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BURCU DURSUN ATASU
BURCU DURSUN ATASU
Hertie Institute for Clinical Brain Research, University of Tübingen
Verified email at medizin.uni-tuebingen.de
Title
Cited by
Cited by
Year
USing exome sequencing to reveal mutations in trem2 presenting as a frontotemporal dementia–like syndrome without bone involvement
RJ Guerreiro, E Lohmann, JM Brás, JR Gibbs, JD Rohrer, N Gurunlian, ...
JAMA neurology 70 (1), 78-84, 2013
3852013
Exome sequencing reveals an unexpected genetic cause of disease: NOTCH3 mutation in a Turkish family with Alzheimer's disease
RJ Guerreiro, E Lohmann, E Kinsella, JM Brás, N Luu, N Gurunlian, ...
Neurobiology of aging 33 (5), 1008. e17-1008. e23, 2012
1172012
Hypomorphic mutations in POLR3A are a frequent cause of sporadic and recessive spastic ataxia
M Minnerop, D Kurzwelly, H Wagner, AS Soehn, J Reichbauer, F Tao, ...
Brain 140 (6), 1561-1578, 2017
982017
HPCA confirmed as a genetic cause of DYT2‐like dystonia phenotype
B Atasu, H Hanagasi, B Bilgic, M Pak, N Erginel‐Unaltuna, AK Hauser, ...
Movement Disorders 33 (8), 1354-1358, 2018
362018
Genetic bases and phenotypes of autosomal recessive Parkinson disease in a Turkish population
E Lohmann, B Dursun, S Lesage, HA Hanagasi, G Sevinc, A Honore, ...
European journal of neurology 19 (5), 769-775, 2012
272012
Differentiating symptomatic Parkin mutations carriers from patients with idiopathic Parkinson’s disease: Contribution of automated segmentation neuroimaging method
B Bilgic, A Bayram, AB Arslan, H Hanagasi, B Dursun, H Gurvit, M Emre, ...
Parkinsonism & related disorders 18 (5), 562-566, 2012
262012
Biallelic variants in TSPOAP1, encoding the active-zone protein RIMBP1, cause autosomal recessive dystonia
NE Mencacci, MM Brockmann, J Dai, S Pajusalu, B Atasu, J Campos, ...
The Journal of Clinical Investigation 131 (7), 2021
232021
A homozygous frameshift mutation of sepiapterin reductase gene causing parkinsonism with onset in childhood
E Lohmann, Ç Köroğlu, HA Hanagasi, B Dursun, E Taşan, A Tolun
Parkinsonism & related disorders 18 (2), 191-193, 2012
192012
Role of LRRK2 and SNCA in autosomal dominant Parkinson's disease in Turkey
C Kessler, B Atasu, H Hanagasi, J Simón-Sánchez, AK Hauser, M Pak, ...
Parkinsonism & related disorders 48, 34-39, 2018
172018
LRRK2 mutations are uncommon in Turkey
HA Hanagasi, E Lohmann, B Dursun, A Honoré, S Lesage, O Dogu, ...
European journal of neurology 18 (10), e137-e137, 2011
122011
Genotype–Phenotype correlations of SCARB2 associated clinical presentation: a case report and in-depth literature review
B Atasu, ANO Acarlı, B Bilgic, B Baykan, E Demir, Y Ozluk, A Turkmen, ...
BMC neurology 22 (1), 122, 2022
32022
BZRAP1 (RIM-BP1) mutations cause a novel autosomal recessive dystonia syndrome
S Pajusalu, NE Mencacci, B Atasu, R Rein, S Puusepp, K Reinson, ...
EUROPEAN JOURNAL OF HUMAN GENETICS 26, 41-41, 2018
12018
Homozygous BZRAP1 Mutations Cause Autosomal Recessive Dystonia (4419)
N Mencacci, M Brockmann, S Pajusalu, B Atasu, PG Latapi, M Schwake, ...
Neurology 94 (15 Supplement), 2020
2020
Frequencies Of Autosomal-recessive Gene Mutations In Turkish Parkinson Patients
B Dursun, E Lohmann, S Lesage, HA Hanagas, G Kayac, H Gürvit, J Yazc, ...
Clinical Genetics 78, 100, 2010
2010
clinic And Genetic Analysis In Five Turkish Families With Restless Legs Syndrome (rls): L20
E Lohmann, H Hanagasi, B Dursun, E Murat, N Unaltuna-erginel, ...
Clinical Genetics 78, 101, 2010
2010
genetic Analysis Of Frequent Lrrk2 Mutations In Turkish Patients With Parkinson Disease: L22
B Dursun, E Lohmann, S Lesage, H Gürvit, J Yazc, N Unaltuna-erginel, ...
Clinical Genetics 78, 101-102, 2010
2010
mutation Analysis In 13 Turkish Patients With Wilson Disease And Identification Of Two Novel Mutations In The: L19atp7b: L19gene: L19
E Lohmann, H Hanagasi, B Dursun, O Dogu, H Kaleagasi, ...
Clinical Genetics 78, 100-101, 2010
2010
LRRK2 Exon 41 mutations are not common in Turkey
HA Hanagasi, E Lohmann, B Dursun, A Honore, S Lesage, O Aydin, ...
MOVEMENT DISORDERS 24, S141-S141, 2009
2009
Autosomal-recessive gene mutation frequencies in Turkish patients with Parkinson's disease
B Dursun, E Lohmann, S Lesage, H Hanagasi, O Aydin, G Babaca, ...
MOVEMENT DISORDERS 24, S137-S138, 2009
2009
OTOZOMAL RESESİF GEÇİŞLİ PARKİNSON HASTALIĞINDA PARKİN (PARK2) GENİ
DRNE ÜNALTUNA, G ORTAK, B DURSUN
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