Denise Anderson

12.9k total citations
51 papers, 1.1k citations indexed

About

Denise Anderson is a scholar working on Molecular Biology, Epidemiology and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Denise Anderson has authored 51 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 10 papers in Epidemiology and 10 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Denise Anderson's work include Epigenetics and DNA Methylation (7 papers), Acute Lymphoblastic Leukemia research (7 papers) and Genomics and Rare Diseases (5 papers). Denise Anderson is often cited by papers focused on Epigenetics and DNA Methylation (7 papers), Acute Lymphoblastic Leukemia research (7 papers) and Genomics and Rare Diseases (5 papers). Denise Anderson collaborates with scholars based in Australia, United Kingdom and United States. Denise Anderson's co-authors include Jenefer M. Blackwell, Sarra E. Jamieson, Timo Lassmann, Kim W. Carter, Prue H. Hart, Craig E. Pennell, Ursula R. Kees, Robyn Lucas, Shyan Vijayasekaran and Harvey Coates and has published in prestigious journals such as Nature Communications, PLoS ONE and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Denise Anderson

50 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Denise Anderson Australia 22 391 188 158 145 144 51 1.1k
Cheongeun Oh United States 20 185 0.5× 170 0.9× 116 0.7× 100 0.7× 148 1.0× 109 1.5k
Sacide Pehlıvan Türkiye 18 330 0.8× 85 0.5× 77 0.5× 100 0.7× 107 0.7× 137 1.1k
Elissa J. Schwartz United States 18 298 0.8× 124 0.7× 132 0.8× 211 1.5× 274 1.9× 65 1.5k
Osama Alsmadi Kuwait 22 623 1.6× 86 0.5× 110 0.7× 186 1.3× 462 3.2× 74 1.6k
Rossella Tomaiuolo Italy 26 354 0.9× 106 0.6× 44 0.3× 110 0.8× 211 1.5× 79 1.6k
Mehmet Baykara Türkiye 20 254 0.6× 212 1.1× 48 0.3× 119 0.8× 130 0.9× 113 1.3k
Ezio Fulcheri Italy 27 252 0.6× 246 1.3× 159 1.0× 215 1.5× 143 1.0× 199 3.3k
Shih‐Hsiang Chen Taiwan 17 253 0.6× 166 0.9× 43 0.3× 88 0.6× 67 0.5× 106 897
Mohamed Abdelhaleem Canada 16 501 1.3× 163 0.9× 69 0.4× 62 0.4× 137 1.0× 87 1.3k

Countries citing papers authored by Denise Anderson

Since Specialization
Citations

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

Fields of papers citing papers by Denise Anderson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Denise Anderson

