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Rudd Garces, Gabriela; Farke, Daniela; Schmidt, Martin J; Letko, Anna; Schirl, Katja; Abitbol, Marie; Leeb, Tosso; Lyons, Leslie A; Lühken, Gesine (2024). PAX3 haploinsufficiency in Maine Coon cats with dominant blue eyes and hearing loss resembling the human Waardenburg syndrome. G3 Genes Genomes Genetics, 14(9) Genetics Society of America 10.1093/g3journal/jkae131
Letko, Anna; Gurtner, Corinne; Jagannathan, Vidhya; Drögemüller, Cord (2024). Renal dysplasia in Leonberger dogs - An emerging recessive congenital disorder? Animal genetics, 55(4), pp. 700-701. Wiley 10.1111/age.13439
Goncalves Pontes Jacinto, Joana; Letko, Anna; Häfliger, Irene Monika; Drögemüller, Cord; Agerholm, Jørgen Steen (2024). Congenital syndromic Chiari-like malformation (CSCM) in Holstein cattle: towards unravelling of possible genetic causes. Acta Veterinaria Scandinavica, 66(29) BioMed Central Ltd. 10.1186/s13028-024-00752-y
Jacinto, J G P; Häfliger, I M; Letko, A; Weber, J; Freick, M; Gentile, A; Drögemüller, C; Agerholm, J S (2024). Multiple independent de novo mutations are associated with the development of schistosoma reflexum, a lethal syndrome in cattle. The veterinary journal, 304, p. 106069. Elsevier 10.1016/j.tvjl.2024.106069
Rudd Garces, Gabriela; Letko, Anna; Häfliger, Irene M; Müller, Jana; Herden, Christiane; Nesseler, Anne; Wagner, Henrik; Schmidt, Martin J; Drögemüller, Cord; Lühken, Gesine (2024). MFSD2A frameshift variant in Kerry Hill sheep with microcephaly. Animal genetics, 55(1), pp. 152-157. Wiley 10.1111/age.13374
Tan, K; Adeniyi, O O; Letko, A; RuddGarces, G; Manz, E; Wagner, H; Zanolari, P; Drögemüller, C; Lühken, G (2024). Identification of genomic regions associated with differences in fleece type in Huacaya and Suri alpacas (Vicugna pacos). Animal genetics, 55(1), pp. 163-167. Wiley 10.1111/age.13377
Kiener, Sarah; Troyer, Heather; Ruvolo, Daniel; Grest, Paula; Soto, Sara; Letko, Anna; Jagannathan, Vidhya; Leeb, Tosso; Mauldin, Elizabeth A; Yang, Ching; Rostaher, Ana (2023). Independent COL17A1 Variants in Cats with Junctional Epidermolysis Bullosa. Genes, 14(10) MDPI 10.3390/genes14101835
Letko, Anna; Brülisauer, Franz; Häfliger, Irene M; Corr, Eilidh; Scholes, Sandra; Drögemüller, Cord (2023). Loss-of-function variant in the ovine TMCO6 gene in north country Cheviot sheep with motor neuron disease. Genomics, 115(5), p. 110689. Elsevier 10.1016/j.ygeno.2023.110689
Brunetti, Barbara; Bacci, Barbara; Abbate, Jessica Maria; Tura, Giorgia; Paciello, Orlando; Vaccaro, Emanuela; Prisco, Francesco; Gandini, Gualtiero; Okonji, Samuel; Paola, Andrea di; Letko, Anna; Drögemüller, Cord; Jagannathan, Vidhya; Turba, Maria Elena; Ogundipe, Tolulope Grace; Lorenzini, Luca; Rosati, Marco; Psalla, Dimitra; Leeb, Tosso and Drögemüller, Michaela (2023). SGCD Missense Variant in a Lagotto Romagnolo Dog with Autosomal Recessively Inherited Limb-Girdle Muscular Dystrophy. Genes, 14(8) MDPI 10.3390/genes14081641
