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Items: 1 to 50 of 146

1.

Identification and validation of genetic variants predictive of gait in standardbred horses.

McCoy AM, Beeson SK, Rubin CJ, Andersson L, Caputo P, Lykkjen S, Moore A, Piercy RJ, Mickelson JR, McCue ME.

PLoS Genet. 2019 May 28;15(5):e1008146. doi: 10.1371/journal.pgen.1008146. eCollection 2019 May.

2.

Evaluation of an HMGA2 variant for pleiotropic effects on height and metabolic traits in ponies.

Norton EM, Avila F, Schultz NE, Mickelson JR, Geor RJ, McCue ME.

J Vet Intern Med. 2019 Mar;33(2):942-952. doi: 10.1111/jvim.15403. Epub 2019 Jan 21.

3.

Associations between endocrine disrupting chemicals and equine metabolic syndrome phenotypes.

Durward-Akhurst SA, Schultz NE, Norton EM, Rendahl AK, Besselink H, Behnisch PA, Brouwer A, Geor RJ, Mickelson JR, McCue ME.

Chemosphere. 2019 Mar;218:652-661. doi: 10.1016/j.chemosphere.2018.11.136. Epub 2018 Nov 26.

PMID:
30502704
4.

Heritability of metabolic traits associated with equine metabolic syndrome in Welsh ponies and Morgan horses.

Norton EM, Schultz NE, Rendahl AK, Mcfarlane D, Geor RJ, Mickelson JR, McCue ME.

Equine Vet J. 2019 Jul;51(4):475-480. doi: 10.1111/evj.13053. Epub 2018 Dec 15.

PMID:
30472742
5.

SNP-based heritability and genetic architecture of tarsal osteochondrosis in North American Standardbred horses.

McCoy AM, Norton EM, Kemper AM, Beeson SK, Mickelson JR, McCue ME.

Anim Genet. 2019 Feb;50(1):78-81. doi: 10.1111/age.12738. Epub 2018 Oct 24.

PMID:
30353927
6.

Genome-Wide Signatures of Selection Reveal Genes Associated With Performance in American Quarter Horse Subpopulations.

Avila F, Mickelson JR, Schaefer RJ, McCue ME.

Front Genet. 2018 Jul 19;9:249. doi: 10.3389/fgene.2018.00249. eCollection 2018.

7.

A Missense Mutation in the Vacuolar Protein Sorting 11 (VPS11) Gene Is Associated with Neuroaxonal Dystrophy in Rottweiler Dogs.

Lucot KL, Dickinson PJ, Finno CJ, Mansour TA, Letko A, Minor KM, Mickelson JR, Drögemüller C, Brown CT, Bannasch DL.

G3 (Bethesda). 2018 Jul 31;8(8):2773-2780. doi: 10.1534/g3.118.200376.

8.

Canine NAPEPLD-associated models of human myelin disorders.

Minor KM, Letko A, Becker D, Drögemüller M, Mandigers PJJ, Bellekom SR, Leegwater PAJ, Stassen QEM, Putschbach K, Fischer A, Flegel T, Matiasek K, Ekenstedt KJ, Furrow E, Patterson EE, Platt SR, Kelly PA, Cassidy JP, Shelton GD, Lucot K, Bannasch DL, Martineau H, Muir CF, Priestnall SL, Henke D, Oevermann A, Jagannathan V, Mickelson JR, Drögemüller C.

Sci Rep. 2018 Apr 11;8(1):5818. doi: 10.1038/s41598-018-23938-7.

9.

A GJA9 frameshift variant is associated with polyneuropathy in Leonberger dogs.

Becker D, Minor KM, Letko A, Ekenstedt KJ, Jagannathan V, Leeb T, Shelton GD, Mickelson JR, Drögemüller C.

BMC Genomics. 2017 Aug 25;18(1):662. doi: 10.1186/s12864-017-4081-z.

10.

Developing a 670k genotyping array to tag ~2M SNPs across 24 horse breeds.

Schaefer RJ, Schubert M, Bailey E, Bannasch DL, Barrey E, Bar-Gal GK, Brem G, Brooks SA, Distl O, Fries R, Finno CJ, Gerber V, Haase B, Jagannathan V, Kalbfleisch T, Leeb T, Lindgren G, Lopes MS, Mach N, da Câmara Machado A, MacLeod JN, McCoy A, Metzger J, Penedo C, Polani S, Rieder S, Tammen I, Tetens J, Thaller G, Verini-Supplizi A, Wade CM, Wallner B, Orlando L, Mickelson JR, McCue ME.

