DOI,IST REx ID,Research Group,Title of publication
10.64898/2026.02.12.705305,21291,"SiHi,LoSw",Lineage origin of spinal cord cell type diversity
10.1016/j.gde.2026.102487,21948,SiHi,Tracing cell lineages in the developing brain: Insights from mosaic analysis and clone-resolved transcriptomics
10.64898/2026.05.01.722191,21963,"SiHi,PreCl,GradSch",Pten orchestrates neurogenic radial glia lineage progression and tunes neocortical astrocyte production
10.1016/j.conb.2025.103046,19718,SiHi,How radial glia progenitor lineages generate cell-type diversity in the developing cerebral cortex
10.1101/2025.05.22.655488,19762,SiHi,Early indirect neurogenesis transitions to late direct neurogenesis in mouse cerebral cortex development
10.15479/AT-ISTA-20737,20737,"GradSch,SiHi",Role of NOTCH signaling in radial glial progenitor lineage progression
10.1016/j.neuron.2023.11.009,12875,"SiHi,RySh",Multipotent progenitors instruct ontogeny of the superior colliculus
10.1016/j.xpro.2023.102771,14683,SiHi,Protocol for sorting cells from mouse brains labeled with mosaic analysis with double markers by flow cytometry
10.1016/j.xpro.2024.103157,17187,SiHi,Protocol for quantitative reconstruction of cell lineage using mosaic analysis with double markers in mice
10.1016/j.xpro.2024.103168,17232,"SiHi,PreCl",Protocol for mapping cell lineage and cell-type identity of clonally-related cells in situ using MADM-CloneSeq
10.1007/978-1-0716-3969-6_19,17425,"GradSch,SiHi",Morphological Analysis of Neurons and Glia Using Mosaic Analysis with Double Markers
10.1016/j.conb.2023.102695,12679,SiHi,Principles of neural stem cell lineage progression: Insights from developing cerebral cortex
10.1016/j.xpro.2021.100939,10321,SiHi,Genetic mosaic dissection of candidate genes in mice using mosaic analysis with double markers
10.1523/jneurosci.1655-20.2020,9073,SiHi,The logic of developing neocortical circuits in health and disease
10.1016/j.xpro.2020.100215,8978,SiHi,Generation and isolation of single cells from mouse brain with mosaic analysis with double markers-induced uniparental chromosome disomy