K. Olek

2.9k citations

106 papers · 2.3k · h-index 25

Impact in

Hematology top 1%
- Hemophilia Treatment and Research
- Blood Coagulation and Thrombosis Mechanisms
- Platelet Disorders and Treatments
Genetics top 5%
- Coagulation, Bradykinin, Polyphosphates, and Angioedema

Papers in

Molecular Biology 61
- Cancer-related gene regulation 19
Hematology 33
- Hemophilia Treatment and Research 28
- Platelet Disorders and Treatments 11
- Blood Coagulation and Thrombosis Mechanisms 11

Co-authors: R. Schwaab (20 shared papers)Johannes Oldenburg (12 shared papers)Edward G. D. Tuddenham (5 shared papers)Michael Kirchgesser (3 shared papers)Miyoko Higuchi (14 shared papers)Michael Ludwig (17 shared papers)J.-P. Faber (7 shared papers)Wolfgang Poller (9 shared papers)
Journals: Human Genetics (20 papers)Nucleic Acids Research (16 papers)Clinical Chemistry and Laboratory Medicine (CCLM) (8 papers)Journal of Molecular Medicine (5 papers)Blood (4 papers)
Partner nations: Germany United Kingdom United States

In The Last Decade

K. Olek

100 papers receiving 2.2k citations

Peers

Countries citing papers authored by K. Olek

Since Specialization

Citations

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

Fields of papers citing papers by K. Olek

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside K. Olek, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with K. Olek Line = papers co-authored together K. Olek links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 106 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Haemophilia A: Mutation Type Determines Risk of Inhibitor Formation Thrombosis and Haemostasis ·R. Schwaab, H.H. Brackmann, Christian Meyer, J. Seehafer, Michael Kirchgesser, Astrid Haack, K. Olek, Edward G. D. Tuddenham, Johannes Oldenburg	1995	261
2	Proteome-wide drug and metabolite interaction mapping by thermal-stability profiling Nature Methods ·K. Huber, K. Olek, André C. Müller, Chris Soon Heng Tan, Keiryn L. Bennett, Jacques Colinge, Giulio Superti‐Furga	2015	171
3	Haemophilia A: database of nucleotide substitutions, deletions, insertions and rearrangements of the factor VIII gene, second edition Nucleic Acids Research ·Edward G. D. Tuddenham, R. Schwaab, J. Seehafer, David Millar, Jane Gitschier, Miyoko Higuchi, Sanjay I. Bidichandani, J. M. Connor, Leon W. Hoyer, Akira Yoshioka, I R Peake, K. Olek, H H Kazazian, J. M. Lavergne, F. Giannelli, Stylianos E. Antonarakis, D.N. Cooper	1994	125
4	Characterization of the factor VIII defect in 147 patients with sporadic hemophilia A: family studies indicate a mutation type-dependent sex ratio of mutation frequencies. PubMed ·Jéfferson Becker, R. Schwaab, A. Möller-Taube, U. Schwaab, W. Schmidt, Hans‐Hermann Brackmann, T. Grimm, K. Olek, Johannes Oldenburg	1996	114
5	Regeneration‐associated high level expression of apolipoprotein D mRNA in endoneurial fibroblasts of peripheral nerve. The EMBO Journal ·P. Spreyer, Heiner Schaal, H. Georg Kuhn, Thomas Rothe, Axel Unterbeck, K. Olek, H. W. Müller	1990	112
6	Molecular characterization of mild-to-moderate hemophilia A: detection of the mutation in 25 of 29 patients by denaturing gradient gel electrophoresis. Proceedings of the National Academy of Sciences ·Miyoko Higuchi, Stylianos E. Antonarakis, L. Kasch, Johannes Oldenburg, E Economou-Petersen, K. Olek, Morio Arai, Hiroshi Inaba, H H Kazazian	1991	111
7	Haemophilia A: database of ncleotide substituttions, deletions, insertions and rearrangements of the factor VIII gene Nucleic Acids Research ·Edward G. D. Tuddenham, D.N. Cooper, Jane Gitschier, Miyoko Higuchi, Leon W. Hoyer, Akira Yoshioka, I. R. Peake, R. Schwaab, K. Olek, H H Kazazian, J. M. Lavergne, F. Giannelli, Stylianos E. Antonarakis	1991	94
8	A Leucine-to-Proline Substitution Causes a Defective α1-Antichymotrypsin Allele Associated with Familial Obstructive Lung Disease Genomics ·Wolfgang Poller, J.-P. Faber, Stephan Weidinger, K. Tief, Sonja W. Scholz, Matthew Fischer, K. Olek, Michael Kirchgesser, H.-H. Heidtmann	1993	87
9	Comparison between intratracheal and intravenous administration of liposome–DNA complexes for cystic fibrosis lung gene therapy Gene Therapy ·Uta Griesenbach, Arcadio Chonn, R Cassady, Vicky Hannam, CA Ackerley, Martin Post, A. Keith Tanswell, K. Olek, Hugh OʼBrodovich, LC Tsui	1998	71
10	Haemophilia B: database of point mutations and short additions and deletions Nucleic Acids Research ·F. Giannelli, P. M. Green, KA High, JN Lozier, David Lillicrap, Michael Ludwig, K. Olek, Pieter H. Reitsma, M. Goossens, Akira Yoshioka, Stefanie Sommer, G.G. Brownlee	1990	61
11	Carnitine palmitoyltransferase II deficiency Neurology ·Thomas Wieser, Marcus Deschauer, K. Olek, Thomas Hermann, S. Zierz	2003	57
12	Identification and DNA sequence analysis of 15 new alpha 1-antitrypsin variants, including two PIQ0 alleles and one deficient PIM allele. PubMed ·J.-P. Faber, Wolfgang Poller, Stephan Weidinger, Michael Kirchgesser, R. Schwaab, F. Bidlingmaier, K. Olek	1994	55
13	Characterization of mutations within the factor VIII gene of 73 unrelated mild and moderate haemophiliacs British Journal of Haematology ·R. Schwaab, Johannes Oldenburg, U. Schwaab, Daniel J. D. Johnson, W. Schmidt, K. Olek, H.‐H. Brackman, E. G. D. Tdddenham	1995	53
14	Allelic dimorphism in the human tissue-type plasminogen activator (TPA) gene as a result of an Alu insertion/deletion event Human Genetics ·Michael Ludwig, K.-D. Wohn, Wolf‐Dieter Schleuning, K. Olek	1992	49
15	Phenylketonuria: distribution of DNA diagnostic patterns in German families Human Genetics ·C. Aulehla‐Scholz, Matthias Vorgerd, E. Sautter, D. Leupold, R. Mahlmann, Kurt Ullrich, K. Olek, J. Horst	1988	41
16	Cloning of the human ?2-macroglobulin gene and detection of mutations in two functional domains: the bait region and the thiolester site Human Genetics ·Wolfgang Poller, J.-P. Faber, Gustav Klobeck, K. Olek	1992	35
17	A novel non-canonical PIP-box mediates PARG interaction with PCNA Nucleic Acids Research ·Tanja Kaufmann, Irina Grishkovskaya, Anton A. Polyansky, Sebastian Kostrhon, Eva Kukolj, K. Olek, Sébastien Herbert, Etienne Beltzung, Karl Mechtler, Thomas Peterbauer, Josef Gotzmann, Lijuan Zhang, Markus Hartl, Bojan Žagrović, Kareem Elsayad, Kristina Djinović‐Carugo, Dea Slade	2017	35
18	Haemophilia B: database of point mutations and short additions and deletions--third edition, 1992 Nucleic Acids Research ·F. Giannelli, P.M. Green, Katherine A. High, S. Sommer, D Lillicrap, Michael Ludwig, K. Olek, Pieter H. Reitsma, M. Goossens, Akira Yoshioka, G. G. Brownlee	1992	34
19	Recurrent mutations in the factor IX gene: founder effect or repeat de novo events Human Genetics ·O Knobloch, Barbara Zoll, Klaus Zerres, Hans‐Hermann Brackmann, K. Olek, Michael Ludwig	1993	33
20	Mapping of DNA markers linked to the cystic fibrosis locus on the long arm of chromosome 7. PubMed ·S. Zengerling, Tsui Lc, Grzeschik Kh, K. Olek, Riordan, Manuel Buchwald	1987	33

