Julie Kaylor
- Co-authors
- Yuri A. ZárateElizabeth A. SellarsCharles SaileyAnne SlavotinekHeather PierceGabriela SchmajukLakshmi MehtaDina Schneidman‐Duhovny
- Topics
- Genomic variations and chromosomal abnormalities (3 papers)Genomics and Rare Diseases (2 papers)Genetics and Neurodevelopmental Disorders (2 papers)
- Journals
- Journal of Clinical OncologyThe American Journal of Human GeneticsCytogenetic and Genome Research
- Partner nations
- United StatesIndiaColombia
In The Last Decade
Julie Kaylor
10 papers receiving 192 citations
Peers
Comparison fields: 5 of 51
- Genetics 104
- Molecular Biology 103
- Pediatrics, Perinatology and Child Health 35
- Cell Biology 23
- Nephrology 21
Countries citing papers authored by Julie Kaylor
This map shows the geographic impact of Julie Kaylor'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 Julie Kaylor with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Julie Kaylor more than expected).
Fields of papers citing papers by Julie Kaylor
This network shows the impact of papers produced by Julie Kaylor. 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 Julie Kaylor. The network helps show where Julie Kaylor may publish in the future.
Co-authorship network of co-authors of Julie Kaylor
This figure shows the co-authorship network connecting the top 25 collaborators of Julie Kaylor. A scholar is included among the top collaborators of Julie Kaylor based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Julie Kaylor. Julie Kaylor is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 0 | |
| 2 | 9 | |
| 3 | 26 | |
| 4 | SATB2-Associated Syndrome | 4 |
| 5 | 13 | |
| 6 | 15 | |
| 7 | 16 | |
| 8 | 25 | |
| 9 | 20 | |
| 10 | 59 | |
| 11 | 19 |
About Julie Kaylor
Julie Kaylor is a scholar working on Genetics, Developmental Neuroscience and Pediatrics, Perinatology and Child Health, having authored 11 papers that have together received 206 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (3 papers), Genomics and Rare Diseases (2 papers) and Genetics and Neurodevelopmental Disorders (2 papers). The work is most often cited by research in Developmental Neuroscience (16 citations), Genetics (104 citations) and Nephrology (21 citations). Julie Kaylor has collaborated with scholars based in United States, India and Colombia. Frequent co-authors include Yuri A. Zárate, Elizabeth A. Sellars, Charles Sailey, Anne Slavotinek, Heather Pierce, Gabriela Schmajuk, Lakshmi Mehta, Dina Schneidman‐Duhovny, Fadi Salem and Stephanie J. DeWard. Their work appears in journals such as Journal of Clinical Oncology, The American Journal of Human Genetics and Cytogenetic and Genome Research.
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.