David Young

2.5k total citations
37 papers, 1.8k citations indexed

About

David Young is a scholar working on Genetics, Molecular Biology and Immunology. According to data from OpenAlex, David Young has authored 37 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 11 papers in Molecular Biology and 10 papers in Immunology. Recurrent topics in David Young's work include Biosimilars and Bioanalytical Methods (9 papers), Inflammatory Bowel Disease (7 papers) and RNA and protein synthesis mechanisms (6 papers). David Young is often cited by papers focused on Biosimilars and Bioanalytical Methods (9 papers), Inflammatory Bowel Disease (7 papers) and RNA and protein synthesis mechanisms (6 papers). David Young collaborates with scholars based in United States, United Kingdom and South Africa. David Young's co-authors include Stanley Fields, Jay Shendure, Frédéric Lynen, M. Daniel Lane, Kenton M. Sanders, Chanjae Park, Wei Yan, Seungil Ro, Dana Pe’er and Rupali P Patwardhan and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and Genes & Development.

In The Last Decade

David Young

35 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
David Young United States 16 1.1k 414 273 223 187 37 1.8k
Robert Boxer United States 17 849 0.8× 205 0.5× 223 0.8× 137 0.6× 110 0.6× 29 1.6k
Nicki Tiffin South Africa 26 604 0.6× 284 0.7× 69 0.3× 178 0.8× 39 0.2× 75 1.6k
Won‐Chul Lee South Korea 20 792 0.7× 94 0.2× 439 1.6× 289 1.3× 42 0.2× 45 2.1k
Enrique Hernández–Lemus Mexico 23 1.1k 1.0× 271 0.7× 259 0.9× 51 0.2× 33 0.2× 150 2.2k
Annie Chung United States 21 888 0.8× 187 0.5× 328 1.2× 99 0.4× 524 2.8× 56 2.3k
Holly Miller United States 24 1.6k 1.5× 167 0.4× 348 1.3× 35 0.2× 54 0.3× 45 2.0k
Julie George Germany 24 705 0.7× 158 0.4× 334 1.2× 86 0.4× 43 0.2× 49 2.3k
Sherry‐Ann Brown United States 24 363 0.3× 154 0.4× 86 0.3× 71 0.3× 44 0.2× 96 2.0k
Akiko Maeda United States 43 4.0k 3.8× 203 0.5× 99 0.4× 264 1.2× 394 2.1× 141 5.6k
Erin M. Green United States 22 1.5k 1.4× 107 0.3× 81 0.3× 61 0.3× 473 2.5× 48 2.4k

Countries citing papers authored by David Young

Since Specialization
Citations

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

Fields of papers citing papers by David Young

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of David Young

This figure shows the co-authorship network connecting the top 25 collaborators of David Young. A scholar is included among the top collaborators of David Young 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 David Young. David Young 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.
Young, David, Cathrine McKenzie, Sanjay Gupta, et al.. (2024). Exploring Antibacterial Usage and Pathogen Surveillance over Five Years in a Tertiary Referral Teaching Hospital Adult General Intensive Care Unit (ICU). Pathogens. 13(11). 961–961. 1 indexed citations
2.
Baumgartner, T., Hishaam Ismael, & David Young. (2024). Management of perforated jejunal diverticulitis: A case series and literature review. 4. 100071–100071. 2 indexed citations
3.
Young, David, Clare Harris, João Gonçalves, et al.. (2024). A randomised, crossover trial exploring the patient perspective and effectiveness of biosimilar adalimumab transition: IBD reference and biosimilar adalimumab cross over study (iBaSS). International Journal of Clinical Pharmacy. 46(5). 1091–1101. 1 indexed citations
4.
Young, David, et al.. (2023). P389 Switching infliximab to subcutaneous from intravenous therapy (SWIMSUIT) – A prospective, real-world, single centre, phase IV interventional study.. Journal of Crohn s and Colitis. 17(Supplement_1). i522–i523. 3 indexed citations
6.
Young, David, et al.. (2023). P96 Patient benefits of switching from intravenous to subcutaneous infliximab. Poster presentations. A104.1–A104. 1 indexed citations
7.
Corominas, Hèctor, David Young, Fraser Cummings, et al.. (2023). Healthcare Professional (HCP) and Patient Usability Evaluation and Preferences of Two Auto-injector Devices for Self-Injection of Biosimilars, SB4 and SB5: A Literature Review. Clinical Drug Investigation. 43(8). 579–593. 4 indexed citations
9.
Young, David, et al.. (2021). P168 Tofacitinib in ulcerative colitis: early real-world experience in Southampton. A130.1–A130. 1 indexed citations
10.
Harris, Clare, Richard Harris, David Young, et al.. (2021). PMO-20 The IBD biosimilar to biosimilar switching study (iBiSS). A87.1–A87.
12.
Kon, Yoshiko, David Young, Michael P. Guy, et al.. (2017). Widespread temperature sensitivity and tRNA decay due to mutations in a yeast tRNA. RNA. 24(3). 410–422. 16 indexed citations
13.
Melamed, Daniel R., et al.. (2015). Combining Natural Sequence Variation with High Throughput Mutational Data to Reveal Protein Interaction Sites. PLoS Genetics. 11(2). e1004918–e1004918. 23 indexed citations
14.
Young, David & Stanley Fields. (2015). The role of functional data in interpreting the effects of genetic variation. Molecular Biology of the Cell. 26(22). 3904–3908. 14 indexed citations
15.
Melamed, Daniel R., et al.. (2013). Deep mutational scanning of an RRM domain of the Saccharomyces cerevisiae poly(A)-binding protein. RNA. 19(11). 1537–1551. 155 indexed citations
16.
Asuzu, David T., Yujiro Hayashi, F Izbéki, et al.. (2011). Generalized neuromuscular hypoplasia, reduced smooth muscle myosin and altered gut motility in the klotho model of premature aging. Neurogastroenterology & Motility. 23(7). e309–e323. 24 indexed citations
17.
Izbéki, F, David T. Asuzu, Andrea Lörincz, et al.. (2010). Loss of Kitlowprogenitors, reduced stem cell factor and high oxidative stress underlie gastric dysfunction in progeric mice. The Journal of Physiology. 588(16). 3101–3117. 45 indexed citations
18.
Patwardhan, Rupali P, Choli Lee, Oren Litvin, et al.. (2009). High-resolution analysis of DNA regulatory elements by synthetic saturation mutagenesis. Nature Biotechnology. 27(12). 1173–1175. 263 indexed citations
19.
Dunt, David, Gerald R. Elsworth, Danielle A. Southern, et al.. (2006). Individual and area factors associated with general practitioner integration in Australia: A multilevel analysis. Social Science & Medicine. 63(3). 680–690. 2 indexed citations
20.
Young, David. (1971). Estradiol- and testosterone-induced alterations in phosphatidylcholine and triglyceride synthesis in hepatic endoplasmic reticulum. Journal of Lipid Research. 12(5). 590–595. 33 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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