Ling T. Guo
ScholarGPS® ID: 94882347965613
Affiliation History
Field
Medicine
Discipline
Pathology
Top Specialties
Muscular Dystrophy | Neuromuscular Disease | Mutation | Birth Defect | Skeletal Muscle | Molecular Genetics | Exome Sequencing
Metrics Summary
Publication Count
64
Predicted Citations
1,774
Predicted h-index
22
Ranking
Publications and Citation History
Publications based on Top Specialties
Types of Publication
- Publications
- Books
- Patents
- NIH/NSF
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Variants in CLCN1 and PDE4C Associated with Muscle Hypertrophy, Dysphagia, and Gait Abnormalities in Young French Bulldogs (journal article) Animals, volume 14, issue 5, pages 722- (2024). |
Precision medicine using whole genome sequencing identifies a novel dystrophin ( DMD ) variant for X ‐linked muscular dystrophy in a cat (journal article) Journal of Veterinary Internal Medicine, volume 38, issue 1, pages 135-144 (2024). |
Novel COL6A3 frameshift variant in American Staffordshire Terrier dogs with Ullrich ‐like congenital muscular dystrophy (journal article) Journal of Veterinary Internal Medicine, volume 37, issue 6, pages 2504-2509 (2023). |
Current Classification of Canine Muscular Dystrophies and Identification of New Variants (journal article) Genes, volume 14, issue 8, pages 1557- (2023). |
Dystrophin-Deficient Muscular Dystrophy in Two Male Juvenile Brittanys (journal article) Journal of the American Animal Hospital Association, volume 58, issue 6, pages 292-296 (2022). |
A Nonsense Variant in the DMD Gene Causes X-Linked Muscular Dystrophy in the Maine Coon Cat (journal article) Animals, volume 12, issue 21, pages 2928- (2022). |
Tandem duplication within the DMD gene in Labrador retrievers with a mild clinical phenotype (journal article) Neuromuscular Disorders, volume 32, issue 10, pages 836-841 (2022). |
Journal of Veterinary Internal Medicine, volume 36, issue 5, pages 1800-1805 (2022). |
An EHPB1L1 Nonsense Mutation Associated with Congenital Dyserythropoietic Anemia and Polymyopathy in Labrador Retriever Littermates (journal article) Genes, volume 13, issue 8, pages 1427- (2022). |
Congenital muscular dystrophy in a dog with a LAMA2 gene deletion (journal article) Journal of Veterinary Internal Medicine, volume 36, issue 1, pages 279-284 (2022). |
Sarcoglycan A mutation in miniature dachshund dogs causes limb-girdle muscular dystrophy 2D (journal article) Skeletal Muscle, volume 11, issue 1 (2021). |
Genes, volume 12, issue 11, pages 1823- (2021). |
Muscular dystrophy-dystroglycanopathy in a family of Labrador retrievers with a LARGE1 mutation (journal article) Neuromuscular Disorders, volume 31, issue 11, pages 1169-1178 (2021). |
Congenital dyserythropoiesis and polymyopathy without cardiac disease in male Labrador retriever littermates (journal article) Journal of Veterinary Internal Medicine, volume 35, issue 5, pages 2409-2414 (2021). |
LATE BREAKING NEWS E-POSTER PRESENTATION (journal article) Neuromuscular Disorders, volume 30 (2020). |
Pathogenic variants in COL6A3 cause Ullrich-like congenital muscular dystrophy in young Labrador Retriever dogs (journal article) Neuromuscular Disorders, volume 30, issue 5, pages 360-367 (2020). |
Neuromuscular Disorders, volume 30, issue 5, pages 353-359 (2020). |
Congenital myasthenic syndrome in Golden Retrievers is associated with a novel COLQ mutation (journal article) Journal of Veterinary Internal Medicine, volume 34, issue 1, pages 258-265 (2020). |
Journal of Neuromuscular Diseases, volume 6, issue 4, pages 485-501 (2019). |
Late‐onset Becker‐type muscular dystrophy in a Border terrier dog (journal article) Journal of Small Animal Practice, volume 60, issue 8, pages 514-517 (2019). |