Andrew Dodd

2.0k total citations · 1 hit paper
29 papers, 1.4k citations indexed

About

Andrew Dodd is a scholar working on Molecular Biology, Genetics and Rheumatology. According to data from OpenAlex, Andrew Dodd has authored 29 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 8 papers in Genetics and 6 papers in Rheumatology. Recurrent topics in Andrew Dodd's work include Osteoarthritis Treatment and Mechanisms (6 papers), Zebrafish Biomedical Research Applications (6 papers) and Peroxisome Proliferator-Activated Receptors (5 papers). Andrew Dodd is often cited by papers focused on Osteoarthritis Treatment and Mechanisms (6 papers), Zebrafish Biomedical Research Applications (6 papers) and Peroxisome Proliferator-Activated Receptors (5 papers). Andrew Dodd collaborates with scholars based in New Zealand, United Kingdom and Spain. Andrew Dodd's co-authors include Donald R. Love, Warren C. McNabb, Rongying Tang, Daniel Lai, Franz B. Pichler, Brent R. Copp, Stephen P. Chambers, John Loughlin, Sophie Laurenson and Liam Williams and has published in prestigious journals such as Blood, Nature Biotechnology and Biochemical and Biophysical Research Communications.

In The Last Decade

Andrew Dodd

28 papers receiving 1.4k citations

Hit Papers

Validation of Zebrafish (<italic>Danio reri... 2007 2026 2013 2019 2007 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Andrew Dodd New Zealand 15 730 377 249 152 131 29 1.4k
Ghislaine Morvan-Dubois France 17 792 1.1× 311 0.8× 298 1.2× 101 0.7× 92 0.7× 22 1.5k
Klaus Röhr Germany 27 965 1.3× 380 1.0× 502 2.0× 62 0.4× 62 0.5× 107 2.4k
Daniel Hesselson Australia 21 887 1.2× 478 1.3× 368 1.5× 141 0.9× 99 0.8× 48 1.7k
Virginia P. Winfrey United States 32 1.2k 1.6× 251 0.7× 446 1.8× 186 1.2× 103 0.8× 64 3.5k
James A. Coffman United States 25 1.2k 1.7× 143 0.4× 164 0.7× 196 1.3× 108 0.8× 60 1.9k
Hisashi Hashimoto Japan 29 1.4k 1.9× 479 1.3× 451 1.8× 255 1.7× 143 1.1× 94 2.5k
Michael J. Gilchrist United Kingdom 25 1.8k 2.5× 226 0.6× 302 1.2× 216 1.4× 279 2.1× 45 2.4k
James F. Catterall United States 30 1.3k 1.8× 164 0.4× 704 2.8× 152 1.0× 75 0.6× 56 2.5k
William J. Larsen United States 31 1.6k 2.1× 476 1.3× 327 1.3× 250 1.6× 97 0.7× 46 3.0k
Shinji Yamaguchi Japan 24 951 1.3× 135 0.4× 243 1.0× 102 0.7× 110 0.8× 89 2.2k

