Sevtap Savas

1.5k total citations
69 papers, 1.1k citations indexed

About

Sevtap Savas is a scholar working on Molecular Biology, Pathology and Forensic Medicine and Oncology. According to data from OpenAlex, Sevtap Savas has authored 69 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 40 papers in Molecular Biology, 23 papers in Pathology and Forensic Medicine and 17 papers in Oncology. Recurrent topics in Sevtap Savas's work include Genetic factors in colorectal cancer (20 papers), RNA modifications and cancer (15 papers) and Cancer Genomics and Diagnostics (9 papers). Sevtap Savas is often cited by papers focused on Genetic factors in colorectal cancer (20 papers), RNA modifications and cancer (15 papers) and Cancer Genomics and Diagnostics (9 papers). Sevtap Savas collaborates with scholars based in Canada, United States and China. Sevtap Savas's co-authors include Hilmi Özçelik, Patrick S. Parfrey, Geoffrey Liu, Bronya J.B. Keats, Elizabeth Dicks, Hamdi Jarjanazi, Wei Xu, Roger Green, Şükrü Tüzmen and H. Banfield Younghusband and has published in prestigious journals such as Journal of Clinical Oncology, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Sevtap Savas

67 papers receiving 1.1k citations

Peers

Sevtap Savas

ONCOL

PFM

GENET

Guillermo Pita Spain

Quan Li China

Berardino Porfirio Italy

Rive Sarfstein Israel

Nathalie Ferrand France

Lara Nonell Spain

Roberto Bomprezzi United States

Håkan Wennbo Sweden

Jacob G. Kirkland United States

Jiang Zhu China

Guillermo Pita Spain

Sevtap Savas

427 ×0.6

350 ×1.4

ONCOL

255 ×1.1

119 ×0.6

PFM

217 ×1.4

GENET

Citations per year, relative to Sevtap Savas Sevtap Savas (= 1×) peers Guillermo Pita

Countries citing papers authored by Sevtap Savas

Since Specialization

Citations

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

Fields of papers citing papers by Sevtap Savas

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sevtap Savas

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

Savas, Sevtap, et al.. (2024). Toward a public outreach and community engagement strategy on cancer in Newfoundland and Labrador: an initial road map and recommendations. 6(4).

Carey, Megan E., et al.. (2023). Multifactor dimensionality reduction method identifies novel SNP interactions in the WNT protein interaction networks that are associated with recurrence risk in colorectal cancer. Frontiers in Oncology. 13. 1122229–1122229. 1 indexed citations

Savas, Sevtap, et al.. (2023). Social stigma associated with cancer in the Newfoundland and Labrador population: an exploratory study. 5(2). 1 indexed citations

Savas, Sevtap, et al.. (2023). Designing and delivering public engagement activities together with patient partners: The experience of Public Conference on Cancer. 5(3). 1 indexed citations

Etchegary, Holly, Katherine E. Watkins, Michael O. Woods, et al.. (2022). Cancer prevention in cancer predisposition syndromes: A protocol for testing the feasibility of building a hereditary cancer research registry and nurse navigator follow up model. PLoS ONE. 17(12). e0279317–e0279317. 3 indexed citations

Carey, Megan E., et al.. (2021). A comprehensive analysis of SNPs and CNVs identifies novel markers associated with disease outcomes in colorectal cancer. Molecular Oncology. 15(12). 3329–3347. 10 indexed citations

Carey, Megan E., William G. Pollett, Jane Green, et al.. (2019). The long-term survival characteristics of a cohort of colorectal cancer patients and baseline variables associated with survival outcomes with or without time-varying effects. BMC Medicine. 17(1). 150–150. 32 indexed citations

Cheng, Dangxiao, et al.. (2018). Two functional indel polymorphisms in the promoter region of the Brahma gene (BRM) and disease risk and progression-free survival in colorectal cancer. PLoS ONE. 13(6). e0198873–e0198873. 5 indexed citations

Shestopaloff, Konstantin, Wei Xu, Elizabeth Dicks, et al.. (2017). Germline INDELs and CNVs in a cohort of colorectal cancer patients: their characteristics, associations with relapse‐free survival time, and potential time‐varying effects on the risk of relapse. Cancer Medicine. 6(6). 1220–1232. 14 indexed citations

10.

Zhu, Yun, Peter Wang, Guangju Zhai, et al.. (2017). Vitamin D receptor and calcium-sensing receptor polymorphisms and colorectal cancer survival in the Newfoundland population. British Journal of Cancer. 117(6). 898–906. 16 indexed citations

11.

Cuffe, Sinéad, Abul Kalam Azad, Xin Qiu, et al.. (2016). ABCC2 polymorphisms and survival in the Princess Margaret cohort study and the NCIC clinical trials group BR.24 trial of platinum-treated advanced stage non-small cell lung cancer patients. Cancer Epidemiology. 41. 50–56. 7 indexed citations

12.

Savas, Sevtap, Konstantin Shestopaloff, Elizabeth Dicks, et al.. (2015). A Survival Association Study of 102 Polymorphisms Previously Associated with Survival Outcomes in Colorectal Cancer. BioMed Research International. 2015. 1–9. 6 indexed citations

13.

Xu, Wei, Konstantin Shestopaloff, Elizabeth Dicks, et al.. (2015). A genome wide association study on Newfoundland colorectal cancer patients’ survival outcomes. Biomarker Research. 3(1). 6–6. 16 indexed citations

14.

Eng, Lawson, Abul Kalam Azad, Xin Qiu, et al.. (2015). Discovery and validation of vascular endothelial growth factor (VEGF) pathway polymorphisms in esophageal adenocarcinoma outcome. Carcinogenesis. 36(9). 956–962. 7 indexed citations

15.

Wang, Jing, Elizabeth Dicks, Ban Younghusband, et al.. (2014). Examining the Polymorphisms in the Hypoxia Pathway Genes in Relation to Outcome in Colorectal Cancer. PLoS ONE. 9(11). e113513–e113513. 6 indexed citations

16.

Eng, Lawson, Abul Kalam Azad, Steven Habbous, et al.. (2012). Vascular Endothelial Growth Factor Pathway Polymorphisms as Prognostic and Pharmacogenetic Factors in Cancer: A Systematic Review and Meta-analysis. Clinical Cancer Research. 18(17). 4526–4537. 45 indexed citations

17.

Savas, Sevtap, et al.. (2012). Serotonin Transporter Gene (SLC6A4) Variations Are Associated with Poor Survival in Colorectal Cancer Patients. PLoS ONE. 7(7). e38953–e38953. 26 indexed citations

18.

Savas, Sevtap, David O. Azorsa, Hamdi Jarjanazi, et al.. (2011). NCI60 Cancer Cell Line Panel Data and RNAi Analysis Help Identify EAF2 as a Modulator of Simvastatin and Lovastatin Response in HCT-116 Cells. PLoS ONE. 6(4). e18306–e18306. 14 indexed citations

19.

Azad, Abul Kalam, Isabelle Bairati, Dangxiao Cheng, et al.. (2011). Genetic sequence variants and the development of secondary primary cancers in patients with head and neck cancers. Cancer. 118(6). 1554–1565. 20 indexed citations

20.

Savas, Sevtap, Nalan Gökgöz, Hülya Kayserili, et al.. (2000). Screening of Deletions in SMN, NAIP and BTF2p44 Genes in Turkish Spinal Muscular Atrophy Patients. Human Heredity. 50(3). 162–165. 11 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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