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Multiple Origins and Genomic Basis of Complex Traits in Sighthounds.
Li WL, Liu YH, Li JX, Ding MT, Adeola AC, Isakova J, Aldashev AA, Peng MS, Huang X, Xie G, Chen X, Yang WK, Zhou WW, Ghanatsaman ZA, Olaogun SC, Sanke OJ, Dawuda PM, Hytönen MK, Lohi H, Esmailizadeh A, Poyarkov AD, Savolainen P, Wang GD, Zhang YP. Li WL, et al. Among authors: lohi h. Mol Biol Evol. 2023 Aug 3;40(8):msad158. doi: 10.1093/molbev/msad158. Mol Biol Evol. 2023. PMID: 37433053 Free PMC article.
Molecular Characterization of Three Canine Models of Human Rare Bone Diseases: Caffey, van den Ende-Gupta, and Raine Syndromes.
Hytönen MK, Arumilli M, Lappalainen AK, Owczarek-Lipska M, Jagannathan V, Hundi S, Salmela E, Venta P, Sarkiala E, Jokinen T, Gorgas D, Kere J, Nieminen P, Drögemüller C, Lohi H. Hytönen MK, et al. Among authors: lohi h. PLoS Genet. 2016 May 17;12(5):e1006037. doi: 10.1371/journal.pgen.1006037. eCollection 2016 May. PLoS Genet. 2016. PMID: 27187611 Free PMC article.
The canine era: the rise of a biomedical model.
van Steenbeek FG, Hytönen MK, Leegwater PA, Lohi H. van Steenbeek FG, et al. Among authors: lohi h. Anim Genet. 2016 Oct;47(5):519-27. doi: 10.1111/age.12460. Epub 2016 Jun 21. Anim Genet. 2016. PMID: 27324307 Review.
Canine models of human rare disorders.
Hytönen MK, Lohi H. Hytönen MK, et al. Among authors: lohi h. Rare Dis. 2016 Sep 28;4(1):e1241362. doi: 10.1080/21675511.2016.1241362. eCollection 2016. Rare Dis. 2016. PMID: 27803843 Free PMC article.
252 results