Arjan de Brouwer

810 total citations
5 papers, 105 citations indexed

About

Arjan de Brouwer is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Arjan de Brouwer has authored 5 papers receiving a total of 105 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 2 papers in Genetics and 1 paper in Pediatrics, Perinatology and Child Health. Recurrent topics in Arjan de Brouwer's work include RNA modifications and cancer (2 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Glycosylation and Glycoproteins Research (1 paper). Arjan de Brouwer is often cited by papers focused on RNA modifications and cancer (2 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Glycosylation and Glycoproteins Research (1 paper). Arjan de Brouwer collaborates with scholars based in Netherlands, Germany and Australia. Arjan de Brouwer's co-authors include Jan Wijnholds, Roelof Ottenhoff, Martin A. van der Valk, Jos H. Beijnen, Anita W. Rijneveld, Ronald P.J. Oude Elferink, Ardy van Helvoort, Tom van der Poll, Piet Borst and Wim F. Voorhout and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Journal of Pediatrics and European Journal of Human Genetics.

In The Last Decade

Arjan de Brouwer

5 papers receiving 105 citations

Peers

Arjan de Brouwer

MB

SURGE

GENET

CR

ONCOL

Danny Létourneau Canada

Guangsuo Xing China

Sebastian Brachtendorf Germany

Navratan Bagwan Spain

Xiazhou Fu China

Mariya Kozenko Canada

Deepthi Telikicherla India

Sarah Pollock United States

Min Qiao China

Danny Létourneau Canada

Arjan de Brouwer

121 ×1.6

MB

33 ×1.6

SURGE

9 ×0.5

GENET

14 ×0.9

CR

16 ×1.1

ONCOL

Citations per year, relative to Arjan de Brouwer Arjan de Brouwer (= 1×) peers Danny Létourneau

Countries citing papers authored by Arjan de Brouwer

Since Specialization

Citations

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

Fields of papers citing papers by Arjan de Brouwer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Arjan de Brouwer. 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 Arjan de Brouwer. The network helps show where Arjan de Brouwer may publish in the future.

Co-authorship network of co-authors of Arjan de Brouwer

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

All Works

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5 of 5 papers shown

1.

Hendriks, Wiljan, N. Bakker, Helma Pluk, et al.. (2019). Certainty-based marking in a formative assessment improves student course appreciation but not summative examination scores. BMC Medical Education. 19(1). 178–178. 7 indexed citations

2.

Guillard, Maïlys, Éva Morava, Tony Roscioli, et al.. (2011). B4GALT1-Congenital Disorders of Glycosylation Presents as a Non-Neurologic Glycosylation Disorder with Hepatointestinal Involvement. The Journal of Pediatrics. 159(6). 1041–1043.e2. 15 indexed citations

3.

Parkel, Sven, Olga Žilina, Priit Palta, et al.. (2007). Screening of 20 patients with X-linked mental retardation using chromosome X-specific array-MAPH. European Journal of Medical Genetics. 50(6). 399–410. 5 indexed citations

4.

Chen, Wei, Lars Riff Jensen, Jozef Gécz, et al.. (2006). Mutation screening of brain-expressed X-chromosomal miRNA genes in 464 patients with nonsyndromic X-linked mental retardation. European Journal of Human Genetics. 15(3). 375–378. 19 indexed citations

5.

Helvoort, Ardy van, Arjan de Brouwer, Roelof Ottenhoff, et al.. (1999). Mice without phosphatidylcholine transfer protein have no defects in the secretion of phosphatidylcholine into bile or into lung airspaces. Proceedings of the National Academy of Sciences. 96(20). 11501–11506. 59 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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