Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 78

1.

Results of a haplotype-based GWAS for recurrent laryngeal neuropathy in the horse.

Dupuis MC, Zhang Z, Druet T, Denoix JM, Charlier C, Lekeux P, Georges M.

Mamm Genome. 2011 Oct;22(9-10):613-20. doi: 10.1007/s00335-011-9337-3. Epub 2011 Jun 23.

PMID:
21698472
2.

Detection of copy number variants in the horse genome and examination of their association with recurrent laryngeal neuropathy.

Dupuis MC, Zhang Z, Durkin K, Charlier C, Lekeux P, Georges M.

Anim Genet. 2013 Apr;44(2):206-8. doi: 10.1111/j.1365-2052.2012.02373.x. Epub 2012 May 14.

PMID:
22582820
3.

Genomic analysis establishes correlation between growth and laryngeal neuropathy in Thoroughbreds.

Boyko AR, Brooks SA, Behan-Braman A, Castelhano M, Corey E, Oliveira KC, Swinburne JE, Todhunter RJ, Zhang Z, Ainsworth DM, Robinson NE.

BMC Genomics. 2014 Apr 3;15:259. doi: 10.1186/1471-2164-15-259.

4.

Genome-wide linkage and association analysis identifies major gene loci for guttural pouch tympany in Arabian and German warmblood horses.

Metzger J, Ohnesorge B, Distl O.

PLoS One. 2012;7(7):e41640. doi: 10.1371/journal.pone.0041640. Epub 2012 Jul 27.

5.

Genome-wide association analysis of osteochondrosis of the tibiotarsal joint in Norwegian Standardbred trotters.

Lykkjen S, Dolvik NI, McCue ME, Rendahl AK, Mickelson JR, Roed KH.

Anim Genet. 2010 Dec;41 Suppl 2:111-20. doi: 10.1111/j.1365-2052.2010.02117.x.

PMID:
21070284
6.

A genome-wide association study for quantitative trait loci of show-jumping in Hanoverian warmblood horses.

Schröder W, Klostermann A, Stock KF, Distl O.

Anim Genet. 2012 Aug;43(4):392-400. doi: 10.1111/j.1365-2052.2011.02265.x. Epub 2011 Oct 12.

PMID:
22497689
7.

Histological and ultrastructural evidence that recurrent laryngeal neuropathy is a bilateral mononeuropathy limited to recurrent laryngeal nerves.

Hahn CN, Matiasek K, Dixon PM, Molony V, Rodenacker K, Mayhew IG.

Equine Vet J. 2008 Nov;40(7):666-72.

PMID:
19165936
8.

A genome-wide association study of osteochondritis dissecans in the Thoroughbred.

Corbin LJ, Blott SC, Swinburne JE, Sibbons C, Fox-Clipsham LY, Helwegen M, Parkin TD, Newton JR, Bramlage LR, McIlwraith CW, Bishop SC, Woolliams JA, Vaudin M.

Mamm Genome. 2012 Apr;23(3-4):294-303. doi: 10.1007/s00335-011-9363-1. Epub 2011 Nov 4.

PMID:
22052004
9.

A genome-wide association study identifies risk loci to equine recurrent uveitis in German warmblood horses.

Kulbrock M, Lehner S, Metzger J, Ohnesorge B, Distl O.

PLoS One. 2013 Aug 14;8(8):e71619. doi: 10.1371/journal.pone.0071619. eCollection 2013.

10.

The prevalence of laryngeal disease in a large population of competition draft horses.

Brakenhoff JE, Holcombe SJ, Hauptman JG, Smith HK, Nickels FA, Caron JP.

Vet Surg. 2006 Aug;35(6):579-83.

PMID:
16911159
11.

Laryngeal paralysis: a study of 375 cases in a mixed-breed population of horses.

Dixon PM, McGorum BC, Railton DI, Hawe C, Tremaine WH, Pickles K, McCann J.

Equine Vet J. 2001 Sep;33(5):452-8.

PMID:
11558739
12.

A genome-wide association study demonstrates significant genetic variation for fracture risk in Thoroughbred racehorses.

Blott SC, Swinburne JE, Sibbons C, Fox-Clipsham LY, Helwegen M, Hillyer L, Parkin TD, Newton JR, Vaudin M.

BMC Genomics. 2014 Feb 21;15:147. doi: 10.1186/1471-2164-15-147.

13.

Whole-genome scan identifies quantitative trait loci for chronic pastern dermatitis in German draft horses.

Mittmann EH, Mömke S, Distl O.

Mamm Genome. 2010 Feb;21(1-2):95-103. doi: 10.1007/s00335-009-9244-z. Epub 2009 Dec 29.

PMID:
20039044
14.

Analysis of six genetic risk factors highly associated with AMD in the region surrounding ARMS2 and HTRA1 on chromosome 10, region q26.

Hadley D, Orlin A, Brown G, Brucker AJ, Ho AC, Regillo CD, Donoso LA, Tian L, Kaderli B, Stambolian D.

Invest Ophthalmol Vis Sci. 2010 Apr;51(4):2191-6. doi: 10.1167/iovs.09-3798. Epub 2009 Nov 20.

PMID:
19933195
15.

Genetic markers in standardbred trotters susceptible to the rhabdomyolysis syndrome.

Collinder E, Lindholm A, Rasmuson M.

Equine Vet J. 1997 Mar;29(2):117-20.

PMID:
9104560
16.

Genome-wide association study of osteochondrosis in the tarsocrural joint of Dutch Warmblood horses identifies susceptibility loci on chromosomes 3 and 10.

Orr N, Hill EW, Gu J, Govindarajan P, Conroy J, van Grevenhof EM, Ducro BJ, van Arendonk JA, Knaap JH, van Weeren PR, Machugh DE, Ennis S, Brama PA.

Anim Genet. 2013 Aug;44(4):408-12. doi: 10.1111/age.12016. Epub 2012 Dec 25.

PMID:
23278111
17.

A combined genome-wide linkage and association approach to find susceptibility loci for platelet function phenotypes in European American and African American families with coronary artery disease.

Mathias RA, Kim Y, Sung H, Yanek LR, Mantese VJ, Hererra-Galeano JE, Ruczinski I, Wilson AF, Faraday N, Becker LC, Becker DM.

BMC Med Genomics. 2010 Jun 7;3:22. doi: 10.1186/1755-8794-3-22.

19.

The association analysis of TBX6 polymorphism with susceptibility to congenital scoliosis in a Chinese Han population.

Fei Q, Wu Z, Wang H, Zhou X, Wang N, Ding Y, Wang Y, Qiu G.

Spine (Phila Pa 1976). 2010 Apr 20;35(9):983-8. doi: 10.1097/BRS.0b013e3181bc963c.

PMID:
20228709
20.

Genetic mapping of recurrent exertional rhabdomyolysis in a population of North American Thoroughbreds.

Fritz KL, McCue ME, Valberg SJ, Rendahl AK, Mickelson JR.

Anim Genet. 2012 Dec;43(6):730-8. doi: 10.1111/j.1365-2052.2012.02351.x. Epub 2012 Mar 23.

Supplemental Content

Support Center