G. Johnson

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A Single IGF1 Allele Is a Major Determinant of Small Size in Dogs

C. Bustamante, E. Ostrander, N. Sutter, 2007, Science.

Genetic Structure of the Purebred Domestic Dog

L. Kruglyak, E. Ostrander, N. Sutter, 2004, Science.

A Simple Genetic Architecture Underlies Morphological Variation in Dogs

Jeremiah D. Degenhardt, A. Auton, J. Novembre, 2010, PLoS biology.

A CLN8 nonsense mutation in the whole genome sequence of a mixed breed dog with neuronal ceroid lipofuscinosis and Australian Shepherd ancestry.

G. Johnson, Jeremy F Taylor, R. Schnabel, 2014, Molecular genetics and metabolism.

A polymorphic (GA)n microsatellite in an intron of the canine endothelin-B receptor gene.

G. Johnson, D. Lubahn, M. Katz, 1998, Animal genetics.

A mutation in the Warburg syndrome gene, RAB3GAP1, causes a similar syndrome with polyneuropathy and neuronal vacuolation in Black Russian Terrier dogs

G. Johnson, Jeremy F Taylor, R. Schnabel, 2016, Neurobiology of Disease.

Chromosome-length genome assembly and structural variations of the primal Basenji dog (Canis lupus familiaris) genome

Richard J. Edwards, Erez Lieberman Aiden, L. Hillier, 2020, bioRxiv.

Immunochemical localization of the Batten disease (CLN3) protein in retina.

G. Johnson, M. Katz, P. Liu, 1997, Investigative ophthalmology & visual science.

A L2HGDH initiator methionine codon mutation in a Yorkshire terrier with L-2-hydroxyglutaric aciduria

G. Johnson, G. Shelton, D. O'brien, 2012, BMC Veterinary Research.

Detection of Babesia bigemina-infected carriers by polymerase chain reaction amplification

G. Johnson, J. V. Figueroa, L. Chieves, 1992, Journal of clinical microbiology.

Binding of Low‐Molecular‐Weight Canine Factor VIII Coagulant from von Willebrand Plasma to Canine Factor VIII‐Related Antigen

G. Johnson, W. Dodds, R. Benson, 1981, British journal of haematology.

Decreased growth in angus steers with a short TG-microsatellite allele in the P1 promoter of the growth hormone receptor gene.

G. Johnson, D. Lubahn, D. Keisler, 2000, Journal of animal science.

Genome-wide association analysis reveals a SOD1 mutation in canine degenerative myelopathy that resembles amyotrophic lateral sclerosis

K. Lindblad-Toh, C. Wade, G. Johnson, 2009, Proceedings of the National Academy of Sciences.

Assessment of retinal function and characterization of lysosomal storage body accumulation in the retinas and brains of Tibetan Terriers with ceroid-lipofuscinosis.

G. Johnson, K. Narfström, M. Katz, 2005, American journal of veterinary research.

Assessment of plasma carnitine concentrations in relation to ceroid lipofuscinosis in Tibetan Terriers.

G. Johnson, M. Katz, Deja A Sanders, 2002, American journal of veterinary research.

Characterization and chromosomal mapping of a mouse ortholog of the late-infantile ceroid-lipofuscinosis gene CLN2

G. Johnson, M. Katz, H. Shibuya, 1999, Mammalian Genome.

Golden Retriever dogs with neuronal ceroid lipofuscinosis have a two-base-pair deletion and frameshift in CLN5.

