Johnson GS - Search Results

1

Resolving the evolution of extant and extinct ruminants with high-throughput phylogenomics.

Decker JE, Pires JC, Conant GC, McKay SD, Heaton MP, Chen K, Cooper A, Vilkki J, Seabury CM, Caetano AR, Johnson GS, Brenneman RA, Hanotte O, Eggert LS, Wiener P, Kim JJ, Kim KS, Sonstegard TS, Van Tassell CP, Neibergs HL, McEwan JC, Brauning R, Coutinho LL, Babar ME, Wilson GA, McClure MC, Rolf MM, Kim J, Schnabel RD, Taylor JF. Decker JE, et al. Among authors: johnson gs. Proc Natl Acad Sci U S A. 2009 Nov 3;106(44):18644-9. doi: 10.1073/pnas.0904691106. Epub 2009 Oct 21. Proc Natl Acad Sci U S A. 2009. PMID: 19846765 Free PMC article.

2

Genetic mapping of canine multiple system degeneration and ectodermal dysplasia loci.

O'Brien DP, Johnson GS, Schnabel RD, Khan S, Coates JR, Johnson GC, Taylor JF. O'Brien DP, et al. Among authors: johnson gs, johnson gc. J Hered. 2005;96(7):727-34. doi: 10.1093/jhered/esi086. Epub 2005 Jun 15. J Hered. 2005. PMID: 15958791

3

A mutation in the cathepsin D gene (CTSD) in American Bulldogs with neuronal ceroid lipofuscinosis.

Awano T, Katz ML, O'Brien DP, Taylor JF, Evans J, Khan S, Sohar I, Lobel P, Johnson GS. Awano T, et al. Among authors: johnson gs. Mol Genet Metab. 2006 Apr;87(4):341-8. doi: 10.1016/j.ymgme.2005.11.005. Epub 2006 Jan 4. Mol Genet Metab. 2006. PMID: 16386934

4

A neonatal encephalopathy with seizures in standard poodle dogs with a missense mutation in the canine ortholog of ATF2.

Chen X, Johnson GS, Schnabel RD, Taylor JF, Johnson GC, Parker HG, Patterson EE, Katz ML, Awano T, Khan S, O'Brien DP. Chen X, et al. Among authors: johnson gs, johnson gc. Neurogenetics. 2008 Feb;9(1):41-9. doi: 10.1007/s10048-007-0112-2. Epub 2007 Dec 12. Neurogenetics. 2008. PMID: 18074159

5

Genome-wide association analysis reveals a SOD1 mutation in canine degenerative myelopathy that resembles amyotrophic lateral sclerosis.

Awano T, Johnson GS, Wade CM, Katz ML, Johnson GC, Taylor JF, Perloski M, Biagi T, Baranowska I, Long S, March PA, Olby NJ, Shelton GD, Khan S, O'Brien DP, Lindblad-Toh K, Coates JR. Awano T, et al. Among authors: johnson gs, johnson gc. Proc Natl Acad Sci U S A. 2009 Feb 24;106(8):2794-9. doi: 10.1073/pnas.0812297106. Epub 2009 Feb 2. Proc Natl Acad Sci U S A. 2009. PMID: 19188595 Free PMC article.

6

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: johnson gs. 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

7

A truncated retrotransposon disrupts the GRM1 coding sequence in Coton de Tulear dogs with Bandera's neonatal ataxia.

Zeng R, Farias FH, Johnson GS, McKay SD, Schnabel RD, Decker JE, Taylor JF, Mann CS, Katz ML, Johnson GC, Coates JR, O'Brien DP. Zeng R, et al. Among authors: johnson gs, johnson gc. J Vet Intern Med. 2011 Mar-Apr;25(2):267-72. doi: 10.1111/j.1939-1676.2010.0666.x. Epub 2011 Jan 31. J Vet Intern Med. 2011. PMID: 21281350 Free article.

8

A truncating mutation in ATP13A2 is responsible for adult-onset neuronal ceroid lipofuscinosis in Tibetan terriers.

Farias FH, Zeng R, Johnson GS, Wininger FA, Taylor JF, Schnabel RD, McKay SD, Sanders DN, Lohi H, Seppälä EH, Wade CM, Lindblad-Toh K, O'Brien DP, Katz ML. Farias FH, et al. Among authors: johnson gs. Neurobiol Dis. 2011 Jun;42(3):468-74. doi: 10.1016/j.nbd.2011.02.009. Epub 2011 Feb 26. Neurobiol Dis. 2011. PMID: 21362476

9

GM2 gangliosidosis associated with a HEXA missense mutation in Japanese Chin dogs: a potential model for Tay Sachs disease.

Sanders DN, Zeng R, Wenger DA, Johnson GS, Johnson GC, Decker JE, Katz ML, Platt SR, O'Brien DP. Sanders DN, et al. Among authors: johnson gs, johnson gc. Mol Genet Metab. 2013 Jan;108(1):70-5. doi: 10.1016/j.ymgme.2012.11.008. Epub 2012 Nov 27. Mol Genet Metab. 2013. PMID: 23266199

10

A homozygous KCNJ10 mutation in Jack Russell Terriers and related breeds with spinocerebellar ataxia with myokymia, seizures, or both.

Gilliam D, O'Brien DP, Coates JR, Johnson GS, Johnson GC, Mhlanga-Mutangadura T, Hansen L, Taylor JF, Schnabel RD. Gilliam D, et al. Among authors: johnson gs, johnson gc. J Vet Intern Med. 2014 May-Jun;28(3):871-7. doi: 10.1111/jvim.12355. Epub 2014 Apr 7. J Vet Intern Med. 2014. PMID: 24708069 Free PMC article.

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