Lista de obras -

1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans

artículo científico publicado en 2021

A Set-Based Mixed Effect Model for Gene-Environment Interaction and Its Application to Neuroimaging Phenotypes

artículo científico publicado en 2017

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 commonly carried genetic variant in the delta opioid receptor gene, OPRD1, is associated with smaller regional brain volumes: replication in elderly and young populations

artículo científico publicado en 2013

A single nucleotide polymorphism associated with reduced alcohol intake in the RASGRF2 gene predicts larger cortical volumes but faster longitudinal ventricular expansion in the elderly

scientific article published on 19 December 2013

Altered regional brain volumes in elderly carriers of a risk variant for drug abuse in the dopamine D2 receptor gene (DRD2)

artículo científico publicado en 2015

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

scientific article published on June 2012

Bivariate Genome-Wide Association Study of Genetically Correlated Neuroimaging Phenotypes from DTI and MRI through a Seemingly Unrelated Regression Model

article

Boosting power for clinical trials using classifiers based on multiple biomarkers

artículo científico publicado en 2010

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

Carriers of a common variant in the dopamine transporter gene have greater dementia risk, cognitive decline, and faster ventricular expansion

artículo científico publicado en 2014

Childhood adversity impacts on brain subcortical structures relevant to depression.

artículo científico publicado en 2016

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 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

Concordance Of Genetic Variation That Increases Risk For Tourette Syndrome And That Influences Its Underlying Neurocircuitry

Cortical Abnormalities Associated With Pediatric and Adult Obsessive-Compulsive Disorder: Findings From the ENIGMA Obsessive-Compulsive Disorder Working Group

artículo científico publicado en 2017

DISCOVERY OF GENES THAT AFFECT HUMAN BRAIN CONNECTIVITY: A GENOME-WIDE ANALYSIS OF THE CONNECTOME.

artículo científico publicado en 2012

Detecting Genetic Risk Factors for Alzheimer's Disease in Whole Genome Sequence Data via Lasso Screening

artículo científico publicado en 2015

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

artículo científico publicado en 2012

Does MRI scan acceleration affect power to track brain change?

artículo científico publicado en 2014

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

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 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 imaging consortium for addiction medicine: From neuroimaging to genes

artículo científico publicado en 2016

Genetic influences on individual differences in longitudinal changes in global and subcortical brain volumes: Results of the ENIGMA plasticity working group

artículo científico publicado en 2017

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

artículo científico publicado en 2016

Genetics of the Connectome and the ENIGMA Project

article

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

Genome-wide scan of healthy human connectome discovers SPON1 gene variant influencing dementia severity

artículo científico publicado en 2013

Heritability and reliability of automatically segmented human hippocampal formation subregions

artículo científico publicado en 2015

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

artículo científico publicado en 2011

Human subcortical brain asymmetries in 15,847 people worldwide reveal effects of age and sex.

artículo científico publicado en 2016

Identification of common variants associated with human hippocampal and intracranial volumes

artículo científico publicado en 2012

Imaging Genomics and ENIGMA

Increasing power for voxel-wise genome-wide association studies: the random field theory, least square kernel machines and fast permutation procedures

artículo científico publicado en 2012

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

artículo científico publicado en 2014

Large-scale classification of major depressive disorder via distributed Lasso

artículo científico publicado en 2017

MRI-based brain atrophy rates in ADNI phase 2: acceleration and enrichment considerations for clinical trials

artículo científico publicado en 2015

Mapping Alzheimer's disease progression in 1309 MRI scans: power estimates for different inter-scan intervals

artículo científico publicado en 2010

Mega-Analysis of Gray Matter Volume in Substance Dependence: General and Substance-Specific Regional Effects

artículo científico publicado en 2018

Multilocus genetic analysis of brain images

artículo científico publicado en 2011

Multilocus genetic profiling to empower drug trials and predict brain atrophy

artículo científico publicado en 2013

NEUROIMAGING OF SUBCORTICAL BRAIN VOLUME ALTERATIONS IN PEADIATRIC AND ADULT OBSESSIVE-COMPULSIVE DISORDER: Preliminary findings from the ENIGMA Obsessive-Compulsive Disorder working group

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 gene NEGR1 associated with white matter integrity in healthy young adults

artículo científico publicado en 2014

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

SPECTRAL GRAPH THEORY AND GRAPH ENERGY METRICS SHOW EVIDENCE FOR THE ALZHEIMER'S DISEASE DISCONNECTION SYNDROME IN APOE-4 RISK GENE CARRIERS.

artículo científico publicado en 2015

Sex and age differences in atrophic rates: an ADNI study with n=1368 MRI scans

artículo científico publicado en 2010

Susceptibility of brain atrophy to in Alzheimer's disease, evidence from functional prioritization in imaging genetics

article published in the Proceedings of the National Academy of Sciences of the United States of America

