Casie A. Genetti
- Genetics top 5%
- Genomics and Rare Diseases 16
- Genomic variations and chromosomal abnormalities 8
- Genetics and Neurodevelopmental Disorders 6
- Clinical Biochemistry top 5%
- Metabolism and Genetic Disorders 5
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- Cancer Genomics and Diagnostics 3
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- Congenital heart defects research 3
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- Cardiomyopathy and Myosin Studies 4
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- Neonatal Respiratory Health Research 3
- Co-authors
- Pankaj B. AgrawalAlan H. BeggsTimothy W. YuMonica H. WojcikTalia S. SchwartzRichard B. ParadRobert C. GreenIngrid A. Holm
- Journals
- PEDIATRICS (1 paper)The American Journal of Human Genetics (1 paper)PLoS Genetics (1 paper)
- Partner nations
- United StatesHong KongNetherlands
In The Last Decade
Casie A. Genetti
34 papers receiving 679 citations
Peers
Comparison fields: 5 of 69
- Genetics 432
- Clinical Biochemistry 101
- Pediatrics, Perinatology and Child Health 154
- Cancer Research 68
- Molecular Biology 274
Countries citing papers authored by Casie A. Genetti
This map shows the geographic impact of Casie A. Genetti'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 Casie A. Genetti with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Casie A. Genetti more than expected).
Fields of papers citing papers by Casie A. Genetti
This network shows the impact of papers produced by Casie A. Genetti. 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 Casie A. Genetti. The network helps show where Casie A. Genetti may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Casie A. Genetti, 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 | 2025 | 0 | |
| 2 | 2025 | 0 | |
| 3 | 2024 | 0 | |
| 4 | 2024 | 4 | |
| 5 | 2024 | 3 | |
| 6 | 2023 | 2 | |
| 7 | 2023 | 5 | |
| 8 | 2023 | 25 | |
| 9 | 2023 | 4 | |
| 10 | 2023 | 1 | |
| 11 | 2021 | 3 | |
| 12 | 2019 | 12 | |
| 13 | 2019 | 25 | |
| 14 | 2019 | 41 | |
| 15 | 2018 | 52 | |
| 16 | 2018 | 62 | |
| 17 | 2018 | 4 | |
| 18 | 2017 | 22 | |
| 19 | 2017 | 7 | |
| 20 | 2016 | 33 |
About Casie A. Genetti
Casie A. Genetti is a scholar working on Genetics, Clinical Biochemistry and Genetics, having authored 37 papers that have together received 689 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (16 papers), Genomic variations and chromosomal abnormalities (8 papers), Genetics and Neurodevelopmental Disorders (6 papers), Metabolism and Genetic Disorders (5 papers), Cardiomyopathy and Myosin Studies (4 papers), Congenital heart defects research (3 papers), Cancer Genomics and Diagnostics (3 papers) and Neonatal Respiratory Health Research (3 papers). The work is most often cited by research in Genetics (432 citations), Clinical Biochemistry (101 citations) and Pediatrics, Perinatology and Child Health (154 citations). Casie A. Genetti has collaborated with scholars based in United States, Hong Kong and Netherlands. Frequent co-authors include Pankaj B. Agrawal, Alan H. Beggs, Timothy W. Yu, Monica H. Wojcik, Talia S. Schwartz, Richard B. Parad, Robert C. Green, Ingrid A. Holm, Amy L. McGuire and Grace E. VanNoy. Their work appears in journals such as PEDIATRICS, The American Journal of Human Genetics and PLoS 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.