Adolfo Correa

发表

Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole genome sequencing studies at scale

Ivana V. Yang, Andrew D. Johnson, Ryan D. Hernandez, 2020, Nature Genetics.

Whole-genome sequencing uncovers two loci for coronary artery calcification and identifies ARSE as a regulator of vascular calcification

May E. Montasser, Nicholette D. Palmer, Caitlin P. McHugh, 2023, Nature Cardiovascular Research.

The trans-ancestral genomic architecture of glycemic traits

Tanya M. Teslovich, May E. Montasser, Nicholette D. Palmer, 2021, Nature Genetics.

Stroke genetics informs drug discovery and risk prediction across ancestries

Sebastian M. Armasu, Laurent F. Thomas, J. Danesh, 2022, Nature.

Association of mitochondrial DNA copy number with cardiometabolic diseases in a large cross-sectional study of multiple ancestries

M. Fornage, G. Abecasis, E. Boerwinkle, 2020, medRxiv.

SMIM1 absence is associated with reduced energy expenditure and excess weight.

Tanya M. Teslovich, May E. Montasser, Nicholette D. Palmer, 2024, i Medicina.

Investigating gene-diet interactions impacting the association between macronutrient intake and glycemic traits

J. Pankow, E. Boerwinkle, J. Meigs, 2022, medRxiv.

Sequence data and association statistics from 12,940 type 2 diabetes cases and controls

Taesung Park, Christian Gieger, Tien Yin Wong, 2017, Scientific Data.

A high-resolution HLA reference panel capturing global population diversity enables multi-ethnic fine-mapping in HIV host response

Nicholette D. Palmer, James T. Elder, P. Gregersen, 2020 .

A multi-ethnic polygenic risk score is associated with hypertension prevalence and progression throughout adulthood

Henry J. Lin, M. Fornage, J. Manson, 2021, medRxiv.