Christine E. Napier

1.2k total citations
41 papers, 802 citations indexed

About

Christine E. Napier is a scholar working on Genetics, Cancer Research and Molecular Biology. According to data from OpenAlex, Christine E. Napier has authored 41 papers receiving a total of 802 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 17 papers in Cancer Research and 14 papers in Molecular Biology. Recurrent topics in Christine E. Napier's work include BRCA gene mutations in cancer (18 papers), Cancer Genomics and Diagnostics (16 papers) and Telomeres, Telomerase, and Senescence (13 papers). Christine E. Napier is often cited by papers focused on BRCA gene mutations in cancer (18 papers), Cancer Genomics and Diagnostics (16 papers) and Telomeres, Telomerase, and Senescence (13 papers). Christine E. Napier collaborates with scholars based in Australia, United States and United Kingdom. Christine E. Napier's co-authors include Roger R. Reddel, Hilda A. Pickett, Axel A. Neumann, Anthony J. Cesare, Scott B. Cohen, Zeenia Kaul, Jane R. Noble, Lily I. Huschtscha, Eric A. Hendrickson and Adam Harvey and has published in prestigious journals such as Nucleic Acids Research, Journal of Clinical Oncology and PLoS ONE.

In The Last Decade

Christine E. Napier

38 papers receiving 797 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Christine E. Napier Australia 14 514 448 121 116 85 41 802
Joshua A. Regal United States 8 349 0.7× 432 1.0× 72 0.6× 82 0.7× 78 0.9× 17 831
Hemanth Tummala United Kingdom 14 406 0.8× 175 0.4× 135 1.1× 50 0.4× 73 0.9× 35 621
Isabelle Guilleret Switzerland 13 615 1.2× 337 0.8× 156 1.3× 77 0.7× 41 0.5× 16 832
Tsun-Po Yang United Kingdom 9 759 1.5× 94 0.2× 297 2.5× 122 1.1× 100 1.2× 16 973
Dustin L. Gable United States 9 226 0.4× 221 0.5× 77 0.6× 61 0.5× 57 0.7× 12 530
T. Zheng United States 13 161 0.3× 136 0.3× 64 0.5× 95 0.8× 179 2.1× 15 715
Marı́a José Ramı́rez Spain 13 478 0.9× 58 0.1× 120 1.0× 151 1.3× 97 1.1× 48 689
Brianne B. Rogers United States 7 285 0.6× 64 0.1× 88 0.7× 130 1.1× 91 1.1× 9 563
Maira Tankimanova United Kingdom 6 257 0.5× 184 0.4× 76 0.6× 65 0.6× 26 0.3× 6 473
Michelle Van Sinderen Australia 17 231 0.4× 54 0.1× 61 0.5× 143 1.2× 90 1.1× 26 756

Countries citing papers authored by Christine E. Napier

Since Specialization
Citations

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

Fields of papers citing papers by Christine E. Napier

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Christine E. Napier. 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 Christine E. Napier. The network helps show where Christine E. Napier may publish in the future.

