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Behavioural Brain Research|May 24, 2026
Beyond Atrophy: Network-Level Functional Disintegration Pattern Along the Cognitive Decline in Parkinson's DiseaseUlaş Ay, Ani Kicik, Emel Erdogdu, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|April 15, 2021
A novel PSEN2 p.Ser175Phe variant in a family with Alzheimer's diseaseGamze Guven, Bedia Samanci, Cagri Gulec, et al.Neurobiology of Aging|April 17, 2012
Identification of PSEN1 and PSEN2 gene mutations and variants in Turkish dementia patientsEbba Lohmann, Rita J Guerreiro, Nihan Erginel-Unaltuna, et al.Brain Topography|June 30, 2026
Diffusion-Informed Joint Segmentation Enhances Detection of Thalamic Atrophy in Parkinson's DiseaseGozde Kizilates-Evin, Ani Kicik, Emel Erdogdu, et al.Tremor and Other Hyperkinetic Movements (New York, N.Y.)|April 30, 2016
PLA2G6 Mutations Related to Distinct Phenotypes: A New Case with Early-onset ParkinsonismAnamika Giri, Gamze Guven, Hasmet Hanagasi, et al.Movement Disorders : Official Journal of the Movement Disorder Society|August 27, 2018
HPCA confirmed as a genetic cause of DYT2-like dystonia phenotypeBurcu Atasu, Hasmet Hanagasi, Basar Bilgic, et al.Human Genomics|July 29, 2021
A comprehensive analysis of copy number variation in a Turkish dementia cohortNadia Dehghani, Gamze Guven, Celia Kun-Rodrigues, et al.Parkinsonism & Related Disorders|December 18, 2017
Role of LRRK2 and SNCA in autosomal dominant Parkinson's disease in TurkeyChristoph Kessler, Burcu Atasu, Hasmet Hanagasi, et al.Journal of Parkinson'S Disease|January 25, 2021
Functional Connectivity Analysis in Heterozygous Glucocerebrosidase Mutation CarriersMine Sezgin, Ani Kicik, Basar Bilgic, et al.European Journal of Radiology|October 7, 2021
Detection of visual and frontoparietal network perfusion deficits in Parkinson's disease dementiaSena Azamat, Dilek Betul Arslan, Emel Erdogdu, et al.Pageof 6