Jaroslav Bendl | Jaroslav Bendl

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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
Common variants contribute to intrinsic human brain functional networks
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 genetic variation influencing human white matter microstructure
Common schizophrenia risk variants are enriched in open chromatin regions of human glutamatergic neurons
decorate: Differential Epigenetic Correlation Test
An atlas of chromatin accessibility in the adult human brain