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ENIGMA 联盟:神经影像学和遗传学数据的大规模合作分析。

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

机构信息

Imaging Genetics Center, Institute for Neuroimaging and Informatics, Keck School of Medicine, University of Southern California, 2001 N. Soto Street, Los Angeles, CA, 90033, USA,

出版信息

Brain Imaging Behav. 2014 Jun;8(2):153-82. doi: 10.1007/s11682-013-9269-5.

Abstract

The Enhancing NeuroImaging Genetics through Meta-Analysis (ENIGMA) Consortium is a collaborative network of researchers working together on a range of large-scale studies that integrate data from 70 institutions worldwide. Organized into Working Groups that tackle questions in neuroscience, genetics, and medicine, ENIGMA studies have analyzed neuroimaging data from over 12,826 subjects. In addition, data from 12,171 individuals were provided by the CHARGE consortium for replication of findings, in a total of 24,997 subjects. By meta-analyzing results from many sites, ENIGMA has detected factors that affect the brain that no individual site could detect on its own, and that require larger numbers of subjects than any individual neuroimaging study has currently collected. ENIGMA's first project was a genome-wide association study identifying common variants in the genome associated with hippocampal volume or intracranial volume. Continuing work is exploring genetic associations with subcortical volumes (ENIGMA2) and white matter microstructure (ENIGMA-DTI). Working groups also focus on understanding how schizophrenia, bipolar illness, major depression and attention deficit/hyperactivity disorder (ADHD) affect the brain. We review the current progress of the ENIGMA Consortium, along with challenges and unexpected discoveries made on the way.

摘要

增强神经影像学遗传学的荟萃分析(ENIGMA)联盟是一个由研究人员组成的合作网络,共同开展一系列大型研究,整合来自全球 70 个机构的数据。ENIGMA 研究组织成处理神经科学、遗传学和医学问题的工作组,分析了来自 12826 名受试者的神经影像学数据。此外,CHARGE 联盟还提供了 12171 名个体的数据,用于对发现结果进行复制,总共有 24997 名受试者。通过对来自多个地点的结果进行荟萃分析,ENIGMA 检测到了一些影响大脑的因素,这些因素是单个地点无法单独检测到的,而且需要比任何单个神经影像学研究目前收集的更多的样本量。ENIGMA 的第一个项目是全基因组关联研究,确定与海马体体积或颅内体积相关的基因组中的常见变异。正在进行的工作还在探索与皮质下体积(ENIGMA2)和白质微观结构(ENIGMA-DTI)的遗传关联。工作组还专注于了解精神分裂症、双相情感障碍、重度抑郁症和注意缺陷/多动障碍(ADHD)如何影响大脑。我们回顾了 ENIGMA 联盟的当前进展,以及在此过程中遇到的挑战和意外发现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5ef/4008818/0998c73651e6/11682_2013_9269_Fig1_HTML.jpg

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