Marion C. Hogg

Genetic variation in RYR1 and malignant hyperthermia phenotypes

Danielle Carpenter, Rachel L. Robinson, Rupert J. Quinnell et al. · British Journal of Anaesthesia · 2009 · 113 citations · Full text

Molecular Physiology, Genetic Disorder, Genetics +5

Elevation of plasma tRNA fragments precedes seizures in human epilepsy

Marion C. Hogg, Rana Raoof, Hany El‐Naggar et al. · Journal of Clinical Investigation · 2019 · 103 citations · Full text

Molecular Neuroscience, Neurophysiology, Specific Trna Fragments +12

A Presenilin 1 Mutation Associated with Familial Frontotemporal Dementia Inhibits γ-Secretase Cleavage of APP and Notch

Zareen Amtul, Patrick A. Lewis, Siân C. Piper et al. · Neurobiology of Disease · 2002 · 89 citations · Full text

Neurodegenerative Diseases, Genetic Disorder, Dementia +10

The L266V tau mutation is associated with frontotemporal dementia and Pick-like 3R and 4R tauopathy

Marion C. Hogg, Zoran Grujic, Matt Baker et al. · Acta Neuropathologica · 2003 · 89 citations

Genetic Disorder, Genetics, Pathology +7

“Preconditioning” with latrepirdine, an adenosine 5′-monophosphate-activated protein kinase activator, delays amyotrophic lateral sclerosis progression in SOD1G93A mice

Karen Coughlan, Mollie R. Mitchem, Marion C. Hogg et al. · Neurobiology of Aging · 2014 · 69 citations

Neurodegenerative Diseases, Amyotrophic Lateral Sclerosis, Molecular Neuroscience +7