Ryan Lorig-Roach
Broad Institute(US)
Publications by Year
Research Areas
Genomics and Phylogenetic Studies, Chromosomal and Genetic Variations, Algorithms and Data Compression, RNA modifications and cancer, Congenital heart defects research
Most-Cited Works
- → Nanopore sequencing and the Shasta toolkit enable efficient de novo assembly of eleven human genomes(2020)645 cited
- → Complete genomic and epigenetic maps of human centromeres(2022)595 cited
- → Human-Specific NOTCH2NL Genes Affect Notch Signaling and Cortical Neurogenesis(2018)552 cited
- → Scalable Nanopore sequencing of human genomes provides a comprehensive view of haplotype-resolved variation and methylation(2023)133 cited
- → Human-specific NOTCH -like genes in a region linked to neurodevelopmental disorders affect cortical neurogenesis(2017)69 cited
- → Expression of transcription factors divides retinal ganglion cells into distinct classes(2017)44 cited
- → Efficient de novo assembly of eleven human genomes using PromethION sequencing and a novel nanopore toolkit(2019)38 cited
- → A common flanking variant is associated with enhanced stability of the FGF14-SCA27B repeat locus(2024)32 cited
- → Phased nanopore assembly with Shasta and modular graph phasing with GFAse(2024)16 cited