Wim Brussel

744 total citations
8 papers, 363 citations indexed

About

Wim Brussel is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Clinical Biochemistry. According to data from OpenAlex, Wim Brussel has authored 8 papers receiving a total of 363 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 2 papers in Pediatrics, Perinatology and Child Health and 2 papers in Clinical Biochemistry. Recurrent topics in Wim Brussel's work include Metabolism and Genetic Disorders (2 papers), Bone Metabolism and Diseases (1 paper) and Tuberous Sclerosis Complex Research (1 paper). Wim Brussel is often cited by papers focused on Metabolism and Genetic Disorders (2 papers), Bone Metabolism and Diseases (1 paper) and Tuberous Sclerosis Complex Research (1 paper). Wim Brussel collaborates with scholars based in Netherlands, United Kingdom and Austria. Wim Brussel's co-authors include Nurten Akarsu, Jacopo Celli, F Skovby, Ellen van Beusekom, Sevim Balcı, E. Ferda Perçin, Han G. Brunner, Hans van Bokhoven, Hülya Kayserili and Ron A. Wevers and has published in prestigious journals such as Nature Genetics, PEDIATRICS and BJOG An International Journal of Obstetrics & Gynaecology.

In The Last Decade

Wim Brussel

8 papers receiving 356 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Wim Brussel Netherlands	6	241	115	71	41	32	8	363
Marjan M. Nezarati Canada	10	232 1.0×	198 1.7×	26 0.4×	40 1.0×	23 0.7×	17	447
Gökhan Yigit Germany	11	207 0.9×	132 1.1×	40 0.6×	18 0.4×	40 1.3×	24	355
Maria Rosaria Piemontese Italy	12	248 1.0×	141 1.2×	23 0.3×	17 0.4×	111 3.5×	23	393
Eri Imagawa Japan	13	250 1.0×	170 1.5×	13 0.2×	26 0.6×	24 0.8×	30	418
Emma Hobson United Kingdom	9	213 0.9×	256 2.2×	23 0.3×	42 1.0×	30 0.9×	24	405
Mary Haddadin United States	6	210 0.9×	103 0.9×	60 0.8×	13 0.3×	24 0.8×	7	343
Hirofumi Ohashi Japan	11	198 0.8×	125 1.1×	16 0.2×	38 0.9×	24 0.8×	12	321
Anju Paudyal United Kingdom	10	325 1.3×	112 1.0×	24 0.3×	24 0.6×	95 3.0×	14	456
Marie‐Ange Delrue France	15	291 1.2×	258 2.2×	28 0.4×	34 0.8×	19 0.6×	30	590
Alka V. Ekbote India	7	136 0.6×	102 0.9×	17 0.2×	22 0.5×	11 0.3×	13	216

Countries citing papers authored by Wim Brussel

Since Specialization

Citations

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

Fields of papers citing papers by Wim Brussel

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Wim Brussel

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

All Works

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8 of 8 papers shown

Wentink, Marjolein, Mark Nellist, Marianne Hoogeveen‐Westerveld, et al.. (2011). Functional characterization of the TSC2 c.3598C>T (p.R1200W) missense mutation that co‐segregates with tuberous sclerosis complex in mildly affected kindreds. Clinical Genetics. 81(5). 453–461. 24 indexed citations

Ott, Claus‐Eric, Gundula Leschik, Louise Brueton, et al.. (2010). Deletions of the RUNX2 gene are present in about 10% of individuals with cleidocranial dysplasia. Human Mutation. 31(8). E1587–E1593. 58 indexed citations

Bech, Anneke, Karin C. Nabbe, Wim Brussel, Darryl Telting, & Hans de Boer. (2010). Elevated Fibroblast Growth Factor 23 Levels in a Newborn With Secondary Hypoparathyroidism. PEDIATRICS. 126(6). e1613–e1616. 3 indexed citations

Engelke, Udo F. H., Maria Tassini, Joussef Hayek, et al.. (2009). Guanidinoacetate methyltransferase (GAMT) deficiency diagnosed by proton NMR spectroscopy of body fluids. NMR in Biomedicine. 22(5). 538–544. 21 indexed citations

Brussel, Wim, André B. P. Kuilenburg, & Pim M.W. Janssens. (2006). A Neonate with Recurrent Vomiting and Generalized Hypotonia Diagnosed with a Deficiency of Dihydropyrimidine Dehydrogenase. Nucleosides Nucleotides & Nucleic Acids. 25(9-11). 1099–1102. 5 indexed citations

Benders, Manon J.N.L., et al.. (2006). Onset of vacuum-related complaints in neonates. European Journal of Pediatrics. 165(6). 374–379. 10 indexed citations

Krapels, Ingrid P.C., Iris A.L.M. van Rooij, Ron A. Wevers, et al.. (2004). Myo‐inositol, glucose and zinc status as risk factors for non‐syndromic cleft lip with or without cleft palate in offspring: a case–control study. BJOG An International Journal of Obstetrics & Gynaecology. 111(7). 661–668. 47 indexed citations

Bokhoven, Hans van, Jacopo Celli, Hülya Kayserili, et al.. (2000). Mutation of the gene encoding the ROR2 tyrosine kinase causes autosomal recessive Robinow syndrome. Nature Genetics. 25(4). 423–426. 195 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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