Heidi Cope
Impact in
- Genetics top 10%
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Cognitive Neuroscience top 10%
- Autism Spectrum Disorder Research
Papers in
- Genetics 13
- Genomics and Rare Diseases 6
- Genetics and Neurodevelopmental Disorders 5
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- Spinal Dysraphism and Malformations 6
- Co-authors
- Allison E. Ashley‐Koch (10 shared papers)Simon G. Gregory (8 shared papers)Michael L. Cuccaro (2 shared papers)Vandana Shashi (7 shared papers)Karen Soldano (6 shared papers)Ruth K. Abramson (1 shared paper)Yujun Shao (1 shared paper)Chantelle M. Wolpert (1 shared paper)
- Journals
- Genetics in Medicine (2 papers)Molecular Genetics and Metabolism (2 papers)Clinical Genetics (2 papers)The Journal of Pediatrics (1 paper)Annals of Human Genetics (1 paper)
- Partner nations
- United StatesGermanyPoland
In The Last Decade
Heidi Cope
33 papers receiving 607 citations
Peers
Comparison fields: 5 of 74
- Genetics 291
- Cognitive Neuroscience 141
- Cellular and Molecular Neuroscience 86
- Public Health, Environmental and Occupational Health 134
- Pediatrics, Perinatology and Child Health 88
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 37 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2002 | 136 | |
| 2 | 2018 | 62 | |
| 3 | 2018 | 49 | |
| 4 | 2013 | 37 | |
| 5 | 2013 | 31 | |
| 6 | 2014 | 23 | |
| 7 | 2018 | 23 | |
| 8 | 2013 | 23 | |
| 9 | 2018 | 22 | |
| 10 | 2015 | 20 | |
| 11 | 2018 | 19 | |
| 12 | 2006 | 18 | |
| 13 | 2020 | 17 | |
| 14 | 2018 | 15 | |
| 15 | 2019 | 15 | |
| 16 | 2017 | 13 | |
| 17 | 2021 | 13 | |
| 18 | 2015 | 10 | |
| 19 | 2022 | 10 | |
| 20 | 2019 | 10 |
About Heidi Cope
Heidi Cope is a scholar working on Genetics, Public Health, Environmental and Occupational Health, Physiology, Molecular Biology and Pediatrics, Perinatology and Child Health, having authored 37 papers that have together received 615 indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (7 papers), Spinal Dysraphism and Malformations (6 papers), Genomics and Rare Diseases (6 papers), Autism Spectrum Disorder Research (5 papers), Genetics and Neurodevelopmental Disorders (5 papers), Family and Disability Support Research (4 papers), Glycogen Storage Diseases and Myoclonus (4 papers) and Hereditary Neurological Disorders (3 papers). The work is most often cited by research in Genetics (291 citations), Cognitive Neuroscience (141 citations), Cellular and Molecular Neuroscience (86 citations), Public Health, Environmental and Occupational Health (134 citations) and Pediatrics, Perinatology and Child Health (88 citations). Heidi Cope has collaborated with scholars based in United States, Germany and Poland. Frequent co-authors include Allison E. Ashley‐Koch, Simon G. Gregory, Michael L. Cuccaro, Vandana Shashi, Karen Soldano, Ruth K. Abramson, Yujun Shao, Chantelle M. Wolpert, Kimberly L. Raiford and John R. Gilbert. Their work appears in journals such as Genetics in Medicine, Molecular Genetics and Metabolism, Clinical Genetics, The Journal of Pediatrics and Annals of 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.