A Missense Variant in SCN8A in Alpine Dachsbracke Dogs Affected by Spinocerebellar Ataxia

per Letko, Anna, Dietschi, Elisabeth, Nieburg, Marco, Jagannathan, Vidhya, Gurtner, Corinne, Oevermann, Anna, Drögemüller, Cord
Publicat a Genes (Basel) (2019)

A large deletion in the COL2A1 gene expands the spectrum of pathogenic variants causing bulldog calf syndrome in cattle

per Jacinto, Joana Gonçalves Pontes, Häfliger, Irene Monika, Letko, Anna, Drögemüller, Cord, Agerholm, Jørgen Steen
Publicat a Acta Vet Scand (2020)

Compound heterozygous PLA2G6 loss-of-function variants in Swaledale sheep with neuroaxonal dystrophy

per Letko, Anna, Strugnell, Ben, Häfliger, Irene M., Paris, Julia M., Waine, Katie, Drögemüller, Cord, Scholes, Sandra
Publicat a Mol Genet Genomics (2020)

Phenotypic and Genomic Analysis of Cystic Hygroma in Pigs

per Letko, Anna, Schauer, Alexandria Marie, Derks, Martijn F. L., Grau-Roma, Llorenç, Drögemüller, Cord, Grahofer, Alexander
Publicat a Genes (Basel) (2021)

Genomic diversity and population structure of the Leonberger dog breed

per Letko, Anna, Minor, Katie M., Jagannathan, Vidhya, Seefried, Franz R., Mickelson, James R., Oliehoek, Pieter, Drögemüller, Cord
Publicat a Genet Sel Evol (2020)

Correction to: Genomic diversity and population structure of the Leonberger dog breed

per Letko, Anna, Minor, Katie M., Jagannathan, Vidhya, Seefried, Franz R., Mickelson, James R., Oliehoek, Pieter, Drögemüller, Cord
Publicat a Genet Sel Evol (2020)

Chromosomal imbalance in pigs showing a syndromic form of cleft palate

per Grahofer, Alexander, Letko, Anna, Häfliger, Irene Monika, Jagannathan, Vidhya, Ducos, Alain, Richard, Olivia, Peter, Vanessa, Nathues, Heiko, Drögemüller, Cord
Publicat a BMC Genomics (2019)

Multiple FGF4 Retrocopies Recently Derived within Canids

per Batcher, Kevin, Dickinson, Peter, Maciejczyk, Kimberly, Brzeski, Kristin, Rasouliha, Sheida Hadji, Letko, Anna, Drögemüller, Cord, Leeb, Tosso, Bannasch, Danika
Publicat a Genes (Basel) (2020)

X-Linked Duchenne-Type Muscular Dystrophy in Jack Russell Terrier Associated with a Partial Deletion of the Canine DMD Gene

per Brunetti, Barbara, Muscatello, Luisa V., Letko, Anna, Papa, Valentina, Cenacchi, Giovanna, Grillini, Marco, Murgiano, Leonardo, Jagannathan, Vidhya, Drögemüller, Cord
Publicat a Genes (Basel) (2020)

A Heterozygous Missense Variant in the COL5A2 in Holstein Cattle Resembling the Classical Ehlers–Danlos Syndrome

per Jacinto, Joana G. P., Häfliger, Irene M., Veiga, Inês M. B., Letko, Anna, Benazzi, Cinzia, Bolcato, Marilena, Drögemüller, Cord
Publicat a Animals (Basel) (2020)

A de novo variant in OTX2 in a lamb with otocephaly

per Paris, Julia Maria, Letko, Anna, Häfliger, Irene Monika, Švara, Tanja, Gombač, Mitja, Klinc, Primož, Škibin, Andrej, Pogorevc, Estera, Drögemüller, Cord
Publicat a Acta Vet Scand (2020)

Whole Genome Sequencing Indicates Heterogeneity of Hyperostotic Disorders in Dogs

per Letko, Anna, Leuthard, Fabienne, Jagannathan, Vidhya, Corlazzoli, Daniele, Matiasek, Kaspar, Schweizer, Daniela, Hytönen, Marjo K., Lohi, Hannes, Leeb, Tosso, Drögemüller, Cord
Publicat a Genes (Basel) (2020)

