Erin P. Carmany
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- BRCA gene mutations in cancer 7
- Genomics and Rare Diseases 2
- Genomic variations and chromosomal abnormalities 2
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- Prenatal Screening and Diagnostics 3
- Ethics and Legal Issues in Pediatric Healthcare 2
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- Racial and Ethnic Identity Research 2
- Family Support in Illness 2
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- LGBTQ Health, Identity, and Policy 2
- Co-authors
- Angela TrepanierErawati V. BawleJaime L. NatoliAlbert E. ChudleyGail E. HermanDavid W. StocktonDavid A. StevensonRobin D. Clark
- Partner nations
- United StatesCanadaUnited Kingdom
In The Last Decade
Erin P. Carmany
16 papers receiving 178 citations
Peers
Comparison fields: 5 of 54
- Genetics 126
- Medical Terminology 1
- Pediatrics, Perinatology and Child Health 45
- Oral Surgery 15
- Dermatology 10
Countries citing papers authored by Erin P. Carmany
This map shows the geographic impact of Erin P. Carmany'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 P. Carmany with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Erin P. Carmany more than expected).
Fields of papers citing papers by Erin P. Carmany
This network shows the impact of papers produced by Erin P. Carmany. 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 P. Carmany. The network helps show where Erin P. Carmany may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Erin P. Carmany, 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 | 2025 | 1 | |
| 2 | 2024 | 0 | |
| 3 | 2023 | 1 | |
| 4 | 2023 | 3 | |
| 5 | 2022 | 10 | |
| 6 | 2021 | 4 | |
| 7 | 2021 | 3 | |
| 8 | 2020 | 3 | |
| 9 | 2020 | 19 | |
| 10 | 2018 | 34 | |
| 11 | 2017 | 11 | |
| 12 | 2015 | 22 | |
| 13 | 2012 | 31 | |
| 14 | 2012 | 1 | |
| 15 | 2011 | 42 | |
| 16 | 2011 | 17 | |
| 17 | 2010 | 1 |
About Erin P. Carmany
Erin P. Carmany is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Social Psychology, having authored 17 papers that have together received 203 indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (7 papers), Prenatal Screening and Diagnostics (3 papers), Genomics and Rare Diseases (2 papers), Racial and Ethnic Identity Research (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Family Support in Illness (2 papers), LGBTQ Health, Identity, and Policy (2 papers) and Ethics and Legal Issues in Pediatric Healthcare (2 papers). The work is most often cited by research in Genetics (126 citations), Medical Terminology (1 citation) and Pediatrics, Perinatology and Child Health (45 citations). Erin P. Carmany has collaborated with scholars based in United States, Canada and United Kingdom. Frequent co-authors include Angela Trepanier, Erawati V. Bawle, Jaime L. Natoli, Albert E. Chudley, Gail E. Herman, David W. Stockton, David A. Stevenson, Robin D. Clark, Joan Atkin and Bryan D. Hall. Their work appears in journals such as Cancer Research, BMC Cancer and Pediatric Pulmonology.
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.