All Stories

  1. Whole Genome Sequencing Reveals Multiple Linked Genetic Variants on Canine Chromosome 12 Associated with Risk for Symmetrical Lupoid Onychodystrophy (SLO) in the Bearded Collie
  2. Dog colour patterns explained by modular promoters of ancient canid origin
  3. Reliability and Validity of Seven Feline Behavior and Personality Traits
  4. Missense variant in LOXHD1 is associated with canine nonsyndromic hearing loss
  5. Reliability and Validity of a Dog Personality and Unwanted Behavior Survey
  6. Gene Panel Screening Across Canine Eye Disorders Highlights Genetic Heterogeneity and the Need for Molecular Discoveries
  7. Missense Variant in LOXHD1 is Associated With Canine Nonsyndromic Hearing Loss
  8. Canine DVL2 variant contributes to brachycephalic phenotype and caudal vertebral anomalies
  9. Intronic variant in POU1F1 associated with canine pituitary dwarfism
  10. Feline tooth resorption findings from a questionnaire survey on 8115 Finnish cats and a case-control study for a more defined population drawn from the survey
  11. Low Pre- and Post-ACTH Stimulation Cortisol Is Associated With Widespread Metabolic Changes in Dogs
  12. Dog color patterns explained by modular promoters of ancient canid origin
  13. Formal commentary
  14. Metabolome of canine and human saliva: a non-targeted metabolomics study
  15. Active and social life is associated with lower non-social fearfulness in pet dogs
  16. Effect of prior general anesthesia or sedation and antiseizure drugs on the diagnostic utility of wireless video electroencephalography in dogs
  17. Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
  18. A Deletion in GDF7 is Associated with a Heritable Forebrain Commissural Malformation Concurrent with Ventriculomegaly and Interhemispheric Cysts in Cats
  19. Mutations in the Kinesin-2 Motor KIF3B Cause an Autosomal-Dominant Ciliopathy
  20. A novel genomic region on chromosome 11 associated with fearfulness in dogs
  21. Assessment of databases to determine the validity of β- and γ-carbonic anhydrase sequences from vertebrates
  22. Elevated blood creatinine -a biomarker of renal function-associates with multiple metabolic perturbations in dogs
  23. Genome wide association study of 40 clinical measurements in eight dog breeds
  24. H1-NMR-based metabolomics provides new insights into canine diabetes mellitus
  25. Recessive missense LAMP3 variant associated with defect in lamellar body biogenesis and fatal neonatal interstitial lung disease in dogs
  26. A putative silencer variant in a spontaneous canine model of retinitis pigmentosa
  27. Prevalence, comorbidity, and breed differences in canine anxiety in 13,700 Finnish pet dogs
  28. webGQT: A Shiny Server for Genotype Query Tools for Model-Based Variant Filtering
  29. Inadequate socialisation, inactivity, and urban living environment are associated with social fearfulness in pet dogs
  30. Whole Genome Sequencing Indicates Heterogeneity of Hyperostotic Disorders in Dogs
  31. A Missense Variant Affecting the C-Terminal Tail of UNC93B1 in Dogs with Exfoliative Cutaneous Lupus Erythematosus (ECLE)
  32. Ventricular arrhythmia and sudden cardiac death in young Leonbergers
  33. Characterisation of canine KCNIP4: A novel gene for cerebellar ataxia identified by whole-genome sequencing two affected Norwegian Buhund dogs
  34. Genetic dissection of canine hip dysplasia phenotypes and osteoarthritis reveals three novel loci
  35. TSEN54 missense variant in Standard Schnauzers with leukodystrophy
  36. A comprehensive biomedical variant catalogue based on whole genome sequences of 582 dogs and eight wolves
  37. NME5 frameshift variant in Alaskan Malamutes with primary ciliary dyskinesia
  38. Novel Locus Associated with Symmetrical Lupoid Onychodystrophy in the Bearded Collie
  39. Novel protective and risk loci in hip dysplasia in German Shepherds
  40. Thoracic high resolution CT using the modified VetMousetrap™ device is a feasible method for diagnosing canine idiopathic pulmonary fibrosis in awake West Highland White Terriers
  41. Breed differences of heritable behaviour traits in cats
