Burçak Özeş

Exome Sequence Analysis Suggests that Genetic Burden Contributes to Phenotypic Variability and Complex Neuropathy

Claudia Gonzaga‐Jauregui, Tamar Harel, Tomasz Gambin et al. · Cell Reports · 2015 · 240 citations · Full text

Motor protein mutations cause a new form of hereditary spastic paraplegia

Andrés Caballero-Oteyza, Esra Battaloğlu, Levent Öcek et al. · Neurology · 2014 · 72 citations · Full text

<scp>PLA2G6</scp> mutations associated with a continuous clinical spectrum from neuroaxonal dystrophy to hereditary spastic paraplegia

Burçak Özeş, N. Karagoz, Rebecca Schüle et al. · Clinical Genetics · 2017 · 45 citations · Full text

Neurological Disorder, Corticobasal Degeneration, Genetics +19

Unraveling the genetic landscape of autosomal recessive Charcot-Marie-Tooth neuropathies using a homozygosity mapping approach

M. Zimoń, Esra Battaloğlu, Yeşim Parman et al. · Neurogenetics · 2014 · 42 citations · Full text

Genetic Landscape, Mendelian Disorder, Genetic Disorder +8

AAV1.NT-3 gene therapy for X-linked Charcot–Marie–Tooth neuropathy type 1

Burçak Özeş, Morgan Myers, Kyle Moss et al. · Gene Therapy · 2021 · 38 citations · Full text