Sarah E. Hemphill

1.1k citations
8 papers · 693 · 1 hit paper · h-index 8

Impact in

Papers in

Sarah E. Hemphill

8 papers receiving 691 citations

Sarah E. Hemphill's Hit Papers

Expert specification of the ACMG/AMP variant interpretation guidelines for genetic hearing loss 2018 · 356 citations
3560+2+5Years since publication100200300

Peers

Sarah E. Hemphill
Comparison fields: 5 of 59
  • Sensory Systems 309
  • Otorhinolaryngology 67
  • Neurology 63
  • Genetics 194
  • Molecular Biology 270
Replace Brandon J. Cushman with:
Brandon J. Cushman United States
Rebecca K. Siegert United States
Alex Chapin United States
Manou Sommen Belgium
Magdalena Beneyto Spain
Asma Ali Khan Pakistan
Cynthia C. Morton United States
Judith B. Kenyon United States
Lingyun Mei China
Clemer Abad United States
Sarah E. Hemphill relative to Brandon J. Cushman United States Brandon J. Cushman's profile →
Citations per field
00.5×1.6×
Brandon J. Cushman · 1×
Citations per year

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-authors

The 20 scholars most cited alongside Sarah E. Hemphill, 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 Sarah E. Hemphill Line = papers co-authored together Sarah E. Hemphill links everyone, so they are left out of the graph.

All Works

8 of 8 papers shown
#Work
1
Expert specification of the ACMG/AMP variant interpretation guidelines for genetic hearing loss
Hit paper breakdown →
2018356
2 201894
3 201971
4 201965
5 201938
6 202130
7 201820
8 201819

About Sarah E. Hemphill

Sarah E. Hemphill is a scholar working on Sensory Systems, Genetics, Cancer Research, Pathology and Forensic Medicine and Otorhinolaryngology, having authored 8 papers that have together received 693 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (4 papers), Cancer Genomics and Diagnostics (2 papers), Genomics and Phylogenetic Studies (2 papers), Hearing, Cochlea, Tinnitus, Genetics (2 papers), Genetic factors in colorectal cancer (2 papers), CRISPR and Genetic Engineering (1 paper), Ear Surgery and Otitis Media (1 paper) and Gene expression and cancer classification (1 paper). The work is most often cited by research in Sensory Systems (309 citations), Otorhinolaryngology (67 citations), Neurology (63 citations), Genetics (194 citations) and Molecular Biology (270 citations). Sarah E. Hemphill has collaborated with scholars based in United States, Israel and Japan. Frequent co-authors include Marina T. DiStefano, Heidi L. Rehm, Steven M. Harrison, Danielle R. Azzariti, Brandon J. Cushman, Karen Eilbeck, Annie Niehaus, Ozlem Senol-Cosar, Jennifer Goldstein and Jonathan S. Berg. Their work appears in journals such as Genetics in Medicine, Human Mutation and Journal of Molecular Diagnostics.

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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