Oliver P. Forman

1.5k citations

37 papers · 805 indexed · h-index 18

Molecular Biology
Genetics top 10%
Neurology top 5%
Cellular and Molecular Neuroscience top 10%
Cell Biology

Co-authors: Cathryn S. Mellersh Louise Pettitt Luisa De Risio M. E. G. Boursnell Mark D. Vaudin Hannes Lohi Keith C. Barnett Elsa Beltrán
Topics: Neurological diseases and metabolism (12 papers)Retinal Development and Disorders (5 papers)Human-Animal Interaction Studies (4 papers)
Cited by: Neurology Genetics Aging
Journals: PLoS ONE Genome biology PLoS Genetics
Partner nations: United Kingdom United States Finland

In The Last Decade

Oliver P. Forman

35 papers receiving 782 citations

Peers

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

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	A splice donor variant in SLAMF1 is associated with canine atopic dermatitis 2025 ·Frontiers in Veterinary Science ·Oliver P. Forman,(unknown),A. G. Kerr,Julia Labadie,M. Denyer,Debbie Gow,Janet E. Alexander,Michelle Daya,(unknown),(unknown),Christian M. Leutenegger,Christian Savard,Jason T. Huff,(unknown)	0
2	Association of FGF4L1 Retrogene Insertion with Prolapsed Gland of the Nictitans (Cherry Eye) in Dogs 2024 ·Genes ·(unknown),Julia Labadie,Jason T. Huff,M. Denyer,Oliver P. Forman,(unknown),Jonas Donner	2
3	A loss-of-function variant in canine GLRA1 associates with a neurological disorder resembling human hyperekplexia 2023 ·Human Genetics ·(unknown),Thomas Flegel,Hanna Müller,Alexandra Kehl,(unknown),Kaspar Matiasek,Andrea Fischer,Jonas Donner,Oliver P. Forman,Hannes Lohi,Marjo K. Hytönen	4
4	Genetic epidemiology of blood type, disease and trait variants, and genome-wide genetic diversity in over 11,000 domestic cats 2022 ·PLoS Genetics ·Heidi Anderson,Stephen Davison,(unknown),(unknown),(unknown),(unknown),Kaisa Kyöstilä,(unknown),(unknown),(unknown),Oliver P. Forman,Hannes Lohi,Jonas Donner	11
5	Large scale across-breed genome-wide association study reveals a variant in HMGA2 associated with inguinal cryptorchidism risk in dogs 2022 ·PLoS ONE ·Matthew Blades,(unknown),Jonas Donner,(unknown),Oliver P. Forman	6
6	Whole Genome Sequencing of Giant Schnauzer Dogs with Progressive Retinal Atrophy Establishes NECAP1 as a Novel Candidate Gene for Retinal Degeneration 2019 ·Genes ·(unknown),(unknown),Ellen Schofield,(unknown),Maria Kaukonen,Oliver P. Forman,Tosso Leeb,Hannes Lohi,(unknown),David R. Sargan,Cathryn S. Mellersh	9
7	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 2019 ·PeerJ ·Nicolas Granger,Alejandro Luján Feliu‐Pascual,(unknown),Sally L. Ricketts,(unknown),Oliver P. Forman,Joshua Hersheson,Henry Houlden	4
8	Frequency and distribution of 152 genetic disease variants in over 100,000 mixed breed and purebred dogs 2018 ·PLoS Genetics ·Jonas Donner,Heidi Anderson,Stephen Davison,Angela M. Hughes,(unknown),Johan Lindqvist,(unknown),Balasubramanian Ganesan,(unknown),(unknown),Maria Kaukonen,Oliver P. Forman,Neale Fretwell,(unknown),Hannes Lohi	70
9	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 2016 ·BMC Genetics ·Joe Fenn,M. E. G. Boursnell,(unknown),(unknown),Rebecca Terry,Simon L. Priestnall,Patrick Kenny,Cathryn S. Mellersh,Oliver P. Forman	19
10	Canine genome assembly correction facilitates identification of a MAP9 deletion as a potential age of onset modifier for RPGRIP1-associated canine retinal degeneration 2016 ·Mammalian Genome ·Oliver P. Forman,(unknown),M. E. G. Boursnell,Keiko Miyadera,David R. Sargan,Cathryn S. Mellersh	21
