Amanda Smith

2.4k citations

31 papers · 1.1k · h-index 18

Impact in

Cell Biology top 5%
- Zebrafish Biomedical Research Applications
- Hippo pathway signaling and YAP/TAZ
Genetics top 10%
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders

Papers in

Molecular Biology 14
- Developmental Biology and Gene Regulation 5
- Congenital heart defects research 3
- Mitochondrial Function and Pathology 3
Genetics 12
- Genomics and Rare Diseases 7
- Genetics and Neurodevelopmental Disorders 4
- Neurogenetic and Muscular Disorders Research 3

Co-authors: Fabien Avaron (3 shared papers)Kym M. Boycott (14 shared papers)М. А. Акименко (3 shared papers)Dennis E. Bulman (13 shared papers)Jacek Majewski (12 shared papers)Bhaja K. Padhi (2 shared papers)Jeremy Schwartzentruber (11 shared papers)Chandree L. Beaulieu (11 shared papers)
Journals: Clinical Genetics (3 papers)Developmental Biology (2 papers)Developmental Dynamics (2 papers)Genetics in Medicine (1 paper)Clinical Epigenetics (1 paper)
Partner nations: Canada United States United Kingdom

In The Last Decade

Amanda Smith

30 papers receiving 1.1k citations

Peers

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-authors

The 25 scholars most cited alongside Amanda Smith, 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 Amanda Smith Line = papers co-authored together Amanda Smith links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 31 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Bone patterning is altered in the regenerating zebrafish caudal fin after ectopic expression of sonic hedgehog and bmp2b or exposure to cyclopamine Proceedings of the National Academy of Sciences ·Elizabeth Quint, Amanda Smith, Fabien Avaron, Lynda Laforest, Jennifer A. Miles, William Gaffield, Marie‐Andrée Akimenko	2002	161
2	Inhibition of BMP signaling during zebrafish fin regeneration disrupts fin growth and scleroblast differentiation and function Developmental Biology ·Amanda Smith, Fabien Avaron, D. Guay, Bhaja K. Padhi, М. А. Акименко	2006	139
3	Mutations in PIK3R1 Cause SHORT Syndrome The American Journal of Human Genetics ·David A. Dyment, Amanda Smith, Diana Alcantara, Jeremy Schwartzentruber, Lina Basel‐Vanagaite, Cynthia J. Curry, I. Karen Temple, William Reardon, Sahar Mansour, Mushfequr R. Haq, Rodney D. Gilbert, Ordan J. Lehmann, Megan R. Vanstone, Chandree L. Beaulieu, Jacek Majewski, Dennis E. Bulman, Mark O’Driscoll, Kym M. Boycott, A. Micheil Innes	2013	132
4	Screen for genes differentially expressed during regeneration of the zebrafish caudal fin Developmental Dynamics ·Bhaja K. Padhi, Lucille Joly, Patricia Tellis, Amanda Smith, Purushothama Nanjappa, Mario Chevrette, Marc Ekker, Marie‐Andrée Akimenko	2004	76
5	Exome Sequencing as a Diagnostic Tool for Pediatric‐Onset Ataxia Human Mutation ·Sarah L. Sawyer, Jeremy Schwartzentruber, Chandree L. Beaulieu, David A. Dyment, Amanda Smith, Jodi Warman‐Chardon, Grace Yoon, Guy A. Rouleau, Oksana Suchowersky, Victoria Mok Siu, Lisa Murphy, Robert A. Hegele, Christian R. Marshall, Dennis E. Bulman, Jacek Majewski, Mark A. Tarnopolsky, Kym M. Boycott	2013	68
6	Gene expression analysis on sections of zebrafish regenerating fins reveals limitations in the whole‐mount in situ hybridization method Developmental Dynamics ·Amanda Smith, J. Zhang, D. Guay, Elizabeth Quint, Amanda M. Johnson, М. А. Акименко	2007	59
7	Identification of a methylation profile for DNMT1-associated autosomal dominant cerebellar ataxia, deafness, and narcolepsy Clinical Epigenetics ·Kristin D. Kernohan, Laila C. Schenkel, Lijia Huang, Amanda Smith, Guillaume Paré, Peter Ainsworth, Kym M. Boycott, Jodi Warman‐Chardon, Bekim Sadiković	2016	51
8	Homozygous nonsense mutation in SYNJ1 associated with intractable epilepsy and tau pathology Neurobiology of Aging ·David A. Dyment, Amanda Smith, Peter Humphreys, Jeremy Schwartzentruber, Chandree L. Beaulieu, Dennis E. Bulman, Jacek Majewski, John Woulfe, Jean Michaud, Kym M. Boycott	2014	51
9	Evidence for clinical, genetic and biochemical variability in spinal muscular atrophy with progressive myoclonic epilepsy Clinical Genetics ·David A. Dyment, Erick Sell, Megan R. Vanstone, Amanda Smith, David Garandeau, Virginie Garcia, Stéphane Carpentier, Emmanuelle Le Trionnaire, Frédérique Sabourdy, Chandree L. Beaulieu, Jeremy Schwartzentruber, Hugh J. McMillan, Jacek Majewski, Dennis E. Bulman, Thierry Levade, Kym M. Boycott	2013	39
