Year |
Citation |
Score |
2020 |
Abrams SR, Hawks AL, Evans JM, Famula TR, Mahaffey M, Johnson GS, Mason JM, Clark LA. Variants in and are associated with small body size and a dental anomaly in dogs. Proceedings of the National Academy of Sciences of the United States of America. PMID 32958658 DOI: 10.1073/Pnas.2009500117 |
0.371 |
|
2019 |
Tsai KL, Evans JM, Noorai RE, Starr-Moss AN, Clark LA. Novel Y Chromosome Retrocopies in Canids Revealed through a Genome-Wide Association Study for Sex. Genes. 10. PMID 31027231 DOI: 10.3390/Genes10040320 |
0.367 |
|
2019 |
Murphy SC, Recio A, de la Fuente C, Guo LT, Shelton GD, Clark LA. A glycine transporter SLC6A5 frameshift mutation causes startle disease in Spanish greyhounds. Human Genetics. PMID 30847549 DOI: 10.1007/S00439-019-01986-X |
0.395 |
|
2018 |
Murphy SC, Evans JM, Tsai KL, Clark LA. Length variations within the retrotransposon of canine : correlating genotype with phenotype. Mobile Dna. 9: 26. PMID 30123327 DOI: 10.1186/S13100-018-0131-6 |
0.332 |
|
2017 |
Evans JM, Noorai RE, Tsai KL, Starr-Moss AN, Hill CM, Anderson KJ, Famula TR, Clark LA. Beyond the MHC: A canine model of dermatomyositis shows a complex pattern of genetic risk involving novel loci. Plos Genetics. 13: e1006604. PMID 28158183 DOI: 10.1371/Journal.Pgen.1006604 |
0.413 |
|
2016 |
Evans JM, Cox ML, Huska J, Li F, Gaitero L, Guo LT, Casal ML, Granzier HL, Shelton GD, Clark LA. Exome sequencing reveals a nebulin nonsense mutation in a dog model of nemaline myopathy. Mammalian Genome : Official Journal of the International Mammalian Genome Society. PMID 27215641 DOI: 10.1007/S00335-016-9644-9 |
0.346 |
|
2015 |
Rinz CJ, Lennon VA, James F, Thoreson JB, Tsai KL, Starr-Moss AN, Humphries HD, Guo LT, Palmer AC, Clark LA, Shelton GD. A CHRNE frameshift mutation causes congenital myasthenic syndrome in young Jack Russell Terriers. Neuromuscular Disorders : Nmd. PMID 26429099 DOI: 10.1016/J.Nmd.2015.09.005 |
0.348 |
|
2015 |
Evans JM, Tsai KL, Starr-Moss AN, Steiner JM, Clark LA. Association of DLA-DQB1 alleles with exocrine pancreatic insufficiency in Pembroke Welsh Corgis. Animal Genetics. PMID 26095904 DOI: 10.1111/Age.12317 |
0.521 |
|
2014 |
Rinz CJ, Levine J, Minor KM, Humphries HD, Lara R, Starr-Moss AN, Guo LT, Williams DC, Shelton GD, Clark LA. A COLQ missense mutation in Labrador Retrievers having congenital myasthenic syndrome. Plos One. 9: e106425. PMID 25166616 DOI: 10.1371/Journal.Pone.0106425 |
0.388 |
|
2013 |
Tsai KL, Starr-Moss AN, Venkataraman GM, Robinson C, Kennedy LJ, Steiner JM, Clark LA. Alleles of the major histocompatibility complex play a role in the pathogenesis of pancreatic acinar atrophy in dogs. Immunogenetics. 65: 501-9. PMID 23604463 DOI: 10.1007/S00251-013-0704-Y |
0.527 |
|
2012 |
Clark LA, Cox ML. Current status of genetic studies of exocrine pancreatic insufficiency in dogs. Topics in Companion Animal Medicine. 27: 109-12. PMID 23148850 DOI: 10.1053/J.Tcam.2012.04.001 |
0.438 |
|
2012 |
Noorai RE, Freese NH, Wright LM, Chapman SC, Clark LA. Genome-wide association mapping and identification of candidate genes for the rumpless and ear-tufted traits of the Araucana Chicken Plos One. 7. PMID 22844420 DOI: 10.1371/Journal.Pone.0040974 |
0.385 |
|
2012 |
Tsai KL, Noorai RE, Starr-Moss AN, Quignon P, Rinz CJ, Ostrander EA, Steiner JM, Murphy KE, Clark LA. Genome-wide association studies for multiple diseases of the German Shepherd Dog. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 23: 203-11. PMID 22105877 DOI: 10.1007/S00335-011-9376-9 |
0.546 |
|
2012 |
Gill JL, Tsai KL, Krey C, Noorai RE, Vanbellinghen JF, Garosi LS, Shelton GD, Clark LA, Harvey RJ. A canine BCAN microdeletion associated with episodic falling syndrome. Neurobiology of Disease. 45: 130-6. PMID 21821125 DOI: 10.1016/j.nbd.2011.07.014 |
0.303 |
|
2011 |
Clark LA, Tsai KL, Starr AN, Nowend KL, Murphy KE. A missense mutation in the 20S proteasome β2 subunit of Great Danes having harlequin coat patterning. Genomics. 97: 244-8. PMID 21256207 DOI: 10.1016/J.Ygeno.2011.01.003 |
0.382 |
|
2010 |
