Genetic network properties of the human cortex based on regional thickness and surface area measures.

作者: Anna R. Docherty , Chelsea K. Sawyers , Matthew S. Panizzon , Michael C. Neale , Lisa T. Eyler

DOI: 10.3389/FNHUM.2015.00440

关键词: Future studiesArtificial intelligenceFuzzy clustering analysisGenetic modelingBiologyPattern recognitionBrain developmentHigh spatial resolutionGenetic covarianceGenetic networkGraph theoryData mining

摘要: We examined network properties of genetic covariance between average cortical thickness (CT) and surface area (SA) within genetically-identified parcellations that we previously derived from human maps using vertex-wise fuzzy clustering analysis with high spatial resolution. There were 24 hierarchical based on CT SA expansion/contraction; in both cases the 12 per hemisphere largely symmetrical. utilized three techniques—biometrical modeling, cluster analysis, graph theory—to examine relationships 48 parcellation measures. Biometrical modeling indicated significant shared size several parcellations. Cluster suggested small distinct groupings covariance; networks highlighted negative positive correlations bilateral Graph theoretical world, but not rich club, may characterize these regional These findings suggest exhibit short characteristic path lengths across a broad connections. This property be protective against failure. In contrast, previous research structural data has observed strong club tightly interconnected hub networks. Future studies might provide powerful phenotypes for normal pathological brain development, aging, function.

参考文章(37)
MCCL Neale, Lon R Cardon, None, Methodology for Genetic Studies of Twins and Families ,(1992)
Christian Dahmann, Andrew C. Oates, Michael Brand, Boundary formation and maintenance in tissue development Nature Reviews Genetics. ,vol. 12, pp. 43- 55 ,(2011) , 10.1038/NRG2902
C.-H. Chen, M. Fiecas, E. D. Gutierrez, M. S. Panizzon, L. T. Eyler, E. Vuoksimaa, W. K. Thompson, C. Fennema-Notestine, D. J. Hagler, T. L. Jernigan, M. C. Neale, C. E. Franz, M. J. Lyons, B. Fischl, M. T. Tsuang, A. M. Dale, W. S. Kremen, Genetic topography of brain morphology Proceedings of the National Academy of Sciences of the United States of America. ,vol. 110, pp. 17089- 17094 ,(2013) , 10.1073/PNAS.1308091110
Sophie Achard, Raymond Salvador, Brandon Whitcher, John Suckling, ED Bullmore, A Resilient, Low-Frequency, Small-World Human Brain Functional Network with Highly Connected Association Cortical Hubs The Journal of Neuroscience. ,vol. 26, pp. 63- 72 ,(2006) , 10.1523/JNEUROSCI.3874-05.2006
Ed Bullmore, Olaf Sporns, Complex brain networks: graph theoretical analysis of structural and functional systems Nature Reviews Neuroscience. ,vol. 10, pp. 186- 198 ,(2009) , 10.1038/NRN2575
Lisa T. Eyler, Eero Vuoksimaa, Matthew S. Panizzon, Christine Fennema-Notestine, Michael C. Neale, Chi-Hua Chen, Amy Jak, Carol E. Franz, Michael J. Lyons, Wesley K. Thompson, Kelly M. Spoon, Bruce Fischl, Anders M. Dale, William S. Kremen, Conceptual and Data-based Investigation of Genetic Influences and Brain Asymmetry: A Twin Study of Multiple Structural Phenotypes Journal of Cognitive Neuroscience. ,vol. 26, pp. 1100- 1117 ,(2014) , 10.1162/JOCN_A_00531
Annica Dominicus, Anders Skrondal, Håkon K. Gjessing, Nancy L. Pedersen, Juni Palmgren, Likelihood ratio tests in behavioral genetics: problems and solutions Behavior Genetics. ,vol. 36, pp. 331- 340 ,(2006) , 10.1007/S10519-005-9034-7
Bruce Fischl, David H. Salat, Evelina Busa, Marilyn Albert, Megan Dieterich, Christian Haselgrove, Andre van der Kouwe, Ron Killiany, David Kennedy, Shuna Klaveness, Albert Montillo, Nikos Makris, Bruce Rosen, Anders M. Dale, Whole Brain Segmentation Neuron. ,vol. 33, pp. 341- 355 ,(2002) , 10.1016/S0896-6273(02)00569-X
M. P. van den Heuvel, O. Sporns, Rich-Club Organization of the Human Connectome The Journal of Neuroscience. ,vol. 31, pp. 15775- 15786 ,(2011) , 10.1523/JNEUROSCI.3539-11.2011
William S. Kremen, Carol E. Franz, Michael J. Lyons, VETSA: The Vietnam Era Twin Study of Aging Twin Research and Human Genetics. ,vol. 16, pp. 399- 402 ,(2013) , 10.1017/THG.2012.86