The rs2175898 Polymorphism in the ESR1 Gene has a Significant Sex-Specific Effect on Obesity
Guclu-Geyik, Filiz, Coban, Neslihan, Can, Gunay, Erginel-Unaltuna, Nihan
Published in Biochemical genetics (01.12.2020)
Published in Biochemical genetics (01.12.2020)
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Journal Article
Association of Estrogen Receptor 1 PvuII and XbaI Polymorphisms and Peripheral Estrogen Receptor 1 mRNA Levels with Alzheimer’s Disease in Turkish Patients
Guven, Gamze, Köseoğlu Büyükkaya, Pinar, Kılıç, Melisa, Uzun, Damla, Cavus, Betül, Güçlü Geyik, Filiz, Lohmann, Ebba, Samancı, Bedia, Gürvit, Hakan, Hanağası, Hasmet, Bilgiç, Başar
Published in Türk nöroloji dergisi (01.09.2023)
Published in Türk nöroloji dergisi (01.09.2023)
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Journal Article
Val109Asp polymorphism in Intelectin 1 gene is associated with coronary artery disease severity in women
Güçlü-Geyik, Filiz, Erkan, Aycan Fahri, Özuynuk, Aybike Sena, Ekici, Berkay, Çoban, Neslihan
Published in Turk Kardiyoloji Dernegi arsivi : Turk Kardiyoloji Derneginin yayin organidir (01.01.2022)
Published in Turk Kardiyoloji Dernegi arsivi : Turk Kardiyoloji Derneginin yayin organidir (01.01.2022)
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Association of polymorphisms in the sex hormone genes with the presence and severity of coronary artery disease
Çoban, Neslihan, Özuynuk, Aybike Sena, Erkan, Aycan Fahri, Kaya, Ayşem, Ekici, Berkay, Güçlü-Geyik, Filiz, Ademoğlu, Evin, Can, Günay, Erginel-Ünaltuna, Nihan
Published in Turk Kardiyoloji Dernegi arsivi : Turk Kardiyoloji Derneginin yayin organidir (01.01.2022)
Published in Turk Kardiyoloji Dernegi arsivi : Turk Kardiyoloji Derneginin yayin organidir (01.01.2022)
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Journal Article
Prevalence of Prader–Willi Syndrome among Infants with Hypotonia
Tuysuz, Beyhan, MD, Kartal, Nuray, MS, Erener-Ercan, Tugba, MD, Guclu-Geyik, Filiz, PhD, Vural, Mehmet, MD, Perk, Yildiz, MD, Erçal, Derya, MD, Erginel-Unaltuna, Nihan, PhD
Published in The Journal of pediatrics (01.05.2014)
Published in The Journal of pediatrics (01.05.2014)
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The relationship between the expression levels of tissue inhibitor of metalloproteinases-3 (timp3) and severity of atherosclerosis
Çelebi,Gizem, Güçlü Geyik,Filiz, Yılmazbayhan,Dilek, Özsoy,Deniz, Yıldız,Cenk Eray, Yıldız,Mustafa, Okşen,Doğaç, Cavlak,Mehmet, Kömürcü Bayrak,Evrim
Published in İstanbul Tıp Fakültesi Dergisi (17.09.2021)
Published in İstanbul Tıp Fakültesi Dergisi (17.09.2021)
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Negative results in screening for possible new sequence variations on ATP-binding cassette transporter A1 gene in Turkish adults with metabolic syndrome
Çoban, Neslihan, Onat, Altan, Geyik, Filiz, Erginel Ünaltuna, Nihan
Published in Türk Kardiyoloji Derneği arşivi (01.09.2014)
Published in Türk Kardiyoloji Derneği arşivi (01.09.2014)
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Examining the effects of coronary artery disease- and mitochondrial biogenesis-related genes’ and microRNAs’ expression levels on metabolic disorders in epicardial adipose tissue
Dogan, Nazli, Ozuynuk-Ertugrul, Aybike S., Balkanay, Ozan O., Yildiz, Cenk E., Guclu-Geyik, Filiz, Kirsan, Cemre B., Coban, Neslihan
Published in Gene (15.02.2024)
Published in Gene (15.02.2024)
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Journal Article
Biallelic frameshift variants in PHLDB1 cause mild-type osteogenesis imperfecta with regressive spondylometaphyseal changes
Tuysuz, Beyhan, Uludag Alkaya, Dilek, Geyik, Filiz, Alaylıoğlu, Merve, Kasap, Busra, Kurugoğlu, Sebuh, Akman, Yunus Emre, Vural, Mehmet, Bilguvar, Kaya
Published in Journal of medical genetics (01.08.2023)
Published in Journal of medical genetics (01.08.2023)
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Investigation of (epi)genotype causes and follow‐up manifestations in the patients with classical and atypical phenotype of Beckwith‐Wiedemann spectrum
Tüysüz, Beyhan, Güneş, Nilay, Geyik, Filiz, Yeşil, Gözde, Celkan, Tiraje, Vural, Mehmet
Published in American journal of medical genetics. Part A (01.06.2021)
Published in American journal of medical genetics. Part A (01.06.2021)
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Journal Article
Association of Intelectin 1 Gene rs2274907 A > T Polymorphism with Obesity, Type 2 Diabetes, Serum Intelectin-1 Levels and Lipid Profiles in Turkish Adults
Guclu-Geyik, Filiz, Koseoglu, Pınar, Guven, Gamze, Can, Gunay, Kaya, Aysem, Coban, Neslihan, Komurcu-Bayrak, Evrim, Erginel-Unaltuna, Nihan
Published in Biochemical genetics (01.12.2023)
Published in Biochemical genetics (01.12.2023)
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Journal Article
Neurofibromatosis type 1: Expanded variant spectrum with multiplex ligation‐dependent probe amplification and genotype–phenotype correlation in 138 Turkish patients
Güneş, Nilay, Yeşil, Gözde, Geyik, Filiz, Kasap, Büşra, Celkan, Tiraje, Kebudi, Rejin, Tüysüz, Beyhan
Published in Annals of human genetics (01.09.2021)
Published in Annals of human genetics (01.09.2021)
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Journal Article
Seven patients with Smith-McCort dysplasia 2: Four novel nonsense variants in RAB33B and follow-up findings
Tüysüz, Beyhan, Geyik, Filiz, Yıldırım, Timur, Alkaya, Dilek Uludağ, Sharifova, Sabine, Kafadar, Ali
Published in European journal of medical genetics (01.07.2021)
Published in European journal of medical genetics (01.07.2021)
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