Oliver Quarrell

4.2k total citations
44 papers, 862 citations indexed

About

Oliver Quarrell is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Oliver Quarrell has authored 44 papers receiving a total of 862 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 22 papers in Cellular and Molecular Neuroscience and 13 papers in Neurology. Recurrent topics in Oliver Quarrell's work include Genetic Neurodegenerative Diseases (21 papers), Mitochondrial Function and Pathology (11 papers) and Neurological disorders and treatments (11 papers). Oliver Quarrell is often cited by papers focused on Genetic Neurodegenerative Diseases (21 papers), Mitochondrial Function and Pathology (11 papers) and Neurological disorders and treatments (11 papers). Oliver Quarrell collaborates with scholars based in United Kingdom, United States and Italy. Oliver Quarrell's co-authors include Sheharyar Baig, Mark Strong, Pradeep Vasudevan, Ferdinando Squitieri, Jonathan A. Smith, Martha Nance, David Craufurd, Peg Nopoulos, Jane S. Paulsen and Peter Hammond and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Neurology and Scientific Reports.

In The Last Decade

Oliver Quarrell

42 papers receiving 837 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Oliver Quarrell United Kingdom 17 369 320 249 237 74 44 862
Katherine A. Fawcett United Kingdom 15 543 1.5× 414 1.3× 205 0.8× 314 1.3× 21 0.3× 27 1.3k
F Ballesta Spain 14 246 0.7× 66 0.2× 37 0.1× 249 1.1× 78 1.1× 28 547
Akira Terao Japan 14 148 0.4× 100 0.3× 123 0.5× 142 0.6× 13 0.2× 51 692
Yasuhiro Arai Japan 19 289 0.8× 80 0.3× 81 0.3× 132 0.6× 10 0.1× 94 1.0k
Christina Raitta Finland 21 355 1.0× 101 0.3× 114 0.5× 157 0.7× 18 0.2× 74 1.4k
Paolo Tacconi Italy 12 636 1.7× 56 0.2× 235 0.9× 199 0.8× 19 0.3× 33 1.2k
Janet Cady United States 10 283 0.8× 88 0.3× 249 1.0× 155 0.7× 8 0.1× 17 933
Athel Hockey Australia 19 833 2.3× 94 0.3× 56 0.2× 500 2.1× 27 0.4× 46 1.5k
Jeffrey Cohn United States 13 111 0.3× 132 0.4× 299 1.2× 16 0.1× 47 0.6× 19 1.5k
Elena Marasco Italy 19 750 2.0× 55 0.2× 28 0.1× 150 0.6× 18 0.2× 37 1.2k

