Cas Simons

7.4k total citations · 1 hit paper
73 papers, 2.8k citations indexed

About

Cas Simons is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Cas Simons has authored 73 papers receiving a total of 2.8k indexed citations (citations by other indexed papers that have themselves been cited), including 58 papers in Molecular Biology, 17 papers in Genetics and 7 papers in Oncology. Recurrent topics in Cas Simons's work include RNA regulation and disease (21 papers), RNA modifications and cancer (14 papers) and RNA Research and Splicing (14 papers). Cas Simons is often cited by papers focused on RNA regulation and disease (21 papers), RNA modifications and cancer (14 papers) and RNA Research and Splicing (14 papers). Cas Simons collaborates with scholars based in Australia, United States and Netherlands. Cas Simons's co-authors include John S. Mattick, Ryan J. Taft, Tim R. Mercer, Giulia Soldà, Marcel E. Dinger, Sean M. Grimmond, Adeline Vanderver, Mark L. Crowe, Marjan Askarian-Amiri and Paulo Amaral and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Genes & Development.

In The Last Decade

Cas Simons

68 papers receiving 2.7k 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.

Long noncoding RNAs in mouse embryonic stem cell pluripotency and differentiation

2008 605 citations Tim R. Mercer, Cas Simons et al. Genome Research profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Cas Simons Australia	25	2.0k	847	368	196	187	73	2.8k
Yan Zhou China	28	1.3k 0.7×	425 0.5×	332 0.9×	123 0.6×	117 0.6×	130	2.3k
Lauro Sumoy Spain	28	2.1k 1.0×	412 0.5×	437 1.2×	323 1.6×	271 1.4×	78	2.9k
Ryan Walsh United States	21	2.8k 1.4×	427 0.5×	322 0.9×	195 1.0×	147 0.8×	62	3.6k
Boris V. Skryabin Germany	28	2.5k 1.2×	675 0.8×	638 1.7×	189 1.0×	359 1.9×	78	3.6k
Jonathan D. Gilthorpe Sweden	23	1.3k 0.7×	363 0.4×	186 0.5×	151 0.8×	152 0.8×	46	2.2k
Ana Dopazo Spain	30	1.5k 0.7×	552 0.7×	312 0.8×	151 0.8×	204 1.1×	83	2.9k
Min Wu China	34	2.7k 1.3×	540 0.6×	344 0.9×	240 1.2×	219 1.2×	121	3.9k
Tamir Alon Israel	11	1.5k 0.7×	356 0.4×	107 0.3×	160 0.8×	215 1.1×	13	2.6k
Andreas W. Kuß Germany	33	1.8k 0.9×	484 0.6×	1.0k 2.8×	275 1.4×	205 1.1×	87	3.2k
Bingbing Yuan United States	20	2.0k 1.0×	1.0k 1.2×	434 1.2×	127 0.6×	475 2.5×	32	3.3k

Countries citing papers authored by Cas Simons

Since Specialization

Citations

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

Fields of papers citing papers by Cas Simons

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Cas Simons

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Parmar, J., Melina Ellis, Samantha J. Bryen, et al.. (2024). A deep intronic variant in MME causes autosomal recessive Charcot–Marie–Tooth neuropathy through aberrant splicing. Journal of the Peripheral Nervous System. 29(2). 262–274. 1 indexed citations

Helman, Guy, Rosalina M.L. van Spaendonk, Cas Simons, et al.. (2024). Megalencephalic leukoencephalopathy with subcortical cysts: a variant update and review of the literature. Frontiers in Genetics. 15. 1352947–1352947. 6 indexed citations

Doggett, Karen, Stephen Mieruszynski, Lachlan Whitehead, et al.. (2023). ahctf1 and kras mutations combine to amplify oncogenic stress and restrict liver overgrowth in a zebrafish model of hepatocellular carcinoma. eLife. 12. 4 indexed citations

Hort, Yvonne, Patricia A. Sullivan, Lindsay Fowles, et al.. (2023). Atypical splicing variants in PKD1 explain most undiagnosed typical familial ADPKD. npj Genomic Medicine. 8(1). 16–16. 8 indexed citations

