Amanda M. Smith

723 total citations
18 papers, 526 citations indexed

About

Amanda M. Smith is a scholar working on Molecular Biology, Hematology and Cancer Research. According to data from OpenAlex, Amanda M. Smith has authored 18 papers receiving a total of 526 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 10 papers in Hematology and 5 papers in Cancer Research. Recurrent topics in Amanda M. Smith's work include Acute Myeloid Leukemia Research (9 papers), Epigenetics and DNA Methylation (7 papers) and Cancer Genomics and Diagnostics (5 papers). Amanda M. Smith is often cited by papers focused on Acute Myeloid Leukemia Research (9 papers), Epigenetics and DNA Methylation (7 papers) and Cancer Genomics and Diagnostics (5 papers). Amanda M. Smith collaborates with scholars based in United States, Australia and Canada. Amanda M. Smith's co-authors include L.D. Middaugh, Vandana Zaman, Barry J. Hoffer, Ann‐Charlotte Granholm, Peng Huang, Ian T. Ryde, Theodore A. Slotkin, Christina M. Powers, Frederic J. Seidler and Nicole M. Verrills and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Investigation and Nature Communications.

In The Last Decade

Amanda M. Smith

17 papers receiving 515 citations

Peers

Amanda M. Smith

HEMAT

CMN

ONCOL

Lene B. Køhler Denmark

Mario Mauri Italy

Massimo Corsaro Italy

S Tadokoro Japan

Jagjit S. Gill United States

Lina Dahl Sweden

Jenny Marzahn Germany

Marie‐Claude Amoureux France

Zhaohua Tang China

Kim Lemmens Belgium

Lene B. Køhler Denmark

Amanda M. Smith

389 ×1.3

52 ×0.4

HEMAT

218 ×1.8

CMN

39 ×0.7

ONCOL

27 ×0.5

Citations per year, relative to Amanda M. Smith Amanda M. Smith (= 1×) peers Lene B. Køhler

Countries citing papers authored by Amanda M. Smith

Since Specialization

Citations

This map shows the geographic impact of Amanda M. 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 M. 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 M. Smith more than expected).

Fields of papers citing papers by Amanda M. Smith

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Amanda M. Smith

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

All Works

Sort: Min cites: Since: Top N: Style:

18 of 18 papers shown

Abel, Haley, et al.. (2024). Rapid and accurate remethylation of DNA in Dnmt3a- deficient hematopoietic cells with restoration of DNMT3A activity. Science Advances. 10(5). eadk8598–eadk8598. 1 indexed citations

Padua, Maria B., et al.. (2024). Non-coding cause of congenital heart defects: Abnormal RNA splicing with multiple isoforms as a mechanism for heterotaxy. Human Genetics and Genomics Advances. 5(4). 100353–100353. 2 indexed citations

Helm, Benjamin M., et al.. (2023). Disruption of FBN1 by an Alu element insertion: A novel genetic cause of Marfan syndrome. European Journal of Medical Genetics. 66(7). 104775–104775.

Smith, Amanda M., Haley Abel, David Y. Chen, et al.. (2022). Somatic Dnmt3a inactivation leads to slow, canonical DNA methylation loss in murine hematopoietic cells. iScience. 25(4). 104004–104004. 3 indexed citations

Chen, David Y., Nichole Helton, Sai Mukund Ramakrishnan, et al.. (2021). Dnmt3a deficiency in the skin causes focal, canonical DNA hypomethylation and a cellular proliferation phenotype. Proceedings of the National Academy of Sciences. 118(16). 8 indexed citations

Smith, Amanda M., Marwan Shinawi, Sai Mukund Ramakrishnan, et al.. (2021). Functional and epigenetic phenotypes of humans and mice with DNMT3A Overgrowth Syndrome. Nature Communications. 12(1). 4549–4549. 32 indexed citations

Ketkar, Shamika, Amanda M. Smith, Elizabeth R. Leight, et al.. (2020). Remethylation of Dnmt3a ^−/− hematopoietic cells is associated with partial correction of gene dysregulation and reduced myeloid skewing. Proceedings of the National Academy of Sciences. 117(6). 3123–3134. 25 indexed citations

Smith, Amanda M., et al.. (2019). DNMT3AR882 Alters the Epigenome of Hematopoietic Cells. Blood. 134(Supplement_1). 112–112. 1 indexed citations

Smith, Amanda M., Christine Zhang, Alexandre S. Cristino, et al.. (2019). PTEN deletion drives acute myeloid leukemia resistance to MEK inhibitors. Oncotarget. 10(56). 5755–5767. 7 indexed citations

10.

Russler‐Germain, David A., Shamika Ketkar, Amanda M. Smith, et al.. (2017). Haploinsufficiency for DNA methyltransferase 3A predisposes hematopoietic cells to myeloid malignancies. Journal of Clinical Investigation. 127(10). 3657–3674. 68 indexed citations

11.

Smith, Amanda M., Matthew D. Dun, Erwin M. Lee, et al.. (2016). Activation of protein phosphatase 2A in FLT3+ acute myeloid leukemia cells enhances the cytotoxicity of FLT3 tyrosine kinase inhibitors. Oncotarget. 7(30). 47465–47478. 35 indexed citations

12.

Smith, Amanda M., et al.. (2015). Targeting Survivin with YM155 (Sepantronium Bromide): A novel therapeutic strategy for paediatric acute myeloid leukaemia. Leukemia Research. 39(4). 435–444. 13 indexed citations

13.

Marcadier, Julien, Amanda M. Smith, Daniela Pohl, et al.. (2013). Mutations in ALDH6A1 encoding methylmalonate semialdehyde dehydrogenase are associated with dysmyelination and transient methylmalonic aciduria. Orphanet Journal of Rare Diseases. 8(1). 98–98. 31 indexed citations

14.

Roberts, Kathryn G., Amanda M. Smith, Fiona McDougall, et al.. (2010). Essential Requirement for PP2A Inhibition by the Oncogenic Receptor c-KIT Suggests PP2A Reactivation as a Strategy to Treat c-KIT+ Cancers. Cancer Research. 70(13). 5438–5447. 100 indexed citations

15.

Powers, Christina M., et al.. (2009). Silver Impairs Neurodevelopment: Studies in PC12 Cells. Environmental Health Perspectives. 118(1). 73–79. 63 indexed citations

16.

Middaugh, L.D., Peng Huang, Vandana Zaman, et al.. (2006). A partial GDNF depletion leads to earlier age-related deterioration of motor function and tyrosine hydroxylase expression in the substantia nigra. Experimental Neurology. 202(2). 336–347. 93 indexed citations

17.

Smith, Amanda M.. (2004). Effects of prenatal marijuana on response inhibition: an fMRI study of young adults. Neurotoxicology and Teratology. 3 indexed citations

18.

Mcdermott, J, Peter R. Dodd, J.A. Edwardson, John Hardy, & Amanda M. Smith. (1983). Pathway of inactivation of cholecystokinin octapeptide (CCK-8) by synaptosomal fractions. Neurochemistry International. 5(5). 641–647. 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.

Explore authors with similar magnitude of impact