Letko, Anna; Hédan, Benoît; Snell, Anna; Harris, Alexander C; Jagannathan, Vidhya; Andersson, Göran; Holst, Bodil S; Ostrander, Elaine A; Quignon, Pascale; André, Catherine; Leeb, Tosso (2023). Genomic Diversity and Runs of Homozygosity in Bernese Mountain Dogs. Genes, 14(3) MDPI 10.3390/genes14030650
Scheemaeker, Stephanie; Inglebert, Marine; Daminet, Sylvie; Dettwiler, Martina; Letko, Anna; Drögemüller, Cord; Kessler, Martin; Ducatelle, Richard; Rottenberg, Sven; Campos, Miguel (2023). Organoids of patient-derived medullary thyroid carcinoma: the first milestone towards a new in vitro model in dogs. Veterinary and comparative oncology, 21(1), pp. 111-122. Wiley 10.1111/vco.12872
Inglebert, Marine; Dettwiler, Martina; Hahn, Kerstin; Letko, Anna; Drögemüller, Cord; Doench, John; Brown, Adam; Memari, Yasin; Davies, Helen R; Degasperi, Andrea; Nik-Zainal, Serena; Rottenberg, Sven (2022). A living biobank of canine mammary tumor organoids as a comparative model for human breast cancer. Scientific Reports, 12(1), p. 18051. Nature Publishing Group 10.1038/s41598-022-21706-2
Inglebert, Marine; Dettwiler, Martina; Hahn, Kerstin; Letko, Anna; Drögemüller, Cord; Doench, John; Brown, Adam; Memari, Yasin; Davies, Helen; Degasperi, Andrea; Nik-Zainal, Serena; Rottenberg, Sven (2022). A living biobank of canine mammary tumor organoids as a comparative model for human breast cancer (bioRxiv). Cold Spring Harbor Laboratory 10.1101/2022.09.02.505845
Letko, Anna; Minor, Katie M.; Norton, Elaine M.; Marinescu, Voichita D.; Drögemüller, Michaela; Ivansson, Emma; Megquier, Kate; Noh, Hyun Ji; Starkey, Mike; Friedenberg, Steven G.; Lindblad-Toh, Kerstin; Mickelson, James R.; Drögemüller, Cord (2021). Genome-Wide Analyses for Osteosarcoma in Leonberger Dogs Reveal the CDKN2A/B Gene Locus as a Major Risk Locus. Genes, 12(12), p. 1964. MDPI 10.3390/genes12121964
Jacinto, Joana G P; Häfliger, Irene M.; Veiga, Inês M. B.; Letko, Anna; Gentile, Arcangelo; Drögemüller, Cord (2021). A frameshift insertion in FA2H causes a recessively inherited form of ichthyosis congenita in Chianina cattle. Molecular genetics and genomics : MGG, 296(6), pp. 1313-1322. Springer 10.1007/s00438-021-01824-8
Letko, Anna; Bützberger, Charis; Hirter, Nathalie; Paris, Julia M.; Abril, Carlos; Drögemüller, Cord (2021). Genetic evaluation of small ruminant lentivirus susceptibility in Valais blacknose sheep. Animal genetics, 52(5), pp. 781-782. Wiley 10.1111/age.13108
Bannasch, Danika L.; Kaelin, Christopher B; Letko, Anna; Loechel, Robert; Hug, Petra; Jagannathan, Vidhya; Henkel, Jan; Roosje, Petra; Hytönen, Marjo K; Lohi, Hannes; Arumilli, Meharji; Minor, Katie M; Mickelson, James R; Drögemüller, Cord; Barsh, Gregory S; Leeb, Tosso (2021). Dog colour patterns explained by modular promoters of ancient canid origin. Nature ecology & evolution, 5(10), pp. 1415-1423. Nature Publishing Group 10.1038/s41559-021-01524-x
