Oliver P. Forman

1.5k total citations
37 papers, 805 citations indexed

About

Oliver P. Forman is a scholar working on Molecular Biology, Neurology and Genetics. According to data from OpenAlex, Oliver P. Forman has authored 37 papers receiving a total of 805 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 12 papers in Neurology and 12 papers in Genetics. Recurrent topics in Oliver P. Forman's work include Neurological diseases and metabolism (12 papers), Retinal Development and Disorders (5 papers) and Human-Animal Interaction Studies (4 papers). Oliver P. Forman is often cited by papers focused on Neurological diseases and metabolism (12 papers), Retinal Development and Disorders (5 papers) and Human-Animal Interaction Studies (4 papers). Oliver P. Forman collaborates with scholars based in United Kingdom, United States and Finland. Oliver P. Forman's co-authors include Cathryn S. Mellersh, Louise Pettitt, Luisa De Risio, M. E. G. Boursnell, Mark D. Vaudin, Hannes Lohi, Keith C. Barnett, N. G. Holmes, Elsa Beltrán and Sally L. Ricketts and has published in prestigious journals such as PLoS ONE, Genome biology and PLoS Genetics.

In The Last Decade

Oliver P. Forman

35 papers receiving 782 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 P. Forman United Kingdom 18 410 321 146 125 84 37 805
W. Schmahl Germany 17 563 1.4× 201 0.6× 57 0.4× 223 1.8× 72 0.9× 74 1.1k
Marie-Anne Colle France 19 524 1.3× 280 0.9× 44 0.3× 145 1.2× 91 1.1× 36 1.0k
Barbara Gandolfi United States 18 306 0.7× 327 1.0× 69 0.5× 30 0.2× 100 1.2× 39 759
Tracey Davey United Kingdom 15 694 1.7× 254 0.8× 20 0.1× 98 0.8× 101 1.2× 30 988
Tara Biagi United States 8 359 0.9× 534 1.7× 77 0.5× 30 0.2× 87 1.0× 12 982
Elaine Kenny Ireland 20 858 2.1× 456 1.4× 64 0.4× 94 0.8× 95 1.1× 37 1.5k
Victor V. Chizhikov United States 24 1.3k 3.1× 502 1.6× 100 0.7× 311 2.5× 181 2.2× 47 2.0k
A Eisenberg United States 11 765 1.9× 513 1.6× 49 0.3× 114 0.9× 52 0.6× 23 1.6k
Rhys Roberts United Kingdom 18 729 1.8× 229 0.7× 65 0.4× 256 2.0× 405 4.8× 40 1.4k
Richard Guyon France 12 329 0.8× 402 1.3× 28 0.2× 50 0.4× 47 0.6× 19 725

Countries citing papers authored by Oliver P. Forman

Since Specialization
Citations

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

Fields of papers citing papers by Oliver P. Forman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Oliver P. Forman

