A. Viluma

发表

Whole-Genome Sequencing of a Canine Family Trio Reveals a FAM83G Variant Associated with Hereditary Footpad Hyperkeratosis

T. Bergström, T. Leeb, G. Andersson, 2016, G3: Genes, Genomes, Genetics.

Equine Multiple Congenital Ocular Anomalies and Silver Coat Colour Result from the Pleiotropic Effects of Mutant PMEL

L. Andersson, G. Cothran, G. Lindgren, 2013, PloS one.

Genomic structure of the horse major histocompatibility complex class II region resolved using PacBio long-read sequencing technology

T. Bergström, S. Mikko, L. Skow, 2017, Scientific Reports.

Whole-genome resequencing of temporally stratified samples reveals substantial loss of haplotype diversity in the highly inbred Scandinavian wolf population

H. Ellegren, H. Sand, Ø. Flagstad, 2022, Genome research.

Evaluation of whole-genome sequencing of four Chinese crested dogs for variant detection using the ion proton system

T. Bergström, S. Mikko, G. Andersson, 2015, Canine Genetics and Epidemiology.

An ABCA4 loss-of-function mutation causes a canine form of Stargardt disease

C. Mellersh, C. Zeiss, T. Bergström, 2018, bioRxiv.

Polymorphism in myostatin gene and athletic performance in Nordic horse breeds

A. Viluma, 2012 .

Frequencies of polymorphisms in myostatin vary in Icelandic horses according to the use of the horses.

L. Andersson, F. Imsland, S. Mikko, 2015, Animal genetics.

Conformation Traits and Gaits in the Icelandic Horse are Associated with Genetic Variants in Myostatin (MSTN).

L. Andersson, F. Imsland, S. Mikko, 2016, The Journal of heredity.