Author details

Full Name

May E Montasser

Affiliation

ORCID

Career Start Year

2007

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37425945	Critical Role for 24-Hydroxylation in Homeostatic Regulation of Vitamin D Metabolism.	medRxiv	2024
37738423	Vitamin D Deficiency Increases Vulnerability to Canagliflozin-induced Adverse Effects on 1,25-Dihydroxyvitamin D and PTH.	J Clin Endocrinol Metab	2024
36945579	Pharmacogenetics of SGLT2 Inhibitors: Validation of a sex-agnostic pharmacodynamic biomarker.	medRxiv	2023
38014529	Type 2 Diabetes Modifies the Association of CAD Genomic Risk Variants With Subclinical Atherosclerosis.	Circ Genom Precis Med	2023
37961350	A statistical framework for powerful multi-trait rare variant analysis in large-scale whole-genome sequencing studies.	bioRxiv	2023
37808823	Acute pharmacodynamic responses to sitagliptin: Drug-induced increase in early insulin secretion in oral glucose tolerance test.	medRxiv	2023
37802043	Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study.	Am J Hum Genet	2023
37608471	Pharmacogenetics of sodium-glucose co-transporter-2 inhibitors: Validation of a sex-agnostic pharmacodynamic biomarker.	Diabetes Obes Metab	2023
37425772	Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed Whole Genome Sequencing Study.	medRxiv	2023
37328064	In-Depth Mass Spectrometry Analysis Reveals the Plasma Proteomic and N-Glycoproteomic Impact of an Amish-Enriched Cardioprotective Variant in B4GALT1.	Mol Cell Proteomics	2023
37264484	Acute pharmacodynamic responses to exenatide: Drug-induced increases in insulin secretion and glucose effectiveness.	Diabetes Obes Metab	2023
37214882	Vitamin D deficiency increases vulnerability to canagliflozin-induced adverse effects on 1,25-dihydroxyvitamin D and PTH.	medRxiv	2023
36993363	Acute pharmacodynamic responses to exenatide: Drug-induced increases in insulin secretion and glucose effectiveness.	medRxiv	2023
36193739	Rare Variants in Genes Encoding Subunits of the Epithelial Na<sup>+</sup> Channel Are Associated With Blood Pressure and Kidney Function.	Hypertension	2022
36050321	Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways.	Nat Commun	2022
35652341	Insights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and Hypertension.	Hypertension	2022
35393526	An Amish founder population reveals rare-population genetic determinants of the human lipidome.	Commun Biol	2022
35119614	Distribution of 54 polygenic risk scores for common diseases in long lived individuals and their offspring.	Geroscience	2022
36477530	Genetic diversity fuels gene discovery for tobacco and alcohol use.	Nature	2022
36220816	Whole genome sequence analysis of blood lipid levels in >66,000 individuals.	Nat Commun	2022
33846329	Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices.	Nat Commun	2021
33720349	Robust, flexible, and scalable tests for Hardy-Weinberg equilibrium across diverse ancestries.	Genetics	2021
33558525	Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.	Nat Commun	2021
33402679	Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.	Nat Commun	2021
34855475	Genetic and functional evidence links a missense variant in <i>B4GALT1</i> to lower LDL and fibrinogen.	Science	2021
34836252	Genomics of Postprandial Lipidomics in the Genetics of Lipid-Lowering Drugs and Diet Network Study.	Nutrients	2021
34230475	Publisher Correction: A multi-ethnic epigenome-wide association study of leukocyte DNA methylation and blood lipids.	Nat Commun	2021
34183656	A multi-ethnic epigenome-wide association study of leukocyte DNA methylation and blood lipids.	Nat Commun	2021
32439900	Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction.	Nat Commun	2020
32586392	A lipidome-wide association study of the lipoprotein insulin resistance index.	Lipids Health Dis	2020
29102571	Multisite Investigation of Outcomes WithÂ Implementation of CYP2C19 Genotype-Guided Antiplatelet Therapy After Percutaneous Coronary Intervention.	JACC Cardiovasc Interv	2018
30140000	Deep-coverage whole genome sequences and blood lipids among 16,324 individuals.	Nat Commun	2018
29593015	An APOO Pseudogene on Chromosome 5q Is Associated With Low-Density Lipoprotein Cholesterol Levels.	Circulation	2018
29198723	DNA Methylation Analysis Identifies Loci for Blood Pressure Regulation.	Am J Hum Genet	2017
29376147	Epigenetic Signature of Impaired Fasting Glucose in the Old Order Amish.	J Clin Epigenet	2017
27355579	Correction: The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study.	PLoS Genet	2016
27876822	A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape.	Nat Commun	2016
27618452	The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals.	Nat Genet	2016
27416945	Genome-Wide Association Study of the Modified Stumvoll Insulin Sensitivity Index Identifies BCL2 and FAM19A2 as Novel Insulin Sensitivity Loci.	Diabetes	2016
25026114	A potentially functional variant in the serotonin transporter gene is associated with premenopausal and perimenopausal hot flashes.	Menopause	2015
26426971	The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study.	PLoS Genet	2015
26131930	Directional dominance on stature and cognition inÂ diverse human populations.	Nature	2015
24658007	Variation in genes that regulate blood pressure are associated with glomerular filtration rate in Chinese.	PLoS ONE	2014
25201834	Disruption of ldlr causes increased LDL-c and vascular lipid accumulation in a zebrafish model of hypercholesterolemia.	J Lipid Res	2014
24097064	Common variants associated with plasma triglycerides and risk for coronary artery disease.	Nat Genet	2013
23583979	Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders.	Nat Genet	2013
24097068	Discovery and refinement of loci associated with lipid levels.	Nat Genet	2013
22199011	Association between chromosome 9p21 variants and the ankle-brachial index identified by a meta-analysis of 21 genome-wide association studies.	Circ Cardiovasc Genet	2012
22885924	Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways.	Nat Genet	2012
22581228	A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.	Nat Genet	2012