Erin E. Conboy
Impact in
- Ophthalmology top 5%
- Retinal Diseases and Treatments
- Clinical Biochemistry top 10%
- Metabolism and Genetic Disorders
Papers in
- Genetics 20
- Genomics and Rare Diseases 10
- Genetics and Neurodevelopmental Disorders 7
- Genomic variations and chromosomal abnormalities 4
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- Metabolism and Genetic Disorders 5
- Co-authors
- Sarah K. Bronson (2 shared papers)Alistair J. Barber (2 shared papers)Matthew J. Gastinger (2 shared papers)Allen R. Kunselman (1 shared paper)David Edward Hartigan (1 shared paper)Vijayaraghavan Rangachari (1 shared paper)Brenda D. Moore (1 shared paper)Dana Kim Reed (1 shared paper)
- Journals
- The American Journal of Human Genetics (4 papers)Investigative Ophthalmology & Visual Science (2 papers)Ophthalmic Genetics (2 papers)American Journal of Physiology-Renal Physiology (2 papers)Clinical Genetics (2 papers)
- Partner nations
- United StatesGermanyAustralia
In The Last Decade
Erin E. Conboy
37 papers receiving 695 citations
Peers
Comparison fields: 5 of 80
- Ophthalmology 111
- Clinical Biochemistry 65
- Physiology 174
- Molecular Biology 319
- Genetics 123
Countries citing papers authored by Erin E. Conboy
This map shows the geographic impact of Erin E. Conboy'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 Erin E. Conboy with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Erin E. Conboy more than expected).
Fields of papers citing papers by Erin E. Conboy
This network shows the impact of papers produced by Erin E. Conboy. 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 Erin E. Conboy. The network helps show where Erin E. Conboy may publish in the future.
Co-authors
The 25 scholars most cited alongside Erin E. Conboy, 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 44 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2008 | 157 | |
| 2 | 2007 | 136 | |
| 3 | 2018 | 65 | |
| 4 | 2019 | 43 | |
| 5 | 2020 | 36 | |
| 6 | 2015 | 32 | |
| 7 | 2017 | 30 | |
| 8 | 2017 | 19 | |
| 9 | 2019 | 17 | |
| 10 | 2017 | 17 | |
| 11 | 2015 | 16 | |
| 12 | 2018 | 15 | |
| 13 | 2017 | 14 | |
| 14 | 2019 | 13 | |
| 15 | 2019 | 13 | |
| 16 | 2009 | 12 | |
| 17 | 2025 | 12 | |
| 18 | 2008 | 8 | |
| 19 | 2018 | 6 | |
| 20 | 2024 | 6 |
About Erin E. Conboy
Erin E. Conboy is a scholar working on Genetics, Clinical Biochemistry, Cell Biology, Molecular Biology and Physiology, having authored 44 papers that have together received 705 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (10 papers), Genetics and Neurodevelopmental Disorders (7 papers), Mitochondrial Function and Pathology (5 papers), Metabolism and Genetic Disorders (5 papers), Lysosomal Storage Disorders Research (5 papers), Genomic variations and chromosomal abnormalities (4 papers), RNA regulation and disease (3 papers) and Immunodeficiency and Autoimmune Disorders (2 papers). The work is most often cited by research in Ophthalmology (111 citations), Clinical Biochemistry (65 citations), Physiology (174 citations), Molecular Biology (319 citations) and Genetics (123 citations). Erin E. Conboy has collaborated with scholars based in United States, Germany and Australia. Frequent co-authors include Sarah K. Bronson, Alistair J. Barber, Matthew J. Gastinger, Allen R. Kunselman, David Edward Hartigan, Vijayaraghavan Rangachari, Brenda D. Moore, Dana Kim Reed, Terrone L. Rosenberry and Filippo Pinto e Vairo. Their work appears in journals such as The American Journal of Human Genetics, Investigative Ophthalmology & Visual Science, Ophthalmic Genetics, American Journal of Physiology-Renal Physiology and Clinical 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.