Casper Shyr

4.1k total citations · 3 hit papers
21 papers, 2.7k citations indexed

About

Casper Shyr is a scholar working on Molecular Biology, Genetics and Physiology. According to data from OpenAlex, Casper Shyr has authored 21 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 8 papers in Genetics and 3 papers in Physiology. Recurrent topics in Casper Shyr's work include Genomics and Rare Diseases (5 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Ion channel regulation and function (3 papers). Casper Shyr is often cited by papers focused on Genomics and Rare Diseases (5 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Ion channel regulation and function (3 papers). Casper Shyr collaborates with scholars based in Canada, United Kingdom and United States. Casper Shyr's co-authors include Wyeth W. Wasserman, David J. Arenillas, Allen W. Zhang, Ge Tan, Chih‐Yu Chen, Albin Sandelin, François Parcy, Anthony Mathelier, Rebecca Worsley-Hunt and Boris Lenhard and has published in prestigious journals such as Nucleic Acids Research, SHILAP Revista de lepidopterología and Neuroscience.

In The Last Decade

Casper Shyr

21 papers receiving 2.6k 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.

JASPAR 2014: an extensively expanded and updated open-access database of transcription factor binding profiles

2013 801 citations Anthony Mathelier, Xiaobei Zhao et al. Nucleic Acids Research profile →
JASPAR 2016: a major expansion and update of the open-access database of transcription factor binding profiles

2015 725 citations Anthony Mathelier, Oriol Fornés et al. Nucleic Acids Research profile →
Global mapping of binding sites for Nrf2 identifies novel targets in cell survival response through ChIP-Seq profiling and network analysis

2010 632 citations Deepti Malhotra, Élodie Portales-Casamar et al. Nucleic Acids Research profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Casper Shyr Canada	14	2.1k	383	363	226	215	21	2.7k
Ty C. Voss United States	23	2.2k 1.0×	477 1.2×	249 0.7×	209 0.9×	253 1.2×	44	3.0k
Manhong Dai United States	13	1.3k 0.6×	269 0.7×	301 0.8×	240 1.1×	199 0.9×	22	2.0k
Marilyn G. Pray-Grant United States	14	2.4k 1.1×	265 0.7×	466 1.3×	276 1.2×	182 0.8×	16	3.0k
Christopher D. Brown United States	29	1.2k 0.6×	567 1.5×	237 0.7×	203 0.9×	136 0.6×	50	2.2k
Jeremy M. Simon United States	29	2.1k 1.0×	700 1.8×	452 1.2×	148 0.7×	213 1.0×	80	2.9k
Bernward Klocke Germany	11	1.5k 0.7×	387 1.0×	256 0.7×	138 0.6×	284 1.3×	14	2.1k
Sang‐Beom Seo South Korea	27	2.3k 1.1×	318 0.8×	298 0.8×	225 1.0×	171 0.8×	73	3.2k
Michael P. Kladde United States	29	2.0k 0.9×	449 1.2×	295 0.8×	189 0.8×	221 1.0×	63	2.5k
Giovanni Perini Italy	33	2.4k 1.2×	427 1.1×	479 1.3×	233 1.0×	217 1.0×	69	3.3k

Countries citing papers authored by Casper Shyr

Since Specialization

Citations

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

Fields of papers citing papers by Casper Shyr

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Casper Shyr

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

All Works

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20 of 20 papers shown

Karnebeek, Clara D. van, Allison Matthews, Britt I. Drögemöller, et al.. (2021). Secondary biogenic amine deficiencies: genetic etiology, therapeutic interventions, and clinical effects. Neurogenetics. 22(4). 251–262. 2 indexed citations

Li, Yanyan, et al.. (2021). Automated thematic analysis of health information technology (HIT) related incident reports. Knowledge Management & E-Learning An International Journal. 408–420. 1 indexed citations

Shyr, Casper, et al.. (2021). Team-based care: A clinical pharmacist and family physicians. Canadian Pharmacists Journal / Revue des Pharmaciens du Canada. 154(4). 242–247. 4 indexed citations

Ye, Xin, Nicole M. Roslin, Andrew D. Paterson, et al.. (2020). Linkage analysis identifies an isolated strabismus locus at 14q12 overlapping with FOXG1 syndrome region. Journal of Medical Genetics. 59(1). 46–55. 2 indexed citations

Horváth, Gabriella, Yulin Zhao, Maja Tarailo‐Graovac, et al.. (2018). Gain-of-function KCNJ6 Mutation in a Severe Hyperkinetic Movement Disorder Phenotype. Neuroscience. 384. 152–164. 20 indexed citations

