Oliver Quarrell

5.3k total citations
47 papers, 1.5k citations indexed

About

Oliver Quarrell is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Genetics. According to data from OpenAlex, Oliver Quarrell has authored 47 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Cellular and Molecular Neuroscience, 23 papers in Molecular Biology and 13 papers in Genetics. Recurrent topics in Oliver Quarrell's work include Genetic Neurodegenerative Diseases (27 papers), Mitochondrial Function and Pathology (11 papers) and Neurological disorders and treatments (8 papers). Oliver Quarrell is often cited by papers focused on Genetic Neurodegenerative Diseases (27 papers), Mitochondrial Function and Pathology (11 papers) and Neurological disorders and treatments (8 papers). Oliver Quarrell collaborates with scholars based in United Kingdom, United States and Germany. Oliver Quarrell's co-authors include Peter S. Harper, Daniela T. Pilz, Jonathan A. Smith, S Youngman, Kirsty O’Donovan, Mark Strong, Oliver Bandmann, Duncan J. Shaw, Susan Michie and Mike Stephenson and has published in prestigious journals such as The Lancet, Nature Genetics and Human Molecular Genetics.

In The Last Decade

Oliver Quarrell

47 papers receiving 1.4k 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 23 729 547 536 258 179 47 1.5k
Kathleen A. Leppig United States 23 662 0.9× 507 0.9× 681 1.3× 310 1.2× 209 1.2× 57 2.0k
Helen Kingston United Kingdom 24 839 1.2× 268 0.5× 645 1.2× 319 1.2× 161 0.9× 63 1.9k
David R. Witt United States 17 694 1.0× 282 0.5× 444 0.8× 106 0.4× 186 1.0× 23 1.9k
Barbara Zoll Germany 22 1.1k 1.6× 460 0.8× 528 1.0× 79 0.3× 210 1.2× 76 1.8k
Julie S. Cohen United States 22 617 0.8× 203 0.4× 578 1.1× 121 0.5× 146 0.8× 44 1.4k
Vandana Shashi United States 27 1.4k 2.0× 174 0.3× 1.3k 2.4× 173 0.7× 230 1.3× 98 2.9k
Jennifer Friedman United States 20 444 0.6× 423 0.8× 526 1.0× 415 1.6× 124 0.7× 57 1.6k
Aurora Sánchez Spain 25 810 1.1× 295 0.5× 862 1.6× 160 0.6× 630 3.5× 91 1.9k
P.S. Harper United Kingdom 31 1.3k 1.7× 1.2k 2.1× 459 0.9× 548 2.1× 161 0.9× 83 2.7k
J. P. Fryns Belgium 24 1.4k 1.9× 335 0.6× 1.7k 3.1× 95 0.4× 598 3.3× 124 2.7k