BMC Genomics. 2017 Jul 27;18(1):565. doi: 10.1186/s12864-017-3943-8.

11.

Border Collie Collapse: Owner Survey Results and Veterinary Description of Videotaped Episodes.

Taylor S, Minor K, Shmon CL, Shelton GD, Patterson EE, Mickelson JR.

J Am Anim Hosp Assoc. 2016 Nov/Dec;52(6):364-370. Epub 2016 Sep 29.

PMID:
27685362
12.

A highly prevalent equine glycogen storage disease is explained by constitutive activation of a mutant glycogen synthase.

Maile CA, Hingst JR, Mahalingan KK, O'Reilly AO, Cleasby ME, Mickelson JR, McCue ME, Anderson SM, Hurley TD, Wojtaszewski JFP, Piercy RJ.

Biochim Biophys Acta Gen Subj. 2017 Jan;1861(1 Pt A):3388-3398. doi: 10.1016/j.bbagen.2016.08.021. Epub 2016 Aug 31.

13.

Heritability of Recurrent Exertional Rhabdomyolysis in Standardbred and Thoroughbred Racehorses Derived From SNP Genotyping Data.

Norton EM, Mickelson JR, Binns MM, Blott SC, Caputo P, Isgren CM, McCoy AM, Moore A, Piercy RJ, Swinburne JE, Vaudin M, McCue ME.

J Hered. 2016 Nov;107(6):537-43. doi: 10.1093/jhered/esw042. Epub 2016 Aug 3.

14.

Identification and validation of risk loci for osteochondrosis in standardbreds.

McCoy AM, Beeson SK, Splan RK, Lykkjen S, Ralston SL, Mickelson JR, McCue ME.

BMC Genomics. 2016 Jan 12;17:41. doi: 10.1186/s12864-016-2385-z.

15.

Genome-wide SNP data show little differentiation between the Appaloosa and other American stock horse breeds.

Petersen JL, Mickelson JR, Valberg SJ, McCue ME.

Anim Genet. 2015 Oct;46(5):585-6. doi: 10.1111/age.12301. Epub 2015 May 22. No abstract available.

PMID:
25997467
16.

The genetics of skeletal muscle disorders in horses.

Mickelson JR, Valberg SJ.

Annu Rev Anim Biosci. 2015;3:197-217. doi: 10.1146/annurev-animal-022114-110653. Epub 2014 Sep 12. Review.

PMID:
25387114
17.

An ARHGEF10 deletion is highly associated with a juvenile-onset inherited polyneuropathy in Leonberger and Saint Bernard dogs.

Ekenstedt KJ, Becker D, Minor KM, Shelton GD, Patterson EE, Bley T, Oevermann A, Bilzer T, Leeb T, Drögemüller C, Mickelson JR.

PLoS Genet. 2014 Oct 2;10(10):e1004635. doi: 10.1371/journal.pgen.1004635. eCollection 2014 Oct.

18.

Haplotype diversity in the equine myostatin gene with focus on variants associated with race distance propensity and muscle fiber type proportions.

Petersen JL, Valberg SJ, Mickelson JR, McCue ME.

Anim Genet. 2014 Dec;45(6):827-35. doi: 10.1111/age.12205. Epub 2014 Aug 26.

19.

Genetic risk factors for insidious equine recurrent uveitis in Appaloosa horses.

Fritz KL, Kaese HJ, Valberg SJ, Hendrickson JA, Rendahl AK, Bellone RR, Dynes KM, Wagner ML, Lucio MA, Cuomo FM, Brinkmeyer-Langford CL, Skow LC, Mickelson JR, Rutherford MS, McCue ME.

Anim Genet. 2014 Jun;45(3):392-9. doi: 10.1111/age.12129. Epub 2014 Jan 28.

PMID:
24467435
20.

The American Quarter Horse: population structure and relationship to the thoroughbred.

Petersen JL, Mickelson JR, Cleary KD, McCue ME.

J Hered. 2014 Mar-Apr;105(2):148-62. doi: 10.1093/jhered/est079. Epub 2013 Nov 29.

21.

Evidence of positive selection for a glycogen synthase (GYS1) mutation in domestic horse populations.

McCoy AM, Schaefer R, Petersen JL, Morrell PL, Slamka MA, Mickelson JR, Valberg SJ, McCue ME.

J Hered. 2014 Mar-Apr;105(2):163-72. doi: 10.1093/jhered/est075. Epub 2013 Nov 8.