G. Johnson, R. Schnabel, T. Mhlanga-Mutangadura, 2015, Molecular genetics and metabolism.

Pathologic characterization of canine multiple system degeneration in the Ibizan hound

G. Johnson, B. Jortner, S. Hancock, 2021, Veterinary pathology.

Accumulation of glial fibrillary acidic protein and histone H4 in brain storage bodies of Tibetan terriers with hereditary neuronal ceroid lipofuscinosis

G. Johnson, B. Mooney, M. Katz, 2007, Journal of Inherited Metabolic Disease.

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

K. Lindblad-Toh, C. Wade, G. Johnson, 2011, Neurobiology of Disease.

Isolation and characterization of the normal canine β-galactosidase gene and its mutation in a dog model of GM1-gangliosidosis

G. Johnson, J. Alroy, G. Pastores, 2000, Journal of Inherited Metabolic Disease.

Variants in FtsJ RNA 2′-O-Methyltransferase 3 and Growth Hormone 1 are associated with small body size and a dental anomaly in dogs

G. Johnson, T. Famula, L. A. Clark, 2020, Proceedings of the National Academy of Sciences.

Mouse gene knockout models for the CLN2 and CLN3 forms of ceroid lipofuscinosis.

G. Johnson, M. Katz, G. Johnson, 2001, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

A rare homozygous MFSD8 single-base-pair deletion and frameshift in the whole genome sequence of a Chinese Crested dog with neuronal ceroid lipofuscinosis

G. Johnson, R. Schnabel, T. Mhlanga-Mutangadura, 2015, BMC Veterinary Research.

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

G. Johnson, M. Katz, D. O'brien, 2010, Molecular genetics and metabolism.

A Homozygous RAB3GAP1:c.743delC Mutation in Rottweilers with Neuronal Vacuolation and Spinocerebellar Degeneration

G. Johnson, T. Mhlanga-Mutangadura, G. Shelton, 2016, Journal of veterinary internal medicine.

An ADAMTS17 splice donor site mutation in dogs with primary lens luxation.

C. Mellersh, G. Johnson, P. Gharahkhani, 2010, Investigative ophthalmology & visual science.

Exploring genetic variation and population structure in a threatened species, Noturus placidus, with whole genome sequence data.

G. Johnson, R. Schnabel, Troy N. Rowan, 2022, G3.

A Missense Mutation in Canine CLN6 in an Australian Shepherd with Neuronal Ceroid Lipofuscinosis

G. Johnson, M. Katz, D. O'brien, 2010, Journal of biomedicine & biotechnology.

Involvement of oxidative pathways in cytokine-induced secretory phospholipase A2-IIA in astrocytes

G. Johnson, Á. Simonyi, Grace Y Sun, 2009, Neurochemistry International.

Heritability and biochemistry of gangliosidosis in emus (Dromaius novaehollandiae).

D. Ledoux, G. Johnson, R. Yu, 1997, Avian diseases.

A homozygous ADAMTS2 nonsense mutation in a Doberman Pinscher dog with Ehlers Danlos syndrome and extreme skin fragility

G. Johnson, T. Mhlanga-Mutangadura, Juyuan Guo, 2019, Animal genetics.

Magnetic Resonance Imaging and Histopathologic Findings From a Standard Poodle With Neonatal Encephalopathy With Seizures

G. Johnson, K. Uchida, D. Hasegawa, 2020, Frontiers in Veterinary Science.

Canine von Willebrand's disease. A heterogeneous group of bleeding disorders.

G. Johnson, K. Kraus, M. Turrentine, 1988, The Veterinary clinics of North America. Small animal practice.

Prepartion of botrocetin, a reagent used to evaluate canine von Willebrand factor activity.

G. Johnson, M. Turrentine, S. Dover, 1987, Veterinary clinical pathology.

Using genetic technologies for promoting canine health and temperament.

G. Johnson, J. Peterson, P. Olson, 2004, Animal reproduction science.

Lysosomal Storage Disease Associated with a CNP Sequence Variant in Dalmatian Dogs.

G. Johnson, S. Goebbels, T. Mhlanga-Mutangadura, 2022, Gene.

Large Animal Models

G. Johnson, C. Drögemüller, M. Katz, 2011 .

Ristocetin cofactor activity of purified canine factor VIII: inhibition by plasma proteins.

