Amanda Smith

2.4k total citations
30 papers, 1.1k citations indexed

About

Amanda Smith is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Amanda Smith has authored 30 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 12 papers in Genetics and 4 papers in Cellular and Molecular Neuroscience. Recurrent topics in Amanda Smith's work include Genomics and Rare Diseases (6 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Developmental Biology and Gene Regulation (5 papers). Amanda Smith is often cited by papers focused on Genomics and Rare Diseases (6 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Developmental Biology and Gene Regulation (5 papers). Amanda Smith collaborates with scholars based in Canada, United States and United Kingdom. Amanda Smith's co-authors include Fabien Avaron, Kym M. Boycott, М. А. Акименко, Dennis E. Bulman, Jacek Majewski, Bhaja K. Padhi, Jeremy Schwartzentruber, Chandree L. Beaulieu, Elizabeth Quint and Marie‐Andrée Akimenko and has published in prestigious journals such as Proceedings of the National Academy of Sciences, SHILAP Revista de lepidopterología and The American Journal of Human Genetics.

In The Last Decade

Amanda Smith

29 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Amanda Smith Canada 17 720 322 233 101 99 30 1.1k
Peter M. Eimon United States 16 1.1k 1.5× 212 0.7× 297 1.3× 119 1.2× 76 0.8× 25 1.6k
Andrea Ciolfi Italy 21 983 1.4× 255 0.8× 112 0.5× 97 1.0× 101 1.0× 55 1.7k
Mohamed A. El-Brolosy Germany 9 1.1k 1.5× 264 0.8× 301 1.3× 121 1.2× 144 1.5× 11 1.5k
Petur H. Petersen Iceland 20 842 1.2× 224 0.7× 187 0.8× 162 1.6× 77 0.8× 31 1.3k
Georgina E. Hollway Australia 19 1.0k 1.4× 502 1.6× 347 1.5× 97 1.0× 133 1.3× 28 1.5k
Maria Doitsidou United States 12 735 1.0× 228 0.7× 216 0.9× 128 1.3× 53 0.5× 17 1.3k
Shih-Lei Lai Taiwan 13 1.1k 1.5× 199 0.6× 394 1.7× 78 0.8× 111 1.1× 18 1.4k
Christopher M. Dooley United Kingdom 14 816 1.1× 187 0.6× 517 2.2× 58 0.6× 122 1.2× 21 1.2k
Álvaro Glavic Chile 18 982 1.4× 188 0.6× 406 1.7× 132 1.3× 79 0.8× 36 1.3k
Claudio Passananti Italy 25 1.2k 1.7× 269 0.8× 102 0.4× 87 0.9× 111 1.1× 66 1.6k

