Linlea Armstrong

3.5k total citations
46 papers, 754 citations indexed

About

Linlea Armstrong is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Linlea Armstrong has authored 46 papers receiving a total of 754 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Genetics, 13 papers in Molecular Biology and 7 papers in Pathology and Forensic Medicine. Recurrent topics in Linlea Armstrong's work include Genomics and Rare Diseases (6 papers), Genomic variations and chromosomal abnormalities (6 papers) and Neurofibromatosis and Schwannoma Cases (6 papers). Linlea Armstrong is often cited by papers focused on Genomics and Rare Diseases (6 papers), Genomic variations and chromosomal abnormalities (6 papers) and Neurofibromatosis and Schwannoma Cases (6 papers). Linlea Armstrong collaborates with scholars based in Canada, United States and United Kingdom. Linlea Armstrong's co-authors include Jan M. Friedman, Tanya N. Nelson, Michael J. Owen, M. Thomas, Sameer M. Zuberi, Arn M. J. M. van den Maagdenberg, Stéphane Supplisson, Seo‐Kyung Chung, Kirsten Harvey and John B.P. Stephenson and has published in prestigious journals such as Nature Genetics, SHILAP Revista de lepidopterología and International Journal of Cancer.

In The Last Decade

Linlea Armstrong

46 papers receiving 724 citations

Peers

Linlea Armstrong

GENET

CMN

NEURO

PFM

Marja Hietala Finland

Rajesh Shinghal United States

Caroline Sevin France

Teruaki Masuda Japan

WILLIAM A. VALENTE United States

Dalia Kasperavičiūtė United Kingdom

Roberta Bombardieri Italy

Oneil G. Bhalala Australia

Britt Johnson United States

Sari Kiuru‐Enari Finland

Marja Hietala Finland

Linlea Armstrong

485 ×1.7

245 ×1.2

GENET

180 ×1.2

CMN

159 ×1.1

NEURO

44 ×0.4

PFM

Citations per year, relative to Linlea Armstrong Linlea Armstrong (= 1×) peers Marja Hietala

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-authorship network of co-authors of Linlea Armstrong

This figure shows the co-authorship network connecting the top 25 collaborators of Linlea Armstrong. A scholar is included among the top collaborators of Linlea Armstrong based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Linlea Armstrong. Linlea Armstrong is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Hebbar, Malavika, Cyrus Boelman, Richard A. Dean, et al.. (2024). Expanding the genotype-phenotype spectrum in SCN8A-related disorders. BMC Neurology. 24(1). 31–31. 2 indexed citations

Jacobsen, Julius O.B., Christèle du Souich, Kent Shefchek, et al.. (2022). The Clinical Variant Analysis Tool: Analyzing the evidence supporting reported genomic variation in clinical practice. Genetics in Medicine. 24(7). 1512–1522. 3 indexed citations

Armstrong, Linlea, Cornelius F. Boerkoel, L. Clarke, et al.. (2021). Somatic mosaicism detected by genome-wide sequencing in 500 parent–child trios with suspected genetic disease: clinical and genetic counseling implications. Molecular Case Studies. 7(6). a006125–a006125. 6 indexed citations

Hubinette, Maria, et al.. (2021). Coaching the coaches: Employing role modeling and coaching as a faculty development strategy. Medical Teacher. 43(8). 918–919. 1 indexed citations

Giampietro, Philip F., Linlea Armstrong, Robert D. Blank, et al.. (2014). Whole exome sequencing identifies a POLRID mutation segregating in a father and two daughters with findings of Klippel–Feil and Treacher Collins syndromes. American Journal of Medical Genetics Part A. 167(1). 95–102. 10 indexed citations

Stevenson, David A., David G. Little, Linlea Armstrong, et al.. (2013). Approaches to Treating NF1 Tibial Pseudarthrosis. Journal of Pediatric Orthopaedics. 33(3). 269–275. 44 indexed citations

Armstrong, Linlea, Kimberly Jett, Patricia Birch, et al.. (2013). The generalized bone phenotype in children with neurofibromatosis 1: A sibling matched case–control study. American Journal of Medical Genetics Part A. 161(7). 1654–1661. 22 indexed citations

Schlade‐Bartusiak, Kamilla, et al.. (2013). Independent post-zygotic breaks of a dicentric chromosome result in mosaicism for an inverted duplication deletion 9p and terminal deletion 9p. European Journal of Medical Genetics. 56(5). 229–235. 6 indexed citations

Richer, Julie, et al.. (2012). CCMG statement on gene patents. Clinical Genetics. 82(5). 405–407. 2 indexed citations

10.

Heran, Manraj K.S., Mary Connolly, Jan M. Friedman, et al.. (2010). Cerebrovasculopathy in NF1 associated with ocular and scalp defects. American Journal of Medical Genetics Part A. 155(2). 380–385. 12 indexed citations

11.

Lehman, Anna, Jan M. Friedman, David Chai, et al.. (2009). A characteristic syndrome associated with microduplication of 8q12, inclusive of CHD7. European Journal of Medical Genetics. 52(6). 436–439. 17 indexed citations

12.

Alfadhel, Majid, D. Pugash, Ashley Robinson, et al.. (2009). Pre‐ and postnatal findings in a boy with duplication of the bladder and intestine: Report and review. American Journal of Medical Genetics Part A. 149A(12). 2795–2802. 9 indexed citations

13.

Langlois, Sylvie, et al.. (2009). Steroid sulfatase deficiency and contiguous gene deletion syndrome amongst pregnant patients with low serum unconjugated estriols. Prenatal Diagnosis. 29(10). 966–974. 18 indexed citations

14.

Monzon, Jose Gerard, Linlea Armstrong, Sean Young, et al.. (2009). Validation of predictive models for germline mutations in DNA mismatch repair genes in colorectal cancer. International Journal of Cancer. 126(4). 930–939. 35 indexed citations

15.

Demos, Michelle, Vincenzo Macri, K Farrell, et al.. (2009). A novel KCNA1 mutation associated with global delay and persistent cerebellar dysfunction. Movement Disorders. 24(5). 778–782. 41 indexed citations

16.

Armstrong, Linlea, Gail E. Graham, R. Neil Schimke, et al.. (2007). The Hunter–MacDonald syndrome with expanded phenotype including risk of meningioma: An update and review. American Journal of Medical Genetics Part A. 146A(1). 83–92. 2 indexed citations

17.

Stevenson, David A., David Viskochil, Elizabeth K. Schorry, et al.. (2007). The use of anterolateral bowing of the lower leg in the diagnostic criteria for neurofibromatosis type 1. Genetics in Medicine. 9(7). 409–412. 15 indexed citations

18.

Rees, Mark I., Kirsten Harvey, Brian R. Pearce, et al.. (2006). Mutations in the gene encoding GlyT2 (SLC6A5) define a presynaptic component of human startle disease. Nature Genetics. 38(7). 801–806. 174 indexed citations

19.

Armstrong, Linlea, et al.. (2005). Unrelated patients with a rearrangement of chromosome 2 causing duplication of 2p23 and deletion of 2q37. American Journal of Medical Genetics Part A. 134A(3). 299–304. 2 indexed citations

20.

Rodger, Marc, Melissa A. Forgie, Nicole Langlois, et al.. (2003). The ACE D/D genotype is protective against the development of idiopathic deep vein thrombosis and pulmonary embolism. Thrombosis and Haemostasis. 90(11). 829–834. 16 indexed citations

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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