G. Johnson, W. Dodds, R. Benson, 1979, Thrombosis research.

Comparison of six activated partial thromboplastin time reagents: intrinsic system factors' sensitivity and responsiveness.

G. Johnson, S. Hales, D. Wagner, 1990, Clinical laboratory science : journal of the American Society for Medical Technology.

Factor VIII coagulant activity and von Willebrand factor in post-exercise plasma from standardbred horses.

G. Johnson, M. Turrentine, P. W. Sculley, 1986, Thrombosis Research.

Evaluation of hemostatic analytes after use of hypertonic saline solution combined with colloids for resuscitation of dogs with hypovolemia.

G. Johnson, A. Jergens, D. Zoran, 1992, American journal of veterinary research.

Plasma von Willebrand factor antigen concentration and buccal mucosal bleeding time in dogs with experimental hypothyroidism.

G. Johnson, D. Panciera, 1996, Journal of veterinary internal medicine.

Effect of desmopressin acetate on bleeding times and plasma von Willebrand factor in Doberman pinscher dogs with von Willebrand's disease.

G. Johnson, K. Kraus, A. Jergens, 1989, Veterinary surgery : VS.

SPECIES SPECIFICITY IN von WILLEBRAND FACTORSUPPORTED PLATELET AGGLUTINATION *

G. Johnson, W. Dodds, T. Rosborough, 1981, Annals of the New York Academy of Sciences.

Ristocetin-induced aggregation of canine platelets.

G. S. Johnson, G. Johnson, G. Johnson, 1980, Thrombosis research.

A Sensitive Autoradlographic Procedure for Factor VIII-Related Antigen in Canine Plasma.

G. Johnson, G. Schlink, 1983, Veterinary clinical pathology.

A bleeding disease (von Willebrand's disease) in a Chesapeake Bay Retriever.

G. Johnson, W. Dodds, R. Benson, 1980, Journal of the American Veterinary Medical Association.

Resolving the evolution of extant and extinct ruminants with high-throughput phylogenomics

Robert D Schnabel, Tad S Sonstegard, Rudiger Brauning, 2009, Proceedings of the National Academy of Sciences.

Multiplex polymerase chain reaction based assay for the detection of Babesia bigemina, Babesia bovis and Anaplasma marginale DNA in bovine blood.

G. Johnson, J. V. Figueroa, L. Chieves, 1993, Veterinary parasitology.

A frame shift mutation in canine TPP1 (the ortholog of human CLN2) in a juvenile Dachshund with neuronal ceroid lipofuscinosis.

G. Johnson, U. Giger, P. Lobel, 2006, Molecular genetics and metabolism.

A mutation in the cathepsin D gene (CTSD) in American Bulldogs with neuronal ceroid lipofuscinosis.

G. Johnson, P. Lobel, M. Katz, 2006, Molecular genetics and metabolism.

Genetic mapping of canine multiple system degeneration and ectodermal dysplasia loci.

G. Johnson, R. Schnabel, G. Johnson, 2005, The Journal of heredity.

A mutation in the CLN8 gene in English Setter dogs with neuronal ceroid-lipofuscinosis.

G. Johnson, M. Katz, S. Shahid, 2005, Biochemical and biophysical research communications.

A diagnostic assay for the endogenous ALV-type provirus ALVE-B2 of broiler chickens.

G. Johnson, M. Katz, H. Shibuya, 1998 .

Meiotic linkage mapping of 52 genes onto the canine map does not identify significant levels of microrearrangement

E. Ostrander, C. Mellersh, G. Johnson, 2001, Mammalian Genome.

Novel Homozygous ADAMTS2 Variants and Associated Disease Phenotypes in Dogs with Dermatosparactic Ehlers–Danlos Syndrome

G. Johnson, T. Mhlanga-Mutangadura, Juyuan Guo, 2022, Genes.

A phosducin (PDC ) gene mutation does not cause progressive retinal atrophy in Korean miniature schnauzers.

