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Items: 16


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.

Oliver JA, Forman OP, Pettitt L, Mellersh CS.

PLoS One. 2016 May 18;11(5):e0156192. doi: 10.1371/journal.pone.0156192. eCollection 2016.


Canine genome assembly correction facilitates identification of a MAP9 deletion as a potential age of onset modifier for RPGRIP1-associated canine retinal degeneration.

Forman OP, Hitti RJ, Boursnell M, Miyadera K, Sargan D, Mellersh C.

Mamm Genome. 2016 Jun;27(5-6):237-45. doi: 10.1007/s00335-016-9627-x. Epub 2016 Mar 26.


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.

Forman OP, Pettitt L, Komáromy AM, Bedford P, Mellersh C.

PLoS One. 2015 Dec 18;10(12):e0143546. doi: 10.1371/journal.pone.0143546. eCollection 2015.


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

Oliver JA, Forman OP, Pettitt L, Mellersh CS.

PLoS One. 2015 Oct 16;10(10):e0140436. doi: 10.1371/journal.pone.0140436. eCollection 2015. Erratum in: PLoS One. 2016;11(5):e0156192.


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

Jenkins CA, Forman OP.

Canine Genet Epidemiol. 2015 May 14;2:7. doi: 10.1186/s40575-015-0019-4. eCollection 2015.


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

Forman OP, De Risio L, Matiasek K, Platt S, Mellersh C.

Mamm Genome. 2015 Feb;26(1-2):108-17. doi: 10.1007/s00335-014-9547-6. Epub 2014 Oct 30.


Investigating inherited diseases in dogs.

Forman OP, Mellersh CS.

Vet Rec. 2014 May 17;174(20):512. doi: 10.1136/vr.g3295. No abstract available.


Missense mutation in CAPN1 is associated with spinocerebellar ataxia in the Parson Russell Terrier dog breed.

Forman OP, De Risio L, Mellersh CS.

PLoS One. 2013 May 31;8(5):e64627. doi: 10.1371/journal.pone.0064627. Print 2013.


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

Forman OP, De Risio L, Stewart J, Mellersh CS, Beltran E.

BMC Genet. 2012 Jul 10;13:55. doi: 10.1186/1471-2156-13-55.


Congenital keratoconjunctivitis sicca and ichthyosiform dermatosis in Cavalier King Charles spaniel dogs. Part II: candidate gene study.

Hartley C, Barnett KC, Pettitt L, Forman OP, Blott S, Mellersh CS.

Vet Ophthalmol. 2012 Sep;15(5):327-32. doi: 10.1111/j.1463-5224.2012.00987.x. Epub 2012 Feb 16.


Parallel mapping and simultaneous sequencing reveals deletions in BCAN and FAM83H associated with discrete inherited disorders in a domestic dog breed.

Forman OP, Penderis J, Hartley C, Hayward LJ, Ricketts SL, Mellersh CS.

PLoS Genet. 2012 Jan;8(1):e1002462. doi: 10.1371/journal.pgen.1002462. Epub 2012 Jan 12.


Primary lens instability in ten related cats: clinical and genetic considerations.

Payen G, Hänninen RL, Mazzucchelli S, Forman OP, Mellersh CS, Savoldelli M, Chahory S.

J Small Anim Pract. 2011 Aug;52(8):402-10. doi: 10.1111/j.1748-5827.2011.01081.x.


An ADAMTS17 splice donor site mutation in dogs with primary lens luxation.

Farias FH, Johnson GS, Taylor JF, Giuliano E, Katz ML, Sanders DN, Schnabel RD, McKay SD, Khan S, Gharahkhani P, O'Leary CA, Pettitt L, Forman OP, Boursnell M, McLaughlin B, Ahonen S, Lohi H, Hernandez-Merino E, Gould DJ, Sargan DR, Mellersh C.

Invest Ophthalmol Vis Sci. 2010 Sep;51(9):4716-21. doi: 10.1167/iovs.09-5142. Epub 2010 Apr 7.


Identification of mutations in HSF4 in dogs of three different breeds with hereditary cataracts.

Mellersh CS, Pettitt L, Forman OP, Vaudin M, Barnett KC.

Vet Ophthalmol. 2006 Sep-Oct;9(5):369-78.


Canine RPGRIP1 mutation establishes cone-rod dystrophy in miniature longhaired dachshunds as a homologue of human Leber congenital amaurosis.

Mellersh CS, Boursnell ME, Pettitt L, Ryder EJ, Holmes NG, Grafham D, Forman OP, Sampson J, Barnett KC, Blanton S, Binns MM, Vaudin M.

Genomics. 2006 Sep;88(3):293-301. Epub 2006 Jun 27.


Characterization of the COMMD1 (MURR1) mutation causing copper toxicosis in Bedlington terriers.

Forman OP, Boursnell ME, Dunmore BJ, Stendall N, van den Sluis B, Fretwell N, Jones C, Wijmenga C, Rothuizen J, van Oost BA, Holmes NG, Binns MM, Jones P.

Anim Genet. 2005 Dec;36(6):497-501.

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