia in two families with sodium channel myotonia. Neurogenetics. 11(2). 257–260. 20 indexed citations

10.

Alfen, Nens van, et al.. (2008). Thought Ripples on Muscle Waves: Recognition of Rippling Muscle Disease. Neuropediatrics. 39(2). 116–118. 1 indexed citations

11.

White, Stefan J., Annemieke Aartsma‐Rus, Kevin M. Flanigan, et al.. (2006). Duplications in theDMD gene. Human Mutation. 27(9). 938–945. 113 indexed citations

12.

Macaya, Alfons, Noèlia Fernàndez‐Castillo, José Antonio Arranz, et al.. (2005). Molybdenum Cofactor Deficiency Presenting as Neonatal Hyperekplexia: A Clinical, Biochemical and Genetic Study. Neuropediatrics. 36(6). 389–394. 21 indexed citations

13.

Ginjaar, H.B., et al.. (2003). Somatic mosaicism of a point mutation in the dystrophin gene in a patient presenting with an asymmetrical muscle weakness and contractures. Neuromuscular Disorders. 13(4). 317–321. 7 indexed citations

14.

Peelen, Tamara, Hans Morreau, Ronald van Eijk, et al.. (2000). Genetic analysis of a breast-ovarian cancer family, with 7 cases of colorectal cancer linked toBRCA1, fails to support a role forBRCA1 in colorectal tumorigenesis. International Journal of Cancer. 88(5). 778–782. 10 indexed citations

15.

Kooi, Anneke J. van der, H.B. Ginjaar, H. F. M. Busch, et al.. (1998). Limb girdle muscular dystrophy: A pathological and immunohistochemical reevaluation. Muscle & Nerve. 21(5). 584–590. 11 indexed citations

16.

Roest, Pauline A.M., H.B. Ginjaar, Rob C. Hoeben, et al.. (1996). Application of in vitro myo-differentiation of non-muscle cells to enhance gene expression and facilitate analysis of muscle proteins. Neuromuscular Disorders. 6(3). 195–202. 21 indexed citations

17.

Kooi, Anneke J. van der, P. G. Barth, H. F. M. Busch, et al.. (1996). The clinical spectrum of limb girdle muscular dystrophy A survey in the Netherlands. Brain. 119(5). 1471–1480. 67 indexed citations

18.

Ginjaar, H.B., Johan T. den Dunnen, Nguyen thi Man, et al.. (1992). Construction of dystrophin fusion proteins to raise targeted antibodies to different epitopes. FEBS Letters. 308(3). 293–297. 3 indexed citations

19.

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

20.

Ommen, G.J.B. van, Corlee J. Bertelson, H.B. Ginjaar, et al.. (1987). Long-range genomic map of the Duchenne muscular dystrophy (DMD) gene: Isolation and use of J66 (DXS268), a distal intragenic marker. Genomics. 1(4). 329–336. 56 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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