Christine Oley

2.3k total citations
21 papers, 954 citations indexed

About

Christine Oley is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, Christine Oley has authored 21 papers receiving a total of 954 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 9 papers in Genetics and 3 papers in Pathology and Forensic Medicine. Recurrent topics in Christine Oley's work include Genetic Syndromes and Imprinting (4 papers), Hedgehog Signaling Pathway Studies (3 papers) and Sexual Differentiation and Disorders (2 papers). Christine Oley is often cited by papers focused on Genetic Syndromes and Imprinting (4 papers), Hedgehog Signaling Pathway Studies (3 papers) and Sexual Differentiation and Disorders (2 papers). Christine Oley collaborates with scholars based in United Kingdom, Australia and United States. Christine Oley's co-authors include M Baraitser, David Ravine, Eric Haan, Georgia Chenevix‐Trench, Carol Wicking, Athel Hockey, Nicholas G. Martin, John W. Ratcliffe, Susan Shanley and Timothy J. Sullivan and has published in prestigious journals such as Ophthalmology, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

Christine Oley

20 papers receiving 914 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Christine Oley United Kingdom 13 572 431 192 191 154 21 954
R J Gorlin Australia 5 667 1.2× 957 2.2× 127 0.7× 65 0.3× 225 1.5× 6 1.7k
Gorlin Rj United States 14 413 0.7× 293 0.7× 91 0.5× 83 0.4× 309 2.0× 42 924
Yangzhu Du United States 13 611 1.1× 366 0.8× 54 0.3× 23 0.1× 64 0.4× 20 979
Sevim Balcı Türkiye 17 552 1.0× 463 1.1× 181 0.9× 33 0.2× 17 0.1× 70 1.2k
Ronald J. Jorgenson United States 19 511 0.9× 379 0.9× 36 0.2× 28 0.1× 282 1.8× 41 1.1k
Carola Durán‐McKinster Mexico 20 245 0.4× 290 0.7× 69 0.4× 332 1.7× 15 0.1× 57 1.2k
P Franceschini Italy 17 357 0.6× 454 1.1× 97 0.5× 34 0.2× 14 0.1× 73 873
J Langdon United Kingdom 12 319 0.6× 105 0.2× 27 0.1× 39 0.2× 61 0.4× 39 690
Robert W. Marion United States 19 520 0.9× 460 1.1× 111 0.6× 17 0.1× 18 0.1× 47 1.2k
Guilherme M. Xavier United Kingdom 20 567 1.0× 235 0.5× 10 0.1× 40 0.2× 353 2.3× 34 1.1k

