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 | 400 | 2013 |
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 | 118 | 2012 |
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 | 105 | 2017 |
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 | 36 | 2018 |
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 | 27 | 2012 |
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 | 27 | 2012 |
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 | 23 | 2021 |
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 | 19 | 2012 |
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 | 17 | 2018 |
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 | 12 | 2011 |
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 | 5 | 2022 |
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 | 1 | 2018 |
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 | | |