Alleene V. Strickland
University of Miami(US)Dr. John T. Macdonald Foundation(US)
Publications by Year
Research Areas
Hereditary Neurological Disorders, Neurological diseases and metabolism, Genetic Neurodegenerative Diseases, Mitochondrial Function and Pathology, Cellular transport and secretion
Most-Cited Works
- → Genetics of Charcot-Marie-Tooth (CMT) Disease within the Frame of the Human Genome Project Success(2014)249 cited
- → Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder(2015)204 cited
- → Mutations in the ER-shaping protein reticulon 2 cause the axon-degenerative disorder hereditary spastic paraplegia type 12(2012)169 cited
- → A novel mutation in VCP causes Charcot–Marie–Tooth Type 2 disease(2014)143 cited
- → Mutation screen reveals novel variants and expands the phenotypes associated with DYNC1H1(2015)69 cited
- → Characterization of the mitofusin 2 R94W mutation in a knock‐in mouse model(2014)55 cited
- → De novo PMP2mutations in families with type 1 Charcot–Marie–Tooth disease(2016)43 cited
- → Variant pathogenicity evaluation in the community-driven Inherited Neuropathy Variant Browser(2018)19 cited
- → Characterizing the molecular phenotype of an Atp7aT985Iconditional knock in mouse model for X-linked distal hereditary motor neuropathy (dHMNX)(2016)11 cited
- → Ex-situ real-time detection of neurotransmitters in perfusion dialysate(2004)