Bottlenecks and selective sweeps during domestication have increased deleterious genetic variation in dogs von Marsden, Clare D., Vecchyo, Diego Ortega-Del, O’Brien, Dennis P., Taylor, Jeremy F., Ramirez, Oscar, Vilà, Carles, Marques-Bonet, Tomas, Schnabel, Robert D., Wayne, Robert K., Lohmueller, Kirk E.

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International veterinary canine dyskinesia task force ECVN consensus statement: Terminology and classification von Cerda‐Gonzalez, Sofia, Packer, Rebecca A., Garosi, Laurent, Lowrie, Mark, Mandigers, Paul J. J., O'Brien, Dennis P., Volk, Holger A.

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Neuronal Ceroid Lipofuscinosis in a Domestic Cat Associated with a DNA Sequence Variant That Creates a Premature Stop Codon in CLN6 von Katz, Martin L, Buckley, Reuben M, Biegen, Vanessa, O'Brien, Dennis P, Johnson, Gayle C, Warren, Wesley C, Lyons, Leslie A

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A mixed breed dog with neuronal ceroid lipofuscinosis is homozygous for a CLN5 nonsense mutation previously identified in Border Collies and Australian Cattle Dogs von Villani, Natalie A., Bullock, Garrett, Michaels, Jennifer R., Yamato, Osamu, O'Brien, Dennis P., Mhlanga-Mutangadura, Tendai, Johnson, Gary S., Katz, Martin L.

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Novel Homozygous ADAMTS2 Variants and Associated Disease Phenotypes in Dogs with Dermatosparactic Ehlers-Danlos Syndrome von Jaffey, Jared A, Bullock, Garrett, Guo, Juyuan, Mhlanga-Mutangadura, Tendai, O'Brien, Dennis P, Coates, Joan R, Morrissey, Rochelle, Hutchison, Robert, Donnelly, Kevin S, Cohn, Leah A, Katz, Martin L, Johnson, Gary S

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Improving Data Acquisition Efficiency: Systematic Accuracy Evaluation of GNSS-Assisted Aerial Triangulation in UAS Operations von Benjamin, Adam R, O’Brien, Dennis, Barnes, Grenville, Wilkinson, Benjamin E, Volkmann, Walter

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A truncating mutation in ATP13A2 is responsible for adult-onset neuronal ceroid lipofuscinosis in Tibetan terriers von Farias, Fabiana H.G, Zeng, Rong, Johnson, Gary S, Wininger, Fred A, Taylor, Jeremy F, Schnabel, Robert D, McKay, Stephanie D, Sanders, Douglas N, Lohi, Hannes, Seppälä, Eija H, Wade, Claire M, Lindblad-Toh, Kerstin, O'Brien, Dennis P, Katz, Martin L

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A novel mutation in CLCN1 associated with feline myotonia congenita von Gandolfi, Barbara, Daniel, Rob J, O'Brien, Dennis P, Guo, Ling T, Youngs, Melanie D, Leach, Stacey B, Jones, Boyd R, Shelton, G Diane, Lyons, Leslie A

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An Inversion Disrupting FAM134B Is Associated with Sensory Neuropathy in the Border Collie Dog Breed von Forman, Oliver P, Hitti, Rebekkah J, Pettitt, Louise, Jenkins, Christopher A, O'Brien, Dennis P, Shelton, G Diane, De Risio, Luisa, Quintana, Rodrigo Gutierrez, Beltran, Elsa, Mellersh, Cathryn

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A homozygous PIGN missense mutation in Soft-Coated Wheaten Terriers with a canine paroxysmal dyskinesia von Kolicheski, Ana L., Johnson, Gary S., Mhlanga-Mutangadura, Tendai, Taylor, Jeremy F., Schnabel, Robert D., Kinoshita, Taroh, Murakami, Yoshiko, O’Brien, Dennis P.

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Smart grid coordination of a chemical processing plant von Feng, Jianyuan, Brown, Avery, O’Brien, Dennis, Chmielewski, Donald J.

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A mutation in the Warburg syndrome gene, RAB3GAP1 , causes a similar syndrome with polyneuropathy and neuronal vacuolation in Black Russian Terrier dogs von Mhlanga-Mutangadura, Tendai, Johnson, Gary S, Schnabel, Robert D, Taylor, Jeremy F, Johnson, Gayle C, Katz, Martin L, Shelton, G. Diane, Lever, Teresa E, Giuliano, Elizabeth, Granger, Nicolas, Shomper, Jeremy, O'Brien, Dennis P

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Case report: MELAS and concomitant presumed antiphospholipid antibody syndrome in an adult woman von Nouduri, Sirisha, Padmanabhan, Rajiv, Hicks, Richard, Abbott, Mary-Alice, O'Brien, Dennis, Schlaug, Gottfried

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A mutation in canine PPT1 causes early onset neuronal ceroid lipofuscinosis in a Dachshund von Sanders, Douglas N., Farias, Fabiana H., Johnson, Gary S., Chiang, Vivian, Cook, James R., O’Brien, Dennis P., Hofmann, Sandra L., Lu, Jui-Yun, Katz, Martin L.

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Canine hereditary ataxia in old english sheepdogs and gordon setters is associated with a defect in the autophagy gene encoding RAB24 von Agler, Caryline, Nielsen, Dahlia M, Urkasemsin, Ganokon, Singleton, Andrew, Tonomura, Noriko, Sigurdsson, Snaevar, Tang, Ruqi, Linder, Keith, Arepalli, Sampath, Hernandez, Dena, Lindblad-Toh, Kerstin, van de Leemput, Joyce, Motsinger-Reif, Alison, O'Brien, Dennis P, Bell, Jerold, Harris, Tonya, Steinberg, Steven, Olby, Natasha J

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A KCNJ10 mutation previously identified in the Russell group of terriers also occurs in Smooth-Haired Fox Terriers with hereditary ataxia and in related breeds von Rohdin, Cecilia, Gilliam, Douglas, O'Leary, Caroline A, O'Brien, Dennis P, Coates, Joan R, Johnson, Gary S, Jäderlund, Karin Hultin

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A rare homozygous MFSD8 single-base-pair deletion and frameshift in the whole genome sequence of a Chinese Crested dog with neuronal ceroid lipofuscinosis von Guo, Juyuan, O'Brien, Dennis P, Mhlanga-Mutangadura, Tendai, Olby, Natasha J, Taylor, Jeremy F, Schnabel, Robert D, Katz, Martin L, Johnson, Gary S

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A CLN8 nonsense mutation in the whole genome sequence of a mixed breed dog with neuronal ceroid lipofuscinosis and Australian Shepherd ancestry von Guo, Juyuan, Johnson, Gary S., Brown, Holly A., Provencher, Michele L., da Costa, Ronaldo C., Mhlanga-Mutangadura, Tendai, Taylor, Jeremy F., Schnabel, Robert D., O'Brien, Dennis P., Katz, Martin L.

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A mutation in the cathepsin D gene ( CTSD) in American Bulldogs with neuronal ceroid lipofuscinosis von Awano, Tomoyuki, Katz, Martin L., O’Brien, Dennis P., Taylor, Jeremy F., Evans, Jason, Khan, Shahnawaz, Sohar, Istvan, Lobel, Peter, Johnson, Gary S.

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Review of the merits of migration and refugee decisions : reflections on the operation of the Migration Review Tribunal and Refugee Review Tribunal in an interconnected world von Dennis O'Brien

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