Countries citing papers authored by Andrew Dodd

Since Specialization
Citations

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

Fields of papers citing papers by Andrew Dodd

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andrew Dodd

This figure shows the co-authorship network connecting the top 25 collaborators of Andrew Dodd. A scholar is included among the top collaborators of Andrew Dodd 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 Andrew Dodd. Andrew Dodd 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.
Dodd, Andrew & Lacey J. Luense. (2024). Contribution of the paternal histone epigenome to the preimplantation embryo. Frontiers in Cell and Developmental Biology. 12. 1476312–1476312. 2 indexed citations
2.
Raine, E.V., Andrew Dodd, Louise N. Reynard, & John Loughlin. (2013). Allelic expression analysis of the osteoarthritis susceptibility gene COL11A1 in human joint tissues. BMC Musculoskeletal Disorders. 14(1). 85–85. 25 indexed citations
3.
Raine, E.V., et al.. (2012). Gene expression analysis reveals HBP1 as a key target for the osteoarthritis susceptibility locus that maps to chromosome 7q22. Annals of the Rheumatic Diseases. 71(12). 2020–2027. 26 indexed citations
5.
Dodd, Andrew, Cristina Rodriguez‐Fontenla, Manuel Calaza, et al.. (2011). Deep sequencing of GDF5 reveals the absence of rare variants at this important osteoarthritis susceptibility locus. Osteoarthritis and Cartilage. 19(4). 430–434. 19 indexed citations
6.
Dodd, Andrew, Cristina Rodriguez‐Fontenla, Manuel Calaza, et al.. (2010). 374 DEEP SEQUENCING OF GDF5 IN OVER 1900 OSTEOARTHRITIS CASES AND CONTROLS REVEALS NOVEL AND POTENTIALLY FUNCTIONAL RARE VARIANTS IN THE PROTEIN CODING AND PROMOTER REGIONS OF THE GENE. Osteoarthritis and Cartilage. 18. S165–S165. 1 indexed citations
7.
Riancho, José A., Carmen García‐Ibarbia, E.V. Raine, et al.. (2010). Common variations in estrogen-related genes are associated with severe large-joint osteoarthritis: a multicenter genetic and functional study. Osteoarthritis and Cartilage. 18(7). 927–933. 32 indexed citations
8.
Millar, Craig D., Andrew Dodd, Jennifer Anderson, et al.. (2008). Mutation and Evolutionary Rates in Adélie Penguins from the Antarctic. PLoS Genetics. 4(10). e1000209–e1000209. 141 indexed citations
9.
Love, Donald R., et al.. (2007). Modeling inflammatory bowel disease: the zebrafish as a way forward. Expert Review of Molecular Diagnostics. 7(2). 177–193. 10 indexed citations
10.
Tang, Rongying, Andrew Dodd, Daniel Lai, Warren C. McNabb, & Donald R. Love. (2007). Validation of Zebrafish (<italic>Danio rerio</italic>) Reference Genes for Quantitative Real-time RT-PCR Normalization. Acta Biochimica et Biophysica Sinica. 39(5). 384–390. 528 indexed citations breakdown →
11.
Dodd, Andrew, David Greenwood, Andrew L. Miller, et al.. (2006). Zebrafish: At the Nexus of Functional and Chemical Genomics. Biotechnology and Genetic Engineering Reviews. 22(1). 77–100. 2 indexed citations
12.
Pichler, Franz B., Andrew Dodd, & Donald R. Love. (2004). Global gene expression analysis in the zebrafish: the challenge and the promise. Drug Discovery Today Technologies. 1(2). 79–84. 5 indexed citations
13.
Dodd, Andrew, Stephen P. Chambers, Peter E. Nielsen, & Donald R. Love. (2004). Modeling Human Disease by Gene Targeting. Methods in cell biology. 76. 593–612. 5 indexed citations
14.
Dodd, Andrew, Stephen P. Chambers, & Donald R. Love. (2004). Short interfering RNA‐mediated gene targeting in the zebrafish. FEBS Letters. 561(1-3). 89–93. 69 indexed citations
15.
Chambers, Stephen P., et al.. (2003). Sarcoglycans of the zebrafish: orthology and localization to the sarcolemma and myosepta of muscle. Biochemical and Biophysical Research Communications. 303(2). 488–495. 18 indexed citations
16.
Chambers, Stephen P., Andrew Dodd, Rupert W. Overall, et al.. (2001). Dystrophin in Adult Zebrafish Muscle. Biochemical and Biophysical Research Communications. 286(3). 478–483. 36 indexed citations
17.
Dodd, Andrew. (2000). Zebrafish: bridging the gap between development and disease. Human Molecular Genetics. 9(16). 2443–2449. 114 indexed citations
18.
Dodd, Andrew, et al.. (1997). Mutations in the adrenoleukodystrophy gene. Human Mutation. 9(6). 500–511. 31 indexed citations
19.
Dodd, Andrew, et al.. (1997). Mutations in the adrenoleukodystrophy gene. Human Mutation. 9(6). 500–511. 4 indexed citations
20.
Kennedy, Martin A., et al.. (1996). Structure and Location of the Murine Adrenoleukodystrophy Gene. Genomics. 32(3). 395–400. 6 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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