Wim Terryn

1.6k total citations
16 papers, 432 citations indexed

About

Wim Terryn is a scholar working on Rheumatology, Physiology and Pathology and Forensic Medicine. According to data from OpenAlex, Wim Terryn has authored 16 papers receiving a total of 432 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Rheumatology, 7 papers in Physiology and 5 papers in Pathology and Forensic Medicine. Recurrent topics in Wim Terryn's work include Lysosomal Storage Disorders Research (7 papers), Glycogen Storage Diseases and Myoclonus (5 papers) and Cellular transport and secretion (3 papers). Wim Terryn is often cited by papers focused on Lysosomal Storage Disorders Research (7 papers), Glycogen Storage Diseases and Myoclonus (5 papers) and Cellular transport and secretion (3 papers). Wim Terryn collaborates with scholars based in Belgium, Spain and France. Wim Terryn's co-authors include Raymond Vanholder, Norbert Lameire, Bruce Poppe, Patrick Peeters, Alberto Ortíz, Wim Van Biesen, Gert De Schoenmakere, Christoph Wanner, Birgitte Wuyts and Kathleen Claes and has published in prestigious journals such as American Journal of Kidney Diseases, Medicine and Nephrology Dialysis Transplantation.

In The Last Decade

Wim Terryn

15 papers receiving 425 citations

Peers

Wim Terryn

PHYSI

EPIDE

RHEUM

Stefanie Reiermann Germany

Jean-Claude Lubanda Czechia

Martina Gaggl Austria

Roshni Vara United Kingdom

Mitsuhiro Abe Japan

Ryuji Okamura Japan

Einar Skulstad Davidsen Norway

Naziha Kaabachi Tunisia

Anwar Al‐Awadhi Kuwait

Anil Bhansali India

Stefanie Reiermann Germany

Wim Terryn

178 ×0.6

PHYSI

73 ×0.5

EPIDE

63 ×0.5

RHEUM

71 ×0.9

45 ×0.7

Citations per year, relative to Wim Terryn Wim Terryn (= 1×) peers Stefanie Reiermann

Countries citing papers authored by Wim Terryn

Since Specialization

Citations

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

Fields of papers citing papers by Wim Terryn

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Wim Terryn

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

All Works

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16 of 16 papers shown

Terryn, Wim, et al.. (2024). INTERMEDIATE UVEITIS IN COMMON VARIABLE IMMUNODEFICIENCY ASSOCIATED WITH A HETEROZYGOUS VARIANT IN THE TNFRSF13B GENE. Retinal Cases & Brief Reports. 19(5). 644–646.

Germain, Dominique P., Gheona Altarescu, Roberto Barriales‐Villa, et al.. (2022). An expert consensus on practical clinical recommendations and guidance for patients with classic Fabry disease. Molecular Genetics and Metabolism. 137(1-2). 49–61. 60 indexed citations

Mulder, Pieter De, Kristof Cokelaere, & Wim Terryn. (2020). Chronic intestinal pseudo-obstruction due to β2microglobulin-amyloidosis in a patient on high-flux haemodialysis. BMJ Case Reports. 13(1). e232201–e232201. 1 indexed citations

Steyaert, Wouter, Steven Callens, Paul Coucke, et al.. (2018). Future perspectives of genome-scale sequencing. Acta Clinica Belgica. 73(1). 7–10. 7 indexed citations

Pauw, Michel De, et al.. (2016). Aggressive extensive cardiac mass in an HIV-1-infected patient: should we go for comfort therapy?. Acta Clinica Belgica. 72(3). 198–200. 1 indexed citations

Dhaese, Sofie, et al.. (2015). Gouty Arthritis of the Spine in a Renal Transplant Patient. Medicine. 94(13). e676–e676. 10 indexed citations

Tol, Linda van der, Einar Svarstad, Alberto Ortíz, et al.. (2014). Chronic kidney disease and an uncertain diagnosis of Fabry disease: Approach to a correct diagnosis. Molecular Genetics and Metabolism. 114(2). 242–247. 44 indexed citations

Vanholder, Raymond, et al.. (2013). SAFETY AND SAMPLE ADEQUACY OF RENAL TRANSPLANT SURVEILLANCE BIOPSIES. Acta Clinica Belgica. 68(3). 161–165. 11 indexed citations

Terryn, Wim, Pierre Cochat, Roseline Froissart, et al.. (2012). Fabry nephropathy: indications for screening and guidance for diagnosis and treatment by the European Renal Best Practice. Nephrology Dialysis Transplantation. 28(3). 505–517. 69 indexed citations

10.

Terryn, Wim, Raymond Vanholder, Dimitri Hemelsoet, et al.. (2012). Questioning the Pathogenic Role of the GLA p.Ala143Thr “Mutation” in Fabry Disease: Implications for Screening Studies and ERT. JIMD Reports. 8. 101–108. 47 indexed citations

11.

Terryn, Wim, Wouter Meersseman, Wim Van Biesen, et al.. (2012). Prevalence of Fabry disease in a predominantly hypertensive population with left ventricular hypertrophy. International Journal of Cardiology. 167(6). 2555–2560. 43 indexed citations

12.

Schoenmakere, Gert De, Bruce Poppe, Birgitte Wuyts, et al.. (2008). Two-tier approach for the detection of alpha-galactosidase A deficiency in kidney transplant recipients. Nephrology Dialysis Transplantation. 23(12). 4044–4048. 14 indexed citations

13.

Terryn, Wim, Bruce Poppe, Birgitte Wuyts, et al.. (2007). Two-tier approach for the detection of alpha-galactosidase A deficiency in a predominantly female haemodialysis population. Nephrology Dialysis Transplantation. 23(1). 294–300. 30 indexed citations

14.

Schoenmakere, Gert De, Jan J. De Waele, Wim Terryn, et al.. (2005). Phenytoin intoxication in critically ill patients. American Journal of Kidney Diseases. 45(1). 189–192. 16 indexed citations

15.

Peeters, Patrick, Wim Terryn, Raymond Vanholder, & Norbert Lameire. (2004). Delayed graft function in renal transplantation. Current Opinion in Critical Care. 10(4). 489–498. 68 indexed citations

16.

Vanbelleghem, Hilde, et al.. (2004). A dramatic case of calciphylaxis 20 years after kidney transplantation. Nephrology Dialysis Transplantation. 19(12). 3183–3185. 11 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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