Publications — Radcliffe Department of Medicine

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Author Correction: Genotyping, sequencing and analysis of 140,000 adults from Mexico City.

Ziyatdinov A. et al, (2024), Nature

Genotyping, sequencing and analysis of 140,000 adults from Mexico City.

Ziyatdinov A. et al, (2023), Nature

A deep catalog of protein-coding variation in 985,830 individuals.

Sun KY. et al, (2023), bioRxiv

Loss of RREB1 in pancreatic beta cells reduces cellular insulin content and affects endocrine cell gene expression.

Mattis KK. et al, (2023), Diabetologia

Human genetics uncovers MAP3K15 as an obesity-independent therapeutic target for diabetes.

Nag A. et al, (2022), Sci Adv, 8

Multiancestry exome sequencing reveals INHBE mutations associated with favorable fat distribution and protection from diabetes.

Akbari P. et al, (2022), Nat Commun, 13

Genotyping, sequencing and analysis of 140,000 adults from the Mexico City Prospective Study

Ziyatdinov A. et al, (2022)

Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation.

Mahajan A. et al, (2022), Nat Genet, 54, 560 - 572

Inferring causal genes at type 2 diabetes GWAS loci through chromosome interactions in islet cells

Torres J. et al, (2022)

TIGER: The gene expression regulatory variation landscape of human pancreatic islets.

Alonso L. et al, (2021), Cell Rep, 37

Association of Kidney Function With NMR-Quantified Lipids, Lipoproteins, and Metabolic Measures in Mexican Adults.

Aguilar-Ramirez D. et al, (2021), J Clin Endocrinol Metab, 106, 2828 - 2839

The type 2 diabetes gene RREB1 plays a role in high-fat diet induced adipogenesis in mice

Yu GZ. et al, (2021), DIABETOLOGIA, 64, 67 - 67

A Multi-omic Integrative Scheme Characterizes Tissues of Action at Loci Associated with Type 2 Diabetes.

Torres JM. et al, (2020), Am J Hum Genet, 107, 1011 - 1028

Deep learning models predict regulatory variants in pancreatic islets and refine type 2 diabetes association signals

Wesolowska-Andersen A. et al, (2019)

Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls.

Flannick J. et al, (2019), Nature, 570, 71 - 76

Developing a network view of type 2 diabetes risk pathways through integration of genetic, genomic and functional data.

Fernández-Tajes J. et al, (2019), Genome Med, 11

Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps.

Mahajan A. et al, (2018), Nat Genet, 50, 1505 - 1513

Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics.

Barbeira AN. et al, (2018), Nat Commun, 9

Integration of human pancreatic islet genomic data refines regulatory mechanisms at Type 2 Diabetes susceptibility loci.

Thurner M. et al, (2018), Elife, 7

Meta-analysis of lipid-traits in Hispanics identifies novel loci, population-specific effects, and tissue-specific enrichment of eQTLs

Below JE. et al, (2016), Scientific Reports, 6

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