Publications & Works

Published journal articles indexed by SCI, SSCI, and AHCI

Articles Published in Other Journals

Refereed Congress / Symposium Publications in Proceedings

Cerebellocerebral and striatocortical functional connectivity changes during implicit associative learning

2nd Joint German-Turkish Symposium on Human Neuroscience (1. Nörogörüntüleme Kongresi kapsamında), Ankara, Turkey, 7 - 09 September 2023

Analysis of copy number variation in a Turkish dementia cohort

Alzheimer's Association International Conference (AAIC) , 27 - 31 July 2020, pp.44868

Alzheı̇mer süreklı̇lı̇ğı̇nde kortikal kalınlık değişimleri

56. Ulusal Nöroloji Kongresi, İstanbul, Turkey, 28 November - 02 December 2020, pp.132 Sustainable Development

Cholesterol related gene polymorphisms in Alzheimer Disease

European Human Genetics Conference 2018, Milan, Italy, 16 - 19 June 2018, pp.1

Cholesterol related gene polymorphisms in Alzheimer Disease

51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG), Milan, Italy, 16 - 19 June 2018, vol.27, pp.958 identifier

TÜRK DEMANS HASTALARINDA FRONTO-TEMPORAL DEMANS İLE İLİŞKİLİ BAŞLICA GENLERDEKİ MUTASYON SIKLIĞI

Uluslararası Katılımlı 13. Ulusal Tıbbi Genetik Kongresi, Antalya, Turkey, 7 - 11 November 2018, pp.142

Cerebrotendinous Xanthomatosis: A Rare Lipid Storage Disease

International Congress of Parkinson's Disease and Movement Disorders, Hong Kong, Hong Kong, 5 - 09 October 2018 identifier

Catatonia as clinical presentation of anti-n-methyl-d-aspartate (anti-NMDA) receptor encephalitis.

Alzheimer’s Association International Conference, Illinois, United States Of America, 22 - 26 July 2018, pp.1467-1468

Geç Tanı Erişkin Mukopolisakkaridozis Tip 1 Olgusu

VI. Uluslararası Katılımlı Lizozomal Hastalıklar Kongresi, Turkey, 11 - 15 April 2018

Resting-state Networks in Adult Patients with Attention Deficit Hyperactivity Disorder

23nd Annual Meeting of the Organization for Human Brain Mapping, Vancouver, Canada, 25 - 29 June 2017, pp.91

Video-Oculography Assessment in Neurodegenerative Ataxias and Neimann Pick Type C

21st International Congress of Parkinson's Disease and Movement Disorders, Vancouver, Canada, 4 - 08 June 2017 identifier

Diffusion discriminant for mild cognitive impairment in Parkinson’s disease

International Society of Magnetic Resonance in Medicine Annual Conference, Honolulu, Hı, United States Of America, 22 - 27 April 2017, pp.1

EFFECTS OF VARIOUS GRN VARIANTS ON MRNA AND SERUM PGRN LEVEL

3th International Conference on Alzheimer’s and Parkinson’s Diseases, Viyana, Austria, 29 March - 02 April 2017, pp.1674

GRN c.708 + 1_+4del TGAG deletion in a large family diagnosed with fronto-temporal dementia

10th International Conference on Frontotemporal Dementias, Münih, Germany, 31 August - 02 September 2016, vol.138, pp.323

GRN c.708+1_+4del TGAG deletion in a large family diagnosed with fronto-temporal dementia

10th International Conference on Frontotemporal Dementias, Munich, Germany, 31 August - 02 September 2016, pp.323 identifier

Clusterin polimorfizmleri ile geç başlangıçlı Alzheimer hastalığı arasındaki ilişki.

14. Ulusal Tıbbi Biyoloji ve Genetik Kongresi, Muğla, Turkey, 27 - 30 October 2015, vol.1, no.1, pp.1

PSEN1 mutation presenting as posterior cortical atrophy

22nd World Congress of Neurology (WCN), Santiago, Chile, 31 October - 05 November 2015, vol.357 identifier

Compromised Regulation of Serum Cytokine Levels and BDNF Due to Low Levels of Vitamin D in Patients with Early or Late Onset Alzheimer’s Disease or Parkinson’s Disease.

