Molecular insights into Wnt3a and Wnt5a gene expression in venous insufficiency von Ageed, Fatima Eltayb M., Tifow, Fadumo Ali, Ibrahim, Leylo Abdullahi, Ismael, Aya B., Balcıoğlu, Özlem, Özcem, Barçın, Cobanogullari, Havva, Yılmaz, Selma, Ergören, Mahmut Çerkez

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Cytotoxic Effects of Verbascoside on MCF-7 and MDA-MB-231 von ŞENOL, Hülya, TULAY, Pinar, ERGÖREN, Mahmut Cerkez, HANOĞLU, Azmi, ÇALIŞ, İhsan, MOCAN, Gamze

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APOE Gene Variation's Impact on Cardiovascular Health: A Case-Control Study von Ismail, Aya Badeea, Balcıoğlu, Özlem, Özcem, Barçın, Ergoren, Mahmut Çerkez

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Caprine Prion Gene Polymorphisms in Main Northern Cyprus Goat Breeds von Betmezoglu, Meryem, Arsoy, Dilek, Ergoren, Mahmut Cerkez

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The association between the chromosome 9p21 CDKN2B-AS1 gene variants and the lipid metabolism: A pre-diagnostic biomarker for coronary artery disease von Temel, Şehime Gülsün, Ergören, Mahmut Çerkez

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The contribution of NOS3 variants to coronary artery disease: A combined genetic epidemiology and computational biochemistry perspective von Teralı, Kerem, Ergören, Mahmut Çerkez

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Mediterranean exposotype: Genomic architecture and plant-based dietary metabolites von Ismail, Aya Badeea, Ergören, Mahmut Çerkez

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Functional coding and non-coding variants in human BRCA1 gene and their use in genetic screening von Tuncel, Gulten, Ergören, Mahmut Çerkez

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Investigation of potential genomic biomarkers for obesity and personalized medicine von Ergören, Mahmut Cerkez, Söyler, Gizem, Sah, Hüseyin, Becer, Eda

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The Association Between APOA5 Gene Polymorphisms and Plasma Lipids in the Turkish Cypriot Population: A Possible Biomarker for Preventing Cardiovascular Diseases von Fahrioğlu, Umut, Ergören, Mahmut Çerkez

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The association between the chromosome 9p21 CDKN2B-AS1 gene variants and the lipid metabolism: A pre-diagnostic biomarker for coronary artery disease von Temel, Şehime Gülsün, Ergören, Mahmut Çerkez

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Unique combination and in silico modeling of biallelic POLR3A variants as a cause of Wiedemann-Rautenstrauch syndrome von Temel, Sehime Gulsun, Ergoren, Mahmut Cerkez, Manara, Elena, Paolacci, Stefano, Tuncel, Gulten, Gul, Seref, Bertelli, Matteo

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Natural selection at work? Vitamin D deficiency rates and rising health problems in young Turkish Cypriot professionals von Kandemiş, Emine, Tuncel, Gülten, Fahrioğlu, Umut, Temel, Şehime Gülsün, Mocan, Gamze, Ergören, Mahmut Çerkez

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The Clinical and Genetic Landscape of Hereditary Cancer: Experience from a Single Clinical Diagnostic Laboratory von TSOULOS, NIKOLAOS, AGIANNITOPOULOS, KONSTANTINOS, POTSKA, KEVISA, KATSELI, ANASTASIA, NTOGKA, CHRISTINA, PEPE, GEORGIA, BOUZARELOU, DIMITRA, PAPATHANASIOU, ATHANASIOS, GRIGORIADIS, DIMITRIOS, TSAOUSIS, GEORGIOS N., GOGAS, HELEN, TROUPIS, THEODORE, PAPAZISIS, KONSTANTINOS, NATSIOPOULOS, IOANNIS, VENIZELOS, VASSILEIOS, AMARANTIDIS, KYRIAKOS, GIASSAS, STYLIANOS, PAPADIMITRIOU, CHRISTOS, FOUNTZILAS, ELENA, STATHOULOPOULOU, MAROULIO, KOUMARIANOU, ANNA, XEPAPADAKIS, GRIGORIOS, BLIDARU, ALEXANDRU, ZOB, DANIELA, VOINEA, OANA, ÖZDOĞAN, MUSTAFA, ERGÖREN, MAHMUT ÇERKEZ, HEGMANE, ALINTA, PAPADOPOULOU, EIRINI, NASIOULAS, GEORGE, MARKOPOULOS, CHRISTOS

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CCR5-Δ32 gene variant frequency in the Nigerian and Zimbabwean populations living in North Cyprus von Chukwuebuka Ndikom, Basil, Cerkez Ergoren, Mahmut, Sayan, Murat, Mocan, Gamze, Fahrioğlu, Umut

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Developing an Online Portal for Determining the Genomic Signature of Archaic DNA that are Associated to Modern Human Genetic Diseases: A Meta-Analysis Study von Senturk, Niyazi, Ergoren, Mahmut Cerkez

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Comparison of Bioinformatics Approaches for Fetal Microdeletions and Monogenic Variations Estimation in Non-invasive Prenatal Testing von Paul, Lizzy Teleboshe, Ergoren, Mahmut Cerkez

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Genetic modifiers of HbF production and effects of elevated HbF levels on clinical phenotype: The case of Turkish Cypriot patients with β-thalassemia von Teralı, Kerem, ErgOren, Mahmut Çerkez, Akdeniz, Esra

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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 von Duman, Nilgun, Tuncel, Gulten, Bisgin, Atil, Bozdogan, Sevcan Tug, Sag, Sebnem Ozemri, Gul, Seref, Kiraz, Aslihan, Balta, Burhan, Erdogan, Murat, Uyanik, Bulent, Canbek, Sezin, Ata, Pinar, Geckinli, Bilgen Bilge, Arslan Ates, Esra, Alavanda, Ceren, Yesim Ozdemir, Sevda, Sezer, Ozlem, Ozgon, Gulay Oner, Gurkan, Hakan, Guler, Kubra, Boga, Ibrahim, Kaya, Niyazi, Alemdar, Adem, Sayan, Murat, Dundar, Munis, Ergoren, Mahmut Cerkez, Temel, Sehime Gulsun

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Structural analysis of M1AP variants associated with severely impaired spermatogenesis causing male infertility von Gerlevik, Umut, Ergoren, Mahmut Cerkez, Sezerman, Osman Uğur, Temel, Sehime Gulsun

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