K. Auberger

886 total citations
22 papers, 574 citations indexed

About

K. Auberger is a scholar working on Hematology, Surgery and Internal Medicine. According to data from OpenAlex, K. Auberger has authored 22 papers receiving a total of 574 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Hematology, 7 papers in Surgery and 6 papers in Internal Medicine. Recurrent topics in K. Auberger's work include Blood Coagulation and Thrombosis Mechanisms (15 papers), Venous Thromboembolism Diagnosis and Management (6 papers) and Hemophilia Treatment and Research (5 papers). K. Auberger is often cited by papers focused on Blood Coagulation and Thrombosis Mechanisms (15 papers), Venous Thromboembolism Diagnosis and Management (6 papers) and Hemophilia Treatment and Research (5 papers). K. Auberger collaborates with scholars based in Germany, Austria and United Kingdom. K. Auberger's co-authors include Ulrike Nowak‐Göttl, N. Münchow, J. Klinge, R. Schobeß, R. Junker, Andreas W. Flemmer, Hans-Georg Koch, S. Ehrenforth, W. Kreuz and Ralf Junker and has published in prestigious journals such as Arteriosclerosis Thrombosis and Vascular Biology, British Journal of Haematology and Thrombosis and Haemostasis.

In The Last Decade

K. Auberger

22 papers receiving 551 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
K. Auberger Germany 13 475 248 143 123 46 22 574
L. Brooker Canada 10 545 1.1× 293 1.2× 162 1.1× 114 0.9× 51 1.1× 10 673
Lawrence Jardine Canada 8 380 0.8× 335 1.4× 128 0.9× 124 1.0× 32 0.7× 11 568
Corrado Sardella Italy 8 485 1.0× 511 2.1× 318 2.2× 94 0.8× 89 1.9× 9 685
Edith Peynaud-Debayle France 10 292 0.6× 181 0.7× 77 0.5× 303 2.5× 38 0.8× 18 500
A. Šrámek Netherlands 9 349 0.7× 154 0.6× 157 1.1× 95 0.8× 102 2.2× 14 533
Vanessa Martlew United Kingdom 9 323 0.7× 85 0.3× 173 1.2× 57 0.5× 63 1.4× 27 559
E Verdy France 9 187 0.4× 128 0.5× 102 0.7× 77 0.6× 19 0.4× 26 374
Alberto Dolce Italy 14 679 1.4× 136 0.5× 108 0.8× 101 0.8× 116 2.5× 30 847
Frits R. Rosendaal Netherlands 5 197 0.4× 120 0.5× 66 0.5× 111 0.9× 130 2.8× 6 440
Janet Brennand United Kingdom 9 307 0.6× 95 0.4× 120 0.8× 43 0.3× 49 1.1× 17 507

