| Year |
Citation |
Score |
| 2024 |
Shelton GD, Mickelson JR, Friedenberg SG, Cullen JN, Graham K, Carpentier MC, Guo LT, Minor KM. Variants in and Associated with Muscle Hypertrophy, Dysphagia, and Gait Abnormalities in Young French Bulldogs. Animals : An Open Access Journal From Mdpi. 14. PMID 38473107 DOI: 10.3390/ani14050722 |
0.307 |
|
| 2023 |
Ekenstedt KJ, Minor KM, Shelton GD, Hammond JJ, Miller AD, Taylor SM, Huang Y, Mickelson JR. A SACS deletion variant in Great Pyrenees dogs causes autosomal recessive neuronal degeneration. Human Genetics. PMID 37758910 DOI: 10.1007/s00439-023-02599-1 |
0.723 |
|
| 2023 |
Jankelunas L, Murthy VD, Chen AV, Minor KM, Friedenberg SG, Cullen JN, Guo LT, Mickelson JR, Shelton GD. Novel COL6A3 frameshift variant in American Staffordshire Terrier dogs with Ullrich-like congenital muscular dystrophy. Journal of Veterinary Internal Medicine. PMID 37706358 DOI: 10.1111/jvim.16862 |
0.306 |
|
| 2022 |
Shelton GD, Minor KM, Vieira NM, Kunkel LM, Friedenberg SG, Cullen JN, Guo LT, Zatz M, Mickelson JR. Tandem duplication within the DMD gene in Labrador retrievers with a mild clinical phenotype. Neuromuscular Disorders : Nmd. PMID 36041985 DOI: 10.1016/j.nmd.2022.08.001 |
0.311 |
|
| 2022 |
Shelton GD, Minor KM, Guo LT, Thomas-Hollands A, Walsh KA, Friedenberg SG, Cullen JN, Mickelson JR. An Nonsense Mutation Associated with Congenital Dyserythropoietic Anemia and Polymyopathy in Labrador Retriever Littermates. Genes. 13. PMID 36011338 DOI: 10.3390/genes13081427 |
0.31 |
|
| 2021 |
Norton EM, Minor KM, Taylor SM, McCue ME, Mickelson JR. Heritability and Genomic Architecture of Episodic Exercise-Induced Collapse in Border Collies. Genes. 12. PMID 34946876 DOI: 10.3390/genes12121927 |
0.638 |
|
| 2021 |
Shelton GD, Minor KM, Thomovsky S, Guo LT, Friedenberg SG, Cullen JN, Mickelson JR. Congenital muscular dystrophy in a dog with a LAMA2 gene deletion. Journal of Veterinary Internal Medicine. PMID 34854126 DOI: 10.1111/jvim.16330 |
0.302 |
|
| 2021 |
Shelton GD, Minor KM, Guo LT, Friedenberg SG, Cullen JN, Hord JM, Venzke D, Anderson ME, Devereaux M, Prouty SJ, Handelman C, Campbell KP, Mickelson JR. Muscular dystrophy-dystroglycanopathy in a family of Labrador retrievers with a LARGE1 mutation. Neuromuscular Disorders : Nmd. PMID 34654610 DOI: 10.1016/j.nmd.2021.07.016 |
0.305 |
|
| 2020 |
Letko A, Minor KM, Friedenberg SG, Shelton GD, Salvador JP, Mandigers PJJ, Leegwater PAJ, Winkler PA, Petersen-Jones SM, Stanley BJ, Ekenstedt KJ, Johnson GS, Hansen L, Jagannathan V, Mickelson JR, et al. A Missense Variant Is Associated with Canine Laryngeal Paralysis and Polyneuropathy. Genes. 11. PMID 33261176 DOI: 10.3390/genes11121426 |
0.727 |
|
| 2020 |
Van Buren SL, Minor KM, Grahn RA, Mickelson JR, Grahn JC, Malvick J, Colangelo JR, Mueller E, Kuehnlein P, Kehl A. A Third Variant Causing Coat Color Dilution in Dogs. Genes. 11. PMID 32531980 DOI: 10.3390/Genes11060639 |
0.308 |
|
| 2020 |
Bolduc V, Minor KM, Hu Y, Kaur R, Friedenberg SG, Van Buren S, Guo LT, Glennon JC, Marioni-Henry K, Mickelson JR, Bönnemann CG, Shelton GD. Pathogenic variants in COL6A3 cause Ullrich-like congenital muscular dystrophy in young Labrador Retriever dogs. Neuromuscular Disorders : Nmd. PMID 32439203 DOI: 10.1016/J.Nmd.2020.03.005 |
0.346 |
|
| 2020 |
Roy MM, Norton EM, Rendahl AK, Schultz NE, McFarlane D, Geor RJ, Mickelson JR, McCue ME. Assessment of the FAM174A 11G allele as a risk allele for equine metabolic syndrome. Animal Genetics. PMID 32412131 DOI: 10.1111/Age.12952 |
0.634 |
|
| 2020 |
Leeb T, Leuthard F, Jagannathan V, Kiener S, Letko A, Roosje P, Welle MM, Gailbreath KL, Cannon A, Linek M, Banovic F, Olivry T, White SD, Batcher K, Bannasch D, ... ... Mickelson JR, et al. A Missense Variant Affecting the C-Terminal Tail of UNC93B1 in Dogs with Exfoliative Cutaneous Lupus Erythematosus (ECLE). Genes. 11. PMID 32028618 DOI: 10.3390/Genes11020159 |
0.369 |
|
| 2020 |
Beeson SK, Mickelson JR, McCue ME. Equine recombination map updated to EquCab3.0 Animal Genetics. 51: 341-342. PMID 31887785 DOI: 10.1111/Age.12898 |
0.581 |
|
| 2019 |
Norton E, Schultz N, Geor R, McFarlane D, Mickelson J, McCue M. Genome-Wide Association Analyses of Equine Metabolic Syndrome Phenotypes in Welsh Ponies and Morgan Horses. Genes. 10. PMID 31698676 DOI: 10.3390/Genes10110893 |
0.661 |
|
| 2019 |
