Cortical thickness or grey matter volume? The importance of selecting the phenotype for imaging genetics studies 由 Winkler, A, Kochunov, P, Blangero, J, Almasy, L, Zilles, K, Fox, P, Duggirala, R, Glahn, D

Analysis of genetic variability and whole genome linkage of whole-brain, subcortical, and ependymal hyperintense white matter volume 由 Kochunov, P, Glahn, D, Winkler, A, Duggirala, R, Olvera, R, Cole, S, Dyer, T, Almasy, L, Fox, P, Blangero, J

Genetics of microstructure of cerebral white matter using diffusion tensor imaging. 由 Kochunov, P, Glahn, D, Lancaster, J, Winkler, A, Smith, S, Thompson, P, Almasy, L, Duggirala, R, Fox, P, Blangero, J

A multimodal assessment of the genetic control over working memory 由 Karlsgodt, K, Kochunov, P, Winkler, A, Laird, A, Almasy, L, Duggirala, R, Olvera, R, Fox, P, Blangero, J, Glahn, D

Whole brain and regional hyperintense white matter volume and blood pressure: overlap of genetic loci produced by bivariate, whole-genome linkage analyses 由 Kochunov, P, Glahn, D, Lancaster, J, Winkler, A, Kent, J, Olvera, R, Cole, SA, Dyer, T, Almasy, L, Duggirala, R, Fox, P, Blangero, J

Testing the hypothesis of accelerated cerebral white matter aging in schizophrenia and major depression 由 Kochunov, P, Glahn, D, Rowland, L, Olvera, R, Winkler, A, Yang, Y, Sampath, H, Carpenter, W, Duggirala, R, Curran, J, Blangero, J, Hong, L

Genetic control over the resting brain. 由 Glahn, D, Winkler, A, Kochunov, P, Almasy, L, Duggirala, R, Carless, M, Curran, J, Olvera, R, Laird, A, Smith, S, Beckmann, C, Fox, P, Blangero, J

Blood pressure and cerebral white matter share common genetic factors in Mexican Americans 由 Kochunov, P, Glahn, D, Lancaster, J, Winkler, A, Karlsgodt, K, Olvera, R, Curran, J, Carless, M, Dyer, T, Almasy, L, Duggirala, R, Fox, P, Blangero, J

Genetic Control Over the Default Mode Network 由 Glahn, D, Winkler, A, Kochunov, P, Almasy, L, Duggirala, R, Carless, M, Curran, J, Olvera, R, Laird, A, Smith, S, Beckmann, C, Fox, P, Blangero, J

Impact of DISC1 variation on neuroanatomical and neurocognitive phenotypes 由 Carless, M, Glahn, D, Johnson, M, Curran, J, Bozaoglu, K, Dyer, T, Winkler, A, Cole, SA, Almasy, L, MacCluer, J, Duggirala, R, Moses, E, Göring, H, Blangero, J

Identification of pleiotropic genetic effects on obesity and brain anatomy. 由 Curran, J, McKay, DR, Winkler, A, Olvera, R, Carless, M, Dyer, T, Kent, J, Kochunov, P, Sprooten, E, Knowles, E, Comuzzie, A, Fox, P, Almasy, L, Duggirala, R, Blangero, J, Glahn, D

Influence of age, sex and genetic factors on the human brain 由 McKay, DR, Knowles, E, Winkler, A, Sprooten, E, Kochunov, P, Olvera, R, Curran, J, Kent, J, Carless, M, Göring, H, Dyer, T, Duggirala, R, Almasy, L, Fox, P, Blangero, J, Glahn, D

High dimensional endophenotype ranking in the search for major depression risk genes 由 Glahn, D, Curran, J, Winkler, A, Carless, M, Kent, J, Charlesworth, J, Johnson, M, Göring, H, Cole, SA, Dyer, T, Moses, E, Olvera, R, Kochunov, P, Duggirala, R, Fox, P, Almasy, L, Blangero, J

Genetic basis of neurocognitive decline and reduced white-matter integrity in normal human brain aging 由 Glahn, D, Kent, J, Sprooten, E, Diego, V, Winkler, A, Curran, J, McKay, DR, Knowles, E, Carless, M, Goring, H, Dyer, T, Olvera, R, Fox, P, Almasy, L, Charlesworth, J, Kochunov, P, Duggirala, R, Blangero, J

