Elizabeth Ormondroyd

Author

Also Known As

Charaka Hadinnapola, E Ormondroyd, E. Ormondroyd, Elizabeth Ormondroyd, Hana Lango Allen, Kevin J. Marchbank, Lisa Willcocks, Liz Ormondroyd, Ormondroyd, Elizabeth, Shahin Moledina

Publications

4.3K

Citations

H-Index

Concepts

All Affiliations

University of Oxford Centre for Human Genetics Oxford University Hospitals NHS Trust John Radcliffe Hospital Churchill Hospital

About

Elizabeth Ormondroyd is an author at University of Oxford specializing in medicine, genetics, and public health.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	14	15	1.4K
2	Public Health	7	7	616
3	Engineering	2	2	46
4	Natural Sciences	2	2	119
5	Biology	1	1	24

Elizabeth Ormondroyd

Publications

2.2K

Citations

H-Index

Page 1

	Year	Citations
Factors influencing success of clinical genome sequencing across a broad spectrum of disorders Jenny C. Taylor, Hilary C. Martin, Stefano Lise, Nature Genetics SequencingPsychiatryClinical GenomeGeneticsMedicine	2015	378
Common genetic variants and modifiable risk factors underpin hypertrophic cardiomyopathy susceptibility and expressivity Andrew R. Harper, Anuj Goel, Christopher Grace, Nature Genetics CardiomyopathyEpidemiologyGenetic DeterminantCardiovascular DiseaseModifiable Risk Factors	2021	317
Molecular Cloning, cDNA Sequence, and Chromosomal Localization of the Human Phosphatidylinositol 3-Kinase p110α (PIK3CA) Gene Stefano Volinia, Ian D. Hiles, Elizabeth Ormondroyd, Genomics Signal TransductionChromosomal LocalizationSignaling PathwayMolecular RegulationMedicine	1994	95
Attitudes to reproductive genetic testing in women who had a positive BRCA test before having children: a qualitative analysis Elizabeth Ormondroyd, Louise S. Donnelly, Clare Moynihan, European Journal of Human Genetics Reproductive Genetic CounselingInfertilityGenetic TestingFertilityPrenatal Genetic Testing	2011	91
Distinct ECG Phenotypes Identified in Hypertrophic Cardiomyopathy Using Machine Learning Associate With Arrhythmic Risk Markers Aurore Lyon, Rina Ariga, Ana Mincholé, Frontiers in Physiology	2018	83
Pre-symptomatic genetic testing for inherited cardiac conditions: a qualitative exploration of psychosocial and ethical implications Elizabeth Ormondroyd, Stephanie Oates, Michael Parker, European Journal of Human Genetics Family MedicineGenetic TestingInherited Cardiac ConditionsCardiovascular GeneticsGenetic Foundation	2013	82
Physical maps of 4p16.3, the area expected to contain the Huntington disease mutation Maja Bućan, Michael Zimmer, William L. Whaley, Genomics Neurodegenerative DiseasesMendelian DisorderGenetic DisorderGeneticsHuntington Disease Mutation	1990	82
Reproductive decision-making in young female carriers of a BRCA mutation Louise S. Donnelly, Maggie Watson, Clare Moynihan, Human Reproduction	2013	82
“Not pathogenic until proven otherwise”: perspectives of UK clinical genomics professionals toward secondary findings in context of a Genomic Medicine Multidisciplinary Team and the 100,000 Genomes Project Elizabeth Ormondroyd, Michael P. Mackley, Edward Blair, Genetics in Medicine Genetic TestingSequencingMedicineGenomes ProjectGenetic Epidemiology	2017	67
Structural and non-coding variants increase the diagnostic yield of clinical whole genome sequencing for rare diseases Alistair T. Pagnamenta, Edoardo Giacopuzzi, John Taylor, Genome Medicine	2023	63

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