Damla Olcaydu

1.4k total citations
15 papers, 955 citations indexed

About

Damla Olcaydu is a scholar working on Genetics, Hematology and Molecular Biology. According to data from OpenAlex, Damla Olcaydu has authored 15 papers receiving a total of 955 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 10 papers in Hematology and 8 papers in Molecular Biology. Recurrent topics in Damla Olcaydu's work include Myeloproliferative Neoplasms: Diagnosis and Treatment (11 papers), Kruppel-like factors research (6 papers) and Chronic Myeloid Leukemia Treatments (5 papers). Damla Olcaydu is often cited by papers focused on Myeloproliferative Neoplasms: Diagnosis and Treatment (11 papers), Kruppel-like factors research (6 papers) and Chronic Myeloid Leukemia Treatments (5 papers). Damla Olcaydu collaborates with scholars based in Austria, Italy and Germany. Damla Olcaydu's co-authors include Róbert Královics, Ashot S. Harutyunyan, Roland Jäger, Heinz Gisslinger, Bettina Gisslinger, Tiina Berg, Ingrid Pabinger, Johannes M. Breuss, Bernd R. Binder and Hannes Stockinger and has published in prestigious journals such as Nature Genetics, Blood and Circulation Research.

In The Last Decade

Damla Olcaydu

14 papers receiving 940 citations

Peers

Damla Olcaydu

GENET

HEMAT

ONCOL

RHEUM

Katherine Waghorn United Kingdom

Hédia Chagraoui France

Philippe Rameau France

Sam Agresta United States

H. M. Kvasnicka Germany

María José Larráyoz Spain

Jack L. Spurbeck United States

Marie Jarošová Czechia

Idoya Lahortiga Spain

Takefumi Ishii United States

Katherine Waghorn United Kingdom

Damla Olcaydu

500 ×1.0

GENET

730 ×1.5

660 ×1.4

HEMAT

72 ×0.3

ONCOL

265 ×1.4

RHEUM

Citations per year, relative to Damla Olcaydu Damla Olcaydu (= 1×) peers Katherine Waghorn

Countries citing papers authored by Damla Olcaydu

Since Specialization

Citations

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

Fields of papers citing papers by Damla Olcaydu

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Damla Olcaydu

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

All Works

Sort: Min cites: Since: Top N: Style:

15 of 15 papers shown

Jäger, Roland, Ashot S. Harutyunyan, Elisa Rumi, et al.. (2014). Common germline variation at the TERT locus contributes to familial clustering of myeloproliferative neoplasms. American Journal of Hematology. 89(12). 1107–1110. 33 indexed citations

Buxhofer‐Ausch, Veronika, Damla Olcaydu, Bettina Gisslinger, et al.. (2014). Decanucleotide insertion polymorphism of F7 significantly influences the risk of thrombosis in patients with essential thrombocythemia. European Journal Of Haematology. 93(2). 103–111. 13 indexed citations

Awad, Ezzat M., Shafaat Yar Khan, Patrick M. Brunner, et al.. (2013). Cold induces reactive oxygen species production and activation of the NF‐kappa B response in endothelial cells and inflammation in vivo. Journal of Thrombosis and Haemostasis. 11(9). 1716–1726. 38 indexed citations

Klampfl, Thorsten, Ashot S. Harutyunyan, Tiina Berg, et al.. (2011). Genome integrity of myeloproliferative neoplasms in chronic phase and during disease progression. Blood. 118(1). 167–176. 128 indexed citations

Jäger, Roland, Heinz Gisslinger, Francesco Passamonti, et al.. (2010). Deletions of the transcription factor Ikaros in myeloproliferative neoplasms. Leukemia. 24(7). 1290–1298. 105 indexed citations

Olcaydu, Damla, Elisa Rumi, Ashot S. Harutyunyan, et al.. (2010). The role of the JAK2 GGCC haplotype and the TET2 gene in familial myeloproliferative neoplasms. Haematologica. 96(3). 367–374. 45 indexed citations

Klampfl, Thorsten, Ashot S. Harutyunyan, Tiina Berg, et al.. (2010). Chromosomal Aberration Network In Myeloproliferative Neoplasms. Blood. 116(21). 318–318. 3 indexed citations

Uhrín, Pavel, Jan Zaujec, Johannes M. Breuss, et al.. (2010). Novel function for blood platelets and podoplanin in developmental separation of blood and lymphatic circulation. Blood. 115(19). 3997–4005. 235 indexed citations

Olcaydu, Damla, Ashot S. Harutyunyan, Roland Jäger, et al.. (2009). A common JAK2 haplotype confers susceptibility to myeloproliferative neoplasms. Nature Genetics. 41(4). 450–454. 244 indexed citations

10.

Jäger, Roland, Heinz Gisslinger, Tiina Berg, et al.. (2009). Deletions of the Transcription Factor Ikaros in Myeloproliferative Neoplasms at Transformation to Acute Myeloid Leukemia.. Blood. 114(22). 435–435. 9 indexed citations

11.

Liu, Kai, Róbert Královics, Zbigniew Rudzki, et al.. (2008). A de novo splice donor mutation in the thrombopoietin gene causes hereditary thrombocythemia in a Polish family. Haematologica. 93(5). 706–714. 32 indexed citations

12.

Olcaydu, Damla, Tiina Berg, Bettina Gisslinger, Heinz Gisslinger, & Róbert Královics. (2008). Deletions of Chromosome 13q in Myeloproliferative Neoplasms: Mapping, Relation to the JAK2-V617F Mutation and Evaluation of Potential Tumor Suppressor Candidates. Blood. 112(11). 3724–3724. 2 indexed citations

13.

Olcaydu, Damla, et al.. (2008). VEGF and AMD3100-Induced Rapid Mobilization of C-Kit/Sca-1 Positive Murine Bone Marrow Cells and of Gr-1+/CD-11b+ Myeloid Cells Is Impaired in Urokinase (uPA) and Urokinase Receptor (uPAR) Deficient Mice.. Blood. 112(11). 1384–1384.

14.

Olcaydu, Damla, Heinz Gisslinger, Harald Esterbauer, Franz Wiesbauer, & Róbert Královics. (2007). Polymorphisms of NOS3 and FCGR2A Genes Contribute to Thrombotic Risk in Essential Thrombocythemia. Blood. 110(11). 1537–1537. 1 indexed citations

15.

Prager, Gerald W., Johannes M. Breuss, Stefan Steurer, et al.. (2004). Vascular Endothelial Growth Factor Receptor-2–Induced Initial Endothelial Cell Migration Depends on the Presence of the Urokinase Receptor. Circulation Research. 94(12). 1562–1570. 67 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.

Explore authors with similar magnitude of impact