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Häfliger, Irene M.; Marchionatti, Emma; Stengard, Michele; Wolf-Hofstetter, Sonja; Paris, Julia M.; Jacinto, Joana G P; Watté, Christine; Voelter, Katrin; Occelli, Laurence M.; Komáromy, András M.; Oevermann, Anna; Goepfert, Christine; Borgo, Angelica; Roduit, Raphaël; Spengeler, Mirjam; Seefried, Franz R.; Drögemüller, Cord (2021). CNGB3 Missense Variant Causes Recessive Achromatopsia in Original Braunvieh Cattle. International journal of molecular sciences, 22(22), p. 12440. MDPI 10.3390/ijms222212440
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
Jacinto, Joana G P; Markey, Alysta D.; Veiga, Inês M. B.; Paris, Julia M.; Welle, Monika; Beever, Jonathan E.; Drögemüller, Cord (2021). A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle. Genes, 12(7), p. 1038. MDPI 10.3390/genes12071038
Kuca, Thibaud; Marron, Brandy M; Jacinto, Joana G P; Paris, Julia M.; Gerspach, Christian; Beever, Jonathan E; Drögemüller, Cord (2021). A Nonsense Variant in Hephaestin Like 1 (HEPHL1) Is Responsible for Congenital Hypotrichosis in Belted Galloway Cattle. Genes, 12(5) MDPI 10.3390/genes12050643
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; 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
