P. Vase

1.5k total citations
25 papers, 1.1k citations indexed

About

P. Vase is a scholar working on Genetics, Pulmonary and Respiratory Medicine and Surgery. According to data from OpenAlex, P. Vase has authored 25 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Genetics, 11 papers in Pulmonary and Respiratory Medicine and 8 papers in Surgery. Recurrent topics in P. Vase's work include Vascular Anomalies and Treatments (16 papers), Tracheal and airway disorders (10 papers) and Sharing Economy and Platforms (4 papers). P. Vase is often cited by papers focused on Vascular Anomalies and Treatments (16 papers), Tracheal and airway disorders (10 papers) and Sharing Economy and Platforms (4 papers). P. Vase collaborates with scholars based in Denmark and United States. P. Vase's co-authors include Anette Drøhse Kjeldsen, Poul Erik Andersen, O. Grove, H Oxhøj, Henrik Arendrup, Klaus Brusgaard, Anders Green, Jens Jacobsen, Bo Elle and Thomas Möller and has published in prestigious journals such as Gastroenterology, CHEST Journal and British Journal of Dermatology.

In The Last Decade

P. Vase

24 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
P. Vase Denmark 14 938 822 319 319 83 25 1.1k
Katharine Henderson United States 17 1.1k 1.2× 985 1.2× 353 1.1× 359 1.1× 128 1.5× 28 1.3k
Maurizio Memeo Italy 11 328 0.3× 348 0.4× 276 0.9× 111 0.3× 33 0.4× 17 587
Anna Cirulli Italy 10 331 0.4× 296 0.4× 140 0.4× 110 0.3× 23 0.3× 15 421
Nelson C. Goldman United States 9 141 0.2× 176 0.2× 134 0.4× 36 0.1× 127 1.5× 26 406
Francesco Chu Italy 10 74 0.1× 107 0.1× 147 0.5× 31 0.1× 22 0.3× 37 339
Ian C. Duncan South Africa 11 46 0.0× 95 0.1× 116 0.4× 5 0.0× 138 1.7× 38 398
O. Merrot France 10 66 0.1× 173 0.2× 91 0.3× 9 0.0× 10 0.1× 29 331
B. Bui France 11 46 0.0× 487 0.6× 176 0.6× 96 1.2× 22 637
Abraham Jacob Australia 13 377 0.4× 93 0.1× 68 0.2× 14 0.2× 32 602
Tarek A. Salam United States 7 56 0.1× 198 0.2× 289 0.9× 30 0.4× 9 472

Countries citing papers authored by P. Vase

Since Specialization
Citations

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

Fields of papers citing papers by P. Vase

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of P. Vase

This figure shows the co-authorship network connecting the top 25 collaborators of P. Vase. A scholar is included among the top collaborators of P. Vase 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 P. Vase. P. Vase 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.
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
2.
Brusgaard, Klaus, Anette Drøhse Kjeldsen, Louise Ladefoged Poulsen, et al.. (2004). Mutations in endoglin and in activin receptor‐like kinase 1 among Danish patients with hereditary haemorrhagic telangiectasia. Clinical Genetics. 66(6). 556–561. 40 indexed citations
3.
Kjeldsen, Anette Drøhse, et al.. (2001). Mutations in theALK-1 gene and the phenotype of hereditary hemorrhagic telangiectasia in two large Danish families. American Journal of Medical Genetics. 98(4). 298–302. 35 indexed citations
4.
Kjeldsen, Anette Drøhse, H Oxhøj, Poul Erik Andersen, Anders Green, & P. Vase. (2000). Prevalence of pulmonary arteriovenous malformations (PAVMs) and occurrence of neurological symptoms in patients with hereditary haemorrhagic telangiectasia (HHT). Journal of Internal Medicine. 248(3). 255–262. 93 indexed citations
5.
Kjeldsen, Anette Drøhse, et al.. (2000). [Hereditary hemorrhagic telangiectasia. A population-based study on prevalence and mortality among Danish HHT patients].. PubMed. 162(25). 3597–601. 33 indexed citations
6.
Kjeldsen, Anette Drøhse, et al.. (1999). Percutaneous transluminal treatment of pulmonary arteriovenous malformations. Journal of interventional radiology. 14. 5 indexed citations
7.
Kjeldsen, Anette Drøhse, et al.. (1999). Hereditary haemorrhagic telangiectasia: a population‐based study of prevalence and mortality in Danish patients. Journal of Internal Medicine. 245(1). 31–39. 311 indexed citations
8.
Kjeldsen, Anette Drøhse, H Oxhøj, Poul Erik Andersen, et al.. (1999). Pulmonary Arteriovenous Malformations. CHEST Journal. 116(2). 432–439. 107 indexed citations
9.
Andersen, Poul Erik, Anette Drøhse Kjeldsen, H Oxhøj, P. Vase, & Robert I. White. (1998). Embolotherapy for Pulmonary Arteriovenous Malformations in Patients with Hereditary Hemorrhagic Telangiectasia (Rendu-Osler-Weber Syndrome). Acta Radiologica. 39(6). 723–726. 25 indexed citations
10.
Kjeldsen, Anette Drøhse, Poul Erik Andersen, H Oxhøj, & P. Vase. (1998). [Percutaneous transluminal embolization of pulmonary arteriovenous malformations].. PubMed. 160(10). 1465–8. 1 indexed citations
11.
Kjeldsen, Anette Drøhse, et al.. (1994). Group Specific Component in Serum and Otosclerosis: No Association. Acta Oto-Laryngologica. 114(3). 303–304.
12.
Vase, P. & O. Grove. (1986). Gastrointestinal Lesions in Hereditary Hemorrhagic Telangiectasia. Gastroenterology. 91(5). 1079–1083. 95 indexed citations
13.
Vase, P., et al.. (1985). Pulmonary Arteriovenous Fistulas in Hereditary Hemorrhagic Telangiectasia. Acta Medica Scandinavica. 218(1). 105–109. 78 indexed citations
14.
Vase, P., et al.. (1983). Identification and functional recording of the recurrent nerve by electrical stimulation during neck surgery. The Laryngoscope. 93(3). 370–373. 9 indexed citations
15.
Vase, P. & Martin Lorentzen. (1983). Histological findings following oestrogen treatment of hereditary haemorrhagic telangiectasia. The Journal of Laryngology & Otology. 97(5). 427–429. 12 indexed citations
16.
Grunnet, Niels, et al.. (1980). HLA Antigens in Atopic Dermatitis. Dermatology. 160(1). 17–20. 5 indexed citations
17.
Vase, P., et al.. (1979). OCULAR LESIONS IN HEREDITARY HAEMORRHAGIC TELANGIECTASIA. Acta Ophthalmologica. 57(6). 1084–1090. 28 indexed citations
18.
Stoksted, Poul & P. Vase. (1978). Perforations of the nasal septum following operative procedures.. PubMed. 16(3). 123–38. 11 indexed citations
19.
Larsen, Finn Schultz, et al.. (1978). Atopic dermatitis and congenital deafness. British Journal of Dermatology. 99(3). 325–328. 1 indexed citations
20.
Vase, P., et al.. (1975). Congenital Stapes Fixation, Symphalangism And Syndactylia. Acta Oto-Laryngologica. 80(1-6). 394–398. 7 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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