Lista de obras - Jason L. Stein - Dominio Público Uruguay

A commonly carried allele of the obesity-related FTO gene is associated with reduced brain volume in the healthy elderly

artículo científico publicado en 2010

A quantitative framework to evaluate modeling of cortical development by neural stem cells

artículo científico publicado en 2014

A validated network of effective amygdala connectivity

artículo científico publicado en 2007

Accurate and High Throughput Cell Segmentation Method for Mouse Brain Nuclei Using Cascaded Convolutional Neural Network

scholarly article by Qian Wang et al published 2017 in Lecture Notes in Computer Science

Active fibers: matching deformable tract templates to diffusion tensor images

artículo científico publicado en 2009

Advancing the understanding of autism disease mechanisms through genetics

artículo científico publicado en 2016

Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susceptibility.

scientific article published on 09 April 2013

Alzheimer's Disease Neuroimaging Initiative biomarkers as quantitative phenotypes: Genetics core aims, progress, and plans

artículo científico publicado en 2010

Alzheimer's disease risk gene, GAB2, is associated with regional brain volume differences in 755 young healthy twins

scientific article published on June 2012

Boosting power to detect genetic associations in imaging using multi-locus, genome-wide scans and ridge regression

Brain structure in healthy adults is related to serum transferrin and the H63D polymorphism in the HFE gene

artículo científico publicado en 2012

Cas9 gene therapy for Angelman syndrome traps Ube3a-ATS long non-coding RNA

artículo científico publicado en 2020

Cell-type-specific effects of genetic variation on chromatin accessibility during human neuronal differentiation

artículo científico publicado en 2021

Cellular Genome-wide Association Study Identifies Common Genetic Variation Influencing Lithium-Induced Neural Progenitor Proliferation

artículo científico publicado en 2022

Chromosome conformation elucidates regulatory relationships in developing human brain.

artículo científico publicado en 2016

Circuit-wide Transcriptional Profiling Reveals Brain Region-Specific Gene Networks Regulating Depression Susceptibility

artículo científico publicado en 2016

Common Alzheimer's disease risk variant within the CLU gene affects white matter microstructure in young adults

artículo científico publicado en 2011

Common folate gene variant, MTHFR C677T, is associated with brain structure in two independent cohorts of people with mild cognitive impairment

scientific article published on 04 October 2012

Common genetic risk variants identified in the SPARK cohort support DDHD2 as a candidate risk gene for autism

artículo científico publicado en 2020

Common genetic variants influence human subcortical brain structures

artículo científico publicado en 2015

Common variants at 12q14 and 12q24 are associated with hippocampal volume

artículo científico publicado en 2012

Comparing 3 T and 1.5 T MRI for tracking Alzheimer's disease progression with tensor-based morphometry

artículo científico publicado en 2010

Copy number variation and brain structure: lessons learned from chromosome 16p11.2.

artículo científico publicado en 2015

De novo mutations revealed by whole-exome sequencing are strongly associated with autism ⬇️

artículo científico publicado el 4 de abril de 2012

Default Patterning Produces Pan-cortical Glutamatergic and CGE/LGE-like GABAergic Neurons from Human Pluripotent Stem Cells

artículo científico publicado en 2017

Discovery and Replication of Gene Influences on Brain Structure Using LASSO Regression

artículo científico publicado en 2012

Discovery and replication of dopamine-related gene effects on caudate volume in young and elderly populations (N=1198) using genome-wide search.

artículo científico publicado en 2011

ENIGMA and the individual: Predicting factors that affect the brain in 35 countries worldwide

artículo científico publicado en 2015

Early developmental gene enhancers affect subcortical volumes in the adult human brain

artículo científico publicado en 2016

EnigmaVis: online interactive visualization of genome-wide association studies of the Enhancing NeuroImaging Genetics through Meta-Analysis (ENIGMA) consortium

artículo científico publicado en 2012

Evaluating brain structure traits as endophenotypes using polygenicity and discoverability

artículo científico publicado en 2020

Exhaustive Search of the SNP-SNP Interactome Identifies Epistatic Effects on Brain Volume in Two Cohorts

artículo científico publicado en 2013

Genetic Architecture of Subcortical Brain Structures in Over 40,000 Individuals Worldwide

scholarly article published 28 August 2017

Genetic Clustering on the Hippocampal Surface for Genome-Wide Association Studies

article by Derrek P Hibar et al published 2013 in Lecture Notes in Computer Science