This figure shows the co-authorship network connecting the top 25 collaborators of Denise Anderson. A scholar is included among the top collaborators of Denise Anderson 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 Denise Anderson. Denise Anderson 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.
Melton, Phillip E., Karen A. Lillycrop, Keith M. Godfrey, et al.. (2023). Differential DNA methylation of steatosis and non-alcoholic fatty liver disease in adolescence. Hepatology International. 17(3). 584–594. 6 indexed citations
2.
Fear, Vanessa S., Catherine A. Forbes, Denise Anderson, et al.. (2022). Functional validation of variants of unknown significance using CRISPR gene editing and transcriptomics: A Kleefstra syndrome case study. Gene. 821. 146287–146287. 7 indexed citations
3.
Jamieson, Sarra E., Michaela Fakiola, Dave Tang, et al.. (2021). Common and Rare Genetic Variants That Could Contribute to Severe Otitis Media in an Australian Aboriginal Population. Clinical Infectious Diseases. 73(10). 1860–1870. 3 indexed citations
4.
Anderson, Denise, Anya C. Jones, Kim W. Carter, et al.. (2020). Differential Gene Expression of Lymphocytes Stimulated with Rhinovirus A and C in Children with Asthma. American Journal of Respiratory and Critical Care Medicine. 202(2). 202–209. 3 indexed citations
5.
Anderson, Denise, Emanuela Ferrari, Jennifer Tickner, et al.. (2020). The bone marrow microenvironment of pre-B acute lymphoblastic leukemia at single-cell resolution. Scientific Reports. 10(1). 19173–19173. 21 indexed citations
6.
Huang, Rae‐Chi, Karen A. Lillycrop, Lawrence J. Beilin, et al.. (2019). Epigenetic Age Acceleration in Adolescence Associates With BMI, Inflammation, and Risk Score for Middle Age Cardiovascular Disease. The Journal of Clinical Endocrinology & Metabolism. 104(7). 3012–3024. 66 indexed citations
7.
Jones, Anya C., Denise Anderson, Sally Galbraith, et al.. (2018). Personalized Transcriptomics Reveals Heterogeneous Immunophenotypes in Children with Viral Bronchiolitis. American Journal of Respiratory and Critical Care Medicine. 199(12). 1537–1549. 26 indexed citations
8.
Anderson, Denise, et al.. (2018). Epigenetic dysregulation of host gene expression in Toxoplasma infection with specific reference to dopamine and amyloid pathways. Infection Genetics and Evolution. 65. 159–162. 17 indexed citations
9.
Stick, Stephen M., Anthony Bosco, Denise Anderson, et al.. (2017). A transcriptomic comparison between nasal and bronchial airway epithelia from children. Genes and Environment. PA1826–PA1826.
10.
Tang, Dave, Denise Anderson, Richard W. Francis, et al.. (2016). Reference genotype and exome data from an Australian Aboriginal population for health-based research. Scientific Data. 3(1). 160023–160023. 13 indexed citations
11.
Anderson, Denise, Michaela Fakiola, Belinda J. Hales, et al.. (2015). Genome-wide association study of IgG1 responses to the choline-binding protein PspC of Streptococcus pneumoniae. Genes and Immunity. 16(5). 289–296. 2 indexed citations
13.
Hart, Prue H., Robyn Lucas, John P. Walsh, et al.. (2014). Vitamin D in Fetal Development: Findings From a Birth Cohort Study. PEDIATRICS. 135(1). e167–e173. 84 indexed citations
14.
Samuels, Lacey, Alex H. Beesley, Rachael A. Papa, et al.. (2014). A pre-clinical model of resistance to induction therapy in pediatric acute lymphoblastic leukemia. Blood Cancer Journal. 4(8). e232–e232. 25 indexed citations
15.
Beesley, Alex H., et al.. (2013). Drug–Gene Modeling in Pediatric T-Cell Acute Lymphoblastic Leukemia Highlights Importance of 6-Mercaptopurine for Outcome. Cancer Research. 73(9). 2749–2759. 12 indexed citations
16.
O’Donnell, Melissa, Denise Anderson, Vera A. Morgan, et al.. (2013). Trends in pre‐existing mental health disorders among parents of infants born in Western Australia from 1990 to 2005. The Medical Journal of Australia. 198(9). 485–488. 15 indexed citations
17.
Miller, Clint L., Denise Anderson, Ramendra K. Kundu, et al.. (2013). Disease-Related Growth Factor and Embryonic Signaling Pathways Modulate an Enhancer of TCF21 Expression at the 6q23.2 Coronary Heart Disease Locus. PLoS Genetics. 9(7). e1003652–e1003652. 51 indexed citations
18.
Kotecha, Rishi S., Jette Ford, Alex H. Beesley, et al.. (2012). Molecular characterization of identical, novel MLL-EPS15 translocation and individual genomic copy number alterations in monozygotic infant twins with acute lymphoblastic leukemia. Haematologica. 97(9). 1447–1450. 3 indexed citations
19.
Genovesi, Laura A., Denise Anderson, Kim W. Carter, Keith M. Giles, & Peter B. Dallas. (2012). Identification of suitable endogenous control genes for microRNA expression profiling of childhood medulloblastoma and human neural stem cells. BMC Research Notes. 5(1). 507–507. 21 indexed citations
20.
Cooper, Matthew N., Nicholas de Klerk, Kathryn R. Greenop, et al.. (2012). Statistical adjustment of genotyping error in a case–control study of childhood leukaemia. BMC Medical Research Methodology. 12(1). 141–141. 2 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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