Meredith Gillespie
Impact in
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- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- BRCA gene mutations in cancer
- Neurogenetic and Muscular Disorders Research
- Genetics and Neurodevelopmental Disorders
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- Cancer Genomics and Diagnostics
Papers in
- Genetics 10
- Genomics and Rare Diseases 10
- Genomic variations and chromosomal abnormalities 2
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- Hereditary Neurological Disorders 2
- Genetic Neurodegenerative Diseases 2
- Co-authors
- Kym M. Boycott (12 shared papers)Taila Hartley (7 shared papers)Deborah A. Marshall (3 shared papers)Karen V. MacDonald (2 shared papers)Christine M. Armour (2 shared papers)Hugh J. McMillan (2 shared papers)François P. Bernier (2 shared papers)Sebastian Heidenreich (1 shared paper)
- Journals
- Genetics in Medicine (6 papers)Human Mutation (1 paper)Fertility and Sterility (1 paper)Journal of Child Neurology (1 paper)Clinical Therapeutics (1 paper)
- Partner nations
- CanadaUnited KingdomUnited States
In The Last Decade
Meredith Gillespie
13 papers receiving 139 citations
Peers
Comparison fields: 5 of 31
- Genetics 86
- Genetics 13
- Cancer Research 13
- Cellular and Molecular Neuroscience 16
- Health Informatics 1
Countries citing papers authored by Meredith Gillespie
This map shows the geographic impact of Meredith Gillespie'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 Meredith Gillespie with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Meredith Gillespie more than expected).
Fields of papers citing papers by Meredith Gillespie
This network shows the impact of papers produced by Meredith Gillespie. 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 Meredith Gillespie. The network helps show where Meredith Gillespie may publish in the future.
Co-authors
The 25 scholars most cited alongside Meredith Gillespie, 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 | 41 | |
| 2 | 2017 | 24 | |
| 3 | 2018 | 16 | |
| 4 | 2018 | 12 | |
| 5 | 2019 | 12 | |
| 6 | 2022 | 11 | |
| 7 | 2022 | 9 | |
| 8 | 2021 | 8 | |
| 9 | 2022 | 2 | |
| 10 | 2023 | 2 | |
| 11 | 2025 | 1 | |
| 12 | 2014 | 1 | |
| 13 | 2023 | 1 | |
| 14 | 2025 | 0 |
About Meredith Gillespie
Meredith Gillespie is a scholar working on Genetics, Cellular and Molecular Neuroscience, Neurology, Surgery and Pathology and Forensic Medicine, having authored 14 papers that have together received 140 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (10 papers), Neurological diseases and metabolism (2 papers), Hereditary Neurological Disorders (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Genetic Neurodegenerative Diseases (2 papers), Cancer Genomics and Diagnostics (1 paper), Congenital Diaphragmatic Hernia Studies (1 paper) and Genetic factors in colorectal cancer (1 paper). The work is most often cited by research in Genetics (86 citations), Genetics (13 citations), Cancer Research (13 citations), Cellular and Molecular Neuroscience (16 citations) and Health Informatics (1 citation). Meredith Gillespie has collaborated with scholars based in Canada, United Kingdom and United States. Frequent co-authors include Kym M. Boycott, Taila Hartley, Deborah A. Marshall, Karen V. MacDonald, Christine M. Armour, Hugh J. McMillan, François P. Bernier, Sebastian Heidenreich, A. Micheil Innes and Brenda McInnes. Their work appears in journals such as Genetics in Medicine, Human Mutation, Fertility and Sterility, Journal of Child Neurology and Clinical Therapeutics.
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.