K. Minor

发表

A novel TYRP1 mutation associated with brown coat color in Siberian huskies.

J. Mickelson, Samantha L Van Buren, K. Minor, 2021, Animal genetics.

Genomic diversity and population structure of the Leonberger dog breed

J. Mickelson, C. Drögemüller, F. Seefried, 2020, Genetics Selection Evolution.

Hereditary xanthinuria in a goat

K. Minor, R. Rech, K. Vail, 2019, Journal of veterinary internal medicine.

Targeted sequencing of candidate gene regions for myelofibrosis in dogs

J. Modiano, D. Seelig, K. Minor, 2022, Journal of veterinary internal medicine.

MTM1 mutation associated with X-linked myotubular myopathy in Labrador Retrievers

L. Kunkel, J. Mickelson, A. Beggs, 2010, Proceedings of the National Academy of Sciences.

Dog colour patterns explained by modular promoters of ancient canid origin

César L. Araujo, J. Kere, G. Barsh, 2020, Nature Ecology & Evolution.

A GJA9 frameshift variant is associated with polyneuropathy in Leonberger dogs

J. Mickelson, C. Drögemüller, T. Leeb, 2017, BMC Genomics.

Sarcoglycan A mutation in miniature dachshund dogs causes limb-girdle muscular dystrophy 2D

Jonah N Cullen, J. Mickelson, Ling T Guo, 2020, Skeletal muscle.

Multiple variants in XDH and MOCOS underlie xanthine urolithiasis in dogs

J. Mickelson, K. Minor, J. Lulich, 2021, Molecular genetics and metabolism reports.

A Third MLPH Variant Causing Coat Color Dilution in Dogs

J. Mickelson, Samantha L Van Buren, K. Minor, 2020, Genes.

A Missense Variant Affecting the C-Terminal Tail of UNC93B1 in Dogs with Exfoliative Cutaneous Lupus Erythematosus (ECLE)

J. Mickelson, T. Leeb, H. Lohi, 2020, Genes.

Congenital muscular dystrophy in a dog with a LAMA2 gene deletion

Jonah N Cullen, J. Mickelson, Ling T Guo, 2021, Journal of veterinary internal medicine.

Muscular dystrophy-dystroglycanopathy in a family of Labrador retrievers with a LARGE1 mutation

Jonah N Cullen, J. Mickelson, Ling T Guo, 2021, Neuromuscular Disorders.

Pathogenic variants in COL6A3 cause Ullrich-like congenital muscular dystrophy in young Labrador Retriever dogs

J. Mickelson, C. Bönnemann, Ling T Guo, 2020, Neuromuscular Disorders.

Sarcoglycan A

Jonah N Cullen, J. Mickelson, Ling T Guo, 2020 .

A Mutation in the Mitochondrial Aspartate/Glutamate Carrier Leads to a More Oxidizing Intramitochondrial Environment and an Inflammatory Myopathy in Dutch Shepherd Dogs

Jonathan M. Monk, R. Naviaux, J. Mickelson, 2019, Journal of Neuromuscular Diseases.

Evaluation of Dogs with Border Collie Collapse, Including Response to Two Standardized Strenuous Exercise Protocols.

E. Patterson, J. Mickelson, G. Shelton, 2016, Journal of the American Animal Hospital Association.

Exercise-induced collapse of Labrador retrievers: survey results and preliminary investigation of heritability.

E. Patterson, J. Mickelson, G. Shelton, 2008, Journal of the American Animal Hospital Association.

An ARHGEF10 Deletion Is Highly Associated with a Juvenile-Onset Inherited Polyneuropathy in Leonberger and Saint Bernard Dogs

E. Patterson, J. Mickelson, C. Drögemüller, 2014, PLoS genetics.

Candidate genes for idiopathic epilepsy in four dog breeds

E. Patterson, J. Mickelson, K. Minor, 2011, BMC Genetics.

Genome-Wide Analyses for Osteosarcoma in Leonberger Dogs Reveal the CDKN2A/B Gene Locus as a Major Risk Locus

Voichita D. Marinescu, K. Lindblad-Toh, J. Mickelson, 2021, Genes.

