Karin Huijben

2.1k total citations
18 papers, 594 citations indexed

About

Karin Huijben is a scholar working on Molecular Biology, Physiology and Organic Chemistry. According to data from OpenAlex, Karin Huijben has authored 18 papers receiving a total of 594 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 6 papers in Physiology and 5 papers in Organic Chemistry. Recurrent topics in Karin Huijben's work include Glycosylation and Glycoproteins Research (14 papers), Carbohydrate Chemistry and Synthesis (5 papers) and Lysosomal Storage Disorders Research (5 papers). Karin Huijben is often cited by papers focused on Glycosylation and Glycoproteins Research (14 papers), Carbohydrate Chemistry and Synthesis (5 papers) and Lysosomal Storage Disorders Research (5 papers). Karin Huijben collaborates with scholars based in Netherlands, United States and Belgium. Karin Huijben's co-authors include Ron A. Wevers, Éva Morava, Suzan Wopereis, Dirk J. Lefeber, Stephanie Grünewald, Johannes Penzien, Paz Briones, M.T. García‐Silva, Gert Matthijs and Pierre N.M. Demacker and has published in prestigious journals such as Nature Communications, Annals of Neurology and International Journal of Molecular Sciences.

In The Last Decade

Karin Huijben

18 papers receiving 582 citations

Peers

Karin Huijben

IMMUN

PHYSI

GENET

Martin Hasilik Germany

Romain Péanne Belgium

Maïlys Guillard Netherlands

Daisy Rymen Belgium

Christina Lam United States

T Orii Japan

Marielle Boonen Belgium

Harold H. Harrison United States

Mei-Shiue Kuo France

C J Pan United States

Martin Hasilik Germany

Karin Huijben

531 ×1.1

192 ×1.1

IMMUN

231 ×1.5

146 ×1.2

PHYSI

77 ×0.6

GENET

Citations per year, relative to Karin Huijben Karin Huijben (= 1×) peers Martin Hasilik

Countries citing papers authored by Karin Huijben

Since Specialization

Citations

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

Fields of papers citing papers by Karin Huijben

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Karin Huijben

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

All Works

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18 of 18 papers shown

Huijben, Karin, Fokje Zijlstra, Joannes F.M. Jacobs, et al.. (2023). Glycoproteomics in Cerebrospinal Fluid Reveals Brain-Specific Glycosylation Changes. International Journal of Molecular Sciences. 24(3). 1937–1937. 11 indexed citations

Conte, Federica, Angel Ashikov, Monique van Scherpenzeel, et al.. (2023). In Vitro Skeletal Muscle Model of PGM1 Deficiency Reveals Altered Energy Homeostasis. International Journal of Molecular Sciences. 24(9). 8247–8247. 6 indexed citations

Linders, Peter, Angel Ashikov, Mari‐Anne Vals, et al.. (2021). Congenital disorder of glycosylation caused by starting site-specific variant in syntaxin-5. Nature Communications. 12(1). 6227–6227. 16 indexed citations

Jansen, Jos C., Bart van Hoek, Herold J. Metselaar, et al.. (2020). Screening for abnormal glycosylation in a cohort of adult liver disease patients. Journal of Inherited Metabolic Disease. 43(6). 1310–1320. 8 indexed citations

Michelakakis, Helen, Peter Van den Bergh, Marina Moraitou, et al.. (2019). Toward understanding tissue‐specific symptoms in dolichol‐phosphate‐mannose synthesis disorders; insight from DPM3‐CDG. Journal of Inherited Metabolic Disease. 42(5). 984–992. 9 indexed citations

Timal, Sharita, Alexander Hoischen, Ludwig Lehle, et al.. (2012). Gene identification in the congenital disorders of glycosylation type I by whole-exome sequencing. Human Molecular Genetics. 21(19). 4151–4161. 122 indexed citations

Grinten, Hedi L. Claahsen‐van der, Antonius E. van Herwaarden, Karin Huijben, et al.. (2012). Thyroid function in PMM2-CDG: Diagnostic approach and proposed management. Molecular Genetics and Metabolism. 105(4). 681–683. 11 indexed citations

Huijben, Karin, et al.. (2011). A novel C2 transferrin variant interfering with the analysis of carbohydrate-deficient transferrin. Clinica Chimica Acta. 412(17-18). 1683–1685. 12 indexed citations

Morava, Éva, Renate Zeevaert, Eckhard Korsch, et al.. (2007). A common mutation in the COG7 gene with a consistent phenotype including microcephaly, adducted thumbs, growth retardation, VSD and episodes of hyperthermia. European Journal of Human Genetics. 15(6). 638–645. 81 indexed citations

10.

Wopereis, Suzan, Umi Marshida Abd Hamid, Louise Royle, et al.. (2006). Abnormal glycosylation with hypersialylated O-glycans in patients with Sialuria. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1762(6). 598–607. 24 indexed citations

11.

Wopereis, Suzan, Stephanie Grünewald, Karin Huijben, et al.. (2006). Transferrin and Apolipoprotein C-III Isofocusing Are Complementary in the Diagnosis of N- and O-Glycan Biosynthesis Defects. Clinical Chemistry. 53(2). 180–187. 47 indexed citations

12.

Wopereis, Suzan, Éva Morava, Stephanie Grünewald, et al.. (2005). Patients with unsolved congenital disorders of glycosylation type II can be subdivided in six distinct biochemical groups. Glycobiology. 15(12). 1312–1319. 23 indexed citations

13.

Wopereis, Suzan, Éva Morava, Stephanie Grünewald, et al.. (2004). A combined defect in the biosynthesis of N- and O-glycans in patients with cutis laxa and neurological involvement: the biochemical characteristics. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1741(1-2). 156–164. 27 indexed citations

14.

Morava, Éva, et al.. (2004). Screening for CDG type Ia in Joubert syndrome.. PubMed. 10(8). CR469–72. 12 indexed citations

15.

Wopereis, Suzan, Stephanie Grünewald, Éva Morava, et al.. (2003). Apolipoprotein C-III Isofocusing in the Diagnosis of Genetic Defects in O-Glycan Biosynthesis. Clinical Chemistry. 49(11). 1839–1845. 108 indexed citations

16.

Huijben, Karin, et al.. (2002). Hemolytic Uremic Syndrome Attributable to Streptococcus pneumoniae Infection: A Novel Cause for Secondary Protein N-Glycan Abnormalities. Clinical Chemistry. 48(5). 781–784. 16 indexed citations

17.

Imbach, Timo, Karin Huijben, M. Estela Rubio‐Gozalbo, et al.. (2000). Clinical and biochemical characteristics of congenital disorder of glycosylation type Ic, the first recognized endoplasmic reticulum defect in N-glycan synthesis. Annals of Neurology. 47(6). 776–781. 60 indexed citations

18.

Vreken, P., H. P. Rusch, Karin Huijben, & Ron A. Wevers. (1998). Anion‐exchange chromatography versus isoelectric focusing of transferrin in diagnosing the carbohydrate‐deficient glycoprotein syndrome. Journal of Inherited Metabolic Disease. 21(4). 447–448. 1 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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