Genetic Determinants of Cortical Structure (Thickness, Surface Area and Volumes) among Disease Free Adults in the CHARGE Consortium

article published in 2018

Genetic Markers of ADHD-Related Variations in Intracranial Volume

artículo científico publicado en 2019

Genetic analysis of cortical thickness and fractional anisotropy of water diffusion in the brain

artículo científico publicado en 2011

Genetic architecture of subcortical brain structures in 38,851 individuals

scientific article published on 21 October 2019

Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adults

scientific article published on 22 September 2020

Genetic influences on schizophrenia and subcortical brain volumes: large-scale proof of concept

artículo científico publicado en 2016

Genetic markers of ADHD-related variations in intracranial volume

Genetics of the Connectome and the ENIGMA Project

article

Genome engineering of isogenic human ES cells to model autism disorders

artículo científico publicado en 2015

Genome-wide analysis reveals novel genes influencing temporal lobe structure with relevance to neurodegeneration in Alzheimer's disease

artículo científico publicado en 2010

Genome-wide association identifies genetic variants associated with lentiform nucleus volume in N = 1345 young and elderly subjects

artículo científico publicado en 2013

Genome-wide interaction analysis reveals replicated epistatic effects on brain structure

artículo científico publicado en 2014

Hippocampal structure and human cognition: key role of spatial processing and evidence supporting the efficiency hypothesis in females

artículo científico publicado en 2013

Hippocampal volume is related to body mass index in Alzheimer's disease

artículo científico publicado en 2011

Human neural stem cell-derived cultures in three-dimensional substrates form spontaneously functional neuronal networks

artículo científico publicado en 2015

Identification of common variants associated with human hippocampal and intracranial volumes

artículo científico publicado en 2012

Imaging Genomics and ENIGMA

Investigation of anatomical thalamo-cortical connectivity and FMRI activation in schizophrenia

artículo científico publicado en 2011

JAKMIP1, a Novel Regulator of Neuronal Translation, Modulates Synaptic Function and Autistic-like Behaviors in Mouse

artículo científico publicado en 2015

Joint genetic analysis of hippocampal size in mouse and human identifies a novel gene linked to neurodegenerative disease

artículo científico publicado en 2014

Know your place: neural processing of social hierarchy in humans

artículo científico publicado en 2008

MRLocus: Identifying causal genes mediating a trait through Bayesian estimation of allelic heterogeneity

artículo científico publicado en 2021

Mapping causal pathways from genetics to neuropsychiatric disorders using genome-wide imaging genetics: Current status and future directions

artículo científico publicado en 2019

Multilocus genetic analysis of brain images

artículo científico publicado en 2011

Neuroimaging and genetics: exploring, searching, and finding

artículo científico publicado en 2012

Novel genetic loci associated with hippocampal volume

scientific article published on 18 January 2017

Novel genetic loci underlying human intracranial volume identified through genome-wide association

artículo científico publicado en 2016

Obesity is linked with lower brain volume in 700 AD and MCI patients

artículo científico publicado en 2010

PREDICTING TEMPORAL LOBE VOLUME ON MRI FROM GENOTYPES USING L(1)-L(2) REGULARIZED REGRESSION.

