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Exome sequencing reveals neurodevelopmental genes in simplex consanguineous Iranian families with syndromic autism.
Ghasemi MR, Sadeghi H, Hashemi-Gorji F, Mirfakhraie R, Gupta V, Ben-Mahmoud A, Bagheri S, Razjouyan K, Salehpour S, Tonekaboni SH, Dianatpour M, Omrani D, Jang MH, Layman LC, Miryounesi M, Kim HG. Ghasemi MR, et al. Among authors: mirfakhraie r. BMC Med Genomics. 2024 Aug 5;17(1):196. doi: 10.1186/s12920-024-01969-6. BMC Med Genomics. 2024. PMID: 39103847 Free PMC article.
Association of β-Secretase Functional Polymorphism with Risk of Schizophrenia.
Rahimi-Aliabadi S, Shahmohammadibeni N, Jamshidi J, Shandiz EE, Mirfakhraie R, Ohadi M, Nejad FR, Mansoori N, Taheri M, Gholipour F, Moudi S, Tayebi G, Divsalar S, Darvish H, Movafagh A. Rahimi-Aliabadi S, et al. Among authors: mirfakhraie r. Genet Test Mol Biomarkers. 2017 Apr;21(4):248-251. doi: 10.1089/gtmb.2016.0262. Epub 2017 Feb 21. Genet Test Mol Biomarkers. 2017. PMID: 28384043
143 results