| Infantile spasms is associated with deletion of the MAGI2 gene on chromosome 7q11. 23-q21. 11 CR Marshall, EJ Young, AM Pani, ML Freckmann, Y Lacassie, C Howald, ... The American Journal of Human Genetics 83 (1), 106-111, 2008 | 149 | 2008 |
| Consanguineous marriages in the province of Antalya, Turkey ÖM Alper, H Erengin, A E Manguoglu, T Bilgen, Z Cetin, N Dedeoglu, ... Annales de génétique 47 (2), 129-138, 2004 | 104 | 2004 |
| AZF microdeletions on the Y chromosome of infertile men from Turkey CF Sargın, S Berker-Karaüzüm, E Manguoğlu, T Erdoğru, Ş Karaveli, ... Annales de genetique 47 (1), 61-68, 2004 | 51 | 2004 |
| Germline mutations in the BRCA1 and BRCA2 genes in Turkish breast/ovarian cancer patients A Esra Manguoǧlu, G Lüleci, T Özçelik, T Çolak, H Schayek, M Akaydın, ... Human Mutation 21 (4), 444-445, 2003 | 45 | 2003 |
| Molecular analysis of beta-thalassemia and sickle cell anemia in Antalya I Keser, AD Sanlioglu, E Manguoglu, O Guzeloglu Kayisli, N Nal, F Sargin, ... Acta haematologica 111 (4), 205-210, 2004 | 41 | 2004 |
| Germline mutations of BRCA1 and BRCA2 genes in Turkish breast, ovarian, and prostate cancer patients E Manguoğlu, Ş Güran, D Yamaç, T Çolak, M Şimşek, M Baykara, ... Cancer Genetics and Cytogenetics 203 (2), 230-237, 2010 | 30 | 2010 |
| Pyridoxine-responsive seizures in infantile hypophosphatasia and a novel homozygous mutation in ALPL gene BG Nur, G Çelmeli, E Manguoğlu, E Soyucen, İ Bircan, E Mıhçı Journal of Clinical Research in Pediatric Endocrinology 8 (3), 360, 2016 | 23 | 2016 |
| Evaluation of ETV6/RUNX1 Fusion and Additional Abnormalities Involving ETV6 and/or RUNX1 Genes Using FISH Technique in Patients with Childhood Acute … C Aydin, Z Cetin, AE Manguoglu, F Tayfun, OA Clark, A Kupesiz, ... Indian Journal of Hematology and Blood Transfusion 32, 154-161, 2016 | 19 | 2016 |
| Analysis of polymorphic patterns in candidate genes in Israeli patients with prostate cancer A Figer, T Friedman, AE Manguoglu, D Flex, A Vazina, I Novikov, ... IMAJ-RAMAT GAN- 5 (10), 741-745, 2003 | 17 | 2003 |
| The value of donor lymphocyte infusions in thalassemia patients at imminent risk of graft rejection following stem cell transplantation GT Karasu, MA Yesilipek, SB Karauzum, V Uygun, E Manguoglu, ... Pediatric Blood & Cancer 58 (3), 453-458, 2012 | 13 | 2012 |
| Prenatal Diagnosis of b-Thalassemia in the Antalya Province I Keser, E Manguoğlu, ÖG Kayişli, F Kurt, I Mendilcioğlu, M Şimşek, ... Turkish journal of medical sciences 35 (4), 253-255, 2005 | 13 | 2005 |
| Donor cell-derived acute myeloblastic leukemia after allogeneic peripheral blood hematopoietic stem cell transplantation for juvenile myelomonocytic leukemia Z Cetin, G Tezcan, SB Karauzum, A Kupesiz, AE Manguoglu, A Yesilipek, ... Journal of Pediatric Hematology/Oncology 28 (11), 763, 2006 | 11 | 2006 |
| Combination of Hb Knossos [Cod 27 (GT)] and IVSII-745 (CG) in a Turkish patient with beta-thalassemia major I Keser, E Manguoglu, O Kayisli, A Yesilipek, G Luleci Genetic Testing 11 (3), 228-230, 2007 | 10 | 2007 |
| A patient with Down syndrome with a de novo derivative chromosome 21 Z Cetin, S Yakut, E Mihci, AE Manguoglu, S Berker, I Keser, G Luleci Gene 507 (2), 159-164, 2012 | 9 | 2012 |
| Genomic Large Rearrangement Screening of BRCA1 and BRCA2 Genes in High-Risk Turkish Breast/Ovarian Cancer Patients by Using Multiplex Ligation … E Manguoğlu, Ş Güran, D Yamaç, M Şimşek, S Akdeniz, T Colak, ... Cancer investigation 29 (1), 73-77, 2011 | 9 | 2011 |
| Lack of association between RNASEL Arg462Gln variant and the risk of breast cancer A Sevinç, D Yannoukakos, I Konstantopoulou, E Manguoglu, G Lüleci, ... Anticancer research 24 (4), 2547-2550, 2004 | 9 | 2004 |
| TCIRG1 and SNX10 gene mutations in the patients with autosomal recessive osteopetrosis G Koçak, BN Güzel, E Mıhçı, OA Küpesiz, K Yalçın, AE Manguoğlu Gene 702, 83-88, 2019 | 8 | 2019 |
| Two rare mutations in Turkey: IVS I. 130 (G–C) and IVS II. 848 (C–A) N Nal, AE Manguoglu, CF Sargin, I Keser, A Kupesiz, A Yesilipek, ... Clinical & Laboratory Haematology 27 (4), 274-277, 2005 | 7 | 2005 |
| A case with de novo interstitial deletion of chromosome 7q21. 1-q22. E Manguoğlu, S Berker-Karaüzüm, A Baumer, E Mihci, S Tacoy, G Lüleci, ... Genetic counseling (Geneva, Switzerland) 16 (2), 155, 2005 | 7 | 2005 |
| Absence of the SLC22A12 gene mutation in Turkish population with primary gout disease S Yakut, Z Cetin, M Arman, H Akbas, AE Manguoglu, G Luleci Rheumatology international 33, 2921-2925, 2013 | 6 | 2013 |
