Samantha Baxter

4.0k total citations
22 papers, 733 citations indexed

About

Samantha Baxter is a scholar working on Genetics, Cardiology and Cardiovascular Medicine and Molecular Biology. According to data from OpenAlex, Samantha Baxter has authored 22 papers receiving a total of 733 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 8 papers in Cardiology and Cardiovascular Medicine and 5 papers in Molecular Biology. Recurrent topics in Samantha Baxter's work include Genomics and Rare Diseases (10 papers), Cardiomyopathy and Myosin Studies (7 papers) and Genomic variations and chromosomal abnormalities (5 papers). Samantha Baxter is often cited by papers focused on Genomics and Rare Diseases (10 papers), Cardiomyopathy and Myosin Studies (7 papers) and Genomic variations and chromosomal abnormalities (5 papers). Samantha Baxter collaborates with scholars based in United States, United Kingdom and Australia. Samantha Baxter's co-authors include Heidi L. Rehm, Birgit Funke, Matthew S. Lebo, Trevor J. Pugh, Neal K. Lakdawala, Emily White, Elizabeth Hynes, Samuel Aronson, Matthew Varugheese and Lawrence Babb and has published in prestigious journals such as Nature Communications, SHILAP Revista de lepidopterología and Journal of Allergy and Clinical Immunology.

In The Last Decade

Samantha Baxter

22 papers receiving 725 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Samantha Baxter United States 11 389 331 264 75 39 22 733
Lisa Mahanta United States 11 231 0.6× 235 0.7× 195 0.7× 73 1.0× 34 0.9× 15 552
Annemieke H. van der Hout Netherlands 8 110 0.3× 227 0.7× 223 0.8× 88 1.2× 15 0.4× 13 451
Lisa Ku United States 11 682 1.8× 585 1.8× 94 0.4× 19 0.3× 21 0.5× 15 1.0k
Tracy N. Hadnott United States 7 65 0.2× 333 1.0× 507 1.9× 66 0.9× 76 1.9× 11 752
Kristin McDonald Gibson United States 8 86 0.2× 272 0.8× 118 0.4× 44 0.6× 10 0.3× 9 424
Alicia S. Martínez Argentina 10 64 0.2× 238 0.7× 256 1.0× 25 0.3× 17 0.4× 16 582
Christian Trolle Denmark 14 86 0.2× 283 0.9× 366 1.4× 51 0.7× 34 0.9× 33 620
Eddy N. de Boer Netherlands 8 54 0.1× 213 0.6× 202 0.8× 90 1.2× 10 0.3× 17 425
Katherine Neas New Zealand 12 158 0.4× 214 0.6× 103 0.4× 14 0.2× 15 0.4× 22 430
Marie‐Ange Delrue France 15 107 0.3× 291 0.9× 258 1.0× 22 0.3× 7 0.2× 30 590