Countries citing papers authored by K. Auberger

Since Specialization
Citations

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

Fields of papers citing papers by K. Auberger

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of K. Auberger

This figure shows the co-authorship network connecting the top 25 collaborators of K. Auberger. A scholar is included among the top collaborators of K. Auberger 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 K. Auberger. K. Auberger 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.
Schobeß, R., R. Junker, K. Auberger, et al.. (1999). Factor V G1691A and prothrombin G20210A in childhood spontaneous venous thrombosis – Evidence of an age-dependent thrombotic onset in carriers of factor V G1691A and prothrombin G20210A mutation. European Journal of Pediatrics. 158(S3). S105–S108. 43 indexed citations
3.
Flemmer, Andreas W., et al.. (1999). The low molecular weight heparin dalteparin for prophylaxis and therapy of thrombosis in childhood: a report on 48 cases. European Journal of Pediatrics. 158(S3). S134–S139. 76 indexed citations
4.
5.
Koch, Hans Georg, R. Junker, K. Auberger, et al.. (1999). The 677T genotype of the common MTHFR thermolabile variant and fasting homocysteine in childhood venous thrombosis. European Journal of Pediatrics. 158(S3). S113–S116. 39 indexed citations
6.
Münchow, N., et al.. (1999). Role of genetic prothrombotic risk factors in childhood caval vein thrombosis. European Journal of Pediatrics. 158(S3). S109–S112. 25 indexed citations
7.
Auberger, K., Susan Halimeh, J. Klinge, et al.. (1999). Thrombolysis in Newborns and Infants. Thrombosis and Haemostasis. 82(S 01). 112–116. 38 indexed citations
8.
Baumeister, F. A. M., et al.. (1999). Obstruktive kongenitale Dakryozystozelen. Monatsschrift Kinderheilkunde. 147(7). 652–654. 1 indexed citations
9.
Harms, H. K., Karl Reiter, K. Auberger, et al.. (1998). PHOSPHOMANNOSE-ISOMERASE (PMI) DEFICIENCY, A NEW DEFECT IN THE SYNTHESIS OF GLYCOPROTEINS, MAINLY MANIFESTS AS GASTROINTESTINAL DISEASE, WHICH CAN BE SUCCESSFULLY TREATED BY ORAL MANNOSE.. Journal of Pediatric Gastroenterology and Nutrition. 26(5). 547–547. 1 indexed citations
10.
Hundt, C., et al.. (1997). Brain Hemangiomas of Infancy. Journal of Neuroimaging. 7(2). 81–85. 3 indexed citations
11.
Nowak‐Göttl, Ulrike, K. Auberger, U. Göbel, et al.. (1996). Inherited defects of the protein C anticoagulant system in childhood thrombo-embolism. European Journal of Pediatrics. 155(11). 921–927. 14 indexed citations
12.
Schlößer, Rolf, K. Auberger, Rüdiger von Kries, Ulrike Nowak‐Göttl, & Dirk Schwabe. (1996). Thrombolyse bei Neugeborenen und Säuglingen. Hämostaseologie. 16(4). 236–238. 1 indexed citations
13.
Klarmann, Dieter, W. Kreuz, Günter Auerswald, et al.. (1995). Hepatitis C and Pasteurised Factor VIII and IX Concentrates. Thrombosis and Haemostasis. 73(4). 736–737. 4 indexed citations
14.
Olds, Robin J., David A. Lane, Vijoy Chowdhury, et al.. (1994). (ATT) trinucleotide repeats in the antithrombin gene and their use in determining the origin of repeated mutations. Human Mutation. 4(1). 31–41. 20 indexed citations
15.
Chowdhury, Vijoy, David A. Lane, K. Auberger, et al.. (1994). Homozygous Antithrombin Deficiency: Report of Two New Cases (99 Leu to Phe) Associated with Arterial and Venous Thrombosis. Thrombosis and Haemostasis. 72(2). 198–202. 39 indexed citations
16.
Auberger, K.. (1992). Evaluation of a new protein-C concentrate and comparison of protein-C assays in a child with congenital protein-C deficiency. Annals of Hematology. 64(3). 146–151. 18 indexed citations
17.
Schmitt, Sarah, et al.. (1992). Hypothalamic failure as a sequela of heterozygous protein C deficiency?. European Journal of Pediatrics. 151(6). 428–431. 2 indexed citations
18.
Kreuz, W., Günter Auerswald, Barbara Zieger, et al.. (1992). Prevention of Hepatitis C Virus Infestion in Children with Haemophilia A and B and von Willebrand’s Disease. Thrombosis and Haemostasis. 67(1). 184–184. 6 indexed citations
19.
Vukovich, Thomas, et al.. (1988). Replacement therapy for a homozygous protein C deficiency‐state using a concentrate of human protein C and S. British Journal of Haematology. 70(4). 435–440. 40 indexed citations
20.
Weil, J., et al.. (1987). Homozygoter Säugling in einer Sippe mit erblichem Protein C-Mangel. Journal of Molecular Medicine. 65(12). 576–580. 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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