Anderegg L, Im Hof Gut M, Hetzel U, Howerth EW, Leuthard F, Kyöstilä K, Lohi H, Pettitt L, Mellersh C, Minor KM, Mickelson JR, Batcher K, Bannasch D, Jagannathan V, Leeb T. NME5 frameshift variant in Alaskan Malamutes with primary ciliary dyskinesia. Plos Genetics. 15: e1008378. PMID 31479451 DOI: 10.1371/Journal.Pgen.1008378 |
0.423 |
|
| 2019 |
Beeson SK, Mickelson JR, McCue ME. Exploration of fine-scale recombination rate variation in the domestic horse. Genome Research. PMID 31434677 DOI: 10.1101/Gr.243311.118 |
0.641 |
|
| 2019 |
McCoy AM, Beeson SK, Rubin CJ, Andersson L, Caputo P, Lykkjen S, Moore A, Piercy RJ, Mickelson JR, McCue ME. Identification and validation of genetic variants predictive of gait in standardbred horses. Plos Genetics. 15: e1008146. PMID 31136578 DOI: 10.1371/Journal.Pgen.1008146 |
0.655 |
|
| 2019 |
Norton EM, Avila F, Schultz NE, Mickelson JR, Geor RJ, McCue ME. Evaluation of an HMGA2 variant for pleiotropic effects on height and metabolic traits in ponies. Journal of Veterinary Internal Medicine. PMID 30666754 DOI: 10.1111/Jvim.15403 |
0.582 |
|
| 2019 |
Durward-Akhurst SA, Schultz NE, Norton EM, Rendahl AK, Besselink H, Behnisch PA, Brouwer A, Geor RJ, Mickelson JR, McCue ME. Associations between endocrine disrupting chemicals and equine metabolic syndrome phenotypes. Chemosphere. 218: 652-661. PMID 30502704 DOI: 10.1016/J.Chemosphere.2018.11.136 |
0.608 |
|
| 2018 |
Norton EM, Schultz NE, Rendahl AK, Geor RJ, Mickelson JR, McCue ME. Heritability of metabolic traits associated with equine metabolic syndrome in Welsh ponies and Morgan horses. Equine Veterinary Journal. PMID 30472742 DOI: 10.1111/Evj.13053 |
0.619 |
|
| 2018 |
McCoy AM, Norton EM, Kemper AM, Beeson SK, Mickelson JR, McCue ME. SNP-based heritability and genetic architecture of tarsal osteochondrosis in North American Standardbred horses. Animal Genetics. PMID 30353927 DOI: 10.1111/Age.12738 |
0.643 |
|
| 2018 |
Avila F, Mickelson JR, Schaefer RJ, McCue ME. Genome-Wide Signatures of Selection Reveal Genes Associated With Performance in American Quarter Horse Subpopulations. Frontiers in Genetics. 9: 249. PMID 30105047 DOI: 10.3389/Fgene.2018.00249 |
0.67 |
|
| 2018 |
Lucot KL, Dickinson PJ, Finno CJ, Mansour TA, Letko A, Minor KM, Mickelson JR, Drögemüller C, Brown CT, Bannasch DL. A Missense Mutation in the Vacuolar Protein Sorting 11 () Gene Is Associated with Neuroaxonal Dystrophy in Rottweiler Dogs. G3 (Bethesda, Md.). PMID 29945969 DOI: 10.1534/G3.118.200376 |
0.43 |
|
| 2018 |
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, ... ... Mickelson JR, et al. Canine NAPEPLD-associated models of human myelin disorders. Scientific Reports. 8: 5818. PMID 29643404 DOI: 10.1038/S41598-018-23938-7 |
0.743 |
|
| 2017 |
Becker D, Minor KM, Letko A, Ekenstedt KJ, Jagannathan V, Leeb T, Shelton GD, Mickelson JR, Drögemüller C. A GJA9 frameshift variant is associated with polyneuropathy in Leonberger dogs. Bmc Genomics. 18: 662. PMID 28841859 DOI: 10.1186/S12864-017-4081-Z |
0.739 |
|
| 2017 |
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, ... ... Mickelson JR, et al. Developing a 670k genotyping array to tag ~2M SNPs across 24 horse breeds. Bmc Genomics. 18: 565. PMID 28750625 DOI: 10.1186/S12864-017-3943-8 |
0.616 |
|
| 2017 |
Bordbari MH, Penedo MCT, Aleman M, Valberg SJ, Mickelson J, Finno CJ. Deletion of 2.7 kb near HOXD3 in an Arabian horse with occipitoatlantoaxial malformation. Animal Genetics. 48: 287-294. PMID 28111759 DOI: 10.1111/Age.12531 |
0.387 |
|
| 2017 |
Norton EM, Avila F, Schultz NS, Mickelson JR, McCue MM. Identification of a genetic locus associated with height and metabolic traits in Welsh ponies Journal of Equine Veterinary Science. 52: 73-74. DOI: 10.1016/J.Jevs.2017.03.090 |
0.336 |
|
| 2017 |
Durward-Akhurst S, Schaefer R, Mickelson J, McCue M. Understanding genetic variation in the equine population Journal of Equine Veterinary Science. 52: 73. DOI: 10.1016/J.Jevs.2017.03.088 |
0.607 |
|
| 2017 |
McDonald M, Norton E, Schultz N, Mickelson J, McCue M. Association of leg length-to-torso ratios and metabolic phenotypes in Welsh ponies and Morgan horses Journal of Equine Veterinary Science. 52: 43-44. DOI: 10.1016/J.Jevs.2017.03.018 |
0.603 |
|
| 2016 |
Finno CJ, Bordbari MH, Valberg SJ, Lee D, Herron J, Hines K, Monsour T, Scott E, Bannasch DL, Mickelson J, Xu L. Transcriptome profiling of equine vitamin E deficient neuroaxonal dystrophy identifies upregulation of liver X receptor target genes. Free Radical Biology & Medicine. PMID 27751910 DOI: 10.1016/J.Freeradbiomed.2016.10.009 |
0.334 |
|
| 2016 |
