Calcium homeostasis in cisplatin resistant epithelial ovarian cancer B Kucukkaya, H Basoglu, D Erdag, F AKBAŞ, S SÜSGÜN, L Yalcintepe General physiology and biophysics 38 (4), 2019 | 18 | 2019 |
Hypomyelinating spastic dyskinesia and ichthyosis caused by a homozygous splice site mutation leading to exon skipping in ELOVL1 T Takahashi, S Mercan, T Sassa, GB Akçapınar, K Yararbaş, S Süsgün, ... Brain and Development 44 (6), 391-400, 2022 | 8 | 2022 |
Investigating of relation between fibromyalgia syndrome and intestinal microbiota B Albayrak, S Süsgün, O Küçükakkaş, F Akbaş, A Yabacı, S Özçelik Mikrobiyoloji Bulteni 55 (2), 146-160, 2021 | 4 | 2021 |
Gene hunting approaches through the combination of linkage analysis with Whole-Exome Sequencing in mendelian diseases: From Darwin to the present day S Susgun, K Kasan, E Yucesan Public health genomics 24 (5-6), 207-217, 2021 | 3 | 2021 |
Evaluation of miR-526b-3p, miR-1179, miR-3529-3p, miR-5011-5p as potential diagnostic biomarkers in isolated cervical dystonia O Gelisin, S Susgun, C Toruntay, A Yabaci, G Baran, AEB Gursoy, ... Revue Neurologique 179 (6), 563-569, 2023 | 2 | 2023 |
Effects of methylprednisolone in the treatment of spinal cord injuries by evaluation of microRNA-21: An experimental study A Abdallah, A Tekin, MN Oztanir, S Süsgün, A Yabacı, İ Çınar, E Can, ... Journal of Neurological Surgery Part A: Central European Neurosurgery 84 (03 …, 2023 | 2 | 2023 |
The rare rs769301934 variant in NHLRC1 is a common cause of Lafora disease in Turkey G Haryanyan, O Ozdemir, K Tutkavul, A Dervent, S Ayta, C Ozkara, ... Journal of human genetics 66 (12), 1145-1151, 2021 | 2 | 2021 |
The utility of serum miRNA-93 and miRNA-191 levels for determining injury severity in adults with multiple blunt trauma. Ö Söğüt, M Metiner, O Kaplan, M Çalık, S Çakmak, TB Ümit, H Ergenç, ... Turkish Journal of Trauma & Emergency Surgery/Ulusal Travma ve Acil Cerrahi …, 2021 | 1 | 2021 |
Optimization of One Step Reverse Transcription Quantitative PCR Method for miRNA Expression Analyses S Süsgün, İ Karacan, E Yücesan Experimed 11 (2), 113-119, 2021 | 1 | 2021 |
Macrocephaly and Digital Anomalies Expand the Phenotypic Spectrum of PGAP2 Variants in Hyperphosphatasia with Impaired Intellectual Development Syndrome … S Susgun, A Ben-Mahmoud, F Rüschendorf, B Ku, SI Hussain, S Schulz, ... Human Mutation 2024, 2024 | | 2024 |
Evaluation of anticancer effects of MAPK6 siRNA loaded PLGA nanoparticles in breast cancer C Toruntay, FS Poyraz, S Susgun, E Yucesan, B Mansuroglu EUROPEAN JOURNAL OF HUMAN GENETICS 32, 253-253, 2024 | | 2024 |
Two rare autosomal recessive neurological disorders identified by combined genetic approaches in a single consanguineous family with multiple offspring S Susgun, E Yucesan, B Goncu, S Hasanoglu Sayin, UY Kina, C Ozgul, ... Neurological Sciences, 1-7, 2023 | | 2023 |
Reanalysis of exome sequencing data reveals a treatable neurometabolic origin in two previously undiagnosed siblings with neurodevelopmental disorder S Susgun, Y Kesim, D Khalilov, NG Sirin, H Gezegen, B Salman, ... Neurological Sciences 44 (7), 2527-2540, 2023 | | 2023 |
Targeted resequencing reveals high-level mosaicism for a novel frameshift variant in WDR45 associated with beta-propeller protein-associated neurodegeneration S Susgun, M Demirel, G Yalcin Cakmakli, B Salman, KK Oguz, B Elibol, ... International Journal of Neuroscience, 1-6, 2023 | | 2023 |
Evaluation of miR-145 and miR-146a as potential biomarkers for diagnosis of Myelodysplastic Syndrome S Süsgün, O Baykara, E Yücesan, RD KURU, BA ÇAKMAK, A YABACI, ... Acta Medica Nicomedia 5 (2), 61-66, 2022 | | 2022 |
Moleküler Biyoloji Güncel Araştırma Teknikleri C Toruntay, S Süsgün | | 2022 |
Assessment of miR-1179 As a Potential Biomarker in Juvenile Myoclonic Epilepsy S Süsgün, C Toruntay, A Bayrakoğlu, U Ferda, E Yücesan Experimed 12 (1), 1-5, 2022 | | 2022 |
Novel WDR45 frameshift variant detected by whole exome sequencing in beta-propeller protein-associated neurodegeneration disease S Susgun, M Demirel, GÜL YALÇIN ÇAKMAKLI, B ELİBOL, S Iseri, ... EUROPEAN JOURNAL OF HUMAN GENETICS 30 (SUPPL 1), 2022 | | 2022 |