Patrick A. Schreiner

The paper describes methylation profiling in the Million Veteran Program, identifies smoking-associated epigenetic signatures, and reports novel probe-smoking associations through ancestry-stratified EWAS.

This study identifies 63 AMD risk loci across multiple ancestries, highlighting ancestry-dependent genetic heterogeneity and potential therapeutic targets.

The paper identifies differences in mtDNA mutation accumulation and selective pressures in pediatric leukemias using bulk and single-cell sequencing, linking these to functional heterogeneity among leukemic cells.

This study identifies 240 novel genetic loci associated with mosaic loss of chromosome Y through a multi-ancestry GWAS of the Million Veteran Program and UK Biobank.

CovidExpress provides an open-access database and tool for exploring SARS-CoV-2 related gene expression data across tissues and conditions, identifying common regulated genes and a potential FURIN feedback loop.

The paper shows that different mutations at Gly 34 of histone H3 cause distinct phenotypes in cancer, affecting DNA repair and genomic stability.

TruePaiR identifies complementary piRNA read pairs in sRNA sequencing data to assess piRNA amplification across species and tissues.

piClusterBusteR classifies and characterizes piRNA cluster loci across species, providing annotated and unannotated sequences for downstream analysis.