Emma Sprooten

Orcid: 0000-0002-1691-9105

According to our database1, Emma Sprooten authored at least 11 papers between 2013 and 2021.

Collaborative distances:
  • Dijkstra number2 of five.
  • Erdős number3 of four.

Timeline

Legend:

Book 
In proceedings 
Article 
PhD thesis 
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Links

Online presence:

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Bibliography

2021
Functional co-activation of the default mode network in APOE ε4-carriers: A replication study.
NeuroImage, 2021

Evaluating the Neuroimaging-Genetic Prediction of Symptom Changes in Individuals with ADHD.
Proceedings of the 43rd Annual International Conference of the IEEE Engineering in Medicine & Biology Society, 2021

2020
Discovering the shared biology of cognitive traits determined by genetic overlap.
NeuroImage, 2020

2019
Depth-dependent intracortical myelin organization in the living human brain determined by in vivo ultra-high field magnetic resonance imaging.
NeuroImage, 2019

2015
Heritability of fractional anisotropy in human white matter: A comparison of Human Connectome Project and ENIGMA-DTI data.
NeuroImage, 2015

2014
Common genetic variants and gene expression associated with white matter microstructure in the human brain.
NeuroImage, 2014

Multi-site study of additive genetic effects on fractional anisotropy of cerebral white matter: Comparing meta and megaanalytical approaches for data pooling.
NeuroImage, 2014

Corrigendum to "Multi-site genetic analysis of diffusion images and voxelwise heritability analysis: A pilot project of the ENIGMA-DTI working group" [NeuroImage 81 (2013) 455-469].
NeuroImage, 2014


2013
Transcriptomics of cortical gray matter thickness decline during normal aging.
NeuroImage, 2013

Multi-site genetic analysis of diffusion images and voxelwise heritability analysis: A pilot project of the ENIGMA-DTI working group.
NeuroImage, 2013


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