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Loss-of-function variants of SETD5 cause intellectual disability and the core phenotype of microdeletion 3p25.3 syndrome.
Kuechler A, Zink AM, Wieland T, Lüdecke HJ, Cremer K, Salviati L, Magini P, Najafi K, Zweier C, Czeschik JC, Aretz S, Endele S, Tamburrino F, Pinato C, Clementi M, Gundlach J, Maylahn C, Mazzanti L, Wohlleber E, Schwarzmayr T, Kariminejad R, Schlessinger A, Wieczorek D, Strom TM, Novarino G, Engels H. Kuechler A, et al. Among authors: najafi k. Eur J Hum Genet. 2015 Jun;23(6):753-60. doi: 10.1038/ejhg.2014.165. Epub 2014 Aug 20. Eur J Hum Genet. 2015. PMID: 25138099 Free PMC article.
5p13 microduplication in a malformed fetus and his unaffected father.
Kariminejad A, Ghaderi-Sohi S, Gholami S, Najafi K, Kariminejad R, Hennekam RCM. Kariminejad A, et al. Among authors: najafi k. Am J Med Genet A. 2023 Feb;191(2):370-377. doi: 10.1002/ajmg.a.63030. Epub 2022 Nov 2. Am J Med Genet A. 2023. PMID: 36322476
Mitral Valve Repair of the Anterior Leaflet: Are We There Yet?
Bahiraie P, Soleimani H, Heydari N, Najafi K, Karlas A, Avgerinos DV, Samanidis G, Kuno T, Doulamis IP, Ioannis I, Spilias N, Hosseini K, Kampaktsis PN. Bahiraie P, et al. Among authors: najafi k. Hellenic J Cardiol. 2024 Feb 13:S1109-9666(24)00025-3. doi: 10.1016/j.hjc.2024.02.001. Online ahead of print. Hellenic J Cardiol. 2024. PMID: 38355045 Free article. Review.
The association between metabolic syndrome and major adverse cardiac and cerebrovascular events in patients with acute coronary syndrome undergoing percutaneous coronary intervention.
Hosseini K, Khalaji A, Behnoush AH, Soleimani H, Mehrban S, Amirsardari Z, Najafi K, Fathian Sabet M, Hosseini Mohammadi NS, Shojaei S, Masoudkabir F, Aghajani H, Mehrani M, Razjouyan H, Hernandez AV. Hosseini K, et al. Among authors: najafi k. Sci Rep. 2024 Jan 6;14(1):697. doi: 10.1038/s41598-024-51157-w. Sci Rep. 2024. PMID: 38184738 Free PMC article.
82 results