Al-Sarraj Y - Search Results

1

The Genetic Architecture of Vitamin D Deficiency among an Elderly Lebanese Middle Eastern Population: An Exome-Wide Association Study.

Hendi NN, Chakhtoura M, Al-Sarraj Y, Basha DS, Albagha O, Fuleihan GE, Nemer G. Hendi NN, et al. Among authors: al sarraj y. Nutrients. 2023 Jul 20;15(14):3216. doi: 10.3390/nu15143216. Nutrients. 2023. PMID: 37513634 Free PMC article.

2

Heterozygous PDGFRB Mutation in a Three-generation Family with Autosomal Dominant Infantile Myofibromatosis.

Lepelletier C, Al-Sarraj Y, Bodemer C, Shaath H, Fraitag S, Kambouris M, Hamel-Teillac D, El Shanti H, Hadj-Rabia S. Lepelletier C, et al. Acta Derm Venereol. 2017 Jul 6;97(7):858-859. doi: 10.2340/00015555-2671. Acta Derm Venereol. 2017. PMID: 28417142 Free article. No abstract available.

3

Host Genetic Variants Potentially Associated With SARS-CoV-2: A Multi-Population Analysis.

Smatti MK, Al-Sarraj YA, Albagha O, Yassine HM. Smatti MK, et al. Front Genet. 2020 Oct 2;11:578523. doi: 10.3389/fgene.2020.578523. eCollection 2020. Front Genet. 2020. PMID: 33133166 Free PMC article.

4

Whole genome sequencing in the Middle Eastern Qatari population identifies genetic associations with 45 clinically relevant traits.

Thareja G, Al-Sarraj Y, Belkadi A, Almotawa M; Qatar Genome Program Research (QGPR) Consortium; Suhre K, Albagha OME. Thareja G, et al. Nat Commun. 2021 Feb 23;12(1):1250. doi: 10.1038/s41467-021-21381-3. Nat Commun. 2021. PMID: 33623009 Free PMC article.

5

Family-Based Genome-Wide Association Study of Autism Spectrum Disorder in Middle Eastern Families.

Al-Sarraj Y, Al-Dous E, Taha RZ, Ahram D, Alshaban F, Tolfat M, El-Shanti H, Albagha OME. Al-Sarraj Y, et al. Genes (Basel). 2021 May 18;12(5):761. doi: 10.3390/genes12050761. Genes (Basel). 2021. PMID: 34069769 Free PMC article.

6

Thousands of Qatari genomes inform human migration history and improve imputation of Arab haplotypes.

Razali RM, Rodriguez-Flores J, Ghorbani M, Naeem H, Aamer W, Aliyev E, Jubran A; Qatar Genome Program Research Consortium; Clark AG, Fakhro KA, Mokrab Y. Razali RM, et al. Nat Commun. 2021 Oct 12;12(1):5929. doi: 10.1038/s41467-021-25287-y. Nat Commun. 2021. PMID: 34642339 Free PMC article.

7

Qatar genome: Insights on genomics from the Middle East.

Mbarek H, Devadoss Gandhi G, Selvaraj S, Al-Muftah W, Badji R, Al-Sarraj Y, Saad C, Darwish D, Alvi M, Fadl T, Yasin H, Alkuwari F, Razali R, Aamer W, Abbaszadeh F, Ahmed I, Mokrab Y, Suhre K, Albagha O, Fakhro K, Badii R, Ismail SI, Althani A; Qatar Genome Program Research Consortium. Mbarek H, et al. Hum Mutat. 2022 Apr;43(4):499-510. doi: 10.1002/humu.24336. Epub 2022 Feb 20. Hum Mutat. 2022. PMID: 35112413

8

Genetic predisposition to cancer across people of different ancestries in Qatar: a population-based, cohort study.

Saad M, Mokrab Y, Halabi N, Shan J, Razali R, Kunji K, Syed N, Temanni R, Subramanian M, Ceccarelli M; Qatar Genome Programme Research Consortium; Rafii Tabrizi A, Bedognetti D, Chouchane L. Saad M, et al. Lancet Oncol. 2022 Mar;23(3):341-352. doi: 10.1016/S1470-2045(21)00752-X. Epub 2022 Feb 9. Lancet Oncol. 2022. PMID: 35150601

9

A population study of clinically actionable genetic variation affecting drug response from the Middle East.

Jithesh PV, Abuhaliqa M, Syed N, Ahmed I, El Anbari M, Bastaki K, Sherif S, Umlai UK, Jan Z, Gandhi G, Manickam C, Selvaraj S, George C, Bangarusamy D, Abdel-Latif R, Al-Shafai M, Tatari-Calderone Z, Estivill X, Pirmohamed M; Qatar Genome Program Research Consortium. Jithesh PV, et al. NPJ Genom Med. 2022 Feb 15;7(1):10. doi: 10.1038/s41525-022-00281-5. NPJ Genom Med. 2022. PMID: 35169154 Free PMC article.

10

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.

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