10	Congenital Visual Impairment and Progressive Microcephaly Due to Lysyl–Transfer Ribonucleic Acid (RNA) Synthetase ( KARS ) Mutations Journal of Child Neurology ·Hugh J. McMillan, Peter Humphreys, Amanda Smith, Jeremy Schwartzentruber, Pranesh Chakraborty, Dennis E. Bulman, Chandree L. Beaulieu, Jacek Majewski, Kym M. Boycott, Michael T. Geraghty	2014	37
11	A family segregating lethal neonatal coenzyme Q₁₀ deficiency caused by mutations in COQ9 Journal of Inherited Metabolic Disease ·Amanda Smith, Yoko Itō, Afsana Ahmed, Jeremy Schwartzentruber, Chandree L. Beaulieu, Erika Aberg, Jacek Majewski, Dennis E. Bulman, Karina Horsting‐Wethly, Diana Vermunt‐de Koning, Richard J. Rodenburg, Kym M. Boycott, Lynette S. Penney	2018	33
12	Compound heterozygous mutations in glycyl-tRNA synthetase are a proposed cause of systemic mitochondrial disease BMC Medical Genetics ·Hugh J. McMillan, Jeremy Schwartzentruber, Amanda Smith, Suzie Lee, Pranesh Chakraborty, Dennis E. Bulman, Chandree L. Beaulieu, Jacek Majewski, Kym M. Boycott, Michael T. Geraghty	2014	33
13	Whole‐exome sequencing in an individual with severe global developmental delay and intractable epilepsy identifies a novel, de novo GRIN2A mutation Epilepsia ·Sunita Venkateswaran, Kenneth A. Myers, Amanda Smith, Chandree L. Beaulieu, Jeremy Schwartzentruber, Jacek Majewski, Dennis E. Bulman, Kym M. Boycott, David A. Dyment	2014	32
14	Reinterpretation of sequence variants: one diagnostic laboratory’s experience, and the need for standard guidelines Genetics in Medicine ·Caitlin Chisholm, Hussein Daoud, Mahdi Ghani, Gabrielle Mettler, Jean McGowan‐Jordan, Liz Sinclair-Bourque, Amanda Smith, Olga Jarinova	2017	32
15	Meconium ileus in a Lebanese family secondary to mutations in the GUCY2C gene European Journal of Human Genetics ·Amanda Smith, Dennis E. Bulman, Claire Goldsmith, Eric Bareke, Jacek Majewski, Kym M. Boycott, Sarah M. Nikkel	2014	25
16	Position dependence of hemiray morphogenesis during tail fin regeneration in Danio rerio Developmental Biology ·Carmen Murciano, Juan A. Pérez‐Claros, Amanda Smith, Fabien Avaron, Tahía D. Fernández, Iván Durán, J. Ruiz-Sánchez, (unknown), José Becerra, М. А. Акименко, Manuel Marí‐Beffa	2007	24
17	Syndrome disintegration: Exome sequencing reveals that Fitzsimmons syndrome is a co‐occurrence of multiple events American Journal of Medical Genetics Part A ·Christine M. Armour, Amanda Smith, Taila Hartley, Jodi Warman‐Chardon, Sarah L. Sawyer, Jeremy Schwartzentruber, Raoul C. M. Hennekam, Jacek Majewski, Dennis E. Bulman, Mohnish Suri, Kym M. Boycott	2016	19
18	Host-Induced Genome Instability Rapidly Generates Phenotypic Variation across Candida albicans Strains and Ploidy States mSphere ·Amanda Smith, Meleah A. Hickman	2020	17
19	Severe Neonatal Presentation of Mitochondrial Citrate Carrier (SLC25A1) Deficiency JIMD Reports ·(unknown), Amanda Smith, Skye McBride, Julien Marcadier, Jean Michaud, Osama Y. Al-Dirbashi, Jeremy Schwartzentruber, Chandree L. Beaulieu, Sherri L. Katz, Jacek Majewski, Dennis E. Bulman, Michael T. Geraghty, Mary‐Ellen Harper, Pranesh Chakraborty, Matthew A. Lines	2016	16
20	LIMS2 mutations are associated with a novel muscular dystrophy, severe cardiomyopathy and triangular tongues Clinical Genetics ·Jodi Warman‐Chardon, Amanda Smith, John Woulfe, Elena Peña, Kawan Rakhra, Carole Dennie, Chandree L. Beaulieu, Lijia Huang, Jeremy Schwartzentruber, Cynthia Hawkins, Matthew B. Harms, Sue Dojeiji, M. Zhang, Jacek Majewski, Dennis E. Bulman, Kym M. Boycott, David A. Dyment	2015	15

About Amanda Smith

Amanda Smith is a scholar working on Molecular Biology, Genetics, Plant Science, Infectious Diseases and Genetics, having authored 31 papers that have together received 1.1k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (7 papers), Developmental Biology and Gene Regulation (5 papers), Genetics and Neurodevelopmental Disorders (4 papers), Antifungal resistance and susceptibility (3 papers), Fungal Infections and Studies (3 papers), Congenital heart defects research (3 papers), Neurogenetic and Muscular Disorders Research (3 papers) and Mitochondrial Function and Pathology (3 papers). The work is most often cited by research in Cell Biology (218 citations), Genetics (288 citations), Molecular Biology (671 citations), Physiology (37 citations) and Genetics (75 citations). Amanda Smith has collaborated with scholars based in Canada, United States and United Kingdom. Frequent 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. Their work appears in journals such as Clinical Genetics, Developmental Biology, Developmental Dynamics, Genetics in Medicine and Clinical Epigenetics.

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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