Stuart Cantsilieris
Impact in
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Ophthalmology top 5%
- Retinal Diseases and Treatments
Papers in
-
- Genomics and Phylogenetic Studies 4
- Retinal Development and Disorders 2
- Genomics and Chromatin Dynamics 2
- Genetics 9
- Genomic variations and chromosomal abnormalities 8
- Co-authors
- Stefan J. White (7 shared papers)Paul N. Baird (9 shared papers)Evan E. Eichler (8 shared papers)Melanie Sorensen (5 shared papers)Bradley J. Nelson (4 shared papers)Richard K. Wilson (3 shared papers)Tina A. Graves-Lindsay (2 shared papers)AnneMarie E. Welch (3 shared papers)
- Journals
- Genomics (2 papers)Nature Communications (1 paper)Journal of Neuroinflammation (1 paper)Cell (1 paper)PLoS ONE (1 paper)
- Partner nations
- AustraliaUnited StatesGermany
In The Last Decade
Stuart Cantsilieris
19 papers receiving 678 citations
Stuart Cantsilieris's Hit Papers
Peers
Comparison fields: 5 of 68
- Genetics 335
- Ophthalmology 54
- Molecular Biology 379
- Cancer Research 60
- Plant Science 159
Countries citing papers authored by Stuart Cantsilieris
This map shows the geographic impact of Stuart Cantsilieris'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 Stuart Cantsilieris with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Stuart Cantsilieris more than expected).
Fields of papers citing papers by Stuart Cantsilieris
This network shows the impact of papers produced by Stuart Cantsilieris. 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 Stuart Cantsilieris. The network helps show where Stuart Cantsilieris may publish in the future.
Co-authors
The 25 scholars most cited alongside Stuart Cantsilieris, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | Characterizing the Major Structural Variant Alleles of the Human Genome Hit paper breakdown → | 2019 | 279 |
| 2 | 2019 | 52 | |
| 3 | 2012 | 44 | |
| 4 | 2018 | 42 | |
| 5 | 2020 | 41 | |
| 6 | 2012 | 40 | |
| 7 | 2014 | 31 | |
| 8 | 2016 | 24 | |
| 9 | 2016 | 21 | |
| 10 | 2012 | 17 | |
| 11 | 2012 | 17 | |
| 12 | 2019 | 16 | |
| 13 | 2019 | 15 | |
| 14 | 2016 | 15 | |
| 15 | 2021 | 9 | |
| 16 | Association of the del443ins54 at the ARMS2 locus in Indian and Australian cohorts with age-related macular degeneration. | 2013 | 7 |
| 17 | 2016 | 7 | |
| 18 | 2009 | 4 | |
| 19 | 2011 | 3 |
About Stuart Cantsilieris
Stuart Cantsilieris is a scholar working on Molecular Biology, Genetics, Plant Science, Ophthalmology and Immunology, having authored 19 papers that have together received 684 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (8 papers), Chromosomal and Genetic Variations (7 papers), Retinal Diseases and Treatments (5 papers), Genomics and Phylogenetic Studies (4 papers), Retinal Imaging and Analysis (2 papers), Retinal Development and Disorders (2 papers), Complement system in diseases (2 papers) and Genomics and Chromatin Dynamics (2 papers). The work is most often cited by research in Genetics (335 citations), Ophthalmology (54 citations), Molecular Biology (379 citations), Cancer Research (60 citations) and Plant Science (159 citations). Stuart Cantsilieris has collaborated with scholars based in Australia, United States and Germany. Frequent co-authors include Stefan J. White, Paul N. Baird, Evan E. Eichler, Melanie Sorensen, Bradley J. Nelson, Richard K. Wilson, Tina A. Graves-Lindsay, AnneMarie E. Welch, Arvis Sulovari and Susan K. Dutcher. Their work appears in journals such as Genomics, Nature Communications, Journal of Neuroinflammation, Cell and PLoS ONE.
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.