Alzheimer’s Association International Conference (AAIC 2015), 17-23 July, 2015 Washington, USA, Washington, United States Of America, 17 - 23 July 2015, pp.1-2

Association Between Clusterin Polymorphisms and Alzheimer’s Disease.

Alzheimer’s Association International Conference (AAIC 2015), 17-23 July, 2015 Washington, USA, Washington, United States Of America, 17 - 23 July 2015, pp.1

Anti-NMDA receptor encephalitis with cancer of unknown primary origin

1st Congress of the European-Academy-of-Neurology, Berlin, Germany, 20 - 23 June 2015, vol.22, pp.526 Sustainable Development identifier

Secondary paroxysmal kinesigenic dyskinesia associated with CLCN2 gene mutation

19th International Congress of Parkinson's Disease and Movement Disorders, California, United States Of America, 14 - 18 June 2015, vol.30 identifier

Adult onset phenylketonuria with rapidly progressive dementia and Parkinsonism

19th International Congress of Parkinson's Disease and Movement Disorders, California, United States Of America, 14 - 18 June 2015, vol.30 identifier

The distinct genetic pattern of ALS in Turkey

Joint Congress of European Neurology, İstanbul, Turkey, 31 May - 03 June 2014, vol.21, pp.63 identifier

Testing of diagnostic criteria for mild cognitive impairment in patients with Parkinson's disease

18th International Congress of Parkinson's Disease and Movement Disorders, Stockholm, Sweden, 8 - 12 June 2014, vol.29 identifier

The distinct genetic pattern of ALS in Turkey

Joint Congress of European Neurology, İstanbul, Turkey, 31 May - 03 June 2014, vol.261 identifier

TREM2 MUTATIONS: RISK FACTOR FOR ALZHEIMER'S DISEASE AND NEW GENETIC CAUSE FOR FAMILIAL FRONTOTEMPORAL LOBAR DEGENERATION

6th International Conference on Alzheimers Disease and Related Disorders in the Middle East, İstanbul, Turkey, 25 - 27 October 2013, vol.35, pp.718 identifier

Serum complement factor H levels in late onset Alzheimer's disease

38th Congress of the Federation-of-European-Biochemical-Societies (FEBS), Saint Peter, Guernsey And Alderney, 6 - 11 July 2013, vol.280, pp.430 identifier

Investigation of SORL1 variants in a Turkish cohort of dementia patients

European Society of Human Genetics Congress, Paris, France, 8 - 11 June 2013, vol.21, pp.219

DYSEXECUTIVE SYNDROME; A SPECIFIC PATTERN OF COGNITIVE IMPAIRMENT IN SSc

2nd Systemic Sclerosis World Congress, Madrid, Spain, 2 - 04 February 2012, vol.51, pp.47-48 identifier

Clinical Features of the "Optineurin" Mutation in familial FTD and ALS

8th International Conference on Frontotemporal Dementias, Manchester, United Kingdom, 5 - 07 September 2012, vol.33, pp.231 identifier

Alzheimer Hastalığı ile İnterlökin-6 Promotör ve VNTR Polimorfizmleri Arasındaki İlişkinin Araştırılması

XI. ULUSAL TIBBİ BİYOLOJİ VE GENETİK KONGRESİ, Antalya, Turkey, 1 - 04 October 2011, vol.31, no.6, pp.161-162

Autosomal-recessive gene mutation frequencies in Turkish patients with Parkinson's disease

13th International Congress of Parkinsons Disease and Movement Disorders, Paris, France, 7 - 11 June 2009, vol.24 identifier

LRRK2 Exon 41 mutations are not common in Turkey

13th International Congress of Parkinsons Disease and Movement Disorders, Paris, France, 7 - 11 June 2009, vol.24 identifier

Event-related brain oscillations associated with color-word interference

10th International Conference on Cognitive Neuroscience, Muğla, Turkey, 1 - 05 September 2008, pp.146 Creative Commons License

Long-term cognitive effect of SCUBA diving

Cognitive V, International Cognitive Neuroscience Meeting, Muğla, Turkey, 17 - 21 May 2008, vol.3, no.2, pp.113 Creative Commons License

Ataxia with vitamin E deficiency in Turkey

12th International Congress of Parkinsons Disease and Movement Disorders, Illinois, United States Of America, 22 - 26 June 2008, vol.23