相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。Association analysis in over 329,000 individuals identifies 116 independent variants influencing neuroticism
Michelle Luciano et al.
NATURE GENETICS (2018)
Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence
Jeanne E. Savage et al.
NATURE GENETICS (2018)
Image processing and Quality Control for the first 10,000 brain imaging datasets from UK Biobank
Fidel Alfaro-Almagro et al.
NEUROIMAGE (2018)
Statistical Challenges in Big Data'' Human Neuroimaging
Stephen M. Smith et al.
NEURON (2018)
The UK Biobank resource with deep phenotyping and genomic data
Clare Bycroft et al.
NATURE (2018)
Genetic effects on gene expression across human tissues
Francois Aguet et al.
NATURE (2017)
Novel genetic loci associated with hippocampal volume
Derrek P. Hibar et al.
NATURE COMMUNICATIONS (2017)
The heritability of multi-modal connectivity in human brain activity
Giles L. Colclough et al.
ELIFE (2017)
Genome-wide association and Mendelian randomization study of NT-proBNP in patients with acute coronary syndrome
Asa Johansson et al.
HUMAN MOLECULAR GENETICS (2016)
A multiple-phenotype imputation method for genetic studies
Andrew Dahl et al.
NATURE GENETICS (2016)
A reference panel of 64,976 haplotypes for genotype imputation
Shane McCarthy et al.
NATURE GENETICS (2016)
Multimodal population brain imaging in the UK Biobank prospective epidemiological study
Karla L. Miller et al.
NATURE NEUROSCIENCE (2016)
Genome-wide association study of schizophrenia in Ashkenazi Jews
Fernando S. Goes et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS (2015)
Heritability of Subcortical and Limbic Brain Volume and Shape in Multiplex-Multigenerational Families with Schizophrenia
David R. Roalf et al.
BIOLOGICAL PSYCHIATRY (2015)
Common genetic variants influence human subcortical brain structures
Derrek P. Hibar et al.
NATURE (2015)
Genetic variance estimation with imputed variants finds negligible missing heritability for human height and body mass index
Jian Yang et al.
NATURE GENETICS (2015)
Partitioning heritability by functional annotation using genome-wide association summary statistics
Hilary K. Finucane et al.
NATURE GENETICS (2015)
An atlas of genetic correlations across human diseases and traits
Brendan Bulik-Sullivan et al.
NATURE GENETICS (2015)
Learning to identify CNS drug action and efficacy using multistudy fMRI data
Eugene P. Duff et al.
SCIENCE TRANSLATIONAL MEDICINE (2015)
UK Biobank: An Open Access Resource for Identifying the Causes of a Wide Range of Complex Diseases of Middle and Old Age
Cathie Sudlow et al.
PLOS MEDICINE (2015)
Exome Sequence Reveals Mutations in CoA Synthase as a Cause of Neurodegeneration with Brain Iron Accumulation
Sabrina Dusi et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2014)
Biological insights from 108 schizophrenia-associated genetic loci
Stephan Ripke et al.
NATURE (2014)
Impact of family structure and common environment on heritability estimation for neuroimaging genetics studies using Sequential Oligogenic Linkage Analysis Routines
Mary Ellen Koran et al.
JOURNAL OF MEDICAL IMAGING (2014)
MR susceptibility imaging
Jeff Duyn
JOURNAL OF MAGNETIC RESONANCE (2013)
Heritability of subcortical brain measures: A perspective for future genome-wide association studies
Anouk den Braber et al.
NEUROIMAGE (2013)
Brain Volumes in Schizophrenia: A Meta-Analysis in Over 18 000 Subjects
Sander V. Haijma et al.
SCHIZOPHRENIA BULLETIN (2013)
NODDI: Practical in vivo neurite orientation dispersion and density imaging of the human brain
Hui Zhang et al.
NEUROIMAGE (2012)
The mystery of missing heritability: Genetic interactions create phantom heritability
Or Zuk et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2012)
UK Biobank: Current status and what it means for epidemiology
Naomi Allen et al.
HEALTH POLICY AND TECHNOLOGY (2012)
101 labeled brain images and a consistent human cortical labeling protocol
Arno Klein et al.
FRONTIERS IN NEUROSCIENCE (2012)
Genome-Wide Association Studies of Cerebral White Matter Lesion Burden: The CHARGE Consortium
Myriam Fornage et al.
ANNALS OF NEUROLOGY (2011)
DTI measures in crossing-fibre areas: Increased diffusion anisotropy reveals early white matter alteration in MCI and mild Alzheimer's disease
Gwenaelle Douaud et al.
NEUROIMAGE (2011)
Genetic and environmental influences on the size of specific brain regions in midlife: The VETSA MRI study
William S. Kremen et al.
NEUROIMAGE (2010)
Whole genome association study of brain-wide imaging phenotypes for identifying quantitative trait loci in MCI and AD: A study of the ADNI cohort
Li Shen et al.
NEUROIMAGE (2010)
Automatic parcellation of human cortical gyri and sulci using standard anatomical nomenclature
Christophe Destrieux et al.
NEUROIMAGE (2010)
A SINGULAR VALUE THRESHOLDING ALGORITHM FOR MATRIX COMPLETION
Jian-Feng Cai et al.
SIAM JOURNAL ON OPTIMIZATION (2010)
The multiple-demand (MD) system of the primate brain: mental programs for intelligent behaviour
John Duncan
TRENDS IN COGNITIVE SCIENCES (2010)
Puzzlingly High Correlations in fMRI Studies of Emotion, Personality, and Social Cognition
Edward Vul et al.
PERSPECTIVES ON PSYCHOLOGICAL SCIENCE (2009)
Analysis of ALDH1A2, CYP26A1, CYP26B1, CRABP1, and CRABP2 in human neural tube defects suggests a possible association with alleles in ALDH1A2
KL Deak et al.
BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY (2005)
Mutations in a human ROBO gene disrupt hindbrain axon pathway crossing and morphogenesis
JC Jen et al.
SCIENCE (2004)
The effects of human population structure on large genetic association studies
J Marchini et al.
NATURE GENETICS (2004)
Human cingulate cortex and autonomic control: converging neuroimaging and clinical evidence
HD Critchley et al.
BRAIN (2003)
Accurate, robust, and automated longitudinal and cross-sectional brain change analysis
SM Smith et al.
NEUROIMAGE (2002)
分享论文
