Sarah E. Noon
Impact in
- Sensory Systems top 10%
- Hearing, Cochlea, Tinnitus, Genetics
Papers in
- Genetics 10
- Genetic Syndromes and Imprinting 4
- Genomic variations and chromosomal abnormalities 4
- Congenital Ear and Nasal Anomalies 2
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- Genomics and Chromatin Dynamics 3
- Congenital heart defects research 2
- Co-authors
- Ian D. Krantz (10 shared papers)Christian P. Schaaf (2 shared papers)Michael D. Fountain (1 shared paper)Robert C. Pedersen (1 shared paper)Weimin Bi (1 shared paper)Fan Xia (1 shared paper)Klementina Fon Tacer (1 shared paper)Ankita Patel (1 shared paper)
- Journals
- American Journal of Medical Genetics Part C Seminars in Medical Genetics (7 papers)Molecular Cell (1 paper)Clinical Cancer Research (1 paper)European Journal of Medical Genetics (1 paper)Otology & Neurotology (1 paper)
- Partner nations
- United StatesJapanFrance
In The Last Decade
Sarah E. Noon
14 papers receiving 376 citations
Peers
Comparison fields: 5 of 57
- Sensory Systems 34
- Otorhinolaryngology 17
- Oncology 91
- Genetics 87
- Molecular Biology 207
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 | 152 | |
| 2 | 2012 | 85 | |
| 3 | 2016 | 36 | |
| 4 | 2016 | 17 | |
| 5 | 2016 | 14 | |
| 6 | 2020 | 13 | |
| 7 | 2014 | 13 | |
| 8 | 2016 | 13 | |
| 9 | 2017 | 10 | |
| 10 | 2016 | 9 | |
| 11 | 2016 | 9 | |
| 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, Genetics and Pediatrics, Perinatology and Child Health, having authored 15 papers that have together received 380 indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (4 papers), Genomic variations and chromosomal abnormalities (4 papers), Genomics and Chromatin Dynamics (3 papers), Hearing, Cochlea, Tinnitus, Genetics (3 papers), Chromosomal and Genetic Variations (2 papers), Congenital heart defects research (2 papers), Prenatal Screening and Diagnostics (2 papers) and Congenital Ear and Nasal Anomalies (2 papers). The work is most often cited by research in Sensory Systems (34 citations), Otorhinolaryngology (17 citations), Oncology (91 citations), Genetics (87 citations) and Molecular Biology (207 citations). Sarah E. Noon has collaborated with scholars based in United States, Japan and France. Frequent co-authors include Ian D. Krantz, Christian P. Schaaf, Michael D. Fountain, Robert C. Pedersen, Weimin Bi, Fan Xia, Klementina Fon Tacer, Ankita Patel, Rocio Moran and Thomas M. Morgan. Their work appears in journals such as American Journal of Medical Genetics Part C Seminars in Medical Genetics, Molecular Cell, Clinical Cancer Research, European Journal of Medical Genetics and Otology & Neurotology.
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.