artículo científico publicado en 2012

Predicting white matter integrity from multiple common genetic variants

artículo científico publicado en 2012

Principal components regression: Multivariate, gene-based tests in imaging genomics

article

Rare inherited variation in autism: beginning to see the forest and a few trees

artículo científico publicado en 2013

Relationship of a variant in the NTRK1 gene to white matter microstructure in young adults

artículo científico publicado en 2012

Sparse reduced-rank regression detects genetic associations with voxel-wise longitudinal phenotypes in Alzheimer's disease

artículo científico publicado en 2011

Structural and functional neuroimaging phenotypes in dysbindin mutant mice

artículo científico publicado en 2012

Ten years of enhancing neuro-imaging genetics through meta-analysis: An overview from the ENIGMA Genetics Working Group

scientific article published on 10 December 2020

The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data

artículo científico publicado en 2014

The contribution of genes to cortical thickness and volume

artículo científico publicado en 2011

The effects of physical activity, education, and body mass index on the aging brain

artículo científico publicado en 2010

The genetic architecture of the human cerebral cortex

artículo científico publicado en 2020

Transcriptomic signatures of neuronal differentiation and their association with risk genes for autism spectrum and related neuropsychiatric disorders.

artículo científico publicado en 2016

Vasopressin modulates medial prefrontal cortex-amygdala circuitry during emotion processing in humans

artículo científico publicado en 2010

Vasopressin modulates social recognition-related activity in the left temporoparietal junction in humans.

artículo científico publicado en 2011

Voxelwise gene-wide association study (vGeneWAS): multivariate gene-based association testing in 731 elderly subjects

artículo científico publicado en 2011

Voxelwise genome-wide association study (vGWAS)

artículo científico publicado en 2010

Lista de obras de Jason L. Stein

A commonly carried allele of the obesity-related FTO gene is associated with reduced brain volume in the healthy elderly

A quantitative framework to evaluate modeling of cortical development by neural stem cells

A validated network of effective amygdala connectivity

Accurate and High Throughput Cell Segmentation Method for Mouse Brain Nuclei Using Cascaded Convolutional Neural Network

Active fibers: matching deformable tract templates to diffusion tensor images

Advancing the understanding of autism disease mechanisms through genetics

Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susceptibility.

Alzheimer's Disease Neuroimaging Initiative biomarkers as quantitative phenotypes: Genetics core aims, progress, and plans

Alzheimer's disease risk gene, GAB2, is associated with regional brain volume differences in 755 young healthy twins

Boosting power to detect genetic associations in imaging using multi-locus, genome-wide scans and ridge regression

Brain structure in healthy adults is related to serum transferrin and the H63D polymorphism in the HFE gene

Cas9 gene therapy for Angelman syndrome traps Ube3a-ATS long non-coding RNA

Cell-type-specific effects of genetic variation on chromatin accessibility during human neuronal differentiation

Cellular Genome-wide Association Study Identifies Common Genetic Variation Influencing Lithium-Induced Neural Progenitor Proliferation

Chromosome conformation elucidates regulatory relationships in developing human brain.

Circuit-wide Transcriptional Profiling Reveals Brain Region-Specific Gene Networks Regulating Depression Susceptibility

Common Alzheimer's disease risk variant within the CLU gene affects white matter microstructure in young adults

Common folate gene variant, MTHFR C677T, is associated with brain structure in two independent cohorts of people with mild cognitive impairment

Common genetic risk variants identified in the SPARK cohort support DDHD2 as a candidate risk gene for autism

Common genetic variants influence human subcortical brain structures

Common variants at 12q14 and 12q24 are associated with hippocampal volume

Comparing 3 T and 1.5 T MRI for tracking Alzheimer's disease progression with tensor-based morphometry

Copy number variation and brain structure: lessons learned from chromosome 16p11.2.

De novo mutations revealed by whole-exome sequencing are strongly associated with autism ⬇️

Default Patterning Produces Pan-cortical Glutamatergic and CGE/LGE-like GABAergic Neurons from Human Pluripotent Stem Cells

Discovery and Replication of Gene Influences on Brain Structure Using LASSO Regression

Discovery and replication of dopamine-related gene effects on caudate volume in young and elderly populations (N=1198) using genome-wide search.