Countries citing papers authored by Amanda Smith

Since Specialization
Citations

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

Fields of papers citing papers by Amanda Smith

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Amanda Smith

This figure shows the co-authorship network connecting the top 25 collaborators of Amanda Smith. A scholar is included among the top collaborators of Amanda Smith 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 Amanda Smith. Amanda Smith 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.
Smith, Amanda, et al.. (2022). Tetraploidy accelerates adaptation under drug selection in a fungal pathogen. SHILAP Revista de lepidopterología. 3. 984377–984377. 9 indexed citations
3.
Smith, Amanda, Levi T. Morran, & Meleah A. Hickman. (2021). Host Defense Mechanisms Induce Genome Instability Leading to Rapid Evolution in an Opportunistic Fungal Pathogen. Infection and Immunity. 90(2). e0032821–e0032821. 8 indexed citations
4.
Smith, Amanda, et al.. (2021). Two Infection Assays to Study Non-Lethal Virulence Phenotypes in <em>C. Albicans</em> using <em>C. Elegans</em>. Journal of Visualized Experiments. 2 indexed citations
5.
Smith, Amanda & Meleah A. Hickman. (2020). Host-Induced Genome Instability Rapidly Generates Phenotypic Variation across Candida albicans Strains and Ploidy States. mSphere. 5(3). 15 indexed citations
6.
Daoud, Hussein, Mahdi Ghani, Nasim Vasli, et al.. (2019). Genetic Diagnostic Testing for Inherited Cardiomyopathies. Journal of Molecular Diagnostics. 21(3). 437–448. 3 indexed citations
7.
Smith, Amanda, Yoko Itō, Jeremy Schwartzentruber, et al.. (2018). A family segregating lethal neonatal coenzyme Q10 deficiency caused by mutations in COQ9. Journal of Inherited Metabolic Disease. 41(4). 719–729. 33 indexed citations
8.
Itō, Yoko, Amanda Smith, Kristin D. Kernohan, et al.. (2018). A ZPR1 mutation is associated with a novel syndrome of growth restriction, distinct craniofacial features, alopecia, and hypoplastic kidneys. Clinical Genetics. 94(3-4). 303–312. 5 indexed citations
9.
Daoud, Hussein, Mahdi Ghani, Gabrielle Mettler, et al.. (2017). Reinterpretation of sequence variants: one diagnostic laboratory’s experience, and the need for standard guidelines. Genetics in Medicine. 20(3). 365–368. 32 indexed citations
10.
Kernohan, Kristin D., Laila C. Schenkel, Lijia Huang, et al.. (2016). Identification of a methylation profile for DNMT1-associated autosomal dominant cerebellar ataxia, deafness, and narcolepsy. Clinical Epigenetics. 8(1). 91–91. 50 indexed citations
11.
Smith, Amanda, Skye McBride, Julien Marcadier, et al.. (2016). Severe Neonatal Presentation of Mitochondrial Citrate Carrier (SLC25A1) Deficiency. JIMD Reports. 30. 73–79. 16 indexed citations
12.
Venkateswaran, Sunita, Kenneth A. Myers, Amanda Smith, et al.. (2014). Whole‐exome sequencing in an individual with severe global developmental delay and intractable epilepsy identifies a novel, de novo GRIN2A mutation. Epilepsia. 55(7). e75–9. 32 indexed citations
13.
Dyment, David A., Amanda Smith, Peter Humphreys, et al.. (2014). Homozygous nonsense mutation in SYNJ1 associated with intractable epilepsy and tau pathology. Neurobiology of Aging. 36(2). 1222.e1–1222.e5. 50 indexed citations
14.
McMillan, Hugh J., Jeremy Schwartzentruber, Amanda Smith, et al.. (2014). Compound heterozygous mutations in glycyl-tRNA synthetase are a proposed cause of systemic mitochondrial disease. BMC Medical Genetics. 15(1). 36–36. 33 indexed citations
15.
McMillan, Hugh J., Peter Humphreys, Amanda Smith, et al.. (2014). Congenital Visual Impairment and Progressive Microcephaly Due to Lysyl–Transfer Ribonucleic Acid (RNA) Synthetase (KARS) Mutations. Journal of Child Neurology. 30(8). 1037–1043. 36 indexed citations
16.
Smith, Amanda, Dennis E. Bulman, Eric Bareke, et al.. (2014). Meconium ileus in a Lebanese family secondary to mutations in the GUCY2C gene. European Journal of Human Genetics. 23(7). 990–992. 25 indexed citations
17.
Dyment, David A., Amanda Smith, Diana Alcantara, et al.. (2013). Mutations in PIK3R1 Cause SHORT Syndrome. The American Journal of Human Genetics. 93(1). 158–166. 130 indexed citations
18.
Dyment, David A., Erick Sell, Megan R. Vanstone, et al.. (2013). Evidence for clinical, genetic and biochemical variability in spinal muscular atrophy with progressive myoclonic epilepsy. Clinical Genetics. 86(6). 558–563. 39 indexed citations
19.
Pérez‐Claros, Juan A., Amanda Smith, Fabien Avaron, et al.. (2007). Position dependence of hemiray morphogenesis during tail fin regeneration in Danio rerio. Developmental Biology. 312(1). 272–283. 23 indexed citations
20.
Smith, Amanda, et al.. (2007). Gene expression analysis on sections of zebrafish regenerating fins reveals limitations in the whole‐mount in situ hybridization method. Developmental Dynamics. 237(2). 417–425. 59 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Peter M. Eimon Breakdown of academic impact, for papers by Andrea Ciolfi Breakdown of academic impact, for papers by Mohamed A. El-Brolosy Breakdown of academic impact, for papers by Petur H. Petersen Breakdown of academic impact, for papers by Georgina E. Hollway Breakdown of academic impact, for papers by Maria Doitsidou Breakdown of academic impact, for papers by Shih-Lei Lai Breakdown of academic impact, for papers by Christopher M. Dooley Breakdown of academic impact, for papers by Álvaro Glavic Breakdown of academic impact, for papers by Claudio Passananti
Rankless by CCL
2026