This figure shows the co-authorship network connecting the top 25 collaborators of Oliver P. Forman. A scholar is included among the top collaborators of Oliver P. Forman 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 P. Forman. Oliver P. Forman 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.
Forman, Oliver P., A. G. Kerr, Julia Labadie, et al.. (2025). A splice donor variant in SLAMF1 is associated with canine atopic dermatitis. Frontiers in Veterinary Science. 12. 1550617–1550617.
2.
Labadie, Julia, et al.. (2024). Association of FGF4L1 Retrogene Insertion with Prolapsed Gland of the Nictitans (Cherry Eye) in Dogs. Genes. 15(2). 198–198. 2 indexed citations
3.
Flegel, Thomas, Hanna Müller, Alexandra Kehl, et al.. (2023). A loss-of-function variant in canine GLRA1 associates with a neurological disorder resembling human hyperekplexia. Human Genetics. 142(8). 1221–1230. 4 indexed citations
4.
Barnaby, Hugh, Oliver P. Forman, Donald A. Wilson, et al.. (2023). Non-Linear Coupling Effects in Fully Depleted SOI Transistors. IEEE Transactions on Nuclear Science. 70(4). 434–441. 4 indexed citations
5.
Blades, Matthew, et al.. (2022). Large scale across-breed genome-wide association study reveals a variant in HMGA2 associated with inguinal cryptorchidism risk in dogs. PLoS ONE. 17(5). e0267604–e0267604. 6 indexed citations
6.
Anderson, Heidi, Stephen Davison, Kaisa Kyöstilä, et al.. (2022). Genetic epidemiology of blood type, disease and trait variants, and genome-wide genetic diversity in over 11,000 domestic cats. PLoS Genetics. 18(6). e1009804–e1009804. 11 indexed citations
7.
Groot, Maarten de, Heidi Anderson, Hans Bauer, et al.. (2021). Standardization of a SNP panel for parentage verification and identification in the domestic cat (Felis silvestris catus). Animal Genetics. 52(5). 675–682. 6 indexed citations
8.
Granger, Nicolas, Alejandro Luján Feliu‐Pascual, Sally L. Ricketts, et al.. (2019). Charcot-Marie-Tooth type 4B2 demyelinating neuropathy in miniature Schnauzer dogs caused by a novel splicing SBF2 (MTMR13) genetic variant: a new spontaneous clinical model. PeerJ. 7. e7983–e7983. 4 indexed citations
9.
Schofield, Ellen, Maria Kaukonen, Oliver P. Forman, et al.. (2019). Whole Genome Sequencing of Giant Schnauzer Dogs with Progressive Retinal Atrophy Establishes NECAP1 as a Novel Candidate Gene for Retinal Degeneration. Genes. 10(5). 385–385. 9 indexed citations
10.
Forman, Oliver P., Amy K. Cain, Carl Robinson, et al.. (2017). Defining the ABC of gene essentiality in streptococci. BMC Genomics. 18(1). 426–426. 23 indexed citations
11.
Fenn, Joe, M. E. G. Boursnell, Rebecca Terry, et al.. (2016). Genome sequencing reveals a splice donor site mutation in the SNX14 gene associated with a novel cerebellar cortical degeneration in the Hungarian Vizsla dog breed. BMC Genetics. 17(1). 123–123. 19 indexed citations
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Forman, Oliver P., Luisa De Risio, & Cathryn S. Mellersh. (2013). Missense Mutation in CAPN1 Is Associated with Spinocerebellar Ataxia in the Parson Russell Terrier Dog Breed. PLoS ONE. 8(5). e64627–e64627. 48 indexed citations
16.
Forman, Oliver P., et al.. (2012). Parallel Mapping and Simultaneous Sequencing Reveals Deletions in BCAN and FAM83H Associated with Discrete Inherited Disorders in a Domestic Dog Breed. PLoS Genetics. 8(1). e1002462–e1002462. 48 indexed citations
17.
Forman, Oliver P., Luisa De Risio, Jennifer Stewart, Cathryn S. Mellersh, & Elsa Beltrán. (2012). Genome-wide mRNA sequencing of a single canine cerebellar cortical degeneration case leads to the identification of a disease associated SPTBN2 mutation. BMC Genetics. 13(1). 55–55. 41 indexed citations
18.
Hartley, Claudia, Keith C. Barnett, Louise Pettitt, et al.. (2012). Congenital keratoconjunctivitis sicca and ichthyosiform dermatosis in Cavalier King Charles spaniel dogs–part II: candidate gene study. Veterinary Ophthalmology. 15(5). 327–332. 6 indexed citations
19.
Mellersh, Cathryn S., Louise Pettitt, Oliver P. Forman, Mark D. Vaudin, & Keith C. Barnett. (2006). Identification of mutations in HSF4 in dogs of three different breeds with hereditary cataracts. Veterinary Ophthalmology. 9(5). 369–378. 49 indexed citations
20.
Forman, Oliver P., M. E. G. Boursnell, Benjamin J. Dunmore, et al.. (2005). Characterization of theCOMMD1(MURR1) mutation causing copper toxicosis in Bedlington terriers. Animal Genetics. 36(6). 497–501. 36 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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