Christine Oley

2.3k citations

21 papers · 954 indexed · h-index 13

Impact in

Dermatology top 2%
- Cancer and Skin Lesions
Oral Surgery top 5%
- Oral and Maxillofacial Pathology

Papers in ⓘ

Molecular Biology 9
- Hedgehog Signaling Pathway Studies 3
- Sexual Differentiation and Disorders 2
Genetics 9
- Genetic Syndromes and Imprinting 4
- Connective tissue disorders research 2
- Genomic variations and chromosomal abnormalities 2

Co-authors: M Baraitser (1 shared paper)Athel Hockey (2 shared papers)Georgia Chenevix‐Trench (2 shared papers)David Ravine (2 shared papers)Eric Haan (2 shared papers)Carol Wicking (2 shared papers)John W. Ratcliffe (1 shared paper)Nicholas G. Martin (1 shared paper)
Journals: Human Genetics (2 papers)Human Mutation (2 papers)European Journal of Human Genetics (1 paper)Human Molecular Genetics (1 paper)Journal of Medical Genetics (1 paper)
Partner nations: United Kingdom Australia United States

In The Last Decade

Christine Oley

20 papers receiving 914 citations

Peers

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-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.

Border = papers with Christine Oley Line = papers co-authored together Christine Oley links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 21 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Nevoid basal cell carcinoma syndrome: Review of 118 affected individuals American Journal of Medical Genetics ·Susan Shanley, John W. Ratcliffe, Athel Hockey, Eric Haan, Christine Oley, David Ravine, Nicholas G. Martin, Carol Wicking, Georgia Chenevix‐Trench	1994	250
2	Clinical and molecular genetic features of Beckwith-Wiedemann syndrome associated with assisted reproductive technologies Human Reproduction ·Derek H.K. Lim, Sarah Bowdin, Louise Tee, Gail Kirby, Edward Blair, Anthony A. Fryer, Wayne Lam, Christine Oley, Tim Cole, L A Brueton, Wolf Reik, Fiona MacDonald, Eamonn R. Maher	2008	160
3	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 ·Neil V. Morgan, Louise Brueton, P. Cox, Marie T. Greally, John Tolmie, Shanaz Pasha, Irene A. Aligianis, Hans van Bokhoven, Tamás Marton, Lihadh Al‐Gazali, Jenny E.V. Morton, Christine Oley, Colin A. Johnson, Richard C. Trembath, Han G. Brunner, Eamonn R. Maher	2006	98
4	Blepharophimosis, ptosis, epicanthus inversus syndrome (BPES syndrome) Journal of Medical Genetics ·Christine Oley, M Baraitser	1988	98
5	Further localization of the gene for nevoid basal cell carcinoma syndrome (NBCCS) in 15 Australasian families: linkage and loss of heterozygosity. PubMed ·Georgia Chenevix‐Trench, Carol Wicking, J. Berkman, Helen Sharpe, Athel Hockey, Eric Haan, Christine Oley, David Ravine, Anne‐Marie W. Turner, (unknown)	1993	71
6	Lacrimal outflow dysgenesis Ophthalmology ·Sonia J. Ahn, Christine Oley, Timothy J. Sullivan	2004	43
7	Blepharophimosis: a recommendation for early surgery in patients with severe ptosis Clinical and Experimental Ophthalmology ·Peter Beckingsale, Timothy J. Sullivan, Vincent Wong, Christine Oley	2003	42
8	Carpenter syndrome: extended RAB23 mutation spectrum and analysis of nonsense‐mediated mRNA decay Human Mutation ·Dagan Jenkins, Gareth Baynam, Luc De Catte, Nursel Elçioǧlu, Michael T. Gabbett, Louanne Hudgins, Jane A. Hurst, Fernanda Sarquis Jehee, Christine Oley, Andrew O.M. Wilkie	2011	32
9	OBSL1mutations in 3-M syndrome are associated with a modulation ofIGFBP2andIGFBP5expression levels Human Mutation ·Céline Huber, MÃ©lanie Fradin, Thomas Édouard, Martine Le Merrer, Yasemin Alanay, Daniela Bezerra Da Silva, Albert David, Hanan Hamamy, Liselotte van Hest, Allan M. Lund, Jacques L. Michaud, Christine Oley, Chirag Patel, Anna Rajab, David Skidmore, Helen Stewart, M. Tauber, Arnold Münnich, Valérie Cormier‐Daire	2009	32
