Burcu Dursun

Using Exome Sequencing to Reveal Mutations in TREM2 Presenting as a Frontotemporal Dementia–like Syndrome Without Bone Involvement

Rita Guerreiro, Ebba Lohmann, José Brás et al. · JAMA Neurology · 2013 · 386 citations · Full text

Life Sciences, Genetics, Neurology +17

Exome sequencing reveals an unexpected genetic cause of disease: NOTCH3 mutation in a Turkish family with Alzheimer's disease

Rita Guerreiro, Ebba Lohmann, Emma Kinsella et al. · Neurobiology of Aging · 2011 · 108 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Genetic bases and phenotypes of autosomal recessive Parkinson disease in a Turkish population

Ebba Lohmann, Burcu Dursun, Suzanne Lesage et al. · European Journal of Neurology · 2012 · 22 citations

Life Sciences, Genetics, Molecular Genetics +17

A homozygous frameshift mutation of sepiapterin reductase gene causing parkinsonism with onset in childhood

Ebba Lohmann, Çiğdem Köroğlu, Haşmet Hanağası et al. · Parkinsonism & Related Disorders · 2011 · 14 citations

Life Sciences, Genetics, Molecular Genetics +14

Differentiating symptomatic Parkin mutations carriers from patients with idiopathic Parkinson’s disease: Contribution of automated segmentation neuroimaging method

Ali Bayram, Ali Bilgin Arslan, Haşmet Hanağası et al. · Parkinsonism & Related Disorders · 2012 · 12 citations

Life Sciences, Neurology, Neuroscience +16