Natalie A. Twine

717 total citations
26 papers, 434 citations indexed

About

Natalie A. Twine is a scholar working on Molecular Biology, Genetics and Epidemiology. According to data from OpenAlex, Natalie A. Twine has authored 26 papers receiving a total of 434 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 8 papers in Genetics and 4 papers in Epidemiology. Recurrent topics in Natalie A. Twine's work include CRISPR and Genetic Engineering (9 papers), Genomics and Phylogenetic Studies (5 papers) and Virus-based gene therapy research (4 papers). Natalie A. Twine is often cited by papers focused on CRISPR and Genetic Engineering (9 papers), Genomics and Phylogenetic Studies (5 papers) and Virus-based gene therapy research (4 papers). Natalie A. Twine collaborates with scholars based in Australia, United Kingdom and Germany. Natalie A. Twine's co-authors include Denis C. Bauer, Aidan R. O’Brien, Armella Zadoorian, Robert Dunne, Gaétan Burgio, Seshadri S. Vasan, Zachary A. Gurard‐Levin, Geneviève Almouzni, Fabien Reyal and Suzanne Scott and has published in prestigious journals such as Bioinformatics, PLoS ONE and Journal of Molecular Biology.

In The Last Decade

Natalie A. Twine

25 papers receiving 432 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Natalie A. Twine Australia 10 320 84 51 42 39 26 434
Peter C. DeWeirdt United States 8 504 1.6× 98 1.2× 49 1.0× 20 0.5× 62 1.6× 8 586
Ruochi Zhang United States 12 676 2.1× 95 1.1× 44 0.9× 76 1.8× 31 0.8× 17 730
Samuel Lessard United States 7 651 2.0× 201 2.4× 49 1.0× 52 1.2× 42 1.1× 19 911
Artur A. Serebrenik United States 12 258 0.8× 50 0.6× 41 0.8× 26 0.6× 98 2.5× 21 416
Jill Henley United States 9 296 0.9× 151 1.8× 71 1.4× 17 0.4× 58 1.5× 13 438
Michelle Brault United States 7 314 1.0× 52 0.6× 173 3.4× 27 0.6× 83 2.1× 8 430
Madina Karimova Germany 7 249 0.8× 86 1.0× 19 0.4× 16 0.4× 25 0.6× 11 328
Huiqiang Cai Denmark 11 496 1.6× 78 0.9× 127 2.5× 194 4.6× 76 1.9× 17 648
Hillary L. Logan United States 6 374 1.2× 49 0.6× 28 0.5× 22 0.5× 151 3.9× 6 519
Nicholas C. Huston United States 10 380 1.2× 27 0.3× 26 0.5× 20 0.5× 16 0.4× 14 546

Countries citing papers authored by Natalie A. Twine

Since Specialization
Citations

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

Fields of papers citing papers by Natalie A. Twine

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Natalie A. Twine. 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 Natalie A. Twine. The network helps show where Natalie A. Twine may publish in the future.