Taylor S, Minor K, Shmon CL, Shelton GD, Patterson EE, Mickelson JR. Border Collie Collapse: Owner Survey Results and Veterinary Description of Videotaped Episodes. Journal of the American Animal Hospital Association. PMID 27685362 DOI: 10.5326/Jaaha-Ms-6436 |
0.311 |
|
| 2016 |
Maile CA, Hingst JR, Mahalingan KK, O'Reilly AO, Cleasby ME, Mickelson JR, McCue ME, Anderson SM, Hurley TD, Wojtaszewski JF, Piercy RJ. A highly prevalent equine glycogen storage disease is explained by constitutive activation of a mutant glycogen synthase. Biochimica Et Biophysica Acta. PMID 27592162 DOI: 10.1016/J.Bbagen.2016.08.021 |
0.661 |
|
| 2016 |
Norton EM, Mickelson JR, Binns MM, Blott SC, Caputo P, Isgren CM, McCoy AM, Moore A, Piercy RJ, Swinburne JE, Vaudin M, McCue ME. Heritability of recurrent exertional rhabdomyolysis in Standardbred and Thoroughbred racehorses derived from SNP genotyping data. The Journal of Heredity. PMID 27489252 DOI: 10.1093/Jhered/Esw042 |
0.659 |
|
| 2016 |
Taylor S, Shmon C, Su L, Epp T, Minor K, Mickelson J, Patterson E, Shelton GD. Evaluation of Dogs with Border Collie Collapse, Including Response to Two Standardized Strenuous Exercise Protocols. Journal of the American Animal Hospital Association. PMID 27487345 DOI: 10.5326/Jaaha-Ms-6361 |
0.767 |
|
| 2016 |
McCoy AM, Beeson SK, Splan RK, Lykkjen S, Ralston SL, Mickelson JR, McCue ME. Identification and validation of risk loci for osteochondrosis in standardbreds. Bmc Genomics. 17: 41. PMID 26753841 DOI: 10.1186/S12864-016-2385-Z |
0.631 |
|
| 2016 |
Tate NM, Minor KM, Mickelson JR, Peterson K, Lulich JP, Furrow E. P6030 Three diverse mutations underlying canine xanthine urolithiasis. Journal of Animal Science. 94: 163-163. DOI: 10.2527/Jas2016.94Supplement4163A |
0.311 |
|
| 2015 |
Petersen JL, Mickelson JR, Valberg SJ, McCue ME. Genome-wide SNP data show little differentiation between the Appaloosa and other American stock horse breeds. Animal Genetics. PMID 25997467 DOI: 10.1111/Age.12301 |
0.661 |
|
| 2015 |
Mickelson JR, Valberg SJ. The genetics of skeletal muscle disorders in horses. Annual Review of Animal Biosciences. 3: 197-217. PMID 25387114 DOI: 10.1146/Annurev-Animal-022114-110653 |
0.379 |
|
| 2014 |
Ekenstedt KJ, Becker D, Minor KM, Shelton GD, Patterson EE, Bley T, Oevermann A, Bilzer T, Leeb T, Drögemüller C, Mickelson JR. An ARHGEF10 deletion is highly associated with a juvenile-onset inherited polyneuropathy in Leonberger and Saint Bernard dogs. Plos Genetics. 10: e1004635. PMID 25275565 DOI: 10.1371/Journal.Pgen.1004635 |
0.759 |
|
| 2014 |
Petersen JL, Valberg SJ, Mickelson JR, McCue ME. Haplotype diversity in the equine myostatin gene with focus on variants associated with race distance propensity and muscle fiber type proportions. Animal Genetics. 45: 827-35. PMID 25160752 DOI: 10.1111/Age.12205 |
0.64 |
|
| 2014 |
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. Genetic risk factors for insidious equine recurrent uveitis in Appaloosa horses. Animal Genetics. 45: 392-9. PMID 24467435 DOI: 10.1111/Age.12129 |
0.657 |
|
| 2014 |
Petersen JL, Mickelson JR, Cleary KD, McCue ME. The American Quarter Horse: population structure and relationship to the thoroughbred. The Journal of Heredity. 105: 148-62. PMID 24293614 DOI: 10.1093/Jhered/Est079 |
0.632 |
|
| 2014 |
McCoy AM, Schaefer R, Petersen JL, Morrell PL, Slamka MA, Mickelson JR, Valberg SJ, McCue ME. Evidence of positive selection for a glycogen synthase (GYS1) mutation in domestic horse populations. The Journal of Heredity. 105: 163-72. PMID 24215078 DOI: 10.1093/Jhered/Est075 |
0.684 |
|
| 2013 |
Teixeira RB, Rendahl AK, Anderson SM, Mickelson JR, Sigler D, Buchanan BR, Coleman RJ, McCue ME. Coat color genotypes and risk and severity of melanoma in gray quarter horses. Journal of Veterinary Internal Medicine / American College of Veterinary Internal Medicine. 27: 1201-8. PMID 23875712 DOI: 10.1111/Jvim.12133 |
0.629 |
|
| 2013 |
Lykkjen S, Dolvik NI, McCue ME, Rendahl AK, Mickelson JR, Røed KH. Equine developmental orthopaedic diseases--a genome-wide association study of first phalanx plantar osteochondral fragments in Standardbred trotters. Animal Genetics. 44: 766-9. PMID 23742657 DOI: 10.1111/Age.12064 |
0.654 |
|
| 2013 |
Furrow E, Minor KM, Taylor SM, Mickelson JR, Patterson EE. Relationship between dynamin 1 mutation status and characteristics of recurrent episodes of exercise-induced collapse in Labrador Retrievers. Journal of the American Veterinary Medical Association. 242: 786-91. PMID 23445289 DOI: 10.2460/Javma.242.6.786 |
