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

Por Letko, Anna, Dietschi, Elisabeth, Nieburg, Marco, Jagannathan, Vidhya, Gurtner, Corinne, Oevermann, Anna, Drögemüller, Cord
Publicado no Genes (Basel) (2019)

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

Por Jacinto, Joana Gonçalves Pontes, Häfliger, Irene Monika, Letko, Anna, Drögemüller, Cord, Agerholm, Jørgen Steen
Publicado no Acta Vet Scand (2020)

Genomic diversity and population structure of the Leonberger dog breed

Por Letko, Anna, Minor, Katie M., Jagannathan, Vidhya, Seefried, Franz R., Mickelson, James R., Oliehoek, Pieter, Drögemüller, Cord
Publicado no Genet Sel Evol (2020)

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

Por Letko, Anna, Minor, Katie M., Jagannathan, Vidhya, Seefried, Franz R., Mickelson, James R., Oliehoek, Pieter, Drögemüller, Cord
Publicado no Genet Sel Evol (2020)

Chromosomal imbalance in pigs showing a syndromic form of cleft palate

Por Grahofer, Alexander, Letko, Anna, Häfliger, Irene Monika, Jagannathan, Vidhya, Ducos, Alain, Richard, Olivia, Peter, Vanessa, Nathues, Heiko, Drögemüller, Cord
Publicado no BMC Genomics (2019)

Multiple FGF4 Retrocopies Recently Derived within Canids

Por Batcher, Kevin, Dickinson, Peter, Maciejczyk, Kimberly, Brzeski, Kristin, Rasouliha, Sheida Hadji, Letko, Anna, Drögemüller, Cord, Leeb, Tosso, Bannasch, Danika
Publicado no Genes (Basel) (2020)

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

Por Brunetti, Barbara, Muscatello, Luisa V., Letko, Anna, Papa, Valentina, Cenacchi, Giovanna, Grillini, Marco, Murgiano, Leonardo, Jagannathan, Vidhya, Drögemüller, Cord
Publicado no Genes (Basel) (2020)

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

Por Jacinto, Joana G. P., Häfliger, Irene M., Veiga, Inês M. B., Letko, Anna, Benazzi, Cinzia, Bolcato, Marilena, Drögemüller, Cord
Publicado no Animals (Basel) (2020)

A de novo variant in OTX2 in a lamb with otocephaly

Por Paris, Julia Maria, Letko, Anna, Häfliger, Irene Monika, Švara, Tanja, Gombač, Mitja, Klinc, Primož, Škibin, Andrej, Pogorevc, Estera, Drögemüller, Cord
Publicado no Acta Vet Scand (2020)

Whole Genome Sequencing Indicates Heterogeneity of Hyperostotic Disorders in Dogs

Por Letko, Anna, Leuthard, Fabienne, Jagannathan, Vidhya, Corlazzoli, Daniele, Matiasek, Kaspar, Schweizer, Daniela, Hytönen, Marjo K., Lohi, Hannes, Leeb, Tosso, Drögemüller, Cord
Publicado no Genes (Basel) (2020)

A GJA9 frameshift variant is associated with polyneuropathy in Leonberger dogs

Por Becker, Doreen, Minor, Katie M., Letko, Anna, Ekenstedt, Kari J., Jagannathan, Vidhya, Leeb, Tosso, Shelton, G. Diane, Mickelson, James R., Drögemüller, Cord
Publicado no BMC Genomics (2017)

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

Por Letko, Anna, Dijkman, Reinie, Strugnell, Ben, Häfliger, Irene M., Paris, Julia M., Henderson, Katrina, Geraghty, Tim, Orr, Hannah, Scholes, Sandra, Drögemüller, Cord
Publicado no Genes (Basel) (2020)

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

Por 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
Publicado no Genes (Basel) (2019)

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

Por 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.
Publicado no G3 (Bethesda) (2018)

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

Por 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
Publicado no Genes (Basel) (2020)

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

Por 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
Publicado no Genes (Basel) (2020)

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

Por 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.
Publicado no Genes (Basel) (2020)

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

Por 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.
Publicado no Genes (Basel) (2020)