Elizabeth Ormondroyd

3.2k total citations
31 papers, 875 citations indexed

About

Elizabeth Ormondroyd is a scholar working on Genetics, Molecular Biology and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Elizabeth Ormondroyd has authored 31 papers receiving a total of 875 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Genetics, 7 papers in Molecular Biology and 7 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Elizabeth Ormondroyd's work include Genomics and Rare Diseases (12 papers), BRCA gene mutations in cancer (10 papers) and Cancer Genomics and Diagnostics (7 papers). Elizabeth Ormondroyd is often cited by papers focused on Genomics and Rare Diseases (12 papers), BRCA gene mutations in cancer (10 papers) and Cancer Genomics and Diagnostics (7 papers). Elizabeth Ormondroyd collaborates with scholars based in United Kingdom, United States and Italy. Elizabeth Ormondroyd's co-authors include Hugh Watkins, Michael P. Mackley, Michael Parker, Edward Blair, Rosalind A. Eeles, Maggie Watson, Clare Moynihan, Jenny C. Taylor, Benjamin Fletcher and N B La Thangue and has published in prestigious journals such as PLoS ONE, Molecular Biology of the Cell and Human Reproduction.

In The Last Decade

Elizabeth Ormondroyd

30 papers receiving 852 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Elizabeth Ormondroyd United Kingdom	16	421	253	180	154	134	31	875
Tracy Dudding Australia	16	276 0.7×	239 0.9×	65 0.4×	49 0.3×	148 1.1×	24	752
Myra Wick United States	16	299 0.7×	397 1.6×	83 0.5×	139 0.9×	170 1.3×	55	1.1k
Julie Richer Canada	13	399 0.9×	202 0.8×	35 0.2×	103 0.7×	89 0.7×	34	670
Sophia B. Hufnagel United States	6	805 1.9×	286 1.1×	70 0.4×	169 1.1×	142 1.1×	6	1.1k
Yadav Sapkota United States	18	167 0.4×	214 0.8×	112 0.6×	158 1.0×	186 1.4×	63	855
Tanya N. Nelson Canada	21	450 1.1×	308 1.2×	38 0.2×	126 0.8×	276 2.1×	51	1.0k
Nicholas Pachter Australia	14	210 0.5×	233 0.9×	30 0.2×	72 0.5×	45 0.3×	30	578
Jacob A. Reiss United States	19	514 1.2×	273 1.1×	18 0.1×	69 0.4×	143 1.1×	43	1.0k
Karen L. David United States	12	491 1.2×	263 1.0×	27 0.1×	127 0.8×	226 1.7×	14	899
Ivan Macciocca Australia	16	319 0.8×	211 0.8×	407 2.3×	66 0.4×	80 0.6×	36	928

Countries citing papers authored by Elizabeth Ormondroyd

Since Specialization

Citations

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

Fields of papers citing papers by Elizabeth Ormondroyd

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Elizabeth Ormondroyd. 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 Elizabeth Ormondroyd. The network helps show where Elizabeth Ormondroyd may publish in the future.

Co-authorship network of co-authors of Elizabeth Ormondroyd

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

All Works

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20 of 20 papers shown

Forrest, Jamie I., et al.. (2024). Additional findings from the 100,000 Genomes Project: A qualitative study of recipient perspectives. Genetics in Medicine. 26(6). 101103–101103. 4 indexed citations

Ormondroyd, Elizabeth, Christopher Grace, Anuj Goel, et al.. (2024). Genetic therapies for cardiomyopathy: survey of attitudes of the patient community for the CureHeart project. European Journal of Human Genetics. 32(9). 1045–1052.

Vears, Danya F., Nina Hallowell, Heidi Beate Bentzen, et al.. (2023). A practical checklist for return of results from genomic research in the European context. European Journal of Human Genetics. 31(6). 687–695. 5 indexed citations

Ormondroyd, Elizabeth, et al.. (2023). Direct‐to‐consumer genetic tests providing health risk information: A systematic review of consequences for consumers and health services. Clinical Genetics. 104(1). 3–21. 7 indexed citations

Raman, Betty, R Smillie, Masliza Mahmod, et al.. (2021). Incremental value of left atrial booster and reservoir strain in predicting atrial fibrillation in patients with hypertrophic cardiomyopathy: a cardiovascular magnetic resonance study. Journal of Cardiovascular Magnetic Resonance. 23(1). 109–109. 22 indexed citations

