Klaus Brusgaard

3.3k total citations
120 papers, 2.3k citations indexed

About

Klaus Brusgaard is a scholar working on Endocrinology, Diabetes and Metabolism, Surgery and Molecular Biology. According to data from OpenAlex, Klaus Brusgaard has authored 120 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 40 papers in Endocrinology, Diabetes and Metabolism, 39 papers in Surgery and 34 papers in Molecular Biology. Recurrent topics in Klaus Brusgaard's work include Hyperglycemia and glycemic control in critically ill and hospitalized patients (30 papers), Pancreatic function and diabetes (17 papers) and Vascular Anomalies and Treatments (14 papers). Klaus Brusgaard is often cited by papers focused on Hyperglycemia and glycemic control in critically ill and hospitalized patients (30 papers), Pancreatic function and diabetes (17 papers) and Vascular Anomalies and Treatments (14 papers). Klaus Brusgaard collaborates with scholars based in Denmark, United Kingdom and Sweden. Klaus Brusgaard's co-authors include Henrik Thybo Christesen, Lilian Bomme Ousager, Anette Drøhse Kjeldsen, Chantal Mathieu, Qihua Tan, Henning Beck‐Nielsen, Dorte Glintborg, Khalid Hussain, Lut Overbergh and Kurt Højlund and has published in prestigious journals such as PLoS ONE, The Journal of Clinical Endocrinology & Metabolism and Diabetes Care.

In The Last Decade

Klaus Brusgaard

115 papers receiving 2.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Klaus Brusgaard Denmark 27 737 652 643 481 351 120 2.3k
Sabrina Corbetta Italy 34 644 0.9× 992 1.5× 1.0k 1.6× 594 1.2× 260 0.7× 145 3.6k
Hiroyuki Koshiyama Japan 26 542 0.7× 1.3k 2.0× 1.1k 1.7× 714 1.5× 225 0.6× 109 3.5k
Mahsa M. Amoli Iran 26 345 0.5× 838 1.3× 371 0.6× 290 0.6× 195 0.6× 186 2.7k
Patrice Rodien France 32 459 0.6× 1.2k 1.8× 2.2k 3.4× 570 1.2× 203 0.6× 107 3.6k
Brigitte Delemer France 32 1.3k 1.8× 536 0.8× 2.0k 3.1× 547 1.1× 150 0.4× 143 3.8k
Fábio R. Faucz United States 28 1.0k 1.4× 901 1.4× 972 1.5× 218 0.5× 71 0.2× 141 2.7k
Sofia Tseleni‐Balafouta Greece 29 1.0k 1.4× 897 1.4× 1.8k 2.7× 304 0.6× 159 0.5× 91 3.4k
Arjen R. Mensenkamp Netherlands 27 409 0.6× 875 1.3× 213 0.3× 351 0.7× 602 1.7× 67 2.2k
Vittorio Tassi Italy 22 271 0.4× 975 1.5× 654 1.0× 395 0.8× 378 1.1× 44 2.2k
Kelly A. Volcik United States 27 473 0.6× 601 0.9× 300 0.5× 729 1.5× 264 0.8× 48 2.8k

