Katherine V. Bricceno

Hereditary Spastic Paraplegia Type 43 (SPG43) is Caused by Mutation in<i>C19orf12</i>

Guida Landouré, Peng-Peng Zhu, Charles Marques Lourenço et al. · Human Mutation · 2013 · 91 citations · Full text

Biology, Rare Diseases, Neurodegenerative Diseases +15

Survival motor neuron protein deficiency impairs myotube formation by altering myogenic gene expression and focal adhesion dynamics

Katherine V. Bricceno, Tara Martinez, Evgenia Leikina et al. · Human Molecular Genetics · 2014 · 75 citations · Full text

Muscle Function, Cytoskeleton, Mechanotransduction +20

Histone deacetylase inhibition suppresses myogenin-dependent atrogene activation in spinal muscular atrophy mice

Katherine V. Bricceno, Paul J. Sampognaro, James P. Van Meerbeke et al. · Human Molecular Genetics · 2012 · 65 citations

Muscle Function, Epigenetic Change, Cytoskeleton +21

Genetics of low spinal muscular atrophy carrier frequency in sub‐Saharan Africa

Modibo Sangaré, Brant C. Hendrickson, Hammadoun Ali sango et al. · Annals of Neurology · 2014 · 40 citations · Full text