J. van Reeuwijk

625 total citations
6 papers, 446 citations indexed

About

J. van Reeuwijk is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Ophthalmology. According to data from OpenAlex, J. van Reeuwijk has authored 6 papers receiving a total of 446 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 2 papers in Cardiology and Cardiovascular Medicine and 1 paper in Ophthalmology. Recurrent topics in J. van Reeuwijk's work include Muscle Physiology and Disorders (3 papers), Cardiomyopathy and Myosin Studies (2 papers) and Signaling Pathways in Disease (2 papers). J. van Reeuwijk is often cited by papers focused on Muscle Physiology and Disorders (3 papers), Cardiomyopathy and Myosin Studies (2 papers) and Signaling Pathways in Disease (2 papers). J. van Reeuwijk collaborates with scholars based in Netherlands, United States and Italy. J. van Reeuwijk's co-authors include Hans van Bokhoven, HG Brunner, Marika Pane, Hans Scheffer, Maria G. van Pampus, Angela Berardinelli, Filippo M. Santorelli, Christa van den Elzen, Alessandra Tessa and Adele D’Amico and has published in prestigious journals such as SHILAP Revista de lepidopterología, Journal of Medical Genetics and Clinical Genetics.

In The Last Decade

J. van Reeuwijk

5 papers receiving 441 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
J. van Reeuwijk Netherlands	5	399	83	77	72	52	6	446
Chris Esapa United Kingdom	8	271 0.7×	48 0.6×	57 0.7×	92 1.3×	34 0.7×	9	320
Hülya Gündeşli Türkiye	7	343 0.9×	75 0.9×	124 1.6×	38 0.5×	32 0.6×	12	417
Anna Corrionero Spain	5	426 1.1×	35 0.4×	20 0.3×	49 0.7×	17 0.3×	6	520
Ashley N. Randle United States	11	187 0.5×	35 0.4×	89 1.2×	148 2.1×	218 4.2×	17	365
Victoria J. McCurdy United States	10	169 0.4×	29 0.3×	81 1.1×	139 1.9×	195 3.8×	12	331
Gerolamo Lanfranchi Italy	8	361 0.9×	44 0.5×	79 1.0×	25 0.3×	94 1.8×	9	423
Brandon L. Brunson United States	12	171 0.4×	17 0.2×	74 1.0×	121 1.7×	220 4.2×	15	385
Darren Murrey United States	11	226 0.6×	39 0.5×	49 0.6×	105 1.5×	133 2.6×	13	351
Dashou Wang United States	7	237 0.6×	36 0.4×	96 1.2×	64 0.9×	96 1.8×	9	433
Dawn H. Catino United States	9	366 0.9×	89 1.1×	120 1.6×	63 0.9×	97 1.9×	9	503

Countries citing papers authored by J. van Reeuwijk

Since Specialization

Citations

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

Fields of papers citing papers by J. van Reeuwijk

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by J. van Reeuwijk. 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 J. van Reeuwijk. The network helps show where J. van Reeuwijk may publish in the future.

Co-authorship network of co-authors of J. van Reeuwijk

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

All Works

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6 of 6 papers shown

1.

Boldt, Karsten, Jungyeon Won, J. van Reeuwijk, et al.. (2012). Disruption of intraflagellar protein transport in photoreceptor cilia causes Leber congenital amaurosis in humans and mice. SHILAP Revista de lepidopterología. 1(S1). 4 indexed citations

2.

Reeuwijk, J. van, Christa van den Elzen, O.F. Brouwer, et al.. (2010). A homozygous FKRP start codon mutation is associated with Walker–Warburg syndrome, the severe end of the clinical spectrum. Clinical Genetics. 78(3). 275–281. 31 indexed citations

3.

Kornak, Uwe, Ellen Reynders, Aikaterini Dimopoulou, et al.. (2008). Mutations in the a2-subunit of the v-type H+-ATPase impair Golgi function and cause a novel congenital disorder of glycosylation with cutix laxa. Medizinische Genetik. 20(1).

4.

Mercuri, Eugenio, Adele D’Amico, Alessandra Tessa, et al.. (2006). POMT2 mutation in a patient with ‘MEB-like’ phenotype. Neuromuscular Disorders. 16(7). 446–448. 34 indexed citations

5.

Reeuwijk, J. van, et al.. (2005). POMT2 mutations cause α-dystroglycan hypoglycosylation and Walker-Warburg syndrome. Journal of Medical Genetics. 42(12). 907–912. 305 indexed citations

6.

Reeuwijk, J. van, HG Brunner, & Hans van Bokhoven. (2004). Glyc‐O‐genetics of Walker–Warburg syndrome. Clinical Genetics. 67(4). 281–289. 72 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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