Ryan Lorig-Roach

机构：Broad Institute · ORCID：0000-0002-8183-9611

发表论文 14 篇 · 总被引 2314 次 · h-index 11

代表论文

• Nanopore sequencing and the Shasta toolkit enable efficient de novo assembly of eleven human genomes (2020 · Nature Biotechnology · 被引 664)
• Complete genomic and epigenetic maps of human centromeres (2022 · Science · 被引 654)
• Human-Specific NOTCH2NL Genes Affect Notch Signaling and Cortical Neurogenesis (2018 · Cell · 被引 582)
• Scalable Nanopore sequencing of human genomes provides a comprehensive view of haplotype-resolved variation and methylation (2023 · Nature Methods · 被引 144)
• Human-specific NOTCH -like genes in a region linked to neurodevelopmental disorders affect cortical neurogenesis (2017 · bioRxiv (Cold Spring Harbor Laboratory) · 被引 72)
• Expression of transcription factors divides retinal ganglion cells into distinct classes (2017 · The Journal of Comparative Neurology · 被引 46)