Teresa Luna-Tusie

Mexico City, DIF, Mexico

Last Updated: 09/26/2026

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Found 52 publications

Improving type 2 diabetes polygenic risk scores by incorporating rare, low-frequency, and population-specific variants.

Improving type 2 diabetes polygenic risk scores by incorporating rare, low-frequency, and population-specific variants.

Journal: medRxiv : the preprint server for health sciences

Published: December 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: medRxiv : the preprint server for health sciences

Published: August 08, 2025

Analysis of a deeply-phenotyped familial hypercholesterolemia cohort from Mexico shows a role for both rare and common alleles across known dyslipidemia genes and reveals structural variation in a novel locus.

Analysis of a deeply-phenotyped familial hypercholesterolemia cohort from Mexico shows a role for both rare and common alleles across known dyslipidemia genes and reveals structural variation in a novel locus.

Journal: Human genomics

Published: July 31, 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 long COVID.

Genome-wide association study of long COVID.

Journal: Nature genetics

Published: June 15, 2024

Metabolomic Profile Alterations Associated with the SLC16A11 Risk Haplotype Following a Lifestyle Intervention in People With Prediabetes.

Metabolomic Profile Alterations Associated with the SLC16A11 Risk Haplotype Following a Lifestyle Intervention in People With Prediabetes.

Journal: Current developments in nutrition

Published: May 27, 2024

Identification and Properties of TRPV4 Mutant Channels Present in Polycystic Kidney Disease Patients.

Identification and Properties of TRPV4 Mutant Channels Present in Polycystic Kidney Disease Patients.

Journal: Function (Oxford, England)

Published: April 21, 2024

Large-scale multi-omics analyses in Hispanic/Latino populations identify genes for cardiometabolic traits.

Large-scale multi-omics analyses in Hispanic/Latino populations identify genes for cardiometabolic traits.

Journal: Nature communications

Published: March 28, 2024

Local Ancestry at the Major Histocompatibility Complex Region is Not a Major Contributor to Disease Heterogeneity in a Multiethnic Lupus Cohort.

Local Ancestry at the Major Histocompatibility Complex Region is Not a Major Contributor to Disease Heterogeneity in a Multiethnic Lupus Cohort.

Journal: Arthritis & rheumatology (Hoboken, N.J.)

Published: November 14, 2023

The fatal contribution of serine protease-related genetic variants to COVID-19 outcomes.

The fatal contribution of serine protease-related genetic variants to COVID-19 outcomes.

Journal: Frontiers in immunology

Published: November 13, 2023

Reversal of high-glucose-induced transcriptional and epigenetic memories through NRF2 pathway activation.

Reversal of high-glucose-induced transcriptional and epigenetic memories through NRF2 pathway activation.

Journal: Life science alliance

Published: September 18, 2023

Author Correction: The power of genetic diversity in genome-wide association studies of lipids.

Author Correction: The power of genetic diversity in genome-wide association studies of lipids.

Journal: Nature

Published: May 26, 2023

Showing 1-12 of 52

Last Updated: 09/26/2026