Publications by authors named "Burcu Atasu"

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Dissecting genetic architecture of rare dystonia: genetic, molecular and clinical insights.
Burcu Atasu, Javier Simón-Sánchez, Hasmet Hanagasi, Basar Bilgic, Ann-Kathrin Hauser

J Med Genet· April 2024

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Pallidal Deep Brain Stimulation Improves HPCA-Linked (DYT 2) Dystonia.
Bedia Samanci, Erdi Şahin, Yavuz Samanci, Başar Bilgiç, Burcu Atasu

Mov Disord Clin Pract· February 2024

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A multi-omics dataset for the analysis of frontotemporal dementia genetic subtypes.
Kevin Menden, Margherita Francescatto, Tenzin Nyima, Cornelis Blauwendraat, Ashutosh Dhingra, Burcu Atasu

Sci Data· December 2023

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Genotype-Phenotype correlations of SCARB2 associated clinical presentation: a case report and in-depth literature review.
Burcu Atasu, Ayse Nur Ozdag Acarlı, Basar Bilgic, Betül Baykan, Erol Demir

BMC Neurol· March 2022

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Biallelic variants in TSPOAP1, encoding the active-zone protein RIMBP1, cause autosomal recessive dystonia.
Niccolò E Mencacci, Marisa M Brockmann, Jinye Dai, Sander Pajusalu, Burcu Atasu

J Clin Invest· April 2021

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HPCA confirmed as a genetic cause of DYT2-like dystonia phenotype.
Burcu Atasu, Hasmet Hanagasi, Basar Bilgic, Meltem Pak, Nihan Erginel-Unaltuna

Mov Disord· August 2018

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Role of LRRK2 and SNCA in autosomal dominant Parkinson's disease in Turkey.
Christoph Kessler, Burcu Atasu, Hasmet Hanagasi, Javier Simón-Sánchez, Ann-Kathrin Hauser

Parkinsonism Relat Disord· March 2018

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Hypomorphic mutations in POLR3A are a frequent cause of sporadic and recessive spastic ataxia.
Martina Minnerop, Delia Kurzwelly, Holger Wagner, Anne S Soehn, Jennifer Reichbauer, Burcu Atasu

Brain· June 2017

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