Co-authorship network of co-authors of Natalie A. Twine

This figure shows the co-authorship network connecting the top 25 collaborators of Natalie A. Twine. A scholar is included among the top collaborators of Natalie A. Twine 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 Natalie A. Twine. Natalie A. Twine 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.
Scott, Suzanne, Adrian Westhaus, Erhua Zhu, et al.. (2024). AAVolve: Concatenated long-read deep sequencing enables whole capsid tracking during shuffled AAV library selection. Molecular Therapy — Methods & Clinical Development. 32(4). 101351–101351. 1 indexed citations
2.
Tay, Aidan P., et al.. (2024). Synsor: a tool for alignment-free detection of engineered DNA sequences. Frontiers in Bioengineering and Biotechnology. 12. 1375626–1375626.
3.
Chandra, Rohitash, et al.. (2023). Unsupervised machine learning framework for discriminating major variants of concern during COVID-19. PLoS ONE. 18(5). e0285719–e0285719. 6 indexed citations
4.
Scott, Suzanne, Felix Hartkopf, Claus V. Hallwirth, et al.. (2022). A bioinformatic pipeline for simulating viral integration data. Data in Brief. 42. 108161–108161. 1 indexed citations
5.
Tay, Aidan P., Joshua J. Hamey, Gabriella E. Martyn, Natalie A. Twine, & Marc R. Wilkins. (2022). Identification of Protein Isoforms Using Reference Databases Built from Long and Short Read RNA-Sequencing. Journal of Proteome Research. 21(7). 1628–1639. 4 indexed citations
6.
Lee, Carol, et al.. (2022). Data-driven platform for identifying variants of interest in COVID-19 virus. Computational and Structural Biotechnology Journal. 20. 2942–2950. 2 indexed citations
7.
O’Brien, Aidan R., et al.. (2021). GOANA: A Universal High-Throughput Web Service for Assessing and Comparing the Outcome and Efficiency of Genome Editing Experiments. The CRISPR Journal. 4(2). 243–252. 2 indexed citations
8.
Cabanes‐Creus, Marti, Erhua Zhu, Sophia H.Y. Liao, et al.. (2021). Novel human liver-tropic AAV variants define transferable domains that markedly enhance the human tropism of AAV7 and AAV8. Molecular Therapy — Methods & Clinical Development. 24. 88–101. 24 indexed citations
9.
Cabanes‐Creus, Marti, Sophia H.Y. Liao, Matthieu Drouyer, et al.. (2021). Single amino acid insertion allows functional transduction of murine hepatocytes with human liver tropic AAV capsids. Molecular Therapy — Methods & Clinical Development. 21. 607–620. 16 indexed citations
10.
Tay, Aidan P., et al.. (2021). INSIDER: alignment-free detection of foreign DNA sequences. Computational and Structural Biotechnology Journal. 19. 3810–3816. 4 indexed citations
11.
Scott, Suzanne, Claus V. Hallwirth, Felix Hartkopf, et al.. (2021). Isling: A Tool for Detecting Integration of Wild-Type Viruses and Clinical Vectors. Journal of Molecular Biology. 434(11). 167408–167408. 3 indexed citations
12.
Bauer, Denis C., Alejandro Metke‐Jimenez, Sebastian Maurer‐Stroh, et al.. (2020). Interoperable medical data: The missing link for understanding COVID‐19. Transboundary and Emerging Diseases. 68(4). 1753–1760. 16 indexed citations
13.
O’Brien, Aidan R., Natalie A. Twine, Gaétan Burgio, & Denis C. Bauer. (2019). Unlocking HDR-mediated nucleotide editing by identifying high-efficiency target sites using machine learning. Scientific Reports. 9(1). 2788–2788. 29 indexed citations
14.
Twine, Natalie A., Sara Hetzel, Christopher Pockrandt, Knut Reinert, & Denis C. Bauer. (2019). VARSCOT: variant-aware detection and scoring enables sensitive and personalized off-target detection for CRISPR-Cas9. BMC Biotechnology. 19(1). 40–40. 9 indexed citations
15.
Twine, Natalie A., et al.. (2018). High Activity Target-Site Identification Using Phenotypic Independent CRISPR-Cas9 Core Functionality. The CRISPR Journal. 1(2). 182–190. 40 indexed citations
16.
Gurard‐Levin, Zachary A., Natalie A. Twine, Véra Pancaldi, et al.. (2016). Chromatin Regulators as a Guide for Cancer Treatment Choice. Molecular Cancer Therapeutics. 15(7). 1768–1777. 15 indexed citations
17.
Williams, Duncan & Natalie A. Twine. (2015). Multi-Criteria Decision Aid Analysis of a Musification Approach to the Auditory Display of Micro-Organism Movement. Journal of the Audio Engineering Society. 1 indexed citations
18.
de, Rocío Montes, Zachary A. Gurard‐Levin, Frédérique Berger, et al.. (2014). The histone chaperone HJURP is a new independent prognostic marker for luminal A breast carcinoma. Molecular Oncology. 9(3). 657–674. 63 indexed citations
19.
Twine, Natalie A., Andrew Spriggs, Jennifer M. Taylor, & Aude M. Fahrer. (2013). A novel splicing outcome reveals more than 2000 new mammalian protein isoforms. Bioinformatics. 30(2). 151–156. 9 indexed citations
20.
Twine, Natalie A., et al.. (2012). Splice variants of the condensin II gene Ncaph2 include alternative reading frame translations of exon 1. FEBS Journal. 279(8). 1422–1432. 4 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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