| Phenotypic spectrum and prevalence of INPP5E mutations in Joubert syndrome and related disorders L Travaglini, F Brancati, J Silhavy, M Iannicelli, E Nickerson, N Elkhartoufi, ... European Journal of Human Genetics 21 (10), 1074-1078, 2013 | 81 | 2013 |
| Investigation of key miRNAs and target genes in bladder cancer using miRNA profiling and bioinformatic tools KM Canturk, M Ozdemir, C Can, S Öner, R Emre, H Aslan, O Cilingir, ... Molecular biology reports 41, 8127-8135, 2014 | 57 | 2014 |
| The association between methylation levels of targeted genes and albuminuria in patients with early diabetic kidney disease O Aldemir, F Turgut, C Gokce Renal failure 39 (1), 597-601, 2017 | 35 | 2017 |
| Methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism in psoriasis in southern Turkey M Izmirli, BB Sen, E Rifaioglu, B Gogebakan, O Aldemir, T Sen, O Ekiz, ... Anais brasileiros de dermatologia 91, 611-613, 2016 | 15 | 2016 |
| Wiedemann–Rautenstrauch syndrome: Report of a variant case A Kiraz, S Ozen, F Tubas, Y Usta, O Aldemir, Y Alanay American Journal of Medical Genetics Part A 158 (6), 1434-1436, 2012 | 12 | 2012 |
| The spectrum of β-thalassemia mutations in Hatay, Turkey: reporting three new mutations O Aldemir, M Izmirli, H Kaya Hemoglobin 38 (5), 325-328, 2014 | 11 | 2014 |
| Early-onset severe obesity with ACTH deficiency and red hair in a boy: the POMC deficiency S Ozen, O Aldemir Genetic Counseling 23 (4), 493, 2012 | 10 | 2012 |
| Urotensin II (U-II), a novel cyclic peptide, possibly associated with the pathophysiology of osteoarthritis B Gögebakan, V Uruc, R Ozden, IG Duman, AE Yagiz, HM Okuyan, ... Peptides 54, 159-161, 2014 | 9 | 2014 |
| Malouf syndrome with hypergonadotropic hypogonadism and cardiomyopathy: two-case report and literature review DB Şilfeler, A Karateke, R Keskin Kurt, Ö Aldemir, A Buğra Nacar, ... Case reports in obstetrics and gynecology 2014, 2014 | 6 | 2014 |
| Are low maternal estriol levels a predictor for pro‐opiomelanocortin (POMC) deficiency caused by POMC mutation during pregnancy? O Aldemir, S Ozen, C Sanlialp, S Ceylaner Prenatal diagnosis 33 (13), 1297-1298, 2013 | 5 | 2013 |
| A new finding in a patient with Mowat Wilson syndrome: peripupillary atrophy and gingival hypertrophy A Kiraz, O Aldemir, Y Karabulut, C Turan, M Dundar Genetic counseling 24 (1), 61, 2013 | 3 | 2013 |
| Ring chromosome 9 in a newborn O Aldemir, IH Celik, K Karaer, G Ceylaner Genet Couns 24, 357-360, 2013 | 2 | 2013 |
| A family diagnosed as MEN2A with a rare mutation D631Y in RET oncogene O Aldemir, M Ozsan, H Gokce West Indian Med J 10, 2016 | 1 | 2016 |
| Unbalanced karyotype with X; 11 translocation associated with SHOX duplication and 11q partial deletion in a girl with amenorrhea and mild mental retardation detected by array … O Aldemir, R Aldemir, Y Sahin, I Ustun, C Gokce Gene Reports 4, 194-197, 2016 | | 2016 |
| A Novel Mutation of SCL26A4 Gene in Turkish Family with Pendred Syndrome O Aldemir, K KARAER, C CEVİK, H DOGAN, C GOKCE The Medical Journal of Mustafa Kemal University 6 (22), 19-24, 2015 | | 2015 |
| A CASE REPORT: SPONDYLOEPIMETAPHSIAL DYSPLASIA, PAKISTANI TYPE CG Ozgur Aldemir, M.Turgut Yıldızoren, İhsan Ustun 12th International Skeletal Dysplasia, PAKISTANI TYPE 1, 102, 2015 | | 2015 |
| Three patients resembling Teebi–Shaltout syndrome O Aldemir, S Ozen, S Erdem, A Kiraz, N Akarsu, Y Alanay American Journal of Medical Genetics Part A 161 (10), 2570-2575, 2013 | | 2013 |
| Skewed X inactivation in a case having partial trisomy 10q with mild phenotype caused by an unbalanced X;10 translocation IÇSA Durak, G. Bademci, Ö. Aldemir, B. Şenel European Cytogenetic Association, Istanbul 15 (1), 94-95p, 2007 | | 2007 |
| The surgical treatment of patellar subluxation in a case of kabuki make-up syndrome I Boyraz, B Koc, O Aldemir, H Sarman | | |
