Stacy Hewson

1.9k total citations
19 papers, 490 citations indexed

About

Stacy Hewson is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Stacy Hewson has authored 19 papers receiving a total of 490 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 7 papers in Genetics and 6 papers in Clinical Biochemistry. Recurrent topics in Stacy Hewson's work include Metabolism and Genetic Disorders (6 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Genomics and Rare Diseases (3 papers). Stacy Hewson is often cited by papers focused on Metabolism and Genetic Disorders (6 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Genomics and Rare Diseases (3 papers). Stacy Hewson collaborates with scholars based in Canada, United States and Netherlands. Stacy Hewson's co-authors include Saadet Mercimek‐Mahmutoglu, Komudi Siriwardena, Jaina Patel, Rosanna Weksberg, Elizabeth Donner, Jeff Kobayashi, David F. Callen, Shelly K. Weiss, Berge A. Minassian and Pekka Kannus and has published in prestigious journals such as SHILAP Revista de lepidopterología, Epilepsia and Patient Education and Counseling.

In The Last Decade

Stacy Hewson

19 papers receiving 479 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Stacy Hewson Canada 10 261 165 99 87 72 19 490
Komudi Siriwardena Canada 13 278 1.1× 279 1.7× 114 1.2× 128 1.5× 255 3.5× 25 671
Yu Kobayashi Japan 13 212 0.8× 173 1.0× 74 0.7× 26 0.3× 21 0.3× 63 503
Noboru Fueki Japan 10 76 0.3× 207 1.3× 44 0.4× 27 0.3× 65 0.9× 24 356
Michal Inbar‐Feigenberg Canada 10 113 0.4× 191 1.2× 23 0.2× 63 0.7× 77 1.1× 30 419
Elena Procopio Italy 16 88 0.3× 407 2.5× 41 0.4× 53 0.6× 164 2.3× 47 670
Janine J. Leffert United States 13 98 0.4× 272 1.6× 80 0.8× 32 0.4× 20 0.3× 16 525
Marion M. Brands Netherlands 11 44 0.2× 93 0.6× 57 0.6× 86 1.0× 26 0.4× 34 438
Mahesh Kamate India 11 39 0.1× 142 0.9× 55 0.6× 38 0.4× 84 1.2× 59 426
Miriam Rigoldi Italy 16 83 0.3× 119 0.7× 42 0.4× 228 2.6× 69 1.0× 29 544
Drago Bratkovic Australia 14 87 0.3× 200 1.2× 17 0.2× 70 0.8× 131 1.8× 48 419

Countries citing papers authored by Stacy Hewson

Since Specialization
Citations

This map shows the geographic impact of Stacy Hewson'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 Stacy Hewson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Stacy Hewson more than expected).

Fields of papers citing papers by Stacy Hewson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Stacy Hewson. 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 Stacy Hewson. The network helps show where Stacy Hewson may publish in the future.

Co-authorship network of co-authors of Stacy Hewson

This figure shows the co-authorship network connecting the top 25 collaborators of Stacy Hewson. A scholar is included among the top collaborators of Stacy Hewson 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 Stacy Hewson. Stacy Hewson is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

