Cortical thickness or grey matter volume? The importance of selecting the phenotype for imaging genetics studies af 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 af 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. af 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 af 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 af 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 af 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. af 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 af 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 af 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 af 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. af 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 af 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 af 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 af 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 af 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 af 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 af 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. af 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. af 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 af 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