Forman OP - Search Results

1

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. Farias FH, et al. Among authors: forman op. Invest Ophthalmol Vis Sci. 2010 Sep;51(9):4716-21. doi: 10.1167/iovs.09-5142. Epub 2010 Apr 7. Invest Ophthalmol Vis Sci. 2010. PMID: 20375329

2

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. Mellersh CS, et al. Among authors: forman op. Genomics. 2006 Sep;88(3):293-301. doi: 10.1016/j.ygeno.2006.05.004. Epub 2006 Jun 27. Genomics. 2006. PMID: 16806805 Free article.

3

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

Mellersh CS, Pettitt L, Forman OP, Vaudin M, Barnett KC. Mellersh CS, et al. Among authors: forman op. Vet Ophthalmol. 2006 Sep-Oct;9(5):369-78. doi: 10.1111/j.1463-5224.2006.00496.x. Vet Ophthalmol. 2006. PMID: 16939467

4

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. Payen G, et al. Among authors: forman op. J Small Anim Pract. 2011 Aug;52(8):402-10. doi: 10.1111/j.1748-5827.2011.01081.x. J Small Anim Pract. 2011. PMID: 21797871

5

ADAMTS17 mutation associated with primary lens luxation is widespread among breeds.

Gould D, Pettitt L, McLaughlin B, Holmes N, Forman O, Thomas A, Ahonen S, Lohi H, O'Leary C, Sargan D, Mellersh C. Gould D, et al. Vet Ophthalmol. 2011 Nov;14(6):378-84. doi: 10.1111/j.1463-5224.2011.00892.x. Epub 2011 Aug 3. Vet Ophthalmol. 2011. PMID: 22050825

6

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. Forman OP, et al. PLoS Genet. 2012 Jan;8(1):e1002462. doi: 10.1371/journal.pgen.1002462. Epub 2012 Jan 12. PLoS Genet. 2012. PMID: 22253609 Free PMC article.

7

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. Hartley C, et al. Among authors: forman op. Vet Ophthalmol. 2012 Sep;15(5):327-32. doi: 10.1111/j.1463-5224.2012.00987.x. Epub 2012 Feb 16. Vet Ophthalmol. 2012. PMID: 22339941 Free article.

8

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. Forman OP, et al. BMC Genet. 2012 Jul 10;13:55. doi: 10.1186/1471-2156-13-55. BMC Genet. 2012. PMID: 22781464 Free PMC article.

9

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

Forman OP, De Risio L, Mellersh CS. Forman OP, et al. PLoS One. 2013 May 31;8(5):e64627. doi: 10.1371/journal.pone.0064627. Print 2013. PLoS One. 2013. PMID: 23741357 Free PMC article.

10

Investigating inherited diseases in dogs.

Forman OP, Mellersh CS. Forman OP, et al. Vet Rec. 2014 May 17;174(20):512. doi: 10.1136/vr.g3295. Vet Rec. 2014. PMID: 24832891 No abstract available.

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