Christine Mannhalter

14.8k total citations
338 papers, 10.9k citations indexed

About

Christine Mannhalter is a scholar working on Hematology, Genetics and Molecular Biology. According to data from OpenAlex, Christine Mannhalter has authored 338 papers receiving a total of 10.9k indexed citations (citations by other indexed papers that have themselves been cited), including 171 papers in Hematology, 75 papers in Genetics and 53 papers in Molecular Biology. Recurrent topics in Christine Mannhalter's work include Blood Coagulation and Thrombosis Mechanisms (97 papers), Venous Thromboembolism Diagnosis and Management (49 papers) and Coagulation, Bradykinin, Polyphosphates, and Angioedema (35 papers). Christine Mannhalter is often cited by papers focused on Blood Coagulation and Thrombosis Mechanisms (97 papers), Venous Thromboembolism Diagnosis and Management (49 papers) and Coagulation, Bradykinin, Polyphosphates, and Angioedema (35 papers). Christine Mannhalter collaborates with scholars based in Austria, Germany and United States. Christine Mannhalter's co-authors include Georg Endler, Ingrid Pabinger, Klaus Lechner, Martin Schillinger, Markus Exner, Oswald Wagner, Gerlinde Mitterbauer, Peter Quehenberger, Wolfgang Lalouschek and Erich Minar and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Clinical Oncology and SHILAP Revista de lepidopterología.

In The Last Decade

Christine Mannhalter

336 papers receiving 10.5k citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author						Papers	Cites
Christine Mannhalter	4.6k	2.2k	2.1k	1.9k	1.9k	338	10.9k
Klaus Lechner	10.8k 2.3×	2.5k 1.1×	3.7k 1.8×	2.4k 1.2×	1.8k 1.0×	453	18.8k
Pieter H. Reitsma	9.0k 1.9×	2.4k 1.1×	2.3k 1.1×	4.5k 2.3×	3.0k 1.6×	248	16.5k
Paolo Gresele	3.8k 0.8×	1.3k 0.6×	678 0.3×	1.0k 0.5×	2.5k 1.3×	311	10.1k
Beng H. Chong	5.6k 1.2×	1.3k 0.6×	925 0.4×	3.1k 1.6×	2.1k 1.1×	211	11.1k
Amiram Eldor	4.0k 0.9×	1.7k 0.8×	1.4k 0.7×	3.1k 1.6×	2.8k 1.5×	226	11.1k
Tatsuya Atsumi	5.0k 1.1×	1.8k 0.8×	719 0.3×	581 0.3×	739 0.4×	512	15.5k
Barbara A. Konkle	4.2k 0.9×	1.6k 0.7×	904 0.4×	920 0.5×	1.1k 0.6×	216	8.0k
Bonno N. Bouma	5.8k 1.2×	1.1k 0.5×	2.8k 1.3×	1.2k 0.6×	1.2k 0.6×	188	9.1k
Uri Seligsohn	7.3k 1.6×	1.1k 0.5×	3.0k 1.4×	1.9k 1.0×	1.7k 0.9×	253	10.9k
Peter Quehenberger	3.0k 0.6×	807 0.4×	604 0.3×	2.8k 1.4×	2.1k 1.1×	204	7.8k

Countries citing papers authored by Christine Mannhalter

Since Specialization

Citations

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

Fields of papers citing papers by Christine Mannhalter

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Christine Mannhalter

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

All Works

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20 of 20 papers shown

Hobl, Eva‐Luise, Thomas Stimpfl, Josef Ebner, et al.. (2013). Morphine Decreases Clopidogrel Concentrations and Effects. Journal of the American College of Cardiology. 63(7). 630–635. 146 indexed citations

Hoke, Matthias, Walter S. Speidl, Martin Schillinger, et al.. (2012). Polymorphism of the complement 5 gene and cardiovascular outcome in patients with atherosclerosis. European Journal of Clinical Investigation. 42(9). 921–926. 22 indexed citations

Streubel, Berthold, Elisabeth Kretschmer‐Chott, Andreas Püspök, et al.. (2011). Primary Follicular Lymphoma of the Duodenum Is a Distinct Mucosal/Submucosal Variant of Follicular Lymphoma: A Retrospective Study of 63 Cases. Journal of Clinical Oncology. 29(11). 1445–1451. 152 indexed citations

Fritsche‐Polanz, Robert, Karl Sotlar, Wolfgang R. Sperr, et al.. (2010). High frequency of concomitant mastocytosis in patients with acute myeloid leukemia exhibiting the transforming KIT mutation D816V. Molecular Oncology. 4(4). 335–346. 35 indexed citations

