selected publications
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Genomes of Three Closely Related Caribbean Amazons Provide Insight for Species History and Conservation.
Genes.
2019
Academic Article
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Times cited: 8 -
Whole-methylome analysis of circulating monocytes in acute diabetic Charcot foot reveals differentially methylated genes involved in the formation of osteoclasts.
Epigenomics.
2018
Academic Article
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Times cited: 11 -
Exome sequencing-based identification of novel type 2 diabetes risk allele loci in the Qatari population.
PloS one.
2018
Academic Article
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Times cited: 7 -
Point-of-care whole-exome sequencing of idiopathic male infertility.
Genetics in medicine : official journal of the American College of Medical Genetics.
2018
Academic Article
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Times cited: 35 -
Whole-exome sequencing identifies common and rare variant metabolic QTLs in a Middle Eastern population.
Nature communications.
2018
Academic Article
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Times cited: 50 -
Rare Synaptogenesis-Impairing Mutations in SLITRK5 Are Associated with Obsessive Compulsive Disorder.
PloS one.
2017
Academic Article
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Times cited: 27 -
Correction: Type 2 Diabetes Risk Allele Loci in the Qatari Population.
2016
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Times cited: 1 -
Type 2 Diabetes Risk Allele Loci in the Qatari Population.
PloS one.
2016
Academic Article
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Times cited: 23 -
The Qatar genome: a population-specific tool for precision medicine in the Middle East.
Human genome variation.
2016
Academic Article
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Times cited: 88 -
Indigenous Arabs are descendants of the earliest split from ancient Eurasian populations.
Genome research.
2016
Academic Article
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Times cited: 72 -
Copy number variations in the genome of the Qatari population.
BMC genomics.
2015
Academic Article
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Times cited: 9 -
Reconstructing Native American migrations from whole-genome and whole-exome data.
PLoS genetics.
2013
Academic Article
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Times cited: 139 -
Exome sequencing identifies potential risk variants for Mendelian disorders at high prevalence in Qatar.
Human mutation.
2013
Academic Article
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Times cited: 43 -
Prevalence of the apolipoprotein E Arg145Cys dyslipidemia at-risk polymorphism in African-derived populations.
The American journal of cardiology.
2013
Academic Article
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Times cited: 14 -
Exome sequencing of only seven Qataris identifies potentially deleterious variants in the Qatari population.
PloS one.
2012
Academic Article
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Times cited: 16 -
Inferring genome-wide patterns of admixture in Qataris using fifty-five ancestral populations.
BMC genetics.
2012
Academic Article
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Times cited: 49 -
RNA-Seq quantification of the human small airway epithelium transcriptome.
BMC genomics.
2012
Academic Article
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Times cited: 96 -
Human dopamine β-hydroxylase promoter variant alters transcription in chromaffin cells, enzyme secretion, and blood pressure.
American journal of hypertension.
2010
Academic Article
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Times cited: 15 -
Common functional genetic variants in catecholamine storage vesicle protein promoter motifs interact to trigger systemic hypertension.
Journal of the American College of Cardiology.
2010
Academic Article
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Times cited: 20 -
Conserved regulatory motifs at phenylethanolamine N-methyltransferase (PNMT) are disrupted by common functional genetic variation: an integrated computational/experimental approach.
Mammalian genome : official journal of the International Mammalian Genome Society.
2010
Academic Article
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Times cited: 6 -
Human tyrosine hydroxylase natural genetic variation: delineation of functional transcriptional control motifs disrupted in the proximal promoter.
Circulation. Cardiovascular genetics.
2010
Academic Article
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Times cited: 30 -
Pro-hormone secretogranin II regulates dense core secretory granule biogenesis in catecholaminergic cells.
The Journal of biological chemistry.
2010
Academic Article
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Times cited: 38 -
Human dopamine beta-hydroxylase (DBH) regulatory polymorphism that influences enzymatic activity, autonomic function, and blood pressure.
Journal of hypertension.
2010
Academic Article
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Times cited: 46 -
Neuropeptide Y(1) Receptor NPY1R discovery of naturally occurring human genetic variants governing gene expression in cella as well as pleiotropic effects on autonomic activity and blood pressure in vivo.
Journal of the American College of Cardiology.
2009
Academic Article
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Times cited: 26 -
Cathepsin L colocalizes with chromogranin a in chromaffin vesicles to generate active peptides.
Endocrinology.
2009
Academic Article
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Times cited: 61 -
Autonomic function in hypertension; role of genetic variation at the catecholamine storage vesicle protein chromogranin B.
Circulation. Cardiovascular genetics.
2009
Academic Article
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Times cited: 21 -
Naturally occurring human genetic variation in the 3'-untranslated region of the secretory protein chromogranin A is associated with autonomic blood pressure regulation and hypertension in a sex-dependent fashion.
Journal of the American College of Cardiology.
2008
Academic Article
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Times cited: 39 -
Common genetic variants in the chromogranin A promoter alter autonomic activity and blood pressure.
Kidney international.
2008
Academic Article
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Times cited: 27 -
Discovery of common human genetic variants of GTP cyclohydrolase 1 (GCH1) governing nitric oxide, autonomic activity, and cardiovascular risk.
The Journal of clinical investigation.
2007
Academic Article
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Times cited: 80 -
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.
2007
Academic Article
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Times cited: 74 - [Treatment of fractures of the proximal epiphysis of the femur using a compression screw and plate designed and constructed in Mexico]. Salud publica de Mexico. 1987 Academic Article GET IT