List of works - Stephanie Valberg

3 Dimensional photonic scans for measuring body volume and muscle mass in the standing horse

scientific article published on 27 February 2020

A glycogen synthase 1 mutation associated with equine polysaccharide storage myopathy and exertional rhabdomyolysis occurs in a variety of UK breeds

scientific article published on 01 July 2009

A high density SNP array for the domestic horse and extant Perissodactyla: utility for association mapping, genetic diversity, and phylogeny studies

scientific article

AGYS1gene mutation is highly associated with polysaccharide storage myopathy in Cob Normand draught horses

article

Abnormal locomotor muscle recruitment activity is present in horses with shivering and Purkinje cell distal axonopathy.

scientific article published on 21 January 2018

An E321G MYH1 mutation is strongly associated with nonexertional rhabdomyolysis in Quarter Horses

scientific article published on 05 August 2018

Biochemical and genetic evaluation of the role of AMP-activated protein kinase in polysaccharide storage myopathy in Quarter Horses

scientific article published on 01 October 2007

Clinical and histopathological features of myofibrillar myopathy in Warmblood horses.

scientific article published on 22 May 2017

Coding sequences of sarcoplasmic reticulum calcium ATPase regulatory peptides and expression of calcium regulatory genes in recurrent exertional rhabdomyolysis

article

Commercial genetic testing for type 2 polysaccharide storage myopathy and myofibrillar myopathy does not correspond to a histopathological diagnosis

scientific article published on 08 September 2020

Comparative skeletal muscle histopathologic and ultrastructural features in two forms of polysaccharide storage myopathy in horses

scientific article published on 15 July 2009

Estimated prevalence of the Type 1 Polysaccharide Storage Myopathy mutation in selected North American and European breeds

scientific article published on 01 December 2010

Evidence of positive selection for a glycogen synthase (GYS1) mutation in domestic horse populations.

scientific article

Genetic risk factors for insidious equine recurrent uveitis in Appaloosa horses.

scientific article

Genome-wide SNP data show little differentiation between the Appaloosa and other American stock horse breeds.

scientific article

Genome-wide analysis reveals selection for important traits in domestic horse breeds.

scientific article published on 17 January 2013

Glycogen synthase (GYS1) mutation causes a novel skeletal muscle glycogenosis.

scientific article published on 20 March 2008

Glycogen synthase 1 (GYS1) mutation in diverse breeds with polysaccharide storage myopathy.

scientific article

Haplotype diversity in the equine myostatin gene with focus on variants associated with race distance propensity and muscle fiber type proportions.

scientific article

Impact of alpha-tocopherol deficiency and supplementation on sacrocaudalis and gluteal muscle fiber histopathology and morphology in horses

scientific article published on 29 October 2019

Pathways of calcium regulation, electron transport, and mitochondrial protein translation are molecular signatures of susceptibility to recurrent exertional rhabdomyolysis in Thoroughbred racehorses

scientific article published on 10 February 2021

Persistent hypoglycemia associated with lipid storage myopathy in a paint foal.

scientific article

Presence of the glycogen synthase 1 (GYS1) mutation causing type 1 polysaccharide storage myopathy in continental European draught horse breeds

scientific article published on 01 November 2010

Prevalence of the E321G MYH1 variant for immune-mediated myositis and nonexertional rhabdomyolysis in performance subgroups of American Quarter Horses

scientific article published on 08 January 2019

Proteome and transcriptome profiling of equine myofibrillar myopathy identifies diminished peroxiredoxin 6 and altered cysteine metabolic pathways

scientific article published on 05 October 2018

Sarcolipin Exhibits Abundant RNA Transcription and Minimal Protein Expression in Horse Gluteal Muscle

scientific article published on 13 November 2020

List of works by Stephanie Valberg

3 Dimensional photonic scans for measuring body volume and muscle mass in the standing horse

A glycogen synthase 1 mutation associated with equine polysaccharide storage myopathy and exertional rhabdomyolysis occurs in a variety of UK breeds

A high density SNP array for the domestic horse and extant Perissodactyla: utility for association mapping, genetic diversity, and phylogeny studies

AGYS1gene mutation is highly associated with polysaccharide storage myopathy in Cob Normand draught horses

Abnormal locomotor muscle recruitment activity is present in horses with shivering and Purkinje cell distal axonopathy.

An E321G MYH1 mutation is strongly associated with nonexertional rhabdomyolysis in Quarter Horses

Biochemical and genetic evaluation of the role of AMP-activated protein kinase in polysaccharide storage myopathy in Quarter Horses

Clinical and histopathological features of myofibrillar myopathy in Warmblood horses.

Coding sequences of sarcoplasmic reticulum calcium ATPase regulatory peptides and expression of calcium regulatory genes in recurrent exertional rhabdomyolysis

Commercial genetic testing for type 2 polysaccharide storage myopathy and myofibrillar myopathy does not correspond to a histopathological diagnosis

Comparative skeletal muscle histopathologic and ultrastructural features in two forms of polysaccharide storage myopathy in horses

Estimated prevalence of the Type 1 Polysaccharide Storage Myopathy mutation in selected North American and European breeds

Evidence of positive selection for a glycogen synthase (GYS1) mutation in domestic horse populations.

Genetic risk factors for insidious equine recurrent uveitis in Appaloosa horses.

Genome-wide SNP data show little differentiation between the Appaloosa and other American stock horse breeds.

Genome-wide analysis reveals selection for important traits in domestic horse breeds.

Glycogen synthase (GYS1) mutation causes a novel skeletal muscle glycogenosis.

Glycogen synthase 1 (GYS1) mutation in diverse breeds with polysaccharide storage myopathy.

Haplotype diversity in the equine myostatin gene with focus on variants associated with race distance propensity and muscle fiber type proportions.

Impact of alpha-tocopherol deficiency and supplementation on sacrocaudalis and gluteal muscle fiber histopathology and morphology in horses

Pathways of calcium regulation, electron transport, and mitochondrial protein translation are molecular signatures of susceptibility to recurrent exertional rhabdomyolysis in Thoroughbred racehorses

Persistent hypoglycemia associated with lipid storage myopathy in a paint foal.

Presence of the glycogen synthase 1 (GYS1) mutation causing type 1 polysaccharide storage myopathy in continental European draught horse breeds

Prevalence of the E321G MYH1 variant for immune-mediated myositis and nonexertional rhabdomyolysis in performance subgroups of American Quarter Horses

Proteome and transcriptome profiling of equine myofibrillar myopathy identifies diminished peroxiredoxin 6 and altered cysteine metabolic pathways

Sarcolipin Exhibits Abundant RNA Transcription and Minimal Protein Expression in Horse Gluteal Muscle