Georg Dewald

1.2k total citations
12 papers, 731 citations indexed

About

Georg Dewald is a scholar working on Genetics, Immunology and Pathology and Forensic Medicine. According to data from OpenAlex, Georg Dewald has authored 12 papers receiving a total of 731 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 5 papers in Immunology and 3 papers in Pathology and Forensic Medicine. Recurrent topics in Georg Dewald's work include Coagulation, Bradykinin, Polyphosphates, and Angioedema (5 papers), Complement system in diseases (4 papers) and Vitamin K Research Studies (3 papers). Georg Dewald is often cited by papers focused on Coagulation, Bradykinin, Polyphosphates, and Angioedema (5 papers), Complement system in diseases (4 papers) and Vitamin K Research Studies (3 papers). Georg Dewald collaborates with scholars based in Germany, France and Denmark. Georg Dewald's co-authors include Konrad Bork, Bettina Fischer, Jochen Hardt, Markus M. Nöthen, Hadas Lahat, Jaime Toribio, Regina C. Betz, Christian Kubisch, Marina Guerrin and Sven Cichon and has published in prestigious journals such as Nature Genetics, Blood and Biochemical and Biophysical Research Communications.

In The Last Decade

Georg Dewald

11 papers receiving 714 citations

Peers

Georg Dewald
Guoan He China
Paula Berkowitz United States
Judit Várkonyi Hungary
Gedeon Loules Greece
Antonella Contri Italy
Carlos A Tirado United States
Andreas M. Boehmler Germany
Sibylle Teurich Germany
Valérie Camara‐Clayette France
Carol Halloran United States
Guoan He China
Georg Dewald
Citations per year, relative to Georg Dewald Georg Dewald (= 1×) peers Guoan He

Countries citing papers authored by Georg Dewald

Since Specialization
Citations

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

Fields of papers citing papers by Georg Dewald

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Georg Dewald

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

All Works

12 of 12 papers shown
1.
Dewald, Georg. (2018). A missense mutation in the plasminogen gene, within the plasminogen kringle 3 domain, in hereditary angioedema with normal C1 inhibitor. Biochemical and Biophysical Research Communications. 498(1). 193–198. 40 indexed citations
2.
Kuijpers, Taco W., C. T. P. Hopman, Ed Nieuwenhuys, et al.. (2009). Complement factor 7 gene mutations in relation to meningococcal infection and clinical recurrence of meningococcal disease. Molecular Immunology. 47(4). 671–677. 10 indexed citations
3.
Bork, Konrad, et al.. (2007). Hereditary Angioedema with Normal C1 Inhibitor: Clinical Symptoms and Course. The American Journal of Medicine. 120(11). 987–992. 106 indexed citations
4.
Dewald, Georg & Konrad Bork. (2006). Missense mutations in the coagulation factor XII (Hageman factor) gene in hereditary angioedema with normal C1 inhibitor. Biochemical and Biophysical Research Communications. 343(4). 1286–1289. 295 indexed citations
5.
6.
Levy‐Nissenbaum, Etgar, Regina C. Betz, Moshe Frydman, et al.. (2003). Hypotrichosis simplex of the scalp is associated with nonsense mutations in CDSN encoding corneodesmosin. Nature Genetics. 34(2). 151–153. 108 indexed citations
7.
Bork, Konrad, Bettina Fischer, & Georg Dewald. (2003). Recurrent episodes of skin angioedema and severe attacks of abdominal pain induced by oral contraceptives or hormone replacement therapy. The American Journal of Medicine. 114(4). 294–298. 132 indexed citations
8.
Schroers, Roland, Marcella Rietschel, Margot Albus, et al.. (1997). Investigation of Complement C4B Deficiency in Schizophrenia. Human Heredity. 47(5). 279–282. 23 indexed citations
9.
Dewald, Georg, et al.. (1996). A HhaI Polymorphism in the Human MEP1A Gene Encoding the Alpha Subunit of the Metalloendopeptidase Meprin. Human Heredity. 46(5). 298–300. 1 indexed citations
10.
Nöthen, Markus M. & Georg Dewald. (1995). Dinucleotide repeat polymorphism at the human CD59 locus. Clinical Genetics. 47(3). 165–166. 1 indexed citations
11.
Dewald, Georg, et al.. (1994). A Common Ser/Thr Polymorphism in the Perforin-Homologous Region of Human Complement Component C7. Human Heredity. 44(6). 301–304. 8 indexed citations
12.
Dewald, Georg, et al.. (1994). Human complement component C8. FEBS Letters. 340(3). 211–215. 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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