| Detection of Y chromosome microdeletions and mitochondrial DNA mutations in male infertility patients A Guney, D Javadova, D Kirac, K Ulucan, G Koc, D Ergec, H Tavukcu, ... Genetics and Molecular Research 11 (2), 2012 | 67 | 2012 |
| Obeziteyle ilişkili beslenme alışkanlıklarının araştırılmasında yeni bir yöntem “Üç faktörlü beslenme anketi” D Kıraç, EÇ Kaspar, T Avcılar, ÖK Çakır, K Ulucan, H Kurtel, O Deyneli, ... Clinical and Experimental Health Sciences 5 (3), 162-169, 2015 | 55 | 2015 |
| Multifactor dimensionality reduction analysis of MTHFR, PAI-1, ACE, PON1, and eNOS gene polymorphisms in patients with early onset coronary artery disease M Agirbasli, AI Guney, HS Ozturhan, D Agirbasli, K Ulucan, D Sevinc, ... European Journal of Cardiovascular Prevention & Rehabilitation 18 (6), 803-809, 2011 | 53 | 2011 |
| Effects of ACE polymorphisms and other risk factors on the severity of coronary artery disease AI Guney, D Ergec, D Kirac, H Ozturhan, M Caner, G Koc, C Kaspar, ... Genet Mol Res 12 (4), 6895-6906, 2013 | 51 | 2013 |
| Lack of SCN1A mutations in familial febrile seizures M Malacarne, F Madia, E Gennaro, D Vacca, AI Güney, S Buono, ... Epilepsia 43 (5), 559-562, 2002 | 40 | 2002 |
| Detection of mitochondrial DNA mutations in nonmuscle invasive bladder cancer AI Guney, DS Ergec, HH Tavukcu, G Koc, D Kirac, K Ulucan, D Javadova, ... Genetic Testing and Molecular Biomarkers 16 (7), 672-678, 2012 | 39 | 2012 |
| New candidate chromosomal regions for chordoma development F Bayrakli, I Guney, T Kilic, M Ozek, MN Pamir Surgical neurology 68 (4), 425-430, 2007 | 37 | 2007 |
| Preliminary findings of α-actinin-3 gene distribution in elite Turkish wind surfers K Ulucan, S Göle, N Altindas, AI Güney Balkan journal of medical genetics 16 (1), 69-72, 2013 | 33 | 2013 |
| Effects of PAX9 and MSX1 gene variants to hypodontia, tooth size and the type of congenitally missing teeth D Kirac, F Eraydin, T Avcilar, K Ulucan, AI Guney, E Keshi, T Isbir Cellular and Molecular Biology 62 (13), 78-84, 2016 | 31 | 2016 |
| A novel heterozygous deletion within the 3’region of the PAX6 gene causing isolated aniridia in a large family group F Bayrakli, I Guney, Y Bayri, AG Ercan-Sencicek, D Ceyhan, T Cankaya, ... Journal of Clinical Neuroscience 16 (12), 1610-1614, 2009 | 31 | 2009 |
| Effect of alpha-actinin-3 gene on trained and untrained Turkish middle-school children’s sprinting performance: a pilot study K Ulucan, GM Bayyurt, M Konuk, AI Güney Biological Rhythm Research 45 (4), 509-514, 2014 | 25 | 2014 |
| Genetic diagnosis in infertile men with numerical and constitutional sperm abnormalities Ç Çinar, C Yazıcı, Ş Ergünsu, Ç Beyazyürek, D Javadova, Y Sağlam, ... Genetic testing 12 (2), 195-202, 2008 | 24 | 2008 |
| The frequency and the effects of 21‐hydroxylase gene defects in congenital adrenal hyperplasia patients D Kirac, AI Guney, T Akcay, T Guran, K Ulucan, S Turan, D Ergec, G Koc, ... Annals of Human Genetics 78 (6), 399-409, 2014 | 23 | 2014 |
| Effects of MC4R, FTO, and NMB gene variants to obesity, physical activity, and eating behavior phenotypes D Kirac, O Kasimay Cakir, T Avcilar, O Deyneli, H Kurtel, D Yazici, ... IUBMB life 68 (10), 806-816, 2016 | 21 | 2016 |
| İlköğretim okulu öğrencilerinin akademik başarıları ile algılanan aile yapısı arasındaki ilişkilerin incelenmesi A Güney Sosyal Bilimler Enstitüsü, 2009 | 21 | 2009 |
| A new method in investigation of obesity-related eating behaviors' three-factor eating questionnaire' D Kiraç, EÇ Kaspar, T Avcilar, OK Çakir, K Ulucan, H Kurtel, O Deyneli, ... Clinical and Experimental Health Sciences 5 (3), 162, 2015 | 19 | 2015 |
| Her-2/neu gene amplification compared with HER-2/neu protein overexpression on ultrasound guided core-needle biopsy specimens of breast carcinoma H Kaya, T Ragazzini, E Aribal, Ý Güney, E Kotilođlu Pathology & Oncology Research 7, 279-283, 2001 | 19 | 2001 |
| Male infertility in Sertoli cell‐only syndrome: an investigation of autosomal gene defects G Koc, AA Ozdemir, G Girgin, C Akbal, D Kirac, T Avcilar, AI Guney International Journal of Urology 26 (2), 292-298, 2019 | 18 | 2019 |
| Autosomal Recessive Idiopathic Epilepsy in an Inbred Family from Turkey: Identification of a Putative Locus on Chromosome 9q32‐33 B Baykan, F Madia, N Bebek, S Gianotti, AI Güney, N Cine, A Bianchi, ... Epilepsia 45 (5), 479-487, 2004 | 16 | 2004 |
| Effect of MDR1 polymorphisms on the blood concentrations of tacrolimus in Turkish renal transplant patients HS Ciftci, TK Ayna, YK Caliskan, I Guney, H Bakkaloglu, I Nane, AE Aydin, ... Transplantation proceedings 45 (3), 895-900, 2013 | 15 | 2013 |
