Sarah E. Hemphill

1.1k total citations
4 papers, 113 citations indexed

About

Sarah E. Hemphill is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, Sarah E. Hemphill has authored 4 papers receiving a total of 113 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 2 papers in Genetics and 1 paper in Pathology and Forensic Medicine. Recurrent topics in Sarah E. Hemphill's work include Genomics and Rare Diseases (2 papers), Genomics and Phylogenetic Studies (2 papers) and Biochemical and Molecular Research (1 paper). Sarah E. Hemphill is often cited by papers focused on Genomics and Rare Diseases (2 papers), Genomics and Phylogenetic Studies (2 papers) and Biochemical and Molecular Research (1 paper). Sarah E. Hemphill collaborates with scholars based in United States, Switzerland and United Arab Emirates. Sarah E. Hemphill's co-authors include Heidi L. Rehm, Brandon J. Cushman, Marina T. DiStefano, Karen Eilbeck, Steven M. Harrison, Danielle R. Azzariti, Jennifer Goldstein, Courtney Thaxton, Jonathan S. Berg and Jennifer McGlaughon and has published in prestigious journals such as Human Mutation, Journal of Molecular Diagnostics and Molecular Case Studies.

In The Last Decade

Sarah E. Hemphill

4 papers receiving 112 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Sarah E. Hemphill United States	4	58	56	25	12	8	4	113
Fabio Sirchia Italy	9	103 1.8×	108 1.9×	16 0.6×	8 0.7×	6 0.8×	35	208
G. C. Chan United Kingdom	2	87 1.5×	129 2.3×	35 1.4×	18 1.5×	6 0.8×	3	193
Kelly Radtke United States	5	71 1.2×	133 2.4×	21 0.8×	25 2.1×	6 0.8×	8	191
Yoko Hiraki Japan	10	97 1.7×	131 2.3×	11 0.4×	13 1.1×	5 0.6×	17	219
Cristina Skrypnyk Bahrain	8	95 1.6×	28 0.5×	48 1.9×	7 0.6×	9 1.1×	17	155
Yanling Teng China	9	130 2.2×	69 1.2×	12 0.5×	7 0.6×	14 1.8×	33	195
Erin Torti United States	7	101 1.7×	51 0.9×	16 0.6×	4 0.3×	7 0.9×	14	159
Julie Kaylor United States	9	103 1.8×	104 1.9×	8 0.3×	11 0.9×	8 1.0×	11	206
Newell Belnap United States	7	84 1.4×	49 0.9×	13 0.5×	6 0.5×	7 0.9×	12	126

Countries citing papers authored by Sarah E. Hemphill

Since Specialization

Citations

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

Fields of papers citing papers by Sarah E. Hemphill

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sarah E. Hemphill. 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 Sarah E. Hemphill. The network helps show where Sarah E. Hemphill may publish in the future.

Co-authorship network of co-authors of Sarah E. Hemphill

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

All Works

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4 of 4 papers shown

1.

Grant, Andrew R., Sarah E. Hemphill, Lisa M. Vincent, & Heidi L. Rehm. (2018). Reclassification of the BRAF p.Ile208Val variant by case-level data sharing. Molecular Case Studies. 4(5). a002675–a002675. 3 indexed citations

2.

DiStefano, Marina T., Sarah E. Hemphill, Brandon J. Cushman, et al.. (2018). Curating Clinically Relevant Transcripts for the Interpretation of Sequence Variants. Journal of Molecular Diagnostics. 20(6). 789–801. 18 indexed citations

3.

McGlaughon, Jennifer, Jennifer Goldstein, Courtney Thaxton, Sarah E. Hemphill, & Jonathan S. Berg. (2018). The progression of the ClinGen gene clinical validity classification over time. Human Mutation. 39(11). 1494–1504. 13 indexed citations

4.

Hemphill, Sarah E., Brandon J. Cushman, Marina T. DiStefano, et al.. (2018). ClinVar Miner: Demonstrating utility of a Web-based tool for viewing and filtering ClinVar data. Human Mutation. 39(8). 1051–1060. 79 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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