Burcu Atasu

Hypomorphic mutations in POLR3A are a frequent cause of sporadic and recessive spastic ataxia

Martina Minnerop, Delia Kurzwelly, Holger Wagner et al. · Brain · 2017 · 121 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

<i>HPCA</i> confirmed as a genetic cause of DYT2‐like dystonia phenotype

Burcu Atasu, Haşmet Hanağası, Meltem Pak et al. · Movement Disorders · 2018 · 39 citations

Life Sciences, Genetics, Neurology +16

Biallelic variants in TSPOAP1, encoding the active-zone protein RIMBP1, cause autosomal recessive dystonia

Niccolò E. Mencacci, Marisa M. Brockmann, Jinye Dai et al. · Journal of Clinical Investigation · 2021 · 38 citations · Full text

Life Sciences, Genetics, Neurology +17

A multi-omics dataset for the analysis of frontotemporal dementia genetic subtypes

Kevin Menden, Margherita Francescatto, Tenzin Nyima et al. · Scientific Data · 2023 · 18 citations · Full text

Life Sciences, Genetics, Neuroscience +14

Role of LRRK2 and SNCA in autosomal dominant Parkinson's disease in Turkey

Burcu Atasu, Haşmet Hanağası, Javier Simón‐Sánchez et al. · Parkinsonism & Related Disorders · 2017 · 16 citations

Life Sciences, Neurology, Neuroscience +12