| Effects of vitamin D receptor gene polymorphisms on the prognosis of COVID‐19 T Apaydin, H Polat, C Dincer Yazan, C Ilgin, O Elbasan, S Dashdamirova, ... Clinical endocrinology 96 (6), 819-830, 2022 | 54 | 2022 |
| Whole-exome sequencing reveals new potential genes and variants in patients with premature ovarian insufficiency A Turkyilmaz, C Alavanda, EA Ates, BB Geckinli, H Polat, M Gokcu, ... Journal of Assisted Reproduction and Genetics 39 (3), 695-710, 2022 | 14 | 2022 |
| Secondary findings in 622 Turkish clinical exome sequencing data E Arslan Ateş, A Türkyilmaz, Ö Yıldırım, C Alavanda, H Polat, Ş Demir, ... Journal of Human Genetics 66 (11), 1113-1119, 2021 | 11 | 2021 |
| Angiotensin-Converting Enzyme (ACE) level, but not ACE gene polymorphism, is associated with prognosis of COVID-19 infection: Implications for diabetes and … O Elbasan, F Bayram, CD Yazan, T Apaydın, S Dashdamirova, H Polat, ... PloS one 18 (7), e0288338, 2023 | 10 | 2023 |
| Genetic and clinical characterization of patients with maturity-onset of diabetes of the young (MODY): identification of novel variations EA Ateş, Ö Üstay, H Polat, T Apaydın, O Elbasan, Ö Yıldırım, Aİ Güney Balkan Medical Journal 38 (5), 272, 2021 | 9 | 2021 |
| When do we need to suspect maturity onset diabetes of the young in patients with type 2 diabetes mellitus? Ö Üstay, EA Ateş, T Apaydin, O Elbasan, H Polat, G Günhan, C Dinçer, ... Archives of Endocrinology and Metabolism 66 (1), 32-39, 2022 | 1 | 2022 |
| Clinical Exome Sequencing in Syndromic Epilepsy Patients Evaluation of Analysis Results. H Polat, BB Geçkinli Gazi Medical Journal 35, 2024 | | 2024 |
| P183 The genetic profile of childhood neuromuscular disorders: a single center experience O Tezel, G Öztürk, O Ünver, H Polat, A Ayaz, SA Özcan, D Türkdoğan Neuromuscular Disorders 33, S111, 2023 | | 2023 |
| Evaluation of Mitochondrial Bioenergetic Function in Mitochondrial and Type 1 Diabetes BG Tosun, A Francisco, CDC Navarro, TS Menevse, H Polat, BO Hismi, ... HORMONE RESEARCH IN PAEDIATRICS 96, 181-182, 2023 | | 2023 |
| Angiotensin-Converting Enzyme (ACE) Level, But Not ACE Gene Polymorphism, Is Associated with Prognosis of COVID-19 Infection: Connection Between Type 2 Diabetes, Hypertension … O Elbasan, F Bayram, YC Dincer, T Apaydin, S Dashdamirova, H Polat, ... Endocrine Abstracts 90, 2023 | | 2023 |
| ALG6-CDG: Epilepsi, Psikomotor Retardasyon, Ataksi Kliniğinde Koagülasyon Testleri Yol Gösterir mi? E GENÇ, EY GÜMÜŞ, H POLAT, B KARAKAYALI, G ÖZTÜRK, BÖ HİŞMİ Turkiye Klinikleri Scientific Meetings 5 (3), 67-69, 2023 | | 2023 |
| Two new cases diagnosed with Hermansky-Pudlak Syndrome C Alavanda, EA Ates, BB Geckinli, S Demir, H Polat, F Uguzdogan, ... EUROPEAN JOURNAL OF HUMAN GENETICS 30 (SUPPL 1), 223-223, 2022 | | 2022 |
| Pelizaeus-merzbacher-benzeri hastalık: GJC 2 gen mutasyonlu pediatrik bir olguda manyetik rezonans görüntüleme bulguları Ö YAPICI, H POLAT, NÇ ÇİMŞİT | | 2021 |
| Characterization of BRCA Genes' Variants in Turkish Hereditary Breast and Ovarian Cancer (HBOC) Patients EA Ates, C Alavanda, H Polat, A Turkyilmaz, MA Soylemez, BB Geckinli, ... EUROPEAN JOURNAL OF HUMAN GENETICS 28 (SUPPL 1), 935-935, 2020 | | 2020 |
| Expanding of mutation spectrum in Muscular Dystrophies: A Turkish Cohort C Alavanda, H Polat, A Ilker, EA Ates, MA Soylemez, BB Geckinli, ... EUROPEAN JOURNAL OF HUMAN GENETICS 28 (SUPPL 1), 435-436, 2020 | | 2020 |
| The use of long-range pcr protocol in the diagnosis of friedreich ataxia C ALAVANDA, H POLAT, MALİ SÖYLEMEZ, BB GEÇKİNLİ, P ATA, ... | | 2020 |
| When do we need to suspect maturity onset diabetes of the young in patients with type 2 diabetes mellitus? Ö Üstay, T Apaydin, O Elbasan, H Polat, G Günhan, C Dinçer, L SÇeker, ... | | |
| Evaluation Of The Mutation Spectrum Of 20 Bardet-Biedl Syndrome Cases In Turkish Population Ş Demir, E Arslan Ateş, A Türkyılmaz, H Polat, B Geçkinli, A Arman | | |
| Adenosine kinase deficiency presenting like Multiple Acyl-coA dehydrogenase deficiency EY Gümüş, E Genç, M Eltan, B Volkan, BS Akkelle, H Polat, EA Ateş, ... | | |
