Syed N - Search Results

1

Ethnic-specific association of amylase gene copy number with adiposity traits in a large Middle Eastern biobank.

Rossi N, Aliyev E, Visconti A, Akil ASA, Syed N, Aamer W, Padmajeya SS, Falchi M, Fakhro KA. Rossi N, et al. Among authors: syed n. NPJ Genom Med. 2021 Feb 9;6(1):8. doi: 10.1038/s41525-021-00170-3. NPJ Genom Med. 2021. PMID: 33563995 Free PMC article.

2

Single-Nucleotide Variations of the Human Nuclear Hormone Receptor Genes in 60,000 Individuals.

Mackeh R, Marr AK, Dargham SR, Syed N, Fakhro KA, Kino T. Mackeh R, et al. Among authors: syed n. J Endocr Soc. 2017 Dec 4;2(1):77-90. doi: 10.1210/js.2017-00406. eCollection 2018 Jan 1. J Endocr Soc. 2017. PMID: 29379896 Free PMC article.

3

Point-of-care whole-exome sequencing of idiopathic male infertility.

Fakhro KA, Elbardisi H, Arafa M, Robay A, Rodriguez-Flores JL, Al-Shakaki A, Syed N, Mezey JG, Abi Khalil C, Malek JA, Al-Ansari A, Al Said S, Crystal RG. Fakhro KA, et al. Among authors: syed n. Genet Med. 2018 Nov;20(11):1365-1373. doi: 10.1038/gim.2018.10. Epub 2018 Apr 12. Genet Med. 2018. PMID: 29790874 Free article.

4

Genetic and Neuroimaging Approaches to Understanding Post-Traumatic Stress Disorder.

Nisar S, Bhat AA, Hashem S, Syed N, Yadav SK, Uddin S, Fakhro K, Bagga P, Thompson P, Reddy R, Frenneaux MP, Haris M. Nisar S, et al. Among authors: syed n. Int J Mol Sci. 2020 Jun 24;21(12):4503. doi: 10.3390/ijms21124503. Int J Mol Sci. 2020. PMID: 32599917 Free PMC article. Review.

5

Genome sequencing unveils mutational landscape of the familial Mediterranean fever: Potential implications of IL33/ST2 signalling.

Umar M, Megarbane A, Shan J, Syed N, Chouery E, Aliyev E, Jithesh P, Temanni R, Mansour I, Chouchane L, Ismail Chouchane A. Umar M, et al. Among authors: syed n. J Cell Mol Med. 2020 Oct;24(19):11294-11306. doi: 10.1111/jcmm.15701. Epub 2020 Aug 27. J Cell Mol Med. 2020. PMID: 32853466 Free PMC article.

6

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.

7

Genetic variations influence brain changes in patients with attention-deficit hyperactivity disorder.

Yadav SK, Bhat AA, Hashem S, Nisar S, Kamal M, Syed N, Temanni MR, Gupta RK, Kamran S, Azeem MW, Srivastava AK, Bagga P, Chawla S, Reddy R, Frenneaux MP, Fakhro K, Haris M. Yadav SK, et al. Among authors: syed n. Transl Psychiatry. 2021 Jun 5;11(1):349. doi: 10.1038/s41398-021-01473-w. Transl Psychiatry. 2021. PMID: 34091591 Free PMC article. Review.

8

Brain microstructural changes support cognitive deficits in HIV uninfected children born to HIV infected mothers.

Yadav SK, Gupta RK, Hashem S, Nisar S, Azeem T, Bhat AA, Syed N, Garg RK, Venkatesh V, Kamal M, Fakhro K, Frenneaux MP, Haris M. Yadav SK, et al. Among authors: syed n. Brain Behav Immun Health. 2020 Jan 26;2:100039. doi: 10.1016/j.bbih.2020.100039. eCollection 2020 Feb. Brain Behav Immun Health. 2020. PMID: 34589830 Free PMC article.

9

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.

10

Maturity-onset diabetes of the young (MODY) due to PDX1 mutation in a sib-pair diabetes family from Qatar.

Haris B, Mohammed I, Syed N, Fakhro K, Hussain K. Haris B, et al. Among authors: syed n. Clin Case Rep. 2021 Dec 11;9(12):e05141. doi: 10.1002/ccr3.5141. eCollection 2021 Dec. Clin Case Rep. 2021. PMID: 34938542 Free PMC article.

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