Katy Phelan
- Genetics top 5%
- Molecular Biology
- Cognitive Neuroscience top 5%
- Pediatrics, Perinatology and Child Health
- Cellular and Molecular Neuroscience
- Co-authors
- Heather E. McDermidKristin M. MaySara M. SarasuaLuigi BoccutoBarbara R. DuPontR. Curtis RogersJonathan D. RollinsAlka Dwivedi
- Topics
- Genomic variations and chromosomal abnormalities (19 papers)Congenital heart defects research (10 papers)Genetics and Neurodevelopmental Disorders (8 papers)
- Partner nations
- United StatesItalyCanada
In The Last Decade
Katy Phelan
31 papers receiving 984 citations
Peers
Comparison fields: 5 of 100
- Genetics 622
- Molecular Biology 562
- Cognitive Neuroscience 312
- Pediatrics, Perinatology and Child Health 85
- Cellular and Molecular Neuroscience 75
Countries citing papers authored by Katy Phelan
This map shows the geographic impact of Katy Phelan'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 Katy Phelan with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Katy Phelan more than expected).
Fields of papers citing papers by Katy Phelan
This network shows the impact of papers produced by Katy Phelan. 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 Katy Phelan. The network helps show where Katy Phelan may publish in the future.
Co-authorship network of co-authors of Katy Phelan
This figure shows the co-authorship network connecting the top 25 collaborators of Katy Phelan. A scholar is included among the top collaborators of Katy Phelan based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Katy Phelan. Katy Phelan is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 1 | |
| 2 | 0 | |
| 3 | 4 | |
| 4 | 3 | |
| 5 | 2 | |
| 6 | 14 | |
| 7 | 6 | |
| 8 | 13 | |
| 9 | 21 | |
| 10 | 6 | |
| 11 | 49 | |
| 12 | 133 | |
| 13 | 62 | |
| 14 | 12 | |
| 15 | 345 | |
| 16 | 104 | |
| 17 | 8 | |
| 18 | 2 | |
| 19 | 3 | |
| 20 | 10 |
About Katy Phelan
Katy Phelan is a scholar working on Genetics, Developmental Biology and Microbiology, having authored 32 papers that have together received 995 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (19 papers), Congenital heart defects research (10 papers) and Genetics and Neurodevelopmental Disorders (8 papers). The work is most often cited by research in Genetics (622 citations), Cognitive Neuroscience (312 citations) and Molecular Biology (562 citations). Katy Phelan has collaborated with scholars based in United States, Italy and Canada. Frequent co-authors include Heather E. McDermid, Kristin M. May, Sara M. Sarasua, Luigi Boccuto, Barbara R. DuPont, R. Curtis Rogers, Jonathan D. Rollins, Alka Dwivedi, Julia L. Sharp and Chih‐Feng Chen. Their work appears in journals such as PLoS ONE, Journal of Medical Genetics and Human 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.