Matthew Harmelink
Impact in
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- Neurogenetic and Muscular Disorders Research
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- Epilepsy research and treatment
Papers in
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- Muscle Physiology and Disorders 5
- Ion channel regulation and function 1
- Surgery 3
- Head and Neck Anomalies 1
- Co-authors
- Dominic B. Fee (1 shared paper)Priya Monrad (1 shared paper)Allison D. Ebert (2 shared papers)Emily Welby (1 shared paper)Donald E. Greydanus (1 shared paper)Michael Weisgerber (1 shared paper)Wei-Liang Chen (1 shared paper)Harry T. Whelan (1 shared paper)
- Journals
- Neuromuscular Disorders (2 papers)Molecular Therapy (1 paper)Clinics in Perinatology (1 paper)Human Molecular Genetics (1 paper)Pediatric Dermatology (1 paper)
- Partner nations
- United StatesCanada
In The Last Decade
Matthew Harmelink
11 papers receiving 96 citations
Peers
Comparison fields: 5 of 35
- Genetics 20
- Psychiatry and Mental health 25
- Neurology 20
- Cellular and Molecular Neuroscience 16
- Pediatrics, Perinatology and Child Health 16
Countries citing papers authored by Matthew Harmelink
This map shows the geographic impact of Matthew Harmelink'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 Matthew Harmelink with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Matthew Harmelink more than expected).
Fields of papers citing papers by Matthew Harmelink
This network shows the impact of papers produced by Matthew Harmelink. 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 Matthew Harmelink. The network helps show where Matthew Harmelink may publish in the future.
Co-authors
The 25 scholars most cited alongside Matthew Harmelink, 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 | 2017 | 27 | |
| 2 | 2021 | 17 | |
| 3 | 2017 | 16 | |
| 4 | 2015 | 13 | |
| 5 | 2022 | 6 | |
| 6 | 2019 | 5 | |
| 7 | 2019 | 4 | |
| 8 | 2020 | 4 | |
| 9 | 2020 | 3 | |
| 10 | 2015 | 3 | |
| 11 | 2024 | 1 | |
| 12 | 2025 | 0 |
About Matthew Harmelink
Matthew Harmelink is a scholar working on Molecular Biology, Surgery, Genetics, Genetics and Cellular and Molecular Neuroscience, having authored 12 papers that have together received 99 indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (5 papers), Neurogenetic and Muscular Disorders Research (3 papers), Neurological and metabolic disorders (2 papers), Genetic Neurodegenerative Diseases (2 papers), Facial Nerve Paralysis Treatment and Research (1 paper), Ion channel regulation and function (1 paper), Head and Neck Anomalies (1 paper) and Biomedical Ethics and Regulation (1 paper). The work is most often cited by research in Genetics (20 citations), Psychiatry and Mental health (25 citations), Neurology (20 citations), Cellular and Molecular Neuroscience (16 citations) and Pediatrics, Perinatology and Child Health (16 citations). Matthew Harmelink has collaborated with scholars based in United States and Canada. Frequent co-authors include Dominic B. Fee, Priya Monrad, Allison D. Ebert, Emily Welby, Donald E. Greydanus, Michael Weisgerber, Wei-Liang Chen, Harry T. Whelan, Jun Ho Kim and Donald Basel. Their work appears in journals such as Neuromuscular Disorders, Molecular Therapy, Clinics in Perinatology, Human Molecular Genetics and Pediatric Dermatology.
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.