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Genomic variants in the FTO gene are associated with sporadic amyotrophic lateral sclerosis in Greek patients.
Hum Genomics. 2017 Dec 8;11(1):30. doi: 10.1186/s40246-017-0126-2.
Hum Genomics. 2017.
PMID: 29216901
Free PMC article.
Genomic variants in members of the Krüppel-like factor gene family are associated with disease severity and hydroxyurea treatment efficacy in β-hemoglobinopathies patients.
Stratopoulos A, Kolliopoulou A, Karamperis K, John A, Kydonopoulou K, Esftathiou G, Sgourou A, Kourakli A, Vlachaki E, Chalkia P, Theodoridou S, Papadakis MN, Gerou S, Symeonidis A, Katsila T, Ali BR, Papachatzopoulou A, Patrinos GP.
Stratopoulos A, et al. Among authors: kydonopoulou k.
Pharmacogenomics. 2019 Jul;20(11):791-801. doi: 10.2217/pgs-2019-0063. Epub 2019 Aug 8.
Pharmacogenomics. 2019.
PMID: 31393228
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Association of GPIa C807T polymorphism with unexplained female infertility and IVF implantation failure.
Kydonopoulou K, Rousso D, Ilonidis G, Mandala E.
Kydonopoulou K, et al.
J Biol Regul Homeost Agents. 2019 May-Jun,;33(3):883-887.
J Biol Regul Homeost Agents. 2019.
PMID: 31184100
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Association of plasminogen activator inhibitor-type 1 (PAI-1) -675 4G/5G polymorphism with unexplained female infertility.
Kydonopoulou K, Delkos D, Rousso D, Ilonidis G, Mandala E.
Kydonopoulou K, et al.
Hippokratia. 2017 Oct-Dec;21(4):180-185.
Hippokratia. 2017.
PMID: 30944508
Free PMC article.
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Novel Pathogenic Variants Leading to Sporadic Amyotrophic Lateral Sclerosis in Greek Patients.
Ivantsik O, John A, Kydonopoulou K, Mitropoulos K, Gerou S, Ali BR, Patrinos GP.
Ivantsik O, et al. Among authors: kydonopoulou k.
Genes (Basel). 2024 Feb 28;15(3):309. doi: 10.3390/genes15030309.
Genes (Basel). 2024.
PMID: 38540370
Free PMC article.
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