About K. Olek

K. Olek is a scholar working on Molecular Biology, Hematology, Clinical Biochemistry, Genetics and Pulmonary and Respiratory Medicine, having authored 106 papers that have together received 2.3k indexed citations. Recurring topics across this work include Hemophilia Treatment and Research (28 papers), Cancer-related gene regulation (19 papers), Metabolism and Genetic Disorders (18 papers), Platelet Disorders and Treatments (11 papers), Blood Coagulation and Thrombosis Mechanisms (11 papers), Cystic Fibrosis Research Advances (10 papers), Analytical Chemistry and Chromatography (8 papers) and Amino Acid Enzymes and Metabolism (7 papers). The work is most often cited by research in Hematology (1.0k citations), Genetics (212 citations), Clinical Biochemistry (140 citations), Molecular Biology (1.1k citations) and Cancer Research (178 citations). K. Olek has collaborated with scholars based in Germany, United Kingdom and United States. Frequent co-authors include R. Schwaab, Johannes Oldenburg, Edward G. D. Tuddenham, Michael Kirchgesser, Miyoko Higuchi, Michael Ludwig, J.-P. Faber, Wolfgang Poller, H.H. Brackmann and Hans‐Hermann Brackmann. Their work appears in journals such as Human Genetics, Nucleic Acids Research, Clinical Chemistry and Laboratory Medicine (CCLM), Journal of Molecular Medicine and Blood.

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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K. Olek

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