Andrew Perez

686 total citations
8 papers, 394 citations indexed

About

Andrew Perez is a scholar working on Molecular Biology, Genetics and Infectious Diseases. According to data from OpenAlex, Andrew Perez has authored 8 papers receiving a total of 394 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 1 paper in Genetics and 0 papers in Infectious Diseases. Recurrent topics in Andrew Perez's work include Genomics and Chromatin Dynamics (6 papers), RNA modifications and cancer (4 papers) and RNA Research and Splicing (4 papers). Andrew Perez is often cited by papers focused on Genomics and Chromatin Dynamics (6 papers), RNA modifications and cancer (4 papers) and RNA Research and Splicing (4 papers). Andrew Perez collaborates with scholars based in United States, Australia and China. Andrew Perez's co-authors include Peggy Farnham, Suhn K. Rhie, Charles M. Nicolet, Shannon Schreiner, Chonghua Ren, David J. Segal, Julian Halmai, Joel P. Mackay, Henriette O’Geen and Yu Guo and has published in prestigious journals such as Cell, Nucleic Acids Research and Nature Communications.

In The Last Decade

Andrew Perez

8 papers receiving 388 citations

Peers

Andrew Perez

MB

GENET

CR

PRM

PS

Eusra Mohammad Germany

William F. Richter United States

Anton Willer Denmark

Eleanor Glancy Ireland

Shinsuke Muto Japan

Krishna Kanchi United States

Sabrina Adam Germany

Hsuan-Cheng Kuo United States

Tamara Beck Australia

Amandine Bemmo Canada

Eusra Mohammad Germany

Andrew Perez

271 ×0.8

MB

74 ×0.8

GENET

62 ×1.3

CR

12 ×0.3

PRM

25 ×1.0

PS

Citations per year, relative to Andrew Perez Andrew Perez (= 1×) peers Eusra Mohammad

Countries citing papers authored by Andrew Perez

Since Specialization

Citations

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

Fields of papers citing papers by Andrew Perez

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andrew Perez

This figure shows the co-authorship network connecting the top 25 collaborators of Andrew Perez. A scholar is included among the top collaborators of Andrew Perez 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 Andrew Perez. Andrew Perez 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:

8 of 8 papers shown

1.

Guo, Jimmy K., Mario R. Blanco, Isabel N. Goronzy, et al.. (2025). SPIDR enables multiplexed mapping of RNA-protein interactions and uncovers a mechanism for selective translational suppression upon cell stress. Cell. 188(19). 5384–5402.e25. 3 indexed citations

2.

Perez, Andrew, et al.. (2024). ChIP-DIP maps binding of hundreds of proteins to DNA simultaneously and identifies diverse gene regulatory elements. Nature Genetics. 56(12). 2827–2841. 7 indexed citations

3.

Perez, Andrew, et al.. (2020). Characterization of the ZFX family of transcription factors that bind downstream of the start site of CpG island promoters. Nucleic Acids Research. 48(11). 5986–6000. 26 indexed citations

4.

Rhie, Suhn K., et al.. (2019). A high-resolution 3D epigenomic map reveals insights into the creation of the prostate cancer transcriptome. Nature Communications. 10(1). 4154–4154. 76 indexed citations

5.

Guo, Yu, Andrew Perez, Dennis J. Hazelett, et al.. (2018). CRISPR-mediated deletion of prostate cancer risk-associated CTCF loop anchors identifies repressive chromatin loops. Genome biology. 19(1). 160–160. 50 indexed citations

6.

Rhie, Suhn K., Lijun Yao, Zhifei Luo, et al.. (2018). ZFX acts as a transcriptional activator in multiple types of human tumors by binding downstream from transcription start sites at the majority of CpG island promoters. Genome Research. 28(3). 310–320. 46 indexed citations

7.

O’Geen, Henriette, Chonghua Ren, Charles M. Nicolet, et al.. (2017). dCas9-based epigenome editing suggests acquisition of histone methylation is not sufficient for target gene repression. Nucleic Acids Research. 45(17). 9901–9916. 161 indexed citations

8.

Chen, Xi, Ruizhe Wang, Xu Liu, et al.. (2017). A Chemical-Genetic Approach Reveals the Distinct Roles of GSK3α and GSK3β in Regulating Embryonic Stem Cell Fate. Developmental Cell. 43(5). 563–576.e4. 25 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.

Explore authors with similar magnitude of impact