Jamie Young

8.5k total citations · 1 hit paper
32 papers, 1.6k citations indexed

About

Jamie Young is a scholar working on Cancer Research, Molecular Biology and Small Animals. According to data from OpenAlex, Jamie Young has authored 32 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Cancer Research, 10 papers in Molecular Biology and 7 papers in Small Animals. Recurrent topics in Jamie Young's work include Carcinogens and Genotoxicity Assessment (8 papers), Animal testing and alternatives (7 papers) and Immunotoxicology and immune responses (5 papers). Jamie Young is often cited by papers focused on Carcinogens and Genotoxicity Assessment (8 papers), Animal testing and alternatives (7 papers) and Immunotoxicology and immune responses (5 papers). Jamie Young collaborates with scholars based in United States, United Kingdom and Japan. Jamie Young's co-authors include Paul C. Francis, Gerald G. Long, John L. Vahle, James B. Nold, Jeffery A. Engelhardt, Young Linda, Masahiko Sato, Michael S. Westmore, Paul Fowler and Laura Jeffrey and has published in prestigious journals such as Nature Genetics, Cancer Research and Genomics.

In The Last Decade

Jamie Young

28 papers receiving 1.5k citations

Hit Papers

Preclinical characterization of the CDK4/6 inhibitor LY28... 2014 2026 2018 2022 2014 100 200 300 400
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. Preclinical characterization of the CDK4/6 inhibitor LY2835219: in-vivo cell cycle-dependent/independent anti-tumor activities alone/in combination with gemcitabine
    2014 446 citations Lawrence M. Gelbert, Shufen Cai et al. Investigational New Drugs profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jamie Young United States 13 727 574 421 414 268 32 1.6k
Kouhei Yamamoto Japan 24 425 0.6× 974 1.7× 308 0.7× 244 0.6× 37 0.1× 107 1.8k
Mariana Ferreira Leal Brazil 28 416 0.6× 1.1k 1.9× 479 1.1× 273 0.7× 51 0.2× 84 1.9k
Yi Shen United States 26 238 0.3× 1.4k 2.4× 858 2.0× 345 0.8× 36 0.1× 49 2.0k
Laura Ottaggio Italy 21 311 0.4× 568 1.0× 257 0.6× 93 0.2× 23 0.1× 53 1.1k
Yisheng Wang China 25 306 0.4× 868 1.5× 400 1.0× 54 0.1× 423 1.6× 71 1.6k
Dorothee Foernzler United States 12 210 0.3× 357 0.6× 88 0.2× 120 0.3× 28 0.1× 20 1.6k
Yaguang Weng China 25 276 0.4× 924 1.6× 549 1.3× 101 0.2× 28 0.1× 53 1.4k
George T. Tkalcevic United States 13 276 0.4× 684 1.2× 177 0.4× 74 0.2× 49 0.2× 14 1.3k
N. Lynn Henry United States 13 704 1.0× 302 0.5× 289 0.7× 147 0.4× 23 0.1× 43 1.1k
Ying Jiang China 23 606 0.8× 1000 1.7× 540 1.3× 212 0.5× 25 0.1× 76 1.9k