Countries citing papers authored by Christine Oley

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Christine Oley

This figure shows the co-authorship network connecting the top 25 collaborators of Christine Oley. A scholar is included among the top collaborators of Christine Oley 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 Christine Oley. Christine Oley is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Vogt, Julie, Shakti Agrawal, T. R. E. Southwood, et al.. (2013). Striking intrafamilial phenotypic variability in Aicardi–Goutières syndrome associated with the recurrent Asian founder mutation in RNASEH2C. American Journal of Medical Genetics Part A. 161(2). 338–342. 23 indexed citations
2.
Brison, Nathalie, Philippe Debeer, Sebastian Fantini, et al.. (2012). An N-terminal G11A mutation in HOXD13 causes synpolydactyly and interferes with Gli3R function during limb pre-patterning†. Human Molecular Genetics. 21(11). 2464–2475. 10 indexed citations
3.
Catte, Luc De, Michael T. Gabbett, Louanne Hudgins, et al.. (2011). Carpenter syndrome: extended RAB23 mutation spectrum and analysis of nonsense‐mediated mRNA decay. Human Mutation. 32(4). E2069–78. 32 indexed citations
4.
Huber, Céline, Thomas Édouard, Martine Le Merrer, et al.. (2009). OBSL1mutations in 3-M syndrome are associated with a modulation ofIGFBP2andIGFBP5expression levels. Human Mutation. 31(1). 20–26. 32 indexed citations
5.
Bowdin, Sarah, Louise Tee, Gail Kirby, et al.. (2008). Clinical and molecular genetic features of Beckwith-Wiedemann syndrome associated with assisted reproductive technologies. Human Reproduction. 24(3). 741–747. 160 indexed citations
6.
Oley, Christine, et al.. (2008). Clinical and radiological findings in Schinzel–Giedion syndrome. European Journal of Pediatrics. 167(12). 1399–1407. 13 indexed citations
7.
Jeske, Y., David Cowley, Christine Oley, et al.. (2007). Androgen Receptor Genotyping in a Large Australasian Cohort with Androgen Insensitivity Syndrom? Identification of Four Novel Mutations. Journal of Pediatric Endocrinology and Metabolism. 20(8). 893–908. 10 indexed citations
8.
Morgan, Neil V., Louise Brueton, P. Cox, et al.. (2006). Mutations in the Embryonal Subunit of the Acetylcholine Receptor (CHRNG) Cause Lethal and Escobar Variants of Multiple Pterygium Syndrome. The American Journal of Human Genetics. 79(2). 390–395. 98 indexed citations
9.
Beysen, Diane, Jean‐Pierre Fryns, Miranda Splitt, et al.. (2004). Genomic deletions account for more than 10% of the FOXL2 mutations in BPES families and can be revealed by MLPA analysis. European Journal of Human Genetics. 12. 248–248. 2 indexed citations
10.
Ahn, Sonia J., Christine Oley, & Timothy J. Sullivan. (2004). Lacrimal outflow dysgenesis. Ophthalmology. 111(9). 1782–1790. 43 indexed citations
11.
Beckingsale, Peter, et al.. (2003). Blepharophimosis: a recommendation for early surgery in patients with severe ptosis. Clinical and Experimental Ophthalmology. 31(2). 138–142. 42 indexed citations
12.
Wyllie, J H, et al.. (2000). Ectrodactyly and glaucoma associated with a 7q21.2-q31.2 interstitial deletion. Clinical Dysmorphology. 9(4). 235–239. 14 indexed citations
13.
Thomas, N. Simon, et al.. (1999). Investigation of a cryptic interstitial duplication involving the Prader-Willi/Angelman syndrome critical region. Human Genetics. 105(5). 384–387. 18 indexed citations
14.
Gedeon, Ági K., et al.. (1999). Gene localization for oral‐facial‐digital syndrome type 1 (OFD1:MIM 311200) proximal to DXS85. American Journal of Medical Genetics. 82(4). 352–354.
15.
Collins, Amanda, et al.. (1995). Crossover analysis in a British family suggests that Coffin‐Lowry syndrome maps to a 3.4‐cM interval in Xp22. American Journal of Medical Genetics. 59(4). 512–516. 12 indexed citations
16.
Shanley, Susan, John W. Ratcliffe, Athel Hockey, et al.. (1994). Nevoid basal cell carcinoma syndrome: Review of 118 affected individuals. American Journal of Medical Genetics. 50(3). 282–290. 250 indexed citations
17.
Reardon, William, et al.. (1994). Femoral hypoplasia unusual facies syndrome with preaxial polydactyly. Clinical Dysmorphology. 3(1). 40???45–40???45. 10 indexed citations
18.
Chenevix‐Trench, Georgia, Carol Wicking, Athel Hockey, et al.. (1993). Further localization of the gene for nevoid basal cell carcinoma syndrome (NBCCS) in 15 Australasian families: linkage and loss of heterozygosity.. PubMed. 53(3). 760–7. 71 indexed citations
19.
Oley, Christine & M Baraitser. (1988). Blepharophimosis, ptosis, epicanthus inversus syndrome (BPES syndrome). Journal of Medical Genetics. 25(1). 47–51. 98 indexed citations
20.
Koo, Winston, Christine Oley, Rosemary Munro, & Peter Tomlinson. (1982). Systemic Haemophilus influenzae infection in childhood. The Medical Journal of Australia. 2(2). 77–80. 11 indexed citations

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.

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