Ulf Drugge

646 total citations
26 papers, 501 citations indexed

About

Ulf Drugge is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Ulf Drugge has authored 26 papers receiving a total of 501 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 5 papers in Cellular and Molecular Neuroscience and 5 papers in Neurology. Recurrent topics in Ulf Drugge's work include Amyloidosis: Diagnosis, Treatment, Outcomes (6 papers), Neurological disorders and treatments (5 papers) and Protein Kinase Regulation and GTPase Signaling (4 papers). Ulf Drugge is often cited by papers focused on Amyloidosis: Diagnosis, Treatment, Outcomes (6 papers), Neurological disorders and treatments (5 papers) and Protein Kinase Regulation and GTPase Signaling (4 papers). Ulf Drugge collaborates with scholars based in Sweden, Portugal and United States. Ulf Drugge's co-authors include Gösta Holmgren, Alda Sousa, Ola Sandgren, Rune Andersson, Lars Forsgren, J. Wahlström, O Sandgren, Gunnar Sanner, Maria Danielsson and B. G. L. Almay and has published in prestigious journals such as Journal of Neurology Neurosurgery & Psychiatry, Movement Disorders and Journal of Medical Genetics.

In The Last Decade

Ulf Drugge

23 papers receiving 477 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ulf Drugge Sweden 11 328 118 101 96 89 26 501
Sari Kiuru Finland 14 466 1.4× 97 0.8× 139 1.4× 269 2.8× 24 0.3× 18 642
H. Goebel Germany 13 263 0.8× 53 0.4× 58 0.6× 29 0.3× 53 0.6× 37 475
Daniela Sommer Belgium 8 159 0.5× 31 0.3× 72 0.7× 203 2.1× 55 0.6× 9 490
Veronika Karcagi Hungary 13 461 1.4× 84 0.7× 79 0.8× 101 1.1× 79 0.9× 32 616
Stayko Sarafov Bulgaria 9 215 0.7× 68 0.6× 37 0.4× 68 0.7× 29 0.3× 20 297
Bianca M. de Graaf Netherlands 9 301 0.9× 41 0.3× 32 0.3× 94 1.0× 135 1.5× 15 458
Ardinger Hh United States 6 192 0.6× 30 0.3× 27 0.3× 124 1.3× 37 0.4× 287 402
Cécile Cauquil France 9 150 0.5× 69 0.6× 46 0.5× 28 0.3× 46 0.5× 20 268
Joshua H. Carey United States 6 305 0.9× 15 0.1× 64 0.6× 137 1.4× 33 0.4× 9 367
Adam Mp 6 180 0.5× 30 0.3× 25 0.2× 113 1.2× 37 0.4× 286 388

Countries citing papers authored by Ulf Drugge

Since Specialization
Citations

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

Fields of papers citing papers by Ulf Drugge

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ulf Drugge

This figure shows the co-authorship network connecting the top 25 collaborators of Ulf Drugge. A scholar is included among the top collaborators of Ulf Drugge 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 Ulf Drugge. Ulf Drugge 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.
2.
Drugge, Ulf. (2007). Krisbiografier. Utfattiga och mindre fattiga förr.
4.
Erikson, Anders, Håkan Forsberg, Ulf Drugge, & Gösta Holmgren. (1995). Outcome of pregnancy in women with myotonic dystrophy and analysis of CTG gene expansion. Acta Paediatrica. 84(4). 416–418. 10 indexed citations
5.
Almeida, Maria Rosário, Yoshiyuki Sakaki, Gösta Holmgren, et al.. (1995). Haplotype analysis of common transthyretin mutations. Human Genetics. 96(3). 350–4. 21 indexed citations
6.
Drugge, Ulf, Monica Holmberg, Gösta Holmgren, B. G. L. Almay, & H Linderholm. (1995). Hereditary myopathy with lactic acidosis, succinate dehydrogenase and aconitase deficiency in northern Sweden: a genealogical study.. Journal of Medical Genetics. 32(5). 344–347. 18 indexed citations
7.
Almqvist, E., Susan E. Andrew, Jane Theilmann, et al.. (1994). Geographical distribution of haplotypes in Swedish families with Huntington's disease. Human Genetics. 94(2). 124–8. 8 indexed citations
8.
Wahlström, J., Laurie J. Ozelius, P. L. Kramer, et al.. (1994). The gene for familial dystonia with myoclonic jerks responsive to alcohol is not located on the distal end of 9q. Clinical Genetics. 45(2). 88–92. 11 indexed citations
9.
Binzer, Michael, Lars Forsgren, Gunnar Holmgren, Ulf Drugge, & S. Fredrikson. (1994). Familial clustering of multiple sclerosis in a northern Swedish rural district.. Journal of Neurology Neurosurgery & Psychiatry. 57(4). 497–499. 19 indexed citations
10.
Sousa, Alda, Rune Andersson, Ulf Drugge, Gösta Holmgren, & Ola Sandgren. (1993). Familial Amyloidotic Polyneuropathy in Sweden: Geographical Distribution, Age of Onset, and Prevalence. Human Heredity. 43(5). 288–294. 120 indexed citations
11.
Drugge, Ulf, Gösta Holmgren, & Bjarne Udd. (1992). The First Case of Familial Amyloidotic Polyneuropathy (FAP Met30) in the Finnish Population. Human Heredity. 42(3). 184–188. 5 indexed citations
13.
Drugge, Ulf & Stefan Svallfors. (1991). Rörelsen, Rotary och storföretagen. Om eliten i en svensk industristad. Sociologisk Forskning. 1. 18–44. 2 indexed citations
14.
Drugge, Ulf, et al.. (1991). Fragile X families in a Northern Swedish County: A genealogical study of possibly affected individuals in the nineteenth century. American Journal of Medical Genetics. 38(2-3). 363–366. 3 indexed citations
15.
Schuback, Deborah E., Laurie J. Ozelius, Gösta Holmgren, et al.. (1991). Dopamine beta-hydroxylase gene excluded in four subtypes of hereditary dystonia. Human Genetics. 87(3). 311–316. 6 indexed citations
16.
Sandgren, Ola, Ulf Drugge, Gösta Holmgren, & Alda Sousa. (1991). Vitreous involvement in familial amyloidotic neuropathy: a genealogical and genetic study. Clinical Genetics. 40(6). 452–460. 38 indexed citations
17.
Forsgren, Lars, et al.. (1990). Alcohol‐responsive myoclonic dystonia in a large family: Dominant inheritance and phenotypic variation. Movement Disorders. 5(4). 270–279. 60 indexed citations
18.
Holmgren, Gösta, Hans K son Blomquist, Ulf Drugge, & Karl‐Henrik Gustavson. (1988). Fragile X families in a Northern Swedish county ‐ a genealogical study demonstrating apparent paternal transmission from the 18th century. American Journal of Medical Genetics. 30(1-2). 673–679. 10 indexed citations
19.
Drugge, Ulf, O Norlander, Per Olsson, & Kjell Rådegran. (1974). Positive End‐Expiratory Pressure Ventilation After Open‐Heart Surgery. Acta Anaesthesiologica Scandinavica. 18(s53). 81–85. 6 indexed citations
20.
Rådegran, Kjell, Ulf Drugge, & Per Olsson. (1974). Pulmonary Venoconstriction by Induced Platelet Aggregation. Acta Anaesthesiologica Scandinavica. 18(3). 243–247. 18 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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