Panos Roussos | Jaroslav Bendl

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Chromatin accessibility provides a window into the genetic etiology of human brain disease
Chromatin accessibility provides a window into the genetic etiology of human brain disease
A multi-region single nucleus transcriptomic atlas of Parkinson's disease
A multi-regional human brain atlas of chromatin accessibility and gene expression facilitates promoter-isoform resolution genetic fine-mapping
Detection and analysis of complex structural variation in human genomes across populations and in brains of donors with psychiatric disorders
Single cell transcriptomes and multiscale networks from persons with and without Alzheimer’s disease
Genetic regulation of cell type–specific chromatin accessibility shapes brain disease etiology
Single-cell genomics and regulatory networks for 388 human brains
Single-cell multi-cohort dissection of the schizophrenia transcriptome
DeepGAMI: deep biologically guided auxiliary learning for multimodal integration and imputation to improve genotype–phenotype prediction
Multi-omic profiling of the developing human cerebral cortex at the single-cell level
Lineage specific 3D genome structure in the adult human brain and neurodevelopmental changes in the chromatin interactome
Multi-omic atlas of the parahippocampal gyrus in Alzheimers disease
The stability of the myelinating oligodendrocyte transcriptome is regulated by the nuclear lamina
Genome-wide analysis of a model-derived binge eating disorder phenotype identifies risk loci and implicates iron metabolism
Activity-Dependent Transcriptional Program in NGN2+ Neurons Enriched for Genetic Risk for Brain-Related Disorders
Genome-wide methylomic regulation of multiscale gene networks in Alzheimers disease
Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains
Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains
Rescue of deficits by Brwd1 copy number restoration in the Ts65Dn mouse model of Down syndrome
The three-dimensional landscape of cortical chromatin accessibility in Alzheimer’s disease
Identification of shared and differentiating genetic architecture for autism spectrum disorder, attention-deficit hyperactivity disorder and case subgroups
Population-level variation in enhancer expression identifies disease mechanisms in the human brain
Impact of schizophrenia GWAS loci converge onto distinct pathways in cortical interneurons vs glutamatergic neurons during development
Chromatin domain alterations linked to 3D genome organization in a large cohort of schizophrenia and bipolar disorder brains
Identification of shared and differentiating genetic architecture for autism spectrum disorder, attention-deficit hyperactivity disorder and case subgroups
Unbiased identification of novel transcription factors in striatal compartmentation and striosome maturation
ATAC-seq and psychiatric disorders
Genetics of the human microglia regulome refines Alzheimer’s disease risk loci
Sex Differences in the Human Brain Transcriptome of Cases With Schizophrenia
Integration of Alzheimer’s disease genetics and myeloid genomics identifies disease risk regulatory elements and genes
Common schizophrenia risk variants are enriched in open chromatin regions of human glutamatergic neurons
decorate: Differential Epigenetic Correlation Test
Functional interpretation of genetic variants using deep learning predicts impact on chromatin accessibility and histone modification
CommonMind Consortium provides transcriptomic and epigenomic data for Schizophrenia and Bipolar Disorder
The Mount Sinai cohort of large-scale genomic, transcriptomic and proteomic data in Alzheimer's disease
An atlas of chromatin accessibility in the adult human brain