Konrad Bork

17.8k total citations · 3 hit papers
209 papers, 9.5k citations indexed

About

Konrad Bork is a scholar working on Genetics, Pathology and Forensic Medicine and Nutrition and Dietetics. According to data from OpenAlex, Konrad Bork has authored 209 papers receiving a total of 9.5k indexed citations (citations by other indexed papers that have themselves been cited), including 141 papers in Genetics, 66 papers in Pathology and Forensic Medicine and 57 papers in Nutrition and Dietetics. Recurrent topics in Konrad Bork's work include Coagulation, Bradykinin, Polyphosphates, and Angioedema (138 papers), Autoimmune Bullous Skin Diseases (63 papers) and Vitamin K Research Studies (57 papers). Konrad Bork is often cited by papers focused on Coagulation, Bradykinin, Polyphosphates, and Angioedema (138 papers), Autoimmune Bullous Skin Diseases (63 papers) and Vitamin K Research Studies (57 papers). Konrad Bork collaborates with scholars based in Germany, United States and Italy. Konrad Bork's co-authors include Jochen Hardt, Petra Staubach, Günther Witzke, Georg Dewald, K. Wulff, Hilary Longhurst, Marco Cicardi, Petra Koch, Heiko Traupe and Henriette Farkas and has published in prestigious journals such as New England Journal of Medicine, The Lancet and Journal of Clinical Investigation.

In The Last Decade

Konrad Bork

198 papers receiving 9.2k citations

Hit Papers

align trajectories

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.

Hereditary Angioedema: New Findings Concerning Symptoms, Affected Organs, and Course

2006 531 citations Konrad Bork, Petra Staubach et al. profile →
ALDEN, an Algorithm for Assessment of Drug Causality in Stevens–Johnson Syndrome and Toxic Epidermal Necrolysis: Comparison With Case–Control Analysis

2010 474 citations Konrad Bork et al. profile →
Classification, diagnosis, and approach to treatment for angioedema: consensus report from the Hereditary Angioedema International Working Group

2014 413 citations Werner Aberer, Konrad Bork et al. Allergy profile →

Peers

Countries citing papers authored by Konrad Bork

Since Specialization

Citations

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

Fields of papers citing papers by Konrad Bork

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Konrad Bork

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

#	Work	Indexed citations
1	Attenuated androgen discontinuation in patients with hereditary angioedema: a commented case series 2022 ·Allergy Asthma and Clinical Immunology ·Marcus Maurer, Markus Magerl, Emel Aygören‐Pürsün, Konrad Bork, Henriette Farkas, Hilary Longhurst, Sorena Kiani‐Alikhan, Laurence Bouillet, Isabelle Boccon‐Gibod, Mauro Cancian, Andrea Zanichelli, David Launay	6
2	Current and Prospective Targets of Pharmacologic Treatment of Hereditary Angioedema Types 1 and 2 2021 ·Clinical Reviews in Allergy & Immunology ·Lauré M. Fijen, Konrad Bork, Danny M. Cohn	21
3	Hereditary angioedema in children and adolescents – A consensus update on therapeutic strategies for German‐speaking countries 2020 ·Pediatric Allergy and Immunology ·V. Wahn, Werner Aberer, (unknown), Konrad Bork, W. Eberl, Maria Faßhauer, Renate Krüger, Markus Magerl, Inmaculada Martinez‐Saguer, Peter Späth, Petra Staubach, (unknown)	12
4	Clinical features of genetically characterized types of hereditary angioedema with normal C1 inhibitor: a systematic review of qualitative evidence 2020 ·Orphanet Journal of Rare Diseases ·Konrad Bork, Thomas Machnig, K. Wulff, Guenther Witzke, (unknown), Jochen Hardt	67
5	Angioedema Due To Acquired C1-Inhibitor Deficiency: Spectrum And Treatment With C1-Inhibitor Concentrate 2019 ·Journal of Allergy and Clinical Immunology ·Konrad Bork, Petra Staubach, Jochen Hardt	1
6	Hereditary angioedema: an update on causes, manifestations and treatment 2019 ·British Journal of Hospital Medicine ·Hilary Longhurst, Konrad Bork	76
7	Hereditary angioedema with a mutation in the plasminogen gene 2017 ·Allergy ·Konrad Bork, K. Wulff, Lars Steinmüller‐Magin, Ingrid Brænne, Petra Staubach, Guenther Witzke, J. Hardt	198
8	Hereditary angioedema with normal C1‐INH with versus without specific F12 gene mutations 2015 ·Allergy ·Konrad Bork, K. Wulff, Günther Witzke, J. Hardt	96
9	Recurrent Angioedema and the Threat of Asphyxiation 2010 ·Deutsches Ärzteblatt international ·Konrad Bork	27
10	Safety Evaluation of Icatibant, a Selective Bradykinin B2 Receptor Antagonist Used in Hereditary Angioedema Due to C1 Inhibitor Deficiency 2009 ·Journal of Allergy and Clinical Immunology ·Petra Staubach, Konrad Bork	1
11	Mutational spectrum of the<i> C1INH (SERPING1) </i>gene in patients with hereditary angioedema 2008 ·Cytogenetic and Genome Research ·(unknown), Arkadius Kocot, (unknown), W. Kreuz, I. Martinez‐Saguer, Emel Aygören‐Pürsün, E. Rusicke, Konrad Bork, Johannes Oldenburg, C. R. Müller	63
12	Hereditary angioedema: causes, manifestations and treatment 2006 ·British Journal of Hospital Medicine ·Hilary Longhurst, Konrad Bork	23
13	Hereditary Angioedema with Normal C1 Inhibitor Activity Including Hereditary Angioedema with Coagulation Factor XII Gene Mutations 2006 ·Immunology and Allergy Clinics of North America ·Konrad Bork	53
14	Hereditary angio-oedema with normal C1 inhibitor in a family with affected women and men 2005 ·British Journal of Dermatology ·Konrad Bork, (unknown), (unknown)	61
15	Treatment of 193 Episodes of Laryngeal Edema With C1 Inhibitor Concentrate in Patients With Hereditary Angioedema 2001 ·Archives of Internal Medicine ·Konrad Bork, (unknown)	164
16	Persistent skin ulcers, mutilations, and acro-osteolysis in hereditary sensory and autonomic neuropathy with phospholipid excretion 1989 ·Journal of the American Academy of Dermatology ·(unknown), (unknown), Konrad Bork	12
17	[Overall progeroid aspect of the Louis-Bar syndrome: pigmentary and keratotic phenomena]. 1979 ·Munich Personal RePEc Archive (Ludwig Maximilian University of Munich) ·(unknown), Konrad Bork	1
18	[Life threatening laryngeal edema after minor dental treatments in hereditary angioneurotic edema]. 1979 ·Munich Personal RePEc Archive (Ludwig Maximilian University of Munich) ·(unknown), Konrad Bork	1
19	Physikalische Grundlagen der Blasenbildung: II. Untersuchung des gesamtosmotischen Druckes in der Blasenflssigkeit von Saugblasen und von ?natrlich? entstandenen Blasen sowie im Serum 1978 ·Archives of Dermatological Research ·Konrad Bork	1
20	[Paget's disease of the vulva and breast carcinoma]. 1976 ·Munich Personal RePEc Archive (Ludwig Maximilian University of Munich) ·Konrad Bork, (unknown)	1

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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