NME5 frameshift variant in Alaskan Malamutes with primary ciliary dyskinesia

C. Mellersh, J. Mickelson, T. Leeb, 2019, PLoS genetics.

Prevalence of the AMHR2 mutation in Miniature Schnauzers and genetic investigation of a Belgian Malinois with persistent Müllerian duct syndrome

K. Minor, P. Leegwater, E. Furrow, 2018, Reproduction in domestic animals = Zuchthygiene.

DNM1 mutation status, sex, and sterilization status of a cohort of Labrador retrievers with and without cranial cruciate ligament rupture

M. Conzemius, A. Rendahl, K. Minor, 2017, Canine Genetics and Epidemiology.

A COLQ Missense Mutation in Labrador Retrievers Having Congenital Myasthenic Syndrome

Ling T Guo, G. Shelton, K. Minor, 2014, PloS one.

Border Collie Collapse: Owner Survey Results and Veterinary Description of Videotaped Episodes.

E. Patterson, J. Mickelson, G. Shelton, 2016, Journal of the American Animal Hospital Association.

An ABCC9 Missense Variant Is Associated with Sudden Cardiac Death and Dilated Cardiomyopathy in Juvenile Dogs

P. Henthorn, K. Minor, M. Sleeper, 2023, Genes.

A Missense Mutation in the Vacuolar Protein Sorting 11 (VPS11) Gene Is Associated with Neuroaxonal Dystrophy in Rottweiler Dogs

C. T. Brown, T. Mansour, J. Mickelson, 2018, G3: Genes, Genomes, Genetics.

Canine NAPEPLD-associated models of human myelin disorders

E. Patterson, J. Mickelson, C. Drögemüller, 2018, Scientific Reports.

An EHPB1L1 Nonsense Mutation Associated with Congenital Dyserythropoietic Anemia and Polymyopathy in Labrador Retriever Littermates

Jonah N Cullen, J. Mickelson, Ling T Guo, 2022, Genes.

Canine models of Charcot-Marie-Tooth: MTMR2, MPZ, and SH3TC2 variants in golden retrievers with congenital hypomyelinating polyneuropathy

G. Shelton, K. Minor, D. C. Williams, 2023, Neuromuscular Disorders.

A CNTNAP1 Missense Variant Is Associated with Canine Laryngeal Paralysis and Polyneuropathy

G. Johnson, J. Mickelson, C. Drögemüller, 2020, Genes.

Current Classification of Canine Muscular Dystrophies and Identification of New Variants

Jonah N Cullen, J. Mickelson, Ling T Guo, 2023, Genes.

P6030 Three diverse mutations underlying canine xanthine urolithiasis.

J. Mickelson, K. Minor, J. Lulich, 2016 .

Canine models of Charcot-Marie-Tooth: MTMR2, MPZ, and SH3TC2 variants in golden retrievers with congenital hypomyelinating polyneuropathy

Jonah N Cullen, G. Shelton, K. Minor, 2023, Neuromuscular Disorders.

A Gly98Val Mutation in the N-Myc Downstream Regulated Gene 1 (NDRG1) in Alaskan Malamutes with Polyneuropathy

S. Cirera, J. Mickelson, M. Fredholm, 2013, PloS one.

Tandem duplication within the DMD gene in Labrador retrievers with a mild clinical phenotype

Jonah N Cullen, L. Kunkel, M. Zatz, 2022, Neuromuscular Disorders.

MTM1 mutation associated with X-linked myotubular myopathy in Labrador Retrievers

L. Kunkel, J. Mickelson, A. Beggs, 2010, Proceedings of the National Academy of Sciences.

A canine DNM1 mutation is highly associated with the syndrome of exercise-induced collapse

K. Minor, K. Ekenstedt, G. D. Shelton, 2008, Nature Genetics.

Multi-Allelic Mitochondrial DNA Deletions in an Adult Dog with Chronic Weakness, Exercise Intolerance and Lactic Acidemia

Jonah N Cullen, Ling T Guo, K. Minor, 2024, Animals : an open access journal from MDPI.

Novel COL6A3 frameshift variant in American Staffordshire Terrier dogs with Ullrich‐like congenital muscular dystrophy

Jonah N Cullen, Ling T Guo, G. Shelton, 2023, Journal of veterinary internal medicine.