Dale Wright

890 total citations
23 papers, 420 citations indexed

About

Dale Wright is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Genetics. According to data from OpenAlex, Dale Wright has authored 23 papers receiving a total of 420 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 6 papers in Pediatrics, Perinatology and Child Health and 6 papers in Genetics. Recurrent topics in Dale Wright's work include Prenatal Screening and Diagnostics (6 papers), Genomic variations and chromosomal abnormalities (4 papers) and Cancer Mechanisms and Therapy (3 papers). Dale Wright is often cited by papers focused on Prenatal Screening and Diagnostics (6 papers), Genomic variations and chromosomal abnormalities (4 papers) and Cancer Mechanisms and Therapy (3 papers). Dale Wright collaborates with scholars based in Australia, United States and Italy. Dale Wright's co-authors include Benjamin M. Nash, Robyn V. Jamieson, Bruce Bennetts, John Grigg, Catherine T. Chung, Narasimhan P. Agaram, Louise Carey, Martha C. Sola, Alan D. Hutson and Robert D. Christensen and has published in prestigious journals such as Blood, The Journal of Immunology and Oncogene.

In The Last Decade

Dale Wright

21 papers receiving 394 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Dale Wright Australia 8 173 160 88 77 56 23 420
Sarah Hale United States 13 36 0.2× 95 0.6× 139 1.6× 20 0.3× 48 0.9× 22 472
Léna Absi France 13 29 0.2× 60 0.4× 8 0.1× 50 0.6× 127 2.3× 25 625
Claudia Cesaretti Italy 12 61 0.4× 61 0.4× 92 1.0× 45 0.6× 197 3.5× 34 504
Gaurav Tyagi India 11 68 0.4× 88 0.6× 27 0.3× 86 1.1× 72 1.3× 48 560
Dhruve S. Jeevan United States 10 43 0.2× 103 0.6× 20 0.2× 63 0.8× 23 0.4× 15 345
Sophie Huybrechts Belgium 12 26 0.2× 158 1.0× 123 1.4× 33 0.4× 235 4.2× 31 515
Mohamed H. Al‐Hamed Saudi Arabia 13 118 0.7× 227 1.4× 38 0.4× 128 1.7× 22 0.4× 44 456
Paola Bolli Italy 9 86 0.5× 59 0.4× 56 0.6× 34 0.4× 30 0.5× 13 328
Shoko Goto Japan 9 22 0.1× 146 0.9× 38 0.4× 42 0.5× 19 0.3× 13 459
Maria Badaracco United States 10 95 0.5× 115 0.7× 24 0.3× 29 0.4× 83 1.5× 11 489

Countries citing papers authored by Dale Wright

Since Specialization
Citations

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

Fields of papers citing papers by Dale Wright

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dale Wright

This figure shows the co-authorship network connecting the top 25 collaborators of Dale Wright. A scholar is included among the top collaborators of Dale Wright 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 Dale Wright. Dale Wright 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.
Hesson, Luke B., Vivian Lin, Dale Wright, et al.. (2024). Microdissection of Distinct Morphological Regions Within Uveal Melanomas Identifies Novel Drug Targets. Cancers. 16(24). 4152–4152.
2.
Wright, Dale, Artur Darmanian, Luke St Heaps, et al.. (2023). Saliva DNA: An alternative biospecimen for single nucleotide polymorphism chromosomal microarray analysis in autism. American Journal of Medical Genetics Part A. 191(12). 2913–2920. 1 indexed citations
3.
Bennetts, Bruce, Artur Darmanian, Luke Jones, et al.. (2023). SNP chromosome microarray genotyping for detection of uniparental disomy in the clinical diagnostic laboratory. Pathology. 55(6). 818–826. 1 indexed citations
4.
Nash, Benjamin M., Alan Ma, Gladys Ho, et al.. (2022). Whole Genome Sequencing, Focused Assays and Functional Studies Increasing Understanding in Cryptic Inherited Retinal Dystrophies. International Journal of Molecular Sciences. 23(7). 3905–3905. 7 indexed citations
5.
McCowage, Geoffrey, et al.. (2021). Neuroblastoma Molecular Risk-Stratification of DNA Copy Number and ALK Genotyping via Cell-Free Circulating Tumor DNA Profiling. Cancers. 13(13). 3365–3365. 10 indexed citations
6.
Chen, Yuyan, Natalie Grima, Federica Saletta, et al.. (2021). Rare germline variants in childhood cancer patients suspected of genetic predisposition to cancer. Genes Chromosomes and Cancer. 61(2). 81–93. 5 indexed citations
7.
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9.
Brown, James, et al.. (2017). Who is and isn't having babies with Down syndrome in western Sydney: a ten year hospital cohort study. Australian and New Zealand Journal of Obstetrics and Gynaecology. 57(2). 146–151. 3 indexed citations
10.
Kao, Yu‐Chien, Yun-Shao Sung, Lei Zhang, et al.. (2016). Recurrent BCOR Internal Tandem Duplication and YWHAE-NUTM2B Fusions in Soft Tissue Undifferentiated Round Cell Sarcoma of Infancy. The American Journal of Surgical Pathology. 40(8). 1009–1020. 139 indexed citations
11.
Wright, Dale, et al.. (2016). Validation of a Chromosomal Microarray for Prenatal Diagnosis Using a Prospective Cohort of Pregnancies with Increased Risk for Chromosome Abnormalities. Genetic Testing and Molecular Biomarkers. 20(12). 791–798. 2 indexed citations
12.
Pangon, Laurent, Marc Giry-Laterrière, Nicola Currey, et al.. (2015). JRK is a positive regulator of β-catenin transcriptional activity commonly overexpressed in colon, breast and ovarian cancer. Oncogene. 35(22). 2834–2841. 21 indexed citations
13.
Nash, Benjamin M., Dale Wright, John Grigg, Bruce Bennetts, & Robyn V. Jamieson. (2015). Retinal dystrophies, genomic applications in diagnosis and prospects for therapy.. PubMed. 4(2). 139–63. 69 indexed citations
14.
Carey, Louise, Benjamin M. Nash, & Dale Wright. (2015). Molecular genetic studies of complete hydatidiform moles.. PubMed. 4(2). 181–8. 18 indexed citations
15.
Carey, Louise, et al.. (2013). Identification of a jumping translocation following pre‐implantation genetic diagnosis. American Journal of Medical Genetics Part A. 164(1). 279–281. 12 indexed citations
16.
Wright, Dale, Stefan Groß, John Robinson, et al.. (2009). Inhibition of T cell function in vitro and in vivo using small molecule antagonists of PIM kinases (35.33). The Journal of Immunology. 182(Supplement_1). 35.33–35.33. 1 indexed citations
17.
18.
Vecchio, Antonio Del, Martha C. Sola, Douglas W. Theriaque, et al.. (2001). Platelet transfusions in the neonatal intensive care unit:factors predicting which patients will require multiple transfusions. Transfusion. 41(6). 803–808. 91 indexed citations
19.
Baumer, J H, et al.. (1997). Illness severity measured by CRIB score: a product of changes in perinatal care?. Archives of Disease in Childhood Fetal & Neonatal. 77(3). F211–F215. 30 indexed citations
20.
Wright, Dale, et al.. (1996). A Precision 96 Channel Dispenser for Microchemical Techniques. 1(3). 19–22. 3 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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