Andrew Colley
Impact in
Papers in
- Genetics 11
- Genomic variations and chromosomal abnormalities 3
- Connective tissue disorders research 3
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- Ion channel regulation and function 2
- Co-authors
- Dian Donnai (5 shared papers)D. Gareth Evans (2 shared papers)R Harris (2 shared papers)Eric Haan (2 shared papers)William G. Newman (1 shared paper)Emily P. McCann (1 shared paper)Dorothy Trump (1 shared paper)Andrew J. Wallace (1 shared paper)
- Journals
- Journal of Medical Genetics (9 papers)Clinical Genetics (2 papers)Human Genetics (2 papers)The Lancet (1 paper)International Journal of Inclusive Education (1 paper)
- Partner nations
- AustraliaUnited KingdomSouth Africa
In The Last Decade
Andrew Colley
27 papers receiving 871 citations
Peers
Comparison fields: 5 of 75
- Neurology 250
- Genetics 319
- Safety Research 49
- Molecular Biology 363
- Developmental Neuroscience 20
Countries citing papers authored by Andrew Colley
This map shows the geographic impact of Andrew Colley'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 Andrew Colley with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Andrew Colley more than expected).
Fields of papers citing papers by Andrew Colley
This network shows the impact of papers produced by Andrew Colley. 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 Andrew Colley. The network helps show where Andrew Colley may publish in the future.
Co-authors
The 25 scholars most cited alongside Andrew Colley, 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 27 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2008 | 136 | |
| 2 | 1996 | 83 | |
| 3 | 1993 | 75 | |
| 4 | The gene for Treacher Collins syndrome maps to the long arm of chromosome 5. | 1991 | 66 |
| 5 | Tandem duplication within a neurofibromatosis type 1 (NF1) gene exon in a family with features of Watson syndrome and Noonan syndrome. | 1993 | 65 |
| 6 | 1996 | 62 | |
| 7 | 1992 | 62 | |
| 8 | 1999 | 56 | |
| 9 | 1990 | 47 | |
| 10 | 2017 | 40 | |
| 11 | 1996 | 25 | |
| 12 | Sport participation in middle childhood: association with styles of play and parental participation. | 1992 | 24 |
| 13 | 2013 | 22 | |
| 14 | 1991 | 20 | |
| 15 | 1999 | 20 | |
| 16 | 2005 | 17 | |
| 17 | 2018 | 16 | |
| 18 | 1997 | 15 | |
| 19 | 1992 | 14 | |
| 20 | 2007 | 12 |
About Andrew Colley
Andrew Colley is a scholar working on Genetics, Molecular Biology, Neurology, Safety Research and Cellular and Molecular Neuroscience, having authored 27 papers that have together received 916 indexed citations. Recurring topics across this work include Neurofibromatosis and Schwannoma Cases (4 papers), Disability Education and Employment (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Connective tissue disorders research (3 papers), Genetic Neurodegenerative Diseases (2 papers), Neurological disorders and treatments (2 papers), Ion channel regulation and function (2 papers) and Family and Disability Support Research (2 papers). The work is most often cited by research in Neurology (250 citations), Genetics (319 citations), Safety Research (49 citations), Molecular Biology (363 citations) and Developmental Neuroscience (20 citations). Andrew Colley has collaborated with scholars based in Australia, United Kingdom and South Africa. Frequent co-authors include Dian Donnai, D. Gareth Evans, R Harris, Eric Haan, William G. Newman, Emily P. McCann, Dorothy Trump, Andrew J. Wallace, Trine Prescott and Kristin Hadfield. Their work appears in journals such as Journal of Medical Genetics, Clinical Genetics, Human Genetics, The Lancet and International Journal of Inclusive Education.
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.