Diane Rushlow

1.1k total citations
11 papers, 496 citations indexed

About

Diane Rushlow is a scholar working on Ophthalmology, Oncology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Diane Rushlow has authored 11 papers receiving a total of 496 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Ophthalmology, 5 papers in Oncology and 4 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Diane Rushlow's work include Ocular Oncology and Treatments (6 papers), Cancer-related Molecular Pathways (4 papers) and Vascular Anomalies and Treatments (3 papers). Diane Rushlow is often cited by papers focused on Ocular Oncology and Treatments (6 papers), Cancer-related Molecular Pathways (4 papers) and Vascular Anomalies and Treatments (3 papers). Diane Rushlow collaborates with scholars based in Canada, United States and Germany. Diane Rushlow's co-authors include Brenda L. Gallie, Katherine Zhang, Beata Piovesan, Tom G.W. Letteboer, Robin D. Clark, C. J. J. Westermann, Antoni Castells, Arupa Ganguly, Carol J. Gallione and Douglas A. Marchuk and has published in prestigious journals such as International Journal of Cancer, Journal of Medical Genetics and Electrophoresis.

In The Last Decade

Diane Rushlow

11 papers receiving 489 citations

Peers

Diane Rushlow

GENET

OPHTH

PRM

ONCOL

MB

Claudia Sampor Argentina

David H. Abramson United States

Julio Manzitti Argentina

Sameh E. Soliman Egypt

Carol L. Shields United States

Annemarie Klingenstein Germany

Lene Dissing Sjø Denmark

Gabriele Prinz Germany

Tatiana Beresneva United States

Atsushi Notoya Japan

Claudia Sampor Argentina

Diane Rushlow

130 ×0.7

GENET

327 ×1.9

OPHTH

138 ×0.8

PRM

131 ×0.8

ONCOL

99 ×0.6

MB

Citations per year, relative to Diane Rushlow Diane Rushlow (= 1×) peers Claudia Sampor

Countries citing papers authored by Diane Rushlow

Since Specialization

Citations

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

Fields of papers citing papers by Diane Rushlow

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Diane Rushlow

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

All Works

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11 of 11 papers shown

1.

Racher, Hilary, Sameh E. Soliman, Bob Argiropoulos, et al.. (2016). Molecular analysis distinguishes metastatic disease from second cancers in patients with retinoblastoma. Cancer Genetics. 209(7-8). 359–363. 8 indexed citations

2.

Kurban, Ghada, Brenda L. Gallie, Michael Leveridge, et al.. (2011). Needle core biopsies provide ample material for genomic and proteomic studies of kidney cancer: Observations on DNA, RNA, protein extractions and VHL mutation detection. Pathology - Research and Practice. 208(1). 22–31. 11 indexed citations

3.

Piovesan, Beata, et al.. (2011). Identification of clinically relevant mosaicism in type I hereditary haemorrhagic telangiectasia. Journal of Medical Genetics. 48(5). 353–357. 12 indexed citations

4.

Dimaras, Helen, Diane Rushlow, William Halliday, et al.. (2010). Using RB1 mutations to assess minimal residual disease in metastatic retinoblastoma. Translational research. 156(2). 91–97. 19 indexed citations

5.

Rushlow, Diane, et al.. (2009). Detection of mosaicRB1mutations in families with retinoblastoma. Human Mutation. 30(5). 842–851. 104 indexed citations

6.

Mitter, Diana, et al.. (2008). Identification of a mutation in exon 27 of the RB1 gene associated with incomplete penetrance retinoblastoma. Familial Cancer. 8(1). 55–58. 8 indexed citations

7.

Zhang, Katherine, et al.. (2008). Patterns of missplicing caused byRB1gene mutations in patients with retinoblastoma and association with phenotypic expression. Human Mutation. 29(4). 475–484. 57 indexed citations

8.

Gillison, Maura L., Renwei Chen, Diane Rushlow, et al.. (2007). Human retinoblastoma is not caused by known pRb‐inactivating human DNA tumor viruses. International Journal of Cancer. 120(7). 1482–1490. 29 indexed citations

9.

Gallione, Carol J., Tom G.W. Letteboer, Diane Rushlow, et al.. (2006). SMAD4 mutations found in unselected HHT patients. Journal of Medical Genetics. 43(10). 793–797. 174 indexed citations

10.

Abdalla, S A, Urszula Cymerman, Diane Rushlow, et al.. (2005). Novel mutations and polymorphisms in genes causing hereditary hemorrhagic telangiectasia. Human Mutation. 25(3). 320–321. 50 indexed citations

11.

Yager, Thomas D., Anne Bouevitch, David C. Chan, et al.. (1999). High performance DNA sequencing, and the detection of mutations and polymorphisms, on the Clipper sequencer. Electrophoresis. 20(6). 1280–1300. 24 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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