Spectral aerosol optical depth from SI-traceable spectral solar irradiance measurements von Gröbner, Julian, Kouremeti, Natalia, Hülsen, Gregor, Zuber, Ralf, Ribnitzky, Mario, Nevas, Saulius, Sperfeld, Peter, Schwind, Kerstin, Schneider, Philipp, Kazadzis, Stelios, Barreto, África, Gardiner, Tom, Mottungan, Kavitha, Medland, David, Coleman, Marc

Volltext

High Resolution Langley von Mottungan, Kavitha, Gardiner, Tom, Medland, David, Coleman, Marc

Volltext bestellen

Bridgeless Super-Arch Top von MEDLAND, PAUL DAVID

Volltext bestellen

Guitar fingerboard defragmentation construct von PAUL DAVID MEDLAND

Volltext bestellen

Guitar fingerboard defragmentation construct von PAUL DAVID MEDLAND

Volltext bestellen

Mapping brain asymmetry in health and disease through the ENIGMA consortium von Kong, Xiang‐Zhen, Postema, Merel C., Guadalupe, Tulio, Kovel, Carolien, Boedhoe, Premika S. W., Hoogman, Martine, Mathias, Samuel R., Rooij, Daan, Schijven, Dick, Glahn, David C., Medland, Sarah E., Jahanshad, Neda, Thomopoulos, Sophia I., Turner, Jessica A., Buitelaar, Jan, Erp, Theo G. M., Franke, Barbara, Fisher, Simon E., Heuvel, Odile A., Schmaal, Lianne, Thompson, Paul M., Francks, Clyde

Volltext

Attention deficit hyperactivity disorder in Australian adults: prevalence, persistence, conduct problems and disadvantage von Ebejer, Jane L, Medland, Sarah E, van der Werf, Julius, Gondro, Cedric, Henders, Anjali K, Lynskey, Michael, Martin, Nicholas G, Duffy, David L

Volltext

Head Motion and Inattention/Hyperactivity Share Common Genetic Influences: Implications for fMRI Studies of ADHD von Couvy-Duchesne, Baptiste, Ebejer, Jane L, Gillespie, Nathan A, Duffy, David L, Hickie, Ian B, Thompson, Paul M, Martin, Nicholas G, de Zubicaray, Greig I, McMahon, Katie L, Medland, Sarah E, Wright, Margaret J

Volltext

Genome-wide meta-analysis of cognitive empathy: heritability, and correlates with sex, neuropsychiatric conditions and cognition von Warrier, V, Grasby, K L, Uzefovsky, F, Toro, R, Smith, P, Chakrabarti, B, Khadake, J, Mawbey-Adamson, E, Litterman, N, Hottenga, J-J, Lubke, G, Boomsma, D I, Martin, N G, Hatemi, P K, Medland, S E, Hinds, D A, Bourgeron, T, Baron-Cohen, S

Volltext

Common genetic variants associated with cognitive performance identified using the proxy-phenotype method von Rietveld, Cornelius A., Esko, Tõnu, Davies, Gail, Pers, Tune H., Turley, Patrick, Benyamin, Beben, Chabris, Christopher F., Emilsson, Valur, Johnson, Andrew D., Lee, James J., de Leeuw, Christiaan, Marioni, Riccardo E., Medland, Sarah E., Miller, Michael B., Rostapshova, Olga, van der Lee, Sven J., Vinkhuyzen, Anna A. E., Amin, Najaf, Conley, Dalton, Derringer, Jaime, van Duijn, Cornelia M., Fehrmann, Rudolf, Franke, Lude, Glaeser, Edward L., Hansell, Narelle K., Hayward, Caroline, Iacono, William G., Ibrahim-Verbaas, Carla, Jaddoe, Vincent, Karjalainen, Juha, Laibson, David, Lichtenstein, Paul, Liewald, David C., Magnusson, Patrik K. E., Martin, Nicholas G., McGue, Matt, McMahon, George, Pedersen, Nancy L., Pinker, Steven, Porteous, David J., Posthuma, Danielle, Rivadeneira, Fernando, Smith, Blair H., Starr, John M., Tiemeier, Henning, Timpson, Nicholas J., Trzaskowski, Maciej, Uitterlinden, André G., Verhulst, Frank C., Ward, Mary E., Wright, Margaret J., Smith, George Davey, Deary, Ian J., Johannesson, Magnus, Plomin, Robert, Visscher, Peter M., Benjamin, Daniel J., Cesarini, David, Koellinger, Philipp D.

Volltext

Subtly altered topological asymmetry of brain structural covariance networks in autism spectrum disorder across 43 datasets from the ENIGMA consortium von Sha, Zhiqiang, van Rooij, Daan, Anagnostou, Evdokia, Arango, Celso, Auzias, Guillaume, Behrmann, Marlene, Bernhardt, Boris, Bolte, Sven, Busatto, Geraldo F., Calderoni, Sara, Calvo, Rosa, Daly, Eileen, Deruelle, Christine, Duan, Meiyu, Duran, Fabio Luis Souza, Durston, Sarah, Ecker, Christine, Ehrlich, Stefan, Fair, Damien, Fedor, Jennifer, Fitzgerald, Jacqueline, Floris, Dorothea L., Franke, Barbara, Freitag, Christine M., Gallagher, Louise, Glahn, David C., Haar, Shlomi, Hoekstra, Liesbeth, Jahanshad, Neda, Jalbrzikowski, Maria, Janssen, Joost, King, Joseph A., Lazaro, Luisa, Luna, Beatriz, McGrath, Jane, Medland, Sarah E., Muratori, Filippo, Murphy, Declan G. M., Neufeld, Janina, O’Hearn, Kirsten, Oranje, Bob, Parellada, Mara, Pariente, Jose C., Postema, Merel C., Remnelius, Karl Lundin, Retico, Alessandra, Rosa, Pedro Gomes Penteado, Rubia, Katya, Shook, Devon, Tammimies, Kristiina, Taylor, Margot J., Tosetti, Michela, Wallace, Gregory L., Zhou, Fengfeng, Thompson, Paul M., Fisher, Simon E., Buitelaar, Jan K., Francks, Clyde

