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Page 1
Beyond the exome: utility of long-read whole genome sequencing in exome-negative autosomal recessive diseases.
Genome Med. 2023 Dec 14;15(1):114. doi: 10.1186/s13073-023-01270-8.
Genome Med. 2023.
PMID: 38098057
Free PMC article.
Gene Expression and Transcriptome Profiling of Changes in a Cancer Cell Line Post-Exposure to Cadmium Telluride Quantum Dots: Possible Implications in Oncogenesis.
Aldughaim MS, Al-Anazi MR, Bohol MFF, Colak D, Alothaid H, Wakil SM, Hagos ST, Ali D, Alarifi S, Rout S, Alkahtani S, Al-Ahdal MN, Al-Qahtani AA.
Aldughaim MS, et al. Among authors: hagos st.
Dose Response. 2021 Jun 11;19(2):15593258211019880. doi: 10.1177/15593258211019880. eCollection 2021 Apr-Jun.
Dose Response. 2021.
PMID: 34177396
Free PMC article.
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The clinical utility of molecular karyotyping for neurocognitive phenotypes in a consanguineous population.
Al-Qattan SM, Wakil SM, Anazi S, Alazami AM, Patel N, Shaheen R, Shamseldin HE, Hagos ST, AlDossari HM, Salih MA, El Khashab HY, Kentab AY, AlNasser MN, Bashiri FA, Kaya N, Hashem MO, Alkuraya FS.
Al-Qattan SM, et al. Among authors: hagos st.
Genet Med. 2015 Sep;17(9):719-25. doi: 10.1038/gim.2014.184. Epub 2014 Dec 11.
Genet Med. 2015.
PMID: 25503496
Free article.
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Autosomal recessive hereditary spastic paraplegia with thin corpus callosum among Saudis.
Wakil SM, Murad HN, Baz BM, Hagos ST, Al-Amr RA, Al-Yamani SA, Al-Wadaee SM, Meyer BF, Bohlega SA.
Wakil SM, et al. Among authors: hagos st.
Neurosciences (Riyadh). 2012 Jan;17(1):48-52.
Neurosciences (Riyadh). 2012.
PMID: 22246010
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