Paul Oei

514 total citations
19 papers, 256 citations indexed

About

Paul Oei is a scholar working on Molecular Biology, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Paul Oei has authored 19 papers receiving a total of 256 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 8 papers in Genetics and 5 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Paul Oei's work include Genomic variations and chromosomal abnormalities (8 papers), Chromosomal and Genetic Variations (5 papers) and Renal cell carcinoma treatment (3 papers). Paul Oei is often cited by papers focused on Genomic variations and chromosomal abnormalities (8 papers), Chromosomal and Genetic Variations (5 papers) and Renal cell carcinoma treatment (3 papers). Paul Oei collaborates with scholars based in New Zealand, Australia and United States. Paul Oei's co-authors include Salim Aftimos, Ingrid Winship, Daniel Ng, Irene Low, Jake Shortt, Lynda J. Campbell, Alice M. George, Julie McGaughran, Pekka Kannus and Philip D. Cotter and has published in prestigious journals such as Journal of Clinical Oncology, Blood and BioMed Research International.

In The Last Decade

Paul Oei

19 papers receiving 243 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Paul Oei New Zealand 11 96 73 50 50 44 19 256
P.M. Chou United States 9 77 0.8× 192 2.6× 36 0.7× 37 0.7× 89 2.0× 17 321
S. Sharif United Kingdom 6 59 0.6× 40 0.5× 20 0.4× 75 1.5× 49 1.1× 7 374
Satoshi Hamanoue Japan 12 127 1.3× 162 2.2× 54 1.1× 24 0.5× 68 1.5× 32 364
Laurence Baranger France 12 49 0.5× 110 1.5× 35 0.7× 40 0.8× 21 0.5× 19 362
Mona S. Jahromi United States 10 27 0.3× 84 1.2× 40 0.8× 32 0.6× 78 1.8× 13 259
Teruaki Akaogi Japan 11 49 0.5× 62 0.8× 50 1.0× 83 1.7× 30 0.7× 19 331
W Tanghe Belgium 10 104 1.1× 118 1.6× 25 0.5× 36 0.7× 80 1.8× 27 355
Emon Elboudwarej United States 7 68 0.7× 146 2.0× 47 0.9× 41 0.8× 26 0.6× 20 291
V. Parlier Switzerland 13 76 0.8× 121 1.7× 27 0.5× 21 0.4× 42 1.0× 19 446
Georg Borgström Finland 15 67 0.7× 95 1.3× 42 0.8× 22 0.4× 18 0.4× 20 517

Countries citing papers authored by Paul Oei

Since Specialization
Citations

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

Fields of papers citing papers by Paul Oei

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Paul Oei

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

All Works

19 of 19 papers shown
1.
Turchini, John, Juliana Andrici, Loretta Sioson, et al.. (2016). NRASQ61R Mutation-specific Immunohistochemistry is Highly Specific for Either NRAS Q61R or KRAS Q61R Mutation in Colorectal Carcinoma. Applied immunohistochemistry & molecular morphology. 25(7). 475–480. 12 indexed citations
2.
Low, Irene, et al.. (2016). USP6 gene rearrangement in nodular fasciitis and histological mimics. Histopathology. 69(5). 784–791. 48 indexed citations
3.
Oei, Paul, et al.. (2014). Analysis of Molecular Cytogenetic Changes in Metastatic Renal Cell Carcinoma in the Setting of Everolimus Treatment: A Pilot Project. Clinical Genitourinary Cancer. 12(4). 256–261. 1 indexed citations
4.
Broom, Reuben, George Dranitsaris, Carol Fraser‐Browne, et al.. (2014). Dovitinib in first-line metastatic renal cell carcinoma and correlation of efficacy with tumor gene status: A phase II clinical trial.. Journal of Clinical Oncology. 32(15_suppl). 4569–4569. 1 indexed citations
5.
Campbell, Lynda J., Paul Oei, Ross Brookwell, et al.. (2013). FISH Detection ofPML-RARAFusion in ins(15;17) Acute Promyelocytic Leukaemia Depends on Probe Size. BioMed Research International. 2013. 1–4. 20 indexed citations
6.
7.
Oei, Paul, et al.. (2009). Retrospective review of prognostic factors, including 1p19q deletion, in low‐grade oligodendrogliomas and a review of recent published works. Journal of Medical Imaging and Radiation Oncology. 53(3). 305–309. 10 indexed citations
8.
Ramsaroop, Reena, et al.. (2009). Cervical intraepithelial neoplasia and aneusomy of TERC: Assessment of liquid‐based cytological preparations. Diagnostic Cytopathology. 37(6). 411–415. 7 indexed citations
9.
10.
Bigby, Susan M., et al.. (2006). Dermatofibrosarcoma protuberans: report of a case with a variant ring chromosome and metastases following pregnancy. Journal of Cutaneous Pathology. 33(5). 383–388. 14 indexed citations
11.
Kannus, Pekka, Paul Oei, Howard R. Slater, Ouda Khammy, & Salim Aftimos. (2006). Epiphyseal dysplasia and other skeletal anomalies in a patient with the 6p25 microdeletion syndrome. American Journal of Medical Genetics Part A. 140A(18). 1955–1959. 18 indexed citations
12.
James, Paul A., Paul Oei, Daniel K. Ng, Pekka Kannus, & Salim Aftimos. (2005). Another case of interstitial del(12) involving the proposed cardio‐facio‐cutaneous candidate region. American Journal of Medical Genetics Part A. 136A(1). 12–16. 11 indexed citations
13.
14.
George, Alice M., Paul Oei, & Ingrid Winship. (2003). False‐positive diagnosis of trisomy 21 using fluorescence in situ hybridisation (FISH) on uncultured amniotic fluid cells. Prenatal Diagnosis. 23(4). 302–305. 17 indexed citations
15.
James, Paul A., Salim Aftimos, & Paul Oei. (2003). Severe musculoskeletal phenotype associated with an unbalanced t(6;10) translocation: Clarification of the locus for this phenotype on distal 6p. American Journal of Medical Genetics Part A. 119A(3). 288–292. 7 indexed citations
16.
Ng, Daniel P. K., et al.. (2002). Supernumerary marker chromosomes 5: Confirmation of a critical region and resultant phenotype. American Journal of Medical Genetics. 111(1). 19–26. 17 indexed citations
17.
George, Alice M., Lavinia Hallam, Paul Oei, & Julie McGaughran. (2002). Prenatal diagnosis of partial tetrasomy 14: a case study. Prenatal Diagnosis. 22(2). 127–130. 4 indexed citations
18.
McGaughran, Julie, Salim Aftimos, & Paul Oei. (2000). Trisomy of 3pter in a patient with apparent C (trigonocephaly) syndrome. American Journal of Medical Genetics. 94(4). 311–315. 15 indexed citations
19.
Glass, Ian A., et al.. (1998). Trisomy 2q11.2-->q21.1 resulting from an unbalanced insertion in two generations.. Journal of Medical Genetics. 35(4). 319–322. 18 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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