Linlea Armstrong
Impact in
- Neurology top 10%
- Neurofibromatosis and Schwannoma Cases
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- Neuroscience and Neuropharmacology Research
Papers in
- Genetics 13
- Genomic variations and chromosomal abnormalities 4
- Genomics and Rare Diseases 4
- Neurogenetic and Muscular Disorders Research 3
- Connective tissue disorders research 3
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- Ion channel regulation and function 3
- Co-authors
- Jan M. Friedman (8 shared papers)Tanya N. Nelson (5 shared papers)Sameer M. Zuberi (1 shared paper)P K Thomas (1 shared paper)Arn M. J. M. van den Maagdenberg (1 shared paper)Stéphane Supplisson (1 shared paper)Marina A.J. Tijssen (1 shared paper)Ian Duguid (1 shared paper)
- Journals
- European Journal of Medical Genetics (2 papers)Prenatal Diagnosis (2 papers)Clinical Genetics (2 papers)Genetics in Medicine (2 papers)American Journal of Medical Genetics Part A (12 papers)
- Partner nations
- CanadaUnited StatesUnited Kingdom
In The Last Decade
Linlea Armstrong
46 papers receiving 728 citations
Peers
Comparison fields: 5 of 74
- Neurology 129
- Cellular and Molecular Neuroscience 141
- Genetics 190
- Pathology and Forensic Medicine 95
- Urology 28
Countries citing papers authored by Linlea Armstrong
This map shows the geographic impact of Linlea Armstrong'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 Linlea Armstrong with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Linlea Armstrong more than expected).
Fields of papers citing papers by Linlea Armstrong
This network shows the impact of papers produced by Linlea Armstrong. 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 Linlea Armstrong. The network helps show where Linlea Armstrong may publish in the future.
Co-authors
The 25 scholars most cited alongside Linlea Armstrong, 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 47 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2006 | 172 | |
| 2 | 2013 | 45 | |
| 3 | 2011 | 42 | |
| 4 | 2009 | 41 | |
| 5 | 2013 | 41 | |
| 6 | 2007 | 38 | |
| 7 | 2009 | 35 | |
| 8 | 2007 | 35 | |
| 9 | 2002 | 27 | |
| 10 | 2013 | 26 | |
| 11 | 2013 | 22 | |
| 12 | 2009 | 18 | |
| 13 | 2009 | 17 | |
| 14 | 2003 | 16 | |
| 15 | 2017 | 15 | |
| 16 | 2007 | 15 | |
| 17 | 2014 | 15 | |
| 18 | 2017 | 14 | |
| 19 | 2015 | 13 | |
| 20 | 2010 | 12 |
About Linlea Armstrong
Linlea Armstrong is a scholar working on Genetics, Molecular Biology, Pulmonary and Respiratory Medicine, Pathology and Forensic Medicine and Neurology, having authored 47 papers that have together received 757 indexed citations. Recurring topics across this work include Neurofibromatosis and Schwannoma Cases (6 papers), Genomic variations and chromosomal abnormalities (4 papers), Genomics and Rare Diseases (4 papers), Neurogenetic and Muscular Disorders Research (3 papers), Prenatal Screening and Diagnostics (3 papers), Connective tissue disorders research (3 papers), Ion channel regulation and function (3 papers) and Genetic factors in colorectal cancer (3 papers). The work is most often cited by research in Neurology (129 citations), Cellular and Molecular Neuroscience (141 citations), Genetics (190 citations), Pathology and Forensic Medicine (95 citations) and Urology (28 citations). Linlea Armstrong has collaborated with scholars based in Canada, United States and United Kingdom. Frequent co-authors include Jan M. Friedman, Tanya N. Nelson, Sameer M. Zuberi, P K Thomas, Arn M. J. M. van den Maagdenberg, Stéphane Supplisson, Marina A.J. Tijssen, Ian Duguid, Rita Shiang and Mark I. Rees. Their work appears in journals such as European Journal of Medical Genetics, Prenatal Diagnosis, Clinical Genetics, Genetics in Medicine and American Journal of Medical Genetics Part A.
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.