0.343 |
|
| 2013 |
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, et al. A Gly98Val mutation in the N-Myc downstream regulated gene 1 (NDRG1) in Alaskan Malamutes with polyneuropathy. Plos One. 8: e54547. PMID 23393557 DOI: 10.1371/Journal.Pone.0054547 |
0.386 |
|
| 2013 |
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, et al. Genetic diversity in the modern horse illustrated from genome-wide SNP data. Plos One. 8: e54997. PMID 23383025 DOI: 10.1371/Journal.Pone.0054997 |
0.631 |
|
| 2013 |
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, et al. Genome-wide analysis reveals selection for important traits in domestic horse breeds. Plos Genetics. 9: e1003211. PMID 23349635 DOI: 10.1371/Journal.Pgen.1003211 |
0.679 |
|
| 2013 |
Mickelson JR, Valberg SJ, Mccue ME, Finno CJ. Genomics of Muscle Disorders Equine Genomics. 171-185. DOI: 10.1002/9781118522158.ch11 |
0.58 |
|
| 2012 |
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, et al. Mutations in DMRT3 affect locomotion in horses and spinal circuit function in mice. Nature. 488: 642-6. PMID 22932389 DOI: 10.1038/Nature11399 |
0.615 |
|
| 2012 |
Fritz KL, McCue ME, Valberg SJ, Rendahl AK, Mickelson JR. Genetic mapping of recurrent exertional rhabdomyolysis in a population of North American Thoroughbreds. Animal Genetics. 43: 730-8. PMID 22497487 DOI: 10.1111/J.1365-2052.2012.02351.X |
0.657 |
|
| 2012 |
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, ... ... Mickelson JR, et al. A high density SNP array for the domestic horse and extant Perissodactyla: utility for association mapping, genetic diversity, and phylogeny studies. Plos Genetics. 8: e1002451. PMID 22253606 DOI: 10.1371/Journal.Pgen.1002451 |
0.654 |
|
| 2012 |
Ekenstedt KJ, Patterson EE, Mickelson JR. Canine epilepsy genetics. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 23: 28-39. PMID 22037590 DOI: 10.1007/S00335-011-9362-2 |
0.728 |
|
| 2011 |
Minor KM, Patterson EE, Keating MK, Gross SD, Ekenstedt KJ, Taylor SM, Mickelson JR. Presence and impact of the exercise-induced collapse associated DNM1 mutation in Labrador retrievers and other breeds. Veterinary Journal (London, England : 1997). 189: 214-9. PMID 21782486 DOI: 10.1016/J.Tvjl.2011.06.022 |
0.738 |
|
| 2011 |
Johlig L, Valberg SJ, Mickelson JR, Klukowska J, Reusser HR, Straub R, Gerber V. Epidemiological and genetic study of exertional rhabdomyolysis in a Warmblood horse family in Switzerland Equine Veterinary Journal. 43: 240-245. PMID 21592222 DOI: 10.1111/J.2042-3306.2010.00161.X |
0.344 |
|
| 2011 |
Ekenstedt KJ, Patterson EE, Minor KM, Mickelson JR. Candidate genes for idiopathic epilepsy in four dog breeds. Bmc Genetics. 12: 38. PMID 21518446 DOI: 10.1186/1471-2156-12-38 |
0.74 |
|
| 2011 |
Shelton G, Ekenstedt K, Drögemüller C, Minor K, Becker D, Leeb T, Patterson N, Mickelson J. P3.24 A deletion in ARHGEF10 is highly associated with early onset inherited polyneuropathy in Leonberger and St. Bernard dogs Neuromuscular Disorders. 21: 689. DOI: 10.1016/J.Nmd.2011.06.918 |
0.701 |
|
| 2011 |
Valberg SJ, McCue ME, Mickelson JR. The Interplay of Genetics, Exercise, and Nutrition in Polysaccharide Storage Myopathy Journal of Equine Veterinary Science. 31: 205-210. DOI: 10.1016/J.Jevs.2011.03.001 |
0.677 |
|
| 2010 |
Baird JD, Valberg SJ, Anderson SM, McCue ME, Mickelson JR. Presence of the glycogen synthase 1 (GYS1) mutation causing type 1 polysaccharide storage myopathy in continental European draught horse breeds. The Veterinary Record. 167: 781-4. PMID 21262610 DOI: 10.1136/Vr.C3447 |
0.663 |
|
| 2010 |
McCue ME, Anderson SM, Valberg SJ, Piercy RJ, Barakzai SZ, Binns MM, Distl O, Penedo MC, Wagner ML, Mickelson JR. Estimated prevalence of the Type 1 Polysaccharide Storage Myopathy mutation in selected North American and European breeds. Animal Genetics. 41: 145-9. PMID 21070288 DOI: 10.1111/J.1365-2052.2010.02124.X |
0.665 |
|
| 2010 |
Lykkjen S, Dolvik NI, McCue ME, Rendahl AK, Mickelson JR, Roed KH. Genome-wide association analysis of osteochondrosis of the tibiotarsal joint in Norwegian Standardbred trotters. Animal Genetics. 41: 111-20. PMID 21070284 DOI: 10.1111/J.1365-2052.2010.02117.X |
0.653 |
|
| 2010 |
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, et al. MTM1 mutation associated with X-linked myotubular myopathy in Labrador Retrievers. Proceedings of the National Academy of Sciences of the United States of America. 107: 14697-702. PMID 20682747 DOI: 10.1073/Pnas.1003677107 |
0.436 |
|
