Stuart Cantsilieris

3.6k total citations · 1 hit paper
19 papers, 665 citations indexed

About

Stuart Cantsilieris is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Stuart Cantsilieris has authored 19 papers receiving a total of 665 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 9 papers in Molecular Biology and 8 papers in Plant Science. Recurrent topics in Stuart Cantsilieris's work include Chromosomal and Genetic Variations (8 papers), Genomic variations and chromosomal abnormalities (8 papers) and Retinal Diseases and Treatments (6 papers). Stuart Cantsilieris is often cited by papers focused on Chromosomal and Genetic Variations (8 papers), Genomic variations and chromosomal abnormalities (8 papers) and Retinal Diseases and Treatments (6 papers). Stuart Cantsilieris collaborates with scholars based in Australia, United States and Italy. Stuart Cantsilieris's co-authors include Stefan J. White, Paul N. Baird, Evan E. Eichler, Melanie Sorensen, Bradley J. Nelson, Richard K. Wilson, Arvis Sulovari, Tina A. Graves-Lindsay, Vincent Magrini and Sean McGrath and has published in prestigious journals such as Science, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Stuart Cantsilieris

19 papers receiving 659 citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Characterizing the Major Structural Variant Alleles of the Human Genome

2019 269 citations Peter A. Audano, Arvis Sulovari et al. Cell profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Stuart Cantsilieris Australia	14	407	352	173	85	62	19	665
Lucy H. Williams United States	7	633 1.6×	227 0.6×	59 0.3×	47 0.6×	23 0.4×	9	807
Qingrun Zhang United States	10	421 1.0×	244 0.7×	196 1.1×	39 0.5×	43 0.7×	23	745
Tina A. Graves-Lindsay United States	5	530 1.3×	367 1.0×	221 1.3×	52 0.6×	9 0.1×	6	720
Carol Jones United States	12	361 0.9×	164 0.5×	68 0.4×	29 0.3×	14 0.2×	19	485
Hidetoshi Inoko Japan	15	313 0.8×	223 0.6×	46 0.3×	233 2.7×	14 0.2×	24	702
Darren Grafham United Kingdom	10	425 1.0×	171 0.5×	94 0.5×	43 0.5×	17 0.3×	11	553
Joseph H. Nadeau United States	13	733 1.8×	530 1.5×	316 1.8×	79 0.9×	6 0.1×	16	1.0k
Theodore G. Drivas United States	12	474 1.2×	187 0.5×	31 0.2×	35 0.4×	22 0.4×	24	635
Chin Thing Ong Singapore	5	755 1.9×	206 0.6×	48 0.3×	31 0.4×	11 0.2×	8	841
L.M. Pertz United States	5	862 2.1×	1.2k 3.5×	625 3.6×	45 0.5×	13 0.2×	6	1.5k

Countries citing papers authored by Stuart Cantsilieris

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Stuart Cantsilieris

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

All Works

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19 of 19 papers shown

Hsieh, PingHsun, Vy Dang, Mitchell R. Vollger, et al.. (2021). Evidence for opposing selective forces operating on human-specific duplicated TCAF genes in Neanderthals and humans. Nature Communications. 12(1). 5118–5118. 9 indexed citations

Porubský, David, Ashley D. Sanders, Wolfram Höps, et al.. (2020). Recurrent inversion toggling and great ape genome evolution. Nature Genetics. 52(8). 849–858. 37 indexed citations

Hsieh, PingHsun, Mitchell R. Vollger, Vy Dang, et al.. (2019). Adaptive archaic introgression of copy number variants and the discovery of previously unknown human genes. Science. 366(6463). 51 indexed citations

Audano, Peter A., Arvis Sulovari, Tina A. Graves-Lindsay, et al.. (2019). Characterizing the Major Structural Variant Alleles of the Human Genome. Cell. 176(3). 663–675.e19. 269 indexed citations breakdown →

