Perry Evans

2.9k total citations
26 papers, 1.1k citations indexed

About

Perry Evans is a scholar working on Molecular Biology, Genetics and Physiology. According to data from OpenAlex, Perry Evans has authored 26 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 9 papers in Genetics and 5 papers in Physiology. Recurrent topics in Perry Evans's work include Genomics and Rare Diseases (5 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genomics and Phylogenetic Studies (4 papers). Perry Evans is often cited by papers focused on Genomics and Rare Diseases (5 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genomics and Phylogenetic Studies (4 papers). Perry Evans collaborates with scholars based in United States, United Arab Emirates and Switzerland. Perry Evans's co-authors include Michael Krauthammer, Harry Ischiropoulos, Lyle Ungar, Ross C. Hardison, Belinda Giardine, Gerd A. Blobel, Aydın Tözeren, Cheryl A. Keller, William Dampier and Aaron J. Stonestrom and has published in prestigious journals such as Nature Communications, Nature Genetics and Genes & Development.

In The Last Decade

Perry Evans

26 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Perry Evans United States 14 793 219 167 136 116 26 1.1k
Martin Augustin Germany 21 946 1.2× 171 0.8× 58 0.3× 191 1.4× 105 0.9× 48 1.4k
Jacky Chi Ki Ngo Hong Kong 19 893 1.1× 81 0.4× 63 0.4× 189 1.4× 59 0.5× 45 1.2k
Weisheng Xu United States 6 1.8k 2.3× 466 2.1× 77 0.5× 98 0.7× 122 1.1× 6 2.0k
Suzanne Graham United States 12 965 1.2× 341 1.6× 97 0.6× 46 0.3× 64 0.6× 20 1.5k
Jiefei Tong Canada 28 1.8k 2.3× 352 1.6× 104 0.6× 157 1.2× 62 0.5× 43 2.3k
Malik M. Keshwani United States 21 1.2k 1.5× 142 0.6× 107 0.6× 39 0.3× 84 0.7× 32 1.6k
Yonghua Yang United States 20 1.5k 1.9× 346 1.6× 213 1.3× 119 0.9× 80 0.7× 30 2.0k
Julianne L. Holleran United States 18 1.0k 1.3× 356 1.6× 51 0.3× 207 1.5× 60 0.5× 55 1.4k
Ron de Jong United States 19 1.1k 1.3× 289 1.3× 54 0.3× 224 1.6× 115 1.0× 33 1.6k
Larry R. Solomon United States 16 1.0k 1.3× 455 2.1× 287 1.7× 106 0.8× 91 0.8× 35 1.6k

