| Materials; incidence of abnormal karyotypes in the Turkish collaborative study MJ KARAOGUZ, E Bal, MA ERGUN, A Balci Genetic counseling 17 (2), 219-230, 2006 | 67 | 2006 |
| Apolipoprotein E gene polymorphism in nonalcoholic fatty liver disease MD Demirag, HI Onen, MY Karaoguz, I Dogan, T Karakan, A Ekmekci, ... Digestive diseases and sciences 52, 3399-3403, 2007 | 40 | 2007 |
| Is cytogenetic diagnosis of 46,XX karyotype spontaneous abortion specimens erroneous? Fluorescence in situ hybridization as a confirmatory technique MY Karaoguz, T Nas, E Konaç, D Ince, E Pala, S Menevse Journal of Obstetrics and Gynaecology Research 31 (6), 508-513, 2005 | 31 | 2005 |
| The apolipoprotein E gene and Taq1A polymorphisms in childhood obesity MA Ergun, MY Karaoguz, A Koc, O Camurdan, A Bideci, AC Yazici, ... Genetic testing and molecular biomarkers 14 (3), 343-345, 2010 | 20 | 2010 |
| The in vitro effect of β-carotene and mitomycin C on SCE frequency in Down's syndrome lymphocyte cultures F Bal, FI Sahin, M Yirmibes, A Balci, S Menevse The Tohoku journal of experimental medicine 184 (4), 295-300, 1998 | 20 | 1998 |
| An unexpected finding in a child with neurological problems: mosaic ring chromosome 18 A Koç, D Kan, K Karaer, MA Ergün, MY Karaoğuz, K Gücüyener, ... European journal of pediatrics 167, 655-659, 2008 | 18 | 2008 |
| Increased frequency of sister chromatid exchanges in peripheral lymphocytes of alcoholics and cigarette smokers MY Karaoğuz, B Coşar, Z Arıkan, F Başaran, A Menevşe, S Menevşe Cell biology international 29 (2), 165-168, 2005 | 18 | 2005 |
| A new syndrome with prenatally diagnosed thoracoschisis, hiatal hernia and extremities' agenesis: case report. A Biri, U Korucuoğlu, A Turp, M Karaoğuz, O Himmetoğlu, S Balci Genetic Counseling (Geneva, Switzerland) 17 (2), 161-165, 2006 | 16 | 2006 |
| A case with a ring chromosome 22 A Koç, K Karaer, MA Ergün, M Yirmibeş-Karaoğuz, D Kan, A Cansu, ... The Turkish Journal of Pediatrics 50 (2), 193-196, 2008 | 13 | 2008 |
| Confirmation of the prenatal mosaic trisomy 2 via fetal USG and cytogenetic analyses E Tuğ, D Karcaaltincaba, M Yirmibeş Karaoğuz, H Saat, A Özek The Journal of Maternal-Fetal & Neonatal Medicine 30 (13), 1579-1583, 2017 | 12 | 2017 |
| Comparison of DRD2 rs1800497 (TaqIA) polymorphism between schizophrenic patients and healthy controls: lack of association in a Turkish sample S Aslan, MY Karaoguz, HY Eser, DK Karaer, E Taner International Journal of Psychiatry in Clinical Practice 14 (4), 257-261, 2010 | 12 | 2010 |
| Gastroschisis with fetal chromosomal abnormality: a case report I Guler, A Erdem, A Biri, G Gunaydin, E Yilmaz, M Erdem, MY Karaoguz Fetal diagnosis and therapy 22 (4), 274-276, 2007 | 11 | 2007 |
| Floating-Harbor syndrome: A first female Turkish patient? K Karaer, MY Karaoguz, MA Ergun, E Yesilkayka, A Bideci, EF Percin GENETIC COUNSELLING 17 (4), 465, 2006 | 11 | 2006 |
| Lack of association between TaqIA RFLP of the Dopamine D2 receptor gene and alcoholism in Type 2 Turkish Alcoholics MY Karaoguz, B Cosar, FI Sahin Genes & Genomics (구 한국유전학회지) 26 (2), 149-154, 2004 | 11 | 2004 |
| Molecular karyotyping of an isolated partial trisomy 11q patient with additional findings G Kayhan, B Cavdarli, MY Karaoguz, EF Percin, AO Kaymak, A Biri, ... Gene 524 (2), 355-360, 2013 | 10 | 2013 |
| İnsandaki genetik hastalıklar MY Karaoğuz Hastalık ve Gen Tedavisi, 2007 | 10 | 2007 |
| Ailesel Resiprokal Translokasyon Olgusu ve Tekrarlayan Düşükler A BALCI, M YİRMİBEŞ, F BAL, S MUTGAN, S MENEVŞE | 10 | 1996 |
| Double aneuploidy in spontaneous miscarriages: two case reports and review of the literature U Korucuoglu, M Erdem, E Pala, MY Karaoguz, A Erdem, A Biri Fetal diagnosis and therapy 24 (2), 106-110, 2008 | 9 | 2008 |
| Prenatal diagnosis of mosaic ring 22 duplication/deletion with terminal 22q13 deletion due to abnormal first trimester screening and choroid plexus cyst detected on ultrasound A Koç, Ö Arısoy, E Pala, M Erdem, AÖ Kaymak, Ö Erkal, MY Karaoğuz Journal of Obstetrics and Gynaecology Research 35 (5), 978-982, 2009 | 8 | 2009 |
| Double aneuploidy involving trisomy 7 with Potter sequence A Biri, MY Karaoğuz, GD İnce, MA Ergün, S Menevşe, B Bingöl European journal of medical genetics 48 (1), 67-73, 2005 | 8 | 2005 |
