Heidi Cope
Impact in
Papers in
- Genetics 34
- Genomics and Rare Diseases 19
- Genetics and Neurodevelopmental Disorders 10
- Genomic variations and chromosomal abnormalities 5
-
- Muscle Physiology and Disorders 7
- RNA Research and Splicing 7
- Co-authors
- Allison E. Ashley‐Koch (10 shared papers)Simon G. Gregory (8 shared papers)Michael L. Cuccaro (2 shared papers)Khanh-Nhat Tran-Viet (2 shared papers)Karen L. Soldano (6 shared papers)Ranga Rama Krishnan (2 shared papers)Jeffery M. Vance (2 shared papers)Hallie C. Wright (2 shared papers)
- Journals
- The American Journal of Human Genetics (22 papers)Genetics in Medicine (16 papers)Brain (3 papers)Clinical Genetics (2 papers)Frontiers in Genetics (2 papers)
- Partner nations
- United StatesFranceGermany
In The Last Decade
Heidi Cope
91 papers receiving 1.9k citations
Peers
Comparison fields: 5 of 111
- Genetics 702
- Aging 36
- Molecular Biology 863
- Cellular and Molecular Neuroscience 207
- Cell Biology 172
Countries citing papers authored by Heidi Cope
This map shows the geographic impact of Heidi Cope'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 Heidi Cope with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Heidi Cope more than expected).
Fields of papers citing papers by Heidi Cope
This network shows the impact of papers produced by Heidi Cope. 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 Heidi Cope. The network helps show where Heidi Cope may publish in the future.
Co-authors
The 25 scholars most cited alongside Heidi Cope, 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 97 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2018 | 106 | |
| 2 | 2006 | 89 | |
| 3 | 2018 | 84 | |
| 4 | 2018 | 80 | |
| 5 | 2015 | 77 | |
| 6 | 2019 | 76 | |
| 7 | 2018 | 74 | |
| 8 | 2018 | 70 | |
| 9 | 2018 | 56 | |
| 10 | 2019 | 53 | |
| 11 | 2020 | 50 | |
| 12 | 2013 | 44 | |
| 13 | 2019 | 42 | |
| 14 | 2020 | 42 | |
| 15 | 2019 | 40 | |
| 16 | 2013 | 37 | |
| 17 | 2021 | 34 | |
| 18 | 2020 | 32 | |
| 19 | 2019 | 31 | |
| 20 | 2021 | 29 |
About Heidi Cope
Heidi Cope is a scholar working on Genetics, Molecular Biology, Cell Biology, Physiology and Cellular and Molecular Neuroscience, having authored 97 papers that have together received 2.0k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (19 papers), Genetics and Neurodevelopmental Disorders (10 papers), Lysosomal Storage Disorders Research (10 papers), Muscle Physiology and Disorders (7 papers), RNA Research and Splicing (7 papers), Cellular transport and secretion (7 papers), Spinal Dysraphism and Malformations (6 papers) and Genomic variations and chromosomal abnormalities (5 papers). The work is most often cited by research in Genetics (702 citations), Aging (36 citations), Molecular Biology (863 citations), Cellular and Molecular Neuroscience (207 citations) and Cell Biology (172 citations). Heidi Cope has collaborated with scholars based in United States, France and Germany. Frequent co-authors include Allison E. Ashley‐Koch, Simon G. Gregory, Michael L. Cuccaro, Khanh-Nhat Tran-Viet, Karen L. Soldano, Ranga Rama Krishnan, Jeffery M. Vance, Hallie C. Wright, Stephan L. Zuchner and Melanie E. Garrett. Their work appears in journals such as The American Journal of Human Genetics, Genetics in Medicine, Brain, Clinical Genetics and Frontiers in 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.