Shane McKee
Impact in
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Pathology and Forensic Medicine top 10%
- Genetic factors in colorectal cancer
Papers in
- Genetics 21
- Genomic variations and chromosomal abnormalities 11
- Genomics and Rare Diseases 6
- Genetics and Neurodevelopmental Disorders 4
- Congenital Ear and Nasal Anomalies 3
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- Inflammasome and immune disorders 3
- Bioinformatics and Genomic Networks 3
- Co-authors
- Eamonn R. Maher (2 shared papers)D. Gareth Evans (1 shared paper)M. Helen Rajpar (1 shared paper)Janusz Jankowski (1 shared paper)D. S. A. Sanders (1 shared paper)Trevor Cole (1 shared paper)Frances M. Richards (1 shared paper)C. McKeown (1 shared paper)
- Journals
- Clinical Genetics (6 papers)The American Journal of Human Genetics (3 papers)Genes (2 papers)Orphanet Journal of Rare Diseases (2 papers)Epilepsia (1 paper)
- Partner nations
- United KingdomUnited StatesNetherlands
In The Last Decade
Shane McKee
44 papers receiving 1.1k citations
Peers
Comparison fields: 5 of 89
- Genetics 452
- Pathology and Forensic Medicine 146
- Developmental Neuroscience 32
- Molecular Biology 530
- Cancer Research 106
Countries citing papers authored by Shane McKee
This map shows the geographic impact of Shane McKee'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 Shane McKee with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Shane McKee more than expected).
Fields of papers citing papers by Shane McKee
This network shows the impact of papers produced by Shane McKee. 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 Shane McKee. The network helps show where Shane McKee may publish in the future.
Co-authors
The 25 scholars most cited alongside Shane McKee, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 44 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1999 | 262 | |
| 2 | 2007 | 127 | |
| 3 | 2014 | 93 | |
| 4 | 2000 | 92 | |
| 5 | 2015 | 85 | |
| 6 | 2004 | 48 | |
| 7 | 1998 | 40 | |
| 8 | 2012 | 40 | |
| 9 | 2017 | 39 | |
| 10 | 2020 | 37 | |
| 11 | 2012 | 35 | |
| 12 | 2019 | 30 | |
| 13 | 2019 | 28 | |
| 14 | 2019 | 26 | |
| 15 | 2011 | 20 | |
| 16 | 2008 | 18 | |
| 17 | 2012 | 18 | |
| 18 | 2013 | 18 | |
| 19 | 2016 | 15 | |
| 20 | 2014 | 15 |
About Shane McKee
Shane McKee is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Immunology and Surgery, having authored 44 papers that have together received 1.2k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (11 papers), Genomics and Rare Diseases (6 papers), Prenatal Screening and Diagnostics (5 papers), Genetics and Neurodevelopmental Disorders (4 papers), Fetal and Pediatric Neurological Disorders (3 papers), Inflammasome and immune disorders (3 papers), Congenital Ear and Nasal Anomalies (3 papers) and Bioinformatics and Genomic Networks (3 papers). The work is most often cited by research in Genetics (452 citations), Pathology and Forensic Medicine (146 citations), Developmental Neuroscience (32 citations), Molecular Biology (530 citations) and Cancer Research (106 citations). Shane McKee has collaborated with scholars based in United Kingdom, United States and Netherlands. Frequent co-authors include Eamonn R. Maher, D. Gareth Evans, M. Helen Rajpar, Janusz Jankowski, D. S. A. Sanders, Trevor Cole, Frances M. Richards, C. McKeown, David Fitzpatrick and Nicholas Nelson. Their work appears in journals such as Clinical Genetics, The American Journal of Human Genetics, Genes, Orphanet Journal of Rare Diseases and Epilepsia.
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.