| Consanguineous marriages in the province of Antalya, Turkey ÖM Alper, H Erengin, AE Manguoğlu, T Bilgen, Z Cetin, N Dedeoğlu, ... Annales de génétique 47 (2), 129-138, 2004 | 103 | 2004 |
| Mutational spectrum of MYO15A: the large N‐terminal extension of myosin XVA is required for hearing N Nal, ZM Ahmed, E Erkal, ÖM Alper, G Lüleci, O Dinç, AM Waryah, Q Ain, ... Human mutation 28 (10), 1014-1019, 2007 | 99 | 2007 |
| Novel insights into c-Src O Alper, ET Bowden Current pharmaceutical design 11 (9), 1119-1130, 2005 | 70 | 2005 |
| Mutation spectrum of the CFTR gene in Taiwanese patients with congenital bilateral absence of the vas deferens CC Wu, ÖM Alper, JF Lu, SP Wang, L Guo, HS Chiang, LJC Wong Human Reproduction 20 (9), 2470-2475, 2005 | 61 | 2005 |
| Recent advances in craniosynostosis E Yilmaz, E Mihci, B Nur, ÖM Alper, Ş Taçoy Pediatric Neurology 99, 7-15, 2019 | 49 | 2019 |
| Identification of novel and rare mutations in California Hispanic and African American cystic fibrosis patients ÖM Alper, LJC Wong, S Young, M Pearl, S Graham, J Sherwin, ... Human Mutation 24 (4), 353-353, 2004 | 46 | 2004 |
| Simultaneous suppression of epidermal growth factor receptor and c-erbB-2 reverses aneuploidy and malignant phenotype of a human ovarian carcinoma cell line SD Pack, OM Alper, K Stromberg, M Augustus, M Ozdemirli, AM Miermont, ... Cancer research 64 (3), 789-794, 2004 | 44 | 2004 |
| Protein kinase A-Iα subunit-directed antisense inhibition of ovarian cancer cell growth: crosstalk with tyrosine kinase signaling pathway OÈ Alper, NF Hacker, YS Cho-Chung Oncogene 18 (35), 4999-5004, 1999 | 39 | 1999 |
| A cystic fibrosis patient with two novel mutations in mitochondrial DNA: mild disease led to delayed diagnosis of both disorders LJC Wong, MH Liang, H Kwon, RK Bai, Ö Alper, A Gropman American journal of medical genetics 113 (1), 59-64, 2002 | 31 | 2002 |
| Clinicogenetic study of Turkish patients with syndromic craniosynostosis and literature review BG Nur, S Pehlivanoğlu, E Mıhçı, M Çalışkan, D Demir, ÖM Alper, ... Pediatric Neurology 50 (5), 482-490, 2014 | 27 | 2014 |
| Two novel null mutations in a Taiwanese cystic fibrosis patient and a survey of East Asian CFTR mutations LJC Wong, ÖM Alper, BT Wang, MH Lee, SY Lo American Journal of Medical Genetics Part A 120 (2), 296-298, 2003 | 26 | 2003 |
| Renkli genetik atlası E Passarge, G Lüleci, M Sakızlı, Ö Alper Nobel Tıp Kitapevleri, 2009 | 25 | 2009 |
| The necessity of complete CFTR mutational analysis of an infertile couple before in vitro fertilization LJC Wong, ÖM Alper, E Hsu, MS Woo, MF Margetis Fertility and sterility 82 (4), 947-949, 2004 | 25 | 2004 |
| Detection of CFTR mutations using temporal temperature gradient gel electrophoresis LJC Wong, ÖM Alper Electrophoresis 25 (15), 2593-2601, 2004 | 20 | 2004 |
| Maternal Serum Screening for Downs Syndrome, Open Neural Tube Defects and Trisomy 18 SH Akbas, T Özben, Ö Alper, A Ugur, G Yücel, G Lüleci Walter de Gruyter 39 (6), 487-490, 2001 | 16 | 2001 |
| Renkli genetik atlası G Lüleci, M Sakızlı, Ö Alper Ġstanbul, Nobel Tıp Kitapevi, 2000 | 14 | 2000 |
| Mitochondrial ATPase subunit 6 and cytochrome B gene variations in obese Turkish children D Demir, D Türkkahraman, AA Samur, G Lüleci, S Akçurin, ÖM Alper Journal of clinical research in pediatric endocrinology 6 (4), 209, 2014 | 8 | 2014 |
| Normal sweat chloride test does not rule out cystic fibrosis AE Başaran, N Karataş-Torun, İC Maslak, A Bingöl, ÖM Alper The Turkish Journal of Pediatrics 59 (1), 68-70, 2017 | 7 | 2017 |
| Initial regional evaluation of the Cystic Fibrosis Newborn Screening Program: data from the Mediterranean coast of Turkey AE Başaran, A Başaran, DF Kocacik, Ö Alper, D Acican, A Bingöl Turkish journal of medical sciences 49 (6), 1655-1661, 2019 | 5 | 2019 |
| Molecular diagnosis of hematological malignancies by RT-PCR. S Berker-Karaüzüm, A Manguoğlu, N Nal, S Yakut, CF Sargin, Ö Alper, ... Turkish Journal of Cancer 35 (3), 2005 | 5 | 2005 |