Luke, May M., Wolfgang Lalouschek, Charles M. Rowland, et al.. (2009). Polymorphisms Associated with Both Noncardioembolic Stroke and Coronary Heart Disease: Vienna Stroke Registry. Cerebrovascular Diseases. 28(5). 499–504. 24 indexed citations

Bach, Jürgen, Georg Endler, Bernhard R. Winkelmann, et al.. (2008). Coagulation factor XII (FXII) activity, activated FXII, distribution of FXII C46T gene polymorphism and coronary risk. Journal of Thrombosis and Haemostasis. 6(2). 291–296. 45 indexed citations

Bach, Jürgen, Georg Endler, Christine Mannhalter, & Peter Hellstern. (2008). Coagulation factor XII activity, activated factor XII, distribution of factor XII C46T gene polymorphism and coronary risk: reply to a rebuttal. Journal of Thrombosis and Haemostasis. 6(6). 1055–1056. 3 indexed citations

Vormittag, Rainer, Cihan Ay, Thomas Vukovich, et al.. (2007). Low‐density lipoprotein receptor‐related protein 1 polymorphism 663 C > T affects clotting factor VIII activity and increases the risk of venous thromboembolism. Journal of Thrombosis and Haemostasis. 5(3). 497–502. 43 indexed citations

Endler, Georg, et al.. (2007). Evidence of a U‐shaped association between factor XII activity and overall survival. Journal of Thrombosis and Haemostasis. 5(6). 1143–1148. 78 indexed citations

10.

Lalouschek, Wolfgang, Martin Schillinger, Kety Hsieh, et al.. (2006). Polymorphisms of the inflammatory system and risk of ischemic cerebrovascular events. Clinical Chemistry and Laboratory Medicine (CCLM). 44(8). 918–23. 58 indexed citations

11.

Brunner, Martin, Oliver Langer, Raute Sunder‐Plaßmann, et al.. (2005). Influence of functional haplotypes in the drug transporter gene on central nervous system drug distribution in humans. Clinical Pharmacology & Therapeutics. 78(2). 182–190. 59 indexed citations

12.

Schillinger, Martin, Markus Exner, Erich Minar, et al.. (2004). Heme oxygenase-1 genotype and restenosis after balloon angioplasty: a novel vascular protective factor. Journal of the American College of Cardiology. 43(6). 950–957. 82 indexed citations

13.

Funk, Marion, Georg Endler, Martin Schillinger, et al.. (2004). The effect of a promoter polymorphism in the heme oxygenase-1 gene on the risk of ischaemic cerebrovascular events. Thrombosis Research. 113(3-4). 217–223. 34 indexed citations

14.

Laczika, Klaus, Iréne Lang, Peter Quehenberger, et al.. (2002). Unilateral Chronic Thromboembolic Pulmonary Disease Associated With Combined Inherited Thrombophilia. CHEST Journal. 121(1). 286–289. 19 indexed citations

15.

Mannhalter, Christine, et al.. (2001). [Practice guidelines for formulation of patient or subject information and for the declaration of consent in genetic studies (inclusive of pharmaceutical genetics].. PubMed. 113(22). 867–9. 2 indexed citations

16.

Kandioler, Daniela, et al.. (1996). Anwendung von P53-Gen-Analysen in der thoraxchirurgischen Onkologie am Beispiel des solitären pulmonalen Rundherdes. European surgery. Supplement/European surgery. 28(2). 103–106. 1 indexed citations

17.

Födinger, Manuela, Heidi Buchmayer, Ilse Schwarzinger, et al.. (1996). Multiplex PCR for rapid detection of T‐cell receptor‐gamma chain gene rearrangements in patients with lymphoproliferative diseases. British Journal of Haematology. 94(1). 136–139. 34 indexed citations

18.

Mitterbauer, Margit, Gerlinde Mitterbauer, Oskar A. Haas, et al.. (1995). Kinetics of minimal residual disease during induction/consolidation therapy in standard-risk adult B-lineage acute lymphoblastic leukemia. Annals of Hematology. 71(4). 155–160. 1 indexed citations

19.

Knapp, Sylvia, et al.. (1993). Mechanism of the chromosomal translocation t(14;18) in lymphoma: detection of a 45-Kd breakpoint binding protein. Blood. 81(7). 1833–1840. 34 indexed citations

20.

Hellstern, Peter, et al.. (1985). Combined Dys-Form of Homozygous Factor XI Deficiency and Heterozygous Factor XII Deficiency. Pathophysiology of Haemostasis and Thrombosis. 15(3). 215–219. 4 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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