about
Discovery of common human genetic variants of GTP cyclohydrolase 1 (GCH1) governing nitric oxide, autonomic activity, and cardiovascular riskRecurring exon deletions in the HP (haptoglobin) gene contribute to lower blood cholesterol levels.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.Common functional genetic variants in catecholamine storage vesicle protein promoter motifs interact to trigger systemic hypertension.Efficient Bayesian mixed-model analysis increases association power in large cohorts.Pancreastatin: multiple actions on human intermediary metabolism in vivo, variation in disease, and naturally occurring functional genetic polymorphism.Dopamine D1 receptor (DRD1) genetic polymorphism: pleiotropic effects on heritable renal traitsProgression of chronic kidney disease: Adrenergic genetic influence on glomerular filtration rate decline in hypertensive nephrosclerosis.Common charge-shift mutation Glu65Lys in K+ channel β₁-Subunit KCNMB1: pleiotropic consequences for glomerular filtration rate and progressive renal diseaseNaturally occurring genetic variants in human chromogranin A (CHGA) associated with hypertension as well as hypertensive renal disease.Direct vasoactive effects of the chromogranin A (CHGA) peptide catestatin in humans in vivo.Genetic risk factors affecting mitochondrial function are associated with kidney disease in people with Type 1 diabetes.Methylenetetrahydrofolate reductase (MTHFR) polymorphism A1298C (Glu429Ala) predicts decline in renal function over time in the African-American Study of Kidney Disease and Hypertension (AASK) Trial and Veterans Affairs Hypertension Cohort (VAHC).Chromogranin A polymorphisms are associated with hypertensive renal disease.Common genetic variants in the chromogranin A promoter alter autonomic activity and blood pressure.MicroRNA-22 and promoter motif polymorphisms at the Chga locus in genetic hypertension: functional and therapeutic implications for gene expression and the pathogenesis of hypertension.G-protein-coupled receptor kinase 4 polymorphisms and blood pressure response to metoprolol among African Americans: sex-specificity and interactionsAdrenergic beta-1 receptor genetic variation predicts longitudinal rate of GFR decline in hypertensive nephrosclerosis.Determinants of Power in Gene-Based Burden Testing for Monogenic Disorders.Renal albumin excretion: twin studies identify influences of heredity, environment, and adrenergic pathway polymorphism.Genetic Evidence That Carbohydrate-Stimulated Insulin Secretion Leads to Obesity.Prospective associations of C-reactive protein (CRP) levels and CRP genetic risk scores with risk of total knee and hip replacement for osteoarthritis in a diverse cohortGenome-Wide Association Study of Diabetic Kidney Disease Highlights Biology Involved in Glomerular Basement Membrane CollagenUsing metabolite profiling to construct and validate a metabolite risk score for predicting future weight gainEvolutionary Pressure against MHC Class II Binding Cancer MutationsInterrogation of human hematopoiesis at single-cell and single-variant resolution
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description
investigador
@es
researcher
@en
wetenschapper
@nl
name
Rany M Salem
@en
Rany M Salem
@nl
type
label
Rany M Salem
@en
Rany M Salem
@nl
prefLabel
Rany M Salem
@en
Rany M Salem
@nl
P31
P496
0000-0001-8816-6862