Search details
1.
Indigenous Arabs are descendants of the earliest split from ancient Eurasian populations.
Genome Res
; 26(2): 151-62, 2016 Feb.
Article
in English
| MEDLINE | ID: mdl-26728717
2.
Point-of-care whole-exome sequencing of idiopathic male infertility.
Genet Med
; 20(11): 1365-1373, 2018 11.
Article
in English
| MEDLINE | ID: mdl-29790874
3.
Reconstructing Native American migrations from whole-genome and whole-exome data.
PLoS Genet
; 9(12): e1004023, 2013.
Article
in English
| MEDLINE | ID: mdl-24385924
4.
Copy number variations in the genome of the Qatari population.
BMC Genomics
; 16: 834, 2015 Oct 22.
Article
in English
| MEDLINE | ID: mdl-26490036
5.
Exome sequencing identifies potential risk variants for Mendelian disorders at high prevalence in Qatar.
Hum Mutat
; 35(1): 105-16, 2014 Jan.
Article
in English
| MEDLINE | ID: mdl-24123366
6.
Cysteine-Altering NOTCH3 Variants Are Associated with an Increased Risk of Autoimmune Diseases.
J Clin Med
; 12(19)2023 Sep 29.
Article
in English
| MEDLINE | ID: mdl-37834922
7.
RNA-Seq quantification of the human small airway epithelium transcriptome.
BMC Genomics
; 13: 82, 2012 Feb 29.
Article
in English
| MEDLINE | ID: mdl-22375630
8.
Inferring genome-wide patterns of admixture in Qataris using fifty-five ancestral populations.
BMC Genet
; 13: 49, 2012 Jun 26.
Article
in English
| MEDLINE | ID: mdl-22734698
9.
The QChip1 knowledgebase and microarray for precision medicine in Qatar.
NPJ Genom Med
; 7(1): 3, 2022 Jan 19.
Article
in English
| MEDLINE | ID: mdl-35046417
10.
Pro-hormone secretogranin II regulates dense core secretory granule biogenesis in catecholaminergic cells.
J Biol Chem
; 285(13): 10030-10043, 2010 Mar 26.
Article
in English
| MEDLINE | ID: mdl-20061385
11.
Mitochondrial haplogroup J associated with higher risk of obesity in the Qatari population.
Sci Rep
; 11(1): 1091, 2021 01 13.
Article
in English
| MEDLINE | ID: mdl-33441698
12.
Large-Scale Identification of Clonal Hematopoiesis and Mutations Recurrent in Blood Cancers.
Blood Cancer Discov
; 2(3): 226-237, 2021 05.
Article
in English
| MEDLINE | ID: mdl-34027416
13.
Genome diversity in Ukraine.
Gigascience
; 10(1)2021 01 13.
Article
in English
| MEDLINE | ID: mdl-33438729
14.
Discovery of common human genetic variants of GTP cyclohydrolase 1 (GCH1) governing nitric oxide, autonomic activity, and cardiovascular risk.
J Clin Invest
; 117(9): 2658-71, 2007 Sep.
Article
in English
| MEDLINE | ID: mdl-17717598
15.
Conserved regulatory motifs at phenylethanolamine N-methyltransferase (PNMT) are disrupted by common functional genetic variation: an integrated computational/experimental approach.
Mamm Genome
; 21(3-4): 195-204, 2010 Apr.
Article
in English
| MEDLINE | ID: mdl-20204374
16.
Human tyrosine hydroxylase natural allelic variation: influence on autonomic function and hypertension.
Cell Mol Neurobiol
; 30(8): 1391-4, 2010 Nov.
Article
in English
| MEDLINE | ID: mdl-20571875
17.
Genomes of Three Closely Related Caribbean Amazons Provide Insight for Species History and Conservation.
Genes (Basel)
; 10(1)2019 01 16.
Article
in English
| MEDLINE | ID: mdl-30654561
18.
Tyrosine hydroxylase, the rate-limiting enzyme in catecholamine biosynthesis: discovery of common human genetic variants governing transcription, autonomic activity, and blood pressure in vivo.
Circulation
; 116(9): 993-1006, 2007 Aug 28.
Article
in English
| MEDLINE | ID: mdl-17698732
19.
Whole-exome sequencing identifies common and rare variant metabolic QTLs in a Middle Eastern population.
Nat Commun
; 9(1): 333, 2018 01 23.
Article
in English
| MEDLINE | ID: mdl-29362361
20.
Exome sequencing-based identification of novel type 2 diabetes risk allele loci in the Qatari population.
PLoS One
; 13(9): e0199837, 2018.
Article
in English
| MEDLINE | ID: mdl-30212457