Emily Glanton
Impact in
-
- Genomics and Rare Diseases
- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
Papers in
- Genetics 6
- Genomics and Rare Diseases 5
- BRCA gene mutations in cancer 5
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- Ethics in Clinical Research 3
- Co-authors
- Kimberly LeBlanc (3 shared papers)Rebecca Signer (2 shared papers)Elly Brokamp (2 shared papers)Kelly Schoch (2 shared papers)Christina G.S. Palmer (2 shared papers)Ellen F. Macnamara (2 shared papers)Elizabeth L. Fieg (1 shared paper)Allyn McConkie‐Rosell (1 shared paper)
- Journals
- Orphanet Journal of Rare Diseases (1 paper)Journal of Genetic Counseling (7 papers)Molecular Genetics & Genomic Medicine (1 paper)
- Partner nations
- United States
In The Last Decade
Emily Glanton
8 papers receiving 55 citations
Peers
Comparison fields: 5 of 25
- Genetics 34
- Anatomy 1
- Family Practice 1
- Developmental Biology 1
- Cancer Research 4
Countries citing papers authored by Emily Glanton
This map shows the geographic impact of Emily Glanton'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 Emily Glanton with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Emily Glanton more than expected).
Fields of papers citing papers by Emily Glanton
This network shows the impact of papers produced by Emily Glanton. 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 Emily Glanton. The network helps show where Emily Glanton may publish in the future.
Co-authors
The 25 scholars most cited alongside Emily Glanton, 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 | 2019 | 20 | |
| 2 | 2020 | 13 | |
| 3 | 2020 | 8 | |
| 4 | 2021 | 4 | |
| 5 | 2020 | 4 | |
| 6 | 2024 | 4 | |
| 7 | 2021 | 3 | |
| 8 | 2024 | 1 | |
| 9 | 2023 | 0 |
About Emily Glanton
Emily Glanton is a scholar working on Genetics, Public Health, Environmental and Occupational Health, Molecular Biology, Cognitive Neuroscience and Social Psychology, having authored 9 papers that have together received 57 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (5 papers), BRCA gene mutations in cancer (5 papers), Ethics in Clinical Research (3 papers), Autism Spectrum Disorder Research (2 papers), Health Policy Implementation Science (1 paper), Childhood Cancer Survivors' Quality of Life (1 paper), Counseling Practices and Supervision (1 paper) and CRISPR and Genetic Engineering (1 paper). The work is most often cited by research in Genetics (34 citations), Anatomy (1 citation), Family Practice (1 citation), Developmental Biology (1 citation) and Cancer Research (4 citations). Emily Glanton has collaborated with scholars based in United States. Frequent co-authors include Kimberly LeBlanc, Rebecca Signer, Elly Brokamp, Kelly Schoch, Christina G.S. Palmer, Ellen F. Macnamara, Elizabeth L. Fieg, Allyn McConkie‐Rosell, Christina Yarrington and Sharyn A. Lincoln. Their work appears in journals such as Orphanet Journal of Rare Diseases, Journal of Genetic Counseling and Molecular Genetics & Genomic Medicine.
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.