  42. Whole Genome Sequencing of Giant Schnauzer Dogs with Progressive Retinal Atrophy Establishes NECAP1 as a Novel Candidate Gene for Retinal Degeneration
  43. Dog10K: an international sequencing effort to advance studies of canine domestication, phenotypes and health
  44. A frameshift insertion in SGK3 leads to recessive hairlessness in Scottish Deerhounds: a candidate gene for human alopecia conditions
  45. Canine models of human amelogenesis imperfecta: identification of novel recessive ENAM and ACP4 variants
  46. Author Correction: Applications and efficiencies of the first cat 63 K DNA array
  47. Breed‐specific reference ranges for standard echocardiographic measurements in salukis
  48. A homozygous missense variant in the alkaline phosphatase gene ALPL is associated with a severe form of canine hypophosphatasia
  49. Correction: Frequency and distribution of 152 genetic disease variants in over 100,000 mixed breed and purebred dogs
  50. Association between dog ownership and type 2 diabetes in later life: the Helsinki birth cohort study
  51. Two novel genomic regions associated with fearfulness in dogs overlap human neuropsychiatric loci
  52. First genome-wide CNV mapping in FELIS CATUS using next generation sequencing data
  53. Interbreed variation of biomarkers of lipid and glucose metabolism in dogs
  54. A novel KRT71 variant in curly-coated dogs
  55. Dog Ownership from a Life Course Perspective and Leisure-time Physical Activity in Late Adulthood: The Helsinki Birth Cohort Study
  56. Fearful dogs have increased plasma glutamine and γ-glutamyl glutamine
  57. Author Correction: Assembly and Analysis of Unmapped Genome Sequence Reads Reveal Novel Sequence and Variation in Dogs
  58. Interbreed variation in serum serotonin (5-hydroxytryptamine) concentration in healthy dogs
  59. Assembly and Analysis of Unmapped Genome Sequence Reads Reveal Novel Sequence and Variation in Dogs
  60. Myotonia congenita in a Labrador Retriever with truncated CLCN1
  61. Two MC1R loss-of-function alleles in cream-coloured Australian Cattle Dogs and white Huskies
  62. Author Correction: Applications and efficiencies of the first cat 63K DNA array
  63. Applications and efficiencies of the first cat 63K DNA array
  64. Maternal Inheritance of a Recessive RBP4 Defect in Canine Congenital Eye Disease
  65. Frequency and distribution of 152 genetic disease variants in over 100,000 mixed breed and purebred dogs
  66. Skin microbiota and allergic symptoms associate with exposure to environmental microbes
  67. MKLN1 splicing defect in dogs with lethal acrodermatitis
  68. The Endo-Lysosomal System of Brain Endothelial Cells Is Influenced by Astrocytes In Vitro
  69. Urban environment predisposes dogs and their owners to allergic symptoms
  70. Absence Seizures as a Feature of Juvenile Myoclonic Epilepsy in Rhodesian Ridgeback Dogs
  71. Toxoplasma gondii seroprevalence varies by cat breed
  72. Early weaning increases aggression and stereotypic behaviour in cats
  73. An intronic LINE-1 insertion in MERTK is strongly associated with retinopathy in Swedish Vallhund dogs
  74. Diagnostic Utility of Wireless Video-Electroencephalography in Unsedated Dogs
  75. Exome sequencing reveals independent SGCD deletions causing limb girdle muscular dystrophy in Boston terriers
  76. Paroxysmal Dyskinesia in Border Terriers: Clinical, Epidemiological, and Genetic Investigations
  77. A Coding Variant in the Gene Bardet-Biedl Syndrome 4 (BBS4) Is Associated with a Novel Form of Canine Progressive Retinal Atrophy
  78. Basal Autophagy Is Altered in Lagotto Romagnolo Dogs with an ATG4D Mutation
  79. Genetic rescue of an endangered domestic animal through outcrossing with closely related breeds: A case study of the Norwegian Lundehund
  80. Nonsense variant in COL7A1 causes recessive dystrophic epidermolysis bullosa in Central Asian Shepherd dogs
  81. Early-Onset Progressive Retinal Atrophy Associated with an IQCB1 Variant in African Black-Footed Cats (Felis nigripes)
  82. AncesTrim - a tool for trimming complex pedigrees
  83. Precision Medicine in Cats: Novel Niemann-Pick Type C1 Diagnosed by Whole-Genome Sequencing
  84. Association study reveals novel risk loci for sporadic inclusion body myositis
