G. H. Glover, B. A. Mueller, J. A. Turner, T. G. Van-erp, T. T. Liu et al., Function biomedical informatics research network recommendations for prospective multicenter functional MRI studies, Journal of Magnetic Resonance Imaging, vol.36, issue.1, pp.39-54, 2012.
DOI : 10.1002/jmri.23572

URL : https://onlinelibrary.wiley.com/doi/pdf/10.1002/jmri.23572

D. Goldman, Our genes, our choices : how genotype and gene interactions affect behavior, 2012.

R. Gollub, J. M. Shoemaker, M. King, T. White, S. Ehrlich et al., The MCIC collection: a shared repository of multimodal, multi-site brain image data from a clinical investigation of schizophrenia, Journal of NeuroInformatics, p.23760817, 2013.

I. I. Gottesman and T. D. Gould, The endophenotype concept in psychiatry: etymology and strategic intentions, The American Journal of Psychiatry, vol.160, pp.636-645, 2003.
DOI : 10.1176/appi.ajp.160.4.636

J. Hall, H. C. Whalley, D. E. Job, B. J. Baig, A. M. Mcintosh et al., A neuregulin 1 variant associated with abnormal cortical function and psychotic symptoms, Nature Neuroscience, vol.9, issue.12, pp.1477-1478, 2006.
DOI : 10.1038/nn1795

A. R. Hariri and D. R. Weinberger, Imaging genomics, British Medical Bulletin, vol.65, pp.259-270, 2003.

D. Harold, R. Abraham, P. Hollingworth, R. Sims, A. Gerrish et al., Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease, Nature Genetics, vol.41, pp.1088-1093, 2009.
DOI : 10.1038/ng.440

URL : http://europepmc.org/articles/pmc2845877?pdf=render

D. P. Hibar, O. Kohannim, J. L. Stein, M. C. Chiang, and P. M. Thompson, Multilocus genetic analysis of brain images, Brain Imaging and Behavior, vol.2, p.73, 2011.
DOI : 10.3389/fgene.2011.00073

URL : https://www.frontiersin.org/articles/10.3389/fgene.2011.00073/pdf

D. P. Hibar, J. L. Stein, O. Kohannim, N. Jahanshad, A. J. Saykin et al., Voxelwise gene-wide association study (vGeneWAS): multivariate gene-based association testing in 731 elderly subjects, NeuroImage, vol.56, pp.1875-1891, 2011.
DOI : 10.1016/j.neuroimage.2011.03.077

URL : http://europepmc.org/articles/pmc3366726?pdf=render

D. P. Hibar, T. G. Van-erp, J. A. Turner, U. K. Haukvik, and I. Agartz, Meta-analysis of structural brain differences in bipolar disorder: the ENIGMA-Bipolar Disorder Project, 2013.

D. P. Hibar, J. L. Stein, A. B. Ryles, O. Kohannim, N. Jahanshad et al., Genome-wide association identifies genetic variants associated with lentiform nucleus volume in N=1345 young and elderly subjects, Brain Imaging and Behavior, vol.7, pp.102-115, 2013.
DOI : 10.1007/s11682-012-9199-7

URL : http://europepmc.org/articles/pmc3779070?pdf=render

D. Hibar, J. L. Stein, N. Jahanshad, A. W. Toga, K. L. Mcmahon et al., Exhaustive search of the SNP-SNP interactome identifies replicated epistatic effects on brain volume, 2013.
DOI : 10.1007/978-3-642-40760-4_75

URL : http://europepmc.org/articles/pmc4109883?pdf=render

L. A. Hindorff, P. Sethupathy, H. A. Junkins, E. M. Ramos, J. P. Mehta et al., Potential etiologic and functional implications of genome-wide association loci for human diseases and traits, vol.106, pp.9362-9367, 2009.
DOI : 10.1073/pnas.0903103106

URL : http://www.pnas.org/content/106/23/9362.full.pdf

P. Hollingworth, D. Harold, R. Sims, A. Gerrish, J. C. Lambert et al., Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease, Nature Genetics, vol.43, issue.5, pp.429-435, 2011.
DOI : 10.1038/ng.803

URL : http://europepmc.org/articles/pmc3084173?pdf=render

A. J. Holmes, P. H. Lee, M. O. Hollinshead, L. Bakst, J. L. Roffman et al., Individual differences in amygdalamedial prefrontal anatomy link negative affect, impaired social function, and polygenic depression risk, Journal of Neuroscience, vol.32, issue.50, pp.18087-18100, 2012.
DOI : 10.1523/jneurosci.2531-12.2012

URL : http://www.jneurosci.org/content/32/50/18087.full.pdf

M. G. Hong, C. A. Reynolds, A. L. Feldman, M. Kallin, J. C. Lambert et al., Genome-wide and gene-based association implicates FRMD6 in Alzheimer disease, Human Mutation, vol.33, pp.521-529, 2012.
DOI : 10.1002/humu.22009

URL : http://europepmc.org/articles/pmc3326347?pdf=render

H. E. Hulshoff-pol, H. G. Schnack, R. C. Mandl, R. G. Brans, N. E. Van-haren et al., Gray and white matter density changes in monozygotic and same-sex dizygotic twins discordant for schizophrenia using voxel-based morphometry, Neuroimage, vol.31, issue.2, pp.482-488, 2006.

M. A. Ikram, M. Fornage, A. V. Smith, S. Seshadri, R. Schmidt et al., Common variants at 6q22 and 17q21 are associated with intracranial volume, Nature Genetics, vol.44, pp.539-544, 2012.
DOI : 10.1038/ng0612-732c

URL : https://www.nature.com/articles/ng0612-732c.pdf

J. P. Ioannidis, Why most published research findings are false, PLoS Medicine, vol.2, p.124, 2005.
DOI : 10.1080/09332480.2005.10722754

URL : http://europepmc.org/articles/pmc1182327?pdf=render

C. R. Jack and . Jr, Alzheimer disease: new concepts on its neurobiology and the clinical role imaging will play, Radiology, vol.263, pp.344-361, 2012.
DOI : 10.1148/radiol.12110433

URL : https://pubs.rsna.org/doi/pdf/10.1148/radiol.12110433

M. W. Weiner, D. P. Veitch, P. S. Aisen, L. A. Beckett, N. J. Cairns et al., The Alzheimer's disease neuroimaging initiative: a review of papers published since its inception, 2012.