Letko, Anna; Strugnell, Ben; Häfliger, Irene M.; Paris, Julia M.; Waine, Katie; Drögemüller, Cord; Scholes, Sandra (2021). Compound heterozygous PLA2G6 loss-of-function variants in Swaledale sheep with neuroaxonal dystrophy. Molecular genetics and genomics : MGG, 296(1), pp. 235-242. Springer 10.1007/s00438-020-01742-1
Letko, Anna; Schauer, Alexandria Marie; Derks, Martijn F. L.; Grau-Roma, Llorenç; Drögemüller, Cord; Grahofer, Alexander (2021). Phenotypic and Genomic Analysis of Cystic Hygroma in Pigs. Genes, 12(2), p. 207. MDPI 10.3390/genes12020207
Paris, J. M.; Letko, A.; Häfliger, I. M.; Ammann, P.; Drögemüller, C. (2020). Ear type in sheep is associated with the MSRB3 locus. Animal genetics, 51(6), pp. 968-972. Wiley 10.1111/age.12994
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, Vidya; Mickelson, James R; Drögemüller, Cord (2020). A CNTNAP1 Missense Variant Is Associated with Canine Laryngeal Paralysis and Polyneuropathy. Genes, 11(12) MDPI 10.3390/genes11121426
Letko, Anna; Minor, Katie M; Jagannathan, Vidhya; Seefried, Franz R; Mickelson, James R; Oliehoek, Pieter; Drögemüller, Cord (2020). Correction to: Genomic diversity and population structure of the Leonberger dog breed. Genetics, selection, evolution, 52(1), p. 70. BioMed Central 10.1186/s12711-020-00590-2
Jacinto, Joana G P; Häfliger, Irene M.; Veiga, Inês M. B.; Letko, Anna; Benazzi, Cinzia; Bolcato, Marilena; Drögemüller, Cord (2020). A Heterozygous Missense Variant in the COL5A2 in Holstein Cattle Resembling the Classical Ehlers–Danlos Syndrome. Animals, 10(11), p. 2002. MDPI 10.3390/ani10112002
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 (2020). SLC19A3 Loss-of-Function Variant in Yorkshire Terriers with Leigh-Like Subacute Necrotizing Encephalopathy. Genes, 11(10), p. 1215. MDPI 10.3390/genes11101215
Letko, Anna; Minor, Katie M.; Jagannathan, Vidya; Seefried, Franz R.; Mickelson, James R.; Oliehoek, Pieter; Drögemüller, Cord (2020). Genomic diversity and population structure of the Leonberger dog breed. Genetics, selection, evolution, 52(1), p. 61. BioMed Central 10.1186/s12711-020-00581-3
Brunetti, Barbara; Muscatello, Luisa V; Letko, Anna; Papa, Valentina; Cenacchi, Giovanna; Grillini, Marco; Murgiano, Leonardo; Jagannathan, Vidya; Drögemüller, Cord (2020). X-Linked Duchenne-Type Muscular Dystrophy in Jack Russell Terrier Associated with a Partial Deletion of the Canine DMD Gene. Genes, 11(10) MDPI 10.3390/genes11101175
Letko, Anna; Dijkman, Reinie; Strugnell, Ben; Häfliger, Irene M.; Paris, Julia M.; Henderson, Katrina; Geraghty, Tim; Orr, Hannah; Scholes, Sandra; Drögemüller, Cord (2020). Deleterious AGXT Missense Variant Associated with Type 1 Primary Hyperoxaluria (PH1) in Zwartbles Sheep. Genes, 11(10) MDPI 10.3390/genes11101147
Pontes Jacinto, Joana Goncalves; Häfliger, Irene Monika; Letko, Anna; Drögemüller, Cord; Agerholm, Jørgen Steen (2020). A large deletion in the COL2A1 gene expands the spectrum of pathogenic variants causing bulldog calf syndrome in cattle. Acta Veterinaria Scandinavica, 62(1), p. 49. BioMed Central Ltd. 10.1186/s13028-020-00548-w