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.. (2023). Dystonia in Pediatric Huntington's Disease; Prominent and Possibly Painful. Movement Disorders Clinical Practice. 10(10). 1552–1553. 1 indexed citations
2.
McNeill, Alisdair, Maria del Mar Amador, Hilary Bekker, et al.. (2022). Predictive genetic testing for Motor neuron disease: time for a guideline?. European Journal of Human Genetics. 30(6). 635–636. 3 indexed citations
3.
Piña-Aguilar, Raúl E., Sheila A Simpson, Angus Clarke, et al.. (2018). 27 years of prenatal diagnosis for Huntington disease in the United Kingdom. Genetics in Medicine. 21(7). 1639–1643. 9 indexed citations
4.
Epping, Eric A., et al.. (2017). A survey-based Study Identifies Common But Unrecognized Symptoms in a Large Series of Juvenile Huntington’s Disease. Neurodegenerative Disease Management. 7(5). 307–315. 24 indexed citations
5.
Hammond, Peter, Shane McKee, Michael Suttie, et al.. (2014). Opposite effects on facial morphology due to gene dosage sensitivity. Human Genetics. 133(9). 1117–1125. 11 indexed citations
6.
Eatough, Virginia, Christine Eiser, Wioletta Krysa, et al.. (2013). The personal experience of parenting a child with Juvenile Huntington’s Disease: perceptions across Europe. European Journal of Human Genetics. 21(10). 1042–1048. 18 indexed citations
7.
Quarrell, Oliver, Olivia Handley, Kirsty O’Donovan, et al.. (2011). Discrepancies in reporting the CAG repeat lengths for Huntington's disease. European Journal of Human Genetics. 20(1). 20–26. 15 indexed citations
8.
Sobey, Glenda, et al.. (2007). Mosaic Chromosome 6 Trisomy in an Epidermal Nevus. Pediatric Dermatology. 24(2). 144–146. 3 indexed citations
9.
Vasudevan, Pradeep & Oliver Quarrell. (2007). Prader–Willi and Klinefelter syndrome: a coincidence or not?. Clinical Dysmorphology. 16(2). 127–129. 5 indexed citations
10.
Squitieri, Ferdinando, Luigi Frati, Andrea Ciarmiello, Secondo Lastoria, & Oliver Quarrell. (2005). Juvenile Huntington's disease: Does a dosage-effect pathogenic mechanism differ from the classical adult disease?. Mechanisms of Ageing and Development. 127(2). 208–212. 59 indexed citations
11.
Clarke, Angus, Martin Richards, L Kerzin-Storrar, et al.. (2005). Genetic professionals' reports of nondisclosure of genetic risk information within families. European Journal of Human Genetics. 13(5). 556–562. 92 indexed citations
12.
Robertson, Stephen P., Stephen R.F. Twigg, Andrew J. Sutherland‐Smith, et al.. (2003). Localized mutations in the gene encoding the cytoskeletal protein filamin A cause diverse malformations in humans. Nature Genetics. 33(4). 487–491. 297 indexed citations
13.
Kamnasaran, Deepak, Patricia C. O’Brien, Simone Schuffenhauer, et al.. (2001). Defining the breakpoints of proximal chromosome 14q rearrangements in nine patients using flow-sorted chromosomes. American Journal of Medical Genetics. 102(2). 173–182. 29 indexed citations
14.
Shah, Ashish, Michael F. Smith, Paul D. Griffiths, & Oliver Quarrell. (1999). Schinzel-Giedion syndrome: Evidence for a neurodegenerative process. American Journal of Medical Genetics. 82(4). 344–347. 22 indexed citations
15.
Pilz, Daniela T. & Oliver Quarrell. (1996). Syndromes with lissencephaly.. Journal of Medical Genetics. 33(4). 319–323. 43 indexed citations
16.
Quarrell, Oliver, et al.. (1990). Interstitial deletion of chromosome 4, del(4)(q12q21.1), in a child with multiple congenital abnormalities.. Journal of Medical Genetics. 27(1). 64–65. 15 indexed citations
17.
Quarrell, Oliver, et al.. (1990). Maxillonasal dysplasia (Binder's syndrome). Journal of Medical Genetics. 27(6). 384–387. 29 indexed citations
18.
Harper, Peter S., Oliver Quarrell, & S Youngman. (1988). Huntington's disease: prediction and prevention. Philosophical transactions of the Royal Society of London. Series B, Biological sciences. 319(1194). 285–298. 6 indexed citations
19.
Quarrell, Oliver, Audrey Tyler, Meena Upadhyaya, et al.. (1988). Exclusion Testing for Huntingtonʼs Disease in Pregnancy with a Closely Linked DNA Marker. Obstetrical & Gynecological Survey. 43(1). 45–46. 1 indexed citations
20.
Quarrell, Oliver, Audrey Tyler, G. Cole, & Peter S. Harper. (1986). The problem of isolated cases of Huntington's disease in South Wales 1974–1984. Clinical Genetics. 30(5). 433–439. 5 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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