Lohi H - Search Results

1

ADAM23 is a common risk gene for canine idiopathic epilepsy.

Koskinen LL, Seppälä EH, Weissl J, Jokinen TS, Viitmaa R, Hänninen RL, Quignon P, Fischer A, André C, Lohi H. Koskinen LL, et al. Among authors: lohi h. BMC Genet. 2017 Jan 31;18(1):8. doi: 10.1186/s12863-017-0478-6. BMC Genet. 2017. PMID: 28143391 Free PMC article.

2

Benign familial juvenile epilepsy in Lagotto Romagnolo dogs.

Jokinen TS, Metsähonkala L, Bergamasco L, Viitmaa R, Syrjä P, Lohi H, Snellman M, Jeserevics J, Cizinauskas S. Jokinen TS, et al. Among authors: lohi h. J Vet Intern Med. 2007 May-Jun;21(3):464-71. doi: 10.1892/0891-6640(2007)21[464:bfjeil]2.0.co;2. J Vet Intern Med. 2007. PMID: 17552452 Free article.

3

Ancestral T-box mutation is present in many, but not all, short-tailed dog breeds.

Hytönen MK, Grall A, Hédan B, Dréano S, Seguin SJ, Delattre D, Thomas A, Galibert F, Paulin L, Lohi H, Sainio K, André C. Hytönen MK, et al. Among authors: lohi h. J Hered. 2009 Mar-Apr;100(2):236-40. doi: 10.1093/jhered/esn085. Epub 2008 Oct 14. J Hered. 2009. PMID: 18854372

4

Genome-wide association mapping identifies multiple loci for a canine SLE-related disease complex.

Wilbe M, Jokinen P, Truvé K, Seppala EH, Karlsson EK, Biagi T, Hughes A, Bannasch D, Andersson G, Hansson-Hamlin H, Lohi H, Lindblad-Toh K. Wilbe M, et al. Among authors: lohi h. Nat Genet. 2010 Mar;42(3):250-4. doi: 10.1038/ng.525. Epub 2010 Jan 31. Nat Genet. 2010. PMID: 20101241

5

Regional occurrence, high frequency but low diversity of mitochondrial DNA haplogroup d1 suggests a recent dog-wolf hybridization in Scandinavia.

Klütsch CF, Seppälä EH, Fall T, Uhlén M, Hedhammar A, Lohi H, Savolainen P. Klütsch CF, et al. Among authors: lohi h. Anim Genet. 2011 Feb;42(1):100-3. doi: 10.1111/j.1365-2052.2010.02069.x. Anim Genet. 2011. PMID: 20497152 Free PMC article.

6

Segregation of point mutation heteroplasmy in the control region of dog mtDNA studied systematically in deep generation pedigrees.

Klütsch CF, Seppälä EH, Uhlén M, Lohi H, Savolainen P. Klütsch CF, et al. Among authors: lohi h. Int J Legal Med. 2011 Jul;125(4):527-35. doi: 10.1007/s00414-010-0524-7. Epub 2010 Nov 4. Int J Legal Med. 2011. PMID: 21049272 Free PMC article. Review.

7

Assessment of the functionality of genome-wide canine SNP arrays and implications for canine disease association studies.

Ke X, Kennedy LJ, Short AD, Seppälä EH, Barnes A, Clements DN, Wood SH, Carter SD, Happ GM, Lohi H, Ollier WE. Ke X, et al. Among authors: lohi h. Anim Genet. 2011 Apr;42(2):181-90. doi: 10.1111/j.1365-2052.2010.02132.x. Epub 2010 Nov 11. Anim Genet. 2011. PMID: 21070295

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: lohi h. 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

LUPA: a European initiative taking advantage of the canine genome architecture for unravelling complex disorders in both human and dogs.

Lequarré AS, Andersson L, André C, Fredholm M, Hitte C, Leeb T, Lohi H, Lindblad-Toh K, Georges M. Lequarré AS, et al. Among authors: lohi h. Vet J. 2011 Aug;189(2):155-9. doi: 10.1016/j.tvjl.2011.06.013. Epub 2011 Jul 12. Vet J. 2011. PMID: 21752675 Free article. Review.

10

Identification of genomic regions associated with phenotypic variation between dog breeds using selection mapping.

Vaysse A, Ratnakumar A, Derrien T, Axelsson E, Rosengren Pielberg G, Sigurdsson S, Fall T, Seppälä EH, Hansen MS, Lawley CT, Karlsson EK; LUPA Consortium; Bannasch D, Vilà C, Lohi H, Galibert F, Fredholm M, Häggström J, Hedhammar A, André C, Lindblad-Toh K, Hitte C, Webster MT. Vaysse A, et al. Among authors: lohi h. PLoS Genet. 2011 Oct;7(10):e1002316. doi: 10.1371/journal.pgen.1002316. Epub 2011 Oct 13. PLoS Genet. 2011. PMID: 22022279 Free PMC article.

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