| 2009 |
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, ... ... Mickelson JR, et al. Genome sequence, comparative analysis, and population genetics of the domestic horse. Science (New York, N.Y.). 326: 865-7. PMID 19892987 DOI: 10.1126/Science.1178158 |
0.337 |
|
| 2009 |
Stanley RL, McCue ME, Valberg SJ, Mickelson JR, Mayhew IG, McGowan C, Hahn CN, Patterson-Kane JC, Piercy RJ. A glycogen synthase 1 mutation associated with equine polysaccharide storage myopathy and exertional rhabdomyolysis occurs in a variety of UK breeds. Equine Veterinary Journal. 41: 597-601. PMID 19803057 DOI: 10.2746/042516409X407611 |
0.643 |
|
| 2009 |
McCue ME, Armién AG, Lucio M, Mickelson JR, Valberg SJ. Comparative skeletal muscle histopathologic and ultrastructural features in two forms of polysaccharide storage myopathy in horses. Veterinary Pathology. 46: 1281-91. PMID 19605906 DOI: 10.1354/Vp.08-Vp-0177-M-Fl |
0.644 |
|
| 2009 |
Taylor SM, Shmon CL, Adams VJ, Mickelson JR, Patterson EN, Shelton GD. Evaluations of labrador retrievers with exercise-induced collapse, including response to a standardized strenuous exercise protocol. Journal of the American Animal Hospital Association. 45: 3-13. PMID 19122058 DOI: 10.5326/0450003 |
0.306 |
|
| 2009 |
Tryon RC, Penedo MC, McCue ME, Valberg SJ, Mickelson JR, Famula TR, Wagner ML, Jackson M, Hamilton MJ, Nooteboom S, Bannasch DL. Evaluation of allele frequencies of inherited disease genes in subgroups of American Quarter Horses. Journal of the American Veterinary Medical Association. 234: 120-5. PMID 19119976 DOI: 10.2460/Javma.234.1.120 |
0.64 |
|
| 2009 |
McCue ME, Valberg SJ, Jackson M, Borgia L, Lucio M, Mickelson JR. Polysaccharide storage myopathy phenotype in quarter horse-related breeds is modified by the presence of an RYR1 mutation. Neuromuscular Disorders : Nmd. 19: 37-43. PMID 19056269 DOI: 10.1016/J.Nmd.2008.10.001 |
0.787 |
|
| 2009 |
Herszberg B, McCue ME, Larcher T, Mata X, Vaiman A, Chaffaux S, Chérel Y, Valberg SJ, Mickelson JR, Guérin G. A GYS1 gene mutation is highly associated with polysaccharide storage myopathy in Cob Normand draught horses. Animal Genetics. 40: 94-6. PMID 18822097 DOI: 10.1111/J.1365-2052.2008.01778.X |
0.695 |
|
| 2009 |
Shelton G, Bohm J, Snead E, Kozlowski M, Minor K, Tiret L, Childers M, Taylor S, Mickelson J, Guo L, Mizisin A, Laporte J, Beggs A. G.P.12.04 A missense variant in the MTM1 gene associated with X-linked myotubular myopathy in Labrador retrievers Neuromuscular Disorders. 19: 636. DOI: 10.1016/J.Nmd.2009.06.288 |
0.313 |
|
| 2009 |
Valberg SJ, MCue ME, Lucio M, Mickelson JR. Breeds of Horses Positive for the GYS1 Mutation Associated with Polysaccharide Storage Myopathy Journal of Equine Veterinary Science. 29: 312-313. DOI: 10.1016/J.Jevs.2009.04.019 |
0.357 |
|
| 2008 |
Taylor SM, Shmon CL, Shelton GD, Patterson EN, Minor K, Mickelson JR. Exercise-induced collapse of Labrador retrievers: survey results and preliminary investigation of heritability. Journal of the American Animal Hospital Association. 44: 295-301. PMID 18981194 DOI: 10.5326/0440295 |
0.305 |
|
| 2008 |
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, ... ... Mickelson JR, et al. A 4,103 marker integrated physical and comparative map of the horse genome. Cytogenetic and Genome Research. 122: 28-36. PMID 18931483 DOI: 10.1159/000151313 |
0.316 |
|
| 2008 |
Patterson EE, Minor KM, Tchernatynskaia AV, Taylor SM, Shelton GD, Ekenstedt KJ, Mickelson JR. A canine DNM1 mutation is highly associated with the syndrome of exercise-induced collapse. Nature Genetics. 40: 1235-9. PMID 18806795 DOI: 10.1038/Ng.224 |
0.76 |
|
| 2008 |
McCue ME, Valberg SJ, Lucio M, Mickelson JR. Glycogen synthase 1 (GYS1) mutation in diverse breeds with polysaccharide storage myopathy. Journal of Veterinary Internal Medicine / American College of Veterinary Internal Medicine. 22: 1228-33. PMID 18691366 DOI: 10.1111/J.1939-1676.2008.0167.X |
0.652 |
|
| 2008 |
McCue ME, Valberg SJ, Miller MB, Wade C, DiMauro S, Akman HO, Mickelson JR. Glycogen synthase (GYS1) mutation causes a novel skeletal muscle glycogenosis. Genomics. 91: 458-66. PMID 18358695 DOI: 10.1016/J.Ygeno.2008.01.011 |
0.682 |
|
| 2007 |
McNiel EA, Griffin KL, Mellett AM, Madrill NJ, Mickelson JR. Microsatellite instability in canine mammary gland tumors. Journal of Veterinary Internal Medicine / American College of Veterinary Internal Medicine. 21: 1034-40. PMID 17939561 DOI: 10.1892/0891-6640(2007)21[1034:Miicmg]2.0.Co;2 |
0.306 |
