Letter to the editor regarding the article "A case of hypertrophic and dilated cardiomyopathic sudden cardiac death: de novo mutation in TTN and SGCD genes" by Ergören, Mahmut Çerkez, Temel, Sehime Gülsün

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Psychomotor Delay in a Child with FGFR3 G380R Pathogenic Mutation Causing Achondroplasia by Ergoren, Mahmut C., Eren, Erdal, Manara, Elena, Paolacci, Stefano, Tulay, Pinar, Sag, Sebnem O., Bertelli, Matteo, Mocan, Gamze, Temel, Sehime Gulsun

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Functional coding/non-coding variants in EGFR, ROS1 and ALK genes and their role in liquid biopsy as a personalized therapy by Ergoren, Mahmut Cerkez, Cobanogulları, Havva, Temel, Sehime Gulsun, Mocan, Gamze

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Characterization and in silico analyses of the BRCA1/2 variants identified in individuals with personal and/or family history of BRCA-related cancers by Pirim, Dilek, Kaya, Niyazi, Yıldırım, Elif Uz, Sag, Sebnem Ozemri, Temel, Sehime Gulsun

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PGT for structural chromosomal rearrangements in 300 couples reveals specific risk factors but an interchromosomal effect is unlikely by Ogur, Cagri, Kahraman, Semra, Griffin, Darren Karl, Cinar Yapan, Cigdem, Tufekci, Mehmet Ali, Cetinkaya, Murat, Temel, Sehime Gulsun, Yilmaz, Alper

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An Endocrinological Perspective on 22q11.2 Deletion Syndrome: A Single-center Experience by Denkboy Ongen, Yasemin, Ozemri Sag, Sebnem, Temel, Sehime Gulsun, Eren, Erdal

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Postmortem genetic testing in sudden cardiac death: To be or not to be? by Temel, Sehime Gulsun, Turkgenc, Burcu, Akcay, Arzu, Koseler, Aylin, Yakicier, Cengiz

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The use of ACE INDEL polymorphism as a biomarker of coronary artery disease (CAD) in humans with Mediterranean-style diet by Temel, Sehime Gulsun, Ergoren, Mahmut Cerkez, Yilmaz, Izel, Oral, Haluk Barbaros

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Alzheimer Disease Associated Loci: IAPOE/I Single Nucleotide Polymorphisms in Marmara Region by Ismail, Aya Badeea, Dundar, Mehmet Sait, Erguzeloglu, Cemre Ornek, Ergoren, Mahmut Cerkez, Alemdar, Adem, Ozemri Sag, Sebnem, Temel, Sehime Gulsun

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Aven blocks DNA damage-induced apoptosis by stabilising Bcl-xL by Kutuk, Ozgur, Temel, Sehime Gulsun, Tolunay, Sahsine, Basaga, Huveyda

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Contribution of genotypes in Prothrombin and Factor V Leiden to COVID‐19 and disease severity in patients at high risk for hereditary thrombophilia by Kiraz, Aslıhan, Sezer, Ozlem, Alemdar, Adem, Canbek, Sezin, Duman, Nilgun, Bisgin, Atıl, Cora, Tulin, Ruhi, Hatice Ilgın, Ergoren, Mahmut Cerkez, Geçkinli, Bilgen Bilge, Sag, Sebnem Ozemri, Gözden, Hilmi Erdem, Oz, Ozlem, Altıntaş, Zuhal Mert, Yalcıntepe, Sinem, Keskin, Adem, Tak, Ayşegül Yabacı, Paskal, Şeyma Aktaş, Yürekli, Uğur Fahri, Demirtas, Mercan, Evren, Emine Unal, Hanta, Abdullah, Başdemirci, Müşerref, Suer, Kaya, Balta, Burhan, Kocak, Nadir, Karabulut, Halil Gürhan, Cobanogulları, Havva, Ateş, Esra Arslan, Bozdoğan, Sevcan Tuğ, Eker, Damla, Ekinci, Sadiye, Nergiz, Süleyman, Tuncalı, Timur, Yagbasan, Serap, Alavanda, Ceren, Kutlay, Nuket Yurur, Evren, Hakan, Erdoğan, Murat, Altıner, Sule, Sanlidag, Tamer, Gonen, Gizem Akıncı, Vicdan, Arzu, Eras, Nazan, Eker, Hatice Koçak, Balasar, Ozgür, Tuncel, Gulten, Dundar, Munis, Gurkan, Hakan, Temel, Sehime Gulsun

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The use of ACE INDEL polymorphism as a biomarker of coronary artery disease (CAD) in humans with Mediterranean-style diet by Temel, Sehime Gulsun, Ergoren, Mahmut Cerkez, Yilmaz, Izel, Oral, Haluk Barbaros

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A Multicenter Study of Genotype Variation/Demographic Patterns in 2475 Individuals Including 1444 Cases With Breast Cancer in Turkey by Boga, Ibrahim, Ozemri Sag, Sebnem, Duman, Nilgun, Ozdemir, Sevda Yesim, Ergoren, Mahmut Cerkez, Dalci, Kubilay, Mujde, Cem, Parsak, Cem Kaan, Rencuzogullari, Cagla, Sonmezler, Ozge, Yalav, Orcun, Alemdar, Adem, Aliyeva, Lamiya, Bozkurt, Ozlem, Cetintas, Sibel, Cubukcu, Erdem, Deligonul, Adem, Dogan, Berkcan, Ornek Erguzeloglu, Cemre, Evrensel, Turkkan, Gokgoz, Sehsuvar, Senol, Kazim, Tolunay, Sahsine, Akyurek, Esra, Basgoz, Neslihan, Gökçe, Nuriye, Dundar, Bilge, Ozturk, Figen, Taskin, Duygu, Demirtas, Mercan, Cag, Murat, Diker, Omer, Olgun, Polat, Tug Bozdogan, Sevcan, Dundar, Munis, Bisgin, Atil, Temel, Sehime Gulsun

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Birt-Hogg-Dubé Syndrome: Diagnostic Journey of Three Cases from Skin to Gene by Eda Hasal, Emel Bulbul Baskan, Seref Gul, Asli Gorek Dilektasli, Sebnem Ozemri Sag, Saduman Balaban Adim, Sehime Gulsun Temel

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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 by Temel, Şehime Gülsün, Ergören, Mahmut Çerkez

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Birt-Hogg-Dubé Syndrome: Diagnostic Journey of Three Cases from Skin to Gene by Hasal, Eda, Baskan, Emel Bulbul, Gul, Seref, Dilektasli, Asli Gorek, Sag, Sebnem Ozemri, Adim, Saduman Balaban, Temel, Sehime Gulsun

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