Melanie Babcock
- Co-authors
- Bernice E. MorrowLisa G. ShafferJoy SamanichMartin J. SomervilleHeather E. McDermidJudy ChernosFrançois P. BernierLionel Willatt
- Topics
- Genomic variations and chromosomal abnormalities (10 papers)Congenital heart defects research (9 papers)Chromosomal and Genetic Variations (4 papers)
- Partner nations
- United StatesUnited KingdomCanada
In The Last Decade
Melanie Babcock
16 papers receiving 491 citations
Peers
Comparison fields: 5 of 45
- Molecular Biology 333
- Genetics 315
- Plant Science 150
- Surgery 65
- Epidemiology 58
Countries citing papers authored by Melanie Babcock
This map shows the geographic impact of Melanie Babcock'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 Melanie Babcock with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Melanie Babcock more than expected).
Fields of papers citing papers by Melanie Babcock
This network shows the impact of papers produced by Melanie Babcock. 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 Melanie Babcock. The network helps show where Melanie Babcock may publish in the future.
Co-authorship network of co-authors of Melanie Babcock
This figure shows the co-authorship network connecting the top 25 collaborators of Melanie Babcock. A scholar is included among the top collaborators of Melanie Babcock 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 Melanie Babcock. Melanie Babcock is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 3 | |
| 2 | 5 | |
| 3 | 0 | |
| 4 | 25 | |
| 5 | 5 | |
| 6 | 19 | |
| 7 | 7 | |
| 8 | 8 | |
| 9 | 27 | |
| 10 | 22 | |
| 11 | 19 | |
| 12 | 5 | |
| 13 | 21 | |
| 14 | 22 | |
| 15 | 170 | |
| 16 | 43 | |
| 17 | 96 |
About Melanie Babcock
Melanie Babcock is a scholar working on Developmental Biology, Genetics and Endocrine and Autonomic Systems, having authored 17 papers that have together received 497 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (10 papers), Congenital heart defects research (9 papers) and Chromosomal and Genetic Variations (4 papers). The work is most often cited by research in Genetics (315 citations), Developmental Neuroscience (21 citations) and Molecular Biology (333 citations). Melanie Babcock has collaborated with scholars based in United States, United Kingdom and Canada. Frequent co-authors include Bernice E. Morrow, Lisa G. Shaffer, Joy Samanich, Martin J. Somerville, Heather E. McDermid, Judy Chernos, François P. Bernier, Lionel Willatt, Karen J. Harrison and Jennifer MacKenzie. Their work appears in journals such as Genome Research, The American Journal of Human Genetics and Human Molecular 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.