L. Engesser

593 total citations
13 papers, 460 citations indexed

About

L. Engesser is a scholar working on Hematology, Genetics and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, L. Engesser has authored 13 papers receiving a total of 460 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Hematology, 3 papers in Genetics and 2 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in L. Engesser's work include Blood Coagulation and Thrombosis Mechanisms (9 papers), Blood properties and coagulation (2 papers) and Coagulation, Bradykinin, Polyphosphates, and Angioedema (2 papers). L. Engesser is often cited by papers focused on Blood Coagulation and Thrombosis Mechanisms (9 papers), Blood properties and coagulation (2 papers) and Coagulation, Bradykinin, Polyphosphates, and Angioedema (2 papers). L. Engesser collaborates with scholars based in Netherlands and Slovakia. L. Engesser's co-authors include E.J.P. Brommer, E Briët, A.W. Broekmans, Cornelis Kluft, R M Bertina, Rogier M. Bertina, Jan Michiels, I K van der Linden, J. Koopman and J.A. de Leeuw and has published in prestigious journals such as Proceedings of the National Academy of Sciences, British Journal of Haematology and Thrombosis and Haemostasis.

In The Last Decade

L. Engesser

13 papers receiving 423 citations

Peers

L. Engesser

HEMAT

PRM

CCM

GENET

Annette Feussner Germany

Vijoy Chowdhury United Kingdom

Akinobu Funatsu Japan

J.H. Lawson United States

UM Marzec United States

Zhong-Fu Huang United States

Josephine P. Ferrel United States

Holleh Husseinzadeh United States

Kálmán Rák Hungary

Kiat Tsong Tan United Kingdom

Annette Feussner Germany

L. Engesser

339 ×0.9

HEMAT

160 ×1.0

57 ×0.6

PRM

200 ×2.3

CCM

145 ×1.9

GENET

Citations per year, relative to L. Engesser L. Engesser (= 1×) peers Annette Feussner

Countries citing papers authored by L. Engesser

Since Specialization

Citations

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

Fields of papers citing papers by L. Engesser

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of L. Engesser

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

All Works

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13 of 13 papers shown

Boomsma, Dorret I., et al.. (1995). An Amino Acid Polymorphism in Histidine-rich Glycoprotein (HRG) Explains 59% of the Variance in Plasma HRG Levels. Thrombosis and Haemostasis. 74(6). 1497–1500. 10 indexed citations

Koopman, J., F. Haverkate, Jos Grimbergen, et al.. (1992). Abnormal fibrinogens IJmuiden (B beta Arg14----Cys) and Nijmegen (B beta Arg44----Cys) form disulfide-linked fibrinogen-albumin complexes.. Proceedings of the National Academy of Sciences. 89(8). 3478–3482. 42 indexed citations

Engesser, L., E.J.P. Brommer, Cornelis Kluft, & E Briët. (1989). Elevated Plasminogen Activator Inhibitor (PAI), a Cause of Thrombophilia? – A Study in 203 Patients with Familial or Sporadic Venous Thrombophilia. Thrombosis and Haemostasis. 62(2). 673–680. 42 indexed citations

Engesser, L., J. Koopman, F. Haverkate, et al.. (1988). Fibrinogen Nijmegen : Congenital Dysfibrinogenemia Associated with Impaired t-PA Mediated Plasminogen Activation and Decreased Binding of t-PA. Thrombosis and Haemostasis. 60(1). 113–120. 33 indexed citations

Engesser, L., Cornelis Kluft, E Briët, & E.J.P. Brommer. (1987). Familial elevation of plasma histidine-rich glycoprotein in a family with thrombophilia. British Journal of Haematology. 67(3). 355–358. 46 indexed citations

Bertina, R M, et al.. (1987). Hereditary Heparin Cofactor II Deficiency and the Risk of Development of Thrombosis. Thrombosis and Haemostasis. 57(2). 196–200. 79 indexed citations

Briët, E, L. Engesser, E.J.P. Brommer, A.W. Broekmans, & Rogier M. Bertina. (1987). THROMBOPHILIA:ITS CAUSES AND A ROUGH ESTIMATE OF ITS PREVALENCE. Thrombosis and Haemostasis. 48 indexed citations

Engesser, L., Cornelis Kluft, E Briët, & E.J.P. Brommer. (1987). Familial elevation of plasma histidine‐rich glycoprotein in a family with thrombophilia. British Journal of Haematology. 67(3). 355–358. 8 indexed citations

Jj, Michiels, et al.. (1987). [A family with venous thrombosis and hereditary protein S deficiency].. Nederlandsch tijdschrift voor geneeskunde/Nederlands tijdschrift voor geneeskunde/NTvG-databank. 131(24). 1043–7. 2 indexed citations

10.

Linden, I K van der, et al.. (1986). Hereditary deficiency in heparin cofactor II (HeCoFII) and the risk for the development of thrombosis. Thrombosis Research. 41. 59–59. 1 indexed citations

11.

Briët, E, L. Engesser, & E.J.P. Brommer. (1985). Regulation of Blood Coagulation and Thrombosis. Pathophysiology of Haemostasis and Thrombosis. 15(4). 228–232. 6 indexed citations

12.

Broekmans, A.W., et al.. (1985). Hereditary Protein S Deficiency and Venous Thrombo-Embolism. Thrombosis and Haemostasis. 53(2). 273–277. 55 indexed citations

13.

Broekmans, A.W., Rogier M. Bertina, L. Engesser, et al.. (1985). Hereditary protein S deficiency and venous thrombo-embolism. A study in three Dutch families.. PubMed. 53(2). 273–7. 88 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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