Countries citing papers authored by Perry Evans

Since Specialization
Citations

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

Fields of papers citing papers by Perry Evans

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Perry Evans

This figure shows the co-authorship network connecting the top 25 collaborators of Perry Evans. A scholar is included among the top collaborators of Perry Evans 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 Perry Evans. Perry Evans 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.
Randall, Michael P., Zalman Vaksman, Minu Samanta, et al.. (2023). BARD1germline variants induce haploinsufficiency and DNA repair defects in neuroblastoma. JNCI Journal of the National Cancer Institute. 116(1). 138–148. 10 indexed citations
2.
Merlo, Lauren M.F., Kathleen Sprouffske, Aleah F. Caulin, et al.. (2020). Application of simultaneous selective pressures slows adaptation. Evolutionary Applications. 13(7). 1615–1625. 3 indexed citations
3.
Wu, Chao, Batsal Devkota, Perry Evans, et al.. (2019). Rapid and accurate interpretation of clinical exomes using Phenoxome: a computational phenotype-driven approach. European Journal of Human Genetics. 27(4). 612–620. 10 indexed citations
4.
Evans, Perry, Chao Wu, Amanda Lindy, et al.. (2019). Genetic variant pathogenicity prediction trained using disease-specific clinical sequencing data sets. Genome Research. 29(7). 1144–1151. 16 indexed citations
5.
Gonzalez, Michael, et al.. (2018). The Development and Validation of Clinical Exome-Based Panels Using ExomeSlicer. Journal of Molecular Diagnostics. 20(5). 643–652. 18 indexed citations
6.
Fazelinia, Hossein, Neal S. Gould, Anastasia K. Yocum, et al.. (2018). Induction of the Immunoproteasome Subunit Lmp7 Links Proteostasis and Immunity in α-Synuclein Aggregation Disorders. EBioMedicine. 31. 307–319. 34 indexed citations
7.
Τενοπούλου, Μαργαρίτα, Paschalis‐Thomas Doulias, Kent Nakamoto, et al.. (2018). Oral nitrite restores age-dependent phenotypes in eNOS-null mice. JCI Insight. 3(16). 11 indexed citations
8.
Chou, Stella T., Perry Evans, Sunitha Vege, et al.. (2018). RH genotype matching for transfusion support in sickle cell disease. Blood. 132(11). 1198–1207. 88 indexed citations
9.
Evans, Perry, Nicole Hamagami, Cheryl A. Keller, et al.. (2018). Exploiting genetic variation to uncover rules of transcription factor binding and chromatin accessibility. Nature Communications. 9(1). 782–782. 30 indexed citations
10.
Hsu, Sarah, Thomas G. Gilgenast, Caroline Bartman, et al.. (2017). The BET Protein BRD2 Cooperates with CTCF to Enforce Transcriptional and Architectural Boundaries. Molecular Cell. 66(1). 102–116.e7. 94 indexed citations
11.
Hsiung, Chris C.‐S., Caroline Bartman, Peng Huang, et al.. (2016). A hyperactive transcriptional state marks genome reactivation at the mitosis–G1 transition. Genes & Development. 30(12). 1423–1439. 77 indexed citations
12.
Gould, Neal S., Perry Evans, Pablo Martínez-Acedo, et al.. (2015). Site-Specific Proteomic Mapping Identifies Selectively Modified Regulatory Cysteine Residues in Functionally Distinct Protein Networks. Chemistry & Biology. 22(7). 965–975. 108 indexed citations
13.
Krauthammer, Michael, Yong Kong, Antonella Bacchiocchi, et al.. (2015). Exome sequencing identifies recurrent mutations in NF1 and RASopathy genes in sun-exposed melanomas. Nature Genetics. 47(9). 996–1002. 274 indexed citations
14.
Raju, Karthik, Paschalis‐Thomas Doulias, Perry Evans, et al.. (2015). Regulation of brain glutamate metabolism by nitric oxide and S-nitrosylation. Science Signaling. 8(384). ra68–ra68. 105 indexed citations
15.
Evans, Perry, Yong Kong, & Michael Krauthammer. (2014). Computational Analysis in Cancer Exome Sequencing. Methods in molecular biology. 1176. 219–227. 1 indexed citations
16.
Mukherjee, Rithun, Perry Evans, Larry N. Singh, & Sridhar Hannenhalli. (2013). Correlated Evolution of Positions within Mammalian cis Elements. PLoS ONE. 8(2). e55521–e55521. 2 indexed citations
17.
Evans, Perry, Ahmet Saçan, Lyle Ungar, & Aydın Tözeren. (2010). Sequence Alignment Reveals Possible MAPK Docking Motifs on HIV Proteins. PLoS ONE. 5(1). e8942–e8942. 7 indexed citations
18.
Dampier, William, Perry Evans, Lyle Ungar, & Aydın Tözeren. (2009). Host sequence motifs shared by HIV predict response to antiretroviral therapy. BMC Medical Genomics. 2(1). 47–47. 11 indexed citations
19.
Evans, Perry, William Dampier, Lyle Ungar, & Aydın Tözeren. (2009). Prediction of HIV-1 virus-host protein interactions using virus and host sequence motifs. BMC Medical Genomics. 2(1). 27–27. 71 indexed citations
20.
Evans, Perry, et al.. (2008). Protein-Protein Interaction Network Alignment by Quantitative Simulation. 325–328. 1 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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