  85. Generalized myoclonic epilepsy with photosensitivity in juvenile dogs caused by a defective DIRAS family GTPase 1
  86. ANLN truncation causes a familial fatal acute respiratory distress syndrome in Dalmatian dogs
  87. ADAM23 is a common risk gene for canine idiopathic epilepsy
  88. Erratum to: A FAS-ligand variant associated with autoimmune lymphoproliferative syndrome in cats
  89. Deep sequencing of a candidate region harboring theSOX9gene for the canine XX disorder of sex development
  90. FEELnc: a tool for long non-coding RNA annotation and its application to the dog transcriptome
  91. Pressure vest on noise phobic dogs
  92. No evidence of prenatal diversifying selection at locus or supertype levels in the dog MHC class II loci
  93. Prevalence, comorbidity, and behavioral variation in canine anxiety
  94. A FAS-ligand variant associated with autoimmune lymphoproliferative syndrome in cats
  95. A non-targeted metabolite profiling pilot study suggests that tryptophan and lipid metabolisms are linked with ADHD-like behaviours in dogs
  96. Investigation of rare and low-frequency variants using high-throughput sequencing with pooled DNA samples
  97. Health and Behavioral Survey of over 8000 Finnish Cats
  98. Genetic Panel Screening of Nearly 100 Mutations Reveals New Insights into the Breed Distribution of Risk Variants for Canine Hereditary Disorders
  99. Globin mRNA reduction for whole-blood transcriptome sequencing
  100. Domesticated Animal Biobanking: Land of Opportunity
  101. The canine era: the rise of a biomedical model
  102. Molecular Characterization of Three Canine Models of Human Rare Bone Diseases: Caffey, van den Ende-Gupta, and Raine Syndromes
  103. Genome-wide association study in mice identifies loci affecting liver-related phenotypes includingSel1linfluencing serum bile acids
  104. A frameshift mutation in ARMC3 is associated with a tail stump sperm defect in Swedish Red (Bos taurus) cattle
  105. Non-targeted metabolite profiling reveals changes in oxidative stress, tryptophan and lipid metabolisms in fearful dogs
  106. Effect of Breed on Plasma Endothelin‐1 Concentration, Plasma Renin Activity, and Serum Cortisol Concentration in Healthy Dogs
  107. Canine models of human rare disorders
  108. Out of southern East Asia: the natural history of domestic dogs across the world
  109. Early Life Experiences and Exercise Associate with Canine Anxieties
  110. Canine MPV17 truncation without clinical manifestations
  111. Identification of a common risk haplotype for canine idiopathic epilepsy in the ADAM23 gene
  112. Multiple Changes of Gene Expression and Function Reveal Genomic and Phenotypic Complexity in SLE-like Disease
  113. The Shepherds’ Tale: A Genome-Wide Study across 9 Dog Breeds Implicates Two Loci in the Regulation of Fructosamine Serum Concentration in Belgian Shepherds
  114. Behavioral Abnormalities in Lagotto Romagnolo Dogs with a History of Benign Familial Juvenile Epilepsy: A Long-Term Follow-Up Study
  115. A Missense Change in the ATG4D Gene Links Aberrant Autophagy to a Neurodegenerative Vacuolar Storage Disease
  116. Correction: A Novel Missense Mutation in ADAMTS10 in Norwegian Elkhound Primary Glaucoma
  117. Increased Expression of MERTK is Associated with a Unique Form of Canine Retinopathy
  118. A Novel Missense Mutation in ADAMTS10 in Norwegian Elkhound Primary Glaucoma
  119. A Novel Form of Progressive Retinal Atrophy in Swedish Vallhund Dogs
  120. Germline Mutation of RPS20, Encoding a Ribosomal Protein, Causes Predisposition to Hereditary Nonpolyposis Colorectal Carcinoma Without DNA Mismatch Repair Deficiency
  121. Reliability and validity of a questionnaire survey in canine anxiety research
  122. Genetics of canine anal furunculosis in the German shepherd dog
  123. Breed Differences in Natriuretic Peptides in Healthy Dogs
  124. Balancing selection and heterozygote advantage in major histocompatibility complex loci of the bottlenecked Finnish wolf population
  125. Exploration of known stereotypic behaviour-related candidate genes in equine crib-biting
  126. In frame exon skipping in UBE3B is associated with developmental disorders and increased mortality in cattle
