about
Genome-Wide Identification and Expression of Xenopus F-Box Family of ProteinsMutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosisLarge-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's diseaseSearching for Grendel: origin and global spread of the C9ORF72 repeat expansionNeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseasesC9ORF72 hexanucleotide repeat exerts toxicity in a stable, inducible motor neuronal cell model, which is rescued by partial depletion of Pten.Genetic architecture of ALS in SardiniaA genome-wide association study of myasthenia gravisAssessment of Parkinson's disease risk loci in GreeceTBK1 is associated with ALS and ALS-FTD in Sardinian patients.Multiplex single cell profiling of chromatin accessibility by combinatorial cellular indexing.Reversed graph embedding resolves complex single-cell trajectories.Genome-wide Analyses Identify KIF5A as a Novel ALS Gene.The cis-regulatory dynamics of embryonic development at single-cell resolution.Joint profiling of chromatin accessibility and gene expression in thousands of single cells.A Single-Cell Atlas of In Vivo Mammalian Chromatin AccessibilityCicero Predicts cis-Regulatory DNA Interactions from Single-Cell Chromatin Accessibility Data.Supervised classification enables rapid annotation of cell atlasesMassively multiplex chemical transcriptomics at single-cell resolutionThe accessible chromatin landscape of the murine hippocampus at single-cell resolution
P50
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P50
description
hulumtuese
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Hannah Pliner
@ast
Hannah Pliner
@en
Hannah Pliner
@es
Hannah Pliner
@nl
Hannah Pliner
@sl
type
label
Hannah Pliner
@ast
Hannah Pliner
@en
Hannah Pliner
@es
Hannah Pliner
@nl
Hannah Pliner
@sl
prefLabel
Hannah Pliner
@ast
Hannah Pliner
@en
Hannah Pliner
@es
Hannah Pliner
@nl
Hannah Pliner
@sl
P1053
F-3608-2015
P21
P31
P3829
P496
0000-0003-1484-6501