P-selectin expression tracks cerebral atrophy in Mexican-Americans 由 Kochunov, P, Glahn, D, Hong, L, Lancaster, J, Curran, J, Johnson, M, Winkler, A, Holcomb, H, Kent, J, Mitchell, B, Kochunov, V, Olvera, R, Cole, SA, Dyer, T, Moses, E, Goring, H, Almasy, L, Duggirala, R, Blangero, J

Transcriptomics of cortical gray matter thickness decline during normal aging 由 Kochunov, P, Charlesworth, J, Winkler, A, Hong, L, Nichols, T, Curran, J, Sprooten, E, Jahanshad, N, Thompson, P, Johnson, M, Kent, J, Landman, B, Mitchell, B, Cole, SA, Dyer, T, Moses, E, Goring, H, Almasy, L, Duggirala, R, Olvera, R, Glahn, D, Blangero, J

Loss-of-function mutations in SLC30A8 protect against type 2 diabetes 由 Flannick, J, Thorleifsson, G, Beer, N, Jacobs, S, Grarup, N, Burtt, N, Mahajan, A, Fuchsberger, C, Atzmon, G, Benediktsson, R, Blangero, J, Bowden, D, Brandslund, I, Brosnan, J, Burslem, F, Chambers, J, Cho, Y, Christensen, C, Douglas, D, Duggirala, R, Dymek, Z, Farjoun, Y, Fennell, T, Fontanillas, P, Forsén, T

Loss-of-function mutations in SLC30A8 protect against type 2 diabetes. 由 Flannick, J, Thorleifsson, G, Beer, N, Jacobs, S, Grarup, N, Burtt, N, Mahajan, A, Fuchsberger, C, Atzmon, G, Benediktsson, R, Blangero, J, Bowden, D, Brandslund, I, Brosnan, J, Burslem, F, Chambers, J, Cho, Y, Christensen, C, Douglas, D, Duggirala, R, Dymek, Z, Farjoun, Y, Fennell, T, Fontanillas, P, Forsén, T

Whole-genome sequencing to understand the genetic architecture of common gene expression and biomarker phenotypes. 由 Wood, A, Tuke, M, Nalls, M, Hernandez, D, Gibbs, JR, Lin, H, Xu, C, Li, Q, Shen, J, Jun, G, Almeida, M, Tanaka, T, Perry, JR, Gaulton, K, Rivas, M, Pearson, R, Curran, J, Johnson, M, Göring, H, Duggirala, R, Blangero, J, Mccarthy, M, Bandinelli, S, Murray, A, Weedon, M

Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees 由 Jun, G, Manning, A, Almeida, M, Zawistowski, M, Wood, AR, Teslovich, TM, Fuchsberger, C, Feng, S, Cingolani, P, Gaulton, KJ, Dyer, T, Blackwell, TW, Chen, H, Chines, PS, Choi, S, Churchhouse, C, Fontanillas, P, King, R, Lee, S, Lincoln, SE, Trubetskoy, V, DePristo, M, Fingerlin, T, Grossman, R, Grundstad, J, Heath, A, Kim, J, Kim, YJ, Laramie, J, Lee, J, Li, H, Liu, X, Livne, O, Locke, AE, Maller, J, Mazur, A, Morris, AP, Pollin, TI, Ragona, D, Reich, D, Rivas, MA, Scott, LJ, Sim, X, Tearle, RG, Teo, YY, Williams, AL, Zöllner, S, Curran, JE, Peralta, J, Akolkar, B, Bell, GI, Burtt, NP, Cox, NJ, Florez, JC, Hanis, CL, McKeon, C, Mohlke, KL, Seielstad, M, Wilson, JG, Atzmon, G, Below, JE, Dupuis, J, Nicolae, DL, Lehman, D, Park, T, Won, S, Sladek, R, Altshuler, D, McCarthy, MI, Duggirala, R, Boehnke, M, Frayling, TM, Abecasis, GR, Blangero, J