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craddockGigascience2014.bib
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@article{Assaf2013,
abstract = {In recent years, diffusion MRI has become an extremely important tool for studying the morphology of living brain tissue, as it provides unique insights into both its macrostructure and microstructure. Recent applications of diffusion MRI aimed to characterize the structural connectome using tractography to infer connectivity between brain regions. In parallel to the development of tractography, additional diffusion MRI based frameworks (CHARMED, AxCaliber, ActiveAx) were developed enabling the extraction of a multitude of micro-structural parameters (axon diameter distribution, mean axonal diameter and axonal density). This unique insight into both tissue microstructure and connectivity has enormous potential value in understanding the structure and organization of the brain as well as providing unique insights to abnormalities that underpin disease states. The CONNECT (Consortium Of Neuroimagers for the Non-invasive Exploration of brain Connectivity and Tracts) project aimed to combine tractography and micro-structural measures of the living human brain in order to obtain a better estimate of the connectome, while also striving to extend validation of these measurements. This paper summarizes the project and describes the perspective of using micro-structural measures to study the connectome.},
author = {Assaf, Yaniv and Alexander, Daniel C and Jones, Derek K and Bizzi, Albero and Behrens, Tim E J and Clark, Chris a and Cohen, Yoram and Dyrby, Tim B and Huppi, Petra S and Knoesche, Thomas R and Lebihan, Denis and Parker, Geoff J M and Poupon, Cyril and Anaby, Debbie and Anwander, Alfred and Bar, Leah and Barazany, Daniel and Blumenfeld-Katzir, Tamar and De-Santis, Silvia and Duclap, Delphine and Figini, Matteo and Fischi, Elda and Guevara, Pamela and Hubbard, Penny and Hofstetter, Shir and Jbabdi, Saad and Kunz, Nicolas and Lazeyras, Francois and Lebois, Alice and Liptrot, Matthew G and Lundell, Henrik and Mangin, Jean-Fran\c{c}ois and Dominguez, David Moreno and Morozov, Darya and Schreiber, Jan and Seunarine, Kiran and Nava, Simone and Riffert, Till and Sasson, Efrat and Schmitt, Benoit and Shemesh, Noam and Sotiropoulos, Stam N and Tavor, Ido and Zhang, Hui Gary and Zhou, Feng-Lei},
doi = {10.1016/j.neuroimage.2013.05.055},
file = {:home/rtungaraza/.local/share/data/Mendeley Ltd./Mendeley Desktop/Downloaded/Assaf et al. - 2013 - The CONNECT project Combining macro- and micro-structure.pdf:pdf},
issn = {1095-9572},
journal = {NeuroImage},
keywords = {Brain,Brain: cytology,Brain: physiology,Connectome,Connectome: methods,Diffusion Tensor Imaging,Diffusion Tensor Imaging: methods,Humans,Image Enhancement,Image Enhancement: methods,Models, Anatomic,Models, Neurological,Nerve Net,Nerve Net: cytology,Nerve Net: physiology},
month = oct,
pages = {273--82},
pmid = {23727318},
publisher = {Elsevier Inc.},
title = {{The CONNECT project: Combining macro- and micro-structure.}},
url = {http://www.ncbi.nlm.nih.gov/pubmed/23727318},
volume = {80},
year = {2013}
}
@article{Biswal2010,
abstract = {Although it is being successfully implemented for exploration of the genome, discovery science has eluded the functional neuroimaging community. The core challenge remains the development of common paradigms for interrogating the myriad functional systems in the brain without the constraints of a priori hypotheses. Resting-state functional MRI (R-fMRI) constitutes a candidate approach capable of addressing this challenge. Imaging the brain during rest reveals large-amplitude spontaneous low-frequency (<0.1 Hz) fluctuations in the fMRI signal that are temporally correlated across functionally related areas. Referred to as functional connectivity, these correlations yield detailed maps of complex neural systems, collectively constituting an individual's "functional connectome." Reproducibility across datasets and individuals suggests the functional connectome has a common architecture, yet each individual's functional connectome exhibits unique features, with stable, meaningful interindividual differences in connectivity patterns and strengths. Comprehensive mapping of the functional connectome, and its subsequent exploitation to discern genetic influences and brain-behavior relationships, will require multicenter collaborative datasets. Here we initiate this endeavor by gathering R-fMRI data from 1,414 volunteers collected independently at 35 international centers. We demonstrate a universal architecture of positive and negative functional connections, as well as consistent loci of inter-individual variability. Age and sex emerged as significant determinants. These results demonstrate that independent R-fMRI datasets can be aggregated and shared. High-throughput R-fMRI can provide quantitative phenotypes for molecular genetic studies and biomarkers of developmental and pathological processes in the brain. To initiate discovery science of brain function, the 1000 Functional Connectomes Project dataset is freely accessible at www.nitrc.org/projects/fcon\_1000/.},
author = {Biswal, Bharat B and Mennes, Maarten and Zuo, Xi-Nian and Gohel, Suril and Kelly, Clare and Smith, Steve M and Beckmann, Christian F and Adelstein, Jonathan S and Buckner, Randy L and Colcombe, Stan and Dogonowski, Anne-Marie and Ernst, Monique and Fair, Damien and Hampson, Michelle and Hoptman, Matthew J and Hyde, James S and Kiviniemi, Vesa J and K\"{o}tter, Rolf and Li, Shi-Jiang and Lin, Ching-Po and Lowe, Mark J and Mackay, Clare and Madden, David J and Madsen, Kristoffer H and Margulies, Daniel S and Mayberg, Helen S and McMahon, Katie and Monk, Christopher S and Mostofsky, Stewart H and Nagel, Bonnie J and Pekar, James J and Peltier, Scott J and Petersen, Steven E and Riedl, Valentin and Rombouts, Serge a R B and Rypma, Bart and Schlaggar, Bradley L and Schmidt, Sein and Seidler, Rachael D and Siegle, Greg J and Sorg, Christian and Teng, Gao-Jun and Veijola, Juha and Villringer, Arno and Walter, Martin and Wang, Lihong and Weng, Xu-Chu and Whitfield-Gabrieli, Susan and Williamson, Peter and Windischberger, Christian and Zang, Yu-Feng and Zhang, Hong-Ying and Castellanos, F Xavier and Milham, Michael P},
doi = {10.1073/pnas.0911855107},
file = {:home/rtungaraza/.local/share/data/Mendeley Ltd./Mendeley Desktop/Downloaded/Biswal et al. - 2010 - Toward discovery science of human brain function(2).pdf:pdf},
issn = {1091-6490},
journal = {Proceedings of the National Academy of Sciences of the United States of America},
keywords = {Adolescent,Adult,Age Factors,Aged,Algorithms,Analysis of Variance,Brain,Brain Mapping,Brain Mapping: methods,Brain: anatomy \& histology,Brain: physiology,Female,Humans,Magnetic Resonance Imaging,Magnetic Resonance Imaging: methods,Male,Middle Aged,Neural Pathways,Neural Pathways: anatomy \& histology,Neural Pathways: physiology,Sex Factors,Young Adult},
month = mar,
number = {10},
pages = {4734--9},
pmid = {20176931},
title = {{Toward discovery science of human brain function.}},
url = {http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=2842060\&tool=pmcentrez\&rendertype=abstract},
volume = {107},
year = {2010}
}
@article{Bogdanov2014,
archivePrefix = {arXiv},
arxivId = {arXiv:1407.5590v1},
author = {Bogdanov, Petko and Dereli, Nazli and Bassett, DS},
eprint = {arXiv:1407.5590v1},
file = {:home/rtungaraza/PapersBooks/LearningAboutLearningSugraphs2014.pdf:pdf},
journal = {arXiv preprint arXiv: \ldots},
title = {{Learning about Learning: Human Brain Sub-Network Biomarkers in fMRI Data}},
url = {http://arxiv.org/abs/1407.5590},
year = {2014}
}
@article{Bullmore2011,
abstract = {Brain graphs provide a relatively simple and increasingly popular way of modeling the human brain connectome, using graph theory to abstractly define a nervous system as a set of nodes (denoting anatomical regions or recording electrodes) and interconnecting edges (denoting structural or functional connections). Topological and geometrical properties of these graphs can be measured and compared to random graphs and to graphs derived from other neuroscience data or other (nonneural) complex systems. Both structural and functional human brain graphs have consistently demonstrated key topological properties such as small-worldness, modularity, and heterogeneous degree distributions. Brain graphs are also physically embedded so as to nearly minimize wiring cost, a key geometric property. Here we offer a conceptual review and methodological guide to graphical analysis of human neuroimaging data, with an emphasis on some of the key assumptions, issues, and trade-offs facing the investigator.},
author = {Bullmore, Edward T and Bassett, Danielle S},
doi = {10.1146/annurev-clinpsy-040510-143934},
file = {:home/rtungaraza/.local/share/data/Mendeley Ltd./Mendeley Desktop/Downloaded/Bullmore, Bassett - 2011 - Brain graphs graphical models of the human brain connectome.pdf:pdf},
issn = {1548-5951},
journal = {Annual review of clinical psychology},
keywords = {Animals,Brain,Brain: anatomy \& histology,Brain: physiology,Humans,Magnetic Resonance Imaging,Models, Neurological,Nerve Net,Nerve Net: anatomy \& histology,Nerve Net: physiology,Neural Networks (Computer)},
