K. Wulff

3.1k total citations
67 papers, 1.9k citations indexed

About

K. Wulff is a scholar working on Hematology, Molecular Biology and Genetics. According to data from OpenAlex, K. Wulff has authored 67 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Hematology, 30 papers in Molecular Biology and 20 papers in Genetics. Recurrent topics in K. Wulff's work include Hemophilia Treatment and Research (27 papers), Blood Coagulation and Thrombosis Mechanisms (21 papers) and Coagulation, Bradykinin, Polyphosphates, and Angioedema (16 papers). K. Wulff is often cited by papers focused on Hemophilia Treatment and Research (27 papers), Blood Coagulation and Thrombosis Mechanisms (21 papers) and Coagulation, Bradykinin, Polyphosphates, and Angioedema (16 papers). K. Wulff collaborates with scholars based in Germany, Costa Rica and Denmark. K. Wulff's co-authors include Konrad Bork, Günther Witzke, Jochen Hardt, Falko H. Herrmann, J. Hardt, Petra Staubach, Guenther Witzke, F. H. Herrmann, Angelika Bátorová and Lars Steinmüller‐Magin and has published in prestigious journals such as The Lancet, The American Journal of Medicine and Journal of Allergy and Clinical Immunology.

In The Last Decade

K. Wulff

65 papers receiving 1.8k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
K. Wulff Germany	19	974	914	368	362	356	67	1.9k
Maria Antonietta Aloe Spiriti Italy	20	598 0.6×	1.0k 1.1×	100 0.3×	247 0.7×	483 1.4×	67	1.5k
Hajnalka Andrikovics Hungary	21	358 0.4×	467 0.5×	141 0.4×	78 0.2×	463 1.3×	90	1.2k
Nicole Watson Australia	14	465 0.5×	567 0.6×	85 0.2×	179 0.5×	199 0.6×	23	1.3k
Angelo Guerrasio Italy	24	547 0.6×	938 1.0×	145 0.4×	159 0.4×	787 2.2×	105	1.7k
Vanessa Ponziani Italy	17	762 0.8×	543 0.6×	357 1.0×	52 0.1×	640 1.8×	24	1.2k
Michael Boxer United States	16	433 0.4×	394 0.4×	164 0.4×	314 0.9×	181 0.5×	43	1.3k
Pascal Mossuz France	16	524 0.5×	499 0.5×	214 0.6×	87 0.2×	463 1.3×	44	1.0k
J A Koedam Netherlands	14	317 0.3×	572 0.6×	68 0.2×	21 0.1×	219 0.6×	19	1.1k
JuCombining Diaeresisrgen Floege Germany	13	275 0.3×	89 0.1×	86 0.2×	148 0.4×	577 1.6×	13	1.6k
Carlo L. Balduini Italy	30	458 0.5×	1.6k 1.7×	56 0.2×	103 0.3×	225 0.6×	67	2.2k

Countries citing papers authored by K. Wulff

Since Specialization

Citations

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

Fields of papers citing papers by K. Wulff

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of K. Wulff

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

Bork, Konrad, et al.. (2020). Clinical features of genetically characterized types of hereditary angioedema with normal C1 inhibitor: a systematic review of qualitative evidence. Orphanet Journal of Rare Diseases. 15(1). 289–289. 67 indexed citations

Bork, Konrad, K. Wulff, Lars Steinmüller‐Magin, et al.. (2017). Hereditary angioedema with a mutation in the plasminogen gene. Allergy. 73(2). 442–450. 198 indexed citations

Bork, Konrad, K. Wulff, Günther Witzke, & J. Hardt. (2015). Hereditary angioedema with normal C1‐INH with versus without specific F12 gene mutations. Allergy. 70(8). 1004–1012. 96 indexed citations

Bork, Konrad, et al.. (2013). Antihistamine-resistant Angioedema in Women with Negative Family History: Estrogens and F12 Gene Mutations. The American Journal of Medicine. 126(12). 1142.e9–1142.e14. 21 indexed citations

