The DOI matches its Crossref record; 24 of the 24 references it cites were found in a registry or an index.
Increased Activity of Coagulation Factor XII (Hageman Factor) Causes Hereditary Angioedema Type III
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Citations
Cites
Mutations of bacteria from virus sensitivity to virus resistance
Luria, S. E., & Delbrück, M. (1943) · Genetics · doi:10.1093/genetics/28.6.491 · Cited by 3,894
A high-resolution recombination map of the human genome
Kong, A., Gudbjartsson, D. F., Sainz, J., Jonsdottir, G. M., Gudjonsson, S. A., Richardsson, B., Sigurdardottir, S., Barnard, J., Hallbeck, B., Masson, G., et al. (2002) · Nature Genetics · doi:10.1038/ng917 · Cited by 1,736
Mutation of human short tandem repeats
Weber, J. L., & Wong, C. (1993) · Human Molecular Genetics · doi:10.1093/hmg/2.8.1123 · Cited by 1,555
Microsatellites: Evolution and Applications
(1999) · doi:10.1093/oso/9780198504085.001.0001 · Cited by 1,047
Defective thrombus formation in mice lacking coagulation factor XII
Renné, T., Pozgajová, M., Grüner, S., Schuh, K., Pauer, H.-U., Burfeind, P., Gailani, D., & Nieswandt, B. (2005) · The Journal of Experimental Medicine · doi:10.1084/jem.20050664 · Cited by 683
Agostoni, A., Aygören-Pürsün, E., Binkley, K. E., Blanch, A., Bork, K., Bouillet, L., Bucher, C., Castaldo, A. J., Cicardi, M., Davis, A. E., et al. (2004) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2004.06.047 · Cited by 646
Self-citationHereditary angioedema with normal C1-inhibitor activity in women
Bork, K., Barnstedt, S.-E., Koch, P., & Traupe, H. (2000) · The Lancet · doi:10.1016/s0140-6736(00)02483-1 · Cited by 557
Self-citationKleinschnitz, C., Stoll, G., Bendszus, M., Schuh, K., Pauer, H.-U., Burfeind, P., Renné, C., Gailani, D., Nieswandt, B., & Renné, T. (2006) · The Journal of Experimental Medicine · doi:10.1084/jem.20052458 · Cited by 452
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Dewald, G., & Bork, K. (2006) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2006.03.092 · Cited by 402
Self-citation
Research works printed but not linked: 4
- Bowen, 2001, A review of the reported defects in the human C1 esterase inhibitor gene producing hereditary angioedema including four new mutations, Clin Immunol, 98, 157, 10.1006/clim.2000.4947 · doi:10.1006/clim.2000.4947
- Martin, 2001, Hereditary angioedema type 3: an additional French pedigree with autosomal dominant transmission, J Allergy Clin Immunol, 107, 747, 10.1067/mai.2001.114242 · doi:10.1067/mai.2001.114242
- Citarella, 1996, Structure/function analysis of human factor XII using recombinant deletion mutants. Evidence for an additional region involved in the binding to negatively charged surfaces, Eur J Biochem, 238, 240, 10.1111/j.1432-1033.1996.0240q.x · doi:10.1111/j.1432-1033.1996.0240q.x
- Gupta, 2004, New-variant hereditary angioedema in three brothers with normal C1 esterase inhibitor level and function, Allergy, 59, 557, 10.1111/j.1398-9995.2004.00428.x · doi:10.1111/j.1398-9995.2004.00428.x
Cited by
HAE Pathophysiology and Underlying Mechanisms
Zuraw, B. L., & Christiansen, S. C. (2016) · Clinical Reviews in Allergy & Immunology · doi:10.1007/s12016-016-8561-8 · Cited by 164
Cilia La Corte, A. L., Carter, A. M., Rice, G. I., Duan, Q. L., Rouleau, G. A., Adam, A., Grant, P. J., & Hooper, N. M. (2011) · Human Mutation · doi:10.1002/humu.21579 · Cited by 154
The Expanding Spectrum of Mutations in Hereditary Angioedema
Veronez, C. L., Csuka, D., Sheikh, F. R., Zuraw, B. L., Farkas, H., & Bork, K. (2021) · The Journal of Allergy and Clinical Immunology: In Practice · doi:10.1016/j.jaip.2021.03.008 · Cited by 57
Self-citationMaroteau, C., Siddiqui, M. K., Veluchamy, A., Carr, F., White, M., Cassidy, A. J., Baranova, E. V., Rasmussen, E. R., Eriksson, N., Bloch, K. M., et al. (2020) · Clinical Pharmacology & Therapeutics · doi:10.1002/cpt.1927 · Cited by 21
Metadata
- Authors
- Cichon, S., Martin, L., Hennies, H. C., Müller, F., Van Driessche, K., Karpushova, A., Stevens, W., Colombo, R., Renné, T., Drouet, C., Bork, K., & Nöthen, M. M.
- Venue
- The American Journal of Human Genetics
- Publisher
- Elsevier BV
- Published
- 2006-12
- Volume
- 79
- Issue
- 6
- Pages
- 1098-1104
- ISSN
- 0002-9297 (ISSN-L)
- OpenAlex
- W1987529569
- Cited by
- 329
- References
- 24
- FWCI
- 6.56
- Type
- journal article
- Language
- en
- Open access
- bronze
- Licence
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- www.elsevier.com/legal/tdmrep-license (tdm)
- www.elsevier.com/open-access/userlicense/1.0/ (vor, 2422 d)
- Funders
- Alfried Krupp von Bohlen und Halbach-Stiftung
- Deutsche Forschungsgemeinschaft (SFB 688)
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- CoChat. (2026). Citation check: Increased Activity of Coagulation Factor XII (Hageman Factor) Causes Hereditary Angioedema Type III. https://app.cochat.ai/papers/10.1086/509899
- The paper
- Cichon, S., Martin, L., Hennies, H. C., Müller, F., Van Driessche, K., Karpushova, A., Stevens, W., Colombo, R., Renné, T., Drouet, C., Bork, K., & Nöthen, M. M. (2006). Increased Activity of Coagulation Factor XII (Hageman Factor) Causes Hereditary Angioedema Type III. The American Journal of Human Genetics. https://doi.org/10.1086/509899
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.