Spadafora D, Hawkins EC, Murphy KE, Clark LA, Ballard ST. Naturally occurring mutations in the canine CFTR gene. Physiological Genomics. 42: 480-5. PMID 20571109 DOI: 10.1152/Physiolgenomics.00092.2010 |
0.355 |
|
2009 |
Strain GM, Clark LA, Wahl JM, Turner AE, Murphy KE. Prevalence of deafness in dogs heterozygous or homozygous for the merle allele. Journal of Veterinary Internal Medicine / American College of Veterinary Internal Medicine. 23: 282-6. PMID 19192156 DOI: 10.1111/J.1939-1676.2008.0257.X |
0.388 |
|
2008 |
Clark LA, Starr AN, Tsai KL, Murphy KE. Genome-wide linkage scan localizes the harlequin locus in the Great Dane to chromosome 9. Gene. 418: 49-52. PMID 18513894 DOI: 10.1016/J.Gene.2008.04.006 |
0.378 |
|
2008 |
Clark LA, Tsai KL, Murphy KE. Alleles of DLA-DRB1 are not unique in German Shepherd dogs having degenerative myelopathy. Animal Genetics. 39: 332. PMID 18410473 DOI: 10.1111/J.1365-2052.2008.01723.X |
0.361 |
|
2008 |
Wahl JM, Clark LA, Skalli O, Ambrus A, Rees CA, Mansell JL, Murphy KE. Analysis of gene transcript profiling and immunobiology in Shetland sheepdogs with dermatomyositis. Veterinary Dermatology. 19: 52-8. PMID 18336421 DOI: 10.1111/J.1365-3164.2008.00655.X |
0.319 |
|
2008 |
Wahl JM, Herbst SM, Clark LA, Tsai KL, Murphy KE. A review of hereditary diseases of the German shepherd dog Journal of Veterinary Behavior. 3: 255-265. DOI: 10.1016/J.Jveb.2008.05.004 |
0.333 |
|
2007 |
Tsai KL, Clark LA, Murphy KE. Understanding hereditary diseases using the dog and human as companion model systems. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 18: 444-51. PMID 17653794 DOI: 10.1007/S00335-007-9037-1 |
0.361 |
|
2007 |
Kerns JA, Cargill EJ, Clark LA, Candille SI, Berryere TG, Olivier M, Lust G, Todhunter RJ, Schmutz SM, Murphy KE, Barsh GS. Linkage and segregation analysis of black and brindle coat color in domestic dogs. Genetics. 176: 1679-89. PMID 17483404 DOI: 10.1534/Genetics.107.074237 |
0.323 |
|
2006 |
Clark LA, Wahl JM, Rees CA, Murphy KE. Retrotransposon insertion in SILV is responsible for merle patterning of the domestic dog. Proceedings of the National Academy of Sciences of the United States of America. 103: 1376-81. PMID 16407134 DOI: 10.1073/Pnas.0506940103 |
0.401 |
|
2005 |
Clark LA, Credille KM, Murphy KE, Rees CA. Linkage of dermatomyositis in the Shetland Sheepdog to chromosome 35. Veterinary Dermatology. 16: 392-4. PMID 16359306 DOI: 10.1111/J.1365-3164.2005.00469.X |
0.396 |
|
2005 |
Clark LA, Wahl JM, Steiner JM, Zhou W, Ji W, Famula TR, Williams DA, Murphy KE. Linkage analysis and gene expression profile of pancreatic acinar atrophy in the German Shepherd Dog. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 16: 955-62. PMID 16341675 DOI: 10.1007/S00335-005-0076-1 |
0.493 |
|
2004 |
Clark LA, Famula TR, Murphy KE. Evaluation of a rapid single multiplex microsatellite-based assay for use in forensic genetic investigations in dogs. American Journal of Veterinary Research. 65: 1446-50. PMID 15524334 DOI: 10.2460/Ajvr.2004.65.1446 |
0.362 |
|
2004 |
Clark LA, Tsai KL, Steiner JM, Williams DA, Guerra T, Ostrander EA, Galibert F, Murphy KE. Chromosome-specific microsatellite multiplex sets for linkage studies in the domestic dog. Genomics. 84: 550-4. PMID 15498461 DOI: 10.1016/J.Ygeno.2004.06.006 |
0.488 |
|
2003 |
Greer KA, Cargill EJ, Cox ML, Clark LA, Tsai KL, Credille KM, Dunstan RW, Venta PJ, Murphy KE. Digging up the canine genome--a tale to wag about. Cytogenetic and Genome Research. 102: 244-8. PMID 14970710 DOI: 10.1159/000075756 |
0.379 |
|
2002 |
Moeller EM, Steiner JM, Clark LA, Murphy KE, Famula TR, Williams DA, Stankovics ME, Vose AS. Inheritance of pancreatic acinar atrophy in German Shepherd Dogs. American Journal of Veterinary Research. 63: 1429-34. PMID 12371772 DOI: 10.2460/Ajvr.2002.63.1429 |
0.439 |
|
2002 |
Cargill EJ, Clark LA, Steiner JM, Murphy KE. Multiplexing of canine microsatellite markers for whole-genome screens. Genomics. 80: 250-3. PMID 12213193 DOI: 10.1006/Geno.2002.6827 |
0.472 |
|
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