month = jan,
pages = {113--40},
pmid = {21128784},
title = {{Brain graphs: graphical models of the human brain connectome.}},
url = {http://www.ncbi.nlm.nih.gov/pubmed/21128784},
volume = {7},
year = {2011}
}
@article{Craddock2009,
abstract = {The application of multivoxel pattern analysis methods has attracted increasing attention, particularly for brain state prediction and real-time functional MRI applications. Support vector classification is the most popular of these techniques, owing to reports that it has better prediction accuracy and is less sensitive to noise. Support vector classification was applied to learn functional connectivity patterns that distinguish patients with depression from healthy volunteers. In addition, two feature selection algorithms were implemented (one filter method, one wrapper method) that incorporate reliability information into the feature selection process. These reliability feature selections methods were compared to two previously proposed feature selection methods. A support vector classifier was trained that reliably distinguishes healthy volunteers from clinically depressed patients. The reliability feature selection methods outperformed previously utilized methods. The proposed framework for applying support vector classification to functional connectivity data is applicable to other disease states beyond major depression.},
author = {Craddock, R Cameron and Holtzheimer, Paul E and Hu, Xiaoping P and Mayberg, Helen S},
doi = {10.1002/mrm.22159},
file = {:home/rtungaraza/.local/share/data/Mendeley Ltd./Mendeley Desktop/Downloaded/Craddock et al. - 2009 - Disease state prediction from resting state functional connectivity.pdf:pdf},
issn = {1522-2594},
journal = {Magnetic resonance in medicine : official journal of the Society of Magnetic Resonance in Medicine / Society of Magnetic Resonance in Medicine},
keywords = {Adult,Algorithms,Artificial Intelligence,Depressive Disorder, Major,Depressive Disorder, Major: diagnosis,Female,Humans,Image Enhancement,Image Enhancement: methods,Image Interpretation, Computer-Assisted,Image Interpretation, Computer-Assisted: methods,Magnetic Resonance Imaging,Magnetic Resonance Imaging: methods,Male,Pattern Recognition, Automated,Pattern Recognition, Automated: methods,Reproducibility of Results,Sensitivity and Specificity},
month = dec,
number = {6},
pages = {1619--28},
pmid = {19859933},
title = {{Disease state prediction from resting state functional connectivity.}},
url = {http://www.ncbi.nlm.nih.gov/pubmed/19859933},
volume = {62},
year = {2009}
}
@article{Craddock2005,
author = {Craddock, R Cameron and James, G Andrew and Holtzheimer, Paul E and Hu, Xiaoping P and Mayberg, Helen S},
file = {:home/rtungaraza/.local/share/data/Mendeley Ltd./Mendeley Desktop/Downloaded/Craddock et al. - 2005 - ROI Atlas Generation from Whole Brain Parcellation of Resting State fMRI Data.pdf:pdf},
journal = {ISMRM},
pages = {77869--77869},
title = {{ROI Atlas Generation from Whole Brain Parcellation of Resting State fMRI Data}},
volume = {25},
year = {2005}
}
@article{Craddock2012,
author = {Craddock, R Cameron and James, G Andrew and Iii, Paul E Holtzheimer and Hu, Xiaoping P and Mayberg, Helen S},
doi = {10.1002/hbm.21333.A},
file = {:home/rtungaraza/.local/share/data/Mendeley Ltd./Mendeley Desktop/Downloaded/Craddock et al. - 2012 - A whole brain fMRI atlas generated via spatially constrained spectral clustering.pdf:pdf},
journal = {Human Brain Mapping},
keywords = {atlas,clustering,functional connectivity,regions of interest,resting state},
number = {8},
title = {{A whole brain fMRI atlas generated via spatially constrained spectral clustering}},
volume = {33},
year = {2012}
}
@article{Craddock2013,
abstract = {At macroscopic scales, the human connectome comprises anatomically distinct brain areas, the structural pathways connecting them and their functional interactions. Annotation of phenotypic associations with variation in the connectome and cataloging of neurophenotypes promise to transform our understanding of the human brain. In this Review, we provide a survey of magnetic resonance imaging–based measurements of functional and structural connectivity. We highlight emerging areas of development and inquiry and emphasize the importance of integrating structural and functional perspectives on brain architecture.},
author = {Craddock, R Cameron and Jbabdi, Saad and Yan, Chao-Gan and Vogelstein, Joshua T and Castellanos, F Xavier and {Di Martino}, Adriana and Kelly, Clare and Heberlein, Keith and Colcombe, Stan and Milham, Michael P},
doi = {10.1038/nmeth.2482},
file = {:home/rtungaraza/.local/share/data/Mendeley Ltd./Mendeley Desktop/Downloaded/Craddock et al. - 2013 - Imaging human connectomes at the macroscale.pdf:pdf},
issn = {1548-7105},
journal = {Nature methods},
keywords = {Brain,Brain: cytology,Brain: physiology,Connectome,Humans,Magnetic Resonance Imaging,Magnetic Resonance Imaging: methods,Phenotype},
month = jun,
number = {6},
pages = {524--39},
pmid = {23722212},
title = {{Imaging human connectomes at the macroscale.}},
url = {http://www.ncbi.nlm.nih.gov/pubmed/23722212},
volume = {10},
year = {2013}
}
@article{DagliMSIngeholmJE1999,
author = {{Dagli MS, Ingeholm JE}, and Haxby JV},
journal = {NeuroImage},
pages = {407--415},
title = {{Localization of cardiac-in- duced signal change in fMRI}},
volume = {9},
year = {1999}
}
@article{Dosenbach2010,
abstract = {Group functional connectivity magnetic resonance imaging (fcMRI) studies have documented reliable changes in human functional brain maturity over development. Here we show that support vector machine-based multivariate pattern analysis extracts sufficient information from fcMRI data to make accurate predictions about individuals' brain maturity across development. The use of only 5 minutes of resting-state fcMRI data from 238 scans of typically developing volunteers (ages 7 to 30 years) allowed prediction of individual brain maturity as a functional connectivity maturation index. The resultant functional maturation curve accounted for 55\% of the sample variance and followed a nonlinear asymptotic growth curve shape. The greatest relative contribution to predicting individual brain maturity was made by the weakening of short-range functional connections between the adult brain's major functional networks.},
author = {Dosenbach, Nico U F and Nardos, Binyam and Cohen, Alexander L and Fair, Damien a and Power, Jonathan D and Church, Jessica a and Nelson, Steven M and Wig, Gagan S and Vogel, Alecia C and Lessov-Schlaggar, Christina N and Barnes, Kelly Anne and Dubis, Joseph W and Feczko, Eric and Coalson, Rebecca S and Pruett, John R and Barch, Deanna M and Petersen, Steven E and Schlaggar, Bradley L},
doi = {10.1126/science.1194144},
file = {:home/rtungaraza/.local/share/data/Mendeley Ltd./Mendeley Desktop/Downloaded/Dosenbach et al. - 2010 - Prediction of individual brain maturity using fMRI.pdf:pdf},
issn = {1095-9203},
journal = {Science (New York, N.Y.)},
keywords = {Adolescent,Adult,Aging,Algorithms,Artificial Intelligence,Brain,Brain Mapping,Brain: growth \& development,Brain: physiology,Cerebellum,Cerebellum: growth \& development,Cerebellum: physiology,Child,Female,Frontal Lobe,Frontal Lobe: growth \& development,Frontal Lobe: physiology,Humans,Magnetic Resonance Imaging,Male,Multivariate Analysis,Neural Pathways,Occipital Lobe,Occipital Lobe: growth \& development,Occipital Lobe: physiology,Young Adult},
month = sep,
number = {5997},
pages = {1358--61},
pmid = {20829489},
title = {{Prediction of individual brain maturity using fMRI.}},
url = {http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=3135376\&tool=pmcentrez\&rendertype=abstract},
volume = {329},
year = {2010}
}
@article{Eloyan2014,
abstract = {Functional magnetic resonance imaging (fMRI) is a thriving field that plays an important role in medical imaging analysis, biological and neuroscience research and practice. This manuscript gives a didactic introduction to the statistical analysis of fMRI data using the R project, along with the relevant R code. The goal is to give statisticians who would like to pursue research in this area a quick tutorial for programming with fMRI data. References of relevant packages and papers are provided for those interested in more advanced analysis.},
author = {Eloyan, Ani and Li, Shanshan and Muschelli, John and Pekar, Jim J and Mostofsky, Stewart H and Caffo, Brian S},
doi = {10.1371/journal.pone.0089470},
file = {:home/rtungaraza/PapersBooks/caffoFMRIpaper.pdf:pdf},
issn = {1932-6203},
journal = {PloS one},
month = jan,
number = {2},
pages = {e89470},
pmid = {24586801},
title = {{Analytic programming with FMRI data: a quick-start guide for statisticians using R.}},
url = {http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=3938835\&tool=pmcentrez\&rendertype=abstract},
volume = {9},
year = {2014}
}
@article{Fornito2014,
