Author details

Full Name

Rany M Salem

Affiliation

ORCID

Career Start Year

2004

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37690116	Pediatric Features of Genetic Predisposition to Polycystic Ovary Syndrome.	J Clin Endocrinol Metab	2024
37292977	Genetics of skeletal proportions in two different populations.	bioRxiv	2023
37239390	Differential Methylation of Telomere-Related Genes Is Associated with Kidney Disease in Individuals with Type 1 Diabetes.	Genes (Basel)	2023
37173324	Germline modifiers of the tumor immune microenvironment implicate drivers of cancer risk and immunotherapy response.	Nat Commun	2023
36550108	Epigenome-wide meta-analysis identifies DNA methylation biomarkers associated with diabetic kidney disease.	Nat Commun	2022
35763030	Genome-wide meta-analysis and omics integration identifies novel genes associated with diabetic kidney disease.	Diabetologia	2022
36002033	Associations of Accelerometer-Measured Physical Activity and Sedentary Time With All-Cause Mortality by Genetic Predisposition for Longevity.	J Aging Phys Act	2022
36131047	Rare copy number variation in posttraumatic stress disorder.	Mol Psychiatry	2022
35477353	Markers of kidney function, genetic variation related to cognitive function, and cognitive performance in the UK Biobank.	BMC Nephrology	2022
34534883	Biomarkers of kidney function and cognitive ability: A Mendelian randomization study.	Journal of the Neurological Sciences	2021
34122051	Similar Genetic Architecture of Alzheimer's Disease and Differential <i>APOE</i> Effect Between Sexes.	Front Aging Neurosci	2021
33933144	Assessment of differentially methylated loci in individuals with end-stage kidney disease attributed to diabetic kidney disease: an exploratory study.	Clin Epigenetics	2021
34334390	Markers of Kidney Function and Longitudinal Cognitive Ability Among Older Community-Dwelling Adults: The Rancho Bernardo Study.	Journal of Alzheimer's Disease	2021
35005200	Causal association of cognitive reserve on Alzheimer's disease with putative sex difference.	Alzheimers Dement (Amst)	2021
31537649	Genome-Wide Association Study of Diabetic Kidney Disease Highlights Biology Involved in Glomerular Basement Membrane Collagen.	J Am Soc Nephrol	2019
31560688	Using metabolite profiling to construct and validate a metabolite risk score for predicting future weight gain.	PLoS One	2019
30858613	Interrogation of human hematopoiesis at single-cell and single-variant resolution.	Nat Genet	2019
29295838	Genetic Evidence That Carbohydrate-Stimulated Insulin Secretion Leads to Obesity.	Clin Chem	2018
30550793	Evolutionary Pressure against MHC Class II Binding Cancer Mutations.	Cell	2018
30245014	Evolutionary Pressure against MHC Class II Binding Cancer Mutations.	Cell	2018
29758352	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 cohort.	Osteoarthritis and Cartilage	2018
29703844	A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes.	Diabetes	2018
28031487	Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanisms.	Proc Natl Acad Sci U S A	2017
27647854	The Genetic Landscape of Renal Complications in Type 1 Diabetes.	J Am Soc Nephrol	2017
27545677	Determinants of Power in Gene-Based Burden Testing for Monogenic Disorders.	Am J Hum Genet	2016
26901066	Recurring exon deletions in the HP (haptoglobin) gene contribute to lower blood cholesterol levels.	Nat Genet	2016
26607381	Targeted Application of Human Genetic Variation Can Improve Red Blood Cell Production from Stem Cells.	Cell Stem Cell	2016
26131930	Directional dominance on stature and cognition inÂ diverse human populations.	Nature	2015
25673413	Genetic studies of body mass index yield new insights for obesity biology.	Nature	2015
25673412	New genetic loci link adipose and insulin biology to body fat distribution.	Nature	2015
25865494	Genome-wide Analysis of Body Proportion Classifies Height-Associated Variants by Mechanism of Action and Implicates Genes Important for Skeletal Development.	Am J Hum Genet	2015
25819010	Genetic risk factors affecting mitochondrial function are associated with kidney disease in people with Type 1 diabetes.	Diabet Med	2015
25642633	Efficient Bayesian mixed-model analysis increases association power in large cohorts.	Nat Genet	2015
26307587	Genetic Evidence for a Causal Role of Obesity in Diabetic Kidney Disease.	Diabetes	2015
24871321	Novel genetic susceptibility loci for diabetic end-stage renal disease identified through robust naive Bayes classification.	Diabetologia	2014
24607388	An excess of risk-increasing low-frequency variants can be a signal of polygenic inheritance in complex diseases.	Am J Hum Genet	2014
25078778	Distribution and medical impact of loss-of-function variants in the Finnish founder population.	PLoS Genet	2014
23674521	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.	Hum Mol Genet	2013
24029427	Chromosome 2q31.1 associates with ESRD in women with type 1 diabetes.	J Am Soc Nephrol	2013
23202124	New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism.	Nat Genet	2013
21613384	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).	Nephrol Dial Transplant	2012
22721967	Association testing of previously reported variants in a large case-control meta-analysis of diabetic nephropathy.	Diabetes	2012
22484627	A genome-wide association meta-analysis identifies new childhood obesity loci.	Nat Genet	2012
23028342	New susceptibility loci associated with kidney disease in type 1 diabetes.	PLoS Genet	2012
20359597	Common functional genetic variants in catecholamine storage vesicle protein promoter motifs interact to trigger systemic hypertension.	J Am Coll Cardiol	2010
21216807	The VA Hypertension Primary Care Longitudinal Cohort: Electronic medical records in the post-genomic era.	Health Informatics J	2010
20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Nature	2010
20838585	Longitudinal genome-wide association of cardiovascular disease risk factors in the Bogalusa heart study.	PLoS Genet	2010
21061160	Naturally occurring genetic variants in human chromogranin A (CHGA) associated with hypertension as well as hypertensive renal disease.	Cell Mol Neurobiol	2010
20861615	Common charge-shift mutation Glu65Lys in K+ channel Î²â¿-Subunit KCNMB1: pleiotropic consequences for glomerular filtration rate and progressive renal disease.	Am J Nephrol	2010