Herrmann, F. H., G. Auerswald, Arlette Ruiz‐Sàez, et al.. (2006). Factor X deficiency: clinical manifestation of 102 subjects from Europe and Latin America with mutations in the factor 10 gene. Haemophilia. 12(5). 479–489. 143 indexed citations

Hennewig, Ulrike, et al.. (2006). LONG-TERM FVII SUBSTITUTION IN A PRETERM INFANT WITH SEVERE GASTROINTESTINAL BLEEDING AND FVII DEFICIENCY DUE TO A HOMOZYGOUS DONOR SPLICE MUTATION IVS4+1G→A. Pediatric Hematology and Oncology. 23(2). 129–133. 5 indexed citations

Meisel, Peter, J. Giebel, Kathrin I. Foerster, et al.. (2002). Expression of N-acetyltransferases in Periodontal Granulation Tissue. Journal of Dental Research. 81(5). 349–353. 12 indexed citations

Wulff, K., et al.. (2000). Identification of a novel large F9 gene mutation?An insertion of an Alu repeated DNA element in exon e of the factor 9 gene. Human Mutation. 15(3). 299–299. 17 indexed citations

Wulff, K. & Falko H. Herrmann. (2000). Twenty two novel mutations of the factor VII gene in factor VII deficiency. Human Mutation. 15(6). 489–496. 76 indexed citations

10.

Wulff, K., et al.. (1998). Molekulare Genanalyse und Gendiagnostik bei Hämophilie B und Faktor-VII-Mangel. Hämostaseologie. 18(3). 129–139. 1 indexed citations

11.

Wulff, K., et al.. (1997). Direct molecular genetic diagnosis and heterozygote identification in X-linked Emery-Dreifuss muscular dystrophy by heteroduplex analysis.. PubMed. 13(2). 77–86. 5 indexed citations

12.

Schröder, W., et al.. (1996). Large-Scale Screening for Factor V Leiden Mutation in a North-Eastern German Population. Pathophysiology of Haemostasis and Thrombosis. 26(5). 233–236. 26 indexed citations

13.

Herrmann, F. H., Manfred Wehnert, & K. Wulff. (1990). RFLP analysis for diagnosis of haemophilia A in the German Democratic Republic. Clinical Genetics. 37(1). 12–17. 6 indexed citations

14.

Herrmann, F. H., K. Wulff, Monika Schütz, & Manfred Wehnert. (1990). Deletion screening and prenatal diagnosis of Duchenne muscular dystrophy using cDNA probes Cf 23a and Cf 56a. European Journal of Pediatrics. 149(4). 263–265. 4 indexed citations

15.

Herrmann, F. H., Brunhilde Wirth, K. Wulff, et al.. (1989). Gene diagnosis in X-linked ichthyosis. Archives of Dermatological Research. 280(8). 457–461. 6 indexed citations

16.

Wulff, K., F. H. Herrmann, Martin C. Wapenaar, & Manfred Wehnert. (1989). Deletion screening in patients with Duchenne muscular dystrophy. Journal of Neurology. 236(8). 470–473. 3 indexed citations

17.

Wulff, K., et al.. (1989). Prenatal diagnosis of phenylketonuria by haplotype analysis. Prenatal Diagnosis. 9(6). 421–425. 4 indexed citations

18.

Herrmann, F. H., et al.. (1988). First experiences in application of RFLP analysis for carrier detection in preparation of prenatal diagnosis of hemophilia A in the GDR.. PubMed. 115(4). 489–93. 1 indexed citations

19.

Herrmann, F. H., et al.. (1988). Haplotype analysis of classical and mild phenotype of phenylketonuria in the German Democratic Republic. Clinical Genetics. 34(3). 176–180. 13 indexed citations

20.

Wirth, Brunhilde, F. H. Herrmann, M. Neugebauer, et al.. (1988). Linkage analysis in X-linked ichthyosis (steroid sulfatase deficiency). Human Genetics. 80(2). 191–192. 14 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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