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The AfrAbia+plus Parkinson's Disease Genomic Consortium.
Mohamed W, Eltantawi MA, Mecheri Y, Zewde YZ, Kamel WA, Al-Mubarak BR, Alzoubi KH, Kissani N, Alghamdi BS, Ben Sassi S; AfrAbia plus Parkinsons Disease Genomic Consortium. Mohamed W, et al. Among authors: al mubarak br. Lancet Neurol. 2024 Feb;23(2):140-141. doi: 10.1016/S1474-4422(23)00453-2. Lancet Neurol. 2024. PMID: 38267182 No abstract available.
Whole exome sequencing in ADHD trios from single and multi-incident families implicates new candidate genes and highlights polygenic transmission.
Al-Mubarak BR, Omar A, Baz B, Al-Abdulaziz B, Magrashi AI, Al-Yemni E, Jabaan A, Monies D, Abouelhoda M, Abebe D, Ghaziuddin M, Al-Tassan NA. Al-Mubarak BR, et al. Eur J Hum Genet. 2020 Aug;28(8):1098-1110. doi: 10.1038/s41431-020-0619-7. Epub 2020 Apr 1. Eur J Hum Genet. 2020. PMID: 32238911 Free PMC article.
Validation of Ion TorrentTM Inherited Disease Panel with the PGMTM Sequencing Platform for Rapid and Comprehensive Mutation Detection.
Mustafa AE, Faquih T, Baz B, Kattan R, Al-Issa A, Tahir AI, Imtiaz F, Ramzan K, Al-Sayed M, Alowain M, Al-Hassnan Z, Al-Zaidan H, Abouelhoda M, Al-Mubarak BR, Al Tassan NA. Mustafa AE, et al. Among authors: al mubarak br. Genes (Basel). 2018 May 22;9(5):267. doi: 10.3390/genes9050267. Genes (Basel). 2018. PMID: 29789446 Free PMC article.
Clinical heterogeneity of PLA2G6-related Parkinsonism: analysis of two Saudi families.
Bohlega SA, Al-Mubarak BR, Alyemni EA, Abouelhoda M, Monies D, Mustafa AE, Khalil DS, Al Haibi S, Abou Al-Shaar H, Faquih T, El-Kalioby M, Tahir AI, Al Tassan NA. Bohlega SA, et al. Among authors: al mubarak br. BMC Res Notes. 2016 Jun 7;9:295. doi: 10.1186/s13104-016-2102-7. BMC Res Notes. 2016. PMID: 27268037 Free PMC article.
12 results