Erick Loomis
Impact in
- Genetics top 10%
- Genetics and Neurodevelopmental Disorders
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- DNA Repair Mechanisms
- RNA modifications and cancer
- Mitochondrial Function and Pathology
- Genomics and Phylogenetic Studies
- RNA and protein synthesis mechanisms
Papers in ⓘ
-
- Epigenetics and DNA Methylation 4
- RNA modifications and cancer 4
- Genomics and Chromatin Dynamics 2
- RNA Research and Splicing 1
- Genetics 6
- Genetics and Neurodevelopmental Disorders 5
- BRCA gene mutations in cancer 1
- Genomics and Rare Diseases 1
- Co-authors
- Paul J. Hagerman (5 shared papers)Frédéric Chédin (1 shared paper)Lionel A. Sanz (1 shared paper)John Eid (4 shared papers)Flora Tassone (3 shared papers)Jun Yin (3 shared papers)Randi J. Hagerman (1 shared paper)David R. Rank (2 shared papers)
- Journals
- Molecular Genetics and Genomics (1 paper)Clinical Epigenetics (1 paper)PLoS Genetics (1 paper)Genome Research (1 paper)Journal of Medical Genetics (1 paper)
- Partner nations
- United StatesUnited Kingdom
In The Last Decade
Erick Loomis
8 papers receiving 404 citations
Peers
Comparison fields: 5 of 63
- Genetics 191
- Molecular Biology 314
- Cellular and Molecular Neuroscience 72
- Cognitive Neuroscience 50
- Cancer Research 27
Countries citing papers authored by Erick Loomis
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
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-authors
The 25 scholars most cited alongside Erick Loomis, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2014 | 173 | |
| 2 | 2012 | 148 | |
| 3 | 2014 | 27 | |
| 4 | 2019 | 18 | |
| 5 | 2016 | 16 | |
| 6 | 2021 | 13 | |
| 7 | 2017 | 11 | |
| 8 | 2013 | 1 |
About Erick Loomis
Erick Loomis is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Pulmonary and Respiratory Medicine and Cognitive Neuroscience, having authored 8 papers that have together received 407 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (5 papers), Epigenetics and DNA Methylation (4 papers), RNA modifications and cancer (4 papers), Genomics and Chromatin Dynamics (2 papers), BRCA gene mutations in cancer (1 paper), Genomics and Rare Diseases (1 paper), RNA Research and Splicing (1 paper) and Prostate Cancer Treatment and Research (1 paper). The work is most often cited by research in Genetics (191 citations), Molecular Biology (314 citations), Cellular and Molecular Neuroscience (72 citations), Cognitive Neuroscience (50 citations) and Cancer Research (27 citations). Erick Loomis has collaborated with scholars based in United States and United Kingdom. Frequent co-authors include Paul J. Hagerman, Frédéric Chédin, Lionel A. Sanz, John Eid, Flora Tassone, Jun Yin, Randi J. Hagerman, David R. Rank, Paul Peluso and Luke Hickey. Their work appears in journals such as Molecular Genetics and Genomics, Clinical Epigenetics, PLoS Genetics, Genome Research and Journal of Medical Genetics.
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.