Zadjali F - Search Results

1

The diagnostic yield, candidate genes, and pitfalls for a genetic study of intellectual disability in 118 middle eastern families.

Al-Kasbi G, Al-Murshedi F, Al-Kindi A, Al-Hashimi N, Al-Thihli K, Al-Saegh A, Al-Futaisi A, Al-Mamari W, Al-Asmi A, Bruwer Z, Al-Kharusi K, Al-Rashdi S, Zadjali F, Al-Yahyaee S, Al-Maawali A. Al-Kasbi G, et al. Among authors: zadjali f. Sci Rep. 2022 Nov 7;12(1):18862. doi: 10.1038/s41598-022-22036-z. Sci Rep. 2022. PMID: 36344539 Free PMC article.

2

Reanalysis of exome sequencing data of intellectual disability samples: Yields and benefits.

Al-Nabhani M, Al-Rashdi S, Al-Murshedi F, Al-Kindi A, Al-Thihli K, Al-Saegh A, Al-Futaisi A, Al-Mamari W, Zadjali F, Al-Maawali A. Al-Nabhani M, et al. Among authors: zadjali f. Clin Genet. 2018 Dec;94(6):495-501. doi: 10.1111/cge.13438. Epub 2018 Sep 12. Clin Genet. 2018. PMID: 30125339

3

Biallelic PTRHD1 Frameshift Variants Associated with Intellectual Disability, Spasticity, and Parkinsonism.

Al-Kasbi G, Al-Saegh A, Al-Qassabi A, Al-Jabry T, Zadjali F, Al-Yahyaee S, Al-Maawali A. Al-Kasbi G, et al. Among authors: zadjali f. Mov Disord Clin Pract. 2021 Sep 20;8(8):1253-1257. doi: 10.1002/mdc3.13342. eCollection 2021 Nov. Mov Disord Clin Pract. 2021. PMID: 34765690 Free PMC article.

4

Homozygosity for FARSB mutation leads to Phe-tRNA synthetase-related disease of growth restriction, brain calcification, and interstitial lung disease.

Zadjali F, Al-Yahyaee A, Al-Nabhani M, Al-Mubaihsi S, Gujjar A, Raniga S, Al-Maawali A. Zadjali F, et al. Hum Mutat. 2018 Oct;39(10):1355-1359. doi: 10.1002/humu.23595. Epub 2018 Jul 30. Hum Mutat. 2018. PMID: 30014610

5

The Parental and Children Report of the Prevalence of Depressive Symptoms in Children and Adolescents Amid the COVID-19 Pandemic: A Cross-Sectional Study From Oman.

Zadjali F, Al-Futaisi A, Al-Hosni A, Al-Huseini S, Crommelin M, Mirza H. Zadjali F, et al. Int J Public Health. 2022 Aug 25;67:1604474. doi: 10.3389/ijph.2022.1604474. eCollection 2022. Int J Public Health. 2022. PMID: 36090839 Free PMC article.

6

Mucolipidosis Type IV in Omani Families with a Novel MCOLN1 Mutation: Search for Evidence of Founder Effect.

Al-Alawi B, Harikrishna B, Al-Thihli K, Al Zuhabi S, Ganesh A, Al Hashami Z, Al Dhamhmani Z, Zadjali R, Al Riyami NB, Zadjali F. Al-Alawi B, et al. Among authors: zadjali r, zadjali f. Genes (Basel). 2022 Jan 28;13(2):248. doi: 10.3390/genes13020248. Genes (Basel). 2022. PMID: 35205297 Free PMC article.

7

The Genetic Spectrum of Familial Hypertriglyceridemia in Oman.

Al-Waili K, Al-Rasadi K, Al-Bulushi M, Habais M, Al-Mujaini A, Al-Yaarubi S, Rimbert A, Zadjali R, Khaniabadi PM, Al-Barwani H, Hasary S, Al-Dahmani ZM, Al-Badi H, Al-Maawali A, Zadjali F. Al-Waili K, et al. Among authors: zadjali r, zadjali f. Front Genet. 2022 May 20;13:886182. doi: 10.3389/fgene.2022.886182. eCollection 2022. Front Genet. 2022. PMID: 35669187 Free PMC article.

8

N-acetyltransferase polymorphism among northern Sudanese.

Al-Yahyaee S, Gaffar U, Al-Ameri MM, Qureshi M, Zadjali F, Ali BH, Bayoumi R. Al-Yahyaee S, et al. Among authors: zadjali f. Hum Biol. 2007 Aug;79(4):445-52. doi: 10.1353/hub.2007.0047. Hum Biol. 2007. PMID: 18075007

9

Utility of large consanguineous family-based model for investigating the genetics of type 2 diabetes mellitus.

Al-Sinani S, Hassan MO, Zadjali F, Al-Yahyaee S, Albarwani S, Rizvi S, Jaju D, Comuzzie A, Voruganti VS, Bayoumi R. Al-Sinani S, et al. Among authors: zadjali f. Gene. 2014 Sep 10;548(1):22-8. doi: 10.1016/j.gene.2014.06.053. Epub 2014 Jun 30. Gene. 2014. PMID: 24993573

10

The ubiquitin ligase Cullin5^SOCS2 regulates NDR1/STK38 stability and NF-κB transactivation.

Paul I, Batth TS, Iglesias-Gato D, Al-Araimi A, Al-Haddabi I, Alkharusi A, Norstedt G, Olsen JV, Zadjali F, Flores-Morales A. Paul I, et al. Among authors: zadjali f. Sci Rep. 2017 Feb 20;7:42800. doi: 10.1038/srep42800. Sci Rep. 2017. PMID: 28216640 Free PMC article.

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