22.

Coat color genotypes and risk and severity of melanoma in gray quarter horses.

Teixeira RB, Rendahl AK, Anderson SM, Mickelson JR, Sigler D, Buchanan BR, Coleman RJ, McCue ME.

J Vet Intern Med. 2013 Sep-Oct;27(5):1201-8. doi: 10.1111/jvim.12133. Epub 2013 Jul 22.

23.

Equine developmental orthopaedic diseases--a genome-wide association study of first phalanx plantar osteochondral fragments in Standardbred trotters.

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

Anim Genet. 2013 Dec;44(6):766-9. doi: 10.1111/age.12064. Epub 2013 Jun 7.

PMID:
23742657
24.

Relationship between dynamin 1 mutation status and characteristics of recurrent episodes of exercise-induced collapse in Labrador Retrievers.

Furrow E, Minor KM, Taylor SM, Mickelson JR, Patterson EE.

J Am Vet Med Assoc. 2013 Mar 15;242(6):786-91. doi: 10.2460/javma.242.6.786.

PMID:
23445289
25.

A Gly98Val mutation in the N-Myc downstream regulated gene 1 (NDRG1) in Alaskan Malamutes with polyneuropathy.

Bruun CS, Jäderlund KH, Berendt M, Jensen KB, Spodsberg EH, Gredal H, Shelton GD, Mickelson JR, Minor KM, Lohi H, Bjerkås I, Stigen O, Espenes A, Rohdin C, Edlund R, Ohlsson J, Cizinauskas S, Leifsson PS, Drögemüller C, Moe L, Cirera S, Fredholm M.

PLoS One. 2013;8(2):e54547. doi: 10.1371/journal.pone.0054547. Epub 2013 Feb 5.

26.

Genetic diversity in the modern horse illustrated from genome-wide SNP data.

Petersen JL, Mickelson JR, Cothran EG, Andersson LS, Axelsson J, Bailey E, Bannasch D, Binns MM, Borges AS, Brama P, da Câmara Machado A, Distl O, Felicetti M, Fox-Clipsham L, Graves KT, Guérin G, Haase B, Hasegawa T, Hemmann K, Hill EW, Leeb T, Lindgren G, Lohi H, Lopes MS, McGivney BA, Mikko S, Orr N, Penedo MC, Piercy RJ, Raekallio M, Rieder S, Røed KH, Silvestrelli M, Swinburne J, Tozaki T, Vaudin M, M Wade C, McCue ME.

PLoS One. 2013;8(1):e54997. doi: 10.1371/journal.pone.0054997. Epub 2013 Jan 30.

27.

Genome-wide analysis reveals selection for important traits in domestic horse breeds.

Petersen JL, Mickelson JR, Rendahl AK, Valberg SJ, Andersson LS, Axelsson J, Bailey E, Bannasch D, Binns MM, Borges AS, Brama P, da Câmara Machado A, Capomaccio S, Cappelli K, Cothran EG, Distl O, Fox-Clipsham L, Graves KT, Guérin G, Haase B, Hasegawa T, Hemmann K, Hill EW, Leeb T, Lindgren G, Lohi H, Lopes MS, McGivney BA, Mikko S, Orr N, Penedo MC, Piercy RJ, Raekallio M, Rieder S, Røed KH, Swinburne J, Tozaki T, Vaudin M, Wade CM, McCue ME.

PLoS Genet. 2013;9(1):e1003211. doi: 10.1371/journal.pgen.1003211. Epub 2013 Jan 17.

28.

Mutations in DMRT3 affect locomotion in horses and spinal circuit function in mice.

Andersson LS, Larhammar M, Memic F, Wootz H, Schwochow D, Rubin CJ, Patra K, Arnason T, Wellbring L, Hjälm G, Imsland F, Petersen JL, McCue ME, Mickelson JR, Cothran G, Ahituv N, Roepstorff L, Mikko S, Vallstedt A, Lindgren G, Andersson L, Kullander K.

Nature. 2012 Aug 30;488(7413):642-6. doi: 10.1038/nature11399.

29.

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.

30.

A high density SNP array for the domestic horse and extant Perissodactyla: utility for association mapping, genetic diversity, and phylogeny studies.

McCue ME, Bannasch DL, Petersen JL, Gurr J, Bailey E, Binns MM, Distl O, Guérin G, Hasegawa T, Hill EW, Leeb T, Lindgren G, Penedo MC, Røed KH, Ryder OA, Swinburne JE, Tozaki T, Valberg SJ, Vaudin M, Lindblad-Toh K, Wade CM, Mickelson JR.

