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)Judith Allanson (2 shared papers)Jean McGowan‐Jordan (1 shared paper)Arn M. J. M. van den Maagdenberg (1 shared paper)Brian R. Pearce (1 shared paper)Gail E. Graham (2 shared papers)Mark I. Rees (1 shared paper)
- Journals
- Prenatal Diagnosis (2 papers)Genetics in Medicine (2 papers)European Journal of Medical Genetics (2 papers)Clinical Genetics (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 778 citations
Peers
Comparison fields: 5 of 76
- Neurology 153
- Cellular and Molecular Neuroscience 154
- Genetics 219
- Pathology and Forensic Medicine 105
- Urology 31
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 48 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2006 | 190 | |
| 2 | 2013 | 49 | |
| 3 | 2007 | 47 | |
| 4 | 2002 | 45 | |
| 5 | 2011 | 44 | |
| 6 | 2009 | 43 | |
| 7 | 2013 | 42 | |
| 8 | 2009 | 37 | |
| 9 | 2007 | 37 | |
| 10 | 2013 | 28 | |
| 11 | 2013 | 24 | |
| 12 | 2007 | 22 | |
| 13 | 2009 | 18 | |
| 14 | 2009 | 18 | |
| 15 | 2003 | 16 | |
| 16 | 2017 | 16 | |
| 17 | 2014 | 16 | |
| 18 | 2017 | 14 | |
| 19 | 2015 | 14 | |
| 20 | 2014 | 12 |
About Linlea Armstrong
Linlea Armstrong is a scholar working on Genetics, Molecular Biology, Neurology, Pulmonary and Respiratory Medicine and Pathology and Forensic Medicine, having authored 48 papers that have together received 840 indexed citations. Recurring topics across this work include Neurofibromatosis and Schwannoma Cases (7 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 Vascular Malformations Diagnosis and Treatment (3 papers). The work is most often cited by research in Neurology (153 citations), Cellular and Molecular Neuroscience (154 citations), Genetics (219 citations), Pathology and Forensic Medicine (105 citations) and Urology (31 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, Judith Allanson, Jean McGowan‐Jordan, Arn M. J. M. van den Maagdenberg, Brian R. Pearce, Gail E. Graham, Mark I. Rees, Marina A.J. Tijssen and John B.P. Stephenson. Their work appears in journals such as Prenatal Diagnosis, Genetics in Medicine, European Journal of Medical Genetics, Clinical Genetics 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.