Jonathan Shortt

3.0k total citations
14 papers, 200 citations indexed

About

Jonathan Shortt is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Jonathan Shortt has authored 14 papers receiving a total of 200 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Genetics, 3 papers in Molecular Biology and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Jonathan Shortt's work include BRCA gene mutations in cancer (2 papers), Immune Cell Function and Interaction (2 papers) and Genomics and Phylogenetic Studies (2 papers). Jonathan Shortt is often cited by papers focused on BRCA gene mutations in cancer (2 papers), Immune Cell Function and Interaction (2 papers) and Genomics and Phylogenetic Studies (2 papers). Jonathan Shortt collaborates with scholars based in United States, China and Australia. Jonathan Shortt's co-authors include Robert P. Ruggiero, Todd A. Castoe, Drew R. Schield, Daren C. Card, Blair W. Perry, Jacobo Reyes‐Velasco, Michael W. Vandewege, Andrew B. Corbin, Giulia Irene Maria Pasquesi and Richard H. Adams and has published in prestigious journals such as Nature Medicine, Nature Communications and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Jonathan Shortt

14 papers receiving 194 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Jonathan Shortt United States	8	92	65	49	34	31	14	200
Reuben M. Buckley United States	10	174 1.9×	128 2.0×	46 0.9×	25 0.7×	20 0.6×	26	308
Christopher Moran Australia	10	84 0.9×	97 1.5×	22 0.4×	14 0.4×	10 0.3×	15	247
Michael Dacre United States	6	176 1.9×	41 0.6×	27 0.6×	16 0.5×	15 0.5×	7	276
Walid H. Gharib Switzerland	9	188 2.0×	93 1.4×	31 0.6×	44 1.3×	10 0.3×	11	299
José Horacio Grau Germany	10	128 1.4×	48 0.7×	29 0.6×	8 0.2×	42 1.4×	27	254
Chase Miller United States	9	164 1.8×	84 1.3×	26 0.5×	76 2.2×	6 0.2×	15	321
Janice Chan Australia	8	121 1.3×	109 1.7×	29 0.6×	65 1.9×	16 0.5×	10	342
Kristina Giorda United States	3	216 2.3×	72 1.1×	74 1.5×	17 0.5×	7 0.2×	5	324
Daniel Marcelo Lombardo Argentina	11	112 1.2×	65 1.0×	13 0.3×	34 1.0×	20 0.6×	53	392
Shrutii Sarda United States	6	172 1.9×	54 0.8×	28 0.6×	11 0.3×	16 0.5×	13	261

Countries citing papers authored by Jonathan Shortt

Since Specialization

Citations

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

Fields of papers citing papers by Jonathan Shortt

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jonathan Shortt

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

All Works

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14 of 14 papers shown

Pozdeyev, Nikita, Manjiri Dighe, Martin Barrio, et al.. (2023). OR32-02 Thyroid Cancer Polygenic Risk Score Improves Risk Stratification Of Thyroid Nodules When Added To Ultrasound Imaging. Journal of the Endocrine Society. 7(Supplement_1). 1 indexed citations

Mefford, Joel, Ella Petter, Alec Chiu, et al.. (2023). Disease risk and healthcare utilization among ancestrally diverse groups in the Los Angeles region. Nature Medicine. 29(7). 1845–1856. 2 indexed citations

Pozdeyev, Nikita, Manjiri Dighe, Martin Barrio, et al.. (2023). Thyroid Cancer Polygenic Risk Score Improves Classification of Thyroid Nodules as Benign or Malignant. The Journal of Clinical Endocrinology & Metabolism. 109(2). 402–412. 11 indexed citations

Julian, Colleen G., Julie A. Houck, Bernardo J. Krause, et al.. (2023). Altered placental ion channel gene expression in preeclamptic high-altitude pregnancies. Physiological Genomics. 55(9). 357–367. 7 indexed citations

Johnson, Randi K., David Mayer, Jonathan Shortt, et al.. (2022). COVID-19 Surveillance in the Biobank at the Colorado Center for Personalized Medicine: Observational Study. JMIR Public Health and Surveillance. 8(6). e37327–e37327. 3 indexed citations

Harrison, Genelle F., Marte K. Viken, Jonathan Shortt, et al.. (2022). Allele imputation for the killer cell immunoglobulin-like receptor KIR3DL1/S1. PLoS Computational Biology. 18(2). e1009059–e1009059. 6 indexed citations

Stanislawski, Maggie A., Leslie A. Lange, Laura M. Raffield, et al.. (2021). Soluble CD14 Levels in the Jackson Heart Study: Associations With Cardiovascular Disease Risk and Genetic Variants. Arteriosclerosis Thrombosis and Vascular Biology. 41(6). e369–e378. 7 indexed citations

Shortt, Jonathan, Laura E. Timm, Nicole R. Hales, et al.. (2021). Population genomic analyses of schistosome parasites highlight critical challenges facing endgame elimination efforts. Scientific Reports. 11(1). 6884–6884. 10 indexed citations

Aquilante, Christina L., et al.. (2021). Applicability of ancestral genotyping in pharmacogenomic research with hormonal contraception. Clinical and Translational Science. 14(5). 1713–1718. 1 indexed citations

10.

Shortt, Jonathan, Robert P. Ruggiero, Corey Cox, Aaron Wacholder, & David D. Pollock. (2020). Finding and extending ancient simple sequence repeat-derived regions in the human genome. Mobile DNA. 11(1). 11–11. 20 indexed citations

11.

Shortt, Jonathan, Sudan Tao, Neda Nemat‐Gorgani, et al.. (2019). Conservation, Extensive Heterozygosity, and Convergence of Signaling Potential All Indicate a Critical Role for KIR3DL3 in Higher Primates. Frontiers in Immunology. 10. 24–24. 20 indexed citations

12.

Pasquesi, Giulia Irene Maria, Richard H. Adams, Daren C. Card, et al.. (2018). Squamate reptiles challenge paradigms of genomic repeat element evolution set by birds and mammals. Nature Communications. 9(1). 2774–2774. 92 indexed citations

13.

Shortt, Jonathan, Daren C. Card, Drew R. Schield, et al.. (2017). Whole Genome Amplification and Reduced-Representation Genome Sequencing of Schistosoma japonicum Miracidia. PLoS neglected tropical diseases. 11(1). e0005292–e0005292. 11 indexed citations

14.

Jiang, Ziqing, Lajos Gera, Colin T. Mant, et al.. (2016). Platform technology to generate broadly cross‐reactive antibodies to α‐helical epitopes in hemagglutinin proteins from influenza A viruses. Biopolymers. 106(2). 144–159. 9 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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