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authFullName_s : Anne Thomas
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MKLN1 splicing defect in dogs with lethal acrodermatitis

Anina Bauer , Vidhya Jagannathan , Sandra Högler , Barbara Richter , Neil A Mcewan et al.
PLoS Genetics, 2018, 14 (3), pp.e1007264. ⟨10.1371/journal.pgen.1007264⟩
Journal articles hal-01744192v1
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Comparison of buccal and blood-derived canine DNA, either native or whole genome amplified, for array-based genome-wide association studies.

Gonzalo Rincon , Katarina Tengvall , Janelle M. Belanger , Laetitia Lagoutte , Juan F. Medrano et al.
BMC Research Notes, 2011, 4 (1), pp.226. ⟨10.1186/1756-0500-4-226⟩
Journal articles inserm-00606991v1

Progressive retinal atrophy in the Border Collie: a new XLPRA.

Thierry Vilboux , Gilles Chaudieu , Patricia Jeannin , Delphine Delattre , Benoît Hédan et al.
BMC Veterinary Research, 2008, 4, pp.10. ⟨10.1186/1746-6148-4-10⟩
Journal articles hal-00277538v1

PNPLA1 mutations cause autosomal recessive congenital ichthyosis in golden retriever dogs and humans.

Anaïs Grall , Eric Guaguère , Sandrine Planchais , Susanne Grond , Emmanuelle Bourrat et al.
Nature Genetics, 2012, 44 (2), pp.140-7. ⟨10.1038/ng.1056⟩
Journal articles inserm-00662852v1

A Spontaneous KRT16 Mutation in a Dog Breed: A Model for Human Focal Non-Epidermolytic Palmoplantar Keratoderma (FNEPPK).

Jocelyn Plassais , Eric Guaguère , Laetitia Lagoutte , Anne-Sophie Guillory , Caroline Dufaure de Citres et al.
Journal of Investigative Dermatology, 2015, 135 (4), pp.1187-90. ⟨10.1038/jid.2014.526⟩
Journal articles hal-01116377v1

Ancestral T-box mutation is present in many, but not all, short-tailed dog breeds.

Marjo K Hytönen , Anaïs Grall , Benoît Hédan , Stéphane Dréano , Samuel J Seguin et al.
The Journal of Heredity, 2009, 100 (2), pp.236-40. ⟨10.1093/jhered/esn085⟩
Journal articles inserm-00353074v1

Modèles spontanés de maladies humaines chez le chien : exemple des ichtyoses [Spontaneous models of human diseases in dogs: ichthyoses as an example]

Catherine Andre , Anaïs Grall , Eric Guaguère , Anne Thomas , Francis Galibert et al.
Bulletin de l'Académie Nationale de Médecine, 2013, 197 (6), pp.1225--1230
Journal articles hal-01157580v1
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A COLQ Missense Mutation in Sphynx and Devon Rex Cats with Congenital Myasthenic Syndrome

Marie Abitbol , Christophe Hitte , Philippe Bossé , Nicolas Blanchard-Gutton , Anne Thomas et al.
PLoS ONE, 2015, 10 (9), pp.e0137019. ⟨10.1371/journal.pone.0137019⟩
Journal articles hal-01196603v1
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A mutation in the FAM83G gene in dogs with hereditary footpad hyperkeratosis (HFH).

Michaela Drögemüller , Vidhya Jagannathan , Doreen Becker , Cord Drögemüller , Claude Schelling et al.
PLoS Genetics, 2014, 10 (5), pp.e1004370. ⟨10.1371/journal.pgen.1004370⟩
Journal articles hal-01024799v1