abstract = {In recent years, pathophysiological models of brain disorders have shifted from an emphasis on understanding pathology in specific brain regions to characterizing disturbances of interconnected neural systems. This shift has paralleled rapid advances in connectomics, a field concerned with comprehensively mapping the neural elements and inter-connections that constitute the brain. Magnetic resonance imaging (MRI) has played a central role in these efforts, as it allows relatively cost-effective in vivo assessment of the macro-scale architecture of brain network connectivity. In this paper, we provide a brief introduction to some of the basic concepts in the field and review how recent developments in imaging connectomics are yielding new insights into brain disease, with a particular focus on Alzheimer's disease and schizophrenia. Specifically, we consider how research into circuit-level, connectome-wide and topological changes is stimulating the development of new aetiopathological theories and biomarkers with potential for clinical translation. The findings highlight the advantage of conceptualizing brain disease as a result of disturbances in an interconnected complex system, rather than discrete pathology in isolated sub-sets of brain regions.},
author = {Fornito, Alex and Bullmore, Edward T},
doi = {10.1016/j.euroneuro.2014.02.011},
file = {:home/rtungaraza/.local/share/data/Mendeley Ltd./Mendeley Desktop/Downloaded/Fornito, Bullmore - 2014 - Connectomics A new paradigm for understanding brain disease.pdf:pdf},
issn = {1873-7862},
journal = {European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology},
month = mar,
pmid = {24726580},
title = {{Connectomics: A new paradigm for understanding brain disease.}},
url = {http://www.ncbi.nlm.nih.gov/pubmed/24726580},
year = {2014}
}
@inproceedings{Fu2013,
author = {Fu, Zenigh and Di, Xiing and Chan, Shing-Chow and Hung, Yeung-Sam and Biswal, B.B. and Zhang, Zhiguo},
booktitle = {Engineering in Medicine and Biology Society (EMBC), 2013 35th Annual International Conference of the IEEE},
pages = {2944--2947},
title = {{Time-varying correlation coefficients estimation and its application to dynamic connectivity analysis of fMRI}},
year = {2013}
}
@article{Gudbjartsson1995,
author = {Gudbjartsson, H and Patz, S},
file = {:home/rtungaraza/PapersBooks/RicianNoiseMRI.pdf:pdf},
journal = {Magnetic resonance in medicine},
keywords = {gaussian,noise,rayleigh,rician},
number = {6},
pages = {910--914},
title = {{The Rician distribution of noisy MRI data}},
url = {http://onlinelibrary.wiley.com/doi/10.1002/mrm.1910340618/full},
volume = {34},
year = {1995}
}
@phdthesis{Hagmann2005,
author = {Hagmann, Patric},
title = {{From diffusion MRI to brain connectomics}},
year = {2005}
}
@article{Iakovidou2013,
abstract = {Complex networks constitute a recurring issue in the analysis of neuroimaging data. Recently, network motifs have been identified as patterns of interconnections since they appear in a significantly higher number than in randomized networks, in a given ensemble of anatomical or functional connectivity graphs. The current approach for detecting and enumerating motifs in brain networks requires a predetermined motif repertoire and can operate only with motifs of small size (consisting of few nodes). There is a growing interest in methodologies for frequent graph-based pattern mining in large graph datasets that can facilitate adaptive design of motifs. The results presented in this paper are based on the graph-based Substructure pattern mining (gSpan) algorithm and introduce a manifold of ways to exploit it for data-driven motif extraction in connectomics research. Functional connectivity graphs from electroencephalographic (EEG) recordings during resting state and mental calculations are used to demonstrate our approach. Relying on either time-invariant or time-evolving graphs, characteristic motifs associated with various frequency bands were derived and compared. With a suitable manipulation, the gSpan discovers motifs which are specific to performing mental arithmetics. Finally, the subject-dependent temporal signatures of motifs' appearance revealed the transient nature of the evolving functional connectivity (math-related motifs "come and go").},
author = {Iakovidou, Nantia D and Dimitriadis, Stavros I and Laskaris, Nikolaos a and Tsichlas, Kostas and Manolopoulos, Yannis},
doi = {10.1016/j.jneumeth.2012.12.018},
file = {:home/rtungaraza/Desktop/Neuro2013idltm.pdf:pdf},
issn = {1872-678X},
journal = {Journal of neuroscience methods},
keywords = {Adult,Algorithms,Brain,Brain: physiology,Computational Biology,Computational Biology: methods,Humans,Models, Neurological,Nerve Net,Nerve Net: physiology},
month = mar,
number = {2},
pages = {204--13},
pmid = {23274947},
publisher = {Elsevier B.V.},
title = {{On the discovery of group-consistent graph substructure patterns from brain networks.}},
url = {http://www.ncbi.nlm.nih.gov/pubmed/23274947},
volume = {213},
year = {2013}
}
@article{Jiang2013,
abstract = {The human brain can be studied as a hierarchy of complex networks on different temporal and spatial scales. On each scale, from gene, protein, synapse, neuron and microcircuit, to area, pathway and the whole brain, many advances have been made with the development of related techniques. Brain network studies on different temporal and spatial scales are booming. However, such studies have focused on single levels, and can only reflect limited aspects of how the brain is formed and how it works. Therefore, it is increasingly urgent to integrate a variety of techniques, methods and models, and to merge fragmented findings into a uniform research framework or platform. To this end, we have proposed the concept of the brainnetome and several related programs/projects have been launched in China. In this paper, we offer a brief review on the methodologies of the brainnetome, which include techniques on different scales, the brainnetome atlas, and methods of brain network analysis. We then take Alzheimer's disease and schizophrenia as examples to show how the brainnetome can be studied in neurological and psychiatric disorders. We also review the studies of how risk genes for brain diseases affect the brain networks. Finally, we summarize the challenges for the brainnetome, and what actions and measures have been taken to address these challenges in China. It is envisioned that the brainnetome will open new avenues and some long-standing issues may be solved by combining the brainnetome with other "omes".},
author = {Jiang, Tianzi},
doi = {10.1016/j.neuroimage.2013.04.002},
file = {:home/rtungaraza/.local/share/data/Mendeley Ltd./Mendeley Desktop/Downloaded/Jiang - 2013 - Brainnetome a new -ome to understand the brain and its disorders.pdf:pdf},
issn = {1095-9572},
journal = {NeuroImage},
keywords = {Brain,Brain Diseases,Brain Diseases: physiopathology,Brain: pathology,Brain: physiopathology,Connectome,Connectome: methods,Humans,Metabolome,Models, Anatomic,Models, Neurological,Nerve Net,Nerve Net: pathology,Nerve Net: physiopathology},
month = oct,
pages = {263--72},
pmid = {23571422},
publisher = {Elsevier Inc.},
title = {{Brainnetome: a new -ome to understand the brain and its disorders.}},
url = {http://www.ncbi.nlm.nih.gov/pubmed/23571422},
volume = {80},
year = {2013}
}
@article{Johansen-Berg2013,
abstract = {Significant resources are now being devoted to large-scale international studies attempting to map the connectome - the brain's wiring diagram. This review will focus on the use of human neuroimaging approaches to map the connectome at a macroscopic level. This emerging field of human connectomics brings both opportunities and challenges. Opportunities arise from the ability to apply a powerful toolkit of mathematical and computational approaches to interrogate these rich datasets, many of which are being freely shared with the scientific community. Challenges arise in methodology, interpretability and biological or clinical validity. This review discusses these challenges and opportunities and highlights potential future directions.},
author = {Johansen-Berg, Heidi},
doi = {10.1016/j.neuroimage.2013.05.082},
file = {:home/rtungaraza/.local/share/data/Mendeley Ltd./Mendeley Desktop/Downloaded/Johansen-Berg - 2013 - Human connectomics - what will the future demand.pdf:pdf},
issn = {1095-9572},
journal = {NeuroImage},
keywords = {Animals,Brain,Brain: anatomy \& histology,Brain: physiology,Connectome,Connectome: trends,Forecasting,Humans,Models, Anatomic,Models, Neurological,Nerve Net,Nerve Net: anatomy \& histology,Nerve Net: physiology},
month = oct,
pages = {541--4},
pmid = {23727322},
publisher = {Elsevier B.V.},
title = {{Human connectomics - what will the future demand?}},
url = {http://www.ncbi.nlm.nih.gov/pubmed/23727322},
volume = {80},
year = {2013}
}
@article{Lee2013,
abstract = {SUMMARY: Resting-state fMRI measures spontaneous low-frequency fluctuations in the BOLD signal to investigate the functional architecture of the brain. Application of this technique has allowed the identification of various RSNs, or spatially distinct areas of the brain that demonstrate synchronous BOLD fluctuations at rest. Various methods exist for analyzing resting-state data, including seed-based approaches, independent component analysis, graph methods, clustering algorithms, neural networks, and pattern classifiers. Clinical applications of resting-state fMRI are at an early stage of development. However, its use in presurgical planning for patients with brain tumor and epilepsy demonstrates early promise, and the technique may have a future role in providing diagnostic and prognostic information for neurologic and psychiatric diseases.},
