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Genes that affect brain structure and function identified by rare variant analyses of Mendelian neurologic disease E Karaca, T Harel, D Pehlivan, SN Jhangiani, T Gambin, ZC Akdemir, ... Neuron 88 (3), 499-513, 2015 | 295 | 2015 |
CEP290 mutations are frequently identified in the oculo-renal form of Joubert syndrome–related disorders F Brancati, G Barrano, JL Silhavy, SE Marsh, L Travaglini, SL Bielas, ... The American Journal of Human Genetics 81 (1), 104-113, 2007 | 227 | 2007 |
Human CLP1 mutations alter tRNA biogenesis, affecting both peripheral and central nervous system function E Karaca, S Weitzer, D Pehlivan, H Shiraishi, T Gogakos, T Hanada, ... Cell 157 (3), 636-650, 2014 | 222* | 2014 |
Mutations in the voltage-gated potassium channel gene KCNH1 cause Temple-Baraitser syndrome and epilepsy C Simons, LD Rash, J Crawford, L Ma, B Cristofori-Armstrong, D Miller, ... Nature genetics 47 (1), 73-77, 2015 | 149 | 2015 |
Evidence that membrane‐bound G protein‐coupled melatonin receptors MT1 and MT2 are not involved in the neuroprotective effects of melatonin in focal cerebral ischemia U Kilic, B Yilmaz, M Ugur, A Yüksel, RJ Reiter, DM Hermann, E Kilic Journal of pineal research 52 (2), 228-235, 2012 | 137 | 2012 |
The effects of carbamazepine and valproic acid on the erythrocyte glutathione, glutathione peroxidase, superoxide dismutase and serum lipid peroxidation in epileptic children M CENGIZ, A YÜKSEL, M Seven Pharmacological Research 41 (4), 423-425, 2000 | 128 | 2000 |
Erythrocyte glutathione, glutathione peroxidase, superoxide dismutase and serum lipid peroxidation in epileptic children with valproate and carbamazepine monotherapy A Yiiksel, M Cengiz, M Seven, T Ulutin Journal of basic and clinical physiology and pharmacology 11 (1), 73-81, 2000 | 99 | 2000 |
Deficiency of selenium and zinc as a causative factor for idiopathic intractable epilepsy M Seven, SY Basaran, M Cengiz, S Unal, A Yuksel Epilepsy research 104 (1-2), 35-39, 2013 | 82 | 2013 |
Effects of memantine and melatonin on signal transduction pathways vascular leakage and brain injury after focal cerebral ischemia in mice U Kilic, B Yilmaz, RJ Reiter, A Yüksel, E Kilic Neuroscience 237, 268-276, 2013 | 79 | 2013 |
Changes in the antioxidant system in epileptic children receiving antiepileptic drugs: two-year prospective studies A Yüksel, M Cengiz, M Seven, T Ulutin Journal of Child Neurology 16 (8), 603-606, 2001 | 78 | 2001 |
Body mass index and complications following major gastrointestinal surgery: a prospective, international cohort study and meta‐analysis EuroSurg Collaborative, R Blanco‐Colino, S Lee, SK Kamarajah, P Vasko, ... Colorectal Disease 20 (8), O215-O225, 2018 | 56 | 2018 |
The drug-transporter gene MDR1 C3435T and G2677T/A polymorphisms and the risk of multidrug-resistant epilepsy in Turkish children M Seven, B Batar, S Unal, G Yesil, A Yuksel, M Guven Molecular biology reports 41, 331-336, 2014 | 45 | 2014 |
Neuroimaging findings of four patients with Sandhoff disease A Yüksel, C Yalçınkaya, C Işlak, E Gündüz, M Seven Pediatric neurology 21 (2), 562-565, 1999 | 44 | 1999 |
Polymorphisms of the DNA repair genes XPD and XRCC1 and the risk of age-related macular degeneration E Görgün, M Güven, M Ünal, B Batar, GS Güven, M Yenerel, S Tatlıpınar, ... Investigative Ophthalmology & Visual Science 51 (9), 4732-4737, 2010 | 42 | 2010 |
Serum thyroid hormones and pituitary response to thyrotropin‐releasing hormone in epileptic children receiving anti‐epileptic medication A Yüksel, A KARTAL, A CENANI, E YALÇIN Pediatrics International 35 (2), 108-112, 1993 | 41 | 1993 |
Molecular genetic screening of MBS1 locus on chromosome 13 for microdeletions and exclusion of FGF9, GSH1 and CDX2 as causative genes in patients with Moebius syndrome A Uzumcu, B Karaman, G Toksoy, ZO Uyguner, S Candan, H Eris, B Tatli, ... European journal of medical genetics 52 (5), 315-320, 2009 | 35 | 2009 |
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Glutathione S-Transferase M1, GSTT1 and GSTP1 Genetic Polymorphisms and the Risk of Age-Related Macular Degeneration M Güven, E Görgün, M Ünal, M Yenerel, B Batar, B Küçümen, UA Dinç, ... Ophthalmic research 46 (1), 31-37, 2011 | 32 | 2011 |