  127. A Mutation in the SUV39H2 Gene in Labrador Retrievers with Hereditary Nasal Parakeratosis (HNPK) Provides Insights into the Epigenetics of Keratinocyte Differentiation
  128. Phenotype, inheritance characteristics, and risk factors for idiopathic epilepsy in Finnish Spitz dogs
  129. Ectopic KIT Copy Number Variation Underlies Impaired Migration of Primordial Germ Cells Associated with Gonadal Hypoplasia in Cattle (Bos taurus)
  130. Canine Chondrodysplasia Caused by a Truncating Mutation in Collagen-Binding Integrin Alpha Subunit 10
  131. A CNGB1 Frameshift Mutation in Papillon and Phalène Dogs with Progressive Retinal Atrophy
  132. Genome-Wide Association Study Identifies a Novel Canine Glaucoma Locus
  133. Fetal growth restriction caused by MIMT1 deletion alters brain transcriptome in cattle
  134. Expression ofFoxi3is regulated by ectodysplasin in skin appendage placodes
  135. A COL11A2 Mutation in Labrador Retrievers with Mild Disproportionate Dwarfism
  136. A Nonsense Mutation in the Acid α-Glucosidase Gene Causes Pompe Disease in Finnish and Swedish Lapphunds
  137. A Gly98Val Mutation in the N-Myc Downstream Regulated Gene 1 (NDRG1) in Alaskan Malamutes with Polyneuropathy
  138. Genetic Diversity in the Modern Horse Illustrated from Genome-Wide SNP Data
  139. Genome-Wide Analysis Reveals Selection for Important Traits in Domestic Horse Breeds
  140. Extent of Linkage Disequilibrium in the Domestic Cat, Felis silvestris catus, and Its Breeds
  141. Truncation of MIMT1 Gene in the PEG3 Domain Leads to Major Changes in Placental Gene Expression and Stillbirth in Cattle1
  142. MHC variability supports dog domestication from a large number of wolves: high diversity in Asia
  143. Feline toxoplasmosis in Finland
  144. Variation in Genes Related to Cochlear Biology Is Strongly Associated with Adult-Onset Deafness in Border Collies
  145. Early-onset Lafora body disease
  146. Environmental Effects on Compulsive Tail Chasing in Dogs
  147. A Novel GUSB Mutation in Brazilian Terriers with Severe Skeletal Abnormalities Defines the Disease as Mucopolysaccharidosis VII
  148. A SEL1L Mutation Links a Canine Progressive Early-Onset Cerebellar Ataxia to the Endoplasmic Reticulum–Associated Protein Degradation (ERAD) Machinery
  149. Phosphorylation prevents polyglucosan transport in Lafora disease
  150. Identification of a Novel Idiopathic Epilepsy Locus in Belgian Shepherd Dogs
  151. Novel origins of copy number variation in the dog genome
  152. Genetics of neurological disease in the dog.
  153. Disease Progression and Treatment Response of Idiopathic Epilepsy in Australian Shepherd Dogs
  154. Evaluation of DLA promoters in Doberman hepatitis
  155. Identification of Genomic Regions Associated with Phenotypic Variation between Dog Breeds using Selection Mapping
  156. Genome-Wide Association Study in Dachshund: Identification of a Major Locus Affecting Intervertebral Disc Calcification
  157. ADAMTS17 mutation associated with primary lens luxation is widespread among breeds
  158. LUPA: A European initiative taking advantage of the canine genome architecture for unravelling complex disorders in both human and dogs
  159. LGI2 Truncation Causes a Remitting Focal Epilepsy in Dogs
  160. Characteristics of epileptic episodes in UK dog breeds: an epidemiological approach
  161. A truncating mutation in ATP13A2 is responsible for adult-onset neuronal ceroid lipofuscinosis in Tibetan terriers
  162. MHC class II risk haplotype associated with Canine chronic superficial keratitis in German Shepherd dogs
  163. Regional occurrence, high frequency but low diversity of mitochondrial DNA haplogroup d1 suggests a recent dog-wolf hybridization in Scandinavia
  164. A Novel Mutation in the Maternally Imprinted PEG3 Domain Results in a Loss of MIMT1 Expression and Causes Abortions and Stillbirths in Cattle (Bos taurus)
  165. Assessment of the functionality of genome-wide canine SNP arrays and implications for canine disease association studies
  166. Segregation of point mutation heteroplasmy in the control region of dog mtDNA studied systematically in deep generation pedigrees
