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

PM Thompson, JL Stein, SE Medland, DP Hibar - Brain imaging and , 2014 - Springer
Abstract The Enhancing NeuroImaging Genetics through Meta-Analysis (ENIGMA)
Consortium is a collaborative network of researchers working together on a range of large 

[HTML][HTML] Genetic studies of quantitative MCI and AD phenotypes in ADNI: Progress, opportunities, and plans

AJ Saykin, L Shen, X Yao, S Kim, K Nho - Alzheimer's & , 2015 - Elsevier
Introduction Genetic data from the Alzheimer's Disease Neuroimaging Initiative (ADNI) have
been crucial in advancing the understanding of Alzheimer's disease (AD) pathophysiology 

Common disorders are quantitative traits

R Plomin, CMA Haworth, OSP Davis - Nature reviews genetics, 2009 - nature.com
After drifting apart for 100 years, the two worlds of genetics—quantitative genetics and
molecular genetics—are finally coming together in genome-wide association (GWA) 

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

AJ Saykin, L Shen, TM Foroud, SG Potkin - Alzheimer's & , 2010 - Elsevier
The role of the Alzheimer's Disease Neuroimaging Initiative Genetics Core is to facilitate the
investigation of genetic influences on disease onset and trajectory as reflected in structural 

Brain imaging genomics: integrated analysis and machine learning

L Shen, PM Thompson - Proceedings of the IEEE, 2019 - ieeexplore.ieee.org
Brain imaging genomics is an emerging data science field, where integrated analysis of
brain imaging and genomics data, often combined with other biomarker, clinical, and 

Whole genome association study of brain-wide imaging phenotypes for identifying quantitative trait loci in MCI and AD: A study of the ADNI cohort

L Shen, S Kim, SL Risacher, K Nho, S Swaminathan - Neuroimage, 2010 - Elsevier
A genome-wide, whole brain approach to investigate genetic effects on neuroimaging
phenotypes for identifying quantitative trait loci is described. The Alzheimer's Disease 

Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease

SG Potkin, G Guffanti, A Lakatos, JA Turner, F Kruggel - PloS one, 2009 - journals.plos.org
Background With the exception of APOE 4 allele, the common genetic risk factors for
sporadic Alzheimer's Disease (AD) are unknown. Methods and Findings We completed a 

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

PM Thompson, OA Andreassen, A Arias-Vasquez - Neuroimage, 2017 - Elsevier
In this review, we discuss recent work by the ENIGMA Consortium (http://enigma. ini. usc.
edu)–a global alliance of over 500 scientists spread across 200 institutions in 35 countries 

APOE and BCHE as modulators of cerebral amyloid deposition: a florbetapir PET genome-wide association study

VK Ramanan, SL Risacher, K Nho, S Kim - Molecular , 2014 - nature.com
Deposition of amyloid- (A) in the cerebral cortex is thought to be a pivotal event in
Alzheimer's disease (AD) pathogenesis with a significant genetic contribution. Molecular 

Genome-wide association study of CSF biomarkers A1-42, t-tau, and p-tau181p in the ADNI cohort

S Kim, S Swaminathan, L Shen, SL Risacher, K Nho - Neurology, 2011 - AAN Enterprises
Objectives: CSF levels of A1-42, t-tau, and p-tau181p are potential early diagnostic
markers for probable Alzheimer disease (AD). The influence of genetic variation on these