Jason Carmichael
Impact in
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- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
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- Congenital heart defects research
- RNA modifications and cancer
- Ubiquitin and proteasome pathways
Papers in
- Genetics 5
- Genomics and Rare Diseases 3
- Genetics and Neurodevelopmental Disorders 3
- Genetic and Kidney Cyst Diseases 1
- BRCA gene mutations in cancer 1
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- Congenital heart defects research 1
- Peroxisome Proliferator-Activated Receptors 1
- Co-authors
- Megan T. Cho (2 shared papers)Kyle Retterer (2 shared papers)Natalie Hauser (1 shared paper)Linshan Shang (1 shared paper)Katrina Haude (1 shared paper)Yvonne W. Wu (1 shared paper)Kristin G. Monaghan (1 shared paper)Donald Petrey (1 shared paper)
- Journals
- Neurogenetics (1 paper)American Journal of Medical Genetics Part A (4 papers)Journal of Genetic Counseling (1 paper)
- Partner nations
- United StatesMexicoIsrael
In The Last Decade
Jason Carmichael
6 papers receiving 101 citations
Peers
Comparison fields: 5 of 42
- Genetics 58
- Molecular Biology 61
- Cell Biology 14
- Health Informatics 1
- Cognitive Neuroscience 11
Countries citing papers authored by Jason Carmichael
This map shows the geographic impact of Jason Carmichael'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 Jason Carmichael with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jason Carmichael more than expected).
Fields of papers citing papers by Jason Carmichael
This network shows the impact of papers produced by Jason Carmichael. 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 Jason Carmichael. The network helps show where Jason Carmichael may publish in the future.
Co-authors
The 25 scholars most cited alongside Jason Carmichael, 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 | 52 | |
| 2 | 2018 | 23 | |
| 3 | 2021 | 12 | |
| 4 | 2018 | 7 | |
| 5 | 2024 | 5 | |
| 6 | 2023 | 4 |
About Jason Carmichael
Jason Carmichael is a scholar working on Genetics, Molecular Biology, Cognitive Neuroscience, Oncology and Clinical Biochemistry, having authored 6 papers that have together received 103 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (3 papers), Genetics and Neurodevelopmental Disorders (3 papers), Congenital heart defects research (1 paper), Peroxisome Proliferator-Activated Receptors (1 paper), Metabolism and Genetic Disorders (1 paper), Genetic and Kidney Cyst Diseases (1 paper), Epilepsy research and treatment (1 paper) and BRCA gene mutations in cancer (1 paper). The work is most often cited by research in Genetics (58 citations), Molecular Biology (61 citations), Cell Biology (14 citations), Health Informatics (1 citation) and Cognitive Neuroscience (11 citations). Jason Carmichael has collaborated with scholars based in United States, Mexico and Israel. Frequent co-authors include Megan T. Cho, Kyle Retterer, Natalie Hauser, Linshan Shang, Katrina Haude, Yvonne W. Wu, Kristin G. Monaghan, Donald Petrey, Chin-To Fong and Natasha Shur. Their work appears in journals such as Neurogenetics, American Journal of Medical Genetics Part A and Journal of Genetic Counseling.
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.