Countries citing papers authored by Oliver Quarrell

Since Specialization
Citations

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

Fields of papers citing papers by Oliver Quarrell

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Oliver Quarrell

This figure shows the co-authorship network connecting the top 25 collaborators of Oliver Quarrell. A scholar is included among the top collaborators of Oliver Quarrell 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 Oliver Quarrell. Oliver Quarrell 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.
Quarrell, Oliver, et al.. (2025). Variation in the reported prevalence of Huntington’s disease: a systematic review and guide to interpretation. Journal of Neurology. 272(8). 534–534.
2.
Oosterloo, Mayke, Lauren M. Byrne, Martha Nance, et al.. (2024). Clinical Review of Juvenile Huntington’s Disease. Journal of Huntington s Disease. 13(2). 149–161. 12 indexed citations
3.
Kotta, Maria‐Christina, Margherita Torchio, Pauline Bayliss, et al.. (2023). Cardiac Genetic Investigation of Sudden Infant and Early Childhood Death: A Study From Victims to Families. Journal of the American Heart Association. 12(17). e029100–e029100. 10 indexed citations
4.
Holden, Simon, Rhona MacLeod, Zosia Miedzybrodzka, et al.. (2019). A case-note review of continued pregnancies found to be at a high risk of Huntington’s disease: considerations for clinical practice. European Journal of Human Genetics. 27(8). 1215–1224. 4 indexed citations
5.
Horton, Mike, Peg Nopoulos, Martha Nance, et al.. (2019). Assessment of the Performance of a Modified Motor Scale as Applied to Juvenile Onset Huntington’s Disease. Journal of Huntington s Disease. 8(2). 181–193. 6 indexed citations
6.
Cohen, Marta C., et al.. (2018). Coinheritance of 2 New Potentially Damaging Heterozygous COL7A1 Variants in a Family With Autosomal Dominant Epidermolysis Bullosa Pruriginosa. Pediatric and Developmental Pathology. 21(6). 580–584. 1 indexed citations
7.
Salway, Sarah, Parveen Ali, Elizabeth Such, et al.. (2016). Responding to the increased genetic risk associated with customary consanguineous marriage among minority ethnic populations: lessons from local innovations in England. Journal of Community Genetics. 7(3). 215–228. 10 indexed citations
8.
Baig, Sheharyar, Mark Strong, Elisabeth Rosser, et al.. (2016). 22 Years of predictive testing for Huntington’s disease: the experience of the UK Huntington’s Prediction Consortium. European Journal of Human Genetics. 24(10). 1396–1402. 57 indexed citations
9.
O’Donovan, Kirsty, Eva Ekblad, Elin Sand, et al.. (2015). Characterization of Gastric Mucosa Biopsies Reveals Alterations in Huntington's Disease. PLoS Currents. 7. 15 indexed citations
10.
Quarrell, Oliver, Elisabeth Rosser, Nicola V. Taverner, et al.. (2014). K06 Uptake of Predictive Tests for Huntington's Disease (HD) in the UK 1993-2012. Journal of Neurology Neurosurgery & Psychiatry. 85(Suppl 1). A80–A81. 1 indexed citations
11.
Hannes, Femke, Peter Hammond, Oliver Quarrell, et al.. (2012). A microdeletion proximal of the critical deletion region is associated with mild Wolf–Hirschhorn syndrome. American Journal of Medical Genetics Part A. 158A(5). 996–1004. 15 indexed citations
12.
Robertson, Lisa, Kirsty O’Donovan, Ferdinando Squitieri, et al.. (2012). Current Pharmacological Management in Juvenile Huntington’s Disease. PLoS Currents. 4. RRN1304–RRN1304. 11 indexed citations
13.
Hammond, Peter, Femke Hannes, Michael Suttie, et al.. (2011). Fine-grained facial phenotype–genotype analysis in Wolf–Hirschhorn syndrome. European Journal of Human Genetics. 20(1). 33–40. 58 indexed citations
14.
Hannes, Femke, Jeroen Van Houdt, Oliver Quarrell, et al.. (2010). Telomere healing following DNA polymerase arrest-induced breakages is likely the main mechanism generating chromosome 4p terminal deletions. Human Mutation. 31(12). 1343–1351. 15 indexed citations
15.
Vasudevan, Pradeep, Marta C. Cohen, Elspeth Whitby, Dilly Anumba, & Oliver Quarrell. (2006). The OEIS complex: two case reports that illustrate the spectrum of abnormalities and a review of the literature. Prenatal Diagnosis. 26(3). 267–272. 22 indexed citations
16.
Curtis, Diana, Miranda Durkie, Anne Goodeve, et al.. (1999). A study of Wilson disease mutations in Britain. Human Mutation. 14(4). 304–311. 64 indexed citations
17.
Clarke, Carl E, M. Lowry, & Oliver Quarrell. (1998). No change in striatal glutamate in Huntington's disease measured by proton magnetic resonance spectroscopy. Parkinsonism & Related Disorders. 4(3). 123–127. 10 indexed citations
18.
Wright, Tracy J., Michele Clemens, Oliver Quarrell, & Michael R. Altherr. (1998). Wolf-Hirschhorn and Pitt-Rogers-Danks syndromes caused by overlapping 4p deletions. American Journal of Medical Genetics. 75(4). 345–350. 31 indexed citations
19.
Quarrell, Oliver, et al.. (1988). Pallister‐Killian mosaic syndrome with emphasis on the adult phenotype. American Journal of Medical Genetics. 31(4). 841–844. 20 indexed citations
20.
Sarfarazi, Mansoor, et al.. (1987). An integrated microcomputer system to maintain a genetic register for Huntington disease. American Journal of Medical Genetics. 28(4). 999–1006. 4 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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