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Phenotypic continuum of NFU1-related disorders.
Ann Clin Transl Neurol. 2022 Dec;9(12):2025-2035. doi: 10.1002/acn3.51679. Epub 2022 Oct 18.
Ann Clin Transl Neurol. 2022.
PMID: 36256512
Free PMC article.
Functional loss of ubiquitin-specific protease 14 may lead to a novel distal arthrogryposis phenotype.
Turgut GT, Altunoglu U, Sivrikoz TS, Toksoy G, Kalaycı T, Avcı Ş, Karaman B, Gulec C, Başaran S, Sayın GY, Kayserili H, Uyguner ZO.
Turgut GT, et al. Among authors: sayin gy.
Clin Genet. 2022 Apr;101(4):421-428. doi: 10.1111/cge.14117. Epub 2022 Jan 31.
Clin Genet. 2022.
PMID: 35066879
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Investigation of genetic and phenotypic heterogeneity in 37 Turkish patients with Kabuki and Kabuki-like phenotype.
Usluer E, Sayın GY, Güneş N, Kasap B, Tüysüz B.
Usluer E, et al. Among authors: sayin gy.
Am J Med Genet A. 2022 Oct;188(10):2976-2987. doi: 10.1002/ajmg.a.62944. Epub 2022 Aug 8.
Am J Med Genet A. 2022.
PMID: 36097644
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Mannose binding lectin gene 2 (rs1800450) missense variant may contribute to development and severity of COVID-19 infection.
Medetalibeyoglu A, Bahat G, Senkal N, Kose M, Avci K, Sayin GY, Isoglu-Alkac U, Tukek T, Pehlivan S.
Medetalibeyoglu A, et al. Among authors: sayin gy.
Infect Genet Evol. 2021 Apr;89:104717. doi: 10.1016/j.meegid.2021.104717. Epub 2021 Jan 27.
Infect Genet Evol. 2021.
PMID: 33515713
Free PMC article.
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Investigation of MBL2 and NOS3 functional gene variants in suspected COVID-19 PCR (-) patients.
Pehlivan S, Köse M, Mese S, Serin I, Senkal N, Oyacı Y, Medetalibeyoglu A, Pehlivan M, Sayın GY, Isoglu-Alkac U, Tukek T.
Pehlivan S, et al. Among authors: sayin gy.
Pathog Glob Health. 2022 May;116(3):178-184. doi: 10.1080/20477724.2021.1984726. Epub 2021 Sep 27.
Pathog Glob Health. 2022.
PMID: 34570692
Free PMC article.
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Clinical and molecular characteristics of 26 fetuses with lethal multiple congenital contractures.
Turgut GT, Altunoglu U, Gulec C, Sarac Sivrikoz T, Kalaycı T, Toksoy G, Avcı Ş, Yıldırım BT, Sayın GY, Kalelioglu IH, Karaman B, Has R, Başaran S, Yuksel A, Kayserili H, Uyguner ZO.
Turgut GT, et al. Among authors: sayin gy.
Clin Genet. 2024 Jun;105(6):596-610. doi: 10.1111/cge.14490. Epub 2024 Jan 26.
Clin Genet. 2024.
PMID: 38278647
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The effect of DNA repair gene variants on COVID-19 disease: susceptibility, severity, and clinical course.
Senkal N, Serin I, Pehlivan S, Pehlivan M, Medetalibeyoglu A, Cebeci T, Konyaoglu H, Oyacı Y, Sayın GY, Isoglu-Alkac U, Tukek T, Kose M.
Senkal N, et al. Among authors: sayin gy.
Nucleosides Nucleotides Nucleic Acids. 2023;42(8):571-585. doi: 10.1080/15257770.2023.2172183. Epub 2023 Jan 28.
Nucleosides Nucleotides Nucleic Acids. 2023.
PMID: 36708261
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The effect of hereditary thrombotic factors and comorbidities on the severity of COVID-19 disease.
Kose M, Senkal N, Konyaoglu H, Emet A, Oyaci Y, Pehlivan S, Sayin GY.
Kose M, et al. Among authors: sayin gy.
Eur Rev Med Pharmacol Sci. 2023 Jan;27(1):395-403. doi: 10.26355/eurrev_202301_30893.
Eur Rev Med Pharmacol Sci. 2023.
PMID: 36647888
Free article.
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