19 of 19 papers shown
1.
Hewson, Stacy, et al.. (2024). Management and Outcomes of Very Long-Chain Acyl-CoA Dehydrogenase Deficiency (VLCAD Deficiency): A Retrospective Chart Review. International Journal of Neonatal Screening. 10(2). 29–29. 1 indexed citations
2.
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Ni, Min, Bushra Afroze, Chao Xing, et al.. (2021). A pathogenic UFSP2 variant in an autosomal recessive form of pediatric neurodevelopmental anomalies and epilepsy. Genetics in Medicine. 23(5). 900–908. 15 indexed citations
4.
Whitney, Robyn, Stacy Hewson, Kimberly Amburgey, et al.. (2021). The Phenotypic Spectrum of Tuberous Sclerosis Complex: A Canadian Cohort. SHILAP Revista de lepidopterología. 8. 2329048X211012817–2329048X211012817. 11 indexed citations
5.
6.
Bourque, Danielle K., Stacy Hewson, Julian Raiman, et al.. (2020). Outcomes of patients with cobalamin C deficiency: A single center experience. JIMD Reports. 57(1). 102–114. 9 indexed citations
7.
Huang, Lijia, Nancy Carson, Jean McGowan‐Jordan, et al.. (2019). ALU transposition induces familial hypertrophic cardiomyopathy. Molecular Genetics & Genomic Medicine. 8(1). e951–e951. 1 indexed citations
8.
Inbar‐Feigenberg, Michal, Susan Blasér, Cynthia Hawkins, et al.. (2018). Mitochondrial POLG related disorder presenting prenatally with fetal cerebellar growth arrest. Metabolic Brain Disease. 33(4). 1369–1373. 6 indexed citations
9.
Costain, Gregory, Rebekah Jobling, Susan Walker, et al.. (2018). Periodic reanalysis of whole-genome sequencing data enhances the diagnostic advantage over standard clinical genetic testing. European Journal of Human Genetics. 26(5). 740–744. 65 indexed citations
10.
Hewson, Stacy, et al.. (2017). Variable expressivity of a likely pathogenic variant in KCNQ2 in a three‐generation pedigree presenting with intellectual disability with childhood onset seizures. American Journal of Medical Genetics Part A. 173(8). 2226–2230. 9 indexed citations
11.
Hewson, Stacy, Ledia Brunga, Jaina Patel, et al.. (2017). Prevalence of Genetic Disorders and GLUT1 Deficiency in a Ketogenic Diet Clinic. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 45(1). 93–96. 6 indexed citations
12.
Sondheimer, Neal, Stacy Hewson, Jessie M. Cameron, et al.. (2017). Novel recessive mutations in COQ4 cause severe infantile cardiomyopathy and encephalopathy associated with CoQ10 deficiency. Molecular Genetics and Metabolism Reports. 12. 23–27. 26 indexed citations
13.
Mercimek‐Mahmutoglu, Saadet, Jaina Patel, Dawn Cordeiro, et al.. (2015). Diagnostic yield of genetic testing in epileptic encephalopathy in childhood. Epilepsia. 56(5). 707–716. 164 indexed citations
14.
Tran, Christel, Stacy Hewson, Steven J. Steinberg, & Saadet Mercimek‐Mahmutoglu. (2014). Late-Onset Zellweger Spectrum Disorder Caused by PEX6 Mutations Mimicking X-Linked Adrenoleukodystrophy. Pediatric Neurology. 51(2). 262–265. 17 indexed citations
15.
Patel, Jaina, Stacy Hewson, Annette Feigenbaum, et al.. (2014). The natural history of glycogen storage disease types VI and IX: Long-term outcome from the largest metabolic center in Canada. Molecular Genetics and Metabolism. 113(3). 171–176. 73 indexed citations
16.
Lines, Matthew A., Stacy Hewson, William Halliday, et al.. (2013). Danon Disease Due to a Novel LAMP2 Microduplication. JIMD Reports. 14. 11–16. 9 indexed citations
17.
Babul‐Hirji, Riyana, et al.. (2009). A sociolinguistic exploration of genetic counseling discourse involving a child with a new genetic diagnosis. Patient Education and Counseling. 78(1). 40–45. 10 indexed citations
18.
Szybowska, Marta, Stacy Hewson, Beverley J. Antle, & Riyana Babul‐Hirji. (2007). Assessing the Informational Needs of Adolescents with a Genetic Condition: What Do They Want to Know?. Journal of Genetic Counseling. 16(2). 201–210. 22 indexed citations
19.
Feigenbaum, Annette, Robert J. Moore, Joe T.R. Clarke, et al.. (2003). Canavan disease: Carrier‐frequency determination in the Ashkenazi Jewish population and development of a novel molecular diagnostic assay. American Journal of Medical Genetics Part A. 124A(2). 142–147. 41 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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