Variants close to NTRK2 gene are associated with birth weight in female twins Dahkki Metrustry, S, Edwards, M, Medland, SE, Holloway, J, Montgomery, G, Martin, N, Spector, T, Cooper, C, Valdes, A

Variants close to NTRK2 gene are associated with birth weight in female twins. Dahkki Metrustry, S, Edwards, M, Medland, SE, Holloway, J, Montgomery, G, Martin, N, Spector, T, Cooper, C, Valdes, A

Patterns of stressful life events and polygenic scores for five mental disorders and neuroticism among adults with depression Dahkki Crouse, JJ, Park, SH, Byrne, EM, Mitchell, BL, Scott, J, Medland, SE, Lin, T, Wray, NR, Martin, NG, Hickie, IB

Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits. Dahkki Yang, J, Ferreira, T, Morris, A, Medland, SE, Madden, P, Heath, A, Martin, N, Montgomery, G, Weedon, M, Loos, R, Frayling, T, McCarthy, M, Hirschhorn, J, Goddard, M, Visscher, P

Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits Dahkki Yang, J, Ferreira, T, Morris, A, Medland, SE, Madden, P, Heath, A, Martin, N, Montgomery, G, Weedon, M, Loos, R, Frayling, T, McCarthy, M, Hirschhorn, J, Goddard, M, Visscher, P

Genomic kinship construction to enhance genetic analyses in the human connectome project data Dahkki Kochunov, P, Donohue, B, Mitchell, BD, Ganjgahi, H, Adhikari, B, Ryan, M, Medland, SE, Jahanshad, N, Thompson, PM, Blangero, J, Fieremans, E, Novikov, DS, Marcus, D, Van Essen, DC, Glahn, DC, Hong, L, Nichols, TE

Hidden heritability due to heterogeneity across seven populations. Dahkki Tropf, FC, Lee, SH, Verweij, RM, Stulp, G, van der Most, PJ, de Vlaming, R, Bakshi, A, Briley, DA, Rahal, C, Hellpap, R, Nyman, A, Esko, T, Metspalu, A, Medland, SE, Martin, NG, Barban, N, Snieder, H, Robinson, MR, Mills, MC

Genome-wide linkage and association analyses implicate FASN in predisposition to Uterine Leiomyomata. Dahkki Eggert, S, Huyck, K, Somasundaram, P, Kavalla, R, Stewart, E, Lu, A, Painter, J, Montgomery, G, Medland, SE, Nyholt, DR, Treloar, SA, Zondervan, K, Heath, A, Madden, P, Rose, L, Buring, J, Ridker, P, Chasman, D, Martin, N, Cantor, R, Morton, C

Hidden heritability due to heterogeneity across seven populations Dahkki Tropf, FC, Lee, SH, Verweij, RM, Stulp, G, van der Moost, PJ, de Vlaming, R, Bakshi, A, Briley, DA, Rahal, C, Hellpap, R, Nyman, A, Esko, T, Metspalu, A, Medland, SE, Martin, NG, Barban, N, Snieder, H, Robinson, MR, Mills, MC

No genetic overlap between circulating iron levels and Alzheimer's disease Dahkki Lupton, MK, Benyamin, B, Proitsi, P, Nyholt, DR, Ferreira, MA, Montgomery, GW, Heath, AC, Madden, PA, Medland, SE, Gordon, SD, GERAD1 Consortium, Alzheimer’s Disease Neuroimaging Initiative, Lovestone, S, Tsolaki, M, Kloszewska, I, Soininen, H, Mecocci, P, Vellas, B, Powell, JF, Bush, AI, Wright, MJ, Martin, NG, Whitfield, JB

The ENIGMA Consortium: Large-scale collaborative analyses of neuroimaging and genetic data Dahkki Thompson, P, Stein, J, Medland, SE, Hibar, D, Vasquez, A, Vasquez, A, Renteria, M, Toro, R, Toro, R, Toro, R, Jahanshad, N, Schumann, G, Franke, B, Franke, B, Wright, M, Martin, N, Agartz, I, Agartz, I, Alda, M, Alhusaini, S, Alhusaini, S, Almasy, L, Almeida, J, Almeida, J, Almeida, J

Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits Dahkki Yang, J, Yang, J, Ferreira, T, Morris, A, Medland, SE, Madden, P, Heath, A, Martin, N, Montgomery, G, Weedon, M, Loos, R, Frayling, T, McCarthy, M, McCarthy, M, Hirschhorn, J, Hirschhorn, J, Hirschhorn, J, Hirschhorn, J, Hirschhorn, J, Goddard, M, Goddard, M, Visscher, P, Visscher, P, Visscher, P