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, Vidya; Drögemüller, Cord; Mansour, Tamer A; ... (2020). A Missense Variant in ALDH5A1 Associated with Canine Succinic Semialdehyde Dehydrogenase Deficiency (SSADHD) in the Saluki Dog. Genes, 11(9) MDPI 10.3390/genes11091033
Batcher, Kevin; Dickinson, Peter; Maciejczyk, Kimberly; Brzeski, Kristin; Hadji Rasouliha, Sheida; Letko, Anna; Drögemüller, Cord; Leeb, Tosso; Bannasch, Danika (2020). Multiple FGF4 Retrocopies Recently Derived within Canids. Genes, 11(8) MDPI 10.3390/genes11080839
Simon, Rebecca; Lischer, H. E. L.; Pieńkowska-Schelling, A.; Keller, I.; Häfliger, I. M.; Letko, A.; Schelling, C; Lühken, G; Drögemüller, C. (2020). New genomic features of the polled intersex syndrome variant in goats unraveled by long-read whole-genome sequencing. Animal genetics, 51(3), pp. 439-448. Wiley 10.1111/age.12918
Häfliger, I. M.; Letko, A.; Murgiano, L.; Drögemüller, C. (2020). De novo stop-lost germline mutation in FGFR3 causes severe chondrodysplasia in the progeny of a Holstein bull. Animal genetics, 51(3), pp. 466-469. Wiley 10.1111/age.12934
Hirter, Nathalie; Letko, Anna; Häfliger, Irene Monika; Becker, Doreen; Greber, Deborah; Drögemüller, Cord (2020). A genome-wide significant association on chromosome 15 for congenital entropion in Swiss White Alpine sheep. Animal genetics, 51(2), pp. 278-283. Wiley 10.1111/age.12903
Letko, Anna; Leuthard, Fabienne; Jagannathan, Vidya; Corlazzoli, Daniele; Matiasek, Kaspar; Schweizer, Daniela; Hytönen, Marjo K; Lohi, Hannes; Leeb, Tosso; Drögemüller, Cord (2020). Whole Genome Sequencing Indicates Heterogeneity of Hyperostotic Disorders in Dogs. Genes, 11(2) MDPI 10.3390/genes11020163
Leeb, Tosso; Leuthard, Fabienne; Jagannathan, Vidya; 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; ... (2020). A Missense Variant Affecting the C-Terminal Tail of UNC93B1 in Dogs with Exfoliative Cutaneous Lupus Erythematosus (ECLE). Genes, 11(2) MDPI 10.3390/genes11020159
Letko, A.; Ammann, B.; Jagannathan, V.; Henkel, J.; Leuthard, F.; Schelling, C.; Carneiro, M.; Drögemüller, C.; Leeb, T. (2020). A deletion spanning the promoter and first exon of the hair cycle-specific ASIP transcript isoform in black and tan rabbits. Animal genetics, 51(1), pp. 137-140. Wiley 10.1111/age.12881
Paris, Julia Maria; Letko, Anna; Häfliger, Irene Monika; Švara, Tanja; Gombač, Mitja; Klinc, Primož; Škibin, Andrej; Pogorevc, Estera; Drögemüller, Cord (2020). A de novo variant in OTX2 in a lamb with otocephaly. Acta Veterinaria Scandinavica, 62(1) BioMed Central Ltd. 10.1186/s13028-020-0503-z
Paris, Julia Maria; Letko, Anna; Häfliger, Irene Monika; Ammann, P; Flury, C; Drögemüller, Cord (2019). Identification of two TYRP1 loss-of-function alleles in Valais Red sheep. Animal genetics, 50(6), pp. 778-782. Wiley 10.1111/age.12863