Co-authorship network of co-authors of Christine E. Napier

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

All Works

20 of 20 papers shown
1.
Sharaf, Radwa, Dexter X. Jin, John P. Grady, et al.. (2023). A pan-sarcoma landscape of telomeric content shows that alterations in RAD51B and GID4 are associated with higher telomeric content. npj Genomic Medicine. 8(1). 26–26. 5 indexed citations
2.
Best, Megan, Nicci Bartley, Christine E. Napier, et al.. (2022). Return of comprehensive tumour genomic profiling results to advanced cancer patients: a qualitative study. Supportive Care in Cancer. 30(10). 8201–8210. 4 indexed citations
3.
Best, Megan, Phyllis Butow, Chris Jacobs, et al.. (2022). Preferences for return of germline genome sequencing results for cancer patients and their genetic relatives in a research setting. European Journal of Human Genetics. 30(8). 930–937. 5 indexed citations
4.
Best, Megan, Christine E. Napier, Timothy E. Schlub, et al.. (2022). Validation of the multidimensional impact of Cancer Risk Assessment Questionnaire to assess impact of waiting for genome sequencing results. Psycho-Oncology. 31(7). 1204–1211. 4 indexed citations
5.
Butow, Phyllis, Megan Best, Timothy E. Schlub, et al.. (2022). Psychological impact of comprehensive tumor genomic profiling results for advanced cancer patients. Patient Education and Counseling. 105(7). 2206–2216. 4 indexed citations
6.
Vatter, Sabina, Timothy E. Schlub, Christine E. Napier, et al.. (2022). Psychological outcomes in advanced cancer patients after receiving genomic tumor profiling results.. Health Psychology. 41(6). 396–408. 4 indexed citations
7.
Meiser, Bettina, Phyllis Butow, Christine E. Napier, et al.. (2021). Psychological predictors of advanced cancer patients’ preferences for return of results from comprehensive tumor genomic profiling. American Journal of Medical Genetics Part A. 188(3). 725–734. 1 indexed citations
8.
Napier, Christine E., Phyllis Butow, Timothy E. Schlub, et al.. (2021). Cancer patient knowledge about and behavioral intentions after germline genome sequencing. Patient Education and Counseling. 105(3). 707–718. 3 indexed citations
9.
Smit, Amelia K., Nicci Bartley, Megan Best, et al.. (2020). Family communication about genomic sequencing: A qualitative study with cancer patients and relatives. Patient Education and Counseling. 104(5). 944–952. 10 indexed citations
10.
Best, Megan, Phyllis Butow, Chris Jacobs, et al.. (2020). Advanced cancer patient preferences for receiving molecular profiling results. Psycho-Oncology. 29(10). 1533–1539. 7 indexed citations
11.
Butow, Phyllis, Christine E. Napier, Nicci Bartley, et al.. (2020). Advanced Cancer Patient Knowledge of and Attitudes towards Tumor Molecular Profiling. Translational Oncology. 13(9). 100799–100799. 9 indexed citations
12.
Bartley, Nicci, Christine E. Napier, Megan Best, & Phyllis Butow. (2020). Patient experience of uncertainty in cancer genomics: a systematic review. Genetics in Medicine. 22(9). 1450–1460. 24 indexed citations
13.
Best, Megan, Phyllis Butow, Chris Jacobs, et al.. (2019). Who should access germline genome sequencing? A mixed methods study of patient views. Clinical Genetics. 97(2). 329–337. 4 indexed citations
14.
Best, Megan, Nicci Bartley, Chris Jacobs, et al.. (2019). Patient perspectives on molecular tumor profiling: “Why wouldn’t you?”. BMC Cancer. 19(1). 753–753. 26 indexed citations
15.
Knezevic, Kathy, Julie A.I. Thoms, Georg von Jonquières, et al.. (2019). DKC1 is a transcriptional target of GATA1 and drives upregulation of telomerase activity in normal human erythroblasts. Haematologica. 105(6). 1517–1526. 22 indexed citations
16.
Khushi, Matloob, Christine E. Napier, Christine M. Smyth, Roger R. Reddel, & Jonathan W. Arthur. (2017). MatCol: a tool to measure fluorescence signal colocalisation in biological systems. Scientific Reports. 7(1). 8879–8879. 16 indexed citations
17.
Lee, Michael, et al.. (2016). Comparative analysis of whole genome sequencing-based telomere length measurement techniques. Methods. 114. 4–15. 29 indexed citations
18.
Napier, Christine E., Sara L. Cole, Rebecca A. Dagg, et al.. (2012). Loss of Wild-Type ATRX Expression in Somatic Cell Hybrids Segregates with Activation of Alternative Lengthening of Telomeres. PLoS ONE. 7(11). e50062–e50062. 63 indexed citations
19.
Napier, Christine E., Lisa Taylor, Jun Yuan, et al.. (2010). Mild hyperoxia limits hTR levels, telomerase activity, and telomere length maintenance in hTERT-transduced bone marrow endothelial cells. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1803(10). 1142–1153. 16 indexed citations
20.
Cesare, Anthony J., Zeenia Kaul, Scott B. Cohen, et al.. (2009). Spontaneous occurrence of telomeric DNA damage response in the absence of chromosome fusions. Nature Structural & Molecular Biology. 16(12). 1244–1251. 212 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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