  167. Association of Doberman hepatitis to canine major histocompatibility complex II
  168. AnADAMTS17Splice Donor Site Mutation in Dogs with Primary Lens Luxation
  169. Exonic mutations in the L2HGDH gene in Staffordshire bull terriers
  170. Individuals with mutations in XPNPEP3, which encodes a mitochondrial protein, develop a nephronophthisis-like nephropathy
  171. Genome-wide association mapping identifies multiple loci for a canine SLE-related disease complex
  172. Association of a dog leukocyte antigen class II haplotype with hypoadrenocorticism in Nova Scotia Duck Tolling Retrievers
  173. Mutation inHSF4is associated with hereditary cataract in the Australian Shepherd
  174. Unlocking the genetic make-up of canine hip dysplasia: We can work it out
  175. MHC class II polymorphism is associated with a canine SLE-related disease complex
  176. Ancestral T-Box Mutation Is Present in Many, but Not All, Short-Tailed Dog Breeds
  177. A Mutation in Hairless Dogs Implicates FOXI3 in Ectodermal Development
  178. Risk of anal furunculosis in German Shepherd dogs is associated with the major histocompatibility complex
  179. The Novel Neuronal Ceroid Lipofuscinosis Gene MFSD8 Encodes a Putative Lysosomal Transporter
  180. Genetic diagnosis in Lafora disease: Genotype-phenotype correlations and diagnostic pitfalls
  181. Benign Familial Juvenile Epilepsy in Lagotto Romagnolo Dogs
  182. Genetic diagnosis in Lafora disease: Genotype-phenotype correlations and diagnostic pitfalls
  183. Conditional nuclear localization of hMLH3 suggests a minor activity in mismatch repair and supports its role as a low-risk gene in HNPCC
  184. Glycogen metabolism in tissues from a mouse model of Lafora disease
  185. CORRECTION
  186. Comprehensive diagnosis of Rett's syndrome relying on genetic, epigenetic and expression evidence of deficiency of the methyl-CpG-binding protein 2 gene: study of a cohort of Israeli patients
  187. Clinical and Genetic Findings in 26 Italian Patients with Lafora Disease
  188. Novel glycogen synthase kinase 3 and ubiquitination pathways in progressive myoclonus epilepsy
  189. Functional Significance and Clinical Phenotype of Nontruncating Mismatch Repair Variants of MLH1
  190. Functional Significance and Clinical Phenotype of Nontruncating Mismatch Repair Variants of
  191. Sacred disease secrets revealed: the genetics of human epilepsy
  192. SLC26A6 and SLC26A7 Anion Exchangers Have a Distinct Distribution in Human Kidney
  193. Functional Comparison of Mouse slc26a6 Anion Exchanger with Human SLC26A6 Polypeptide Variants
  194. Expanded Repeat in Canine Epilepsy
  195. Lafora progressive myoclonus epilepsy mutation database-EPM2A and NHLRC1 (EMP2B) genes
  196. Restoring mismatch repair does not stop the formation of reciprocal translocations in the colon cancer cell line HCA7 but further destabilizes chromosome number
  197. Novel splicing associations of hereditary colon cancer related DNA mismatch repair gene mutations
  198. Laforin preferentially binds the neurotoxic starch-like polyglucosans, which form in its absence in progressive myoclonus epilepsy
  199. A previously unidentified MECP2 open reading frame defines a new protein isoform relevant to Rett syndrome
  200. Altered Expression of MLH1, MSH2, and MSH6 in Predisposition to Hereditary Nonpolyposis Colorectal Cancer
  201. Identification of a basolateral Cl−/HCO 3 − exchanger specific to gastric parietal cells
  202. Isoforms of SLC26A6 mediate anion transport and have functional PDZ interaction domains
  203. Matrix metalloproteinase-21, the human orthologue for XMMP, is expressed during fetal development and in cancer
  204. Upregulation of CFTR expression but not SLC26A3 and SLC9A3 in ulcerative colitis
  205. Functional Characterization of Three Novel Tissue-specific Anion Exchangers SLC26A7, -A8, and -A9
  206. Mapping of Five New Putative Anion Transporter Genes in Human and Characterization of SLC26A6, A Candidate Gene for Pancreatic Anion Exchanger
  207. The congenital chloride diarrhea gene is expressed in seminal vesicle, sweat gland, inflammatory colon epithelium, and in some dysplastic colon cells