Author details

Full Name

Panos Roussos

Affiliation

ORCID

Career Start Year

2007

Papers

183

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37454787	Activity-Dependent Transcriptional Program in NGN2+ Neurons Enriched for Genetic Risk for Brain-Related Disorders.	Biol Psychiatry	2024
37546856	Dopaminoceptive D1 and D2 neurons in ventral hippocampus arbitrate approach and avoidance in anxiety.		2023
36123423	Comment on: What genes are differentially expressed in individuals with schizophrenia? A systematic review.	Mol Psychiatry	2023
37824614	Multi-omic profiling of the developing human cerebral cortex at the single-cell level.		2023
37811875	Lineage specific 3D genome structure in the adult human brain and neurodevelopmental changes in the chromatin interactome.		2023
37904203	DeepGAMI: deep biologically guided auxiliary learning for multimodal integration and imputation to improve genotype-phenotype prediction.	Genome Med	2023
37886514	The neuronal chromatin landscape in adult schizophrenia brains is linked to early fetal development.	Res Sq	2023
38076956	Long-read RNA-seq atlas of novel microglia isoforms elucidates disease-associated genetic regulation of splicing.	medRxiv	2023
37562536	Neuroimmune Mechanisms of Opioid Use Disorder and Recovery: Translatability to Human Studies, and Future Research Directions.		2023
37873320	The neuronal chromatin landscape in adult schizophrenia brains is linked to early fetal development.	medRxiv	2023
37961404	A public resource of single cell transcriptomes and multiscale networks from persons with and without Alzheimer's disease.	bioRxiv	2023
37550530	Genome-wide analysis of a model-derived binge eating disorder phenotype identifies risk loci and implicates iron metabolism.	Nat Genet	2023
37684260	Multi-omic atlas of the parahippocampal gyrus in Alzheimer's disease.	Sci Data	2023
37160117	Interleukin-3 coordinates glial-peripheral immune crosstalk to incite multiple sclerosis.	Immunity	2023
37090548	Genetic regulation of cell-type specific chromatin accessibility shapes the etiology of brain diseases.	bioRxiv	2023
37464041	Depression pathophysiology, risk prediction of recurrence and comorbid psychiatric disorders using genome-wide analyses.	Nat Med	2023
37020048	Applications of artificial intelligence-machine learning for detection of stress: a critical overview.		2023
37205394	ZBTB7A regulates MDD-specific chromatin signatures and astrocyte-mediated stress vulnerability in orbitofrontal cortex.		2023
37205331	Efficient differential expression analysis of large-scale single cell transcriptomics data using dreamlet.	Res Sq	2023
36811307	Genome-wide methylomic regulation of multiscale gene networks in Alzheimer's disease.	Alzheimers Dement	2023
37191946	Basal forebrain cholinergic neurons are vulnerable in a mouse model of Down syndrome and their molecular fingerprint is rescued by maternal choline supplementation.		2023
36993743	Evaluating performance and applications of sample-wise cell deconvolution methods on human brain transcriptomic data.	bioRxiv	2023
36993704	Efficient differential expression analysis of large-scale single cell transcriptomics data using dreamlet.	bioRxiv	2023
36543923	African ancestry GWAS of dementia in a large military cohort identifies significant risk loci.	Mol Psychiatry	2023
37425708	Diversity and Scale: Genetic Architecture of 2,068 Traits in the VA Million Veteran Program.	medRxiv	2023
37515770	The stability of the myelinating oligodendrocyte transcriptome is regulated by the nuclear lamina.		2023
35138379	Transcriptome-wide association study in UK Biobank Europeans identifies associations with blood cell traits.	Hum Mol Genet	2022
35396580	Mapping genomic loci implicates genes and synaptic biology in schizophrenia.	Nature	2022
36103194	Penetrance and Pleiotropy of Polygenic Risk Scores for Schizophrenia, Bipolar Disorder, and Depression Among Adults in the US Veterans Affairs Health Care System.	JAMA Psychiatry	2022
35388222	A complete temporal transcription factor series in the fly visual system.	Nature	2022
36171428	The three-dimensional landscape of cortical chromatin accessibility in Alzheimer's disease.	Nat Neurosci	2022
35701597	Impact of schizophrenia GWAS loci converge onto distinct pathways in cortical interneurons vs glutamatergic neurons during development.	Mol Psychiatry	2022
36163277	Identification of shared and differentiating genetic architecture for autism spectrum disorder, attention-deficit hyperactivity disorder and case subgroups.	Nat Genet	2022
36289231	Rescue of deficits by Brwd1 copy number restoration in the Ts65Dn mouse model of Down syndrome.	Nature Communications	2022
35750513	The Neuroepigenome: Implications of Chemical and Physical Modifications of Genomic DNA in Schizophrenia.	Biological Psychiatry	2022
36276926	A mechanistic framework for cardiometabolic and coronary artery diseases.	Nat Cardiovasc Res	2022
36206733	Analysis of Transcriptional Variability in a Large Human iPSC Library Reveals Genetic and Non-genetic Determinants of Heterogeneity.	Cell Stem Cell	2022
35931864	Genetics of the human microglia regulome refines Alzheimer's disease risk loci.	Nat Genet	2022
36064543	A translational genomics approach identifies IL10RB as the top candidate gene target for COVID-19 susceptibility.	NPJ Genom Med	2022
34154796	Sex Differences in the Human Brain Transcriptome of Cases With Schizophrenia.	Biol Psychiatry	2022
33934884	Sex Differences in Molecular Rhythms in the Human Cortex.	Biol Psychiatry	2022
35045295	A bidirectional competitive interaction between circHomer1 and Homer1b within the orbitofrontal cortex regulates reversal learning.	Cell Rep	2022
35332326	Chromatin domain alterations linked to 3D genome organization in a large cohort of schizophrenia and bipolar disorder brains.	Nat Neurosci	2022
34837629	Correction to: Profiling Basal Forebrain Cholinergic Neurons Reveals a Molecular Basis for Vulnerability Within the Ts65Dn Model of Down Syndrome and Alzheimer's Disease.	Molecular Neurobiology	2022
35180380	Non-cell-autonomous disruption of nuclear architecture as a potential cause of COVID-19-induced anosmia.	Cell	2022
34758195	Engagement of vascular early response genes typifies mild cognitive impairment.	Alzheimer's and Dementia	2022
35058635	Multi-ancestry eQTL meta-analysis of human brain identifies candidate causal variants for brain-related traits.	Nat Genet	2022
35177824	Altered gene expression and PTSD symptom dimensions in World Trade Center responders.	Mol Psychiatry	2022
34609283	Unbiased identification of novel transcription factors in striatal compartmentation and striosome maturation.	Elife	2021
34281603	Single-nucleus transcriptome analysis of human brain immune response in patients with severe COVID-19.	Genome Med	2021