Sharon Keers
Newcastle University(GB)
Publications by Year
Research Areas
Muscle Physiology and Disorders, Mitochondrial Function and Pathology, Genetic Neurodegenerative Diseases, Metabolism and Genetic Disorders, Cardiomyopathy and Myosin Studies
Most-Cited Works
- → A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B(1998)682 cited
- → Dysferlin is a Plasma Membrane Protein and is Expressed Early in Human Development(1999)295 cited
- → A gene for autosomal recessive limb-girdle muscular dystrophy maps to chromosome 2p(1994)194 cited
- → Identification of an X-Chromosomal Locus and Haplotype Modulating the Phenotype of a Mitochondrial DNA Disorder(2005)191 cited
- → Identical Mutation in Patients with Limb Girdle Muscular Dystrophy Type 2B Or Miyoshi Myopathy Suggests a Role for Modifier Gene(s)(1999)179 cited
- → Mitochondrial DNA haplogroup cluster UKJT reduces the risk of PD(2005)176 cited
- → Mitochondrial DNA and survival after sepsis: a prospective study(2005)175 cited
- → Secondary reduction in calpain 3 expression in patients with limb girdle muscular dystrophy type 2B and Miyoshi myopathy (primary dysferlinopathies)(2000)164 cited
- → Genomic organization of the dysferlin gene and novel mutations in Miyoshi myopathy(2001)146 cited
- → Muscular dystrophy due to dysferlin deficiency in Libyan Jews(2000)107 cited