ENIGMA and the individual: Predicting factors that affect the brain in 35 countries worldwide

Early developmental gene enhancers affect subcortical volumes in the adult human brain

EnigmaVis: online interactive visualization of genome-wide association studies of the Enhancing NeuroImaging Genetics through Meta-Analysis (ENIGMA) consortium

Evaluating brain structure traits as endophenotypes using polygenicity and discoverability

Exhaustive Search of the SNP-SNP Interactome Identifies Epistatic Effects on Brain Volume in Two Cohorts

Genetic Architecture of Subcortical Brain Structures in Over 40,000 Individuals Worldwide

Genetic Clustering on the Hippocampal Surface for Genome-Wide Association Studies

Genetic Determinants of Cortical Structure (Thickness, Surface Area and Volumes) among Disease Free Adults in the CHARGE Consortium

Genetic Markers of ADHD-Related Variations in Intracranial Volume

Genetic analysis of cortical thickness and fractional anisotropy of water diffusion in the brain

Genetic architecture of subcortical brain structures in 38,851 individuals

Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adults

Genetic influences on schizophrenia and subcortical brain volumes: large-scale proof of concept

Genetic markers of ADHD-related variations in intracranial volume

Genetics of the Connectome and the ENIGMA Project

Genome engineering of isogenic human ES cells to model autism disorders

Genome-wide analysis reveals novel genes influencing temporal lobe structure with relevance to neurodegeneration in Alzheimer's disease

Genome-wide association identifies genetic variants associated with lentiform nucleus volume in N = 1345 young and elderly subjects

Genome-wide interaction analysis reveals replicated epistatic effects on brain structure

Hippocampal structure and human cognition: key role of spatial processing and evidence supporting the efficiency hypothesis in females

Hippocampal volume is related to body mass index in Alzheimer's disease

Human neural stem cell-derived cultures in three-dimensional substrates form spontaneously functional neuronal networks

Identification of common variants associated with human hippocampal and intracranial volumes

Imaging Genomics and ENIGMA

Investigation of anatomical thalamo-cortical connectivity and FMRI activation in schizophrenia

JAKMIP1, a Novel Regulator of Neuronal Translation, Modulates Synaptic Function and Autistic-like Behaviors in Mouse

Joint genetic analysis of hippocampal size in mouse and human identifies a novel gene linked to neurodegenerative disease

Know your place: neural processing of social hierarchy in humans

MRLocus: Identifying causal genes mediating a trait through Bayesian estimation of allelic heterogeneity

Mapping causal pathways from genetics to neuropsychiatric disorders using genome-wide imaging genetics: Current status and future directions

Multilocus genetic analysis of brain images

Neuroimaging and genetics: exploring, searching, and finding

Novel genetic loci associated with hippocampal volume

Novel genetic loci underlying human intracranial volume identified through genome-wide association

Obesity is linked with lower brain volume in 700 AD and MCI patients

PREDICTING TEMPORAL LOBE VOLUME ON MRI FROM GENOTYPES USING L(1)-L(2) REGULARIZED REGRESSION.

Predicting white matter integrity from multiple common genetic variants

Principal components regression: Multivariate, gene-based tests in imaging genomics

Rare inherited variation in autism: beginning to see the forest and a few trees

Relationship of a variant in the NTRK1 gene to white matter microstructure in young adults

Sparse reduced-rank regression detects genetic associations with voxel-wise longitudinal phenotypes in Alzheimer's disease

Structural and functional neuroimaging phenotypes in dysbindin mutant mice

Ten years of enhancing neuro-imaging genetics through meta-analysis: An overview from the ENIGMA Genetics Working Group

The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data

The contribution of genes to cortical thickness and volume

The effects of physical activity, education, and body mass index on the aging brain

The genetic architecture of the human cerebral cortex

The genetic architecture of the human cerebral cortex

Transcriptomic signatures of neuronal differentiation and their association with risk genes for autism spectrum and related neuropsychiatric disorders.

Vasopressin modulates medial prefrontal cortex-amygdala circuitry during emotion processing in humans

Vasopressin modulates social recognition-related activity in the left temporoparietal junction in humans.

Voxelwise gene-wide association study (vGeneWAS): multivariate gene-based association testing in 731 elderly subjects