A GJA9 frameshift variant is associated with polyneuropathy in Leonberger dogs

per Becker, Doreen, Minor, Katie M., Letko, Anna, Ekenstedt, Kari J., Jagannathan, Vidhya, Leeb, Tosso, Shelton, G. Diane, Mickelson, James R., Drögemüller, Cord
Publicat a BMC Genomics (2017)

Deleterious AGXT Missense Variant Associated with Type 1 Primary Hyperoxaluria (PH1) in Zwartbles Sheep

per Letko, Anna, Dijkman, Reinie, Strugnell, Ben, Häfliger, Irene M., Paris, Julia M., Henderson, Katrina, Geraghty, Tim, Orr, Hannah, Scholes, Sandra, Drögemüller, Cord
Publicat a Genes (Basel) (2020)

Identification of a Missense Variant in MFSD12 Involved in Dilution of Phaeomelanin Leading to White or Cream Coat Color in Dogs

per Hédan, Benoit, Cadieu, Edouard, Botherel, Nadine, Dufaure de Citres, Caroline, Letko, Anna, Rimbault, Maud, Drögemüller, Cord, Jagannathan, Vidhya, Derrien, Thomas, Schmutz, Sheila, Leeb, Tosso, André, Catherine
Publicat a Genes (Basel) (2019)

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

per Lucot, Katherine L., Dickinson, Peter J., Finno, Carrie J., Mansour, Tamer A., Letko, Anna, Minor, Katherine M., Mickelson, James R., Drögemüller, Cord, Brown, C. Titus, Bannasch, Danika L.
Publicat a G3 (Bethesda) (2018)

SLC19A3 Loss-of-Function Variant in Yorkshire Terriers With Leigh-Like Subacute Necrotizing Encephalopathy

per Drögemüller, Michaela, Letko, Anna, Matiasek, Kaspar, Jagannathan, Vidhya, Corlazzoli, Daniele, Rosati, Marco, Jurina, Konrad, Medl, Susanne, Gödde, Thomas, Rupp, Stefan, Fischer, Andrea, Luján Feliu-Pascual, Alejandro, Drögemüller, Cord
Publicat a Genes (Basel) (2020)

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

per Letko, Anna, Minor, Katie M., Friedenberg, Steven G., Shelton, G. Diane, Salvador, Jill Pesayco, Mandigers, Paul J. J., Leegwater, Peter A. J., Winkler, Paige A., Petersen-Jones, Simon M., Stanley, Bryden J., Ekenstedt, Kari J., Johnson, Gary S., Hansen, Liz, Jagannathan, Vidhya, Mickelson, James R., Drögemüller, Cord
Publicat a Genes (Basel) (2020)

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

per Leeb, Tosso, Leuthard, Fabienne, Jagannathan, Vidhya, Kiener, Sarah, Letko, Anna, Roosje, Petra, Welle, Monika M., Gailbreath, Katherine L., Cannon, Andrea, Linek, Monika, Banovic, Frane, Olivry, Thierry, White, Stephen D., Batcher, Kevin, Bannasch, Danika, Minor, Katie M., Mickelson, James R., Hytönen, Marjo K., Lohi, Hannes, Mauldin, Elizabeth A., Casal, Margret L.
Publicat a Genes (Basel) (2020)

A Missense Variant in ALDH5A1 Associated with Canine Succinic Semialdehyde Dehydrogenase Deficiency (SSADHD) in the Saluki Dog

per Vernau, Karen M., Struys, Eduard, Letko, Anna, Woolard, Kevin D., Aguilar, Miriam, Brown, Emily A., Cissell, Derek D., Dickinson, Peter J., Shelton, G. Diane, Broome, Michael R., Gibson, K. Michael, Pearl, Phillip L., König, Florian, Van Winkle, Thomas J., O’Brien, Dennis, Roos, B., Matiasek, Kaspar, Jagannathan, Vidhya, Drögemüller, Cord, Mansour, Tamer A., Brown, C. Titus, Bannasch, Danika L.
Publicat a Genes (Basel) (2020)