author = {Lee, M H and Smyser, C D and Shimony, J S},
doi = {10.3174/ajnr.A3263},
file = {:home/rtungaraza/PapersBooks/1866.full.pdf:pdf},
issn = {1936-959X},
journal = {AJNR. American journal of neuroradiology},
keywords = {Algorithms,Brain,Brain Mapping,Brain Mapping: methods,Brain: physiology,Humans,Magnetic Resonance Imaging,Magnetic Resonance Imaging: methods,Preoperative Care,Preoperative Care: methods,Rest,Rest: physiology},
month = oct,
number = {10},
pages = {1866--72},
pmid = {22936095},
title = {{Resting-state fMRI: a review of methods and clinical applications.}},
url = {http://www.ncbi.nlm.nih.gov/pubmed/22936095},
volume = {34},
year = {2013}
}
@article{Mennes2013,
abstract = {Over a decade ago, the fMRI Data Center (fMRIDC) pioneered open-access data sharing in the task-based functional neuroimaging community. Well ahead of its time, the fMRIDC effort encountered logistical, sociocultural and funding barriers that impeded the field-wise instantiation of open-access data sharing. In 2009, ambitions for open-access data sharing were revived in the resting state functional MRI community in the form of two grassroots initiatives: the 1000 Functional Connectomes Project (FCP) and its successor, the International Neuroimaging Datasharing Initiative (INDI). Beyond providing open access to thousands of clinical and non-clinical imaging datasets, the FCP and INDI have demonstrated the feasibility of large-scale data aggregation for hypothesis generation and testing. Yet, the success of the FCP and INDI should not be confused with widespread embracement of open-access data sharing. Reminiscent of the challenges faced by fMRIDC, key controversies persist and include participant privacy, the role of informatics, and the logistical and cultural challenges of establishing an open science ethos. We discuss the FCP and INDI in the context of these challenges, highlighting the promise of current initiatives and suggesting solutions for possible pitfalls.},
author = {Mennes, Maarten and Biswal, Bharat B and Castellanos, F Xavier and Milham, Michael P},
doi = {10.1016/j.neuroimage.2012.10.064},
file = {:home/rtungaraza/PapersBooks/mennesINDI2013.pdf:pdf},
issn = {1095-9572},
journal = {NeuroImage},
keywords = {Databases, Factual,Humans,Information Dissemination,Information Dissemination: ethics,Information Dissemination: methods,Magnetic Resonance Imaging,Medical Informatics,Medical Informatics: ethics,Medical Informatics: methods,Medical Informatics: organization \& administration},
month = nov,
pages = {683--91},
pmid = {23123682},
publisher = {Elsevier Inc.},
title = {{Making data sharing work: the FCP/INDI experience.}},
url = {http://www.ncbi.nlm.nih.gov/pubmed/23123682},
volume = {82},
year = {2013}
}
@article{Meskaldji2013,
abstract = {Brain connectivity can be represented by a network that enables the comparison of the different patterns of structural and functional connectivity among individuals. In the literature, two levels of statistical analysis have been considered in comparing brain connectivity across groups and subjects: 1) the global comparison where a single measure that summarizes the information of each brain is used in a statistical test; 2) the local analysis where a single test is performed either for each node/connection which implies a multiplicity correction, or for each group of nodes/connections where each subset is summarized by one single test in order to reduce the number of tests to avoid a penalizing multiplicity correction. We comment on the different levels of analysis and present some methods that have been proposed at each scale. We highlight as well the possible factors that could influence the statistical results and the questions that have to be addressed in such an analysis.},
author = {Meskaldji, Djalel Eddine and Fischi-Gomez, Elda and Griffa, Alessandra and Hagmann, Patric and Morgenthaler, Stephan and Thiran, Jean-Philippe},
doi = {10.1016/j.neuroimage.2013.04.084},
file = {:home/rtungaraza/.local/share/data/Mendeley Ltd./Mendeley Desktop/Downloaded/Meskaldji et al. - 2013 - Comparing connectomes across subjects and populations at different scales.pdf:pdf},
issn = {1095-9572},
journal = {NeuroImage},
keywords = {Animals,Brain,Brain: physiology,Connectome,Connectome: methods,Data Interpretation, Statistical,Humans,Models, Anatomic,Models, Neurological,Models, Statistical,Nerve Net,Nerve Net: physiology},
month = oct,
pages = {416--25},
pmid = {23631992},
publisher = {Elsevier Inc.},
title = {{Comparing connectomes across subjects and populations at different scales.}},
url = {http://www.ncbi.nlm.nih.gov/pubmed/23631992},
volume = {80},
year = {2013}
}
@article{Milham2012,
abstract = {The neuroimaging community is at a crossroads. Long characterized by individualism, the data and computational and analytic needs of the connectome-wide association era necessitate cultural reform. Emerging initiatives have demonstrated the feasibility and utility of adopting an open neuroscience model to accelerate the pace and success of scientific discovery.},
author = {Milham, Michael Peter},
doi = {10.1016/j.neuron.2011.11.004},
file = {:home/rtungaraza/.local/share/data/Mendeley Ltd./Mendeley Desktop/Downloaded/Milham - 2012 - Open neuroscience solutions for the connectome-wide association era.pdf:pdf},
issn = {1097-4199},
journal = {Neuron},
keywords = {Interdisciplinary Communication,Neurosciences,Software},
month = jan,
number = {2},
pages = {214--8},
pmid = {22284177},
title = {{Open neuroscience solutions for the connectome-wide association era.}},
url = {http://www.sciencedirect.com/science/article/pii/S0896627311010038},
volume = {73},
year = {2012}
}
@article{Richiardi2013,
author = {Richiardi, Jonas and Achard, Sophie and Bunke, Horst and Ville, Dimitri Van De},
file = {:home/rtungaraza/.local/share/data/Mendeley Ltd./Mendeley Desktop/Downloaded/Richiardi et al. - 2013 - Machine Learning with Brain Graphs.pdf:pdf},
number = {April},
pages = {58--70},
title = {{Machine Learning with Brain Graphs}},
year = {2013}
}
@article{Richiardi2011,
abstract = {Functional connectivity analysis of fMRI data can reveal synchronised activity between anatomically distinct brain regions. Here, we extract the characteristic connectivity signatures of different brain states to perform classification, allowing us to decode the different states based on the functional connectivity patterns. Our approach is based on polythetic decision trees, which combine powerful discriminative ability with interpretability of results. We also propose to use ensemble of classifiers within specific frequency subbands, and show that they bring systematic improvement in classification accuracy. Exploiting multi-band classification of connectivity graphs is also proposed, and we explain theoretical reasons why the technique could bring further improvement in classification performance. The choice of decision trees as classifier is shown to provide a practical way to identify a subset of connections that distinguishes best between the conditions, permitting the extraction of very compact representations for differences between brain states, which we call discriminative graphs. Our experimental results based on strict train/test separation at all stages of processing show that the method is applicable to inter-subject brain decoding with relatively low error rates for the task considered.},
author = {Richiardi, Jonas and Eryilmaz, Hamdi and Schwartz, Sophie and Vuilleumier, Patrik and {Van De Ville}, Dimitri},
doi = {10.1016/j.neuroimage.2010.05.081},
file = {:home/rtungaraza/.local/share/data/Mendeley Ltd./Mendeley Desktop/Downloaded/Richiardi et al. - 2011 - Decoding brain states from fMRI connectivity graphs.pdf:pdf},
issn = {1095-9572},
journal = {NeuroImage},
keywords = {Artificial Intelligence,Brain,Brain Mapping,Brain Mapping: methods,Brain: anatomy \& histology,Brain: physiology,Decision Trees,Humans,Image Processing, Computer-Assisted,Image Processing, Computer-Assisted: methods,Magnetic Resonance Imaging,Nerve Net,Nerve Net: anatomy \& histology,Nerve Net: physiology},
month = may,
number = {2},
pages = {616--26},
pmid = {20541019},
publisher = {Elsevier Inc.},
title = {{Decoding brain states from fMRI connectivity graphs.}},
url = {http://www.ncbi.nlm.nih.gov/pubmed/20541019},
volume = {56},
year = {2011}
}
@book{Riesen2010,
address = {Singapore},
author = {Riesen, Kaspar and Bunke, Horst},
publisher = {World Scientific},
title = {{Graph Classification and Clustering based on Vector space embedding}},
year = {2010}
}
@article{Rubinov2010,
abstract = {Brain connectivity datasets comprise networks of brain regions connected by anatomical tracts or by functional associations. Complex network analysis-a new multidisciplinary approach to the study of complex systems-aims to characterize these brain networks with a small number of neurobiologically meaningful and easily computable measures. In this article, we discuss construction of brain networks from connectivity data and describe the most commonly used network measures of structural and functional connectivity. We describe measures that variously detect functional integration and segregation, quantify centrality of individual brain regions or pathways, characterize patterns of local anatomical circuitry, and test resilience of networks to insult. We discuss the issues surrounding comparison of structural and functional network connectivity, as well as comparison of networks across subjects. Finally, we describe a Matlab toolbox (http://www.brain-connectivity-toolbox.net) accompanying this article and containing a collection of complex network measures and large-scale neuroanatomical connectivity datasets.},
