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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2010 2
2011 2
2012 9
2013 9
2014 9
2015 7
2016 7
2017 10
2018 13
2019 16
2020 10
2021 10
2022 10
2023 13
2024 4

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114 results

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Page 1
Whole exome sequencing revealed variants in four genes underlying X-linked intellectual disability in four Iranian families: novel deleterious variants and clinical features with the review of literature.
Mir A, Song Y, Lee H, Khanahmad H, Khorram E, Nasiri J, Tabatabaiefar MA. Mir A, et al. Among authors: tabatabaiefar ma. BMC Med Genomics. 2023 Oct 11;16(1):239. doi: 10.1186/s12920-023-01680-y. BMC Med Genomics. 2023. PMID: 37821930 Free PMC article. Review.
Monogenic etiologies of persistent human papillomavirus infections: A comprehensive systematic review.
Biglari S, Moghaddam AS, Tabatabaiefar MA, Sherkat R, Youssefian L, Saeidian AH, Vahidnezhad F, Tsoi LC, Gudjonsson JE, Hakonarson H, Casanova JL, Béziat V, Jouanguy E, Vahidnezhad H. Biglari S, et al. Among authors: tabatabaiefar ma. Genet Med. 2024 Feb;26(2):101028. doi: 10.1016/j.gim.2023.101028. Epub 2023 Nov 14. Genet Med. 2024. PMID: 37978863 Review.
Griscelli syndrome type 1: a novel pathogenic variant, and review of literature.
Khorram E, Tabatabaiefar MA, Yaghini O, Khorrami M, Yazdani V, Fakhr F, Amini M, Kheirollahi M. Khorram E, et al. Among authors: tabatabaiefar ma. Mol Genet Genomics. 2023 Mar;298(2):485-493. doi: 10.1007/s00438-022-01971-6. Epub 2023 Jan 18. Mol Genet Genomics. 2023. PMID: 36651988 Review.
Epigenetics and Common Non Communicable Disease.
Tabatabaiefar MA, Sajjadi RS, Narrei S. Tabatabaiefar MA, et al. Adv Exp Med Biol. 2019;1121:7-20. doi: 10.1007/978-3-030-10616-4_2. Adv Exp Med Biol. 2019. PMID: 31392648
A novel TECTA mutation causes ARNSHL.
Asgharzade S, Tabatabaiefar MA, Modarressi MH, Ghahremani MH, Reiisi S, Tahmasebi P, Abdollahnejad F, Chaleshtori MH. Asgharzade S, et al. Among authors: tabatabaiefar ma. Int J Pediatr Otorhinolaryngol. 2017 Jan;92:88-93. doi: 10.1016/j.ijporl.2016.11.010. Epub 2016 Nov 15. Int J Pediatr Otorhinolaryngol. 2017. PMID: 28012541 Free article.
A deleterious frameshift insertion mutation in the ZNF142 gene leads to intellectual developmental disorder with impaired speech in three affected siblings: Clinical features and literature review.
Mir A, Song Y, Lee H, Montazer-Zohouri M, Reisi M, Tabatabaiefar MA. Mir A, et al. Among authors: tabatabaiefar ma. Mol Genet Genomic Med. 2023 Dec;11(12):e2261. doi: 10.1002/mgg3.2261. Epub 2023 Jul 26. Mol Genet Genomic Med. 2023. PMID: 37496384 Free PMC article. Review.
114 results