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Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium.
Dundar M, Fahrioglu U, Yildiz SH, Bakir-Gungor B, Temel SG, Akin H, Artan S, Cora T, Sahin FI, Dursun A, Sezer O, Gurkan H, Erdogan M, Gunduz CNS, Bisgin A, Ozdemir O, Ulgenalp A, Percin EF, Yildirim ME, Tekes S, Bagis H, Yuce H, Duman N, Bozkurt G, Yararbas K, Yildirim MS, Arman A, Mihci E, Eraslan S, Altintas ZM, Aymelek HS, Ruhi HI, Tatar A, Ergoren MC, Cetin GO, Altunoglu U, Caglayan AO, Yuksel B, Ozkul Y, Saatci C, Kenanoglu S, Karasu N, Dundar B, Ozcelik F, Demir M, Siniksaran BS, Kulak H, Kiranatlioglu K, Baysal K, Kazimli U, Akalin H, Dundar A, Boz M, Bayram A, Subasioglu A, Colak FK, Karaduman N, Gunes MC, Kandemir N, Aynekin B, Emekli R, Sahin IO, Ozdemir SY, Onal MG, Senel AS, Poyrazoglu MH, Kisaarslan ANP, Gursoy S, Baskol M, Calis M, Demir H, Zararsiz GE, Erdogan MO, Elmas M, Solak M, Ulu MS, Thahir A, Aydin Z, Atasever U, Sag SO, Aliyeva L, Alemdar A, Dogan B, Erguzeloglu CO, Kaya N, Ozkinay F, Cogulu O, Durmaz A, Onay H, Karaca E, Durmaz B, Aykut A, Cilingir O, Aras BD, Gokalp EE, Arslan S, Temena A, Haziyeva K, Kocagil S, Bas H, Susam E, Keklikci AR, Sarac E, Kocak N, Nergiz S, Terzi YK, Dincer SA, Baskin ES, Genc GC, Bahadir O, Sanri A, Yigit S, Tozkir H, Y… See abstract for full author list ➔ Dundar M, et al. Among authors: arslan s. Funct Integr Genomics. 2022 Jun;22(3):291-315. doi: 10.1007/s10142-021-00819-3. Epub 2022 Jan 31. Funct Integr Genomics. 2022. PMID: 35098403
Genetic variants associated with atrial fibrillationand long-term recurrence after catheter ablation for atrialfibrillation in Turkish patients.
Ulus T, Dural M, Meşe P, Yetmiş F, Mert KU, Görenek B, Çilingir O, Erzurumluoglu Gökalp E, Arslan S, Artan S, Aykaç Ö, Çolak E, Yorgun H, Canpolat U, Aytemir K. Ulus T, et al. Among authors: arslan s. Anatol J Cardiol. 2021 Feb;25(2):129-138. doi: 10.14744/AnatolJCardiol.2020.44082. Anatol J Cardiol. 2021. PMID: 33583820 Free PMC article.
Patient with Mal de Meleda in whom a Novel Gene Mutation was Identified.
Gurel G, Cilingir O, Kutluay O, Arslan S, Sahin S, Colgecen E. Gurel G, et al. Among authors: arslan s. Eurasian J Med. 2019 Jun;51(2):206-208. doi: 10.5152/eurasianjmed.2018.18215. Epub 2018 Nov 30. Eurasian J Med. 2019. PMID: 31258365 Free PMC article.
The relationship of retinopathy of prematurity with brain-derivated neurotrophic factor, vascular endotelial growth factor-A, endothelial PAD domain protein 1 and nitric oxide synthase 3 gene polymorphisms.
Ilguy S, Cilingir O, Bilgec MD, Ozalp O, Erzurumluoglu Gokalp E, Arslan S, Tekin N, Aydemir O, Erol N, Colak E, Gursoy H. Ilguy S, et al. Among authors: arslan s. Ophthalmic Genet. 2021 Dec;42(6):725-731. doi: 10.1080/13816810.2021.1961279. Epub 2021 Aug 4. Ophthalmic Genet. 2021. PMID: 34346275
Retrospective evaluation of pregnant women with celiac disease.
Beksaç K, Örgül G, Çağan M, Karaağaoğlu E, Arslan S, Beksaç MS. Beksaç K, et al. Among authors: arslan s. J Turk Ger Gynecol Assoc. 2017 Mar 15;18(1):56-59. doi: 10.4274/jtgga.2016.0198. J Turk Ger Gynecol Assoc. 2017. PMID: 28506952 Free PMC article.
1,031 results