PLoS Genet. 2012 Jan;8(1):e1002451. doi: 10.1371/journal.pgen.1002451. Epub 2012 Jan 12.

31.

Canine epilepsy genetics.

Ekenstedt KJ, Patterson EE, Mickelson JR.

Mamm Genome. 2012 Feb;23(1-2):28-39. doi: 10.1007/s00335-011-9362-2. Epub 2011 Oct 30. Review.

PMID:
22037590
32.

Presence and impact of the exercise-induced collapse associated DNM1 mutation in Labrador retrievers and other breeds.

Minor KM, Patterson EE, Keating MK, Gross SD, Ekenstedt KJ, Taylor SM, Mickelson JR.

Vet J. 2011 Aug;189(2):214-9. doi: 10.1016/j.tvjl.2011.06.022. Epub 2011 Jul 22.

PMID:
21782486
33.

Epidemiological and genetic study of exertional rhabdomyolysis in a Warmblood horse family in Switzerland.

Johlig L, Valberg SJ, Mickelson JR, Klukowska J, Reusser HR, Straub R, Gerber V.

Equine Vet J. 2011 Mar;43(2):240-5. doi: 10.1111/j.2042-3306.2010.00161.x.

PMID:
21592222
34.

Candidate genes for idiopathic epilepsy in four dog breeds.

Ekenstedt KJ, Patterson EE, Minor KM, Mickelson JR.

BMC Genet. 2011 Apr 25;12:38. doi: 10.1186/1471-2156-12-38.

35.

Presence of the glycogen synthase 1 (GYS1) mutation causing type 1 polysaccharide storage myopathy in continental European draught horse breeds.

Baird JD, Valberg SJ, Anderson SM, McCue ME, Mickelson JR.

Vet Rec. 2010 Nov 13;167(20):781-4. doi: 10.1136/vr.c3447.

PMID:
21262610
36.

Estimated prevalence of the Type 1 Polysaccharide Storage Myopathy mutation in selected North American and European breeds.

McCue ME, Anderson SM, Valberg SJ, Piercy RJ, Barakzai SZ, Binns MM, Distl O, Penedo MC, Wagner ML, Mickelson JR.

Anim Genet. 2010 Dec;41 Suppl 2:145-9. doi: 10.1111/j.1365-2052.2010.02124.x.

PMID:
21070288
37.

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
38.

MTM1 mutation associated with X-linked myotubular myopathy in Labrador Retrievers.

Beggs AH, Böhm J, Snead E, Kozlowski M, Maurer M, Minor K, Childers MK, Taylor SM, Hitte C, Mickelson JR, Guo LT, Mizisin AP, Buj-Bello A, Tiret L, Laporte J, Shelton GD.

Proc Natl Acad Sci U S A. 2010 Aug 17;107(33):14697-702. doi: 10.1073/pnas.1003677107. Epub 2010 Aug 3.

39.

Genome sequence, comparative analysis, and population genetics of the domestic horse.

Wade CM, Giulotto E, Sigurdsson S, Zoli M, Gnerre S, Imsland F, Lear TL, Adelson DL, Bailey E, Bellone RR, Blöcker H, Distl O, Edgar RC, Garber M, Leeb T, Mauceli E, MacLeod JN, Penedo MC, Raison JM, Sharpe T, Vogel J, Andersson L, Antczak DF, Biagi T, Binns MM, Chowdhary BP, Coleman SJ, Della Valle G, Fryc S, Guérin G, Hasegawa T, Hill EW, Jurka J, Kiialainen A, Lindgren G, Liu J, Magnani E, Mickelson JR, Murray J, Nergadze SG, Onofrio R, Pedroni S, Piras MF, Raudsepp T, Rocchi M, Røed KH, Ryder OA, Searle S, Skow L, Swinburne JE, Syvänen AC, Tozaki T, Valberg SJ, Vaudin M, White JR, Zody MC; Broad Institute Genome Sequencing Platform; Broad Institute Whole Genome Assembly Team, Lander ES, Lindblad-Toh K.

Science. 2009 Nov 6;326(5954):865-7. doi: 10.1126/science.1178158.

40.

A glycogen synthase 1 mutation associated with equine polysaccharide storage myopathy and exertional rhabdomyolysis occurs in a variety of UK breeds.