|
| 2007 |
Dranchak PK, Leiper FC, Valberg SJ, Piercy RJ, Carling D, McCue ME, Mickelson JR. Biochemical and genetic evaluation of the role of AMP-activated protein kinase in polysaccharide storage myopathy in Quarter Horses. American Journal of Veterinary Research. 68: 1079-84. PMID 17916014 DOI: 10.2460/Ajvr.68.10.1079 |
0.802 |
|
| 2007 |
Goh G, Raudsepp T, Durkin K, Wagner ML, Schäffer AA, Agarwala R, Tozaki T, Mickelson JR, Chowdhary BP. High-resolution gene maps of horse chromosomes 14 and 21: additional insights into evolution and rearrangements of HSA5 homologs in mammals. Genomics. 89: 89-112. PMID 16916595 DOI: 10.1016/J.Ygeno.2006.06.012 |
0.328 |
|
| 2006 |
Wagner ML, Valberg SJ, Ames EG, Bauer MM, Wiseman JA, Penedo MC, Kinde H, Abbitt B, Mickelson JR. Allele frequency and likely impact of the glycogen branching enzyme deficiency gene in Quarter Horse and Paint Horse populations. Journal of Veterinary Internal Medicine / American College of Veterinary Internal Medicine. 20: 1207-11. PMID 17063718 DOI: 10.1892/0891-6640(2006)20[1207:Afalio]2.0.Co;2 |
0.397 |
|
| 2006 |
Dranchak PK, Valberg SJ, Onan GW, Gallant EM, Binns MM, Swinburne JE, Mickelson JR. Exclusion of linkage of the RYR1, CACNA1S, and ATP2A1 genes to recurrent exertional rhabdomyolysis in Thoroughbreds. American Journal of Veterinary Research. 67: 1395-400. PMID 16881852 DOI: 10.2460/Ajvr.67.8.1395 |
0.715 |
|
| 2006 |
Dranchak PK, Ekenstedt KJ, Valberg SJ, Chowdhary BP, Raudsepp T, Mickelson JR. Chromosomal assignments for the equine AMPK family genes. Animal Genetics. 37: 293-4. PMID 16734697 DOI: 10.1111/J.1365-2052.2006.01431.X |
0.76 |
|
| 2006 |
Wagner ML, Raudsepp T, Goh G, Agarwala R, Schaffer AA, Dranchak PK, Brinkmeyer-Langford C, Skow LC, Chowdhary BP, Mickelson JR. A 1.3-Mb interval map of equine homologs of HSA2. Cytogenetic and Genome Research. 112: 227-34. PMID 16484777 DOI: 10.1159/000089875 |
0.712 |
|
| 2006 |
Swinburne JE, Boursnell M, Hill G, Pettitt L, Allen T, Chowdhary B, Hasegawa T, Kurosawa M, Leeb T, Mashima S, Mickelson JR, Raudsepp T, Tozaki T, Binns M. Single linkage group per chromosome genetic linkage map for the horse, based on two three-generation, full-sibling, crossbred horse reference families. Genomics. 87: 1-29. PMID 16314071 DOI: 10.1016/J.Ygeno.2005.09.001 |
0.351 |
|
| 2005 |
Brinkmeyer-Langford C, Raudsepp T, Lee EJ, Goh G, Schäffer AA, Agarwala R, Wagner ML, Tozaki T, Skow LC, Womack JE, Mickelson JR, Chowdhary BP. A high-resolution physical map of equine homologs of HSA19 shows divergent evolution compared with other mammals. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 16: 631-49. PMID 16180145 DOI: 10.1007/S00335-005-0023-1 |
0.336 |
|
| 2005 |
Dranchak PK, Valberg SJ, Onan GW, Gallant EM, MacLeay JM, McKenzie EC, De La Corte FD, Ekenstedt K, Mickelson JR. Inheritance of recurrent exertional rhabdomyolysis in thoroughbreds. Journal of the American Veterinary Medical Association. 227: 762-7. PMID 16178398 DOI: 10.2460/Javma.2005.227.762 |
0.768 |
|
| 2005 |
Gustafson-Seabury A, Raudsepp T, Goh G, Kata SR, Wagner ML, Tozaki T, Mickelson JR, Womack JE, Skow LC, Chowdhary BP. High-resolution RH map of horse chromosome 22 reveals a putative ancestral vertebrate chromosome. Genomics. 85: 188-200. PMID 15676277 DOI: 10.1016/J.Ygeno.2004.10.012 |
0.345 |
|
| 2005 |
Patterson EE, Armstrong PJ, O'Brien DP, Roberts MC, Johnson GS, Mickelson JR. Clinical description and mode of inheritance of idiopathic epilepsy in English springer spaniels. Journal of the American Veterinary Medical Association. 226: 54-8. PMID 15646572 DOI: 10.2460/Javma.2005.226.54 |
0.514 |
|
| 2004 |
Ward TL, Valberg SJ, Adelson DL, Abbey CA, Binns MM, Mickelson JR. Glycogen branching enzyme (GBE1) mutation causing equine glycogen storage disease IV. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 15: 570-7. PMID 15366377 DOI: 10.1007/S00335-004-2369-1 |
0.611 |
|
| 2004 |
Tay SK, Akman HO, Chung WK, Pike MG, Muntoni F, Hays AP, Shanske S, Valberg SJ, Mickelson JR, Tanji K, DiMauro S. Fatal infantile neuromuscular presentation of glycogen storage disease type IV. Neuromuscular Disorders : Nmd. 14: 253-60. PMID 15019703 DOI: 10.1016/J.Nmd.2003.12.006 |
0.339 |
|
| 2004 |
Raudsepp T, Lee EJ, Kata SR, Brinkmeyer C, Mickelson JR, Skow LC, Womack JE, Chowdhary BP. Exceptional conservation of horse-human gene order on X chromosome revealed by high-resolution radiation hybrid mapping. Proceedings of the National Academy of Sciences of the United States of America. 101: 2386-91. PMID 14983019 DOI: 10.1073/Pnas.0308513100 |