G. Johnson, K. Narfström, K. Seo, 2008, Animal genetics.

Activated partial thromboplastin time of owl monkey (Aotus trivirgatus) plasma.

G. Johnson, J. Mrema, S. Kelley, 1984, Laboratory animal science.

Clinical characteristics and inheritance of idiopathic epilepsy in Vizslas.

P. J. Armstrong, E. Patterson, G. Johnson, 2003, Journal of veterinary internal medicine.

10 Animal models for the ceroid lipofuscinoses

G. Johnson, M. Katz, H. Shibuya, 2001 .

A mouse gene knockout model for juvenile ceroid‐lipofuscinosis (batten disease)

G. Johnson, S. Kaur, M. Katz, 1999, Journal of neuroscience research.

Histopathologic and immunocytochemical analysis of the retina and ocular tissues in Batten disease.

A. Milam, G. Johnson, M. Katz, 2000, Ophthalmology.

Phenotypic characterization of a mouse model of juvenile neuronal ceroid lipofuscinosis

G. Johnson, G. Tullis, M. Katz, 2008, Neurobiology of Disease.

Coding sequence and exon/intron organization of the canine CLN3 (batten disease) gene and its exclusion as the locus for ceroid‐lipofuscinosis in english setter dogs

G. Johnson, D. Nonneman, M. Katz, 1998, Journal of neuroscience research.

Two polymorphic microsatellites in a coding segment of the canine androgen receptor gene.

G. Johnson, H. Shibuya, V. Ganjam, 2009, Animal genetics.

Allele Is a Major Determinant of Small Size in Dogs IGF 1 A Single

C. Bustamante, E. Ostrander, N. Sutter, 2011 .

A mixed breed dog with neuronal ceroid lipofuscinosis is homozygous for a CLN5 nonsense mutation previously identified in Border Collies and Australian Cattle Dogs.

G. Johnson, T. Mhlanga-Mutangadura, M. Katz, 2019, Molecular genetics and metabolism.

Neuronal ceroid lipofuscinosis associated with an MFSD8 mutation in Chihuahuas.

G. Johnson, T. Mhlanga-Mutangadura, Juyuan Guo, 2016, Molecular genetics and metabolism.

Homozygous PPT1 Splice Donor Mutation in a Cane Corso Dog With Neuronal Ceroid Lipofuscinosis

G. Johnson, T. Mhlanga-Mutangadura, D. O'brien, 2016, Journal of veterinary internal medicine.

Rapid communication: polymorphic (GT)n microsatellite in the bovine somatotropin receptor gene promoter.

G. Johnson, M. Lucy, H. Shibuya, 1998, Journal of animal science.

Cytochemical properties of chicken blood cells resembling both thrombocytes and lymphocytes.

G. Johnson, D. Swayne, S. Stockham, 1986, Veterinary clinical pathology.

A polymorphic (AGGAAT)n tandem repeat in an intron of the canine von Willebrand factor gene.

G. Johnson, H. Shibuya, B. K. Collins, 2009, Animal genetics.

Coagulation of plasma from the chicken (Gallus domesticus): phospholipids influence clotting rates induced by components from Russell's viper venom.

G. Johnson, D. Swayne, M. Turrentine, 1985, Comparative biochemistry and physiology. B, Comparative biochemistry.

Long‐term Treatment with Methylene Blue in a Dog with Hereditary Methemoglobinemia Caused by Cytochrome b5 Reductase Deficiency

G. Johnson, U. Giger, J. Jaffey, 2017, Journal of veterinary internal medicine.

A BstUI PCR/RFLP in the bovine tyrosinase-related protein-1 (TYRP1) gene.

G. Johnson, H. Shibuya, D. Nonneman, 2009, Animal genetics.

Oral Mucosa Bleeding Times of Normal Cats and Cats with Chediak-Higashi Syndrome or Hageman Trait (Factor XII Deficiency).

