| Mutation analysis in Turkish phenylketonuria patients AS Ozgüç M, Ozalp I, Coşkun T, Yilmaz E, Erdem H J Med Genet. 30 (2), 129-30., 1993 | 66 | 1993 |
| Familial segmental neurofibromatosis S Oguzkan, M Cinbis, S Ayter, B Anlar, S Aysun Journal of child neurology 19 (5), 392-394, 2004 | 33 | 2004 |
| Possible modifier genes in the variation of neurofibromatosis type 1 clinical phenotypes PSS Ayter Journal of Neurogenetics, 2018 | 25 | 2018 |
| Two neurofibromatosis type 1 cases associated with rhabdomyosarcoma of bladder, one with a large deletion in the NF1 gene S Oguzkan, YK Terzi, E Güler, M Derbent, PI Agras, U Saatci, S Ayter Cancer genetics and cytogenetics 164 (2), 159-163, 2006 | 24 | 2006 |
| Reproductive decisions after prenatal dianosis in neurofibromatosis type 1: Importance of genetic counseling YK Terzi, S Oguzkan-Balci, B Anlar, S Aysun, S Guran, S Ayter Genetic Counseling 20 (2), 195, 2009 | 22 | 2009 |
| Molecular genetic analyses in neurofibromatosis type 1 patients with tumors S Oguzkan, YK Terzi, M Cinbis, B Anlar, S Aysun, S Ayter Cancer genetics and cytogenetics 165 (2), 167-171, 2006 | 20 | 2006 |
| Heightened CXCR4 and CXCL12 expression in NF1-associated neurofibromas B Karaosmanoglu, ÇY Kocaefe, F Söylemezoğlu, B Anlar, A Varan, ... Child's Nervous System 34, 877-882, 2018 | 19 | 2018 |
| Molecular deletion patterns in Turkish Duchenne and Becker muscular dystrophy patients RY Dinçer P, Topaloğlu H, Ayter S, Ozgüç M, Taşdemir HA Brain Dev. 18 (2), 91-4., 1996 | 19 | 1996 |
| Spinal neurofibromatosis associated with classical neurofibromatosis type 1: genetic characterisation of an atypical case K bora Carman, A Yakut, B Anlar, S Ayter Case Reports 2013, bcr2012008468, 2013 | 16* | 2013 |
| Neurofibromatosis: novel and recurrent mutations in Turkish patients YK Terzi, S Oguzkan, B Anlar, S Aysun, S Ayter Pediatric neurology 37 (6), 421-425, 2007 | 16 | 2007 |
| Neurofibromatosis—Noonan's syndrome with associated rhabdomyosarcoma of the urinary bladder in an infant: case report PI Agras, E Baskin, AE Sakallioglu, IS Arda, S Ayter, S Oguzkan, ... Journal of child neurology 18 (1), 68-72, 2003 | 16 | 2003 |
| Coronin 1A inhibits neurite outgrowth in PC12 cells. AS Terzi YK, Kocaefe YC Neurosci Lett. 17 (582), 38-42, 2014 | 14* | 2014 |
| Two pathogenic NF1 gene mutations identified in DNA from a child with mild phenotype YK Terzi, B Sirin, G Hosgor, E Serdaroglu, B Anlar, S Aysun, S Ayter Child's Nervous System 28, 943-946, 2012 | 9 | 2012 |
| Learning disability and oligodendrocyte myelin glycoprotein (OMGP) gene in neurofibromatosis type 1 YK Terzi, S Oğuzkan-Balci, B Anlar, E Erdoğan-Bakar, S Ayter The Turkish Journal of Pediatrics 53 (1), 75-78, 2011 | 9 | 2011 |
| Molecular analysis of neurofibromatosis type 1 in Turkish families using polymorphic markers. AS Oğuzkan S, Cinbiş M, Ayter S, Anlar B Turk J Pediatr 45 (3), 192-7, 2003 | 9 | 2003 |
| Frequency of the IVS-10nt546 mutation in 44 Turkish phenylketonuria patients AS Ozgüç M, Ozalp I, Coşkun T, Yilmaz E, Erdem H Turk J Pediatr. 35 (1), 11-4., 1993 | 7 | 1993 |
| Clinical findings and mutation analysis of NF1 patients in Turkey AS Terzi YK, Oğuzkan-Balcı S, Anlar B, Varan A, Ersoy-Evanse S, Sharafi P Meta Gene 15, 80-83, 2018 | 5 | 2018 |
| Distribution of F508 mutation on the XV2C/KM19 haplotypes in Turkish cystic fibrosis mutant alleles M Özgüç, E Yilmaz, H Erdem, Ş Ayter, T Coskun, I Özalp, A Göçmen Doĝa Tr J Med Sci 16, 523-531, 1992 | 5 | 1992 |
| Absence of exon 17 c. 2970-2872delAAT mutation in Turkish NF1 patients with mild phenotype YK Terzi, B Sirin, E Serdaroglu, B Anlar, S Aysun, G Hosgor, EA Arslan, ... Child's Nervous System 27, 2113-2116, 2011 | 4 | 2011 |
| Analysis of ΔF508 mutation in cystic fibrosis pathology specimens M Özgüç, A Tekin, H Erdem, E Yılmaz, Ş Ayter, T Coşkun, A Can, S Gögüş, ... Pediatric Pathology 14 (3), 491-496, 1994 | 4 | 1994 |