0.341 |
|
| 2003 |
Park HB, Marklund S, Jeon JT, Mickelson JR, Valberg SJ, Sandberg K, Andersson L. Molecular characterization and mutational screening of the PRKAG3 gene in the horse Cytogenetic and Genome Research. 102: 211-216. PMID 14970705 DOI: 10.1159/000075751 |
0.436 |
|
| 2003 |
Ward TL, Valberg SJ, Lear TL, Guérin G, Milenkovic D, Swinburne JE, Binns MM, Raudsepp T, Skow L, Chowdhary BP, Mickelson JR. Genetic mapping of GBE1 and its association with glycogen storage disease IV in American Quarter horses. Cytogenetic and Genome Research. 102: 201-6. PMID 14970703 DOI: 10.1159/000075749 |
0.65 |
|
| 2003 |
Patterson EE, Mickelson JR, Da Y, Roberts MC, McVey AS, O'Brien DP, Johnson GS, Armstrong PJ. Clinical characteristics and inheritance of idiopathic epilepsy in Vizslas. Journal of Veterinary Internal Medicine / American College of Veterinary Internal Medicine. 17: 319-25. PMID 12774973 DOI: 10.1111/J.1939-1676.2003.Tb02455.X |
0.563 |
|
| 2003 |
Chowdhary BP, Raudsepp T, Kata SR, Goh G, Millon LV, Allan V, Piumi F, Guérin G, Swinburne J, Binns M, Lear TL, Mickelson J, Murray J, Antczak DF, Womack JE, et al. The first-generation whole-genome radiation hybrid map in the horse identifies conserved segments in human and mouse genomes. Genome Research. 13: 742-51. PMID 12671008 DOI: 10.1101/Gr.917503 |
0.321 |
|
| 2003 |
Roberts MC, Hitte CC, Hendrickson JA, Hoffmann DE, Flickinger GH, Rutherford MS, Guyon RS, Galibert FS, Mickelson JR. Characterization and radiation hybrid mapping of expressed sequence tags from the canine brain. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 14: 203-13. PMID 12647243 DOI: 10.1007/S00335-002-2207-2 |
0.588 |
|
| 2003 |
Mickelson JR, Wu JT, Morrison LY, Swinburne JE, Binns MM, Reed KM, Alexander LJ. Eighty-three previously unreported equine microsatellite loci Animal Genetics. 34: 71-74. PMID 12580794 DOI: 10.1046/J.1365-2052.2003.00951_4.X |
0.371 |
|
| 2003 |
Sponseller BT, Valberg SJ, Ward TL, Fales-Williams AJ, Mickelson JR. Muscular weakness and recumbency in a Quarter Horse colt due to glycogen branching enzyme deficiency Equine Veterinary Education. 15: 182-187. DOI: 10.1111/J.2042-3292.2003.Tb00240.X |
0.518 |
|
| 2002 |
De La Corte FD, Valberg SJ, MacLeay JM, Mickelson JR. Developmental onset of polysaccharide storage myopathy in 4 Quarter Horse foals. Journal of Veterinary Internal Medicine / American College of Veterinary Internal Medicine. 16: 581-7. PMID 12322710 DOI: 10.1111/J.1939-1676.2002.Tb02391.X |
0.379 |
|
| 2001 |
Valberg SJ, Ward TL, Rush B, Kinde H, Hiraragi H, Nahey D, Fyfe J, Mickelson JR. Glycogen branching enzyme deficiency in quarter horse foals. Journal of Veterinary Internal Medicine / American College of Veterinary Internal Medicine. 15: 572-80. PMID 11817063 DOI: 10.1111/J.1939-1676.2001.Tb01593.X |
0.571 |
|
| 2001 |
Mlekoday JA, Mickelson JR, Valberg SJ, Horton JH, Gallant EM, Thompson LV. Calcium sensitivity of force production and myofibrillar ATPase activity in muscles from thoroughbreds with recurrent exertional rhabdomyolysis American Journal of Veterinary Research. 62: 1647-1652. PMID 11592334 DOI: 10.2460/Ajvr.2001.62.1647 |
0.3 |
|
| 2001 |
Roberts MC, Mickelson JR, Patterson EE, Nelson TE, Armstrong PJ, Brunson DB, Hogan K. Autosomal dominant canine malignant hyperthermia is caused by a mutation in the gene encoding the skeletal muscle calcium release channel (RYR1). Anesthesiology. 95: 716-25. PMID 11575546 DOI: 10.1097/00000542-200109000-00026 |
0.601 |
|
| 2000 |
Swinburne J, Gerstenberg C, Breen M, Aldridge V, Lockhart L, Marti E, Antczak D, Eggleston-Stott M, Bailey E, Mickelson J, Røed K, Lindgren G, Von Haeringen W, Guérin G, Bjarnason J, et al. First comprehensive low-density horse linkage map based on two 3- generation, full-sibling, cross-bred horse reference families Genomics. 66: 123-134. PMID 10860657 DOI: 10.1006/Geno.2000.6207 |
0.34 |
|
| 2000 |
Roberts MC, Murtaugh J, Valberg SJ, Mickelson JR, Alexander LJ. Twenty-one new equine dinucleotide repeat microsatellites. Animal Genetics. 31: 141. PMID 10782217 DOI: 10.1046/J.1365-2052.2000.00574.X |
0.528 |
|
| 2000 |
Ward TL, Valberg SJ, Gallant EM, Mickelson JR. Calcium regulation by skeletal muscle membranes of horses with recurrent exertional rhabdomyolysis. American Journal of Veterinary Research. 61: 242-7. PMID 10714513 DOI: 10.2460/Ajvr.2000.61.242 |
0.558 |
|
| 1999 |
