Bernhard Lämmle

19.0k total citations · 1 hit paper
288 papers, 12.6k citations indexed

About

Bernhard Lämmle is a scholar working on Hematology, Immunology and Genetics. According to data from OpenAlex, Bernhard Lämmle has authored 288 papers receiving a total of 12.6k indexed citations (citations by other indexed papers that have themselves been cited), including 151 papers in Hematology, 128 papers in Immunology and 89 papers in Genetics. Recurrent topics in Bernhard Lämmle's work include Complement system in diseases (111 papers), Coagulation, Bradykinin, Polyphosphates, and Angioedema (68 papers) and Platelet Disorders and Treatments (63 papers). Bernhard Lämmle is often cited by papers focused on Complement system in diseases (111 papers), Coagulation, Bradykinin, Polyphosphates, and Angioedema (68 papers) and Platelet Disorders and Treatments (63 papers). Bernhard Lämmle collaborates with scholars based in Switzerland, Germany and United States. Bernhard Lämmle's co-authors include Johanna A. Kremer Hovinga, Miha Furlan, Rodolfo Robles, James N. George, Sara K. Vesely, Lorenzo Alberio, Max Solenthaler, Deirdra R. Terrell, Walter A. Wuillemin and M Furlan and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and The Lancet.

In The Last Decade

Bernhard Lämmle

280 papers receiving 12.3k citations

Hit Papers

align trajectories sort by overperformance

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

von Willebrand Factor–Cleaving Protease in Thrombotic Thrombocytopenic Purpura and the Hemolytic–Uremic Syndrome

1998 1.3k citations I. Scharrer, Bernhard Lämmle et al. profile →

Author Peers

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

Author						Papers	Cites
Bernhard Lämmle	8.1k	6.8k	3.9k	3.6k	1.1k	288	12.6k
Joel L. Moake	5.9k 0.7×	5.9k 0.9×	2.5k 0.7×	1.9k 0.5×	585 0.5×	146	10.4k
Marie Scully	5.0k 0.6×	3.9k 0.6×	2.6k 0.7×	1.9k 0.5×	507 0.5×	185	7.7k
I. Scharrer	2.1k 0.3×	6.0k 0.9×	1.1k 0.3×	1.4k 0.4×	1.5k 1.4×	180	10.1k
Klaus Lechner	4.9k 0.6×	10.8k 1.6×	445 0.1×	3.7k 1.0×	2.4k 2.2×	453	18.8k
Jane E. Salmon	6.8k 0.8×	3.2k 0.5×	1.9k 0.5×	530 0.1×	174 0.2×	211	14.6k
Tatsuya Atsumi	4.2k 0.5×	5.0k 0.7×	1.7k 0.4×	719 0.2×	581 0.5×	512	15.5k
John G. Kelton	2.5k 0.3×	9.2k 1.3×	1.5k 0.4×	1.4k 0.4×	4.7k 4.3×	236	16.3k
Hannah Cohen	1.7k 0.2×	3.7k 0.5×	1.1k 0.3×	805 0.2×	1.1k 1.1×	195	9.4k
Paul Knöbl	2.0k 0.2×	3.2k 0.5×	913 0.2×	1.2k 0.3×	396 0.4×	159	5.6k
James B. Bussel	3.8k 0.5×	17.2k 2.5×	1.6k 0.4×	3.4k 1.0×	327 0.3×	514	21.1k

Countries citing papers authored by Bernhard Lämmle

Since Specialization

Citations

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

Fields of papers citing papers by Bernhard Lämmle

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bernhard Lämmle

This figure shows the co-authorship network connecting the top 25 collaborators of Bernhard Lämmle. A scholar is included among the top collaborators of Bernhard Lämmle 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 Bernhard Lämmle. Bernhard Lämmle 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

Barco, Stefano, Alice Trinchero, Chiara Ambaglio, et al.. (2023). Severe high-molecular-weight kininogen deficiency: clinical characteristics, deficiency–causing KNG1 variants, and estimated prevalence. Journal of Thrombosis and Haemostasis. 21(2). 237–254. 7 indexed citations

Häuser, Friederike, Heidi Rossmann, Claudia Paret, et al.. (2023). Hereditary Spherocytosis: Can Next-Generation Sequencing of the Five Most Frequently Affected Genes Replace Time-Consuming Functional Investigations?. International Journal of Molecular Sciences. 24(23). 17021–17021. 5 indexed citations

Sakai, Kazuya, Ilaria Mancini, György Sinkovits, et al.. (2023). Open ADAMTS-13 conformation index predicts earlier relapse in immune-mediated thrombotic thrombocytopenic purpura. Journal of Thrombosis and Haemostasis. 22(2). 493–502. 7 indexed citations

