| New Record of Tuta absoluta (Meyrick) (Lepidoptera: Gelechiidae) on Greenhouse-Grown Tomato in Southwestern Turkey (Antalya) F Erler, M Can, M Erdogan, AO Ates, T Pradier Journal of Entomological Science 45 (4), 392-393, 2010 | 70 | 2010 |
| The incidence of cystic fibrosis in the central region of Anatolia in Turkey between 2015 and 2016 M Hangül, S Pekcan, M Köse, D Acıcan, TE Şahlar, M Erdoğan, ... Balkan medical journal 36 (3), 179, 2019 | 31 | 2019 |
| Expectation of accounting professionals from accounting education: An Antalya research FA Kutluk, A Donmez, BD Utku, M Erdogan Procedia-Social and Behavioral Sciences 62, 418-423, 2012 | 29 | 2012 |
| Increased vitamin D receptor gene expression and rs11568820 and rs4516035 promoter polymorphisms in autistic disorder B Balta, H Gumus, R Bayramov, K Korkmaz Bayramov, M Erdogan, ... Molecular biology reports 45, 541-546, 2018 | 21 | 2018 |
| A comprehensive molecular analysis and genotype–phenotype correlation in patients with familial mediterranean fever B Balta, M Erdogan, A Kiraz, T Akalın, F Baştug, A Bayram Molecular Biology Reports 47, 1835-1843, 2020 | 16 | 2020 |
| Prediction, prevention and personalisation of medication for the prenatal period: genetic prenatal tests for both rare and common diseases M Dundar, AS Uzak, M Erdogan, Y Akbarova EPMA journal 2, 181-195, 2011 | 15 | 2011 |
| Partial trisomy 3q in a child with sacrococcygeal teratoma and Cornelia de Lange syndrome phenotype M Dundar, A Uzak, M Erdogan, C Saatci, S Akdeniz, G Luleci, I Keser, ... Genetic Counseling 22 (2), 199, 2011 | 13 | 2011 |
| Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium M Dundar, U Fahrioglu, SH Yildiz, B Bakir-Gungor, SG Temel, H Akin, ... Functional & integrative genomics 22 (3), 291-315, 2022 | 10 | 2022 |
| A novel PTCH1 gene mutation in a pediatric patient associated multiple keratocystic odontogenic tumors of the jaws and Gorlin–Goltz syndrome G Ozcan, B Balta, AE Sekerci, OA Etoz, C Martinuzzi, O Kara, L Pastorino, ... Indian Journal of Pathology and Microbiology 59 (3), 335-338, 2016 | 9 | 2016 |
| Analysis of ACE2 and TMPRSS2 coding variants as a risk factor for SARS‐CoV‐2 from 946 whole‐exome sequencing data in the Turkish population N Duman, G Tuncel, A Bisgin, ST Bozdogan, SO Sag, S Gul, A Kiraz, ... Journal of medical virology 94 (11), 5225-5243, 2022 | 8 | 2022 |
| Does thiol–disulphide balance show oxidative stress in different MEFV mutations? B Balta, M Erdogan, M Alisik, A Kiraz, T Akalin, F Bastug, O Erel Rheumatology International 38, 97-104, 2018 | 7 | 2018 |
| Contribution of genotypes in Prothrombin and Factor V Leiden to COVID‐19 and disease severity in patients at high risk for hereditary thrombophilia A Kiraz, O Sezer, A Alemdar, S Canbek, N Duman, A Bisgin, T Cora, ... Journal of medical virology 95 (2), e28457, 2023 | 6 | 2023 |
| The genetic analysis of cystic fibrosis patients with seven novel mutations in the CFTR gene in the central Anatolian region of Turkey M Erdoğan, M Köse, S Pekcan, M Hangül, B Balta, A Kiraz, GA Gönen, ... Balkan medical journal 38 (6), 357, 2021 | 6 | 2021 |
| Maturity‐onset diabetes of the young: Different diabetes in an infant with cystic fibrosis M Hangül, M Erdoğan, N Hatipoğlu, M Köse Pediatric Pulmonology 55 (5), E5-E7, 2020 | 5 | 2020 |
| Congenital myasthenic syndromes in Turkey: clinical and molecular characterization of 16 cases with three novel mutations S Öztürk, A Güleç, M Erdoğan, M Demir, M Canpolat, H Gümüş, ... Pediatric Neurology 136, 43-49, 2022 | 4 | 2022 |
| Genotype-phenotype correlations in ocular manifestations of Marinesco–Sjögren syndrome: Case report and literature review N Bayram, A Kaçar Bayram, HS Daimagüler, HS Dafsari, D Bamborschke, ... European journal of ophthalmology 32 (3), NP92-NP97, 2022 | 2 | 2022 |
| Tubulopathy and hepatomegaly in a 2-year-old boy: Answers PS Ustkoyuncu, F Bastug, A Kiraz, M Erdogan, E Eren, G Yıldız Pediatric Nephrology 36 (7), 2083-2084, 2021 | 2 | 2021 |
| A Frequent Mutation in the FTL Gene Causing Hyperferritinemia Cataract Syndrome in Turkish Population Is c.-160A> G B Balta, M Erdoğan, A Kiraz, S Korkmaz, A Ağadayı Turkish Journal of Hematology 36 (1), 25, 2019 | 2 | 2019 |
| Tc-99m MDP bone SPECT/CT findings of a patient detected with a new mutation in LEMD3 gene: a case of osteopoikilosis G Silov, Z Erdoğan, M Erdoğan, A Özdal, H Gençer, T Akalın, S Karaçavuş Molecular Imaging and Radionuclide Therapy 27 (1), 48, 2018 | 2 | 2018 |
| Yaşlılar İçin Egzersiz Eğitimlerinde Güncel Yaklaşımlar; Amerika Birleşik Devletleri (ABD) Örneği M ERDOĞAN Başkent Üniversitesi Sağlık Bilimleri Fakültesi Dergisi 2 (2), 174-185, 2017 | 2 | 2017 |
