A O'Rourke

528 total citations
10 papers, 383 citations indexed

About

A O'Rourke is a scholar working on Genetics, Molecular Biology and Clinical Biochemistry. According to data from OpenAlex, A O'Rourke has authored 10 papers receiving a total of 383 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 5 papers in Molecular Biology and 2 papers in Clinical Biochemistry. Recurrent topics in A O'Rourke's work include Craniofacial Disorders and Treatments (3 papers), Cleft Lip and Palate Research (3 papers) and Genomics and Rare Diseases (2 papers). A O'Rourke is often cited by papers focused on Craniofacial Disorders and Treatments (3 papers), Cleft Lip and Palate Research (3 papers) and Genomics and Rare Diseases (2 papers). A O'Rourke collaborates with scholars based in United Kingdom, Netherlands and India. A O'Rourke's co-authors include Andrew O.M. Wilkie, Steven A. Wall, Ans M. M. van Pelt, Dirk G. de Rooij, Anne Goriely, A Seller, Gil McVean, Tracy Lester, Jane A. Hurst and Indira B. Taylor and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Human Molecular Genetics and Epilepsia.

In The Last Decade

A O'Rourke

10 papers receiving 373 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
A O'Rourke United Kingdom	7	237	236	43	27	26	10	383
Shane C. Quinonez United States	11	172 0.7×	221 0.9×	60 1.4×	11 0.4×	23 0.9×	29	396
Patricia Bretones France	8	128 0.5×	165 0.7×	11 0.3×	16 0.6×	21 0.8×	14	301
Mary Willis United States	10	197 0.8×	200 0.8×	72 1.7×	11 0.4×	16 0.6×	17	361
Philip L. Beales United Kingdom	7	152 0.6×	102 0.4×	16 0.4×	22 0.8×	19 0.7×	8	263
Machteld Baetens Belgium	9	212 0.9×	126 0.5×	5 0.1×	28 1.0×	24 0.9×	16	392
Rafael Loch Batista Brazil	13	252 1.1×	461 2.0×	14 0.3×	41 1.5×	62 2.4×	44	668
John Hutson Australia	4	119 0.5×	149 0.6×	6 0.1×	17 0.6×	15 0.6×	6	201
Jean P. Pfotenhauer United States	8	156 0.7×	211 0.9×	4 0.1×	23 0.9×	12 0.5×	9	438
Emily C. Lisi United States	13	182 0.8×	142 0.6×	35 0.8×	11 0.4×	23 0.9×	22	411

Countries citing papers authored by A O'Rourke

Since Specialization

Citations

This map shows the geographic impact of A O'Rourke'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 A O'Rourke with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites A O'Rourke more than expected).

Fields of papers citing papers by A O'Rourke

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by A O'Rourke. 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 A O'Rourke. The network helps show where A O'Rourke may publish in the future.

Co-authorship network of co-authors of A O'Rourke

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

All Works

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10 of 10 papers shown

Uusimaa, Johanna, Vasantha Gowda, Conrad Smith, et al.. (2013). Prospective study of POLG mutations presenting in children with intractable epilepsy: Prevalence and clinical features. Epilepsia. 54(6). 1002–1011. 34 indexed citations

Bowman, Michael, Michael Oldridge, A O'Rourke, et al.. (2012). Gross deletions in TCOF1 are a cause of Treacher–Collins–Franceschetti syndrome. European Journal of Human Genetics. 20(7). 769–777. 39 indexed citations

Harrison, Victoria, Jane A. Hurst, Tracy Lester, et al.. (2012). Segmental paternal uniparental disomy of chromosome 14 in a 4-year-old boy. Clinical Dysmorphology. 21(4). 208–211. 1 indexed citations

Ashley, Neil, A O'Rourke, Conrad Smith, et al.. (2008). Depletion of mitochondrial DNA in fibroblast cultures from patients with POLG1 mutations is a consequence of catalytic mutations. Human Molecular Genetics. 17(16). 2496–2506. 45 indexed citations

Ashley, Neil, Sandeep Jayawant, Jeremy Parr, et al.. (2007). Mutations in the mitochondrial DNA gamma polymerase (POLG-G) may cause Alpers syndrome, mitochondrial DNA depletion and apparent non-syndromic status epilepticus: implications for valproate therapy. Journal of Medical Genetics. 44. 1 indexed citations

Wilkie, Andrew O.M., Elena G. Bochukova, Indira B. Taylor, et al.. (2007). Clinical dividends from the molecular genetic diagnosis of craniosynostosis†. American Journal of Medical Genetics Part A. 143A(16). 1941–1949. 66 indexed citations

Fratter, Carl, A O'Rourke, Jackie Marchington, et al.. (2006). Molecular genetic diagnosis of mitochondrial DNA depletion syndrome and Alpers syndrome. Journal of Medical Genetics. 43. 1 indexed citations

Wilkie, Andrew O.M., Elena G. Bochukova, Indira B. Taylor, et al.. (2006). Clinical dividends from the molecular genetic diagnosis of craniosynostosis. American Journal of Medical Genetics Part A. 140A(23). 2631–2639. 80 indexed citations

Goriely, Anne, Gil McVean, Ans M. M. van Pelt, et al.. (2005). Gain-of-function amino acid substitutions drive positive selection of FGFR2 mutations in human spermatogonia. Proceedings of the National Academy of Sciences. 102(17). 6051–6056. 107 indexed citations

10.

O'Rourke, A. (1986). Bone marrow procedure guide.. PubMed. 13(1). 66–7. 9 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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