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Seda SUSGUN
Seda SUSGUN
Istanbul University; Bezmialem Vakif University
Verified email at bezmialem.edu.tr - Homepage
Title
Cited by
Cited by
Year
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
182019
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
82022
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
42021
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
32021
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
22023
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
22023
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
22021
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
12021
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
12021
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
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