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Unbiased targeted next-generation sequencing molecular approach for primary immunodeficiency diseases.
J Allergy Clin Immunol. 2016 Jun;137(6):1780-1787. doi: 10.1016/j.jaci.2015.12.1310. Epub 2016 Feb 23.
J Allergy Clin Immunol. 2016.
PMID: 26915675
Association of a mutation in LACC1 with a monogenic form of systemic juvenile idiopathic arthritis.
Wakil SM, Monies DM, Abouelhoda M, Al-Tassan N, Al-Dusery H, Naim EA, Al-Younes B, Shinwari J, Al-Mohanna FA, Meyer BF, Al-Mayouf S.
Wakil SM, et al. Among authors: al dusery h.
Arthritis Rheumatol. 2015 Jan;67(1):288-95. doi: 10.1002/art.38877.
Arthritis Rheumatol. 2015.
PMID: 25220867
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New Insights into the Impact of Genome-Wide Copy Number Variations on Complex Congenital Heart Disease in Saudi Arabia.
Dasouki MJ, Wakil SM, Al-Harazi O, Alkorashy M, Muiya NP, Andres E, Hagos S, Aldusery H, Dzimiri N, Colak D.
Dasouki MJ, et al.
OMICS. 2020 Jan;24(1):16-28. doi: 10.1089/omi.2019.0165. Epub 2019 Dec 19.
OMICS. 2020.
PMID: 31855513
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New or vanishing frontiers: LACC1-associated juvenile arthritis.
Al-Mayouf SM, Yateem M, Al-Dusery H, Monies D, Wakil S, AlShiakh M, AlEnazi A, Aladaileh B, Alzyoud R, Meyer B.
Al-Mayouf SM, et al. Among authors: al dusery h.
Int J Pediatr Adolesc Med. 2021 Mar;8(1):44-47. doi: 10.1016/j.ijpam.2020.11.005. Epub 2020 Nov 12.
Int J Pediatr Adolesc Med. 2021.
PMID: 33718577
Free PMC article.
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Comprehensive gene panels provide advantages over clinical exome sequencing for Mendelian diseases.
Saudi Mendeliome Group.
Saudi Mendeliome Group.
Genome Biol. 2015 Jun 26;16(1):134. doi: 10.1186/s13059-015-0693-2.
Genome Biol. 2015.
PMID: 26112015
Free PMC article.
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