| Bilateral maxillary dentigerous cysts: a case report E Ustuner, S Fitoz, C Atasoy, I Erden, S Akyar Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and …, 2003 | 200 | 2003 |
| Takayasu arteritis in children. N Cakar, F Yalcinkaya, A Duzova, S Caliskan, A Sirin, A Oner, E Baskin, ... The Journal of rheumatology 35 (5), 913-919, 2008 | 150 | 2008 |
| Homozygous mutations in fibroblast growth factor 3 are associated with a new form of syndromic deafness characterized by inner ear agenesis, microtia, and microdontia M Tekin, BÖ Hişmi, S Fitoz, H Özdağ, FB Cengiz, A Sırmacı, İ Aslan, ... The American Journal of Human Genetics 80 (2), 338-344, 2007 | 143 | 2007 |
| High frequency of kidney and urinary tract anomalies in asymptomatic first-degree relatives of patients with CAKUT B Bulum, ZB Özçakar, E Üstüner, E Düşünceli, A Kavaz, D Duman, K Walz, ... Pediatric nephrology 28, 2143-2147, 2013 | 97 | 2013 |
| Nutcracker syndrome in children: the role of upright position examination and superior mesenteric artery angle measurement in the diagnosis S Fitoz, M Ekim, ZB Ozcakar, AH Elhan, F Yalcinkaya Journal of ultrasound in medicine 26 (5), 573-580, 2007 | 87 | 2007 |
| Magnetic resonance cholangiopancreatography of biliary system abnormalities in children S Fitoz, A Erden, S Boruban Clinical imaging 31 (2), 93-101, 2007 | 87 | 2007 |
| Frequency of mtDNA A1555G and A7445G mutations among children with prelingual deafness in Turkey M Tekin, T Duman, G Boğoçlu, A Incesulu, E Comak, S Fitoz, E Yılmaz, ... European journal of pediatrics 162, 154-158, 2003 | 83 | 2003 |
| Efficacy of transrectal ultrasonography in the evaluation of hematospermia C Yagci, S Kupeli, C Tok, S Fitoz, S Baltaci, O Gogus Clinical imaging 28 (4), 286-290, 2004 | 77 | 2004 |
| Three-dimensional CT of congenital esophageal atresia and distal tracheoesophageal fistula in neonates: preliminary results S Fitoz, C Atasoy, A Yagmurlu, S Akyar, A Erden, H Dindar American Journal of Roentgenology 175 (5), 1403-1407, 2000 | 76 | 2000 |
| Hypertension induced reversible posterior leukoencephalopathy syndrome: a report of two cases ZB Özcakar, M Ekim, S Fitoz, S Teber, S Hizel, B Acar, S Yüksel, ... European journal of pediatrics 163, 728-730, 2004 | 74 | 2004 |
| Abdominal confluence of lymph trunks: detectability and morphology on heavily T2-weighted images A Erden, S Fitoz, B Yagmurlu, I Erden American Journal of Roentgenology 184 (1), 35-40, 2005 | 70 | 2005 |
| Homozygous FGF3 mutations result in congenital deafness with inner ear agenesis, microtia, and microdontia M Tekin, H Öztürkmen Akay, S Fitoz, S Birnbaum, FB Cengiz, ... Clinical genetics 73 (6), 554-565, 2008 | 62 | 2008 |
| Mutations in TMC1 contribute significantly to nonsyndromic autosomal recessive sensorineural hearing loss: a report of five novel mutations A Sırmacı, D Duman, H Öztürkmen-Akay, S Erbek, A İncesulu, ... International journal of pediatric otorhinolaryngology 73 (5), 699-705, 2009 | 59 | 2009 |
| Virtual cystoscopy in the evaluation of bladder tumors C Yazgan, S Fitoz, C Atasoy, K Turkolmez, C Yagci, S Akyar Clinical imaging 28 (2), 138-142, 2004 | 56 | 2004 |
| Gray‐scale and color Doppler sonographic findings in intratesticular varicocele C Atasoy, S Fitoz Journal of clinical ultrasound 29 (7), 369-373, 2001 | 55 | 2001 |
| Diagnostic tools in the preoperative evaluation of children with anomalous pulmonary venous connections T Uçar, S Fitoz, E Tutar, S Atalay, A Uysalel The international journal of cardiovascular imaging 24, 229-235, 2008 | 53 | 2008 |
| ROR1 is essential for proper innervation of auditory hair cells and hearing in humans and mice O Diaz-Horta, C Abad, L Sennaroglu, J Foster, A DeSmidt, G Bademci, ... Proceedings of the National Academy of Sciences 113 (21), 5993-5998, 2016 | 48 | 2016 |
| A complex TFAP2A allele is associated with branchio‐oculo‐facial syndrome and inner ear malformation in a deaf child M Tekin, A Sırmacı, B Yüksel‐Konuk, S Fitoz, L Sennaroğlu American Journal of Medical Genetics Part A 149 (3), 427-430, 2009 | 48 | 2009 |
| Familial neonatal Marfan syndrome due to parental mosaicism of a missense mutation in the FBN1 gene M Tekin, FB Cengiz, E Ayberkin, T Kendirli, S Fitoz, E Tutar, E Çiftçi, ... American journal of medical genetics Part A 143 (8), 875-880, 2007 | 47 | 2007 |
| The" nutcracker phenomenon" with orthostatic proteinuria M Ekim, ZB Özçakar, S Fitoz, T Soygür, S Yüksel, B Acar, F Yalçinkaya, ... Clinical nephrology 65 (4), 2006 | 45 | 2006 |