10	Striking intrafamilial phenotypic variability in Aicardi–Goutières syndrome associated with the recurrent Asian founder mutation in RNASEH2C American Journal of Medical Genetics Part A ·Julie Vogt, Shakti Agrawal, Zala Ibrahim, T. R. E. Southwood, Sunny Philip, Lesley MacPherson, Malini Bhole, Yanick J. Crow, Christine Oley	2013	23
11	Investigation of a cryptic interstitial duplication involving the Prader-Willi/Angelman syndrome critical region Human Genetics ·N. Simon Thomas, C.E. Browne, Christine Oley, S. Healey, John A. Crolla	1999	18
12	Ectrodactyly and glaucoma associated with a 7q21.2-q31.2 interstitial deletion Clinical Dysmorphology ·T. L. Montgomery, J H Wyllie, Christine Oley	2000	14
13	Clinical and radiological findings in Schinzel–Giedion syndrome European Journal of Pediatrics ·Mudaffer Al-Mudaffer, Christine Oley, Sue Price, Ian Hayes, A Stewart, Christine M Hall, William Reardon	2008	13
14	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 ·Helen Bird, Amanda Collins, Christine Oley, Susan Lindsay	1995	12
15	Systemic Haemophilus influenzae infection in childhood The Medical Journal of Australia ·Winston Koo, Christine Oley, Rosemary Munro, Peter Tomlinson	1982	11
16	An N-terminal G11A mutation in HOXD13 causes synpolydactyly and interferes with Gli3R function during limb pre-patterning† Human Molecular Genetics ·Nathalie Brison, Philippe Debeer, Sebastian Fantini, Christine Oley, Vincenzo Zappavigna, Frank P. Luyten, Przemko Tylżanowski	2012	10
17	Androgen Receptor Genotyping in a Large Australasian Cohort with Androgen Insensitivity Syndrom? Identification of Four Novel Mutations Journal of Pediatric Endocrinology and Metabolism ·Y. Jeske, Ivan McGown, David Cowley, Christine Oley, M. J. THOMSETT, Catherine S. Choong, Andrew Cotterill	2007	10
18	Femoral hypoplasia unusual facies syndrome with preaxial polydactyly Clinical Dysmorphology ·M. BARAITSER, William Reardon, Christine Oley, J. A. Fixsen	1994	10
19	Investigation of a cryptic interstitial duplication involving the Prader-Willi/Angelman syndrome critical region Human Genetics ·N. Simon Thomas, C.E. Browne, Christine Oley, S. Healey, John A. Crolla	1999	5
20	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 ·Diane Beysen, MK Fellous, Jean‐Pierre Fryns, Miranda Splitt, Philippe Bouchard, Sophie Christin‐Maître, RA Veitia, Anders O.H. Nygren, Jan Schouten, Emmanuelle Lemyre, Christine Oley, Helle Hjalgrim, PA Koivisto, Ludwine Messiaen, Annick De Paepe, E De Baerer	2004	2

About Christine Oley

Christine Oley is a scholar working on Molecular Biology, Genetics, Pathology and Forensic Medicine, Cellular and Molecular Neuroscience and Infectious Diseases, having authored 21 papers that have together received 954 indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (4 papers), Hedgehog Signaling Pathway Studies (3 papers), Connective tissue disorders research (2 papers), Prenatal Screening and Diagnostics (2 papers), Genetic Neurodegenerative Diseases (2 papers), Parvovirus B19 Infection Studies (2 papers), Sexual Differentiation and Disorders (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). The work is most often cited by research in Dermatology (191 citations), Oral Surgery (154 citations), Genetics (431 citations), Pediatrics, Perinatology and Child Health (192 citations) and Genetics (94 citations). Christine Oley has collaborated with scholars based in United Kingdom, Australia and United States. Frequent co-authors include M Baraitser, Athel Hockey, Georgia Chenevix‐Trench, David Ravine, Eric Haan, Carol Wicking, John W. Ratcliffe, Nicholas G. Martin, Susan Shanley and Timothy J. Sullivan. Their work appears in journals such as Human Genetics, Human Mutation, European Journal of Human Genetics, Human Molecular Genetics and Journal of Medical Genetics.

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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