Countries citing papers authored by Klaus Brusgaard

Since Specialization
Citations

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

Fields of papers citing papers by Klaus Brusgaard

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Klaus Brusgaard

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

All Works

20 of 20 papers shown
1.
Hao, Qin, Klaus Brusgaard, Martin J. Larsen, et al.. (2025). Multiple lesion-specific somatic mutations and bi-allelic loss of ACVRL1 in a single patient with hereditary haemorrhagic telangiectasia. European Journal of Human Genetics. 34(2). 236–242.
2.
3.
Kareva, Maria, Anatoly Tiulpakov, Yuri Sokolov, et al.. (2023). Insulinoma in childhood: a retrospective review of 22 patients from one referral centre. Frontiers in Endocrinology. 14. 1127173–1127173. 6 indexed citations
4.
Hansen, Stinus, et al.. (2022). Bone Deformities and Kidney Failure: Coincidence of PHEX-Related Hypophosphatemic Rickets and m.3243A>G Mitochondrial Disease. Calcified Tissue International. 111(6). 641–645.
5.
Tan, Ming, Klaus Brusgaard, Anne‐Marie Gerdes, et al.. (2021). Whole genome sequencing identifies rare germline variants enriched in cancer related genes in first degree relatives of familial pancreatic cancer patients. Clinical Genetics. 100(5). 551–562. 8 indexed citations
6.
Lines, Matthew A., Klaus Brusgaard, Diva D. De León, et al.. (2021). PHKA2 variants expand the phenotype of phosphorylase B kinase deficiency to include patients with ketotic hypoglycemia only. American Journal of Medical Genetics Part A. 185(10). 2959–2975. 5 indexed citations
7.
Globa, Evgenia, Sönke Detlefsen, Lars Melholt Rasmussen, et al.. (2020). The difficult management of persistent, non‐focal congenital hyperinsulinism: A retrospective review from a single, tertiary center. Pediatric Diabetes. 21(3). 441–455. 13 indexed citations
8.
Busiah, Kanetee, Μαρία Αντωνίου, E Jacot, et al.. (2020). Congenital hyperinsulinism: 2 case reports with different rare variants in ABCC8. Annals of Pediatric Endocrinology & Metabolism. 26(1). 60–65. 3 indexed citations
9.
Brusgaard, Klaus, et al.. (2018). A Novel Mutation in Phka2: Idiopathic Ketotic Hypoglycaemia May Represent Mild Gsdixa. University of Southern Denmark Research Portal (University of Southern Denmark). 1 indexed citations
10.
Tørring, Pernille Mathiesen, Christine í Dali, Poul Erik Andersen, et al.. (2017). Familial cerebral abscesses caused by hereditary hemorrhagic telangiectasia. Clinical Case Reports. 5(6). 805–808. 1 indexed citations
11.
Tørring, Pernille Mathiesen, Martin J. Larsen, Anette Drøhse Kjeldsen, et al.. (2015). Global gene expression profiling of telangiectasial tissue from patients with hereditary hemorrhagic telangiectasia. Microvascular Research. 99. 118–126. 7 indexed citations
12.
Tørring, Pernille Mathiesen, Anette Drøhse Kjeldsen, Lilian Bomme Ousager, Charlotte Brasch‐Andersen, & Klaus Brusgaard. (2012). Allelic Dropout in the ENG Gene, Affecting the Results of Genetic Testing in Hereditary Hemorrhagic Telangiectasia. Genetic Testing and Molecular Biomarkers. 16(12). 1419–1423. 3 indexed citations
13.
Overbergh, L., Conny Gysemans, Klaus Brusgaard, et al.. (2012). Unraveling the effects of 1,25(OH)2D3 on global gene expression in pancreatic islets. The Journal of Steroid Biochemistry and Molecular Biology. 136. 68–79. 41 indexed citations
14.
Christesen, Henrik Thybo, Klaus Brusgaard, & Khalid Hussain. (2011). Recurrent spontaneous hypoglycaemia causes loss of neurogenic and neuroglycopaenic signs in infants with congenital hyperinsulinism. Clinical Endocrinology. 76(4). 548–554. 19 indexed citations
15.
Tan, Qihua, Mette Nyegaard, Klaus Brusgaard, et al.. (2007). Arrayed Primer Extension in the “Array of Arrays” Format: A Rational Approach for Microarray-Based SNP Genotyping. Genetic Testing. 11(2). 160–166. 2 indexed citations
16.
Brusgaard, Klaus, et al.. (2006). A TCF1 mutation may cause transient congenital hyperinsulinism followed by MODY3. 4 indexed citations
17.
Brusgaard, Klaus, et al.. (2006). Molecular genetic analysis of 1053 Danish individuals with clinical signs of familial hypercholesterolemia. Clinical Genetics. 69(3). 277–283. 15 indexed citations
18.
Christesen, Henrik Thybo, Klaus Brusgaard, Jan Alm, et al.. (2006). Rapid Genetic Analysis in Congenital Hyperinsulinism. Hormone Research in Paediatrics. 67(4). 184–188. 16 indexed citations
19.
Kjeldsen, Anette Drøhse, Thomas Möller, Klaus Brusgaard, P. Vase, & Poul Erik Andersen. (2005). Clinical symptoms according to genotype amongst patients with hereditary haemorrhagic telangiectasia. Journal of Internal Medicine. 258(4). 349–355. 73 indexed citations
20.
Holm, Lars‐Erik, et al.. (1996). A polymorphic trinucleotide microsatellite in cattle: BtDIASI. Animal Genetics. 27(5). 373–373. 2 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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