1. A CHRNB1 frameshift mutation is associated with familial arthrogryposis multiplex congenita in Red dairy cattle. (December 2016) Authors: Agerholm, Jørgen; McEvoy, Fintan; Menzi, Fiona; Jagannathan, Vidhya; Drögemüller, Cord Journal: BMC genomics Issue: Volume 17:Number 1(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A COL2A1 de novo variant in a Holstein bulldog calf. (31st October 2018) Authors: Häfliger, Irene Monika; Behn, Holger; Freick, Markus; Jagannathan, Vidhya; Drögemüller, Cord Journal: Animal genetics Issue: Volume 50:Number 1(2019) Page Start: 113 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. A de novo germline mutation of DLX3 in a Brown Swiss calf with tricho‐dento‐osseus‐like syndrome. Issue 6 (2nd July 2017) Authors: Hofstetter, Sonja; Welle, Monika; Gorgas, Daniela; Balmer, Pierre; Roosje, Petra; Mock, Thomas; Meylan, Mireille; Jagannathan, Vidhya; Drögemüller, Cord Journal: Veterinary dermatology Issue: Volume 28:Issue 6(2017:Dec.) Page Start: 616 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. A de novo in‐frame duplication in the COL1A2 gene in a Lagotto Romagnolo dog with osteogenesis imperfecta. (29th August 2019) Authors: Letko, Anna; Zdora, Isabel; Hitzler, Valerie; Jagannathan, Vidhya; Beineke, Andreas; Möhrke, Carola; Drögemüller, Cord Journal: Animal genetics Issue: Volume 50:Number 6(2019) Page Start: 786 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. A frameshift mutation in MOCOS is associated with familial renal syndrome (xanthinuria) in Tyrolean Grey cattle. Issue 1 (December 2016) Authors: Murgiano, Leonardo; Jagannathan, Vidhya; Piffer, Christian; Diez-Prieto, Inmaculada; Bolcato, Marilena; Gentile, Arcangelo; Drögemüller, Cord Journal: BMC veterinary research Issue: Volume 12:Issue 1(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. A frameshift mutation in the cubilin gene (CUBN) in Beagles with Imerslund–Gräsbeck syndrome (selective cobalamin malabsorption). (27th October 2013) Authors: Drögemüller, Michaela; Jagannathan, Vidhya; Howard, Judith; Bruggmann, Rémy; Drögemüller, Cord; Ruetten, Maja; Leeb, Tosso; Kook, Peter H. Journal: Animal genetics Issue: Volume 45:Number 1(2014:Feb.) Page Start: 148 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. A Large Deletion in the NSDHL Gene in Labrador Retrievers with a Congenital Cornification Disorder. Issue 9 (1st September 2017) Authors: Bauer, Anina; De Lucia, Michela; Jagannathan, Vidhya; Mezzalira, Giorgia; Casal, Margret L; Welle, Monika M; Leeb, Tosso Journal: G3 Issue: Volume 7:Issue 9(2017) Page Start: 3115 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. A major facilitator superfamily domain 8 frameshift variant in a cat with suspected neuronal ceroid lipofuscinosis. (20th December 2019) Authors: Guevar, Julien; Hug, Petra; Giebels, Felix; Durand, Alexane; Jagannathan, Vidhya; Leeb, Tosso Journal: Journal of veterinary internal medicine Issue: Volume 34:Number 1(2020) Page Start: 289 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. A Missense Variant in KCNJ10 in Belgian Shepherd Dogs Affected by Spongy Degeneration with Cerebellar Ataxia (SDCA1). Issue 2 (1st February 2017) Authors: Mauri, Nico; Kleiter, Miriam; Leschnik, Michael; Högler, Sandra; Dietschi, Elisabeth; Wiedmer, Michaela; Dietrich, Joëlle; Henke, Diana; Steffen, Frank; Schuller, Simone; Gurtner, Corinne; Stokar-Regenscheit, Nadine; O'Toole, Donal; Bilzer, Thomas; Herden, Christiane; Oevermann, Anna; Jagannathan... Journal: G3 Issue: Volume 7:Issue 2(2017) Page Start: 663 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. A Nonsense Variant in COL6A1 in Landseer Dogs with Muscular Dystrophy. Issue 12 (1st December 2015) Authors: Steffen, Frank; Bilzer, Thomas; Brands, Jan; Golini, Lorenzo; Jagannathan, Vidhya; Wiedmer, Michaela; Drögemüller, Michaela; Drögemüller, Cord; Leeb, Tosso Journal: G3 Issue: Volume 5:Issue 12(2015) Page Start: 2611 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