Kory Keller
Impact in
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- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetic Syndromes and Imprinting
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- Autism Spectrum Disorder Research
Papers in
- Genetics 7
- Genetics and Neurodevelopmental Disorders 5
- Genomic variations and chromosomal abnormalities 4
- Genomics and Rare Diseases 2
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- Congenital heart defects research 3
- Renal and related cancers 1
- Co-authors
- Brian A. Gray (2 shared papers)Roberto T. Zori (1 shared paper)Heather J. Stalker (1 shared paper)Urvashi Surti (1 shared paper)Beth S. Torchia (1 shared paper)Christine Erdie-Lalena (1 shared paper)Jonathan Zonana (1 shared paper)Wendy S. Meschino (1 shared paper)
- Journals
- Genetics in Medicine (1 paper)Human Genetics (1 paper)Developmental Medicine & Child Neurology (1 paper)American Journal of Medical Genetics Part A (4 papers)
- Partner nations
- United StatesNetherlandsGermany
In The Last Decade
Kory Keller
7 papers receiving 154 citations
Peers
Comparison fields: 5 of 35
- Genetics 129
- Cognitive Neuroscience 34
- Developmental Neuroscience 7
- Reproductive Medicine 13
- Molecular Biology 102
Countries citing papers authored by Kory Keller
This map shows the geographic impact of Kory Keller'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 Kory Keller with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Kory Keller more than expected).
Fields of papers citing papers by Kory Keller
This network shows the impact of papers produced by Kory Keller. 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 Kory Keller. The network helps show where Kory Keller may publish in the future.
Co-authors
The 25 scholars most cited alongside Kory Keller, 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 | 2009 | 55 | |
| 2 | 2007 | 38 | |
| 3 | 2002 | 19 | |
| 4 | 2020 | 16 | |
| 5 | 2002 | 15 | |
| 6 | 2018 | 10 | |
| 7 | 2018 | 7 |
About Kory Keller
Kory Keller is a scholar working on Genetics, Molecular Biology, Neurology, Pediatrics, Perinatology and Child Health and Cognitive Neuroscience, having authored 7 papers that have together received 160 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (5 papers), Genomic variations and chromosomal abnormalities (4 papers), Congenital heart defects research (3 papers), Genomics and Rare Diseases (2 papers), Williams Syndrome Research (1 paper), Chromosomal and Genetic Variations (1 paper), Neurofibromatosis and Schwannoma Cases (1 paper) and Renal and related cancers (1 paper). The work is most often cited by research in Genetics (129 citations), Cognitive Neuroscience (34 citations), Developmental Neuroscience (7 citations), Reproductive Medicine (13 citations) and Molecular Biology (102 citations). Kory Keller has collaborated with scholars based in United States, Netherlands and Germany. Frequent co-authors include Brian A. Gray, Roberto T. Zori, Heather J. Stalker, Urvashi Surti, Beth S. Torchia, Christine Erdie-Lalena, Jonathan Zonana, Wendy S. Meschino, Heidi Thiese and Bassem A. Bejjani. Their work appears in journals such as Genetics in Medicine, Human Genetics, Developmental Medicine & Child Neurology and American Journal of Medical Genetics Part A.
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.