Falter, Tanja, Heidi Rossmann, Charis von Auer, et al.. (2023). A novel von Willebrand factor multimer ratio as marker of disease activity in thrombotic thrombocytopenic purpura. Blood Advances. 7(17). 5091–5102. 5 indexed citations

Bütikofer, Lukas, Kenneth D. Friedman, James N. George, et al.. (2021). Annual incidence and severity of acute episodes in hereditary thrombotic thrombocytopenic purpura. Blood. 137(25). 3563–3575. 41 indexed citations

Cuker, Adam, Spero R. Cataland, Paul Coppo, et al.. (2021). Redefining outcomes in immune TTP: an international working group consensus report. Blood. 137(14). 1855–1861. 121 indexed citations

Barco, Stefano, Alice Trinchero, Hassan Abolghasemi, et al.. (2020). Severe plasma prekallikrein deficiency: Clinical characteristics, novel KLKB1 mutations, and estimated prevalence. Journal of Thrombosis and Haemostasis. 18(7). 1598–1617. 17 indexed citations

Barco, Stefano, Alice Trinchero, Dagmar Laubert‐Reh, et al.. (2020). c.451dupT in KLKB1 is common in Nigerians, confirming a higher prevalence of severe prekallikrein deficiency in Africans compared to Europeans. Journal of Thrombosis and Haemostasis. 19(1). 147–152.

Falter, Tanja, Veronika Weyer, Charis von Auer, et al.. (2017). Depression and cognitive deficits as long‐term consequences of thrombotic thrombocytopenic purpura. Transfusion. 57(5). 1152–1162. 40 indexed citations

10.

Lämmle, Bernhard. (2016). Caplacizumab accelerates resolution of acute acquired TTP. Nature Reviews Nephrology. 12(5). 259–260. 5 indexed citations

11.

Jiménez-Alcázar, Miguel, Markus Napirei, Rachita Panda, et al.. (2014). Impaired DNase1‐mediated degradation of neutrophil extracellular traps is associated with acute thrombotic microangiopathies. Journal of Thrombosis and Haemostasis. 13(5). 732–742. 114 indexed citations

12.

Stroka, Deborah, Adrian Keogh, Dũng Chí Vũ, et al.. (2014). In vitro rescue of FGA deletion by lentiviral transduction of an afibrinogenemic patient's hepatocytes. Journal of Thrombosis and Haemostasis. 12(11). 1874–1879. 4 indexed citations

13.

Hovinga, Johanna A. Kremer & Bernhard Lämmle. (2012). Role of ADAMTS13 in the pathogenesis, diagnosis, and treatment of thrombotic thrombocytopenic purpura. Hematology. 2012(1). 610–616. 55 indexed citations

14.

George, JN, Sara K. Vesely, Deirdra R. Terrell, et al.. (2011). Evidence for a role of anti-ADAMTS13 autoantibodies despite normal ADAMTS13 activity in recurrent thrombotic thrombocytopenic purpura. Haematologica. 97(2). 297–303. 55 indexed citations

15.

Isenegger, Jörg, Niklaus Meier, Bernhard Lämmle, et al.. (2009). D-Dimers Predict Stroke Subtype when Assessed Early. Cerebrovascular Diseases. 29(1). 82–86. 48 indexed citations

16.

Terrell, Deirdra R., Lauren A. Williams, Sara K. Vesely, et al.. (2005). The incidence of thrombotic thrombocytopenic purpura‐hemolytic uremic syndrome: all patients, idiopathic patients, and patients with severe ADAMTS‐13 deficiency. Journal of Thrombosis and Haemostasis. 3(7). 1432–1436. 231 indexed citations

17.

Studt, Jan–Dirk, Johanna A. Kremer Hovinga, Gerhard Antoine, et al.. (2004). Fatal congenital thrombotic thrombocytopenic purpura with apparent ADAMTS13 inhibitor: in vitro inhibition of ADAMTS13 activity by hemoglobin. Blood. 105(2). 542–544. 117 indexed citations

18.

Alberio, Lorenzo, et al.. (2003). Rapid determination of anti-heparin/platelet factor 4 antibody titers in the diagnosis of heparin-induced thrombocytopenia. The American Journal of Medicine. 114(7). 528–536. 49 indexed citations

19.

Zeerleder, Sacha, et al.. (2002). Effect of low-molecular weight dextran sulfate on coagulation and platelet function tests. Thrombosis Research. 105(5). 441–446. 48 indexed citations

20.

Lämmle, Bernhard, et al.. (1978). [Pathophysiology and surgery of the parathyroid glands].. PubMed. 44(5-6). 767–77. 1 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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