Identification of a novel frameshift mutation in the DMD gene as the cause of muscular dystrophy in a Norfolk terrier dog

por Jenkins, Christopher A, Forman, Oliver P
Publicado 2015

Missense Mutation in CAPN1 Is Associated with Spinocerebellar Ataxia in the Parson Russell Terrier Dog Breed

por Forman, Oliver P., De Risio, Luisa, Mellersh, Cathryn S.
Publicado 2013

Two Independent Mutations in ADAMTS17 Are Associated with Primary Open Angle Glaucoma in the Basset Hound and Basset Fauve de Bretagne Breeds of Dog

por Oliver, James A. C., Forman, Oliver P., Pettitt, Louise, Mellersh, Cathryn S.
Publicado 2015

Correction: Two Independent Mutations in ADAMTS17 Are Associated with Primary Open Angle Glaucoma in the Basset Hound and Basset Fauve de Bretagne Breeds of Dog

por Oliver, James A. C., Forman, Oliver P., Pettitt, Louise, Mellersh, Cathryn S.
Publicado 2016

Genome-wide mRNA sequencing of a single canine cerebellar cortical degeneration case leads to the identification of a disease associated SPTBN2 mutation

por Forman, Oliver P, De Risio, Luisa, Stewart, Jennifer, Mellersh, Cathryn S, Beltran, Elsa
Publicado 2012

Spinocerebellar ataxia in the Italian Spinone dog is associated with an intronic GAA repeat expansion in ITPR1

por Forman, Oliver P., De Risio, Luisa, Matiasek, Kaspar, Platt, Simon, Mellersh, Cathryn
Publicado 2014

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 ADA...

por Forman, Oliver P., Pettitt, Louise, Komáromy, András M., Bedford, Peter, Mellersh, Cathryn
Publicado 2015

Large scale across-breed genome-wide association study reveals a variant in HMGA2 associated with inguinal cryptorchidism risk in dogs

por Blades, Matthew, Freyer, Jamie, Donner, Jonas, Chodroff Foran, Rebecca, Forman, Oliver P.
Publicado 2022

Parallel Mapping and Simultaneous Sequencing Reveals Deletions in BCAN and FAM83H Associated with Discrete Inherited Disorders in a Domestic Dog Breed

por Forman, Oliver P., Penderis, Jacques, Hartley, Claudia, Hayward, Louisa J., Ricketts, Sally L., Mellersh, Cathryn S.
Publicado 2012

A loss-of-function variant in canine GLRA1 associates with a neurological disorder resembling human hyperekplexia

por Heinonen, Tiina, Flegel, Thomas, Müller, Hanna, Kehl, Alexandra, Hundi, Sruthi, Matiasek, Kaspar, Fischer, Andrea, Donner, Jonas, Forman, Oliver P., Lohi, Hannes, Hytönen, Marjo K.
Publicado 2023

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

por Fenn, Joe, Boursnell, Mike, Hitti, Rebekkah J., Jenkins, Christopher A., Terry, Rebecca L., Priestnall, Simon L., Kenny, Patrick J., Mellersh, Cathryn S., Forman, Oliver P.
Publicado 2016

Defining the ABC of gene essentiality in streptococci

por Charbonneau, Amelia R. L., Forman, Oliver P., Cain, Amy K., Newland, Graham, Robinson, Carl, Boursnell, Mike, Parkhill, Julian, Leigh, James A., Maskell, Duncan J., Waller, Andrew S.
Publicado 2017

Genetic prevalence and clinical relevance of canine Mendelian disease variants in over one million dogs

por Donner, Jonas, Freyer, Jamie, Davison, Stephen, Anderson, Heidi, Blades, Matthew, Honkanen, Leena, Inman, Laura, Brookhart-Knox, Casey A., Louviere, Annette, Forman, Oliver P., Chodroff Foran, Rebecca
Publicado 2023

An Inversion Disrupting FAM134B Is Associated with Sensory Neuropathy in the Border Collie Dog Breed

por Forman, Oliver P., Hitti, Rebekkah J., Pettitt, Louise, Jenkins, Christopher A., O’Brien, Dennis P., Shelton, G. Diane, De Risio, Luisa, Quintana, Rodrigo Gutierrez, Beltran, Elsa, Mellersh, Cathryn
Publicado 2016

Whole Genome Sequencing of Giant Schnauzer Dogs with Progressive Retinal Atrophy Establishes NECAP1 as a Novel Candidate Gene for Retinal Degeneration

por Hitti, Rebekkah J., Oliver, James A. C., Schofield, Ellen C., Bauer, Anina, Kaukonen, Maria, Forman, Oliver P., Leeb, Tosso, Lohi, Hannes, Burmeister, Louise M., Sargan, David, Mellersh, Cathryn S.
Publicado 2019

An intronic LINE-1 insertion in MERTK is strongly associated with retinopathy in Swedish Vallhund dogs

por Everson, Richard, Pettitt, Louise, Forman, Oliver P., Dower-Tylee, Olivia, McLaughlin, Bryan, Ahonen, Saija, Kaukonen, Maria, Komáromy, András M., Lohi, Hannes, Mellersh, Cathryn S., Sansom, Jane, Ricketts, Sally L.
Publicado 2017

Genetic epidemiology of blood type, disease and trait variants, and genome-wide genetic diversity in over 11,000 domestic cats

por Anderson, Heidi, Davison, Stephen, Lytle, Katherine M., Honkanen, Leena, Freyer, Jamie, Mathlin, Julia, Kyöstilä, Kaisa, Inman, Laura, Louviere, Annette, Chodroff Foran, Rebecca, Forman, Oliver P., Lohi, Hannes, Donner, Jonas
Publicado 2022

Frequency and distribution of 152 genetic disease variants in over 100,000 mixed breed and purebred dogs

por Donner, Jonas, Anderson, Heidi, Davison, Stephen, Hughes, Angela M., Bouirmane, Julia, Lindqvist, Johan, Lytle, Katherine M., Ganesan, Balasubramanian, Ottka, Claudia, Ruotanen, Päivi, Kaukonen, Maria, Forman, Oliver P., Fretwell, Neale, Cole, Cynthia A., Lohi, Hannes
Publicado 2018

Correction: Frequency and distribution of 152 genetic disease variants in over 100,000 mixed breed and purebred dogs

por Donner, Jonas, Anderson, Heidi, Davison, Stephen, Hughes, Angela M., Bouirmane, Julia, Lindqvist, Johan, Lytle, Katherine M., Ganesan, Balasubramanian, Ottka, Claudia, Ruotanen, Päivi, Kaukonen, Maria, Forman, Oliver P., Fretwell, Neale, Cole, Cynthia A., Lohi, Hannes
Publicado 2019