Linlea Armstrong

3.5k citations
46 papers · 754 · h-index 16

Impact in

Papers in

    • Genomic variations and chromosomal abnormalities 6
    • Genomics and Rare Diseases 6
    • BRCA gene mutations in cancer 3
    • Connective tissue disorders research 3

Linlea Armstrong

46 papers receiving 724 citations

Peers

Linlea Armstrong
Comparison fields: 5 of 81
  • Neurology 141
  • Cellular and Molecular Neuroscience 152
  • Genetics 212
  • Pathology and Forensic Medicine 110
  • Rheumatology 82
Replace Martina Witsch‐Baumgartner with:
Martina Witsch‐Baumgartner Austria
Joseph J. Pinzone United States
Hagit Baris Israel
Isabelle Thiffault United States
Sally Heywood United Kingdom
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Citations per field
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Martina Witsch‐Baumgartner · 1×
Citations per year

Countries citing papers authored by Linlea Armstrong

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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.

Border = papers with Linlea Armstrong Line = papers co-authored together Linlea Armstrong links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 46 papers — load more, or switch the sort, to bring in the rest.

#Work
1 2006174
2 201344
3 201142
4 200941
5 201340
6 200738
7 200735
8 200935
9 200227
10 201326
11 201322
12 200918
13 200917
14 200316
15 201715
16 200715
17 201415
18 201714
19 201513
20 201012

About Linlea Armstrong

Linlea Armstrong is a scholar working on Genetics, Molecular Biology, Pathology and Forensic Medicine, Neurology and Pulmonary and Respiratory Medicine, having authored 46 papers that have together received 754 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (6 papers), Neurofibromatosis and Schwannoma Cases (6 papers), Genomics and Rare Diseases (6 papers), Prenatal Screening and Diagnostics (4 papers), Genetic factors in colorectal cancer (3 papers), BRCA gene mutations in cancer (3 papers), Soft tissue tumor case studies (3 papers) and Connective tissue disorders research (3 papers). The work is most often cited by research in Neurology (141 citations), Cellular and Molecular Neuroscience (152 citations), Genetics (212 citations), Pathology and Forensic Medicine (110 citations) and Rheumatology (82 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, Arn M. J. M. van den Maagdenberg, Victoria L. Harvey, Kirsten Harvey, Rita Shiang, P K Thomas, Gail E. Graham, Seo‐Kyung Chung and Brian R. Pearce. Their work appears in journals such as Genetics in Medicine, European Journal of Medical Genetics, Prenatal Diagnosis, 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.

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