Bauer, Anina

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2019

Bauer, Anina; de Lucia, M; Leuthard, Fabienne Nadja; Jagannathan, Vidya; Leeb, Tosso (2019). Compound heterozygosity for TNXB genetic variants in a mixed-breed dog with Ehlers-Danlos syndrome. Animal genetics, 50(5), pp. 546-549. Wiley 10.1111/age.12830

Woolley, S A; Eager, K L M; Häfliger, Irene Monika; Bauer, Anina; Drögemüller, Cord; Leeb, Tosso; O'Rourke, B A; Tammen, I (2019). An ABCA12 missense variant in a Shorthorn calf with ichthyosis fetalis. (In Press). Animal genetics Wiley 10.1111/age.12856

Bauer, Anina; Bateman, John F; Lamandé, Shireen R; Hanssen, Eric; Kirejczyk, Shannon G M; Yee, Mark; Ramiche, Ali; Jagannathan, Vidya; Welle, Monika; Leeb, Tosso; Bateman, Fiona L (2019). Identification of Two Independent COL5A1 Variants in Dogs with Ehlers-Danlos Syndrome. Genes, 10(10) MDPI, Molecular Diversity Preservation International 10.3390/genes10100731

De Lucia, Michela; Angileri, Martina; Bauer, Anina; Spycher, Melina; Jagannathan, Vidya; Denti, Daria; Di Diodoro, Francesca; Ferro, Silvia; Mezzalira, Giorgia; Welle, Monika; Leeb, Tosso (2019). X-linked cutaneous mosaicism in a dog. Veterinary dermatology, 30(4), pp. 361-362. Wiley 10.1111/vde.12748

Hitti, Rebekkah J; Oliver, James A C; Schofield, Ellen C; Bauer, Anina; Kaukonen, Maria; Forman, Oliver P; Leeb, Tosso; Lohi, Hannes; Burmeister, Louise M; Sargan, David; Mellersh, Cathryn S (2019). Whole Genome Sequencing of Giant Schnauzer Dogs with Progressive Retinal Atrophy Establishes NECAP1 as a Novel Candidate Gene for Retinal Degeneration. Genes, 10(5) MDPI, Molecular Diversity Preservation International 10.3390/genes10050385

Brunner, Magdalena; Rüfenacht, Silvia; Bauer, Anina; Erpel, Susanne; Buchs, Natasha; Braga, Sophie Marie-Pierre; Heller, Manfred; Leeb, Tosso; Jagannathan, Vidya; Wiener, Dominique Judith; Welle, Monika Maria (2019). Bald thigh syndrome in sighthounds - Revisiting the cause of a well-known disease. PLoS ONE, 14(2), e0212645. Public Library of Science 10.1371/journal.pone.0212645

Bauer, Anina; Hadji Rasouliha, Sheida; Brunner, Magdalena; Jagannathan, Vidya; Bucher, I; Bannöhr, Jeanette; Varjonen, K; Bond, R; Bergvall, K; Welle, Monika Maria; Roosje, Petra; Leeb, Tosso (2019). A second KRT71 allele in curly coated dogs. Animal genetics, 50(1), pp. 97-100. Blackwell 10.1111/age.12743

De Lucia, Michela; Bauer, Anina; Spycher, Melina; Jagannathan, Vidya; Romano, Erica; Welle, Monika Maria; Leeb, Tosso (2019). Genetic variant in the NSDHL gene in a cat with multiple congenital lesions resembling inflammatory linear verrucous epidermal nevi. Veterinary dermatology, 30(1), 64-e18. Blackwell Science 10.1111/vde.12699

2018

Spycher, M; Bauer, Anina; Jagannathan, Vidhya; Frizzi, M; De Lucia, M; Leeb, Tosso (2018). A frameshift variant in the COL5A1 gene in a cat with Ehlers-Danlos syndrome. Animal genetics, 49(6), pp. 641-644. Wiley 10.1111/age.12727

Hadji Rasouliha, S; Bauer, Anina; Dettwiler, Martina Andrea; Welle, Monika Maria; Leeb, Tosso (2018). A frameshift variant in the EDA gene in Dachshunds with X-linked hypohidrotic ectodermal dysplasia. Animal genetics, 49(6), pp. 651-654. Wiley 10.1111/age.12729

Bauer, Anina; Nimmo, J; Newman, R; Brunner, Magdalena Anna Theresa; Welle, Monika Maria; Jagannathan, Vidhya; Leeb, Tosso (2018). A splice site variant in the SUV39H2 gene in Greyhounds with nasal parakeratosis. Animal genetics, 49(2), pp. 137-140. Blackwell 10.1111/age.12643

Bauer, Anina; Jagannathan, Vidhya; Högler, Sandra; Richter, Barbara; McEwan, Neil A; Thomas, Anne; Cadieu, Edouard; André, Catherine; Hytönen, Marjo K; Lohi, Hannes; Welle, Monika Maria; Roosje, Petra; Mellersh, Cathryn; Casal, Margret L; Leeb, Tosso (2018). MKLN1 splicing defect in dogs with lethal acrodermatitis. PLoS genetics, 14(3), e1007264. Public Library of Science 10.1371/journal.pgen.1007264

Bauer, Anina; Kehl, A; Jagannathan, Vidhya; Leeb, Tosso (2018). A novel MLPH variant in dogs with coat colour dilution. Animal genetics, 49(1), pp. 94-97. Blackwell 10.1111/age.12632

2017

Caduff, M; Bauer, Anina; Jagannathan, Vidhya; Leeb, Tosso (2017). A single base deletion in the SLC45A2 gene in a Bullmastiff with oculocutaneous albinism. Animal genetics, 48(5), pp. 619-621. Blackwell 10.1111/age.12582

Bauer, Anina; De Lucia, Michela; Jagannathan, Vidhya; Mezzalira, Giorgia; Casal, Margaret L; Welle, Monika Maria; Leeb, Tosso (2017). A Large Deletion in the NSDHL Gene in Labrador Retrievers with a Congenital Cornification Disorder. G3 Genes Genomes Genetics, 7(9), pp. 3115-3121. Genetics Society of America 10.1534/g3.117.1124

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