G. Johnson, A. Kier, M. Parker, 1988, Veterinary clinical pathology.

Clinical Phenotype of Musladin‐Lueke Syndrome in 2 Beagles

G. Johnson, Ling T Guo, G. Shelton, 2017, Journal of veterinary internal medicine.

The coding sequence of the bovine ferrochelatase gene.

G. Johnson, H. Shibuya, D. Nonneman, 1995, Biochimica et biophysica acta.

GM2 Gangliosidosis in Shiba Inu Dogs with an In‐Frame Deletion in HEXB

G. Johnson, T. Mhlanga-Mutangadura, J. Taylor, 2017, Journal of veterinary internal medicine.

Plasma von Willebrand factor antigen concentration in dogs with hypothyroidism.

G. Johnson, D. Panciera, 1994, Journal of the American Veterinary Medical Association.

Plasma from donor dogs, pretreated with DDAVP, transfused into a German shorthair pointer with type II von Willebrand's disease.

G. Johnson, K. Kraus, M. Turrentine, 1988, The Veterinary clinics of North America. Small animal practice.

Buccal mucosa bleeding times of healthy dogs and of dogs in various pathologic states, including thrombocytopenia, uremia, and von Willebrand's disease.

G. Johnson, K. Kraus, A. Jergens, 1987, American journal of veterinary research.

Hemorrhage from the cosmetic otoplasty of Doberman Pinschers with von Willebrand's disease.

G. Johnson, C. P. Moore, G. Schlink, 1985, American journal of veterinary research.

A BseRI PCR/RFLP in an intron of the canine phenol sulfotransferase gene.

G. Johnson, M. Katz, P. Liu, 1998, Animal genetics.

An AvaII PCR/RFLP in an exon of the canine gene for the beta subunit of the amiloride-sensitive sodium channel (SCNN1B).

G. Johnson, P. Liu, H. Shibuya, 1998, Animal genetics.

A polymorphic (TG)n microsatellite in an intron of the canine angiotensin I converting enzyme gene.

G. Johnson, H. Shibuya, M. W. Cassells, 1998, Animal genetics.

A polymorphic (CT)n microsatellite in an intron of the canine SA-hypertension gene.

G. Johnson, D. Lubahn, P. Liu, 1998, Animal genetics.

A BstUI PCR/RFLP marker in an intron of the canine fibrillin 1 gene.

G. Johnson, M. Katz, P. Liu, 1998, Animal genetics.

A BsmFI PCR/RFLP in the canine CD19 gene.

G. Johnson, M. Katz, P. Liu, 1998, Animal genetics.

A polymorphic (GAAA)n microsatellite in a canine Wilms tumor 1 (WT1) gene intron.

G. Johnson, H. Shibuya, B. K. Collins, 2009, Animal genetics.

Two polymorphisms in the canine beta-A3/A1-crystallin gene, detectable by PCR-RFLP analysis.

G. Johnson, H. Shibuya, B. K. Collins, 1995, Animal genetics.

Australian Cattle Dogs with Neuronal Ceroid Lipofuscinosis are Homozygous for a CLN5 Nonsense Mutation Previously Identified in Border Collies

G. Johnson, T. Mhlanga-Mutangadura, Juyuan Guo, 2016, Journal of veterinary internal medicine.

Clinical, metabolic, and molecular genetic characterization of hereditary methemoglobinemia caused by cytochrome b5 reductase deficiency in 30 dogs

G. Johnson, U. Giger, T. Mhlanga-Mutangadura, 2020, Scientific Reports.

Multimeric analysis of von Willebrand factor before and after desmopressin acetate (DDAVP) administration intravenously and subcutaneously in male beagle dogs.

G. Johnson, K. Kraus, M. Turrentine, 1987, American journal of veterinary research.

DDAVP-induced increases in coagulation factor VIII and von Willebrand factor in the plasma of conscious dogs.

