Madeline L. Page

The paper identifies tau as an m6A-associated RNA binding protein that causes RNA dysregulation in MAPT coding-variant patients and V337M iNeurons.

The paper develops a computational framework to contextualize novel isoforms identified through long-read single-cell RNA sequencing by integrating pathway analysis with expression-based neighborhoods.

The paper identifies contextual biases in the SegmentNT model, showing how input sequence length and nucleotide position affect predictions and suggests ways to mitigate these biases.

This study uses long-read single-cell sequencing to analyze isoform-level diversity in human PBMCs, identifying novel isoforms and cell-type-specific patterns.

The paper evaluates how long-read sequencing reduces dark genomic regions in the CHM13 reference genome compared to shorter-read references.

RNApysoforms provides an interactive, customizable Python tool for visualizing RNA isoform structures and expression data using plotly and polars.

The paper uses long-read RNAseq to identify new RNA isoforms in Alzheimer's disease brain tissue and demonstrates their medical relevance.

This study surveys RNA isoform diversity and expression across nine GTEx tissues using long-read sequencing, revealing significant tissue-specific isoform variation and validating new isoforms.

The paper identifies rare genetic variants associated with exceptional longevity through pedigree analysis and genomic screening in Utah populations.