Author details

Full Name

Jason L Stein

Affiliation

ORCID

Career Start Year

2007

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37693466	The pivotal role of the X-chromosome in the genetic architecture of the human brain.	medRxiv	2024
36798360	Wnt activity reveals context-specific genetic effects on gene regulation in neural progenitors.		2023
35994039	Inference of putative cell-type-specific imprinted regulatory elements and genes during human neuronal differentiation.	Human Molecular Genetics	2023
36442731	Genetic variations within human gained enhancer elements affect human brain sulcal morphology.	NeuroImage	2023
36824893	Eye-brain connections revealed by multimodal retinal and brain imaging genetics in the UK Biobank.	medRxiv	2023
37262162	Heart-brain connections: Phenotypic and genetic insights from magnetic resonance images.	Science	2023
36945630	Cross-ancestry, cell-type-informed atlas of gene, isoform, and splicing regulation in the developing human brain.	medRxiv	2023
36629315	MicroRNA-eQTLs in the developing human neocortex link miR-4707-3p expression to brain size.	Elife	2023
37254169	Inferring cell-type-specific causal gene regulatory networks during human neurogenesis.		2023
33300665	Ten years of enhancing neuro-imaging genetics through meta-analysis: An overview from the ENIGMA Genetics Working Group.	Hum Brain Mapp	2022
35393594	Common variants contribute to intrinsic human brain functional networks.	Nat Genet	2022
36161899	Using neuroimaging genomics to investigate the evolution of human brain structure.	Proceedings of the National Academy of Sciences of the United States of America	2022
36085003	Focus on your locus with a massively parallel reporter assay.	Journal of Neurodevelopmental Disorders	2022
35812078	ToxCast chemical library Wnt screen identifies diethanolamine as an activator of neural progenitor proliferation.	FASEB BioAdvances	2022
33098356	Evaluating brain structure traits as endophenotypes using polygenicity and discoverability.	Hum Brain Mapp	2022
34416157	Brain-trait-associated variants impact cell-type-specific gene regulation during neurogenesis.	Am J Hum Genet	2021
34017130	Cell-type-specific effects of genetic variation on chromatin accessibility during human neuronal differentiation.	Nat Neurosci	2021
33875895	From base pair to brain.	Nature Neuroscience	2021
34140357	Common genetic variation influencing human white matter microstructure.	Science	2021
33872308	MRLocus: Identifying causal genes mediating a trait through Bayesian estimation of allelic heterogeneity.	PLoS Genet	2021
34022787	Segmentor: a tool for manual refinement of 3D microscopy annotations.	BMC Bioinformatics	2021
34644582	NuMorph: Tools for cortical cellular phenotyping in tissue-cleared whole-brain images.	Cell Reports	2021
32963231	Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adults.	Nat Commun	2020
32198361	ENIGMA and global neuroscience: A decade of large-scale studies of the brain in health and disease across more than 40 countries.	Transl Psychiatry	2020
32359439	Genetic Control of Expression and Splicing in Developing Human Brain Informs Disease Mechanisms.	Cell	2020
32302575	Genetic Control of Expression and Splicing in Developing Human Brain Informs Disease Mechanisms.	Cell	2020
33087932	Cas9 gene therapy for Angelman syndrome traps Ube3a-ATS long non-coding RNA.	Nature	2020
32747698	Common genetic risk variants identified in the SPARK cohort support DDHD2 as a candidate risk gene for autism.	Transl Psychiatry	2020
30864184	Mapping causal pathways from genetics to neuropsychiatric disorders using genome-wide imaging genetics: Current status and future directions.	Psychiatry and Clinical Neurosciences	2019
32154516	Cross Modality Microscopy Segmentation via Adversarial Adaptation.		2019
34046647	SAU-Net: A Universal Deep Network for Cell Counting.		2019
31303374	A Single-Cell Transcriptomic Atlas of Human Neocortical Development during Mid-gestation.	Neuron	2019
30818988	Genetic Markers of ADHD-Related Variations in Intracranial Volume.	Am J Psychiatry	2019
29307494	The Dynamic Landscape of Open Chromatin during Human Cortical Neurogenesis.	Cell	2018
28098162	Novel genetic loci associated with hippocampal volume.	Nat Commun	2017
29107596	Default Patterning Produces Pan-cortical Glutamatergic and CGE/LGE-like GABAergic Neurons from Human Pluripotent Stem Cells.	Stem Cell Reports	2017
25712225	Human neural stem cell-derived cultures in three-dimensional substrates form spontaneously functional neuronal networks.	J Tissue Eng Regen Med	2017
26658930	ENIGMA and the individual: Predicting factors that affect the brain in 35 countries worldwide.	Neuroimage	2017
27694991	Novel genetic loci underlying human intracranial volume identified through genome-wide association.	Nat Neurosci	2016
26890892	Early developmental gene enhancers affect subcortical volumes in the adult human brain.	Hum Brain Mapp	2016
27181059	Circuit-wide Transcriptional Profiling Reveals Brain Region-Specific Gene Networks Regulating Depression Susceptibility.	Neuron	2016
27050589	Advancing the understanding of autism disease mechanisms through genetics.	Nat Med	2016
26854805	Genetic influences on schizophrenia and subcortical brain volumes: large-scale proof of concept.	Nat Neurosci	2016
27483382	Transcriptomic signatures of neuronal differentiation and their association with risk genes for autism spectrum and related neuropsychiatric disorders.	Transl Psychiatry	2016
27760116	Chromosome conformation elucidates regulatory relationships in developing human brain.	Nature	2016
26627310	JAKMIP1, a Novel Regulator of Neuronal Translation, Modulates Synaptic Function and Autistic-like Behaviors in Mouse.	Neuron	2015
25688292	Copy number variation and brain structure: lessons learned from chromosome 16p11.2.	Genome Medicine	2015
25264344	Genome-wide interaction analysis reveals replicated epistatic effects on brain structure.	Neurobiol Aging	2015
25607358	Common genetic variants influence human subcortical brain structures.	Nature	2015
25765640	Genome engineering of isogenic human ES cells to model autism disorders.	Nucleic Acids Res	2015