Author details

Full Name

Maggie C Y Ng

Affiliation

ORCID

Career Start Year

1996

Papers

171

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37034649	Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications.	medRxiv	2023
37558891	Methods for estimating insulin resistance from untargeted metabolomics data.		2023
37148359	The power of TOPMed imputation for the discovery of Latino-enriched rare variants associated with type 2 diabetes.	Diabetologia	2023
37005925	Metabolomic profiling of glucose homeostasis in African Americans: the Insulin Resistance Atherosclerosis Family Study (IRAS-FS).	Metabolomics	2023
34166655	Gene Set Enrichment Analsyes Identify Pathways Involved in Genetic Risk for Diabetic Retinopathy.	Am J Ophthalmol	2022
35393509	Identification of genetic effects underlying type 2 diabetes in South Asian and European populations.	Commun Biol	2022
35513483	Author Correction: Identification of genetic effects underlying type 2 diabetes in South Asian and European populations.	Commun Biol	2022
35765100	Development and validation of a trans-ancestry polygenic risk score for type 2 diabetes in diverse populations.	Genome Med	2022
35551307	Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation.	Nat Genet	2022
35659450	Erratum to Gene Set Enrichment Analyses Identify Pathways Involved in Genetic Risk for Diabetic Retinopathy. Am J Ophthalmol 2022;233:111-123.	Am J Ophthalmol	2022
34604815	Genetic discovery and risk characterization in type 2 diabetes across diverse populations.	HGG Adv	2021
34241534	Multiethnic Genome-Wide Association Study of Subclinical Atherosclerosis in Individuals With Type 2 Diabetes.	Circ Genom Precis Med	2021
34014961	Genome-wide association study of vitamin D concentrations and bone mineral density in the African American-Diabetes Heart Study.	PLoS One	2021
34108472	Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes.	Nat Commun	2021
33608049	Development of genome-wide polygenic risk scores for lipid traits and clinical applications for dyslipidemia, subclinical atherosclerosis, and diabetes cardiovascular complications among East Asians.	Genome Med	2021
33713608	Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry.	Am J Hum Genet	2021
34563731	Metabolomic architecture of obesity implicates metabolonic lactone sulfate in cardiometabolic disease.	Mol Metab	2021
34717821	Predicting diabetes risk in diverse populations: what next?	Lancet Diabetes and Endocrinology,The	2021
32242986	Magnetic Phase Transitions in a Ni O -Cubane-Based Metal-Organic Framework.	Chemistry - A European Journal	2020
31160809	Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.	Nat Genet	2019
31688885	Association of Genetic Variants With Primary Open-Angle Glaucoma Among Individuals With African Ancestry.	JAMA	2019
30352225	Genetic Architecture of Primary Open-Angle Glaucoma in Individuals of African Descent: The African Descent and Glaucoma Evaluation Study III.	Ophthalmology	2019
30487263	Multiethnic Genome-Wide Association Study of Diabetic Retinopathy Using Liability Threshold Modeling of Duration of Diabetes and Glycemic Control.	Diabetes	2019
30415941	Progression of diabetic kidney disease and trajectory of kidney function decline in Chinese patients with Type 2 diabetes.	Kidney Int	2019
29361356	The African Descent and Glaucoma Evaluation Study (ADAGES) III: Contribution of Genotype to Glaucoma Phenotype in African Americans: Study Design and Baseline Data.	Ophthalmology	2019
29273807	Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.	Nat Genet	2018
29885931	Genome-wide association studies suggest that APOL1-environment interactions more likely trigger kidney disease in African Americans with nondiabetic nephropathy than strong APOL1-second gene interactions.	Kidney Int	2018
30297969	Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps.	Nat Genet	2018
29989002	An Exome-wide Association Study for Type 2 Diabetes-Attributed End-Stage Kidney Disease in African Americans.	Kidney International Reports	2018
30317457	Genome-wide association study of primary open-angle glaucoma in continental and admixed African populations.	Hum Genet	2018
29691896	Genome-wide interaction with the insulin secretion locus MTNR1B reveals CMIP as a novel type 2 diabetes susceptibility gene in African Americans.	Genet Epidemiol	2018
29549330	Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.	Nat Genet	2018
29549329	Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.	Nat Genet	2018
29417738	Genetic variants in sex hormone pathways and the risk of type 2 diabetes among African American, Hispanic American, and European American postmenopausal women in the US.	J Diabetes	2018
29546329	Metabolomics Identifies Distinctive Metabolite Signatures for Measures of Glucose Homeostasis: The Insulin Resistance Atherosclerosis Family Study (IRAS-FS).	J Clin Endocrinol Metab	2018
29360107	Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.	Sci Data	2018
27535031	Genome-wide linkage and association analysis of cardiometabolic phenotypes in Hispanic Americans.	J Hum Genet	2017
28430825	Discovery and fine-mapping of adiposity loci using high density imputation of genome-wide association studies in individuals of African ancestry: African Ancestry Anthropometry Genetics Consortium.	PLoS Genet	2017
28341696	A Low-Frequency Inactivating <i>AKT2</i> Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk.	Diabetes	2017
28945282	High risk of conversion to diabetes in first-degree relatives of individuals with young-onset type 2 diabetes: a 12-year follow-up analysis.	Diabetic Medicine	2017
28666119	Type 2 Diabetes Variants Disrupt Function of SLC16A11 through Two Distinct Mechanisms.	Cell	2017
29257133	Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.	Sci Data	2017
28254843	Genetics of Type 2 Diabetes in U.S. Hispanic/Latino Individuals: Results From the Hispanic Community Health Study/Study of Latinos (HCHS/SOL).		2017
28253288	A novel TCF7L2 type 2 diabetes SNP identified from fine mapping in African American women.	PLoS ONE	2017
28067407	Analysis of Whole Exome Sequencing with Cardiometabolic Traits Using Family-Based Linkage and Association in the IRAS Family Study.	Ann Hum Genet	2017
27896979	GENOME-WIDE INTERACTION WITH SELECTED TYPE 2 DIABETES LOCI REVEALS NOVEL LOCI FOR TYPE 2 DIABETES IN AFRICAN AMERICANS.	Pac Symp Biocomput	2017
28146470	Rare and low-frequency coding variants alter human adult height.	Nature	2017
27398621	The genetic architecture of type 2 diabetes.	Nature	2016
27197912	Association Analysis of the Cubilin (CUBN) and Megalin (LRP2) Genes with ESRD in African Americans.	Clinical journal of the American Society of Nephrology : CJASN	2016
26806836	Genetic and clinical variables identify predictors for chronic kidney disease in type 2 diabetes.	Kidney Int	2016