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

由 Letko, Anna, Dietschi, Elisabeth, Nieburg, Marco, Jagannathan, Vidhya, Gurtner, Corinne, Oevermann, Anna, Drögemüller, Cord
發表在 Genes (Basel) (2019)

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

由 Jacinto, Joana Gonçalves Pontes, Häfliger, Irene Monika, Letko, Anna, Drögemüller, Cord, Agerholm, Jørgen Steen
發表在 Acta Vet Scand (2020)

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

由 Letko, Anna, Strugnell, Ben, Häfliger, Irene M., Paris, Julia M., Waine, Katie, Drögemüller, Cord, Scholes, Sandra
發表在 Mol Genet Genomics (2020)

Phenotypic and Genomic Analysis of Cystic Hygroma in Pigs

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

Genomic diversity and population structure of the Leonberger dog breed

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

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

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

Chromosomal imbalance in pigs showing a syndromic form of cleft palate

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

Multiple FGF4 Retrocopies Recently Derived within Canids

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

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

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

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

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

A de novo variant in OTX2 in a lamb with otocephaly

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

Whole Genome Sequencing Indicates Heterogeneity of Hyperostotic Disorders in Dogs

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

A GJA9 frameshift variant is associated with polyneuropathy in Leonberger dogs

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

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

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

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

由 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
發表在 Genes (Basel) (2019)

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

由 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.
發表在 G3 (Bethesda) (2018)

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

由 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
發表在 Genes (Basel) (2020)

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

由 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
發表在 Genes (Basel) (2020)

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

由 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.
發表在 Genes (Basel) (2020)

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

由 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.
發表在 Genes (Basel) (2020)