| Year |
Citation |
Score |
| 2021 |
Vural A, Şimşir G, Tekgül Ş, Koçoğlu C, Akçimen F, Kartal E, Şen NE, Lahut S, Ömür Ö, Saner N, Gül T, Bayraktar E, Palvadeau R, Tunca C, Pirkevi Çetinkaya C, et al. The Complex Genetic Landscape of Hereditary Ataxias in Turkey and Implications in Clinical Practice. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 33624863 DOI: 10.1002/mds.28518 |
0.448 |
|
| 2017 |
Lahut S, Gispert S, Ömür Ö, Depboylu C, Seidel K, Domínguez-Bautista JA, Brehm N, Tireli H, Hackmann K, Pirkevi C, Leube B, Ries V, Reim K, Brose N, den Dunnen WF, et al. Blood RNA biomarkers in prodromal PARK4 and REM sleep behavior disorder show role of complexin-1 loss for risk of Parkinson's disease. Disease Models & Mechanisms. PMID 28108469 DOI: 10.1242/Dmm.028035 |
0.481 |
|
| 2015 |
Özo?uz A, Uyan Ö, Birdal G, Iskender C, Kartal E, Lahut S, Ömür Ö, Agim ZS, Eken AG, Sen NE, Kavak P, Sayg? C, Sapp PC, Keagle P, Parman Y, et al. The distinct genetic pattern of ALS in Turkey and novel mutations. Neurobiology of Aging. 36: 1764.e9-18. PMID 25681989 DOI: 10.1016/J.Neurobiolaging.2014.12.032 |
0.414 |
|
| 2014 |
Lahut S, Vadasz D, Depboylu C, Ries V, Krenzer M, Stiasny-Kolster K, Basak AN, Oertel WH, Auburger G. The PD-associated alpha-synuclein promoter Rep1 allele 2 shows diminished frequency in restless legs syndrome. Neurogenetics. 15: 189-92. PMID 24863655 DOI: 10.1007/S10048-014-0407-Z |
0.585 |
|
| 2012 |
Lahut S, Ömür Ö, Uyan Ö, Ağım ZS, Özoğuz A, Parman Y, Deymeer F, Oflazer P, Koç F, Özçelik H, Auburger G, Başak AN. ATXN2 and its neighbouring gene SH2B3 are associated with increased ALS risk in the Turkish population. Plos One. 7: e42956. PMID 22916186 DOI: 10.1371/Journal.Pone.0042956 |
0.471 |
|
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