Jones, Sarah A., Stuart Cantsilieris, Huapeng Fan, et al.. (2019). Rare variants in non-coding regulatory regions of the genome that affect gene expression in systemic lupus erythematosus. Scientific Reports. 9(1). 15433–15433. 15 indexed citations

Maggiolini, Flavia Angela Maria, Stuart Cantsilieris, Pietro D’Addabbo, et al.. (2019). Genomic inversions and GOLGA core duplicons underlie disease instability at the 15q25 locus. PLoS Genetics. 15(3). e1008075–e1008075. 16 indexed citations

Cantsilieris, Stuart, Bradley J. Nelson, John Huddleston, et al.. (2018). Recurrent structural variation, clustered sites of selection, and disease risk for the complement factor H ( CFH ) gene family. Proceedings of the National Academy of Sciences. 115(19). 42 indexed citations

Mohajeri, Kiana, Stuart Cantsilieris, John Huddleston, et al.. (2016). Interchromosomal core duplicons drive both evolutionary instability and disease susceptibility of the Chromosome 8p23.1 region. Genome Research. 26(11). 1453–1467. 20 indexed citations

Cantsilieris, Stuart, Holly A.F. Stessman, Jay Shendure, & Evan E. Eichler. (2016). Targeted Capture and High-Throughput Sequencing Using Molecular Inversion Probes (MIPs). Methods in molecular biology. 1492. 95–106. 15 indexed citations

10.

Graßmann, Felix, Stuart Cantsilieris, Stefan J. White, et al.. (2016). Multiallelic copy number variation in the complement component 4A (C4A) gene is associated with late-stage age-related macular degeneration (AMD). Journal of Neuroinflammation. 13(1). 81–81. 24 indexed citations

11.

White, Stefan J. & Stuart Cantsilieris. (2016). Genotyping. Methods in molecular biology. 6 indexed citations

12.

Cantsilieris, Stuart, Patrick Western, Paul N. Baird, & Stefan J. White. (2014). Technical considerations for genotyping multi-allelic copy number variation (CNV), in regions of segmental duplication. BMC Genomics. 15(1). 329–329. 30 indexed citations

13.

Kaur, Inderjeet, Stuart Cantsilieris, Andrea J. Richardson, et al.. (2013). Association of the del443ins54 at the ARMS2 locus in Indian and Australian cohorts with age-related macular degeneration.. PubMed. 19. 822–8. 7 indexed citations

14.

Cantsilieris, Stuart, Paul N. Baird, & Stefan J. White. (2012). Molecular methods for genotyping complex copy number polymorphisms. Genomics. 101(2). 86–93. 39 indexed citations

15.

Cantsilieris, Stuart & Stefan J. White. (2012). Correlating Multiallelic Copy Number Polymorphisms with Disease Susceptibility. Human Mutation. 34(1). 1–13. 44 indexed citations

16.

Adams, Madeleine, J. A. Simpson, Andrea J. Richardson, et al.. (2012). Can genetic associations change with age? CFH and age-related macular degeneration. Human Molecular Genetics. 21(23). 5229–5236. 17 indexed citations

17.

Cantsilieris, Stuart, Stefan J. White, Andrea J. Richardson, Robyn H. Guymer, & Paul N. Baird. (2012). Comprehensive Analysis of Copy Number Variation of Genes at Chromosome 1 and 10 Loci Associated with Late Age Related Macular Degeneration. PLoS ONE. 7(4). e35255–e35255. 17 indexed citations

18.

Williamson, J., et al.. (2011). Almost total protection from age-related macular degeneration by haplotypes of the Regulators of Complement Activation. Genomics. 98(6). 412–421. 3 indexed citations

19.

Cantsilieris, Stuart, et al.. (2009). Recent Patents Relating to Diagnostic Advances in Age Related Macular Degeneration (AMD). PubMed. 3(2). 102–113. 4 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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