| The Arg753GLn polymorphism of the human toll-like receptor 2 gene in tuberculosis disease AC Ogus, B Yoldas, T Ozdemir, A Uguz, S Olcen, I Keser, M Coskun, ... European Respiratory Journal 23 (2), 219-223, 2004 | 556 | 2004 |
| Normal phenotype with maternal isodisomy in a female with two isochromosomes: i (2p) and i (2q) F Bernasconi, A Karagüzel, F Celep, I Keser, G Lüleci, F Dutly, ... American journal of human genetics 59 (5), 1114, 1996 | 77 | 1996 |
| The effect of MDR1 (ABCB1) polymorphism on the pharmacokinetic of tacrolimus in Turkish renal transplant recipients SH Akbas, T Bilgen, I Keser, M Tuncer, L Yucetin, O Tosun, M Gultekin, ... Transplantation proceedings 38 (5), 1290-1292, 2006 | 58 | 2006 |
| The effect of CYP1A2 gene polymorphisms on Theophylline metabolism and chronic obstructive pulmonary disease in Turkish patients A Uslu, C Ogus, T ÖZDEMİR, T Bilgen, O Tosun, I Keser BMB reports 43 (8), 2010 | 57 | 2010 |
| Evaluation of congenital heart diseases and thyroid abnormalities in children with Down syndrome. E Mıhçı, G Akçurin, E Eren, F Kardelen, S Akçurin, İ Keser, H Ertuğ Anatolian Journal of Cardiology/Anadolu Kardiyoloji Dergisi 10 (5), 2010 | 49 | 2010 |
| Clinical evaluation of R202Q alteration of MEFV genes in Turkish children E Comak, S Akman, M Koyun, CS Dogan, AU Gokceoglu, Y Arikan, ... Clinical rheumatology 33, 1765-1771, 2014 | 47 | 2014 |
| Molecular analysis of beta-thalassemia and sickle cell anemia in Antalya I Keser, AD Sanlioglu, E Manguoglu, O Guzeloglu Kayisli, N Nal, F Sargin, ... Acta haematologica 111 (4), 205-210, 2004 | 43 | 2004 |
| MEFV gene mutations in Turkish children with juvenile idiopathic arthritis E Comak, CS Dogan, S Akman, M Koyun, AU Gokceoglu, I Keser European journal of pediatrics 172, 1061-1067, 2013 | 41 | 2013 |
| Effects of hormone replacement therapy on bone mineral density in Turkish patients with or without COL1A1 Sp1 binding site polymorphism M Simsek, Z Cetin, T Bilgen, O Taskin, G Luleci, I Keser Journal of Obstetrics and Gynaecology Research 34 (1), 73-77, 2008 | 36 | 2008 |
| The association between intragenic SNP haplotypes and mutations of the beta globin gene in a Turkish population T Bilgen, Y Arikan, D Canatan, A Yeşilipek, I Keser Blood Cells, Molecules, and Diseases 46 (3), 226-229, 2011 | 31 | 2011 |
| Prenatal diagnosis of β-thalassemia and other hemoglobinopathies in southwestern Turkey I Mendilcioglu, S Yakut, I Keser, M Simsek, A Yesilipek, G Bagci, G Luleci Hemoglobin 35 (1), 47-55, 2011 | 27 | 2011 |
| Psychological effects of amniocentesis on women and their spouses: importance of the testing period and genetic counseling K Kukulu, K Buldukoglu, İ Keser, İ Keser, M Şi˙ mŞek, İÇ Mendi˙ lci˙ oĞlu, ... Journal of Psychosomatic Obstetrics & Gynecology 27 (1), 9-15, 2006 | 26 | 2006 |
| Germline hMSH2and hMLH1 gene mutations in incomplete HNPCC families Q Wang, F Desseigne, C Lasset, JC Saurin, C Navarro, T Yagci, I Keser, ... International journal of cancer 73 (6), 831-836, 1997 | 26 | 1997 |
| Sitogenetik uygulama yöntemleri G Lüleci, S Başaran, G Bağcı, İ Keser Metaksan AŞ Ankara, 1-18, 1990 | 25 | 1990 |
| Two novel mutations in the 3′ untranslated region of the beta‐globin gene that are associated with the mild phenotype of beta thalassemia T Bilgen, OA Clark, Z Ozturk, M Akif Yesilipek, I Keser International Journal of Laboratory Hematology 35 (1), 26-30, 2013 | 24 | 2013 |
| Insertion/deletion polymorphism and serum activity of the angiotensin-converting enzyme in Turkish patients with obstructive sleep apnea syndrome C Ogus, S Ket, T Bilgen, I Keser, A Cilli, AY Gocmen, O Tosun, S Gumuslu Biochemical genetics 48, 516-523, 2010 | 24 | 2010 |
| Relationship between SP1 polymorphism and osteoporosis in β‐thalassemia major patients O Guzeloglu‐Kayisli, Z Cetin, I Keser, Z Ozturk, T Tuncer, D Canatan, ... Pediatrics International 50 (4), 474-476, 2008 | 24 | 2008 |
| Frequencies of four genetic polymorphisms in the CYP1A2 gene in Turkish population T Bilgen, O Tosun, G Luleci, I Keser Russian Journal of Genetics 44, 989-992, 2008 | 23 | 2008 |
| Primary atypical teratoid/rhabdoid tumor of the clival region: case report S Kazan, E Göksu, E Mihci, G Gökhan, I Keser, I Gürer Journal of Neurosurgery: Pediatrics 106 (4), 308-311, 2007 | 22 | 2007 |
| Neutrophil oxidative metabolism in Down syndrome patients with congenital heart defects O Akinci, E Mihci, S Tacoy, F Kardelen, I Keser, M Aslan Environmental and molecular mutagenesis 51 (1), 57-63, 2010 | 20 | 2010 |
