Paul Kalitsis

4.3k total citations
59 papers, 3.3k citations indexed

About

Paul Kalitsis is a scholar working on Molecular Biology, Plant Science and Genetics. According to data from OpenAlex, Paul Kalitsis has authored 59 papers receiving a total of 3.3k indexed citations (citations by other indexed papers that have themselves been cited), including 50 papers in Molecular Biology, 31 papers in Plant Science and 23 papers in Genetics. Recurrent topics in Paul Kalitsis's work include Chromosomal and Genetic Variations (31 papers), Genomics and Chromatin Dynamics (24 papers) and Genomic variations and chromosomal abnormalities (16 papers). Paul Kalitsis is often cited by papers focused on Chromosomal and Genetic Variations (31 papers), Genomics and Chromatin Dynamics (24 papers) and Genomic variations and chromosomal abnormalities (16 papers). Paul Kalitsis collaborates with scholars based in Australia, United States and United Kingdom. Paul Kalitsis's co-authors include K. H. Andy Choo, Kerry J. Fowler, Elizabeth D. Earle, K.H. Andy Choo, Damien F. Hudson, Richard Saffery, Emily V. Howman, Bryce Vissel, Tao Zhang and Ainsley J. Newson and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Paul Kalitsis

58 papers receiving 3.2k 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 Kalitsis Australia 30 2.6k 1.7k 854 804 272 59 3.3k
Dale Dorsett United States 41 4.5k 1.7× 1.2k 0.7× 865 1.0× 380 0.5× 145 0.5× 79 4.9k
Kei‐ichiro Ishiguro Japan 22 2.8k 1.1× 629 0.4× 412 0.5× 1.1k 1.3× 252 0.9× 62 3.2k
Janet F. Partridge United States 28 5.2k 2.0× 1.5k 0.9× 445 0.5× 387 0.5× 344 1.3× 43 5.6k
Ian R. Adams United Kingdom 29 3.2k 1.2× 517 0.3× 809 0.9× 535 0.7× 297 1.1× 55 3.7k
Francisco Antequera Spain 24 3.0k 1.2× 517 0.3× 740 0.9× 139 0.2× 164 0.6× 48 3.4k
K. H. Andy Choo Australia 37 3.7k 1.4× 3.1k 1.9× 1.4k 1.7× 1.1k 1.3× 150 0.6× 68 4.6k
Michaela Pagani Austria 16 4.0k 1.5× 610 0.4× 718 0.8× 101 0.1× 150 0.6× 25 4.3k
Marek Bartkuhn Germany 28 2.5k 0.9× 551 0.3× 515 0.6× 115 0.1× 234 0.9× 65 3.0k
Michael Bulger United States 25 3.4k 1.3× 477 0.3× 448 0.5× 235 0.3× 120 0.4× 42 3.9k
Bettina A. Moser United States 27 2.0k 0.8× 212 0.1× 636 0.7× 158 0.2× 205 0.8× 50 2.5k

