Association of the C677T and A1298C polymorphisms in the 5, 10 methylenetetrahydrofolate reductase gene in patients with migraine risk I Kara, A Sazci, E Ergul, G Kaya, G Kilic Molecular Brain Research 111 (1-2), 84-90, 2003 | 234 | 2003 |
Detection of cellulolytic fungi by using Congo red as an indicator: a comparative study with the dinitrosalicyclic acid reagent method A Sazci, K Erenler, A Radford Journal of Applied Microbiology 61 (6), 559-562, 1986 | 162 | 1986 |
Methylenetetrahydrofolate reductase gene polymorphisms are associated with ischemic and hemorrhagic stroke: Dual effect of MTHFR polymorphisms C677T and A1298C A Sazci, E Ergul, N Tuncer, G Akpinar, I Kara Brain research bulletin 71 (1-3), 45-50, 2006 | 146 | 2006 |
Genotype and allele frequencies of the polymorphic methylenetetrahydrofolate reductase gene in Turkey A Sazci, E Ergul, G Kaya, I Kara Cell Biochemistry and Function: Cellular biochemistry and its modulation by …, 2005 | 127 | 2005 |
Polymorphisms in the MTHFR gene are associated with breast cancer E Ergul, A Sazci, Z Utkan, NZ Canturk Tumor biology 24 (6), 286-290, 2004 | 116 | 2004 |
Association of apolipoprotein E polymorphisms in patients with non-alcoholic steatohepatitis A Sazci, G Akpinar, C Aygun, E Ergul, O Senturk, S Hulagu Digestive diseases and sciences 53, 3218-3224, 2008 | 106 | 2008 |
Association of the C677T and A1298C polymorphisms of methylenetetrahydrofolate reductase gene with schizophrenia: association is significant in men but not in women A Sazci, E Ergul, I Kucukali, I Kara, G Kaya Progress in Neuro-Psychopharmacology and Biological Psychiatry 29 (7), 1113-1123, 2005 | 80 | 2005 |
Methylenetetrahydrofolate reductase gene polymorphisms in patients with schizophrenia A Sazci, E Ergül, Y Güzelhan, G Kaya, I Kara Molecular Brain Research 117 (1), 104-107, 2003 | 79 | 2003 |
Catechol-O-methyltransferase gene Val108/158Met polymorphism, and susceptibility to schizophrenia: association is more significant in women A Sazci, E Ergul, I Kucukali, G Kilic, G Kaya, I Kara Molecular brain research 132 (1), 51-56, 2004 | 76 | 2004 |
Heteromorphic variants of chromosome 9 N Kosyakova, A Grigorian, T Liehr, M Manvelyan, I Simonyan, ... Molecular cytogenetics 6, 1-11, 2013 | 72 | 2013 |
Evaluation of the angiotensin-converting enzyme insertion/deletion polymorphism and the risk of ischaemic stroke N Tuncer, S Tuglular, G Kılıç, A Sazcı, Ö Us, I Kara Journal of clinical neuroscience 13 (2), 224-227, 2006 | 68 | 2006 |
Methylenetetrahydrofolate reductase gene polymorphisms in patients with nonalcoholic steatohepatitis (NASH) A Sazci, E Ergul, C Aygun, G Akpinar, O Senturk, S Hulagu Cell Biochemistry and Function: Cellular biochemistry and its modulation by …, 2008 | 61 | 2008 |
Effect of the methylenetetrahydrofolate reductase gene polymorphisms on homocysteine, folate and vitamin B12 in patients with bipolar disorder and relatives Z Ozbek, CI Kucukali, E Ozkok, N Orhan, M Aydin, G Kilic, A Sazci, I Kara Progress in Neuro-Psychopharmacology and Biological Psychiatry 32 (5), 1331-1337, 2008 | 60 | 2008 |
Association of the C677T and A1298C polymorphisms of methylenetetrahydrofolate reductase gene in patients with essential tremor in Turkey A Sazci, E Ergul, K Bayulkem Movement Disorders 19 (12), 1472-1476, 2004 | 44 | 2004 |
Catechol-O-methyltransferase Val 108/158 Met polymorphism in premenopausal breast cancer patients A Sazci, E Ergul, NZ Utkan, NZ Canturk, G Kaya Toxicology 204 (2-3), 197-202, 2004 | 43 | 2004 |
Liposome-mediated genetic transformation of Neurospora crassa A Radford, S Pope, A Sazci, MJ Fraser, JH Parish Molecular and General Genetics MGG 184, 567-569, 1981 | 42 | 1981 |
Association of the nibrin gene (NBN) variants with breast cancer H Uzunoglu, T Korak, E Ergul, N Uren, A Sazci, NZ Utkan, E Kargi, ... Biomedical reports 4 (3), 369-373, 2016 | 35 | 2016 |
Association of nicotinamide-N-methyltransferase gene rs694539 variant with patients with nonalcoholic steatohepatitis A Sazci, MD Ozel, E Ergul, C Aygun Genetic testing and molecular biomarkers 17 (11), 849-853, 2013 | 35 | 2013 |
Using global team science to identify genetic Parkinson’s disease worldwide EJ Vollstedt, M Kasten, C Klein Annals of neurology 86 (2), 153, 2019 | 29 | 2019 |
Association of nicotinamide-N-methyltransferase (NNMT) gene rs694539 variant with bipolar disorder A Sazci, MD Ozel, E Ergul, ME Onder Gene 532 (2), 272-275, 2013 | 23 | 2013 |