Whole Animal Genome Sequencing: user-friendly, rapid, containerized pipelines for processing, variant discovery, and annotation of short-read whole genome sequencing data

por Cullen, Jonah N, Friedenberg, Steven G
Publicado 2023

Special Issue “Molecular Basis of Inherited Diseases in Companion Animals”

por Friedenberg, Steven G., Bannasch, Danika L.
Publicado 2021

A scoping review of autoantibodies as biomarkers for canine autoimmune disease

por Treeful, Amy E., Coffey, Emily L., Friedenberg, Steven G.
Publicado 2022

RNA sequencing of whole blood in dogs with primary immune-mediated hemolytic anemia (IMHA) reveals novel insights into disease pathogenesis

por Borchert, Corie, Herman, Adam, Roth, Megan, Brooks, Aimee C., Friedenberg, Steven G.
Publicado 2020

A novel mutation of the CLCN1 gene in a cat with myotonia congenita: Diagnosis and treatment

por Woelfel, Christian, Meurs, Kathryn, Friedenberg, Steven, DeBruyne, Nicole, Olby, Natasha J.
Publicado 2022

An SNN retrocopy insertion upstream of GPR22 is associated with dark red coat color in Poodles

por Batcher, Kevin, Varney, Scarlett, Affolter, Verena K, Friedenberg, Steven G, Bannasch, Danika
Publicado 2022

Deafness and vestibular dysfunction in a Doberman Pinscher puppy associated with a mutation in the PTPRQ gene

por Guevar, Julien, Olby, Natasha J., Meurs, Kathryn M., Yost, Oriana, Friedenberg, Steven G.
Publicado 2018

A defect in the NOG gene increases susceptibility to spontaneous superficial chronic corneal epithelial defects (SCCED) in boxer dogs

por Meurs, Kathryn M., Montgomery, Keith, Friedenberg, Steven G., Williams, Brian, Gilger, Brian C.
Publicado 2021

A novel missense mutation of the NAT10 gene in a juvenile Schnauzer dog with chronic respiratory tract infections

por Hedgespeth, Barry A., Birkenheuer, Adam J., Friedenberg, Steven G., Olby, Natasha J., Meurs, Kathryn M.
Publicado 2021

Current Classification of Canine Muscular Dystrophies and Identification of New Variants

por Shelton, G. Diane, Minor, Katie M., Friedenberg, Steven G., Cullen, Jonah N., Guo, Ling T., Mickelson, James R.
Publicado 2023

Development and application of a next-generation sequencing protocol and bioinformatics pipeline for the comprehensive analysis of the canine immunoglobulin repertoire

por Cullen, Jonah N., Martin, Jolyon, Vilella, Albert J., Treeful, Amy, Sargan, David, Bradley, Allan, Friedenberg, Steven G.
Publicado 2022

A case‐control survey study of environmental risk factors for primary hypoadrenocorticism in dogs

por Treeful, Amy E., Searle, Kelly M., Carroll, Dana M., Yost, Kathleen J., Hedger, Anna L., Friedenberg, Steven G.
Publicado 2023

A QIL1 Variant Associated with Ventricular Arrhythmias and Sudden Cardiac Death in the Juvenile Rhodesian Ridgeback Dog

por Meurs, Kathryn M., Friedenberg, Steven G., Olby, Natasha J., Condit, Julia, Weidman, Jess, Rosenthal, Steve, Shelton, G. Diane
Publicado 2019

A de novo mutation in the EXT2 gene associated with osteochondromatosis in a litter of American Staffordshire Terriers

por Friedenberg, Steven G., Vansteenkiste, Daniella, Yost, Oriana, Treeful, Amy E., Meurs, Kathryn M., Tokarz, Debra A., Olby, Natasha J.
Publicado 2018

Congenital muscular dystrophy in a dog with a LAMA2 gene deletion

por Shelton, G. Diane, Minor, Katie M., Thomovsky, Stephanie, Guo, Ling T., Friedenberg, Steven G., Cullen, Jonah N., Mickelson, James R.
Publicado 2021

Targeted sequencing of candidate gene regions for myelofibrosis in dogs

por Campbell, Amelia G., Seelig, Davis M., Beckman, Joan D., Minor, Katie M., Heinrich, Daniel A., Friedenberg, Steven G., Modiano, Jaime F., Furrow, Eva
Publicado 2022

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

por Shelton, G. Diane, Minor, Katie M., Guo, Ling T., Thomas-Hollands, Alison, Walsh, Koranda A., Friedenberg, Steven G., Cullen, Jonah N., Mickelson, James R.
Publicado 2022

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

por Shelton, G. Diane, Minor, Katie M., Vieira, Natassia M., Kunkel, Louis M., Friedenberg, Steven G., Cullen, Jonah N., Guo, Ling T., Zatz, Mayana, Mickelson, James R.
Publicado 2022

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

por Jankelunas, Leanne, Murthy, Vishal D., Chen, Annie V., Minor, Katie M., Friedenberg, Steven G., Cullen, Jonah N., Guo, Ling T., Mickelson, James R., Shelton, G. Diane
Publicado 2023

A deleterious mutation in the ALMS1 gene in a naturally occurring model of hypertrophic cardiomyopathy in the Sphynx cat

por Meurs, Kathryn M., Williams, Brian G., DeProspero, Dylan, Friedenberg, Steven G., Malarkey, David E., Ezzell, J. Ashley, Keene, Bruce W., Adin, Darcy B., DeFrancesco, Teresa C., Tou, Sandra
Publicado 2021