Christine Oley
Impact in
- Developmental Biology top 2%
- Congenital limb and hand anomalies
- Genetics top 2%
- Genomics and Rare Diseases
- Ocular Disorders and Treatments
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
Papers in
-
- Congenital limb and hand anomalies 6
- Genetics 15
- Genomics and Rare Diseases 7
- Genomic variations and chromosomal abnormalities 6
- Ocular Disorders and Treatments 5
- Genetics and Neurodevelopmental Disorders 2
- Genetic Syndromes and Imprinting 2
- Co-authors
- Michael Baraitser (2 shared papers)David Ravine (2 shared papers)Georgia Chenevix‐Trench (2 shared papers)Carol Wicking (2 shared papers)Athel Hockey (2 shared papers)Eric Haan (2 shared papers)Timothy J. Sullivan (2 shared papers)Susan Shanley (1 shared paper)
- Journals
- The American Journal of Human Genetics (3 papers)Human Mutation (2 papers)European Journal of Human Genetics (2 papers)Ophthalmology (1 paper)Neuromuscular Disorders (1 paper)
- Partner nations
- United KingdomAustraliaBelgium
In The Last Decade
Christine Oley
26 papers receiving 1.7k citations
Peers
Comparison fields: 5 of 64
- Developmental Biology 106
- Genetics 940
- Oral Surgery 82
- Developmental Neuroscience 42
- Reproductive Medicine 104
Countries citing papers authored by Christine Oley
This map shows the geographic impact of Christine Oley'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 Christine Oley with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Christine Oley more than expected).
Fields of papers citing papers by Christine Oley
This network shows the impact of papers produced by Christine Oley. 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 Christine Oley. The network helps show where Christine Oley may publish in the future.
Co-authors
The 25 scholars most cited alongside Christine Oley, 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 26 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1994 | 277 | |
| 2 | 2003 | 203 | |
| 3 | 2008 | 198 | |
| 4 | 2009 | 161 | |
| 5 | 2011 | 142 | |
| 6 | 2006 | 123 | |
| 7 | 2003 | 113 | |
| 8 | 2005 | 109 | |
| 9 | 1988 | 106 | |
| 10 | Further localization of the gene for nevoid basal cell carcinoma syndrome (NBCCS) in 15 Australasian families: linkage and loss of heterozygosity. | 1993 | 78 |
| 11 | 2004 | 60 | |
| 12 | 2003 | 48 | |
| 13 | 2011 | 37 | |
| 14 | 2009 | 34 | |
| 15 | 2013 | 27 | |
| 16 | 1999 | 21 | |
| 17 | 2008 | 16 | |
| 18 | 2000 | 15 | |
| 19 | 1999 | 14 | |
| 20 | 1995 | 12 |
About Christine Oley
Christine Oley is a scholar working on Developmental Biology, Genetics, Molecular Biology, Developmental Neuroscience and Microbiology, having authored 26 papers that have together received 1.8k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (7 papers), Congenital limb and hand anomalies (6 papers), Genomic variations and chromosomal abnormalities (6 papers), Ocular Disorders and Treatments (5 papers), Genetics and Neurodevelopmental Disorders (2 papers), Hedgehog Signaling Pathway Studies (2 papers), Genetic Syndromes and Imprinting (2 papers) and Nasolacrimal Duct Obstruction Treatments (1 paper). The work is most often cited by research in Developmental Biology (106 citations), Genetics (940 citations), Oral Surgery (82 citations), Developmental Neuroscience (42 citations) and Reproductive Medicine (104 citations). Christine Oley has collaborated with scholars based in United Kingdom, Australia and Belgium. Frequent co-authors include Michael Baraitser, David Ravine, Georgia Chenevix‐Trench, Carol Wicking, Athel Hockey, Eric Haan, Timothy J. Sullivan, Susan Shanley, John WT Ratcliffe and Eamonn Richard Maher. Their work appears in journals such as The American Journal of Human Genetics, Human Mutation, European Journal of Human Genetics, Ophthalmology and Neuromuscular Disorders.
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.