Graham, Mackenzie, Nina Hallowell, Berge Solberg, et al.. (2021). Taking it to the bank: the ethical management of individual findings arising in secondary research. Journal of Medical Ethics. 47(10). 689–696. 3 indexed citations

Ormondroyd, Elizabeth, et al.. (2021). Genomic health data generation in the UK: a 360 view. European Journal of Human Genetics. 30(7). 782–789. 8 indexed citations

Taylor, John, E Blair, Sarah Wordsworth, et al.. (2019). Implementation of a genomic medicine multi-disciplinary team approach for rare disease in the clinical setting: a prospective exome sequencing case series. Genome Medicine. 11(1). 46–46. 21 indexed citations

Buchanan, James, Edward Blair, Kate Thomson, et al.. (2019). Do health professionals value genomic testing? A discrete choice experiment in inherited cardiovascular disease. European Journal of Human Genetics. 27(11). 1639–1648. 11 indexed citations

10.

Mackley, Michael P., Edward Blair, Michael Parker, et al.. (2018). Views of rare disease participants in a UK whole-genome sequencing study towards secondary findings: a qualitative study. European Journal of Human Genetics. 26(5). 652–659. 25 indexed citations

11.

Lyon, Aurore, Rina Ariga, Ana Mincholé, et al.. (2018). Distinct ECG Phenotypes Identified in Hypertrophic Cardiomyopathy Using Machine Learning Associate With Arrhythmic Risk Markers. Frontiers in Physiology. 9. 213–213. 62 indexed citations

12.

Hastings, Robert, Charlotte Hooper, Elizabeth Ormondroyd, et al.. (2016). Combination of Whole Genome Sequencing, Linkage, and Functional Studies Implicates a Missense Mutation in Titin as a Cause of Autosomal Dominant Cardiomyopathy With Features of Left Ventricular Noncompaction. Circulation Cardiovascular Genetics. 9(5). 426–435. 43 indexed citations

13.

Mackley, Michael P., Benjamin Fletcher, Michael Parker, Hugh Watkins, & Elizabeth Ormondroyd. (2016). Stakeholder views on secondary findings in whole-genome and whole-exome sequencing: a systematic review of quantitative and qualitative studies. Genetics in Medicine. 19(3). 283–293. 101 indexed citations

14.

Donnelly, Louise S., Maggie Watson, Clare Moynihan, et al.. (2013). Reproductive decision-making in young female carriers of a BRCA mutation. Human Reproduction. 28(4). 1006–1012. 63 indexed citations

15.

Ormondroyd, Elizabeth, et al.. (2013). Pre-symptomatic genetic testing for inherited cardiac conditions: a qualitative exploration of psychosocial and ethical implications. European Journal of Human Genetics. 22(1). 88–93. 54 indexed citations

16.

Ormondroyd, Elizabeth, Louise S. Donnelly, Clare Moynihan, et al.. (2011). Attitudes to reproductive genetic testing in women who had a positive BRCA test before having children: a qualitative analysis. European Journal of Human Genetics. 20(1). 4–10. 68 indexed citations

17.

Volinia, Stefano, Nicoletta Mascellani, Jlenia Marchesini, et al.. (2008). Genome Wide Identification of Recessive Cancer Genes by Combinatorial Mutation Analysis. PLoS ONE. 3(10). e3380–e3380. 12 indexed citations

18.

Ormondroyd, Elizabeth, Clare Moynihan, Audrey Ardern‐Jones, et al.. (2008). Communicating genetics research results to families: problems arising when the patient participant is deceased. Psycho-Oncology. 17(8). 804–811. 15 indexed citations

19.

Girling, Rowena, Lasantha R. Bandara, Elizabeth Ormondroyd, et al.. (1994). Molecular characterization of Xenopus laevis DP proteins.. Molecular Biology of the Cell. 5(10). 1081–1092. 22 indexed citations

20.

Volinia, Stefano, Ian D. Hiles, Elizabeth Ormondroyd, et al.. (1994). Molecular Cloning, cDNA Sequence, and Chromosomal Localization of the Human Phosphatidylinositol 3-Kinase p110α (PIK3CA) Gene. Genomics. 24(3). 472–477. 82 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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