This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. The overall aim of this project is to develop and build on our earlier funded work on the segmentation and spatial normalisation for regional morphometry at 1.5T, to make use of novel new imaging contrasts becoming available in higher field imaging.
Aim 1 : Multi-Sequence Fusion and High Resolution Tissue Segmentation: Development of automated tissue segmentation methods which estimate a voxel by voxel map of both the fractional occupancy and the probability of tissue types from multi-acquisition variable T1 weighted imaging data. This willincorporate inter-frame co-alignment, motion frame rejection, intensity inhomogeneity correction of the frames, and co-alignment and fusion of this data with other MRI sequences (such as DTI and FLAIR) acquired in a typical study.
Aim 2 : Improved Whole Brain Spatial Normalisation: Develop and refine multi-sequence fine-scalespatial normalisation methods for novel image contrasts, which make use of multiple-contrasts at high isotropic resolution. This will employ large scale diffeomorphic and symmetric image registration driven by robust regionalized entropy based registration criteria. We will also construct and use a high-resolution target template for spatial normalisation.
Aim 3 : High Resolution Map of T1 values in the Aging Adult Brain: Construction of a population based statistical map capturing the expected T1 values and their variance with location over a set of normal control subjects using the tissue segmentation and spatial normalisation methods developed in aims 1 and 2, together with the acquisition and reconstruction methods developed in this resource proposal. This statistical map will be published on the web as a resource for other researchers to make use of.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Biotechnology Resource Grants (P41)
Project #
5P41RR023953-02
Application #
7957227
Study Section
Special Emphasis Panel (ZRG1-SBIB-J (40))
Project Start
2009-07-01
Project End
2010-06-30
Budget Start
2009-07-01
Budget End
2010-06-30
Support Year
2
Fiscal Year
2009
Total Cost
$76,919
Indirect Cost
Name
Northern California Institute Research & Education
Department
Type
DUNS #
613338789
City
San Francisco
State
CA
Country
United States
Zip Code
94121
Kuceyeski, A; Shah, S; Dyke, J P et al. (2016) The application of a mathematical model linking structural and functional connectomes in severe brain injury. Neuroimage Clin 11:635-647
Lam, Fan; Liu, Ding; Song, Zhuang et al. (2016) A fast algorithm for denoising magnitude diffusion-weighted images with rank and edge constraints. Magn Reson Med 75:433-40
Pannetier, Nicolas A; Stavrinos, Theano; Ng, Peter et al. (2016) Quantitative framework for prospective motion correction evaluation. Magn Reson Med 75:810-6
Kuceyeski, Amy; Navi, Babak B; Kamel, Hooman et al. (2016) Structural connectome disruption at baseline predicts 6-months post-stroke outcome. Hum Brain Mapp 37:2587-601
Friedman, Eric J; Young, Karl; Tremper, Graham et al. (2015) Directed network motifs in Alzheimer's disease and mild cognitive impairment. PLoS One 10:e0124453
Kuceyeski, Amy; Navi, Babak B; Kamel, Hooman et al. (2015) Exploring the brain's structural connectome: A quantitative stroke lesion-dysfunction mapping study. Hum Brain Mapp 36:2147-60
Ma, Chao; Liang, Zhi-Pei (2015) Design of multidimensional Shinnar-Le Roux radiofrequency pulses. Magn Reson Med 73:633-45
Zhao, Bo; Lu, Wenmiao; Hitchens, T Kevin et al. (2015) Accelerated MR parameter mapping with low-rank and sparsity constraints. Magn Reson Med 74:489-98
Lu, Zhao-Hua; Zhu, Hongtu; Knickmeyer, Rebecca C et al. (2015) Multiple SNP Set Analysis for Genome-Wide Association Studies Through Bayesian Latent Variable Selection. Genet Epidemiol 39:664-77
Raj, Ashish; LoCastro, Eve; Kuceyeski, Amy et al. (2015) Network Diffusion Model of Progression Predicts Longitudinal Patterns of Atrophy and Metabolism in Alzheimer's Disease. Cell Rep :

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