author = {Rubinov, Mikail and Sporns, Olaf},
doi = {10.1016/j.neuroimage.2009.10.003},
file = {:home/rtungaraza/.local/share/data/Mendeley Ltd./Mendeley Desktop/Downloaded/Rubinov, Sporns - 2010 - Complex network measures of brain connectivity uses and interpretations.pdf:pdf},
issn = {1095-9572},
journal = {NeuroImage},
keywords = {Brain,Brain: physiology,Models, Neurological,Nerve Net,Nerve Net: physiology,Neural Networks (Computer)},
month = sep,
number = {3},
pages = {1059--69},
pmid = {19819337},
publisher = {Elsevier Inc.},
title = {{Complex network measures of brain connectivity: uses and interpretations.}},
url = {http://www.ncbi.nlm.nih.gov/pubmed/19819337},
volume = {52},
year = {2010}
}
@article{Smith1999,
abstract = {Low frequency drift (0.0-0.015 Hz) has often been reported in time series fMRI data. This drift has often been attributed to physiological noise or subject motion, but no studies have been done to test this assumption. Time series T*2-weighted volumes were acquired on two clinical 1.5 T MRI systems using spiral and EPI readout gradients from cadavers, a normal volunteer, and nonhomogeneous and homogeneous phantoms. The data were tested for significant differences (P = 0.001) from Gaussian noise in the frequency range 0.0-0.015 Hz. The percentage of voxels that were significant in data from the cadaver, normal volunteer, nonhomogeneous and homogeneous phantoms were 13.7-49.0\%, 22.1-61.9\%, 46.4-68.0\%, and 1.10\%, respectively. Low frequency drift was more pronounced in regions with high spatial intensity gradients. Significant drifting was present in data acquired from cadavers and nonhomogeneous phantoms and all pulse sequences tested, implying that scanner instabilities and not motion or physiological noise may be the major cause of the drift.},
author = {Smith, a M and Lewis, B K and Ruttimann, U E and Ye, F Q and Sinnwell, T M and Yang, Y and Duyn, J H and Frank, J a},
doi = {10.1006/nimg.1999.0435},
file = {:home/rtungaraza/PapersBooks/driftfmrisignalSmith1999.pdf:pdf},
issn = {1053-8119},
journal = {NeuroImage},
keywords = {Adult,Aged,Artifacts,Cadaver,Case-Control Studies,Humans,Magnetic Resonance Imaging,Magnetic Resonance Imaging: methods,Male,Middle Aged,Motion,Normal Distribution,Phantoms, Imaging},
month = may,
number = {5},
pages = {526--33},
pmid = {10329292},
title = {{Investigation of low frequency drift in fMRI signal.}},
url = {http://www.ncbi.nlm.nih.gov/pubmed/10329292},
volume = {9},
year = {1999}
}
@article{Sotiropoulos2013,
abstract = {The Human Connectome Project (HCP) is a collaborative 5-year effort to map human brain connections and their variability in healthy adults. A consortium of HCP investigators will study a population of 1200 healthy adults using multiple imaging modalities, along with extensive behavioral and genetic data. In this overview, we focus on diffusion MRI (dMRI) and the structural connectivity aspect of the project. We present recent advances in acquisition and processing that allow us to obtain very high-quality in-vivo MRI data, whilst enabling scanning of a very large number of subjects. These advances result from 2 years of intensive efforts in optimising many aspects of data acquisition and processing during the piloting phase of the project. The data quality and methods described here are representative of the datasets and processing pipelines that will be made freely available to the community at quarterly intervals, beginning in 2013.},
author = {Sotiropoulos, Stamatios N and Jbabdi, Saad and Xu, Junqian and Andersson, Jesper L and Moeller, Steen and Auerbach, Edward J and Glasser, Matthew F and Hernandez, Moises and Sapiro, Guillermo and Jenkinson, Mark and Feinberg, David a and Yacoub, Essa and Lenglet, Christophe and {Van Essen}, David C and Ugurbil, Kamil and Behrens, Timothy E J},
doi = {10.1016/j.neuroimage.2013.05.057},
file = {:home/rtungaraza/.local/share/data/Mendeley Ltd./Mendeley Desktop/Downloaded/Sotiropoulos et al. - 2013 - Advances in diffusion MRI acquisition and processing in the Human Connectome Project.pdf:pdf},
issn = {1095-9572},
journal = {NeuroImage},
keywords = {Brain,Brain: anatomy \& histology,Brain: physiology,Connectome,Connectome: trends,Diffusion Tensor Imaging,Diffusion Tensor Imaging: trends,Humans,Models, Anatomic,Models, Neurological,Nerve Net,Nerve Net: anatomy \& histology,Nerve Net: physiology},
month = oct,
pages = {125--43},
pmid = {23702418},
publisher = {Elsevier Inc.},
title = {{Advances in diffusion MRI acquisition and processing in the Human Connectome Project.}},
url = {http://www.ncbi.nlm.nih.gov/pubmed/23702418},
volume = {80},
year = {2013}
}
@article{Sporns2013,
abstract = {The human connectome refers to a map of the brain's structural connections, rendered as a connection matrix or network. This article attempts to trace some of the historical origins of the connectome, in the process clarifying its definition and scope, as well as its putative role in illuminating brain function. Current efforts to map the connectome face a number of significant challenges, including the issue of capturing network connectivity across multiple spatial scales, accounting for individual variability and structural plasticity, as well as clarifying the role of the connectome in shaping brain dynamics. Throughout, the article argues that these challenges require the development of new approaches for the statistical analysis and computational modeling of brain network data, and greater collaboration across disciplinary boundaries, especially with researchers in complex systems and network science.},
author = {Sporns, Olaf},
doi = {10.1016/j.neuroimage.2013.03.023},
file = {:home/rtungaraza/.local/share/data/Mendeley Ltd./Mendeley Desktop/Downloaded/Sporns - 2013 - The human connectome origins and challenges.pdf:pdf},
issn = {1095-9572},
journal = {NeuroImage},
keywords = {Brain,Brain: anatomy \& histology,Brain: physiology,Connectome,Connectome: methods,Humans,Models, Anatomic,Models, Neurological,Nerve Net,Nerve Net: anatomy \& histology,Nerve Net: physiology},
month = oct,
pages = {53--61},
pmid = {23528922},
publisher = {Elsevier Inc.},
title = {{The human connectome: origins and challenges.}},
url = {http://www.ncbi.nlm.nih.gov/pubmed/23528922},
volume = {80},
year = {2013}
}
@article{Sporns2005,
abstract = {The connection matrix of the human brain (the human "connectome") represents an indispensable foundation for basic and applied neurobiological research. However, the network of anatomical connections linking the neuronal elements of the human brain is still largely unknown. While some databases or collations of large-scale anatomical connection patterns exist for other mammalian species, there is currently no connection matrix of the human brain, nor is there a coordinated research effort to collect, archive, and disseminate this important information. We propose a research strategy to achieve this goal, and discuss its potential impact.},
author = {Sporns, Olaf and Tononi, Giulio and K\"{o}tter, Rolf},
doi = {10.1371/journal.pcbi.0010042},
file = {:home/rtungaraza/.local/share/data/Mendeley Ltd./Mendeley Desktop/Downloaded/Sporns, Tononi, K\"{o}tter - 2005 - The human connectome A structural description of the human brain.pdf:pdf},
issn = {1553-7358},
journal = {PLoS computational biology},
keywords = {Animals,Brain,Brain: anatomy \& histology,Brain: cytology,Brain: metabolism,Humans,Nerve Net,Neurons,Neurons: metabolism,Synapses,Synapses: metabolism},
month = sep,
number = {4},
pages = {e42},
pmid = {16201007},
title = {{The human connectome: A structural description of the human brain.}},
url = {http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=1239902\&tool=pmcentrez\&rendertype=abstract},
volume = {1},
year = {2005}
}
@article{VanEssen2012,
abstract = {The opportunity to explore the human connectome using cutting-edge neuroimaging methods has elicited widespread interest. How far will the field be able to progress in deciphering long-distance connectivity patterns and in relating differences in connectivity to phenotypic characteristics in health and disease? We discuss the daunting nature of this challenge in relation to specific complexities of brain circuitry and known limitations of in vivo imaging methods. We also discuss the excellent prospects for continuing improvements in data acquisition and analysis. Accordingly, we are optimistic that major insights will emerge from human connectomics in the coming decade.},
author = {{Van Essen}, D C and Ugurbil, K},
doi = {10.1016/j.neuroimage.2012.01.032},
file = {:home/rtungaraza/.local/share/data/Mendeley Ltd./Mendeley Desktop/Downloaded/Van Essen, Ugurbil - 2012 - The future of the human connectome.pdf:pdf},
issn = {1095-9572},
journal = {NeuroImage},
