Aaron S. Leong

Internal Medicine
50 Staniford St Fl 9
Boston, MA 02114

Last Updated: 09/26/2026

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Found 83 publications

Common genetic variants near SLC2A2 and glycemic response to glimepiride in the GRADE comparative effectiveness clinical trial.

Common genetic variants near SLC2A2 and glycemic response to glimepiride in the GRADE comparative effectiveness clinical trial.

Journal: medRxiv : the preprint server for health sciences
Published: November 24, 2025

Multi-ancestry polygenic risk scores for the prediction of type 2 diabetes and complications in diverse ancestries.

Multi-ancestry polygenic risk scores for the prediction of type 2 diabetes and complications in diverse ancestries.

Journal: medRxiv : the preprint server for health sciences
Published: August 08, 2025

Multi-ancestry polygenic risk scores for the prediction of type 2 diabetes and complications in diverse ancestries.

Multi-ancestry polygenic risk scores for the prediction of type 2 diabetes and complications in diverse ancestries.

Journal: The lancet. Diabetes & endocrinology
Published: July 17, 2025

Genome-Wide Association Study of Hypoglycemia in Adults With Diabetes in the Million Veteran Program.

Genome-Wide Association Study of Hypoglycemia in Adults With Diabetes in the Million Veteran Program.

Journal: Diabetes
Published: March 28, 2025

Author Correction: Rare variant analyses in 51,256 type 2 diabetes cases and 370,487 controls reveal the pathogenicity spectrum of monogenic diabetes genes.

Author Correction: Rare variant analyses in 51,256 type 2 diabetes cases and 370,487 controls reveal the pathogenicity spectrum of monogenic diabetes genes.

Journal: Nature genetics
Published: March 26, 2025

Publisher Correction: Rare variant analyses in 51,256 type 2 diabetes cases and 370,487 controls reveal the pathogenicity spectrum of monogenic diabetes genes.

Publisher Correction: Rare variant analyses in 51,256 type 2 diabetes cases and 370,487 controls reveal the pathogenicity spectrum of monogenic diabetes genes.

Journal: Nature genetics
Published: October 22, 2024

Adaptive selection at G6PD and disparities in diabetes complications.

Adaptive selection at G6PD and disparities in diabetes complications.

Journal: Nature medicine
Published: February 16, 2024

Rare variant analyses in 51,256 type 2 diabetes cases and 370,487 controls reveal the pathogenicity spectrum of monogenic diabetes genes.

Rare variant analyses in 51,256 type 2 diabetes cases and 370,487 controls reveal the pathogenicity spectrum of monogenic diabetes genes.

Journal: Nature genetics
Published: October 31, 2023

Type 1 Diabetes Genetic Risk in 109,954 Veterans With Adult-Onset Diabetes: The Million Veteran Program (MVP).

Type 1 Diabetes Genetic Risk in 109,954 Veterans With Adult-Onset Diabetes: The Million Veteran Program (MVP).

Journal: Diabetes care
Published: October 13, 2023

Rare variant association analysis in 51,256 type 2 diabetes cases and 370,487 controls informs the spectrum of pathogenicity of monogenic diabetes genes.

Rare variant association analysis in 51,256 type 2 diabetes cases and 370,487 controls informs the spectrum of pathogenicity of monogenic diabetes genes.

Journal: medRxiv : the preprint server for health sciences
Published: October 09, 2023

Large-scale exome array summary statistics resources for glycemic traits to aid effector gene prioritization.

Large-scale exome array summary statistics resources for glycemic traits to aid effector gene prioritization.

Journal: Wellcome open research
Published: October 02, 2023

Polygenic scores for longitudinal prediction of incident type 2 diabetes in an ancestrally and medically diverse primary care physician network: a patient cohort study.

Polygenic scores for longitudinal prediction of incident type 2 diabetes in an ancestrally and medically diverse primary care physician network: a patient cohort study.

Journal: Genome medicine
Published: September 27, 2023
Showing 1-12 of 83

Last Updated: 09/26/2026