Emma Bedoukian
Impact in
- Sensory Systems top 5%
- Hearing, Cochlea, Tinnitus, Genetics
- Developmental Biology top 10%
- Congenital limb and hand anomalies
Papers in
-
- Retinal Development and Disorders 6
- Genetics 10
- Genomics and Rare Diseases 5
- Genomic variations and chromosomal abnormalities 4
- Genetics and Neurodevelopmental Disorders 3
- Genetic Syndromes and Imprinting 2
- Co-authors
- Ian D. Krantz (9 shared papers)Matthew A. Deardorff (7 shared papers)Cara Skraban (11 shared papers)Xiaosong Zhu (5 shared papers)Tomás S. Alemán (9 shared papers)Bart P. Leroy (4 shared papers)Alisha Wilkens (3 shared papers)Emily Place (2 shared papers)
- Journals
- Genetics in Medicine (4 papers)Ophthalmic Genetics (2 papers)American Journal of Medical Genetics Part A (10 papers)The Journal of Pediatrics (1 paper)Proceedings of the National Academy of Sciences (1 paper)
- Partner nations
- United StatesBelgiumCanada
In The Last Decade
Emma Bedoukian
31 papers receiving 391 citations
Peers
Comparison fields: 5 of 59
- Sensory Systems 57
- Developmental Biology 24
- Otorhinolaryngology 23
- Ophthalmology 41
- Genetics 115
Countries citing papers authored by Emma Bedoukian
This map shows the geographic impact of Emma Bedoukian'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 Emma Bedoukian with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Emma Bedoukian more than expected).
Fields of papers citing papers by Emma Bedoukian
This network shows the impact of papers produced by Emma Bedoukian. 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 Emma Bedoukian. The network helps show where Emma Bedoukian may publish in the future.
Co-authors
The 25 scholars most cited alongside Emma Bedoukian, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 31 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2016 | 41 | |
| 2 | 2020 | 36 | |
| 3 | 2016 | 36 | |
| 4 | 2018 | 27 | |
| 5 | 2019 | 25 | |
| 6 | 2018 | 24 | |
| 7 | 2021 | 21 | |
| 8 | 2020 | 18 | |
| 9 | 2019 | 17 | |
| 10 | 2018 | 17 | |
| 11 | 2017 | 16 | |
| 12 | The importance of genetic testing as demonstrated by two cases of CACNA1F-associated retinal generation misdiagnosed as LCA. | 2017 | 16 |
| 13 | 2019 | 14 | |
| 14 | 2019 | 10 | |
| 15 | 2021 | 10 | |
| 16 | 2021 | 9 | |
| 17 | 2020 | 7 | |
| 18 | 2020 | 7 | |
| 19 | 2020 | 6 | |
| 20 | 2022 | 5 |
About Emma Bedoukian
Emma Bedoukian is a scholar working on Molecular Biology, Genetics, Cell Biology, Sensory Systems and Otorhinolaryngology, having authored 31 papers that have together received 393 indexed citations. Recurring topics across this work include Retinal Development and Disorders (6 papers), Genomics and Rare Diseases (5 papers), Genomic variations and chromosomal abnormalities (4 papers), Genetics and Neurodevelopmental Disorders (3 papers), Cellular transport and secretion (3 papers), Hearing, Cochlea, Tinnitus, Genetics (2 papers), Retinal Diseases and Treatments (2 papers) and Genetic Syndromes and Imprinting (2 papers). The work is most often cited by research in Sensory Systems (57 citations), Developmental Biology (24 citations), Otorhinolaryngology (23 citations), Ophthalmology (41 citations) and Genetics (115 citations). Emma Bedoukian has collaborated with scholars based in United States, Belgium and Canada. Frequent co-authors include Ian D. Krantz, Matthew A. Deardorff, Cara Skraban, Xiaosong Zhu, Tomás S. Alemán, Bart P. Leroy, Alisha Wilkens, Emily Place, Elaine H. Zackai and Eric A. Pierce. Their work appears in journals such as Genetics in Medicine, Ophthalmic Genetics, American Journal of Medical Genetics Part A, The Journal of Pediatrics and Proceedings of the National Academy of Sciences.
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.