Carrie J Finno, BSc; DVM; PhD

Associate Professor

  • 576 Citations
  • 15 h-Index
20032019
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Fingerprint Dive into the research topics where Carrie J Finno is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 14 Similar Profiles
Horses Medicine & Life Sciences
horses Agriculture & Biology
Neuroaxonal Dystrophies Medicine & Life Sciences
rhabdomyolysis Agriculture & Biology
Rhabdomyolysis Medicine & Life Sciences
Quarter Horse Agriculture & Biology
myeloencephalopathy Agriculture & Biology
Horse Diseases Medicine & Life Sciences

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Research Output 2003 2019

  • 576 Citations
  • 15 h-Index
  • 56 Article
  • 3 Chapter
  • 1 Review article

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

Valberg, S. J., Soave, K., Williams, Z. J., Perumbakkam, S., Schott, M., Finno, C. J., Petersen, J. L., Fenger, C., Autry, J. M. & Thomas, D. D., Jan 1 2019, In : Journal of Veterinary Internal Medicine.

Research output: Contribution to journalArticle

Sarcoplasmic Reticulum Calcium-Transporting ATPases
rhabdomyolysis
Rhabdomyolysis
sarcoplasmic reticulum
Ca2-transporting ATPase

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

Gianino, G. M., Valberg, S. J., Perumbakkam, S., Henry, M. L., Gardner, K., Penedo, C. & Finno, C. J., Jan 1 2019, (Accepted/In press) In : Journal of Veterinary Internal Medicine.

Research output: Contribution to journalArticle

rhabdomyolysis
myositis
Quarter Horse
Rhabdomyolysis
Myositis

Previously Identified Genetic Variants in ADGRL3 Are not Associated with Risk for Equine Degenerative Myeloencephalopathy across Breeds

Marquardt, S. A., Wilcox, C. V., Burns, E. N., Peterson, J. A. & Finno, C. J., Sep 5 2019, In : Genes. 10, 9

Research output: Contribution to journalArticle

Open Access
G-Protein-Coupled Receptors
Horses
Neuroaxonal Dystrophies
Single Nucleotide Polymorphism
Missense Mutation
4 Citations (Scopus)

A missense mutation in MYH1 is associated with susceptibility to immune-mediated myositis in Quarter Horses

Finno, C. J., Gianino, G., Perumbakkam, S., Williams, Z. J., Bordbari, M. H., Gardner, K. L., Burns, E., Peng, S., Durward-Akhurst, S. A. & Valberg, S. J., Mar 6 2018, In : Skeletal Muscle. 8, 1, 7.

Research output: Contribution to journalArticle

Myositis
Missense Mutation
Horses
Mutation
Skeletal Muscle Myosins
2 Citations (Scopus)

A missense mutation in the vacuolar protein sorting 11 (VPS11) gene is associated with neuroaxonal dystrophy in rottweiler dogs

Lucot, K. L., Dickinson, P. J., Finno, C. J., Mansour, T. A., Letko, A., Minor, K. M., Mickelson, J. R., Drögemüller, C., Brown, C. & Bannasch, D. L., Aug 1 2018, In : G3: Genes, Genomes, Genetics. 8, 8, p. 2773-2780 8 p.

Research output: Contribution to journalArticle

Neuroaxonal Dystrophies
Protein Transport
Missense Mutation
Dogs
Genes