Identification of a Novel Idiopathic Epilepsy Locus in Belgian Shepherd Dogs

Candidate genes for idiopathic epilepsy in four dog breeds

(2011) Kari J Ekenstedt et al.   BMC GENETICS

A truncating mutation in ATP13A2 is responsible for adult-onset neuronal ceroid lipofuscinosis in Tibetan terriers

(2011) Fabiana H.G. Farias et al.   NEUROBIOLOGY OF DISEASE

LGI2 Truncation Causes a Remitting Focal Epilepsy in Dogs

(2011) Eija H. Seppälä et al.   PLoS Genetics

Genome-wide linkage scan for loci associated with epilepsy in Belgian shepherd dogs

(2010) Anita M Oberbauer et al.   BMC GENETICS

Familial partial epilepsy with variable foci: A new family with suggestion of linkage to chromosome 22q12

(2010) José Morales-Corraliza et al.   EPILEPSIA

Revised terminology and concepts for organization of seizures and epilepsies: Report of the ILAE Commission on Classification and Terminology, 2005-2009

(2010) Anne T. Berg et al.   EPILEPSIA

Krüppel-like factor 7 is required for olfactory bulb dopaminergic neuron development

(2010) Massimiliano Caiazzo et al.   EXPERIMENTAL CELL RESEARCH

Epilepsy in Border Collies: Clinical Manifestation, Outcome, and Mode of Inheritance

(2010) V. Hülsmeyer et al.   JOURNAL OF VETERINARY INTERNAL MEDICINE

A mutation in canine PPT1 causes early onset neuronal ceroid lipofuscinosis in a Dachshund

(2010) Douglas N. Sanders et al.   MOLECULAR GENETICS AND METABOLISM

Novel mutations in the NDUFS1 gene cause low residual activities in human complex I deficiencies

(2010) Saskia J.G. Hoefs et al.   MOLECULAR GENETICS AND METABOLISM

Genome-wide association mapping identifies multiple loci for a canine SLE-related disease complex

(2010) Maria Wilbe et al.   NATURE GENETICS

A method and server for predicting damaging missense mutations

(2010) Ivan A Adzhubei et al.   NATURE METHODS

A canine Arylsulfatase G (ARSG) mutation leading to a sulfatase deficiency is associated with neuronal ceroid lipofuscinosis

(2010) M. Abitbol et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Disruption of LGI1–linked synaptic complex causes abnormal synaptic transmission and epilepsy

(2010) Yuko Fukata et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Focal epilepsy in the Belgian shepherd: evidence for simple Mendelian inheritance

(2009) M. Berendt et al.   JOURNAL OF SMALL ANIMAL PRACTICE

LGI1-associated epilepsy through altered ADAM23-dependent neuronal morphology

(2009) Katherine Owuor et al.   MOLECULAR AND CELLULAR NEUROSCIENCE

FASTKD2 Nonsense Mutation in an Infantile Mitochondrial Encephalomyopathy Associated with Cytochrome C Oxidase Deficiency

(2008) Daniele Ghezzi et al.   AMERICAN JOURNAL OF HUMAN GENETICS

A Mutation in Hairless Dogs Implicates FOXI3 in Ectodermal Development

(2008) Cord Drögemüller et al.   SCIENCE

Evaluating candidate genes in common epilepsies and the nature of evidence

(2007) Deb K. Pal et al.   EPILEPSIA