Anna Szuto

1.3k total citations
20 papers, 361 citations indexed

About

Anna Szuto is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Anna Szuto has authored 20 papers receiving a total of 361 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 8 papers in Molecular Biology and 6 papers in Genetics. Recurrent topics in Anna Szuto's work include Genomics and Rare Diseases (7 papers), Neurogenetic and Muscular Disorders Research (6 papers) and Neurological diseases and metabolism (4 papers). Anna Szuto is often cited by papers focused on Genomics and Rare Diseases (7 papers), Neurogenetic and Muscular Disorders Research (6 papers) and Neurological diseases and metabolism (4 papers). Anna Szuto collaborates with scholars based in Canada, United States and France. Anna Szuto's co-authors include Patrick A. Dion, Guy A. Rouleau, Nicolas Dupré, Hussein Daoud, Jean‐Pierre Bouchard, William Camu, Claire S. Leblond, Annie Levert, Anne Noreau and Véronique Belzil and has published in prestigious journals such as Neurology, Biophysical Journal and Human Molecular Genetics.

In The Last Decade

Anna Szuto

15 papers receiving 357 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Anna Szuto Canada 10 219 160 110 58 57 20 361
Mukesh Gautam United States 12 214 1.0× 184 1.1× 120 1.1× 65 1.1× 81 1.4× 18 472
Janel O. Johnson United States 10 153 0.7× 163 1.0× 73 0.7× 94 1.6× 58 1.0× 11 364
Sayaka Teramoto Japan 11 274 1.3× 218 1.4× 115 1.0× 81 1.4× 27 0.5× 14 407
Tao Qiao United States 6 152 0.7× 228 1.4× 150 1.4× 44 0.8× 22 0.4× 7 310
Claire Guissart France 12 174 0.8× 65 0.4× 40 0.4× 76 1.3× 73 1.3× 22 301
Maximilian Naujock Germany 10 154 0.7× 120 0.8× 58 0.5× 96 1.7× 27 0.5× 14 290
Yevgeniya Abramzon United States 6 216 1.0× 327 2.0× 161 1.5× 71 1.2× 46 0.8× 7 506
Roberto Miguez United States 6 243 1.1× 216 1.4× 124 1.1× 49 0.8× 15 0.3× 6 342
Catherine Antar France 9 194 0.9× 100 0.6× 95 0.9× 26 0.4× 36 0.6× 11 288
Xiaohong Zi China 11 192 0.9× 59 0.4× 42 0.4× 155 2.7× 31 0.5× 25 355