keywords = {Animals,Brain,Brain Mapping,Brain Mapping: methods,Brain Mapping: trends,Brain: physiology,History, 20th Century,History, 21st Century,Humans,Image Processing, Computer-Assisted,Image Processing, Computer-Assisted: history,Image Processing, Computer-Assisted: methods,Image Processing, Computer-Assisted: trends,Nerve Net,Nerve Net: physiology,Neuroimaging,Neuroimaging: history,Neuroimaging: methods,Neuroimaging: trends},
month = aug,
number = {2},
pages = {1299--310},
pmid = {22245355},
title = {{The future of the human connectome.}},
url = {http://www.sciencedirect.com/science/article/pii/S1053811912000493},
volume = {62},
year = {2012}
}
@article{VanHorn2013,
abstract = {Neuroimaging and the discipline of cognitive neuroscience have grown together in lock-step with each pushing the other toward an improved ability to explore and examine brain function and form. However successful neuroimaging and the examination of cognitive processes may seem today, the culture of data sharing in these fields remains underdeveloped. In this article, we discuss our own experience in the development of the fMRI Data Center (fMRIDC) - a large-scale effort to gather, curate, and openly share the complete data sets from published research articles of brain activation studies using fMRI. We outline the fMRIDC effort's beginnings, how it operated, note some of the sociological reactions we received, and provide several examples of prominent new studies performed using data drawn from the archive. Finally, we provide comment on what considerations are needed for successful neuroimaging databasing and data sharing as existing and emerging efforts take the next steps in archiving and disseminating the field's valuable and irreplaceable data.},
author = {{Van Horn}, John Darrell and Gazzaniga, Michael S},
doi = {10.1016/j.neuroimage.2012.11.010},
file = {:home/rtungaraza/.local/share/data/Mendeley Ltd./Mendeley Desktop/Downloaded/Van Horn, Gazzaniga - 2013 - Why share data Lessons learned from the fMRIDC.pdf:pdf},
issn = {1095-9572},
journal = {NeuroImage},
keywords = {Databases as Topic,Databases as Topic: organization \& administration,Humans,Information Dissemination,Magnetic Resonance Imaging},
month = nov,
pages = {677--82},
pmid = {23160115},
title = {{Why share data? Lessons learned from the fMRIDC.}},
url = {http://www.sciencedirect.com/science/article/pii/S1053811912011068},
volume = {82},
year = {2013}
}
@article{Varoquaux2013,
author = {Varoquaux, Ga\"{e}l and Craddock, R. Cameron},
doi = {10.1016/j.neuroimage.2013.04.007},
file = {:home/rtungaraza/.local/share/data/Mendeley Ltd./Mendeley Desktop/Downloaded/Varoquaux, Craddock - 2013 - Learning and comparing functional connectomes across subjects.pdf:pdf},
issn = {10538119},
journal = {NeuroImage},
keywords = {Connectome,Effective connectivity,Group study,Resting-state,fMRI,functional connectivity},
month = oct,
pages = {405--415},
publisher = {Elsevier Inc.},
title = {{Learning and comparing functional connectomes across subjects}},
url = {http://linkinghub.elsevier.com/retrieve/pii/S1053811913003340},
volume = {80},
year = {2013}
}
@article{Vogelstein2013,
author = {J. T. Vogelstein and W. G. Roncal and R. J. Vogelstein and C. E. Priebe},
title = {Graph Classification Using Signal-Subgraphs: Applications in Statistical Connectomics},
journal ={IEEE Transactions on Pattern Analysis and Machine Intelligence},
volume = {35},
number = {7},
issn = {0162-8828},
year = {2013},
pages = {1539-1551},
doi = {http://doi.ieeecomputersociety.org/10.1109/TPAMI.2012.235},
publisher = {IEEE Computer Society},
address = {Los Alamitos, CA, USA},
}
@article{Zalesky2012,
abstract = {The scenario considered here is one where brain connectivity is represented as a network and an experimenter wishes to assess the evidence for an experimental effect at each of the typically thousands of connections comprising the network. To do this, a univariate model is independently fitted to each connection. It would be unwise to declare significance based on an uncorrected threshold of $\alpha$=0.05, since the expected number of false positives for a network comprising N=90 nodes and N(N-1)/2=4005 connections would be 200. Control of Type I errors over all connections is therefore necessary. The network-based statistic (NBS) and spatial pairwise clustering (SPC) are two distinct methods that have been used to control family-wise errors when assessing the evidence for an experimental effect with mass univariate testing. The basic principle of the NBS and SPC is the same as supra-threshold voxel clustering. Unlike voxel clustering, where the definition of a voxel cluster is unambiguous, 'clusters' formed among supra-threshold connections can be defined in different ways. The NBS defines clusters using the graph theoretical concept of connected components. SPC on the other hand uses a more stringent pairwise clustering concept. The purpose of this article is to compare the pros and cons of the NBS and SPC, provide some guidelines on their practical use and demonstrate their utility using a case study involving neuroimaging data.},
author = {Zalesky, Andrew and Cocchi, Luca and Fornito, Alex and Murray, Micah M and Bullmore, Ed},
doi = {10.1016/j.neuroimage.2012.01.068},
file = {:home/rtungaraza/.local/share/data/Mendeley Ltd./Mendeley Desktop/Downloaded/Zalesky et al. - 2012 - Connectivity differences in brain networks.pdf:pdf},
issn = {1095-9572},
journal = {NeuroImage},
keywords = {Brain connectivity,Brain network,Connectome,Family-wise errors,Network-based statistic,Spatial pairwise clustering},
month = jan,
number = {2},
pages = {1055--1062},
pmid = {22273567},
publisher = {Elsevier Inc.},
title = {{Connectivity differences in brain networks.}},
url = {http://www.ncbi.nlm.nih.gov/pubmed/22273567},
volume = {60},
year = {2012}
}
@article{DagliMSIngeholmJE1999,
author = {{Dagli MS, Ingeholm JE}, and Haxby JV},
journal = {NeuroImage},
pages = {407--415},
title = {{Localization of cardiac-in- duced signal change in fMRI}},
volume = {9},
year = {1999}
}
@article{Eloyan2014,
abstract = {Functional magnetic resonance imaging (fMRI) is a thriving field that plays an important role in medical imaging analysis, biological and neuroscience research and practice. This manuscript gives a didactic introduction to the statistical analysis of fMRI data using the R project, along with the relevant R code. The goal is to give statisticians who would like to pursue research in this area a quick tutorial for programming with fMRI data. References of relevant packages and papers are provided for those interested in more advanced analysis.},
author = {Eloyan, Ani and Li, Shanshan and Muschelli, John and Pekar, Jim J and Mostofsky, Stewart H and Caffo, Brian S},
doi = {10.1371/journal.pone.0089470},
file = {:home/rtungaraza/PapersBooks/caffoFMRIpaper.pdf:pdf},
issn = {1932-6203},
journal = {PloS one},
month = jan,
number = {2},
pages = {e89470},
pmid = {24586801},
title = {{Analytic programming with FMRI data: a quick-start guide for statisticians using R.}},
url = {http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=3938835\&tool=pmcentrez\&rendertype=abstract},
volume = {9},
year = {2014}
}
@article{Fornito2014,
abstract = {In recent years, pathophysiological models of brain disorders have shifted from an emphasis on understanding pathology in specific brain regions to characterizing disturbances of interconnected neural systems. This shift has paralleled rapid advances in connectomics, a field concerned with comprehensively mapping the neural elements and inter-connections that constitute the brain. Magnetic resonance imaging (MRI) has played a central role in these efforts, as it allows relatively cost-effective in vivo assessment of the macro-scale architecture of brain network connectivity. In this paper, we provide a brief introduction to some of the basic concepts in the field and review how recent developments in imaging connectomics are yielding new insights into brain disease, with a particular focus on Alzheimer's disease and schizophrenia. Specifically, we consider how research into circuit-level, connectome-wide and topological changes is stimulating the development of new aetiopathological theories and biomarkers with potential for clinical translation. The findings highlight the advantage of conceptualizing brain disease as a result of disturbances in an interconnected complex system, rather than discrete pathology in isolated sub-sets of brain regions.},
author = {Fornito, Alex and Bullmore, Edward T},
doi = {10.1016/j.euroneuro.2014.02.011},
file = {:home/rtungaraza/.local/share/data/Mendeley Ltd./Mendeley Desktop/Downloaded/Fornito, Bullmore - 2014 - Connectomics A new paradigm for understanding brain disease.pdf:pdf},
issn = {1873-7862},
journal = {European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology},
month = mar,
pmid = {24726580},
title = {{Connectomics: A new paradigm for understanding brain disease.}},
url = {http://www.ncbi.nlm.nih.gov/pubmed/24726580},
year = {2014}
}
@article{Lee2013,