Countries citing papers authored by Paul Kalitsis

Since Specialization
Citations

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

Fields of papers citing papers by Paul Kalitsis

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Paul Kalitsis

This figure shows the co-authorship network connecting the top 25 collaborators of Paul Kalitsis. A scholar is included among the top collaborators of Paul Kalitsis 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 Kalitsis. Paul Kalitsis 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.
Kalitsis, Paul, Florence Petit, Judith M.A. Verhagen, et al.. (2025). AP2M1 Is a Candidate Gene for Microcephaly and Intellectual Disability in 3q27.1 Deletions. American Journal of Medical Genetics Part A. 197(11). e64153–e64153.
2.
Francis, David, Samantha Ayres, Nicole J. Van Bergen, et al.. (2023). De novo enhancer deletion of LMX1B produces a mild nail‐patella clinical phenotype. Clinical Genetics. 105(2). 214–219. 2 indexed citations
3.
Nielsen, Christian Friberg, Tao Zhang, Marin Barišić, Paul Kalitsis, & Damien F. Hudson. (2020). Topoisomerase IIα is essential for maintenance of mitotic chromosome structure. Proceedings of the National Academy of Sciences. 117(22). 12131–12142. 94 indexed citations
4.
Zhang, Tao, et al.. (2019). Loss of TOP3B leads to increased R-loop formation and genome instability. Open Biology. 9(12). 190222–190222. 49 indexed citations
5.
Tremblay, Cédric S., Nicholas C. Wong, Kirill Tsyganov, et al.. (2018). Restricted cell cycle is essential for clonal evolution and therapeutic resistance of pre-leukemic stem cells. Nature Communications. 9(1). 3535–3535. 17 indexed citations
6.
McKay, Michael J., Jeffrey M. Craig, Paul Kalitsis, et al.. (2018). A Roberts Syndrome Individual With Differential Genotoxin Sensitivity and a DNA Damage Response Defect. International Journal of Radiation Oncology*Biology*Physics. 103(5). 1194–1202. 10 indexed citations
7.
Kuek, Li Eon, et al.. (2018). Identification of an Immortalized Human Airway Epithelial Cell Line with Dyskinetic Cilia. American Journal of Respiratory Cell and Molecular Biology. 59(3). 375–382. 4 indexed citations
8.
Kalitsis, Paul, et al.. (2017). The Role of Centromere Defects in Cancer. Progress in molecular and subcellular biology. 56. 541–554. 7 indexed citations
9.
Hudson, Damien F., David J. Amor, Amber Boys, et al.. (2016). Loss of RMI2 Increases Genome Instability and Causes a Bloom-Like Syndrome. PLoS Genetics. 12(12). e1006483–e1006483. 56 indexed citations
10.
Jacobs, Shelley, Deidre M Mattiske, Shu Ly Lim, et al.. (2015). Contribution of the Two Genes Encoding Histone Variant H3.3 to Viability and Fertility in Mice. PLoS Genetics. 11(2). e1004964–e1004964. 87 indexed citations
11.
Kalitsis, Paul, et al.. (2014). Chromosome Y Centromere Array Deletion Leads to Impaired Centromere Function. PLoS ONE. 9(1). e86875–e86875. 1 indexed citations
12.
Loesch, Danuta Z., HR Slater, Justin P. Rubio, et al.. (2009). Small CGG repeat expansion alleles of FMR1 gene are associated with parkinsonism. Clinical Genetics. 76(5). 471–476. 55 indexed citations
13.
Pertile, Mark D., et al.. (2009). Rapid evolution of mouse Y centromere repeat DNA belies recent sequence stability. Genome Research. 19(12). 2202–2213. 41 indexed citations
14.
Kalitsis, Paul, et al.. (2003). Partially functional Cenpa–GFP fusion protein causes increased chromosome missegregation and apoptosis during mouse embryogenesis. Chromosome Research. 11(4). 345–357. 26 indexed citations
15.
Saffery, Richard, et al.. (2000). Components of the human spindle checkpoint control mechanism localize specifically to the active centromere on dicentric chromosomes. Human Genetics. 107(4). 376–384. 18 indexed citations
16.
Howman, Emily V., Kerry J. Fowler, Ainsley J. Newson, et al.. (2000). Early disruption of centromeric chromatin organization in centromere protein A (Cenpa) null mice. Proceedings of the National Academy of Sciences. 97(3). 1148–1153. 327 indexed citations
17.
Kalitsis, Paul, Andrew Macdonald, Ainsley J. Newson, Damien F. Hudson, & K. H. Andy Choo. (1998). Gene Structure and Sequence Analysis of Mouse Centromere Proteins A and C. Genomics. 47(1). 108–114. 23 indexed citations
18.
Kalitsis, Paul, E. D. Earle, Bryce Vissel, Lisa G. Shaffer, & K.H. Andy Choo. (1993). A Chromosome 13-Specific Human Satellite I DNA Subfamily with Minor Presence on Chromosome 21: Further Studies on Robertsonian Translocations. Genomics. 16(1). 104–112. 32 indexed citations
19.
Sart, Desirée du, Paul Kalitsis, & Malgorzata Schmidt. (1992). Noninactivation of a portion of Xq28 in a balanced X‐autosome translocation. American Journal of Medical Genetics. 42(2). 156–160. 25 indexed citations
20.
Schmidt, Malgorzata, Desirée du Sart, Paul Kalitsis, et al.. (1991). X chromosome inactivation in fibroblasts of mentally retarded female carriers of the fragile site Xq27.3: Application of the probe M27β to evaluate X inactivation status. American Journal of Medical Genetics. 38(2-3). 411–415. 8 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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