Countries citing papers authored by Anna Szuto

Since Specialization
Citations

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

Fields of papers citing papers by Anna Szuto

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anna Szuto

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

All Works

20 of 20 papers shown
1.
2.
Lauffer, Marlen C., Kimberly Amburgey, Danique Beijer, et al.. (2025). Screening rare genetic diagnoses for amenability to bespoke antisense oligonucleotide therapy development: A retrospective cohort study. Genetics in Medicine. 28(1). 101597–101597.
3.
Ungar, Wendy J., Christian R. Marshall, Robin Z. Hayeems, et al.. (2025). A microcosting and cost consequence analysis from a randomized controlled trial comparing genome sequencing with exome sequencing for genetic diagnosis. Genetics in Medicine. 28(2). 101561–101561. 1 indexed citations
4.
Hayeems, Robin Z., Wendy J. Ungar, Christian R. Marshall, et al.. (2025). Comparing the performance of exome and genome sequencing for rare disease diagnostics: A randomized implementation effectiveness trial. Genetics in Medicine. 28(1). 101605–101605.
5.
Morton, Sarah U., Gregory Costain, Courtney E. French, et al.. (2024). Exome and Genome Sequencing to Diagnose the Genetic Basis of Neonatal Hypotonia. Neurology. 104(1). e210106–e210106.
6.
Shugar, Andrea, Anna Szuto, Miriam Weinstein, et al.. (2024). Genome sequencing reveals novel IKBKG structural variants associated with incontinentia pigmenti. British Journal of Dermatology. 192(5). 933–935.
7.
Ungar, Wendy J., Robin Z. Hayeems, Christian R. Marshall, et al.. (2023). Protocol for a Prospective, Observational Cost-effectiveness Analysis of Returning Secondary Findings of Genome Sequencing for Unexplained Suspected Genetic Conditions. Clinical Therapeutics. 45(8). 702–709. 1 indexed citations
8.
Hayeems, Robin Z., Christian R. Marshall, Anna Szuto, et al.. (2022). Comparing genome sequencing technologies to improve rare disease diagnostics: a protocol for the evaluation of a pilot project, Genome-wide Sequencing Ontario. CMAJ Open. 10(2). E460–E465. 9 indexed citations
9.
Morton, Sarah U., John Christodoulou, Gregory Costain, et al.. (2022). Multicenter Consensus Approach to Evaluation of Neonatal Hypotonia in the Genomic Era: A Review. JAMA Neurology. 79(4). 405–405. 17 indexed citations
10.
Chad, Lauren, et al.. (2022). Rapid Genetic Testing in Pediatric and Neonatal Critical Care: A Scoping Review of Emerging Ethical Issues. Hospital Pediatrics. 12(10). e347–e359. 8 indexed citations
11.
Diomedi, Marina, Ziv Gan‐Or, Fabio Placidi, et al.. (2016). A 23 years follow-up study identifies GLUT1 deficiency syndrome initially diagnosed as complicated hereditary spastic paraplegia. European Journal of Medical Genetics. 59(11). 564–568. 8 indexed citations
12.
Leblond, Claire S., Ziv Gan‐Or, Dan Spiegelman, et al.. (2015). Replication study of MATR3 in familial and sporadic amyotrophic lateral sclerosis. Neurobiology of Aging. 37. 209.e17–209.e21. 58 indexed citations
13.
Jouan, Loubna, Bouchra Ouled Amar Bencheikh, Hussein Daoud, et al.. (2015). Exome sequencing identifies recessive CDK5RAP2 variants in patients with isolated agenesis of corpus callosum. European Journal of Human Genetics. 24(4). 607–610. 17 indexed citations
14.
Kaneb, Hannah, Andrew W. Folkmann, Véronique Belzil, et al.. (2014). Deleterious mutations in the essential mRNA metabolism factor, hGle1, in amyotrophic lateral sclerosis. Human Molecular Genetics. 24(5). 1363–1373. 101 indexed citations
15.
Szuto, Anna, et al.. (2014). An 18 Alanine Repeat in a Severe Form of Oculopharyngeal Muscular Dystrophy. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 41(4). 508–511. 12 indexed citations
16.
Noreau, Anne, Cynthia V. Bourassa, Anna Szuto, et al.. (2013). SYNE1Mutations in Autosomal Recessive Cerebellar Ataxia. JAMA Neurology. 70(10). 1296–31. 45 indexed citations
17.
Daoud, Hussein, Anna Szuto, William Camu, et al.. (2012). UBQLN2 mutations are rare in French and French–Canadian amyotrophic lateral sclerosis. Neurobiology of Aging. 33(9). 2230.e1–2230.e5. 39 indexed citations
18.
Daoud, Hussein, Mike Sabbagh, Véronique Belzil, et al.. (2012). C9orf72 Hexanucleotide Repeat Expansions as the Causative Mutation for Chromosome 9p21–Linked Amyotrophic Lateral Sclerosis and Frontotemporal Dementia. Archives of Neurology. 69(9). 1159–63. 22 indexed citations
19.
Noreau, Anne, Patrick A. Dion, Anna Szuto, et al.. (2012). CYP7B1 Mutations in French-Canadian Hereditary Spastic Paraplegia Subjects. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 39(1). 91–94. 1 indexed citations
20.
Batenchuk, Cory, et al.. (2011). Chromosomal Position Effects Are Linked to Sir2-Mediated Variation in Transcriptional Burst Size. Biophysical Journal. 100(10). L56–L58. 22 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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