Publications by authors named "Feride Sahin"

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Effect of resveratrol on the antioxidant enzyme pathway and alveolar bone loss in experimental periodontitis.
Yasemin Sezgin, Mehtap Bilgin Çetin, Yunus Kasim Terzi, Özlem Darcansoy İşeri, Hilal Erinanç

Acta Odontol Scand· December 2025

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Short and Long-Term Outcomes of Liver Transplantation in Pediatric Patients With Inborn Errors of Metabolism: A Single-Center Study.
Hazel Delal Dara Kar, Halil İbrahim Aydın, Figen Özçay, Oya Balcı Sezer, Esra Baskın

Pediatr Transplant· May 2025

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Rare STAT3 haplotypes cause a predisposition to developing congenital anomalies of the kidney and urinary tract disorder.
Mert Polat, Feride İffet Şahin, Esra Baskin, Uğur Toprak, Kaan Savaş Gülleroğlu

Turk J Med Sci· December 2024

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Homologous recombination deficiency gene panel analysis results in synchronous endometrial and ovarian cancers.
Ferah Kazanci, Zerrin Yılmaz Çelik, Mert Polat, Ferhat Karademir, Ozlem Erdem

Rev Assoc Med Bras (1992)· October 2024

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Determination of the Frequency of BCL-2 Polymorphisms (c.-717C>A and c.*2364G>A) and LIF Polymorphism (c.*1414T>G) in Patients with Congenital Anomalies of the Kidney and Urinary Tract.
Tugce Oztepe, Feride Iffet Sahin, Aysun Caltik Yilmaz, Esra Baskin, Mehmet Haberal

Mol Syndromol· October 2024

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Impact of Matrix Metalloproteinases 2 and 9 and Tissue Inhibitor of Metalloproteinase 2 Gene Polymorphisms on Allograft Rejection in Pediatric Renal Transplant Recipients.
Selin Akad Dincer, Feride Iffet Sahin, Yunus Kasim Terzi, Kaan Gulleroglu, Esra Baskin

Exp Clin Transplant· April 2023

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BRCA, infertility, and fertility preservation: a review for counseling.
Ege Baltacı, Ferah Kazancı, Feride İffet Şahin

J Assist Reprod Genet· March 2023

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The impact of developmental genes in non-syndromic cleft lip and/or palate.
Nihal Şahin Uysal, Feride İffet Şahin, Yunus Kasım Terzi

J Turk Ger Gynecol Assoc· March 2023

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Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium.
Munis Dundar, Umut Fahrioglu, Saliha Handan Yildiz, Burcu Bakir-Gungor, Sehime Gulsun Temel, Feride Iffet Sahin, Izem Olcay Sahin

Funct Integr Genomics· June 2022

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Comparison of diagnostic criteria for children with familial Mediterranean fever.
Esra Nagehan Akyol Onder, Kudret Ebru Ozcan, Feride Iffet Sahin, Kaan Savas Gulleroglu, Esra Baskin

Eur J Pediatr· April 2022

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Evaluation of silent information regulator T (SIRT) 1 and Forkhead Box O (FOXO) transcription factor 1 and 3a genes in glaucoma.
Derya Yaman, Tamer Takmaz, Nilay Yüksel, Selin Akad Dinçer, Feride İffet Şahin

Mol Biol Rep· December 2020

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Antibacterial efficacy and remineralization capacity of glycyrrhizic acid added casein phosphopeptide-amorphous calcium phosphate.
Feride Sahin, Fatih Oznurhan

Microsc Res Tech· July 2020

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The Role of Heredity and the Prevalence of Strabismus in Families with Accommodative, Partial Accommodative, and Infantile Esotropia.
Fatma Çorak Eroğlu, Sibel Oto, Feride İffet Şahin, Yunus Terzi, Özge Özer Kaya

Turk J Ophthalmol· June 2020

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Vitamin D receptor gene TaqI single nucleotide polymorphism is not associated with lead levels in maternal and umbilical cord blood.
Yusuf Aytac Tohma, Selin Akad, Eser Colak, Sevsen Kulaksizoglu, Mesut Akyol, Feride Iffet Sahin

J Matern Fetal Neonatal Med· August 2019

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The differences in the expression of fractalkine and its receptor in conditions of tonsillar hypertrophy and chronic tonsillitis.
Elif Koclu Hetemoglu, Seda Turkoglu Babakurban, Yunus Kasım Terzi, Feride Iffet Sahin, Selim Sermed Erbek

Auris Nasus Larynx· August 2019

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No Interaction Between Childhood Maltreatment and Serotonin Transporter Gene in Recurrent Major Depressive Disorder: A Clinical Sample.
Gamze Özçürümez, Hasan Talha Yurdakul, Yunus Terzi, Neşe Direk, Altan Eşsizoğlu

Noro Psikiyatr Ars· June 2019

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Odontogenic effects of two calcium silicate-based biomaterials in human dental pulp cells.
Emel Olga Önay, Erkan Yurtcu, Yunus Kasim Terzi, Mete Üngör, Yener Oguz

Adv Clin Exp Med· November 2018

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Causative Mutations and Mechanism of Androgenetic Hydatidiform Moles.
Ngoc Minh Phuong Nguyen, Zhao-Jia Ge, Ramesh Reddy, Somayyeh Fahiminiya, Philippe Sauthier, Feride Iffet Sahin

Am J Hum Genet· November 2018

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Corchorus olitorius and Urtica pilulifera extracts alleviate copper induced oxidative damage and genotoxicity in tomato.
Özlem Darcansoy İşeri, Dİdem Aksoy Körpe, Feride Iffet Sahin, Mehmet Haberal

Acta Biol Hung· September 2018

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Effect of Hereditary Hemochromatosis Gene H63D and C282Y Mutations on Iron Overload in Sickle Cell Disease Patients.
Yunus Kasım Terzi, Tuğçe Bulakbaşı Balcı, Can Boğa, Zafer Koç, Zerrin Yılmaz Çelik

Turk J Haematol· December 2016

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FCN2 c.772G>T polymorphism is associated with chronic adenoiditis and/or tonsillitis, but not -4 A>G and -602 G>A.
Alper N Erkan, Isilay Oz, Yunus K Terzi, Erdinc Aydin, Murat Ozkale, Feride Iffet Sahin

Int J Pediatr Otorhinolaryngol· August 2016

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BRCA1 and BRCA2 sequence variations detected with next-generation sequencing in patients with premature ovarian insufficiency.
Nafiye Karakaş Yılmaz, Peren Hatice Karagin, Yunus Kasım Terzi, İnci Kahyaoğlu, Saynur Yılmaz

J Turk Ger Gynecol Assoc· July 2016

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Lack of association of matrix metalloproteinase-9 promoter gene polymorphism in obstructive sleep apnea syndrome.
Mustafa Yalcınkaya, Selim S Erbek, Seda Turkoglu Babakurban, Elif Kupeli, Serife Bozbas, Feride Iffet Sahin

J Craniomaxillofac Surg· September 2015

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Fractalkine receptor polymorphism may not be associated with the development and clinical course of ulcerative colitis.
Hale Gokcan, Erkan Yurtcu, Haldun Selcuk, Feride I Sahin

Bosn J Basic Med Sci· May 2015

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West syndrome associated with a novel chromosomal anomaly; partial trisomy 8P together with partial monosomy 9P, resulting from a familial unbalanced reciprocal translocation.
Ilknur Erol, Semra Saygı, Şenay Demir, Fusun Alehan, Feride Iffet Sahin

J Pediatr Neurosci· April 2015

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