Countries citing papers authored by Jamie Young

Since Specialization
Citations

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

Fields of papers citing papers by Jamie Young

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jamie Young

This figure shows the co-authorship network connecting the top 25 collaborators of Jamie Young. A scholar is included among the top collaborators of Jamie 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 Jamie Young. Jamie 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.
Koh, Ching Chiek, Arjun S. Nanda, Andrea Degasperi, et al.. (2025). A redefined InDel taxonomy provides insights into mutational signatures. Nature Genetics. 57(5). 1132–1141.
2.
Power, Colm, Xinqi Liu, Jamie Young, & Diana Munteanu. (2024). Taxane-based chemotherapy-induced peripheral neuropathy: a prospective cohort study. 4. 3–3. 1 indexed citations
3.
Thomas, Luke W., Cinzia Esposito, Rachel Morgan, et al.. (2021). Genome-wide CRISPR/Cas9 deletion screen defines mitochondrial gene essentiality and identifies routes for tumour cell viability in hypoxia. Communications Biology. 4(1). 615–615. 14 indexed citations
4.
Stokes, Alan H., Benoit Laffont, Guillaume Dubois, et al.. (2020). Nonclinical safety assessment of repeated administration and biodistribution of a novel rabies self-amplifying mRNA vaccine in rats. Regulatory Toxicology and Pharmacology. 113. 104648–104648. 52 indexed citations
5.
Bolon, Brad, Karyn Colman, Sabine Francke, et al.. (2020). Opinion on Current Use of Non-Blinded Versus Blinded Histopathologic Evaluation in Animal Toxicity Studies. Toxicologic Pathology. 48(4). 549–559. 3 indexed citations
6.
Degasperi, Andrea, Tauanne Dias Amarante, Jan Czarnecki, et al.. (2020). A practical framework and online tool for mutational signature analyses show intertissue variation and driver dependencies. Nature Cancer. 1(2). 249–263. 127 indexed citations
7.
Wagner, Nicole, et al.. (2019). Bioinformatic analysis suggests potential mechanisms underlying parasitoid venom evolution and function. Genomics. 112(2). 1096–1104. 12 indexed citations
8.
Gelbert, Lawrence M., Shufen Cai, Xi Lin, et al.. (2014). Preclinical characterization of the CDK4/6 inhibitor LY2835219: in-vivo cell cycle-dependent/independent anti-tumor activities alone/in combination with gemcitabine. Investigational New Drugs. 32(5). 825–837. 446 indexed citations breakdown →
9.
Fowler, Paul, Robert Smith, Katie Smith, et al.. (2014). Reduction of misleading (“false”) positive results in mammalian cell genotoxicity assays. III: Sensitivity of human cell types to known genotoxic agents. Mutation Research/Genetic Toxicology and Environmental Mutagenesis. 767. 28–36. 43 indexed citations
10.
Fowler, Paul, Robert Smith, Katie Smith, et al.. (2012). Reduction of misleading (“false”) positive results in mammalian cell genotoxicity assays. II. Importance of accurate toxicity measurement. Mutation Research/Genetic Toxicology and Environmental Mutagenesis. 747(1). 104–117. 59 indexed citations
11.
Fowler, Paul, Katie Smith, Jamie Young, et al.. (2011). Reduction of misleading (“false”) positive results in mammalian cell genotoxicity assays. I. Choice of cell type. Mutation Research/Genetic Toxicology and Environmental Mutagenesis. 742(1-2). 11–25. 160 indexed citations
12.
Gelbert, Lawrence M., Shufen Cai, Xi Lin, et al.. (2011). Abstract B233: Identification and characterization of LY2835219: A potent oral inhibitor of the cyclin-dependent kinases 4 and 6 (CDK4/6) with broad in vivo antitumor activity.. Molecular Cancer Therapeutics. 10(11_Supplement). B233–B233. 14 indexed citations
13.
Young, Jamie, Robert L. Hall, Peter J. O’Brien, Volker Strauss, & John L. Vahle. (2011). Best Practices for Clinical Pathology Testing in Carcinogenicity Studies. Toxicologic Pathology. 39(2). 429–434. 8 indexed citations
14.
Whitwell, James, Paul Fowler, Katie Smith, et al.. (2010). 5-Fluorouracil, colchicine, benzo[a]pyrene and cytosine arabinoside tested in the in vitro mammalian cell micronucleus test (MNvit) in Chinese hamster V79 cells at Covance Laboratories, Harrogate, UK in support of OECD draft Test Guideline 487. Mutation Research/Genetic Toxicology and Environmental Mutagenesis. 702(2). 230–236. 2 indexed citations
15.
Fowler, Paul, James Whitwell, Laura Jeffrey, et al.. (2010). Etoposide; colchicine; mitomycin C and cyclophosphamide tested in the in vitro mammalian cell micronucleus test (MNvit) in Chinese hamster lung (CHL) cells at Covance laboratories; Harrogate UK in support of OECD draft Test Guideline 487. Mutation Research/Genetic Toxicology and Environmental Mutagenesis. 702(2). 175–180. 12 indexed citations
16.
17.
Fowler, Paul, James Whitwell, Laura Jeffrey, et al.. (2010). Cadmium chloride, benzo[a]pyrene and cyclophosphamide tested in the in vitro mammalian cell micronucleus test (MNvit) in the human lymphoblastoid cell line TK6 at Covance laboratories, Harrogate UK in support of OECD draft Test Guideline 487. Mutation Research/Genetic Toxicology and Environmental Mutagenesis. 702(2). 171–174. 18 indexed citations
18.
Young, Jamie. (2007). Nietzsche on Art. The British Journal of Aesthetics. 47(4). 442–444. 9 indexed citations
19.
Young, Jamie, et al.. (2004). Toxicity of single-dose oral gemcitibine in mice.. Cancer Research. 64. 486–487. 1 indexed citations
20.
Vahle, John L., Masahiko Sato, Gerald G. Long, et al.. (2002). Skeletal Changes in Rats Given Daily Subcutaneous Injections of Recombinant Human Parathyroid Hormone (1-34) for 2 Years and Relevance to Human Safety. Toxicologic Pathology. 30(3). 312–321. 497 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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