Amanda Springer

751 total citations
7 papers, 116 citations indexed

About

Amanda Springer is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Amanda Springer has authored 7 papers receiving a total of 116 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 4 papers in Molecular Biology and 1 paper in Pediatrics, Perinatology and Child Health. Recurrent topics in Amanda Springer's work include Genomics and Rare Diseases (5 papers), RNA modifications and cancer (3 papers) and RNA Research and Splicing (2 papers). Amanda Springer is often cited by papers focused on Genomics and Rare Diseases (5 papers), RNA modifications and cancer (3 papers) and RNA Research and Splicing (2 papers). Amanda Springer collaborates with scholars based in Australia, Italy and Ireland. Amanda Springer's co-authors include Timothy B. Niewold, David L. Boone, Wesley A. Grimm, Urszula Dougherty, Jeannette S. Messer, Christopher R. Weber, Stephen F. Murphy, Dezheng Huo, Nathan A. Ellis and Sonia S. Kupfer and has published in prestigious journals such as SHILAP Revista de lepidopterología, Gut and Human Mutation.

In The Last Decade

Amanda Springer

7 papers receiving 116 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Amanda Springer Australia	5	62	49	30	18	17	7	116
Debbie Hughes United Kingdom	6	32 0.5×	29 0.6×	13 0.4×	14 0.8×	16 0.9×	14	116
Stephanie Nance United States	7	73 1.2×	14 0.3×	10 0.3×	17 0.9×	13 0.8×	9	125
Kaido Lepik Switzerland	6	77 1.2×	13 0.3×	56 1.9×	13 0.7×	12 0.7×	9	141
Kelly Shaffer United States	5	100 1.6×	15 0.3×	26 0.9×	7 0.4×	9 0.5×	7	140
Anna Barbara Mancuso Italy	4	80 1.3×	11 0.2×	26 0.9×	16 0.9×	13 0.8×	4	119
Lisa Davey United States	2	45 0.7×	23 0.5×	15 0.5×	21 1.2×	9 0.5×	2	219
Shengcheng Dong United States	5	103 1.7×	7 0.1×	49 1.6×	14 0.8×	26 1.5×	7	142
Zhengbo Xue China	6	56 0.9×	27 0.6×	14 0.5×	11 0.6×	28 1.6×	7	125
Jiin Ying Lim Singapore	7	29 0.5×	15 0.3×	52 1.7×	23 1.3×	12 0.7×	20	110
Barbara Pazdrak United States	5	62 1.0×	13 0.3×	16 0.5×	30 1.7×	30 1.8×	7	146

Countries citing papers authored by Amanda Springer

Since Specialization

Citations

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

Fields of papers citing papers by Amanda Springer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Amanda Springer

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

All Works

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7 of 7 papers shown

Boggs, Kirsten, Fiona Lynch, Michelle C. Ward, et al.. (2024). Rapid genomic testing in critically ill pediatric patients: Genetic counseling lessons from a national program. SHILAP Revista de lepidopterología. 2(Suppl 2). 101878–101878. 2 indexed citations

Brett, Gemma R., Elizabeth E. Palmer, Kirsten Boggs, et al.. (2022). Co-design, implementation, and evaluation of plain language genomic test reports. npj Genomic Medicine. 7(1). 61–61. 6 indexed citations

Horton, Ari, Meredith A. Allen, Stacy Goergen, et al.. (2022). Ethylmalonic encephalopathy masquerading as meningococcemia. Molecular Case Studies. 8(2). mcs.a006193–mcs.a006193. 4 indexed citations

Akesson, Lauren, Adam Bournazos, Andrew Fennell, et al.. (2020). Rapid exome sequencing and adjunct RNA studies confirm the pathogenicity of a novel homozygous ASNS splicing variant in a critically ill neonate. Human Mutation. 41(11). 1884–1891. 8 indexed citations

Akesson, Lauren, Adam Bournazos, Andrew Fennell, et al.. (2020). Rapid exome sequencing and adjunct rna studies confirm pathogenicity of a novel homozygous asns splicing variant in a critically ill neonate. Pathology. 52. S106–S106. 2 indexed citations

Loveday, Chey, Anna Zachariou, Lucy‐Ann Behan, et al.. (2019). EED and EZH2 constitutive variants: A study to expand the Cohen‐Gibson syndrome phenotype and contrast it with Weaver syndrome. American Journal of Medical Genetics Part A. 179(4). 588–594. 23 indexed citations

Grimm, Wesley A., Jeannette S. Messer, Stephen F. Murphy, et al.. (2015). The Thr300Ala variant in ATG16L1 is associated with improved survival in human colorectal cancer and enhanced production of type I interferon. Gut. 65(3). 456–464. 71 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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