David J. Dow

5.6k total citations · 1 hit paper
15 papers, 1.1k citations indexed

About

David J. Dow is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, David J. Dow has authored 15 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 6 papers in Genetics and 3 papers in Oncology. Recurrent topics in David J. Dow's work include CRISPR and Genetic Engineering (4 papers), Virus-based gene therapy research (2 papers) and CAR-T cell therapy research (2 papers). David J. Dow is often cited by papers focused on CRISPR and Genetic Engineering (4 papers), Virus-based gene therapy research (2 papers) and CAR-T cell therapy research (2 papers). David J. Dow collaborates with scholars based in United Kingdom, United States and Germany. David J. Dow's co-authors include Allen D. Roses, Linda M. Thurmond, Katherine L. Baker-Neblett, Denise Shortino, Michael Mosteller, Eric Lai, Seth Hetherington, Arlene R. Hughes, Michael Stocum and William Spreen and has published in prestigious journals such as The Lancet, Nature Communications and Human Molecular Genetics.

In The Last Decade

David J. Dow

15 papers receiving 1.1k citations

Hit Papers

Genetic variations in HLA-B region and hypersensitivity r... 2002 2026 2010 2018 2002 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
David J. Dow United Kingdom 11 399 327 185 173 136 15 1.1k
María Isidoro‐García Spain 18 310 0.8× 68 0.2× 87 0.5× 57 0.3× 185 1.4× 90 1.1k
Shaomin Yang China 18 316 0.8× 52 0.2× 54 0.3× 47 0.3× 60 0.4× 56 816
Roscoe D. Atkinson United States 12 259 0.6× 46 0.1× 52 0.3× 38 0.2× 249 1.8× 18 1.1k
V Rossi Italy 12 487 1.2× 25 0.1× 57 0.3× 37 0.2× 197 1.4× 18 1.4k
Paul Frohna United States 17 403 1.0× 57 0.2× 318 1.7× 128 0.7× 263 1.9× 47 1.3k
Dan Lehmann Israel 19 169 0.4× 70 0.2× 158 0.9× 45 0.3× 598 4.4× 36 1.2k
Eiichi Suematsu Japan 19 630 1.6× 29 0.1× 35 0.2× 156 0.9× 139 1.0× 79 1.3k
Asim Diab Sweden 15 472 1.2× 73 0.2× 36 0.2× 74 0.4× 530 3.9× 26 1.1k
Joon Seol Bae South Korea 23 573 1.4× 204 0.6× 463 2.5× 69 0.4× 245 1.8× 111 1.7k
María Eugenia Sáez Spain 21 455 1.1× 30 0.1× 239 1.3× 61 0.4× 201 1.5× 67 1.3k

Countries citing papers authored by David J. Dow

Since Specialization
Citations

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

Fields of papers citing papers by David J. Dow

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of David J. Dow

This figure shows the co-authorship network connecting the top 25 collaborators of David J. Dow. A scholar is included among the top collaborators of David J. Dow 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 J. Dow. David J. Dow is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

15 of 15 papers shown
1.
Picco, Gabriele, Elisabeth Chen, Luz García‐Alonso, et al.. (2019). Functional linkage of gene fusions to cancer cell fitness assessed by pharmacological and CRISPR-Cas9 screening. Nature Communications. 10(1). 2198–2198. 78 indexed citations
2.
Rittié, Laure, Takis Athanasopoulos, Marie Davies, et al.. (2019). The Landscape of Early Clinical Gene Therapies outside of Oncology. Molecular Therapy. 27(10). 1706–1717. 21 indexed citations
3.
Lu, Quinn, et al.. (2017). Applications of CRISPR genome editing technology in drug target identification and validation. Expert Opinion on Drug Discovery. 12(6). 541–552. 12 indexed citations
4.
Woollard, Peter, Nalini Mehta, Jessica Vamathevan, et al.. (2011). The application of next-generation sequencing technologies to drug discovery and development. Drug Discovery Today. 16(11-12). 512–519. 31 indexed citations
5.
Dow, David J., Julie Huxley‐Jones, Clyde Francks, et al.. (2011). ADAMTSL3 as a candidate gene for schizophrenia: Gene sequencing and ultra-high density association analysis by imputation. Schizophrenia Research. 127(1-3). 28–34. 38 indexed citations
6.
Dow, David J., Alex D. McMahon, Ian C. Gray, Chris J. Packard, & Pieter H.E. Groot. (2010). CCR2 and coronary artery disease: a woscops substudy. BMC Research Notes. 3(1). 31–31. 6 indexed citations
7.
Parry, David, et al.. (2006). Improved management in threatened preterm labour with rapid fetal fibronectin testing. Australian and New Zealand Journal of Obstetrics and Gynaecology. 46(3). 240–241. 6 indexed citations
8.
Spraggs, Colin F., Sreekumar Pillai, David J. Dow, et al.. (2005). Pharmacogenetics and obesity: common gene variants influence weight loss response of the norepinephrine/dopamine transporter inhibitor GW320659 in obese subjects. Pharmacogenetics and Genomics. 15(12). 883–889. 11 indexed citations
9.
Hetherington, Seth, Arlene R. Hughes, Michael Mosteller, et al.. (2002). Genetic variations in HLA-B region and hypersensitivity reactions to abacavir. The Lancet. 359(9312). 1121–1122. 583 indexed citations breakdown →
10.
Farndon, Peter, et al.. (1999). Prenatal diagnosis of tuberous sclerosis with intracerebral signs at 14 weeks' gestation. Prenatal Diagnosis. 19(6). 575–579. 11 indexed citations
11.
Camacho, Nancy P., David J. Dow, Joseph M. Gertner, et al.. (1998). Identification of the oim mutation by dye terminator chemistry combined with automated direct DNA sequencing. Journal of Orthopaedic Research®. 16(1). 38–42. 8 indexed citations
12.
Dow, David J., David C. Rubinsztein, John R.W. Yates, David Barton, & M.A. Ferguson‐Smith. (1997). Instability of normal (CTG)n alleles in the DM kinase gene.. Journal of Medical Genetics. 34(10). 871–873. 4 indexed citations
13.
Knight, Samantha J.L., Rachael J. Ritchie, Lisa Chakrabarti, et al.. (1996). A study of FRAXE in mentally retarded individuals referred for fragile X syndrome (FRAXA) testing in the United Kingdom.. PubMed. 58(5). 906–13. 37 indexed citations
14.
Warner, Jon, et al.. (1996). A general method for the detection of large CAG repeat expansions by fluorescent PCR.. Journal of Medical Genetics. 33(12). 1022–1026. 208 indexed citations
15.
Sargent, Carole A., N. Affara, Elizabeth Bentley, et al.. (1993). Cloning of the X-linked glycerol kinase deficiency gene and its identification by sequence comparison to the Bacillus subtilis homologue. Human Molecular Genetics. 2(2). 97–106. 31 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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