Penny Clouston

1.5k total citations
34 papers, 850 citations indexed

About

Penny Clouston is a scholar working on Molecular Biology, Ophthalmology and Genetics. According to data from OpenAlex, Penny Clouston has authored 34 papers receiving a total of 850 indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Molecular Biology, 23 papers in Ophthalmology and 6 papers in Genetics. Recurrent topics in Penny Clouston's work include Retinal Development and Disorders (27 papers), Retinal Diseases and Treatments (22 papers) and RNA regulation and disease (4 papers). Penny Clouston is often cited by papers focused on Retinal Development and Disorders (27 papers), Retinal Diseases and Treatments (22 papers) and RNA regulation and disease (4 papers). Penny Clouston collaborates with scholars based in United Kingdom, Australia and Germany. Penny Clouston's co-authors include Jiannis Ragoussis, A Seller, Robert E. MacLaren, Morag Shanks, Christopher Yau, Stefano Colella, Ghazala Mirza, Helen Butler, Chris Holmes and Anne S. Bassett and has published in prestigious journals such as Nucleic Acids Research, The American Journal of Human Genetics and American Journal of Ophthalmology.

In The Last Decade

Penny Clouston

32 papers receiving 846 citations

Peers

Countries citing papers authored by Penny Clouston

Since Specialization

Citations

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

Fields of papers citing papers by Penny Clouston

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Penny Clouston

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

#	Work	Indexed citations
1	Myoclonus-dystonia due to novel mutation in the guanine nucleotide-binding protein (GNB1) gene 2025 ·Parkinsonism & Related Disorders ·Duncan Street, (unknown), Teodora Georgieva, (unknown), Suzanne Broadgate, Penny Clouston, Mary O’Driscoll	0
2	A hypomorphic variant of choroideremia is associated with a novel intronic mutation that leads to exon skipping 2024 ·Ophthalmic Genetics ·(unknown), Laura J. Taylor, (unknown), (unknown), Cristina Martínez-Fernández de la Cámara, (unknown), Penny Clouston, Imran H. Yusuf, Robert E. MacLaren	1
3	Expanding the genotypic and phenotypic spectra with a novel variant in the ciliopathy gene, CFAP410 , associated with selective cone degeneration 2024 ·Ophthalmic Genetics ·(unknown), Morag Shanks, (unknown), Penny Clouston, (unknown), (unknown), Jennifer A. Thompson, Kanmin Xue, Samantha R. De Silva, Susan M. Downes, Robert E. MacLaren, Jasmina Cehajic‐Kapetanovic	1
4	A Carrier Female Manifesting an Unusual X-Linked Retinoschisis Phenotype Associated with the Pathogenic Variant c.266delA, p.(Tyr89LeufsTer37) in RS1, and Skewed X-Inactivation 2023 ·Genes ·(unknown), Stephanie Halford, Morag Shanks, Anthony T. Moore, (unknown), Lucy Jenkins, Penny Clouston, Chetan K. Patel, Susan M. Downes	4
5	Phenotypic and Genetic Characteristics in a Cohort of Patients with Usher Genes 2022 ·Genes ·(unknown), (unknown), Mital Shah, Suzanne Broadgate, Morag Shanks, Archith Kamath, Jing Yu, Jasleen K. Jolly, Robert E. MacLaren, Penny Clouston, Stephanie Halford, Susan M. Downes	5
6	Compound dominant-null heterozygosity in a family with RP1-related retinal dystrophy 2022 ·American Journal of Ophthalmology Case Reports ·(unknown), Jasmina Cehajic‐Kapetanovic, Morag Shanks, Penny Clouston, Robert E. MacLaren	2
7	MERTK missense variants in three patients with retinitis pigmentosa 2022 ·Ophthalmic Genetics ·(unknown), Imran H. Yusuf, Penny Clouston, Morag Shanks, (unknown), Peter Charbel Issa, Robert E. MacLaren	6