TREM2 and neurodegenerative disease

artículo científico publicado en 2013

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

artículo científico publicado en 2014

The effect of increased genetic risk for Alzheimer's disease on hippocampal and amygdala volume

artículo científico publicado en 2016

The genetic architecture of the human cerebral cortex

artículo científico publicado en 2020

Unbiased tensor-based morphometry: improved robustness and sample size estimates for Alzheimer's disease clinical trials

artículo científico publicado en 2012

Using structural MRI to identify bipolar disorders - 13 site machine learning study in 3020 individuals from the ENIGMA Bipolar Disorders Working Group

scholarly article by Abraham Nunes et al published 31 August 2018 in Molecular Psychiatry

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

artículo científico publicado en 2011

Lista de obras de

1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans

A Set-Based Mixed Effect Model for Gene-Environment Interaction and Its Application to Neuroimaging Phenotypes

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

A commonly carried genetic variant in the delta opioid receptor gene, OPRD1, is associated with smaller regional brain volumes: replication in elderly and young populations

A single nucleotide polymorphism associated with reduced alcohol intake in the RASGRF2 gene predicts larger cortical volumes but faster longitudinal ventricular expansion in the elderly

Altered regional brain volumes in elderly carriers of a risk variant for drug abuse in the dopamine D2 receptor gene (DRD2)

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

Bivariate Genome-Wide Association Study of Genetically Correlated Neuroimaging Phenotypes from DTI and MRI through a Seemingly Unrelated Regression Model

Boosting power for clinical trials using classifiers based on multiple biomarkers

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

Carriers of a common variant in the dopamine transporter gene have greater dementia risk, cognitive decline, and faster ventricular expansion

Childhood adversity impacts on brain subcortical structures relevant to depression.

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

Common genetic variants influence human subcortical brain structures

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

Concordance Of Genetic Variation That Increases Risk For Tourette Syndrome And That Influences Its Underlying Neurocircuitry

Cortical Abnormalities Associated With Pediatric and Adult Obsessive-Compulsive Disorder: Findings From the ENIGMA Obsessive-Compulsive Disorder Working Group

DISCOVERY OF GENES THAT AFFECT HUMAN BRAIN CONNECTIVITY: A GENOME-WIDE ANALYSIS OF THE CONNECTOME.

Detecting Genetic Risk Factors for Alzheimer's Disease in Whole Genome Sequence Data via Lasso Screening

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

Does MRI scan acceleration affect power to track brain change?

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

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 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 imaging consortium for addiction medicine: From neuroimaging to genes

Genetic influences on individual differences in longitudinal changes in global and subcortical brain volumes: Results of the ENIGMA plasticity working group

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

Genetics of the Connectome and the ENIGMA Project

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

Genome-wide scan of healthy human connectome discovers SPON1 gene variant influencing dementia severity

Heritability and reliability of automatically segmented human hippocampal formation subregions

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

Human subcortical brain asymmetries in 15,847 people worldwide reveal effects of age and sex.

Identification of common variants associated with human hippocampal and intracranial volumes

Imaging Genomics and ENIGMA

Increasing power for voxel-wise genome-wide association studies: the random field theory, least square kernel machines and fast permutation procedures

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

Large-scale classification of major depressive disorder via distributed Lasso

MRI-based brain atrophy rates in ADNI phase 2: acceleration and enrichment considerations for clinical trials

Mapping Alzheimer's disease progression in 1309 MRI scans: power estimates for different inter-scan intervals

Mega-Analysis of Gray Matter Volume in Substance Dependence: General and Substance-Specific Regional Effects

Multilocus genetic analysis of brain images

Multilocus genetic profiling to empower drug trials and predict brain atrophy

NEUROIMAGING OF SUBCORTICAL BRAIN VOLUME ALTERATIONS IN PEADIATRIC AND ADULT OBSESSIVE-COMPULSIVE DISORDER: Preliminary findings from the ENIGMA Obsessive-Compulsive Disorder working group

Novel genetic loci associated with hippocampal volume

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

Obesity gene NEGR1 associated with white matter integrity in healthy young adults

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

SPECTRAL GRAPH THEORY AND GRAPH ENERGY METRICS SHOW EVIDENCE FOR THE ALZHEIMER'S DISEASE DISCONNECTION SYNDROME IN APOE-4 RISK GENE CARRIERS.

Sex and age differences in atrophic rates: an ADNI study with n=1368 MRI scans

Susceptibility of brain atrophy to in Alzheimer's disease, evidence from functional prioritization in imaging genetics

TREM2 and neurodegenerative disease

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

The effect of increased genetic risk for Alzheimer's disease on hippocampal and amygdala volume

The genetic architecture of the human cerebral cortex

The genetic architecture of the human cerebral cortex

Unbiased tensor-based morphometry: improved robustness and sample size estimates for Alzheimer's disease clinical trials

Using structural MRI to identify bipolar disorders - 13 site machine learning study in 3020 individuals from the ENIGMA Bipolar Disorders Working Group

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

Workflow Reuse in Practice: A Study of Neuroimaging Pipeline Users