Robert L. Ross

The paper benchmarks cross-platform RNA modification quantification using LC-MS/MS and finds that harmonized workflows and SILIS normalization improve reproducibility across different instrument types.

The paper benchmarks MS-Seq for human 28S rRNA analysis, showing reproducible results across platforms but highlighting gaps in coverage and ambiguity.

This study demonstrates that hydrogen bond donating alkylamines improve the purity analysis of oligonucleotides using LC-MS by reducing the need for fluoroalcohol reagents.

This study identifies m6A RNA methylation by Mettl3 as essential for developmental pausing in mice by maintaining transcriptional dormancy through mRNA destabilization and suppression of N-Myc.

This paper develops a sensitive nLC-MS method using capillary porous graphitic carbon columns to quantify chemically modified ribonucleosides at attomol levels in complex samples.