LRRTM1 protein is located in the endoplasmic reticulum (ER) in mammalian cells Dahkki Francks, C, Maegawa, S, Laurén, J, Abrahams, B, Velayos-Baeza, A, Medland, SE, Colella, S, Groszer, M, McAuley, E, Caffrey, T, Timmusk, T, Pruunsild, P, Koppel, I, Lind, P, Matsumoto-Itaba, N, Nicod, J, Xiong, L, Joober, R, Enard, W, Krinsky, B, Nanba, E, Richardson, A, Riley, B, Martin, N, Strittmatter, S

The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data. Dahkki Thompson, P, Stein, J, Medland, SE, Hibar, D, Vasquez, A, Renteria, M, Toro, R, Jahanshad, N, Schumann, G, Franke, B, Wright, M, Martin, N, Agartz, I, Alda, M, Alhusaini, S, Almasy, L, Almeida, J, Alpert, K, Andreasen, N, Andreassen, O, Apostolova, L, Appel, K, Armstrong, N, Aribisala, B, Bastin, M

LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia. Dahkki Francks, C, Maegawa, S, Laurén, J, Abrahams, B, Velayos-Baeza, A, Medland, SE, Colella, S, Groszer, M, McAuley, E, Caffrey, T, Timmusk, T, Pruunsild, P, Koppel, I, Lind, P, Matsumoto-Itaba, N, Nicod, J, Xiong, L, Joober, R, Enard, W, Krinsky, B, Nanba, E, Richardson, A, Riley, B, Martin, N, Strittmatter, S

Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis Dahkki Gallagher, CS, Mäkinen, N, Harris, HR, Rahmioglu, N, Uimari, O, Cook, JP, Shigesi, N, Ferreira, T, Velez-Edwards, DR, Edwards, TL, Mortlock, S, Ruhioglu, Z, Day, F, Becker, CM, Karhunen, V, Martikainen, H, Järvelin, M-R, Cantor, RM, Ridker, PM, Terry, KL, Buring, JE, Gordon, SD, Medland, SE, Montgomery, GW, Nyholt, DR

FTO genotype is associated with phenotypic variability of body mass index. Dahkki Yang, J, Loos, R, Powell, J, Medland, SE, Speliotes, E, Chasman, D, Rose, L, Thorleifsson, G, Steinthorsdottir, V, Mägi, R, Waite, L, Smith, A, Yerges-Armstrong, L, Monda, K, Hadley, D, Mahajan, A, Li, G, Kapur, K, Vitart, V, Huffman, J, Wang, SR, Palmer, C, Esko, T, Fischer, K, Zhao, J

Identification of common variants associated with human hippocampal and intracranial volumes Dahkki Stein, J, Medland, SE, Vasquez, A, Hibar, D, Senstad, R, Winkler, A, Toro, R, Appel, K, Bartecek, R, Bergmann, O, Bernard, M, Brown, A, Cannon, D, Chakravarty, M, Christoforou, A, Domin, M, Grimm, O, Hollinshead, M, Holmes, A, Homuth, G, Hottenga, J, Langan, C, Lopez, L, Hansell, N, Hwang, K

Metabolomics reveals a link between homocysteine and lipid metabolism and leukocyte telomere length: The ENGAGE consortium Dahkki Van Der Spek, A, Broer, L, Draisma, HHM, Pool, R, Albrecht, E, Beekman, M, Mangino, M, Raag, M, Nyholt, DR, Dharuri, HK, Codd, V, Amin, N, De Geus, EJC, Deelen, J, Demirkan, A, Yet, I, Fischer, K, Haller, T, Henders, AK, Isaacs, A, Medland, SE, Montgomery, GW, Mooijaart, SP, Strauch, K, Suchiman, HED

FTO genotype is associated with phenotypic variability of body mass index Dahkki Yang, J, Loos, R, Powell, J, Medland, SE, Speliotes, E, Chasman, D, Rose, L, Thorleifsson, G, Steinthorsdottir, V, Mägi, R, Waite, L, Vernon Smith, A, Yerges-Armstrong, L, Monda, K, Hadley, D, Mahajan, A, Li, G, Kapur, K, Vitart, V, Huffman, J, Wang, SR, Palmer, C, Esko, T, Fischer, K, Hua Zhao, J