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Funda Tayfun Kupesiz

As seen in: Wiley Online Library
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Articles

Advanced Molecular Analysis in Hemophilia A in a Single Step: Next Generation Sequencing (NGS) and Copy Number Variation (CNV) Analysis

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By Enise Avci Durmusalioglu, Esra Isik, Basak Durmus Ozen, Mehmet Mert Topaloglu, Nihal Karadaş, Kaan Kavakli, Melike Sezgin Evim, Tolga Aslan, Erşen Kavak, Adalet Meral Güneş, Funda Tayfun Kupesiz, Alphan Küpesiz, Fahri Şahin, Tahir Atik
| Wiley Online Library Verified
1 Introduction Hemophilia A is an X-linked inherited bleeding disorder with a wide clinical spectrum ranging from mild to severe forms, with an estimated prevalence of 24.6 per 100 000 male births [1]. It is caused by pathogenic variants in the F8 gene, which encodes the coagulation factor VIII (FVIII) [2]. The type of underlying genetic alteration strongly correlates with plasma factor activity, bleeding phenotype, disease severity, and the risk of developing inhibitors during treatment [3-5].
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The First Phylogenetically Confirmed Hemorrhagic Cystitis Outbreak Among Pediatric Hematopoietic Stem Cell Transplant Recipients

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By Tugba Nukte Tezel, Derya Mutlu, Nazli Gurkan, Funda Tayfun Kupesiz
| Wiley Online Library Verified
Conflicts of Interest The authors declare no conflicts of interest. Data Availability Statement The data that support the findings of this study are available from the corresponding author upon reasonable request. References 1, , , and , “Seroprevalence of Fourteen Human Polyomaviruses Determined in Blood Donors,” PLoS One 13, no. 10 (2018): e0206273, https://doi.org/10.1371/journal.pone.0206273.
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