G. Johnson, K. Kraus, M. Turrentine, 1986, Journal of veterinary pharmacology and therapeutics.

Afibrinogenemia and a circulating antibody against fibrinogen in a Bichon Frise dog.

G. Johnson, S. Stockham, L. Riley, 2005, Veterinary clinical pathology.

Prekallikrein deficiency in a family of miniature horses.

G. Johnson, E. Green, M. Turrentine, 1986, American journal of veterinary research.

A homozygous PIGN missense mutation in Soft-Coated Wheaten Terriers with a canine paroxysmal dyskinesia

G. Johnson, R. Schnabel, T. Kinoshita, 2016, neurogenetics.

Clinical description and mode of inheritance of idiopathic epilepsy in English springer spaniels.

P. J. Armstrong, E. Patterson, G. Johnson, 2005, Journal of the American Veterinary Medical Association.

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

G. Johnson, J. Coates, D. O'brien, 2015, Acta veterinaria Scandinavica.

Clinical characterization of a familial degenerative myelopathy in Pembroke Welsh Corgi dogs.

G. Johnson, R. Berghaus, J. Keating, 2007, Journal of veterinary internal medicine.

Characterization of Neuronal Ceroid-Lipofuscinosis in 3 Cats

G. Johnson, M. Katz, R. Zeng, 2014, Veterinary pathology.

The relationships among mitochondrial uncoupling protein 2 and 3 expression, mitochondrial deoxyribonucleic acid single nucleotide polymorphisms, and residual feed intake in Angus steers.

G. Johnson, M. Kerley, J. W. Golden, 2006, Journal of animal science.

Genome-Wide Association Study Identifies a Novel Canine Glaucoma Locus

C. Mellersh, G. Johnson, S. Ahonen, 2013, PloS one.

A Bsm AI PCRRFLP in the bovine microtubule‐associated protein‐5 (MAPIB) gene

G. Johnson, H. Shibuya, D. Nonneman, 2009 .

A One Health overview, facilitating advances in comparative medicine and translational research

Dongsheng Duan, Ubadah Sabbagh, James P. Calvet, 2016, Clinical and Translational Medicine.

A CNTNAP1 Missense Variant Is Associated with Canine Laryngeal Paralysis and Polyneuropathy

G. Johnson, J. Mickelson, C. Drögemüller, 2020, Genes.

Polymerase chain reaction-based diagnostic assay to detect cattle chronically infected with Babesia bovis.

G. Johnson, W. Goff, J. V. Figueroa, 1994, Revista latinoamericana de microbiologia.

A polymorphic (TG)n microsatellite in an intron of the canine tyrosine transaminase gene.

G. Johnson, P. Liu, H. Shibuya, 1998, Animal genetics.

AMissenseMutation in Canine CLN 6 in an Australian Shepherd with Neuronal Ceroid Lipofuscinosis

G. Johnson, M. Katz, D. O'brien, 2014 .

Neuronal ceroid lipofuscinosis in a German Shorthaired Pointer associated with a previously reported CLN8 nonsense variant

G. Johnson, R. Schnabel, T. Mhlanga-Mutangadura, 2019, Molecular genetics and metabolism reports.

Familial cataracts and concurrent ocular anomalies in chow chows.

G. Johnson, C. P. Moore, H. Shibuya, 1992, Journal of the American Veterinary Medical Association.

PCR/RFLP markers in the canine gamma-D-crystallin gene.

G. Johnson, H. Shibuya, B. K. Collins, 2009, Animal Genetics.

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

K. Lindblad-Toh, C. Wade, G. Johnson, 2011, Neurobiology of Disease.

Evaluation of microwave-thawed canine plasma for transfusion.

G. Johnson, M. Turrentine, T. S. Hurst, 1987, Journal of the American Veterinary Medical Association.

Amylaceous (Polyglucosan) Bodies in Familial Cerebral Atrophy of Early Onset

G. Johnson, S. Crawford, C. Darling, 1996, Journal of child neurology.