Valberg SJ, Mickelson JR, Gallant EM, MacLeay JM, Lentz L, de la Corte F. Exertional rhabdomyolysis in quarter horses and thoroughbreds: one syndrome, multiple aetiologies Equine Veterinary Journal. Supplement. 30: 533-538. PMID 10659313 DOI: 10.1111/J.2042-3306.1999.Tb05279.X |
0.324 |
|
| 1999 |
Guérin G, Bailey E, Bernoco D, Anderson I, Antczak DF, Bell K, Binns MM, Bowling AT, Brandon R, Cholewinski G, Cothran EG, Ellegren H, Förster M, Godard S, Horin P, ... ... Mickelson JR, et al. Report of the International Equine Gene Mapping Workshop: male linkage map. Animal Genetics. 30: 341-54. PMID 10582279 DOI: 10.1046/J.1365-2052.1999.00510.X |
0.331 |
|
| 1999 |
Shiue YL, Bickel LA, Caetano AR, Millon LV, Clark RS, Eggleston ML, Michelmore R, Bailey E, Guérin G, Godard S, Mickelson JR, Valberg SJ, Murray JD, Bowling AT. A synteny map of the horse genome comprised of 240 microsatellite and RAPD markers. Animal Genetics. 30: 1-9. PMID 10050277 DOI: 10.1046/J.1365-2052.1999.00377.X |
0.347 |
|
| 1999 |
Valberg SJ, Macleay JM, Billstrom JA, Hower-Moritz MA, Mickelson JR. Skeletal muscle metabolic response to exercise in horses with 'tying-up' due to polysaccharide storage myopathy Equine Veterinary Journal. 31: 43-47. PMID 9952328 DOI: 10.1111/J.2042-3306.1999.Tb03789.X |
0.317 |
|
| 1998 |
Santschi EM, Purdy AK, Valberg SJ, Vrotsos PD, Kaese H, Mickelson JR. Endothelin receptor B polymorphism associated with lethal white foal syndrome in horses. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 9: 306-9. PMID 9530628 DOI: 10.1007/S003359900754 |
0.367 |
|
| 1998 |
Bilstrom JA, Valberg SJ, Bernoco D, Mickelson JR. Genetic test for myophosphorylase deficiency in Charolais cattle American Journal of Veterinary Research. 59: 267-270. PMID 9522942 |
0.316 |
|
| 1997 |
O'Rourke KI, Holyoak GR, Clark WW, Mickelson JR, Wang S, Melco RP, Besser TE, Foote WC. PrP genotypes and experimental scrapie in orally inoculated Suffolk sheep in the United States Journal of General Virology. 78: 975-978. PMID 9129673 DOI: 10.1099/0022-1317-78-4-975 |
0.304 |
|
| 1996 |
O'Rourke KI, Melco RP, Mickelson JR. Allelic frequencies of an ovine scrapie susceptibility gene Animal Biotechnology. 7: 155-162. DOI: 10.1080/10495399609525856 |
0.366 |
|
| 1995 |
Paszek AA, Schook LB, Louis CF, Mickelson JR, Flickinger GH, Murtaugh J, Mendiola JR, Janzen MA, Beattie CW, Rohrer GA. First international workshop on porcine chromosome 6. Report and abstracts. Animal Genetics. 26: 377-401. PMID 8572361 DOI: 10.1111/J.1365-2052.1995.Tb02689.X |
0.315 |
|
| 1995 |
Rempel WE, lu My, Mickelson JR, Louis CF. The effect of skeletal muscle ryanodine receptor genotype on pig performance and carcass quality traits Animal Science. 60: 249-257. DOI: 10.1017/S1357729800008419 |
0.323 |
|
| 1994 |
Mickelson JR, Ervasti JM, Litterer LA, Campbell KP, Louis CF. Skeletal muscle junctional membrane protein content in pigs with different ryanodine receptor genotypes. The American Journal of Physiology. 267: C282-92. PMID 8048487 DOI: 10.1152/Ajpcell.1994.267.1.C282 |
0.311 |
|
| 1993 |
Rempel WE, Lu M, el Kandelgy S, Kennedy CF, Irvin LR, Mickelson JR, Louis CF. Relative accuracy of the halothane challenge test and a molecular genetic test in detecting the gene for porcine stress syndrome Journal of Animal Science. 71: 1395-1399. PMID 8392044 DOI: 10.2527/1993.7161395X |
0.366 |
|
| 1991 |
Ervasti JM, Strand MA, Hanson TP, Mickelson JR, Louis CF. Ryanodine receptor in different malignant hyperthermia-susceptible porcine muscles. The American Journal of Physiology. 260: C58-66. PMID 1824808 DOI: 10.1152/Ajpcell.1991.260.1.C58 |
0.303 |
|
| 1989 |
Mickelson JR, Gallant EM, Rempel WE, Johnson KM, Litterer LA, Jacobson BA, Louis CF. Effects of the halothane-sensitivity gene on sarcoplasmic reticulum function American Journal of Physiology - Cell Physiology. 257: 26/4. PMID 2801927 DOI: 10.1152/Ajpcell.1989.257.4.C787 |
0.322 |
|
| 1989 |
Gallant EM, Mickelson JR, Roggow BD, Donaldson SK, Louis CF, Rempel WE. Halothane-sensitivity gene and muscle contractile properties in malignant hyperthermia American Journal of Physiology - Cell Physiology. 257: 26/4. PMID 2801926 DOI: 10.1152/Ajpcell.1989.257.4.C781 |
0.381 |
|
| 1984 |
Soman G, Mickelson JR, Louis CF, Graves DJ. NAD: Guanidino group specific mono ADP-ribosyltransferase activity in skeletal muscle Biochemical and Biophysical Research Communications. 120: 973-980. PMID 6329192 DOI: 10.1016/S0006-291X(84)80202-8 |
0.303 |
|
| Show low-probability matches. |