Stanley RL, McCue ME, Valberg SJ, Mickelson JR, Mayhew IG, McGowan C, Hahn CN, Patterson-Kane JC, Piercy RJ.

Equine Vet J. 2009 Jul;41(6):597-601.

PMID:
19803057
41.

Comparative skeletal muscle histopathologic and ultrastructural features in two forms of polysaccharide storage myopathy in horses.

McCue ME, Armién AG, Lucio M, Mickelson JR, Valberg SJ.

Vet Pathol. 2009 Nov;46(6):1281-91. doi: 10.1354/vp.08-VP-0177-M-FL. Epub 2009 Jul 15.

PMID:
19605906
42.

Evaluations of labrador retrievers with exercise-induced collapse, including response to a standardized strenuous exercise protocol.

Taylor SM, Shmon CL, Adams VJ, Mickelson JR, Patterson EN, Shelton GD.

J Am Anim Hosp Assoc. 2009 Jan-Feb;45(1):3-13.

PMID:
19122058
43.

Evaluation of allele frequencies of inherited disease genes in subgroups of American Quarter Horses.

Tryon RC, Penedo MC, McCue ME, Valberg SJ, Mickelson JR, Famula TR, Wagner ML, Jackson M, Hamilton MJ, Nooteboom S, Bannasch DL.

J Am Vet Med Assoc. 2009 Jan 1;234(1):120-5. doi: 10.2460/javma.234.1.120.

PMID:
19119976
44.

Polysaccharide storage myopathy phenotype in quarter horse-related breeds is modified by the presence of an RYR1 mutation.

McCue ME, Valberg SJ, Jackson M, Borgia L, Lucio M, Mickelson JR.

Neuromuscul Disord. 2009 Jan;19(1):37-43. doi: 10.1016/j.nmd.2008.10.001. Epub 2008 Dec 3.

PMID:
19056269
45.

Assessment of the transformation of equine skin-derived fibroblasts to multinucleated skeletal myotubes following lentiviral-induced expression of equine myogenic differentiation 1.

Fernandez-Fuente M, Ames EG, Wagner ML, Zhou H, Strom M, Zammit PS, Mickelson JR, Muntoni F, Brown SC, Piercy RJ.

Am J Vet Res. 2008 Dec;69(12):1637-45. doi: 10.2460/ajvr.69.12.1637.

PMID:
19046012
46.

Exercise-induced collapse of Labrador retrievers: survey results and preliminary investigation of heritability.

Taylor SM, Shmon CL, Shelton GD, Patterson EN, Minor K, Mickelson JR.

J Am Anim Hosp Assoc. 2008 Nov-Dec;44(6):295-301.

PMID:
18981194
47.

A 4,103 marker integrated physical and comparative map of the horse genome.

Raudsepp T, Gustafson-Seabury A, Durkin K, Wagner ML, Goh G, Seabury CM, Brinkmeyer-Langford C, Lee EJ, Agarwala R, Stallknecht-Rice E, Schäffer AA, Skow LC, Tozaki T, Yasue H, Penedo MC, Lyons LA, Khazanehdari KA, Binns MM, MacLeod JN, Distl O, Guérin G, Leeb T, Mickelson JR, Chowdhary BP.

Cytogenet Genome Res. 2008;122(1):28-36. doi: 10.1159/000151313. Epub 2008 Oct 14.

48.

A GYS1 gene mutation is highly associated with polysaccharide storage myopathy in Cob Normand draught horses.

Herszberg B, McCue ME, Larcher T, Mata X, Vaiman A, Chaffaux S, Chérel Y, Valberg SJ, Mickelson JR, Guérin G.

Anim Genet. 2009 Feb;40(1):94-6. doi: 10.1111/j.1365-2052.2008.01778.x. Epub 2008 Sep 24.

PMID:
18822097
49.

A canine DNM1 mutation is highly associated with the syndrome of exercise-induced collapse.

Patterson EE, Minor KM, Tchernatynskaia AV, Taylor SM, Shelton GD, Ekenstedt KJ, Mickelson JR.

Nat Genet. 2008 Oct;40(10):1235-9. doi: 10.1038/ng.224. Epub 2008 Sep 21.

PMID:
18806795
50.

Glycogen synthase 1 (GYS1) mutation in diverse breeds with polysaccharide storage myopathy.

McCue ME, Valberg SJ, Lucio M, Mickelson JR.

J Vet Intern Med. 2008 Sep-Oct;22(5):1228-33. doi: 10.1111/j.1939-1676.2008.0167.x. Epub 2008 Aug 6.

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