Sarah E. Noon
Impact in
- Sensory Systems top 10%
- Hearing, Cochlea, Tinnitus, Genetics
- Otorhinolaryngology top 10%
Papers in
- Genetics 10
- Genomic variations and chromosomal abnormalities 4
- Genetic Syndromes and Imprinting 4
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- Genomics and Chromatin Dynamics 3
- Congenital heart defects research 2
- Co-authors
- Ian D. Krantz (10 shared papers)Bertrand Isidor (1 shared paper)Michael D. Fountain (1 shared paper)Jean P. Pfotenhauer (1 shared paper)Patrick Ryan Potts (1 shared paper)Thomas M. Morgan (1 shared paper)Rocio Moran (1 shared paper)Christian P. Schaaf (2 shared papers)
- Journals
- American Journal of Medical Genetics Part C Seminars in Medical Genetics (7 papers)Clinical Cancer Research (1 paper)Otology & Neurotology (1 paper)European Journal of Medical Genetics (1 paper)Molecular Cell (1 paper)
- Partner nations
- United StatesJapanFrance
In The Last Decade
Sarah E. Noon
14 papers receiving 367 citations
Peers
Comparison fields: 5 of 64
- Sensory Systems 37
- Otorhinolaryngology 25
- Neurology 29
- Oncology 95
- Molecular Biology 226
Countries citing papers authored by Sarah E. Noon
This map shows the geographic impact of Sarah E. Noon'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. Noon 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. Noon more than expected).
Fields of papers citing papers by Sarah E. Noon
This network shows the impact of papers produced by Sarah E. Noon. 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. Noon. The network helps show where Sarah E. Noon may publish in the future.
Co-authors
The 25 scholars most cited alongside Sarah E. Noon, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2015 | 149 | |
| 2 | 2012 | 85 | |
| 3 | 2016 | 36 | |
| 4 | 2016 | 17 | |
| 5 | 2016 | 14 | |
| 6 | 2014 | 12 | |
| 7 | 2016 | 12 | |
| 8 | 2020 | 12 | |
| 9 | 2017 | 10 | |
| 10 | 2016 | 9 | |
| 11 | 2016 | 8 | |
| 12 | 2016 | 4 | |
| 13 | 2015 | 3 | |
| 14 | 2016 | 2 | |
| 15 | 2016 | 0 |
About Sarah E. Noon
Sarah E. Noon is a scholar working on Genetics, Molecular Biology, Sensory Systems, Otorhinolaryngology and Genetics, having authored 15 papers that have together received 373 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (4 papers), Genetic Syndromes and Imprinting (4 papers), Genomics and Chromatin Dynamics (3 papers), Hearing, Cochlea, Tinnitus, Genetics (3 papers), Prenatal Screening and Diagnostics (2 papers), Chromosomal and Genetic Variations (2 papers), Ear Surgery and Otitis Media (2 papers) and Congenital heart defects research (2 papers). The work is most often cited by research in Sensory Systems (37 citations), Otorhinolaryngology (25 citations), Neurology (29 citations), Oncology (95 citations) and Molecular Biology (226 citations). Sarah E. Noon has collaborated with scholars based in United States, Japan and France. Frequent co-authors include Ian D. Krantz, Bertrand Isidor, Michael D. Fountain, Jean P. Pfotenhauer, Patrick Ryan Potts, Thomas M. Morgan, Rocio Moran, Christian P. Schaaf, Robert C. Pedersen and Alisha Wilkens. Their work appears in journals such as American Journal of Medical Genetics Part C Seminars in Medical Genetics, Clinical Cancer Research, Otology & Neurotology, European Journal of Medical Genetics and Molecular Cell.
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.