Koopman, Charlotte D., Jessica De Angelis, Arie O. Verkerk, et al.. (2021). The zebrafishgrimemutant uncovers an evolutionarily conserved role for Tmem161b in the control of cardiac rhythm. Proceedings of the National Academy of Sciences. 118(9). 14 indexed citations

Helman, Guy, Marzena Walkiewicz, Stefanie Eggers, et al.. (2021). Aberrant splicing and transcriptional activity of TPP1 result in CLN2-like disorder. European Journal of Medical Genetics. 64(8). 104259–104259. 2 indexed citations

Helman, Guy, Ayelet Zerem, Sarah Woidill, et al.. (2021). Further Delineation of the Clinical and Pathologic Features of HIKESHI-Related Hypomyelinating Leukodystrophy. Pediatric Neurology. 121. 11–19. 4 indexed citations

Robevska, Gorjana, Jocelyn van den Bergen, Emanuele Pelosi, et al.. (2018). Identification of Candidate Genes for Mayer-Rokitansky-Küster-Hauser Syndrome Using Genomic Approaches. Sexual Development. 13(1). 26–34. 29 indexed citations

Forbes, Thomas, Sara E. Howden, Kynan T. Lawlor, et al.. (2018). Patient-iPSC-Derived Kidney Organoids Show Functional Validation of a Ciliopathic Renal Phenotype and Reveal Underlying Pathogenetic Mechanisms. The American Journal of Human Genetics. 102(5). 816–831. 155 indexed citations

10.

Curiel, Julian, Guillermo Rodríguez Bey, Asako Takanohashi, et al.. (2017). TUBB4A mutations result in specific neuronal and oligodendrocytic defects that closely match clinically distinct phenotypes. Human Molecular Genetics. 26(22). 4506–4518. 53 indexed citations

11.

Tétreault, Martine, Luan T. Tran, Myriam Srour, et al.. (2017). Recessive Mutations in NDUFA2 Cause Mitochondrial Leukoencephalopathy. Annals of Neurology. 82.

12.

Angelis, Jessica De, Anne K. Lagendijk, Huijun Chen, et al.. (2017). Tmem2 Regulates Embryonic Vegf Signaling by Controlling Hyaluronic Acid Turnover. Developmental Cell. 40(4). 421–421. 12 indexed citations

13.

Mallett, Andrew J., Dylan Mordaunt, A M Walker, et al.. (2015). Rmnd1 Mutations Are Associated with Autosomal Recessive Syndromic Nephropathy. Nephrology. 20. 42–42. 1 indexed citations

14.

Koltowska, Katarzyna, Scott Paterson, Neil I. Bower, et al.. (2015). mafba is a downstream transcriptional effector of Vegfc signaling essential for embryonic lymphangiogenesis in zebrafish. Genes & Development. 29(15). 1618–1630. 49 indexed citations

15.

Miller, David K., Minal Menezes, Cas Simons, et al.. (2014). Rapid Identification of a Novel Complex I MT-ND3 m.10134C>A Mutation in a Leigh Syndrome Patient. PLoS ONE. 9(8). e104879–e104879. 9 indexed citations

16.

Prokudin, Ivan, Cas Simons, John Grigg, et al.. (2013). Exome sequencing in developmental eye disease leads to identification of causal variants in GJA8, CRYGC, PAX6 and CYP1B1. European Journal of Human Genetics. 22(7). 907–915. 52 indexed citations

17.

Thu, Yee Mon, Yan Ru Su, Jinming Yang, et al.. (2011). NF-κB inducing kinase (NIK) modulates melanoma tumorigenesis by regulating expression of pro-survival factors through the β-catenin pathway. Oncogene. 31(20). 2580–2592. 40 indexed citations

18.

Taft, Ryan J., Cas Simons, Satu Nahkuri, et al.. (2010). Nuclear-localized tiny RNAs are associated with transcription initiation and splice sites in metazoans. Nature Structural & Molecular Biology. 17(8). 1030–1034. 128 indexed citations

19.

Simons, Cas, Michael Pheasant, Igor V. Makunin, & John S. Mattick. (2005). Transposon-free regions in mammalian genomes. Genome Research. 16(2). 164–172. 97 indexed citations

20.

Tebbutt, Scott J. & Cas Simons. (2002). Gene sequences from New Zealand's extinct huia. Journal of the Royal Society of New Zealand. 32(2). 327–335. 6 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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