Alleene V. Strickland

Genetics of Charcot-Marie-Tooth (CMT) Disease within the Frame of the Human Genome Project Success

Vincent Timmerman, Alleene V. Strickland, Stephan Züchner · Genes · 2014 · 249 citations · Full text

Genetics, Genetic Epidemiology, Pathology +16

Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder

Alexander J. Abrams, Robert B. Hufnagel, Adriana Rebelo et al. · Nature Genetics · 2015 · 200 citations · Full text

Somatic Variant, Mendelian Disorder, Genetic Disorder +7

Mutations in the ER-shaping protein reticulon 2 cause the axon-degenerative disorder hereditary spastic paraplegia type 12

Gladys Montenegro, Adriana Rebelo, James W. Connell et al. · Journal of Clinical Investigation · 2012 · 168 citations

Neurodegenerative Diseases, Mendelian Disorder, Er Localization +14

A novel mutation in VCP causes Charcot–Marie–Tooth Type 2 disease

Michael Gonzalez, Shawna Feely, Fiorella Speziani et al. · Brain · 2014 · 138 citations · Full text

Mutation screen reveals novel variants and expands the phenotypes associated with DYNC1H1

Alleene V. Strickland, Maria Schabhüttl, H. Offenbacher et al. · Journal of Neurology · 2015 · 69 citations · Full text

Genome Instability, Engineering, Somatic Variant +8