Kelly E. Jackson
Impact in
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Ophthalmology top 10%
Papers in
- Genetics 8
- Genomic variations and chromosomal abnormalities 5
- BRCA gene mutations in cancer 2
- Genomics and Rare Diseases 2
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- Prenatal Screening and Diagnostics 4
- Neonatal Health and Biochemistry 2
- Co-authors
- Corry M.R. Weemaes (1 shared paper)Melanie Ehrlich (1 shared paper)Alexander Asamoah (3 shared papers)Gordon C. Gowans (3 shared papers)Pamela Brock (2 shared papers)Bassem A. Bejjani (2 shared papers)Lisa G. Shaffer (2 shared papers)Līvija Medne (1 shared paper)
- Journals
- Genetics in Medicine (2 papers)Nature Genetics (1 paper)Ophthalmology (1 paper)Molecular Genetics and Metabolism (1 paper)Orphanet Journal of Rare Diseases (1 paper)
- Partner nations
- United StatesItalyNetherlands
In The Last Decade
Kelly E. Jackson
15 papers receiving 365 citations
Peers
Comparison fields: 5 of 61
- Genetics 211
- Ophthalmology 30
- Genetics 33
- Molecular Biology 204
- Pediatrics, Perinatology and Child Health 50
Countries citing papers authored by Kelly E. Jackson
This map shows the geographic impact of Kelly E. Jackson'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 Kelly E. Jackson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Kelly E. Jackson more than expected).
Fields of papers citing papers by Kelly E. Jackson
This network shows the impact of papers produced by Kelly E. Jackson. 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 Kelly E. Jackson. The network helps show where Kelly E. Jackson may publish in the future.
Co-authors
The 25 scholars most cited alongside Kelly E. Jackson, 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 | 2007 | 140 | |
| 2 | 2006 | 94 | |
| 3 | 1995 | 50 | |
| 4 | 2019 | 14 | |
| 5 | 2003 | 13 | |
| 6 | 2002 | 13 | |
| 7 | 2022 | 13 | |
| 8 | 2012 | 11 | |
| 9 | 2021 | 7 | |
| 10 | Trisomy 1q43 syndrome: a consistent phenotype with macrocephaly, characteristic face, developmental delay and cardiac anomalies. | 2004 | 6 |
| 11 | 2009 | 5 | |
| 12 | 2021 | 4 | |
| 13 | 2000 | 3 | |
| 14 | 2008 | 1 | |
| 15 | 2004 | 1 |
About Kelly E. Jackson
Kelly E. Jackson is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Clinical Biochemistry and Pathology and Forensic Medicine, having authored 15 papers that have together received 375 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (5 papers), Prenatal Screening and Diagnostics (4 papers), Metabolism and Genetic Disorders (3 papers), BRCA gene mutations in cancer (2 papers), Chromosomal and Genetic Variations (2 papers), Neurological diseases and metabolism (2 papers), Neonatal Health and Biochemistry (2 papers) and Genomics and Rare Diseases (2 papers). The work is most often cited by research in Genetics (211 citations), Ophthalmology (30 citations), Genetics (33 citations), Molecular Biology (204 citations) and Pediatrics, Perinatology and Child Health (50 citations). Kelly E. Jackson has collaborated with scholars based in United States, Italy and Netherlands. Frequent co-authors include Corry M.R. Weemaes, Melanie Ehrlich, Alexander Asamoah, Gordon C. Gowans, Pamela Brock, Bassem A. Bejjani, Lisa G. Shaffer, Līvija Medne, Urvashi Surti and Peggy S. Eis. Their work appears in journals such as Genetics in Medicine, Nature Genetics, Ophthalmology, Molecular Genetics and Metabolism and Orphanet Journal of Rare Diseases.
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.