Erica E. Davis
Impact in
- Genetics top 0.2%
- Genetic and Kidney Cyst Diseases
- Genetic Syndromes and Imprinting
- Molecular Biology top 1%
- Renal and related cancers
- Hedgehog Signaling Pathway Studies
- Protist diversity and phylogeny
- Epigenetics and DNA Methylation
Papers in
- Genetics 92
- Genetic and Kidney Cyst Diseases 52
- Genetic Syndromes and Imprinting 24
- Genetics and Neurodevelopmental Disorders 14
- Genomics and Rare Diseases 12
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- Protist diversity and phylogeny 18
- Renal and related cancers 17
- Hedgehog Signaling Pathway Studies 15
- Co-authors
- Nicholas Katsanis (44 shared papers)Jantje M. Gerdes (1 shared paper)Adrian Gherman (1 shared paper)Michel Georges (5 shared papers)Noelle Cockett (4 shared papers)Carole Charlier (5 shared papers)Martina K. Brueckner (1 shared paper)Eyal Banin (3 shared papers)
- Journals
- The American Journal of Human Genetics (29 papers)Nature Genetics (10 papers)Nature Communications (7 papers)Genetics in Medicine (5 papers)Human Mutation (4 papers)
- Partner nations
- United StatesFranceUnited Kingdom
In The Last Decade
Erica E. Davis
133 papers receiving 8.4k citations
Erica E. Davis's Hit Papers
Peers
Comparison fields: 5 of 134
- Genetics 5.5k
- Molecular Biology 5.6k
- Cell Biology 1.2k
- Pediatrics, Perinatology and Child Health 846
- Aging 60
Countries citing papers authored by Erica E. Davis
This map shows the geographic impact of Erica E. Davis'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 Erica E. Davis with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Erica E. Davis more than expected).
Fields of papers citing papers by Erica E. Davis
This network shows the impact of papers produced by Erica E. Davis. 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 Erica E. Davis. The network helps show where Erica E. Davis may publish in the future.
Co-authors
The 25 scholars most cited alongside Erica E. Davis, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 135 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | The Vertebrate Primary Cilium in Development, Homeostasis, and Disease Hit paper breakdown → | 2009 | 601 |
| 2 | 2008 | 339 | |
| 3 | 2011 | 290 | |
| 4 | 2010 | 288 | |
| 5 | 2005 | 267 | |
| 6 | 2006 | 254 | |
| 7 | 2010 | 239 | |
| 8 | 2009 | 236 | |
| 9 | 2006 | 225 | |
| 10 | 2008 | 204 | |
| 11 | 2016 | 200 | |
| 12 | A cross-disorder dosage sensitivity map of the human genome Hit paper breakdown → | 2022 | 197 |
| 13 | 2011 | 193 | |
| 14 | 2006 | 190 | |
| 15 | 2013 | 180 | |
| 16 | 2011 | 160 | |
| 17 | 2013 | 130 | |
| 18 | 2017 | 122 | |
| 19 | 2012 | 121 | |
| 20 | 2006 | 119 |
About Erica E. Davis
Erica E. Davis is a scholar working on Genetics, Molecular Biology, Cell Biology, Pediatrics, Perinatology and Child Health and Genetics, having authored 135 papers that have together received 8.5k indexed citations. Recurring topics across this work include Genetic and Kidney Cyst Diseases (52 papers), Genetic Syndromes and Imprinting (24 papers), Protist diversity and phylogeny (18 papers), Renal and related cancers (17 papers), Hedgehog Signaling Pathway Studies (15 papers), Genetics and Neurodevelopmental Disorders (14 papers), Genomics and Rare Diseases (12 papers) and Microtubule and mitosis dynamics (9 papers). The work is most often cited by research in Genetics (5.5k citations), Molecular Biology (5.6k citations), Cell Biology (1.2k citations), Pediatrics, Perinatology and Child Health (846 citations) and Aging (60 citations). Erica E. Davis has collaborated with scholars based in United States, France and United Kingdom. Frequent co-authors include Nicholas Katsanis, Jantje M. Gerdes, Adrian Gherman, Michel Georges, Noelle Cockett, Carole Charlier, Martina K. Brueckner, Eyal Banin, Xavier Tordoir and Anne C. Ferguson‐Smith. Their work appears in journals such as The American Journal of Human Genetics, Nature Genetics, Nature Communications, Genetics in Medicine and Human Mutation.
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.