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Genetic profiling of children with advanced cholestatic liver disease.
Shagrani M, Burkholder J, Broering D, Abouelhoda M, Faquih T, El-Kalioby M, Subhani SN, Goljan E, Albar R, Monies D, Mazhar N, AlAbdulaziz BS, Abdelrahman KA, Altassan N, Alkuraya FS. Shagrani M, et al. Among authors: alabdulaziz bs. Clin Genet. 2017 Jul;92(1):52-61. doi: 10.1111/cge.12959. Epub 2017 Mar 17. Clin Genet. 2017. PMID: 28039895
Parkinson's Disease in Saudi Patients: A Genetic Study.
Al-Mubarak BR, Bohlega SA, Alkhairallah TS, Magrashi AI, AlTurki MI, Khalil DS, AlAbdulaziz BS, Abou Al-Shaar H, Mustafa AE, Alyemni EA, Alsaffar BA, Tahir AI, Al Tassan NA. Al-Mubarak BR, et al. Among authors: alabdulaziz bs. PLoS One. 2015 Aug 14;10(8):e0135950. doi: 10.1371/journal.pone.0135950. eCollection 2015. PLoS One. 2015. PMID: 26274610 Free PMC article. Clinical Trial.
Integrated Analysis of Whole Exome Sequencing and Copy Number Evaluation in Parkinson's Disease.
Yemni EA, Monies D, Alkhairallah T, Bohlega S, Abouelhoda M, Magrashi A, Mustafa A, AlAbdulaziz B, Alhamed M, Baz B, Goljan E, Albar R, Jabaan A, Faquih T, Subhani S, Ali W, Shinwari J, Al-Mubarak B, Al-Tassan N. Yemni EA, et al. Among authors: alabdulaziz b. Sci Rep. 2019 Mar 4;9(1):3344. doi: 10.1038/s41598-019-40102-x. Sci Rep. 2019. PMID: 30833663 Free PMC article.
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.