Skip to main content
TOPMed

Publications

Submitting Author Title Journal Name Publication Date PMID
Lubitz, Steven Rare Coding Variants Associated With Electrocardiographic Intervals Identify Monogenic Arrhythmia Susceptibility Genes: A Multi-Ancestry Analysis Circulation: Genomic and Precision Medicine 34319147
Manichaikul, Ani Whole genome sequence analysis of pulmonary function and COPD in 19,996 multi-ethnic participants Nature Communications 33057025
Battle, Stephanie A bioinformatics pipeline for estimating mitochondrial DNA copy number and heteroplasmy levels from whole genome sequencing data NAR Genom Bioinform 35591888
Hu, Yao A common TCN1 loss of function variant is associated with lower vitamin B12 level in African Americans Blood 29764838
Li, Zilin A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies Nat Methods 36303018
Sofer, Tamar A Fully-Adjusted Two-Stage Procedure for Rank Normalization in Genetic Association Studies Genetic Epidemiology 30653739
de Vries, Paul A genetic association study of circulating coagulation Factor VIII and von Willebrand Factor levels Blood 38320121
Luo, Yang A high-resolution HLA reference panel capturing global population diversity enables multi-ethnic fine-mapping in HIV host response Nature Genetics 34611364
Minster, Ryan L A loss-of-function IFNAR1 allele in Polynesia underlies severe viral diseases in homozygotes J. Exp. Med. 35442418
Sofer, Tamar A multi-ethnic polygenic risk score is associated with hypertension prevalence and progression throughout adulthood Nat Commun. 35729114

Contact Us

* Required field
Reason of Contact
Back to top