Townsend, Katelin N., Casper Shyr, Allison Matthews, et al.. (2016). Optic atrophy, cataracts, lipodystrophy/lipoatrophy, and peripheral neuropathy caused by a de novo OPA3 mutation. Molecular Case Studies. 3(1). a001156–a001156. 10 indexed citations

Santra, Saikat, Jessie M. Cameron, Casper Shyr, et al.. (2016). Cytosolic phosphoenolpyruvate carboxykinase deficiency presenting with acute liver failure following gastroenteritis. Molecular Genetics and Metabolism. 118(1). 21–27. 22 indexed citations

Lee, Jessica J. Y., Clara van Karnebeek, Britt I. Drögemöller, et al.. (2016). Further Validation of the SIGMAR1 c.151+1G>T Mutation as Cause of Distal Hereditary Motor Neuropathy. SHILAP Revista de lepidopterología. 3. 2329048X16669912–2329048X16669912. 13 indexed citations

Janer, Alexandre, Clara DM van Karnebeek, Florin Sasarman, et al.. (2015). RMND1 deficiency associated with neonatal lactic acidosis, infantile onset renal failure, deafness, and multiorgan involvement. European Journal of Human Genetics. 23(10). 1301–1307. 23 indexed citations

10.

Tarailo‐Graovac, Maja, Graham Sinclair, Sylvia Stöckler‐Ipsiroglu, et al.. (2015). The genotypic and phenotypic spectrum of PIGA deficiency. Orphanet Journal of Rare Diseases. 10(1). 23–23. 58 indexed citations

11.

Mathelier, Anthony, Oriol Fornés, David J. Arenillas, et al.. (2015). JASPAR 2016: a major expansion and update of the open-access database of transcription factor binding profiles. Nucleic Acids Research. 44(D1). D110–D115. 725 indexed citations breakdown →

12.

Sirrs, Sandra, Clara DM van Karnebeek, Xiaoxue Peng, et al.. (2015). Defects in fatty acid amide hydrolase 2 in a male with neurologic and psychiatric symptoms. Orphanet Journal of Rare Diseases. 10(1). 38–38. 19 indexed citations

13.

Horváth, Gabriella, Michelle Demos, Casper Shyr, et al.. (2015). Secondary neurotransmitter deficiencies in epilepsy caused by voltage-gated sodium channelopathies: A potential treatment target?. Molecular Genetics and Metabolism. 117(1). 42–48. 33 indexed citations

14.

Shyr, Casper, André Kushniruk, Clara van Karnebeek, & Wyeth W. Wasserman. (2015). Dynamic software design for clinical exome and genome analyses: insights from bioinformaticians, clinical geneticists, and genetic counselors. Journal of the American Medical Informatics Association. 23(2). 257–268. 8 indexed citations

15.

Demos, Michelle, Clara DM van Karnebeek, Colin J.D. Ross, et al.. (2014). A novel recurrent mutation in ATP1A3 causes CAPOS syndrome. Orphanet Journal of Rare Diseases. 9(1). 15–15. 135 indexed citations

16.

Shyr, Casper, André Kushniruk, & Wyeth W. Wasserman. (2014). Usability study of clinical exome analysis software: Top lessons learned and recommendations. Journal of Biomedical Informatics. 51. 129–136. 11 indexed citations

17.

Shyr, Casper, Maja Tarailo‐Graovac, Michael Gottlieb, et al.. (2014). FLAGS, frequently mutated genes in public exomes. BMC Medical Genomics. 7(1). 64–64. 100 indexed citations

18.

Armstrong, Linlea, Roberta Biancheri, Casper Shyr, et al.. (2014). AIMP1 deficiency presents as a cortical neurodegenerative disease with infantile onset. Neurogenetics. 15(3). 157–159. 15 indexed citations

19.

Mathelier, Anthony, Xiaobei Zhao, Allen W. Zhang, et al.. (2013). JASPAR 2014: an extensively expanded and updated open-access database of transcription factor binding profiles. Nucleic Acids Research. 42(D1). D142–D147. 801 indexed citations breakdown →

20.

Malhotra, Deepti, Élodie Portales-Casamar, Anju Singh, et al.. (2010). Global mapping of binding sites for Nrf2 identifies novel targets in cell survival response through ChIP-Seq profiling and network analysis. Nucleic Acids Research. 38(17). 5718–5734. 632 indexed citations breakdown →

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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