abstract = {SUMMARY: Resting-state fMRI measures spontaneous low-frequency fluctuations in the BOLD signal to investigate the functional architecture of the brain. Application of this technique has allowed the identification of various RSNs, or spatially distinct areas of the brain that demonstrate synchronous BOLD fluctuations at rest. Various methods exist for analyzing resting-state data, including seed-based approaches, independent component analysis, graph methods, clustering algorithms, neural networks, and pattern classifiers. Clinical applications of resting-state fMRI are at an early stage of development. However, its use in presurgical planning for patients with brain tumor and epilepsy demonstrates early promise, and the technique may have a future role in providing diagnostic and prognostic information for neurologic and psychiatric diseases.},
author = {Lee, M H and Smyser, C D and Shimony, J S},
doi = {10.3174/ajnr.A3263},
file = {:home/rtungaraza/PapersBooks/1866.full.pdf:pdf},
issn = {1936-959X},
journal = {AJNR. American journal of neuroradiology},
keywords = {Algorithms,Brain,Brain Mapping,Brain Mapping: methods,Brain: physiology,Humans,Magnetic Resonance Imaging,Magnetic Resonance Imaging: methods,Preoperative Care,Preoperative Care: methods,Rest,Rest: physiology},
month = oct,
number = {10},
pages = {1866--72},
pmid = {22936095},
title = {{Resting-state fMRI: a review of methods and clinical applications.}},
url = {http://www.ncbi.nlm.nih.gov/pubmed/22936095},
volume = {34},
year = {2013}
}
@article{Sporns2013,
abstract = {The human connectome refers to a map of the brain's structural connections, rendered as a connection matrix or network. This article attempts to trace some of the historical origins of the connectome, in the process clarifying its definition and scope, as well as its putative role in illuminating brain function. Current efforts to map the connectome face a number of significant challenges, including the issue of capturing network connectivity across multiple spatial scales, accounting for individual variability and structural plasticity, as well as clarifying the role of the connectome in shaping brain dynamics. Throughout, the article argues that these challenges require the development of new approaches for the statistical analysis and computational modeling of brain network data, and greater collaboration across disciplinary boundaries, especially with researchers in complex systems and network science.},
author = {Sporns, Olaf},
doi = {10.1016/j.neuroimage.2013.03.023},
file = {:home/rtungaraza/.local/share/data/Mendeley Ltd./Mendeley Desktop/Downloaded/Sporns - 2013 - The human connectome origins and challenges.pdf:pdf},
issn = {1095-9572},
journal = {NeuroImage},
keywords = {Brain,Brain: anatomy \& histology,Brain: physiology,Connectome,Connectome: methods,Humans,Models, Anatomic,Models, Neurological,Nerve Net,Nerve Net: anatomy \& histology,Nerve Net: physiology},
month = oct,
pages = {53--61},
pmid = {23528922},
publisher = {Elsevier Inc.},
title = {{The human connectome: origins and challenges.}},
url = {http://www.ncbi.nlm.nih.gov/pubmed/23528922},
volume = {80},
year = {2013}
}
Buckner, Randy L.; Roffman, Joshua L. ; Smoller, Jordan W. , 2014, "Brain Genomics Superstruct Project (GSP)", <a href="http://dx.doi.org/10.7910/DVN/25833">doi:10.7910/DVN/25833</a> Harvard Dataverse Network [Distributor] V9 [Version]
@ELECTRONIC{BucknerGSP2014,
author = {Randy L. Buckner and Joshua L. Roffman and Jordan W. Smoller},
year = {2014},
title = {{B}rain {G}enomics {S}uperstruct {P}roject {(GSP)}},
language = {English},
howpublished = {\url=http://dx.doi.org/10.7910/DVN/25833},
doi = {10.7910/DVN/25833}
}
@misc{NDAR,
author = {{NIMH}},
title = {{N}ational {D}atabase for {A}utism {R}esearch {(NDAR)}},
language = {English},
url = {http://ndar.nih.gov},
note = {Accessed 12 13 2014}
}
@misc{JerniganPING,
author = {Terry L. Jernigan and Connor McCabe and Linda Chang and Natacha Akshoomoff and Erik Newman and Anders M. Dale and Thomas Ernst and Peter Van Zijl and Joshua Kuperman and Sarah Murray and Cinnamon Bloss and Nicholas J. Schork and Mark Appelbaum and Anthony Gamst and Wesley Thompson and Hauke Bartsch and Brian Keating and David Amaral and Elizabeth Sowell and Walter Kaufmann and Peter Van Zijl and Stewart Mostofsky and B.J. Casey and Erika J. Ruberry and Alisa Powers and Bruce Rosen and Tal Kenet and Jean Frazier and M.D. and David Kennedy and Jeffrey Gruen},
title = {{P}ediatric {I}maging, {N}eurocognition, and {G}enetics {(PING)} Study},
language = {English},
url = {http://pingstudy.ucsd.edu},
note = {Accessed 12 13 2014}
}
@INPROCEEDINGS{RosenHCP2010,
author = {Bruce Rosen and Van J. Wedeen and John D. Van Horn and Bruce Fischl and Randy L. Buckner and Lawrence Wald and Matti Hamalainen and Steven Stufflebeam and Joshua Roffman and David W. Shattuck and Thompson PM and Roger P. Woods and Nelson Freimer and Robert Bilder and and Arthur W. Toga},
title = {The {H}uman {C}onnectome {P}roject},
booktitle = {Proceedings Organization for Human Brain Mapping 16th Annual Meeting},
year = {2010},
address = {Barcelona},
owner = {Richard Craddock},
}
@Article{Satterthwaite2014,
Author="Satterthwaite, T. D. and Elliott, M. A. and Ruparel, K. and Loughead, J. and Prabhakaran, K. and Calkins, M. E. and Hopson, R. and Jackson, C. and Keefe, J. and Riley, M. and Mentch, F. D. and Sleiman, P. and Verma, R. and Davatzikos, C. and Hakonarson, H. and Gur, R. C. and Gur, R. E. ",
Title="{{N}euroimaging of the {P}hiladelphia neurodevelopmental cohort}",
Journal="Neuroimage",
Year="2014",
Volume="86",
Pages="544--553",
Month="Feb",
Note={[PubMed Central:\href{http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3947233}{PMC3947233}] [DOI:\href{http://dx.doi.org/10.1016/j.neuroimage.2013.07.064}{10.1016/j.neuroimage.2013.07.064}] [PubMed:\href{http://www.ncbi.nlm.nih.gov/pubmed/23921101}{23921101}] }
}
@Article{Varela2001,
Author="Varela, F. and Lachaux, J. P. and Rodriguez, E. and Martinerie, J. ",
Title="{{T}he brainweb: phase synchronization and large-scale integration}",
Journal="Nat. Rev. Neurosci.",
Year="2001",
Volume="2",
Number="4",
Pages="229--239",
Month="Apr",
Note={[DOI:\href{http://dx.doi.org/10.1038/35067550}{10.1038/35067550}] [PubMed:\href{http://www.ncbi.nlm.nih.gov/pubmed/11283746}{11283746}] }
}
% 21908183
@Article{Behrens2012,
Author="Behrens, T. E. and Sporns, O. ",
Title="{{H}uman connectomics}",
Journal="Curr. Opin. Neurobiol.",
Year="2012",
Volume="22",
Number="1",
Pages="144--153",
Month="Feb",
Note={[PubMed Central:\href{http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3294015}{PMC3294015}] [DOI:\href{http://dx.doi.org/10.1016/j.conb.2011.08.005}{10.1016/j.conb.2011.08.005}] [PubMed:\href{http://www.ncbi.nlm.nih.gov/pubmed/21908183}{21908183}] }
}
@Article{Kapur2012,
Author="Kapur, S. and Phillips, A. G. and Insel, T. R. ",
Title="{{W}hy has it taken so long for biological psychiatry to develop clinical tests and what to do about it?}",
Journal="Mol. Psychiatry",
Year="2012",
Volume="17",
Number="12",
Pages="1174--1179",
Month="Dec",
Note={[DOI:\href{http://dx.doi.org/10.1038/mp.2012.105}{10.1038/mp.2012.105}] [PubMed:\href{http://www.ncbi.nlm.nih.gov/pubmed/22869033}{22869033}] }
}
@Article{Biswal1995,
Author="Biswal, B. and Yetkin, F. Z. and Haughton, V. M. and Hyde, J. S. ",
Title="{{F}unctional connectivity in the motor cortex of resting human brain using echo-planar {M}{R}{I}}",
Journal="Magn Reson Med",
Year="1995",
Volume="34",
Number="4",
Pages="537--541",
Month="Oct",
Note={[PubMed:\href{http://www.ncbi.nlm.nih.gov/pubmed/8524021}{8524021}] }
}
@Article{Kelly2012,
Author="Kelly, C. and Biswal, B. B. and Craddock, R. C. and Castellanos, F. X. and Milham, M. P. ",
Title="{{C}haracterizing variation in the functional connectome: promise and pitfalls}",
Journal="Trends Cogn. Sci. (Regul. Ed.)",
Year="2012",
Volume="16",
Number="3",
Pages="181--188",
Month="Mar",
Note={[PubMed Central:\href{http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3882689}{PMC3882689}] [DOI:\href{http://dx.doi.org/10.1016/j.tics.2012.02.001}{10.1016/j.tics.2012.02.001}] [PubMed:\href{http://www.ncbi.nlm.nih.gov/pubmed/22341211}{22341211}] }
}
% 23523803
@Article{Blumensath2013,
Author="Blumensath, T. and Jbabdi, S. and Glasser, M. F. and Van Essen, D. C. and Ugurbil, K. and Behrens, T. E. and Smith, S. M. ",
Title="{{S}patially constrained hierarchical parcellation of the brain with resting-state f{M}{R}{I}}",
Journal="Neuroimage",
Year="2013",
Volume="76",
Pages="313--324",
Month="Aug",
Note={[PubMed Central:\href{http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3758955}{PMC3758955}] [DOI:\href{http://dx.doi.org/10.1016/j.neuroimage.2013.03.024}{10.1016/j.neuroimage.2013.03.024}] [PubMed:\href{http://www.ncbi.nlm.nih.gov/pubmed/23523803}{23523803}] }
}
@Article{Bellec2006,
Author="Bellec, P. and Perlbarg, V. and Jbabdi, S. and Pelegrini-Issac, M. and Anton, J. L. and Doyon, J. and Benali, H. ",
Title="{{I}dentification of large-scale networks in the brain using f{M}{R}{I}}",
Journal="Neuroimage",
Year="2006",
Volume="29",
Number="4",
Pages="1231--1243",
Month="Feb",
Note={[DOI:\href{http://dx.doi.org/10.1016/j.neuroimage.2005.08.044}{10.1016/j.neuroimage.2005.08.044}] [PubMed:\href{http://www.ncbi.nlm.nih.gov/pubmed/16246590}{16246590}] }
}
@Article{Thirion2006,
Author="Thirion, B. and Flandin, G. and Pinel, P. and Roche, A. and Ciuciu, P. and Poline, J. B. ",
Title="{{D}ealing with the shortcomings of spatial normalization: multi-subject parcellation of f{M}{R}{I} datasets}",
Journal="Hum Brain Mapp",
Year="2006",
Volume="27",
Number="8",
Pages="678--693",
Month="Aug",
