| A new subtype of brachydactyly type B caused by point mutations in the bone morphogenetic protein antagonist NOGGIN K Lehmann, P Seemann, F Silan, TO Goecke, S Irgang, KW Kjaer, ... The American Journal of Human Genetics 81 (2), 388-396, 2007 | 129 | 2007 |
| A new mutation of the fukutin gene in a non‐Japanese patient F Silan, M Yoshioka, K Kobayashi, E Simsek, M Tunc, M Alper, M Cam, ... Annals of Neurology: Official Journal of the American Neurological …, 2003 | 122 | 2003 |
| SALL4 deletions are a common cause of Okihiro and acro-renal-ocular syndromes and confirm haploinsufficiency as the pathogenic mechanism W Borozdin, D Boehm, M Leipoldt, C Wilhelm, W Reardon, ... Journal of medical genetics 41 (9), e113-e113, 2004 | 101 | 2004 |
| Protective effect of melatonin on β-cell damage in streptozotocin-induced diabetes in rats O Yavuz, M Cam, N Bukan, A Guven, F Silan Acta histochemica 105 (3), 261-266, 2003 | 101 | 2003 |
| Recurrent pregnancy loss and its relation to combined parental thrombophilic gene mutations O Ozdemir, GI Yenicesu, F Silan, B Köksal, S Atik, F Ozen, M Göl, A Cetin Genetic Testing and Molecular Biomarkers 16 (4), 279-286, 2012 | 100 | 2012 |
| The genomics of arthrogryposis, a complex trait: candidate genes and further evidence for oligogenic inheritance D Pehlivan, Y Bayram, N Gunes, ZC Akdemir, A Shukla, T Bierhals, ... The American Journal of Human Genetics 105 (1), 132-150, 2019 | 84 | 2019 |
| Vitamin D receptor gene BSMI, FOKI, APAI, and TAQI polymorphisms and the risk of atopic dermatitis. S Kılıç, F Sılan, MM Hız, S Işık, Z Ögretmen, Ö Özdemir Journal of investigational allergology & clinical immunology 26 (2), 106-110, 2016 | 49 | 2016 |
| The prevelance of human papillomavirus (HPV) genotypes detected by PCR in women with normal and abnormal cervico-vaginal cytology F Beyazit, F Sılan, M Gencer, B Aydin, B Paksoy, MA Unsal, O Ozdemir Ginekologia polska 89 (2), 62-67, 2018 | 43 | 2018 |
| Etiology of deafness at the Yeditepe school for the deaf in Istanbul E Egeli, G Çiçekci, F Silan, Ö Öztürk, U Harputluoğlu, A Onur, A Egeli, ... International journal of pediatric otorhinolaryngology 67 (5), 467-471, 2003 | 42 | 2003 |
| Evaluation of deaf children in a large series in Turkey O Ozturk, F Silan, F Oghan, E Egeli, S Belli, A Tokmak, A Egeli, ... International journal of pediatric otorhinolaryngology 69 (3), 367-373, 2005 | 40 | 2005 |
| Association between ABCB1 (MDR1) Gene 3435 C>T Polymorphism and Colchicine Unresponsiveness of FMF Patients F Ozen, C Silan, A Uludag, F Candan, F Silan, S Ozdemir, S Atik, ... Renal failure 33 (9), 899-903, 2011 | 33 | 2011 |
| Effects of CYP2C19 and P2Y12 gene polymorphisms on clinical results of patients using clopidogrel after acute ischemic cerebrovascular disease HM Sen, F Silan, Y Degirmenci, OHI Kamaran Balkan Journal of Medical Genetics 17 (2), 37-41, 2014 | 32 | 2014 |
| Association between FokI, ApaI and TaqI RFLP polymorphisms in VDR gene and Hashimoto's thyroiditis: preliminary data from female patients in Serbia J Djurovic, O Stojkovic, O Ozdemir, F Silan, C Akurut, J Todorovic, K Savic, ... International Journal of Immunogenetics 42 (3), 190-194, 2015 | 31 | 2015 |
| Congenital sialoblastoma (embryoma) associated with premature centromere division and high level of alpha‐fetoprotein I Ozdemir, E Simsek, F Silan, F Demirci Prenatal diagnosis 25 (8), 687-689, 2005 | 31 | 2005 |
| The relationship between obstructive sleep apnea syndrome and apolipoprotein E genetic variants E Uyrum, O Balbay, AN Annakkaya, E Gulec Balbay, F Silan, P Arbak Respiration 89 (3), 195-200, 2015 | 29 | 2015 |
| Germ-line MTHFR C677T, FV H1299R and PAI-1 5G/4G variations in breast carcinoma F ÖZEN, EDA ERDİŞ, E Sik, F Silan, A ULUDAĞ, Ö ÖZDEMİR Asian Pacific Journal of Cancer Prevention 14 (5), 2013 | 27 | 2013 |
| Syndromic etiology in children at schools for the deaf in Turkey F Silan, L Demirci, A Egeli, E Egeli, HI Onder, O Ozturk, ZS Unal International journal of pediatric otorhinolaryngology 68 (11), 1399-1406, 2004 | 26 | 2004 |
| Endothelial function and germ-line ACE I/D, eNOS and PAI-1 gene profiles in patients with coronary slow flow in the Canakkale population: multiple thrombophilic gene profiles … E Gazi, A Temiz, B Altun, A Barutcu, F Silan, Y Colkesen, O Ozdemir Cardiovascular journal of Africa 25 (1), 9-14, 2014 | 24 | 2014 |
| MPZL2 is a novel gene associated with autosomal recessive nonsyndromic moderate hearing loss G Bademci, C Abad, A Incesulu, A Rad, O Alper, SM Kolb, FB Cengiz, ... Human genetics 137, 479-486, 2018 | 23 | 2018 |
| Multiple inherited thrombophilic gene polymorphisms in spontaneous abortions in Turkish population S Yalcintepe, O Ozdemir, SO Hacivelioglu, C Akurut, E Koc, A Uludag, ... International Journal of Molecular and Cellular Medicine 4 (2), 120, 2015 | 23 | 2015 |