11	Identification of a novel frameshift mutation in the DMD gene as the cause of muscular dystrophy in a Norfolk terrier dog 2015 ·PubMed ·(unknown),Oliver P. Forman	12
12	Two Independent Mutations in ADAMTS17 Are Associated with Primary Open Angle Glaucoma in the Basset Hound and Basset Fauve de Bretagne Breeds of Dog 2015 ·PLoS ONE ·(unknown),Oliver P. Forman,Louise Pettitt,Cathryn S. Mellersh	29
13	A Novel Genome-Wide Association Study Approach Using Genotyping by Exome Sequencing Leads to the Identification of a Primary Open Angle Glaucoma Associated Inversion Disrupting ADAMTS17 2015 ·PLoS ONE ·Oliver P. Forman,Louise Pettitt,András M. Komáromy,P. G. C. Bedford,Cathryn S. Mellersh	29
14	Spinocerebellar ataxia in the Italian Spinone dog is associated with an intronic GAA repeat expansion in ITPR1 2014 ·Mammalian Genome ·Oliver P. Forman,Luisa De Risio,Kaspar Matiasek,Simon R. Platt,Cathryn S. Mellersh	19
15	Parallel Mapping and Simultaneous Sequencing Reveals Deletions in BCAN and FAM83H Associated with Discrete Inherited Disorders in a Domestic Dog Breed 2012 ·PLoS Genetics ·Oliver P. Forman,Jacques Penderis,Claudia Hartley,(unknown),Sally L. Ricketts,Cathryn S. Mellersh	48
16	Genome-wide mRNA sequencing of a single canine cerebellar cortical degeneration case leads to the identification of a disease associated SPTBN2 mutation 2012 ·BMC Genetics ·Oliver P. Forman,Luisa De Risio,Jennifer Stewart,Cathryn S. Mellersh,Elsa Beltrán	41
17	Congenital keratoconjunctivitis sicca and ichthyosiform dermatosis in Cavalier King Charles spaniel dogs–part II: candidate gene study 2012 ·Veterinary Ophthalmology ·Claudia Hartley,Keith C. Barnett,Louise Pettitt,Oliver P. Forman,Sarah Blott,Cathryn S. Mellersh	6
18	Primary lens instability in ten related cats: clinical and genetic considerations 2011 ·Journal of Small Animal Practice ·(unknown),(unknown),Serena Mazzucchelli,Oliver P. Forman,Cathryn S. Mellersh,Michèle Savoldelli,Sabine Chahory	9
19	ADAMTS17 mutation associated with primary lens luxation is widespread among breeds 2011 ·Veterinary Ophthalmology ·David Gould,Louise Pettitt,Bryan McLaughlin,Nigel G. Holmes,Oliver P. Forman,Anne Thomas,Saija Ahonen,Hannes Lohi,Caroline A. O’Leary,David R. Sargan,Cathryn S. Mellersh	39
20	Identification of mutations in HSF4 in dogs of three different breeds with hereditary cataracts 2006 ·Veterinary Ophthalmology ·Cathryn S. Mellersh,Louise Pettitt,Oliver P. Forman,Mark D. Vaudin,Keith C. Barnett	49

About Oliver P. Forman

Oliver P. Forman is a scholar working on Equine, Neurology and Cell Biology, having authored 37 papers that have together received 805 indexed citations. Recurring topics across this work include Neurological diseases and metabolism (12 papers), Retinal Development and Disorders (5 papers) and Human-Animal Interaction Studies (4 papers). The work is most often cited by research in Neurology (146 citations), Genetics (321 citations) and Aging (18 citations). Oliver P. Forman has collaborated with scholars based in United Kingdom, United States and Finland. Frequent co-authors include Cathryn S. Mellersh, Louise Pettitt, Luisa De Risio, M. E. G. Boursnell, Mark D. Vaudin, Hannes Lohi, Keith C. Barnett, Elsa Beltrán, N. G. Holmes and M. M. Binns. Their work appears in journals such as PLoS ONE, Genome biology and PLoS Genetics.

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.

Explore authors with similar magnitude of impact