| WRN Mutation Update: Mutation Spectrum, Patient Registries, and Translational Prospects K Yokote, S Chanprasert, L Lee, K Eirich, M Takemoto, A Watanabe, ... Human mutation 38 (1), 7-15, 2017 | 115 | 2017 |
| WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterations K Friedrich, L Lee, DF Leistritz, G Nürnberg, B Saha, FM Hisama, ... Human genetics 128, 103-111, 2010 | 108 | 2010 |
| Mutations in RAD21 disrupt regulation of APOB in patients with chronic intestinal pseudo-obstruction E Bonora, F Bianco, L Cordeddu, M Bamshad, L Francescatto, D Dowless, ... Gastroenterology 148 (4), 771-782. e11, 2015 | 95 | 2015 |
| Multidisciplinary treatment of non-syndromic oligodontia C Bural, E Oztas, S Ozturk, G Bayraktar European journal of dentistry 6 (02), 218-226, 2012 | 61 | 2012 |
| The phenotypic and molecular genetic spectrum of Alström syndrome in 44 Turkish kindreds and a literature review of Alström syndrome in Turkey A Ozantürk, JD Marshall, GB Collin, S Düzenli, RP Marshall, Ş Candan, ... Journal of human genetics 60 (1), 1-9, 2015 | 60 | 2015 |
| REST final-exon-truncating mutations cause hereditary gingival fibromatosis Y Bayram, JJ White, N Elcioglu, MT Cho, N Zadeh, A Gedikbasi, ... The American Journal of Human Genetics 101 (1), 149-156, 2017 | 57 | 2017 |
| Radiosynovectomy in hemophilic synovitis: correlation of therapeutic response and blood-pool changes C Türkmen, B Zülflkar, Ö Taşer, H Tokmak, Ö Kílíčoǧlu, A Mudun, S Ünal, ... Cancer biotherapy & radiopharmaceuticals 20 (3), 363-370, 2005 | 52 | 2005 |
| The genotoxic effects in lymphocyte cultures of children treated with radiosynovectomy by using yttrium-90 citrate colloid C Turkmen, S Ozturk, SN Unal, B Zulfikar, O Taser, Y Sanli, K Cefle, ... Cancer biotherapy & radiopharmaceuticals 22 (3), 393-399, 2007 | 47 | 2007 |
| Molecular diagnosis of analbuminemia: a novel mutation identified in two Amerindian and two Turkish families M Galliano, M Campagnoli, A Rossi, CH Wirsing von König, AW Lyon, ... Clinical chemistry 48 (6), 844-849, 2002 | 46 | 2002 |
| In VitroChromosomal Radiosensitivity in common variable immune deficiency S Palanduz, A Palanduz, I Yalcin, A Somer, U Ones, D Ustek, S Ozturk, ... Clinical immunology and immunopathology 86 (2), 180-182, 1998 | 44 | 1998 |
| Clinical and molecular characterization of two adults with autosomal recessive Robinow syndrome F Tufan, K Cefle, S Türkmen, A Türkmen, U Zorba, M Dursun, S Oztürk, ... American Journal of Medical Genetics Part A 136 (2), 185-189, 2005 | 43 | 2005 |
| Monitoring the genotoxic effects of radiosynovectomy with Re‐186 in paediatric age group undergoing therapy for haemophilic synovitis C Turkmen, S Ozturk, SN Unal, B Zulfikar, O Taser, Y Sanli, K Cefle, ... Haemophilia 13 (1), 57-64, 2007 | 39 | 2007 |
| Familial visceral myopathy with pseudo-obstruction, megaduodenum, Barrett's esophagus, and cardiac abnormalities Z Mungan, F Akyüz, Z Bugra, O Yönal, S Öztürk, A Acar, U Çevikbas Official journal of the American College of Gastroenterology| ACG 98 (11 …, 2003 | 37 | 2003 |
| Treatment of acquired severe aplastic anemia with antilymphocyte globulin, cyclosporin A, methyprednisolone, and granulocyte colony‐stimulating factor G Dinçol, M Aktan, R Diz‐Küçükkaya, S Yavuz, M Nalcacı, Ş Öztürk, ... American journal of hematology 82 (9), 783-786, 2007 | 30 | 2007 |
| Increased sister chromatid exchange frequency in young women with breast cancer and in their first-degree relatives K Cefle, A Ucur, N Guney, S Ozturk, S Palanduz, F Tas, O Asoglu, ... Cancer genetics and cytogenetics 171 (1), 65-67, 2006 | 28 | 2006 |
| Atrial and ventricular arryhthmogenic potential in Turner Syndrome AB Sozen, K Cefle, H Kudat, S Ozturk, H Oflaz, B Pamukcu, V Akkaya, ... Pacing and clinical electrophysiology 31 (9), 1140-1145, 2008 | 27 | 2008 |
| Loss of heterozygosity at chromosome 14q is associated with poor prognosis in head and neck squamous cell carcinomas D Pehlivan, E Gunduz, M Gunduz, H Nagatsuka, LB Beder, B Cengiz, ... Journal of cancer research and clinical oncology 134, 1267-1276, 2008 | 25 | 2008 |
| Investigation of Arg399Gln and Arg194Trp Polymorphisms of the XRCC1 (X-Ray Cross-Complementing Group 1) Gene and Its Correlation to Sister Chromatid … N Duman, M Aktan, S Ozturk, S Palanduz, A Cakiris, D Ustek, U Ozbek, ... Genetic testing and molecular biomarkers 16 (4), 287-291, 2012 | 24 | 2012 |
| The effects of etodolac, nimesulid and naproxen sodium on the frequency of sister chromatid exchange after enclused third molars surgery. BG Koseoglu, S Ozturk, H Koçak, S Palanduz, K Çefle Yonsei Medical Journal 49 (5), 742-747, 2008 | 23 | 2008 |
| Acute wood or coal exposure with carbon monoxide intoxication induces sister chromatid exchange Ş Öztürk, S Vatansever, K Çefle, Ş Palanduz, K Güler, N Erten, O Erk, ... Journal of Toxicology: Clinical Toxicology 40 (2), 115-120, 2002 | 23 | 2002 |
