Quincy Prescott

456 total citations
10 papers, 296 citations indexed

About

Quincy Prescott is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Quincy Prescott has authored 10 papers receiving a total of 296 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 2 papers in Cellular and Molecular Neuroscience and 2 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Quincy Prescott's work include Connexins and lens biology (3 papers), RNA regulation and disease (2 papers) and Corneal surgery and disorders (2 papers). Quincy Prescott is often cited by papers focused on Connexins and lens biology (3 papers), RNA regulation and disease (2 papers) and Corneal surgery and disorders (2 papers). Quincy Prescott collaborates with scholars based in United Kingdom, Canada and Spain. Quincy Prescott's co-authors include Shomi S. Bhattacharya, Siladitya Bhattacharya, Tanya Moore, Thomas M. Magin, Petra Lišková, Stephen J. Tuft, Melanie Müller, Harald Herrmann, Tatjana Wedig and Vanita Berry and has published in prestigious journals such as Journal of Applied Physics, Human Molecular Genetics and British Journal of Ophthalmology.

In The Last Decade

Quincy Prescott

10 papers receiving 290 citations

Peers

Quincy Prescott

OPHTH

RNMI

GENET

Natsuko Nakamura Japan

Firoz Kabir United States

Eric Souied France

Betsy Campochiaro United States

Romana Kucerova United Kingdom

Rosario Fernández‐Godino United States

Radwan Ajlan United States

Chloë M. Stanton United Kingdom

Sara D. Ragi United States

Natsuko Nakamura Japan

Quincy Prescott

241 ×1.3

158 ×1.7

OPHTH

51 ×0.6

RNMI

43 ×0.6

22 ×0.5

GENET

Citations per year, relative to Quincy Prescott Quincy Prescott (= 1×) peers Natsuko Nakamura

Countries citing papers authored by Quincy Prescott

Since Specialization

Citations

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

Fields of papers citing papers by Quincy Prescott

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Quincy Prescott

This figure shows the co-authorship network connecting the top 25 collaborators of Quincy Prescott. A scholar is included among the top collaborators of Quincy Prescott 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 Quincy Prescott. Quincy Prescott 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

Berry, Vanita, Nikolas Pontikos, Vincent Plagnol, et al.. (2017). A recurrent splice-site mutation in EPHA2 causing congenital posterior nuclear cataract. Ophthalmic Genetics. 39(2). 236–241. 15 indexed citations

Berry, Vanita, Cheryl Y. Gregory‐Evans, Warren Emmett, et al.. (2013). Wolfram gene (WFS1) mutation causes autosomal dominant congenital nuclear cataract in humans. European Journal of Human Genetics. 21(12). 1356–1360. 47 indexed citations

Cherninkova, Sylvia, Quincy Prescott, Vanio Mitev, et al.. (2012). A novel locus for autosomal dominant cone-rod dystrophy maps to chromosome 10q. European Journal of Human Genetics. 21(3). 338–342. 4 indexed citations

Berry, Vanita, Peter J. Francis, Quincy Prescott, et al.. (2011). A novel 1-bp deletion in PITX3 causing congenital posterior polar cataract.. PubMed. 17. 1249–53. 17 indexed citations

Müller, Melanie, Siladitya Bhattacharya, Tanya Moore, et al.. (2009). Dominant cataract formation in association with a vimentin assembly disrupting mutation. Human Molecular Genetics. 18(6). 1052–1057. 82 indexed citations

Lišková, Petra, Stephen J. Tuft, Rhian Gwilliam, et al.. (2007). Novel mutations in theZEB1 gene identified in Czech and British patients with posterior polymorphous corneal dystrophy. Human Mutation. 28(6). 638–638. 64 indexed citations

Lišková, Petra, Quincy Prescott, Shomi S. Bhattacharya, & Stephen J. Tuft. (2007). British family with early-onset Fuchs' endothelial corneal dystrophy associated with p.L450W mutation in the COL8A2 gene. British Journal of Ophthalmology. 91(12). 1717–1718. 30 indexed citations

Papaioannou, Myrto, Christina Chakarova, Quincy Prescott, et al.. (2005). A new locus (RP31) for autosomal dominant retinitis pigmentosa maps to chromosome 9p. Human Genetics. 118(3-4). 501–503. 12 indexed citations

Prescott, Quincy, S. K. Haywood, David A. Pattison, et al.. (1998). Carrier lifetime and exciton saturation in a strain-balanced InGaAs/InAsP multiple quantum well. Journal of Applied Physics. 83(1). 306–309. 3 indexed citations

10.

McKoy, Godfrina, et al.. (1997). Characterisation of phosphoglycerate kinase genes in Leishmania major and evidence for the absence of a third closely related gene or isoenzyme1Note: Nucleotide sequence data reported in this paper are available in the EMBL, GenBank™ and DDJB data bases under the accession numbers L12520 (PGK gene B) and L12521 (PGK gene C).1. Molecular and Biochemical Parasitology. 90(1). 169–181. 22 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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