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Page 1
Identification of Novel Circulating miRNAs in Patients with Acute Ischemic Stroke.
Aldous EK, Toor SM, Parray A, Al-Sarraj Y, Diboun I, Abdelalim EM, Arredouani A, El-Agnaf O, Thornalley PJ, Akhtar N, Pananchikkal SV, Shuaib A, Alajez NM, Albagha OME. Aldous EK, et al. Int J Mol Sci. 2022 Mar 21;23(6):3387. doi: 10.3390/ijms23063387. Int J Mol Sci. 2022. PMID: 35328807 Free PMC article.
De novo genome sequencing and comparative genomics of date palm (Phoenix dactylifera).
Al-Dous EK, George B, Al-Mahmoud ME, Al-Jaber MY, Wang H, Salameh YM, Al-Azwani EK, Chaluvadi S, Pontaroli AC, DeBarry J, Arondel V, Ohlrogge J, Saie IJ, Suliman-Elmeer KM, Bennetzen JL, Kruegger RR, Malek JA. Al-Dous EK, et al. Nat Biotechnol. 2011 May 29;29(6):521-7. doi: 10.1038/nbt.1860. Nat Biotechnol. 2011. PMID: 21623354
Mutation in noncoding RNA RNU12 causes early onset cerebellar ataxia.
Elsaid MF, Chalhoub N, Ben-Omran T, Kumar P, Kamel H, Ibrahim K, Mohamoud Y, Al-Dous E, Al-Azwani I, Malek JA, Suhre K, Ross ME, Aleem AA. Elsaid MF, et al. Among authors: al dous e. Ann Neurol. 2017 Jan;81(1):68-78. doi: 10.1002/ana.24826. Ann Neurol. 2017. PMID: 27863452
Connecting genetic risk to disease end points through the human blood plasma proteome.
Suhre K, Arnold M, Bhagwat AM, Cotton RJ, Engelke R, Raffler J, Sarwath H, Thareja G, Wahl A, DeLisle RK, Gold L, Pezer M, Lauc G, El-Din Selim MA, Mook-Kanamori DO, Al-Dous EK, Mohamoud YA, Malek J, Strauch K, Grallert H, Peters A, Kastenmüller G, Gieger C, Graumann J. Suhre K, et al. Among authors: al dous ek. Nat Commun. 2017 Feb 27;8:14357. doi: 10.1038/ncomms14357. Nat Commun. 2017. PMID: 28240269 Free PMC article.
Whole genome sequencing identifies a novel occludin mutation in microcephaly with band-like calcification and polymicrogyria that extends the phenotypic spectrum.
Elsaid MF, Kamel H, Chalhoub N, Aziz NA, Ibrahim K, Ben-Omran T, George B, Al-Dous E, Mohamoud Y, Malek JA, Ross ME, Aleem AA. Elsaid MF, et al. Am J Med Genet A. 2014 Jun;164A(6):1614-7. doi: 10.1002/ajmg.a.36485. Epub 2014 Mar 25. Am J Med Genet A. 2014. PMID: 24668585 No abstract available.
Deep molecular phenotypes link complex disorders and physiological insult to CpG methylation.
Zaghlool SB, Mook-Kanamori DO, Kader S, Stephan N, Halama A, Engelke R, Sarwath H, Al-Dous EK, Mohamoud YA, Roemisch-Margl W, Adamski J, Kastenmüller G, Friedrich N, Visconti A, Tsai PC, Spector T, Bell JT, Falchi M, Wahl A, Waldenberger M, Peters A, Gieger C, Pezer M, Lauc G, Graumann J, Malek JA, Suhre K. Zaghlool SB, et al. Among authors: al dous ek. Hum Mol Genet. 2018 Mar 15;27(6):1106-1121. doi: 10.1093/hmg/ddy006. Hum Mol Genet. 2018. PMID: 29325019 Free PMC article.
18 results