Countries citing papers authored by Samantha Baxter

Since Specialization
Citations

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

Fields of papers citing papers by Samantha Baxter

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Samantha Baxter

This figure shows the co-authorship network connecting the top 25 collaborators of Samantha Baxter. A scholar is included among the top collaborators of Samantha Baxter 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 Samantha Baxter. Samantha Baxter 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.
Wilson, Michael W., Grace Tiao, Katherine R. Chao, et al.. (2025). Improved allele frequencies in gnomAD through local ancestry inference. Nature Communications. 16(1). 8734–8734. 1 indexed citations
2.
Chong, Jessica X., Seth Berger, Samantha Baxter, et al.. (2024). Considerations for reporting variants in novel candidate genes identified during clinical genomic testing. Genetics in Medicine. 26(10). 101199–101199. 3 indexed citations
3.
Kurtović-Kozarić, Amina, Moriel Singer‐Berk, Jordan C. Wood, et al.. (2024). An estimation of global genetic prevalence of PLA2G6-associated neurodegeneration. Orphanet Journal of Rare Diseases. 19(1). 388–388. 1 indexed citations
4.
Singer‐Berk, Moriel, Sanna Gudmundsson, Samantha Baxter, et al.. (2023). Advanced variant classification framework reduces the false positive rate of predicted loss-of-function variants in population sequencing data. The American Journal of Human Genetics. 110(9). 1496–1508. 7 indexed citations
5.
Huang, Zhengping, Samantha Baxter, Yuelong Huang, et al.. (2021). Comprehensive analysis of ADA2 genetic variants and estimation of carrier frequency driven by a function-based approach. Journal of Allergy and Clinical Immunology. 149(1). 379–387. 30 indexed citations
6.
Xiang, Jiale, Jiguang Peng, Samantha Baxter, & Zhiyu Peng. (2020). AutoPVS1: An automatic classification tool for PVS1 interpretation of null variants. Human Mutation. 41(9). 1488–1498. 36 indexed citations
7.
Arachchi, Harindra, Monica H. Wojcik, Julius O.B. Jacobsen, et al.. (2018). matchbox: An open-source tool for patient matching via the Matchmaker Exchange. Human Mutation. 39(12). 1827–1834. 7 indexed citations
8.
Volk, Lynn A., Lisa P. Newmark, Matthew Varugheese, et al.. (2016). Evaluation: A Qualitative Pilot Study of Novel Information Technology Infrastructure to Communicate Genetic Variant Updates. Applied Clinical Informatics. 7(2). 461–476. 9 indexed citations
9.
Pugh, Trevor J., Melissa Kelly, Sivakumar Gowrisankar, et al.. (2014). The landscape of genetic variation in dilated cardiomyopathy as surveyed by clinical DNA sequencing. Genetics in Medicine. 16(8). 601–608. 245 indexed citations
10.
Baxter, Samantha, et al.. (2014). Fos expression in monoaminergic cell groups in response to sociosexual interactions in male and female Japanese quail.. Behavioral Neuroscience. 128(1). 48–60. 7 indexed citations
11.
Lebo, Matthew S. & Samantha Baxter. (2014). New Molecular Genetic Tests in the Diagnosis of Heart Disease. Clinics in Laboratory Medicine. 34(1). 137–156. 5 indexed citations
12.
Wilcox, Allison R., Pamela M. Neri, Lynn A. Volk, et al.. (2013). A novel clinician interface to improve clinician access to up-to-date genetic results. Journal of the American Medical Informatics Association. 21(e1). e117–e121. 13 indexed citations
13.
Neri, Pamela M., Lynn A. Volk, Lisa P. Newmark, et al.. (2012). Usability of a novel clinician interface for genetic results. Journal of Biomedical Informatics. 45(5). 950–957. 22 indexed citations
14.
Lakdawala, Neal K., Birgit Funke, Samantha Baxter, et al.. (2012). Genetic Testing for Dilated Cardiomyopathy in Clinical Practice. Journal of Cardiac Failure. 18(4). 296–303. 116 indexed citations
15.
Aronson, Samuel, Eugene Clark, Matthew Varugheese, et al.. (2012). Communicating new knowledge on previously reported genetic variants. Genetics in Medicine. 14(8). 713–719. 66 indexed citations
16.
Jordan, Daniel M., Adam Kieżun, Samantha Baxter, et al.. (2011). Development and Validation of a Computational Method for Assessment of Missense Variants in Hypertrophic Cardiomyopathy. The American Journal of Human Genetics. 88(2). 183–192. 58 indexed citations
17.
Aronson, Samuel, Eugene Clark, Lawrence Babb, et al.. (2011). The GeneInsight suite: a platform to support laboratory and provider use of DNA-based genetic testing. Human Mutation. 32(5). 532–536. 53 indexed citations
18.
Caleshu, Colleen, Sharlene M. Day, Heidi L. Rehm, & Samantha Baxter. (2010). Use and interpretation of genetic tests in cardiovascular genetics. Heart. 96(20). 1669–1675. 29 indexed citations
19.
Skrzynia, Cécile, et al.. (2009). Genetic Counseling and Testing for Hypertrophic Cardiomyopathy: An Adult Perspective. Journal of Cardiovascular Translational Research. 2(4). 493–499. 7 indexed citations
20.
Shearman, C.P., Samantha Baxter, G.E. Morris, et al.. (2008). Level of Ex Vivo Interleukin 6 Expression in Human Peripheral Fat Compared with Other Tissues. European Journal of Vascular and Endovascular Surgery. 35(3). 314–319. 3 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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