8	Targeted next generation sequencing and family survey enable correct genetic diagnosis in CRX associated macular dystrophy – a case report 2021 ·BMC Ophthalmology ·(unknown), K Hudspith, Suzanne Broadgate, Morag Shanks, Penny Clouston, Andrea H. Németh, Stephanie Halford, Susan M. Downes	3
9	Genetic and Clinical Findings in an Ethnically Diverse Cohort with Retinitis Pigmentosa Associated with Pathogenic Variants in CERKL 2020 ·Genes ·Susan M. Downes, (unknown), Vicky Tai, Suzanne Broadgate, Mital Shah, (unknown), Robert E. MacLaren, Morag Shanks, Penny Clouston, Stephanie Halford	6
10	Novel Pathogenic Sequence Variants in NR2E3 and Clinical Findings in Three Patients 2020 ·Genes ·(unknown), Suzanne Broadgate, Stephanie Halford, Jasleen K. Jolly, Morag Shanks, Penny Clouston, Susan M. Downes	7
11	“Genetic and clinical findings in an ethnically diverse retinitis pigmentosa cohort associated with pathogenic variants in EYS” 2020 ·Eye ·(unknown), Suzanne Broadgate, Stephanie Halford, Robert E. MacLaren, Morag Shanks, Penny Clouston, Michael James Gilhooley, Susan M. Downes	7
12	Next generation sequencing using phenotype-based panels for genetic testing in inherited retinal diseases 2020 ·Ophthalmic Genetics ·Mital Shah, Morag Shanks, (unknown), Jonathan Williams, (unknown), Robert E. MacLaren, Andrea H. Németh, Penny Clouston, Susan M. Downes	23
13	Infantile Onset of Spinocerebellar Ataxia Type 5 (SCA-5) in a 6 Month Old with Ataxic Cerebral Palsy 2019 ·The Cerebellum ·Gillian Rea, Sandya Tirupathi, Jonathan Williams, Penny Clouston, Patrick J. Morrison	7
14	The Location of Exon 4 Mutations in RP1 Raises Challenges for Genetic Counseling and Gene Therapy 2019 ·American Journal of Ophthalmology ·Anika Nanda, Michelle E. McClements, Penny Clouston, Morag Shanks, Robert E. MacLaren	17
15	Slowly progressive retinitis pigmentosa caused by two novel mutations in the MAK gene 2018 ·Ophthalmic Genetics ·Joanna Gray, Harry O. Orlans, Morag Shanks, Penny Clouston, Robert E. MacLaren	4
16	Electrophysiological verification of enhanced S-cone syndrome caused by a novel c.755T>C NR2E3 missense variant 2018 ·Ophthalmic Genetics ·Jasmina Cehajic‐Kapetanovic, Charles L. Cottriall, Jasleen K. Jolly, Morag Shanks, Penny Clouston, Peter Charbel Issa, Robert E. MacLaren	5
17	Dominant Mutations in GRM1 Cause Spinocerebellar Ataxia Type 44 2017 ·The American Journal of Human Genetics ·Lauren M. Watson, (unknown), Ricardo Parolin Schnekenberg, Jonathan P. Williams, Conceição Bettencourt, (unknown), Sandeep Jayawant, Katherine A. Fawcett, Samuel Clokie, Yvonne Wallis, Penny Clouston, David Sims, Henry Houlden, Esther B. E. Becker, Andrea H. Németh	55
18	Two Novel CAPN5 Variants Associated with Mild and Severe Autosomal Dominant Neovascular Inflammatory Vitreoretinopathy Phenotypes 2017 ·Ocular Immunology and Inflammation ·(unknown), Morag Shanks, Penny Clouston, Robert E. MacLaren	15
19	Next-generation sequencing (NGS) as a diagnostic tool for retinal degeneration reveals a much higher detection rate in early-onset disease 2012 ·European Journal of Human Genetics ·Morag Shanks, Susan M. Downes, Richard R. Copley, Stefano Lise, John Broxholme, (unknown), (unknown), Wayne I. L. Davies, Mark W. Hankins, (unknown), Penny Clouston, A Seller, Andrew O.M. Wilkie, Jenny C. Taylor, Jiannis Ragoussis, Andrea H. Németh	104
20	QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data 2007 ·Nucleic Acids Research ·Stefano Colella, Christopher Yau, Jennifer M. Taylor, Ghazala Mirza, Helen Butler, Penny Clouston, Anne S. Bassett, A Seller, Chris Holmes, Jiannis Ragoussis	400

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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