Elyse B. Mitchell
Impact in
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 10
- Genomic variations and chromosomal abnormalities 9
- Genomics and Rare Diseases 4
- Genetics and Neurodevelopmental Disorders 4
- Congenital Ear and Nasal Anomalies 1
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- Prenatal Screening and Diagnostics 3
- Co-authors
- Jennelle C. Hodge (2 shared papers)Michael E. Talkowski (1 shared paper)Matthew R. Stone (1 shared paper)Ryan L. Collins (1 shared paper)Harrison Brand (1 shared paper)Carrie Hanscom (1 shared paper)Jill A. Rosenfeld (1 shared paper)James F. Gusella (1 shared paper)
- Journals
- The American Journal of Human Genetics (2 papers)Nature Genetics (1 paper)Molecular Psychiatry (1 paper)Human Molecular Genetics (1 paper)European Journal of Human Genetics (1 paper)
- Partner nations
- United StatesNetherlandsUnited Kingdom
In The Last Decade
Elyse B. Mitchell
11 papers receiving 574 citations
Peers
Comparison fields: 5 of 60
- Genetics 418
- Pediatrics, Perinatology and Child Health 79
- Molecular Biology 276
- Cognitive Neuroscience 72
- Cellular and Molecular Neuroscience 51
Countries citing papers authored by Elyse B. Mitchell
This map shows the geographic impact of Elyse B. Mitchell'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 Elyse B. Mitchell with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Elyse B. Mitchell more than expected).
Fields of papers citing papers by Elyse B. Mitchell
This network shows the impact of papers produced by Elyse B. Mitchell. 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 Elyse B. Mitchell. The network helps show where Elyse B. Mitchell may publish in the future.
Co-authors
The 25 scholars most cited alongside Elyse B. Mitchell, 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 | 2016 | 240 | |
| 2 | 2013 | 127 | |
| 3 | 2013 | 59 | |
| 4 | 2013 | 58 | |
| 5 | 2015 | 49 | |
| 6 | 2015 | 35 | |
| 7 | 2017 | 28 | |
| 8 | 2014 | 13 | |
| 9 | 2012 | 11 | |
| 10 | 2016 | 6 | |
| 11 | Ready reference to common segmental aneusomies by syndromic names, major features and chromosomal locations. | 2008 | 1 |
| 12 | 2016 | 0 |
About Elyse B. Mitchell
Elyse B. Mitchell is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Plant Science, Molecular Biology and Immunology and Allergy, having authored 12 papers that have together received 627 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (9 papers), Genomics and Rare Diseases (4 papers), Genetics and Neurodevelopmental Disorders (4 papers), Chromosomal and Genetic Variations (3 papers), Prenatal Screening and Diagnostics (3 papers), Congenital heart defects research (2 papers), Congenital Ear and Nasal Anomalies (1 paper) and interferon and immune responses (1 paper). The work is most often cited by research in Genetics (418 citations), Pediatrics, Perinatology and Child Health (79 citations), Molecular Biology (276 citations), Cognitive Neuroscience (72 citations) and Cellular and Molecular Neuroscience (51 citations). Elyse B. Mitchell has collaborated with scholars based in United States, Netherlands and United Kingdom. Frequent co-authors include Jennelle C. Hodge, Michael E. Talkowski, Matthew R. Stone, Ryan L. Collins, Harrison Brand, Carrie Hanscom, Jill A. Rosenfeld, James F. Gusella, Stephan Sanders and Vamsee K. Pillalamarri. Their work appears in journals such as The American Journal of Human Genetics, Nature Genetics, Molecular Psychiatry, Human Molecular Genetics and European Journal of Human Genetics.
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.