Note={[DOI:\href{http://dx.doi.org/10.1002/hbm.20210}{10.1002/hbm.20210}] [PubMed:\href{http://www.ncbi.nlm.nih.gov/pubmed/16281292}{16281292}] }
}
@Article{Zalesky2010,
Author="Zalesky, A. and Fornito, A. and Harding, I. H. and Cocchi, L. and Yucel, M. and Pantelis, C. and Bullmore, E. T. ",
Title="{{W}hole-brain anatomical networks: does the choice of nodes matter?}",
Journal="Neuroimage",
Year="2010",
Volume="50",
Number="3",
Pages="970--983",
Month="Apr",
Note={[DOI:\href{http://dx.doi.org/10.1016/j.neuroimage.2009.12.027}{10.1016/j.neuroimage.2009.12.027}] [PubMed:\href{http://www.ncbi.nlm.nih.gov/pubmed/20035887}{20035887}] }
}
@INPROCEEDINGS{Flandin2002,
author={Flandin, G. and Kherif, F. and Pennec, X. and Riviere, D. and Ayache, N. and Poline, J.-B.},
booktitle={Biomedical Imaging, 2002. Proceedings. 2002 IEEE International Symposium on},
title={Parcellation of brain images with anatomical and functional constraints for fMRI data analysis},
year={2002},
month={},
pages={907-910},
keywords={biomedical MRI;brain;differential geometry;image resolution;image segmentation;medical image processing;3D cortex;K-means clustering adaptation;adjustable resolution;anatomical constraints;automatic parcellation;brain image parcellation;connectivity studies;fMRI data analysis;functional constraints;geodesic distances;intermediate dimensionality;modality fusion;multivariate analyses;nonconvex domain;region of interest;voxel;weighted geodesic distances;Anatomy;Brain;Clustering algorithms;Data analysis;Image analysis;Image resolution;Magnetic analysis;Signal resolution;Spatial resolution;Testing},
doi={10.1109/ISBI.2002.1029408},}
@Article{Thirion2014,
Author="Thirion, B. and Varoquaux, G. and Dohmatob, E. and Poline, J. B. ",
Title="{{W}hich f{M}{R}{I} clustering gives good brain parcellations?}",
Journal="Front Neurosci",
Year="2014",
Volume="8",
Pages="167",
Note={[PubMed Central:\href{http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4076743}{PMC4076743}] [DOI:\href{http://dx.doi.org/10.3389/fnins.2014.00167}{10.3389/fnins.2014.00167}] [PubMed:\href{http://www.ncbi.nlm.nih.gov/pubmed/25071425}{25071425}] }
}
@article{Desikan2006,
title = "An automated labeling system for subdividing the human cerebral cortex on \{MRI\} scans into gyral based regions of interest ",
journal = "NeuroImage ",
volume = "31",
number = "3",
pages = "968 - 980",
year = "2006",
note = "",
issn = "1053-8119",
doi = "http://dx.doi.org/10.1016/j.neuroimage.2006.01.021",
url = "http://www.sciencedirect.com/science/article/pii/S1053811906000437",
author = "Rahul S. Desikan and Florent Ségonne and Bruce Fischl and Brian T. Quinn and Bradford C. Dickerson and Deborah Blacker and Randy L. Buckner and Anders M. Dale and R. Paul Maguire and Bradley T. Hyman and Marilyn S. Albert and Ronald J. Killiany"
}
@ARTICLE{Klein2012,
AUTHOR={Klein, Arno and Tourville, Jason},
TITLE={101 labeled brain images and a consistent human cortical labeling protocol},
JOURNAL={Frontiers in Neuroscience},
VOLUME={6},
YEAR={2012},
NUMBER={171},
URL={http://www.frontiersin.org/brain_imaging_methods/10.3389/fnins.2012.00171/abstract},
DOI={10.3389/fnins.2012.00171},
ISSN={1662-453X}
}
@Article{AAL2002,
Author="Tzourio-Mazoyer, N. and Landeau, B. and Papathanassiou, D. and Crivello, F. and Etard, O. and Delcroix, N. and Mazoyer, B. and Joliot, M. ",
Title="{{A}utomated anatomical labeling of activations in {S}{P}{M} using a macroscopic anatomical parcellation of the {M}{N}{I} {M}{R}{I} single-subject brain}",
Journal="Neuroimage",
Year="2002",
Volume="15",
Number="1",
Pages="273--289",
Month="Jan",
Abstract={An anatomical parcellation of the spatially normalized single-subject high-resolution T1 volume provided by the Montreal Neurological Institute (MNI) (D. L. Collins et al., 1998, Trans. Med. Imag. 17, 463-468) was performed. The MNI single-subject main sulci were first delineated and further used as landmarks for the 3D definition of 45 anatomical volumes of interest (AVOI) in each hemisphere. This procedure was performed using a dedicated software which allowed a 3D following of the sulci course on the edited brain. Regions of interest were then drawn manually with the same software every 2 mm on the axial slices of the high-resolution MNI single subject. The 90 AVOI were reconstructed and assigned a label. Using this parcellation method, three procedures to perform the automated anatomical labeling of functional studies are proposed: (1) labeling of an extremum defined by a set of coordinates, (2) percentage of voxels belonging to each of the AVOI intersected by a sphere centered by a set of coordinates, and (3) percentage of voxels belonging to each of the AVOI intersected by an activated cluster. An interface with the Statistical Parametric Mapping package (SPM, J. Ashburner and K. J. Friston, 1999, Hum. Brain Mapp. 7, 254-266) is provided as a freeware to researchers of the neuroimaging community. We believe that this tool is an improvement for the macroscopical labeling of activated area compared to labeling assessed using the Talairach atlas brain in which deformations are well known. However, this tool does not alleviate the need for more sophisticated labeling strategies based on anatomical or cytoarchitectonic probabilistic maps.}
}
@article{Eickhoff2008,
author = {Eickhoff, Simon B. and Rottschy, Claudia and Kujovic, Milenko and Palomero-Gallagher, Nicola and Zilles, Karl},
title = {Organizational Principles of Human Visual Cortex Revealed by Receptor Mapping},
volume = {18},
number = {11},
pages = {2637-2645},
year = {2008},
doi = {10.1093/cercor/bhn024},
abstract ={This receptorarchitectonic study of the human visual cortex investigated interareal differences in mean receptor concentrations and laminar distribution patterns of 16 neurotransmitter receptors in the dorsal and ventral parts of areas V1, V2, V3 as well as in adjoining areas V4 (ventrally) and V3A (dorsally). Both the functional hierarchy of these areas and a distinction between dorsal and ventral visual cortices were reflected by significant receptorarchitectonic differences. The observation that dorso-ventral differences existed in all extrastriate areas (including V2) is particularly important for the discussion about the relationship between dorsal and ventral V3 as it indicates that a receptorarchitectonic distinction between the ventral and dorsal visual cortices is present in but not specific to V3. This molecular specificity is mirrored by previously reported differences in retinal microstructure and functional differences as revealed in behavioral experiments demonstrating differential advantages for stimulus processing in the upper and lower visual fields. We argue that these anatomical and functional differences may be regarded as the result of an evolutionary optimization adapting to the processing of the most relevant stimuli occurring in the upper and lower visual fields.},
URL = {http://cercor.oxfordjournals.org/content/18/11/2637.abstract},
eprint = {http://cercor.oxfordjournals.org/content/18/11/2637.full.pdf+html},
journal = {Cerebral Cortex}
}
@Article{Smith2011,
Author="Smith, S. M. and Miller, K. L. and Salimi-Khorshidi, G. and Webster, M. and Beckmann, C. F. and Nichols, T. E. and Ramsey, J. D. and Woolrich, M. W. ",
Title="{{N}etwork modelling methods for {F}{M}{R}{I}}",
Journal="Neuroimage",
Year="2011",
Volume="54",
Number="2",
Pages="875--891",
Month="Jan",
Note={[DOI:\href{http://dx.doi.org/10.1016/j.neuroimage.2010.08.063}{10.1016/j.neuroimage.2010.08.063}] [PubMed:\href{http://www.ncbi.nlm.nih.gov/pubmed/20817103}{20817103}] }
}
@Article{Friston2011,
Author="Friston, K. J. ",
Title="{{F}unctional and effective connectivity: a review}",
Journal="Brain Connect",
Year="2011",
Volume="1",
Number="1",
Pages="13--36",
Note={[DOI:\href{http://dx.doi.org/10.1089/brain.2011.0008}{10.1089/brain.2011.0008}] [PubMed:\href{http://www.ncbi.nlm.nih.gov/pubmed/22432952}{22432952}] }
}
@Article{Friston2003,
Author="Friston, K. J. and Harrison, L. and Penny, W. ",
Title="{{D}ynamic causal modelling}",
Journal="Neuroimage",
Year="2003",
Volume="19",
Number="4",
Pages="1273--1302",
Month="Aug",
Note={[PubMed:\href{http://www.ncbi.nlm.nih.gov/pubmed/12948688}{12948688}] }
}
@article {Friston1994,
author = {Friston, Karl J.},
title = {Functional and effective connectivity in neuroimaging: A synthesis},
journal = {Human Brain Mapping},
volume = {2},
number = {1-2},
publisher = {Wiley Subscription Services, Inc., A Wiley Company},
issn = {1097-0193},
url = {http://dx.doi.org/10.1002/hbm.460020107},
doi = {10.1002/hbm.460020107},
pages = {56--78},
keywords = {functional connectivity, effective connectivity, PET, fMRI, eigenimages, spatial modes, multidimensional scaling, word generation, visual, modulation},
year = {1994},
}
@Article{Buchel1997,
Author="Buchel, C. and Friston, K. J. ",
Title="{{M}odulation of connectivity in visual pathways by attention: cortical interactions evaluated with structural equation modelling and f{M}{R}{I}}",
Journal="Cereb. Cortex",
Year="1997",
Volume="7",
Number="8",
Pages="768--778",
Month="Dec",
Note={[PubMed:\href{http://www.ncbi.nlm.nih.gov/pubmed/9408041}{9408041}] }
}
@article{Lohmann2012,
title = "Critical comments on dynamic causal modelling ",
journal = "NeuroImage ",
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