A non-coding genomic duplication at the HMX1 locus is associated with crop ears in highland cattle.

por Caroline Tina Koch, Rémy Bruggmann, Jens Tetens, Cord Drögemüller
Publicado 2013

A COL7A1 mutation causes dystrophic epidermolysis bullosa in Rotes Höhenvieh cattle.

por Annie Menoud, Monika Welle, Jens Tetens, Peter Lichtner, Cord Drögemüller
Publicado 2012

Looking the cow in the eye: deletion in the NID1 gene is associated with recessive inherited cataract in Romagnola cattle.

por Leonardo Murgiano, Vidhya Jagannathan, Valerio Calderoni, Monika Joechler, Arcangelo Gentile, Cord Drögemüller
Publicado 2014

A frameshift mutation in the cubilin gene (CUBN) in Border Collies with Imerslund-Gräsbeck syndrome (selective cobalamin malabsorption).

por Marta Owczarek-Lipska, Vidhya Jagannathan, Cord Drögemüller, Sabina Lutz, Barbara Glanemann, Tosso Leeb, Peter H Kook
Publicado 2013

Independent polled mutations leading to complex gene expression differences in cattle.

por Natalie Wiedemar, Jens Tetens, Vidhya Jagannathan, Annie Menoud, Samuel Neuenschwander, Rémy Bruggmann, Georg Thaller, Cord Drögemüller
Publicado 2014

KDM2B is implicated in bovine lethal multi-organic developmental dysplasia.

por Stefania Testoni, Elena Bartolone, Marco Rossi, Andrea Patrignani, Rémy Bruggmann, Peter Lichtner, Jens Tetens, Arcangelo Gentile, Cord Drögemüller
Publicado 2012

<i>KCNG1</i>-Related Syndromic Form of Congenital Neuromuscular Channelopathy in a Crossbred Calf

por Joana G. P. Jacinto, Irene M. Häfliger, Eylem Emek Akyürek, Roberta Sacchetto, Cinzia Benazzi, Arcangelo Gentile, Cord Drögemüller
Publicado 2021

Microphthalmia in Texel sheep is associated with a missense mutation in the paired-like homeodomain 3 (PITX3) gene.

por Doreen Becker, Jens Tetens, Adrian Brunner, Daniela Bürstel, Martin Ganter, James Kijas, International Sheep Genomics Consortium, Cord Drögemüller
Publicado 2010

Deletion in the EVC2 gene causes chondrodysplastic dwarfism in Tyrolean Grey cattle.

por Leonardo Murgiano, Vidhya Jagannathan, Cinzia Benazzi, Marilena Bolcato, Barbara Brunetti, Luisa Vera Muscatello, Keren Dittmer, Christian Piffer, Arcangelo Gentile, Cord Drögemüller
Publicado 2014

A locus on chromosome 5 is associated with dilated cardiomyopathy in Doberman Pinschers.

por Theresa-Bernadette Mausberg, Gerhard Wess, Julia Simak, Lisa Keller, Michaela Drögemüller, Cord Drögemüller, Matthew T Webster, Hannah Stephenson, Joanna Dukes-McEwan, Tosso Leeb
Publicado 2011

A nonsense mutation in the IKBKG gene in mares with incontinentia pigmenti.

por Rachel E Towers, Leonardo Murgiano, David S Millar, Elise Glen, Ana Topf, Vidhya Jagannathan, Cord Drögemüller, Judith A Goodship, Angus J Clarke, Tosso Leeb
Publicado 2013

A deletion in the N-myc downstream regulated gene 1 (NDRG1) gene in Greyhounds with polyneuropathy.

por Cord Drögemüller, Doreen Becker, Barbara Kessler, Elisabeth Kemter, Jens Tetens, Konrad Jurina, Karin Hultin Jäderlund, Annette Flagstad, Michele Perloski, Kerstin Lindblad-Toh, Kaspar Matiasek
Publicado 2010

A COL11A2 mutation in Labrador retrievers with mild disproportionate dwarfism.

por Mirjam Frischknecht, Helena Niehof-Oellers, Vidhya Jagannathan, Marta Owczarek-Lipska, Cord Drögemüller, Elisabeth Dietschi, Gaudenz Dolf, Bernd Tellhelm, Johann Lang, Katriina Tiira, Hannes Lohi, Tosso Leeb
Publicado 2013

An unusual splice defect in the mitofusin 2 gene (MFN2) is associated with degenerative axonopathy in Tyrolean Grey cattle.

por Cord Drögemüller, Ursula Reichart, Torsten Seuberlich, Anna Oevermann, Martin Baumgartner, Kathrin Kühni Boghenbor, Michael H Stoffel, Claudia Syring, Mireille Meylan, Simone Müller, Mathias Müller, Birgit Gredler, Johann Sölkner, Tosso Leeb
Publicado 2011

<i>CNGB3</i> Missense Variant Causes Recessive Achromatopsia in Original Braunvieh Cattle

por Irene M. Häfliger, Emma Marchionatti, Michele Stengård, Sonja Wolf-Hofstetter, Julia M. Paris, Joana G. P. Jacinto, Christine Watté, Katrin Voelter, Laurence M. Occelli, András M. Komáromy, Anna Oevermann, Christine Goepfert, Angelica Borgo, Raphaël Roduit, Mirjam Spengeler, Franz R. Seefried, Cord Drögemüller
Publicado 2021

A Gly98Val mutation in the N-Myc downstream regulated gene 1 (NDRG1) in Alaskan Malamutes with polyneuropathy.

por Camilla S Bruun, Karin H Jäderlund, Mette Berendt, Kristine B Jensen, Eva H Spodsberg, Hanne Gredal, G Diane Shelton, James R Mickelson, Katie M Minor, Hannes Lohi, Inge Bjerkås, Oyvind Stigen, Arild Espenes, Cecilia Rohdin, Rebecca Edlund, Jennie Ohlsson, Sigitas Cizinauskas, Páll S Leifsson, Cord Drögemüller, Lars Moe, Susanna Cirera, Merete Fredholm
Publicado 2013