Erick Loomis

656 total citations
8 papers, 407 citations indexed

About

Erick Loomis is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Erick Loomis has authored 8 papers receiving a total of 407 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 6 papers in Genetics and 1 paper in Pediatrics, Perinatology and Child Health. Recurrent topics in Erick Loomis's work include Genetics and Neurodevelopmental Disorders (5 papers), RNA modifications and cancer (4 papers) and Epigenetics and DNA Methylation (4 papers). Erick Loomis is often cited by papers focused on Genetics and Neurodevelopmental Disorders (5 papers), RNA modifications and cancer (4 papers) and Epigenetics and DNA Methylation (4 papers). Erick Loomis collaborates with scholars based in United States and United Kingdom. Erick Loomis's co-authors include Paul J. Hagerman, Frédéric Chédin, Lionel A. Sanz, John Eid, Flora Tassone, Jun Yin, Luke Hickey, Paul Peluso, David R. Rank and Randi J. Hagerman and has published in prestigious journals such as Biophysical Journal, Genome Research and PLoS Genetics.

In The Last Decade

Erick Loomis

8 papers receiving 404 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Erick Loomis United States 7 314 191 72 50 27 8 407
Huiping Tan China 14 301 1.0× 120 0.6× 93 1.3× 35 0.7× 15 0.6× 19 431
Seth M. Kelly United States 11 425 1.4× 92 0.5× 34 0.5× 39 0.8× 18 0.7× 14 475
Meghan A. Rego United States 8 271 0.9× 87 0.5× 54 0.8× 19 0.4× 17 0.6× 12 356
Arikuni Uchimura Japan 8 163 0.5× 101 0.5× 38 0.5× 46 0.9× 25 0.9× 12 294
James H. Notwell United States 8 277 0.9× 76 0.4× 34 0.5× 31 0.6× 79 2.9× 8 372
Kerry J. Woodford United States 7 512 1.6× 164 0.9× 83 1.2× 17 0.3× 24 0.9× 8 547
Heather R. Glatt-Deeley United States 7 319 1.0× 244 1.3× 18 0.3× 38 0.8× 9 0.3× 10 433
Nima Mousavi United States 5 216 0.7× 181 0.9× 111 1.5× 18 0.4× 22 0.8× 9 312
Kirsten Cremer Germany 10 326 1.0× 144 0.8× 26 0.4× 17 0.3× 11 0.4× 14 436
Catherine B. Carr United Kingdom 5 356 1.1× 131 0.7× 53 0.7× 14 0.3× 21 0.8× 6 421

Countries citing papers authored by Erick Loomis

Since Specialization
Citations

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

Fields of papers citing papers by Erick Loomis

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Erick Loomis

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

All Works

8 of 8 papers shown
1.
Gallon, John, Erick Loomis, Edward Curry, et al.. (2021). Chromatin accessibility changes at intergenic regions are associated with ovarian cancer drug resistance. Clinical Epigenetics. 13(1). 122–122. 13 indexed citations
2.
Dunaway, Keith W., Erick Loomis, Stephen Riffle, et al.. (2019). Genetic counseling, 2030: An on‐demand service tailored to the needs of a price conscious, genetically literate, and busy world. Journal of Genetic Counseling. 28(2). 456–465. 18 indexed citations
4.
Pham, Thang, Jun Yin, John Eid, et al.. (2016). Single-locus enrichment without amplification for sequencing and direct detection of epigenetic modifications. Molecular Genetics and Genomics. 291(3). 1491–1504. 16 indexed citations
5.
Loomis, Erick, Lionel A. Sanz, Frédéric Chédin, & Paul J. Hagerman. (2014). Transcription-Associated R-Loop Formation across the Human FMR1 CGG-Repeat Region. PLoS Genetics. 10(4). e1004294–e1004294. 173 indexed citations
6.
Pretto, Dalyir, John Eid, Carolyn M. Yrigollen, et al.. (2014). Differential increases of specific FMR1 mRNA isoforms in premutation carriers. Journal of Medical Genetics. 52(1). 42–52. 27 indexed citations
7.
Hagerman, Paul J., John Eid, Paul Peluso, et al.. (2013). Sequencing the Unsequenceable: Expanded CGG Repeats in the Human FMR1 Gene. Biophysical Journal. 104(2). 377a–377a. 1 indexed citations
8.
Loomis, Erick, John Eid, Paul Peluso, et al.. (2012). Sequencing the unsequenceable: Expanded CGG-repeat alleles of the fragile X gene. Genome Research. 23(1). 121–128. 148 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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