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Imaging Genetics

  • Ge, T., Feng, J., Hibar, D. P., Thompson, P. M., & Nichols, T. E. (2012). Increasing Power for Voxel-wise Genome-wide Association Studies: The Random Field Theory, Least Square Kernel Machines and Fast Permutation Procedures. NeuroImage, 63(2), 858–873. doi:10.1016/j.neuroimage.2012.07.012
  • Stein, J. L., Medland, S. E., Vasquez, A. A., Hibar, D. P., Senstad, R. E., Winkler, A. M., Toro, R., et al. (2012). Identification of common variants associated with human hippocampal and intracranial volumes. Nature Genetics, 44, 552–561. doi:10.1038/ng.2250
  • Inkster, B., Rao, A. W., Ridler, K., Nichols, T. E., Saemann, P. G., Auer, D. P., Holsboer, F., et al. (2011). Structural brain changes in patients with recurrent major depressive disorder presenting with anxiety symptoms. Journal of neuroimaging : official journal of the American Society of Neuroimaging, 21(4), 375–82. doi:10.1111/j.1552-6569.2010.00515.x
  • Silver, M., Montana, G., & Nichols, T. E. (2010). False positives in neuroimaging genetics using voxel-based morphometry data. NeuroImage, 54(2), 992–1000. doi:10.1016/j.neuroimage.2010.08.049
  • Vounou, M., Nichols, T. E., & Montana, G. (2010). Discovering genetic associations with high-dimensional neuroimaging phenotypes: A sparse reduced-rank regression approach. NeuroImage, 53(3), 1147–59. doi:10.1016/j.neuroimage.2010.07.002
  • Inkster, B., Nichols, T. E., Saemann, P. G., Auer, D. P., Holsboer, F., Muglia, P., & Matthews, P. M. (2010). Pathway-based approaches to imaging genetics association studies: Wnt signaling, GSK3beta substrates and major depression. NeuroImage, 53(3), 908–917. doi:10.1016/j.neuroimage.2010.02.065
  • Inkster, B., Nichols, T. E., Saemann, P. G., Auer, D. P., Holsboer, F., Muglia, P., & Matthews, P. M. (2009). Association of GSK3 Polymorphisms With Brain Structural Changes in Major Depressive Disorder. Archives of general psychiatry, 66(7), 721–728. doi:10.1002/bdra.20744
  • Meyer-Lindenberg, a, Nichols, T., Callicott, J. H., Ding, J., Kolachana, B., Buckholtz, J., Mattay, V. S., et al. (2006). Impact of complex genetic variation in COMT on human brain function. Molecular psychiatry, 11(9), 867–77, 797. doi:10.1038/
  • Abecasis, G. R., Ghosh, D., & Nichols, T. E. (2005). Linkage disequilibrium: ancient history drives the new genetics. Human heredity, 59(2), 118–24. doi:10.1159/000085226
  • Filippini, N., Rao, A., Wetten, S., Gibson, R. A., Borrie, M., Guzman, D., Kertesz, A., et al. (2009). NeuroImage Anatomically-distinct genetic associations of APOE ɛ4 allele load with regional cortical atrophy in Alzheimer ’ s disease. NeuroImage, 44(3), 724–728. doi:10.1016/j.neuroimage.2008.10.003
  • Ossadtchi, A., Brown, V. M., Khan, A. H., Cherry, S. R., Nichols, T. E., Leahy, R. M., & Smith, D. J. (2002). Statistical analysis of multiplex brain gene expression datasets. Neurochemical Research, 27(10), 1113–1121.doi:10.1023/A:1020965107124


Contact Info

Room D0.03
Deptment of Statistics
University of Warwick
United Kingdom

Tel: +44(0)24 761 51086
Email: t.e.nichols 'at'
Blog: NISOx blog

[Book Cover]

Handbook of fMRI Data Analysis by Russ Poldrack, Thomas Nichols and Jeanette Mumford