Volltext

Mining the human phenome using allelic scores that index biological intermediates von Evans, David M, Brion, Marie Jo A, Paternoster, Lavinia, Kemp, John P, McMahon, George, Munafò, Marcus, Whitfield, John B, Medland, Sarah E, Montgomery, Grant W, Timpson, Nicholas J, St Pourcain, Beate, Lawlor, Debbie A, Martin, Nicholas G, Dehghan, Abbas, Hirschhorn, Joel, Smith, George Davey

Volltext

Genome-wide association study identifies nine novel loci for 2D:4D finger ratio, a putative retrospective biomarker of testosterone exposure in utero von Warrington, Nicole M, Shevroja, Enisa, Hemani, Gibran, Hysi, Pirro G, Jiang, Yunxuan, Auton, Adam, Boer, Cindy G, Mangino, Massimo, Wang, Carol A, Kemp, John P, McMahon, George, Medina-Gomez, Carolina, Hickey, Martha, Trajanoska, Katerina, Wolke, Dieter, Ikram, M Arfan, Montgomery, Grant W, Felix, Janine F, Wright, Margaret J, Mackey, David A, Jaddoe, Vincent W, Martin, Nicholas G, Tung, Joyce Y, Davey Smith, George, Pennell, Craig E, Spector, Tim D, van Meurs, Joyce, Rivadeneira, Fernando, Medland, Sarah E, Evans, David M

Volltext

Uncovering the complex relationship between balding, testosterone and skin cancers in men von Ong, Jue-Sheng, Seviiri, Mathias, Dusingize, Jean Claude, Wu, Yeda, Han, Xikun, Shi, Jianxin, Olsen, Catherine M., Neale, Rachel E., Thompson, John F., Saw, Robyn P. M., Shannon, Kerwin F., Mann, Graham J., Martin, Nicholas G., Medland, Sarah E., Gordon, Scott D., Scolyer, Richard A., Long, Georgina V., Iles, Mark M., Landi, Maria Teresa, Whiteman, David C., MacGregor, Stuart, Law, Matthew H.

Volltext

Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability von Hysi, Pirro G., Valdes, Ana M., Liu, Fan, Furlotte, Nicholas A., Evans, David M., Bataille, Veronique, Visconti, Alessia, Hemani, Gibran, McMahon, George, Ring, Susan M., Smith, George Davey, Duffy, David L., Zhu, Gu, Gordon, Scott D., Medland, Sarah E., Lin, Bochao D., Willemsen, Gonneke, Jan Hottenga, Jouke, Vuckovic, Dragana, Girotto, Giorgia, Gandin, Ilaria, Sala, Cinzia, Concas, Maria Pina, Brumat, Marco, Gasparini, Paolo, Toniolo, Daniela, Cocca, Massimiliano, Robino, Antonietta, Yazar, Seyhan, Hewitt, Alex W., Chen, Yan, Zeng, Changqing, Uitterlinden, Andre G., Ikram, M. Arfan, Hamer, Merel A., van Duijn, Cornelia M., Nijsten, Tamar, Mackey, David A., Falchi, Mario, Boomsma, Dorret I., Martin, Nicholas G., Hinds, David A., Kayser, Manfred, Spector, Timothy D.

Volltext

Characteristics of recently arrived Asian men who have sex with men diagnosed with HIV through sexual health services in Melbourne and Sydney von Blackshaw, Lucinda C.D., Chow, Eric P.F., Varma, Rick, Healey, Loretta, Templeton, David J., Basu, Ashna, Turner, Dane, Medland, Nick A., Rix, Suzanne, Fairley, Christopher K., Chen, Marcus Y.

Volltext

Association Between Population Density and Genetic Risk for Schizophrenia von Colodro-Conde, Lucía, Couvy-Duchesne, Baptiste, Whitfield, John B, Streit, Fabian, Gordon, Scott, Kemper, Kathryn E, Yengo, Loic, Zheng, Zhili, Trzaskowski, Maciej, de Zeeuw, Eveline L, Nivard, Michel G, Das, Marjolijn, Neale, Rachel E, MacGregor, Stuart, Olsen, Catherine M, Whiteman, David C, Boomsma, Dorret I, Yang, Jian, Rietschel, Marcella, McGrath, John J, Medland, Sarah E, Martin, Nicholas G

Volltext

The Australian Genetics of Depression Study: new risk loci and dissecting heterogeneity between subtypes von Mitchell, Brittany L., Campos, Adrian I., Whiteman, David C., Olsen, Catherine M., Gordon, Scott D., Walker, Adam J., Dean, Olivia M., Berk, Michael, Hickie, Ian B., Medland, Sarah E., Wray, Naomi R., Martin, Nicholas G., Byrne, Enda M.

Volltext

Polygenic Risk Scores Derived From Varying Definitions of Depression and Risk of Depression von Mitchell, Brittany L, Thorp, Jackson G, Wu, Yeda, Campos, Adrian I, Nyholt, Dale R, Gordon, Scott D, Whiteman, David C, Olsen, Catherine M, Hickie, Ian B, Martin, Nicholas G, Medland, Sarah E, Wray, Naomi R, Byrne, Enda M

Volltext

Introduction to the Special Issue on Statistical Genetic Methods for Human Complex Traits von Evans, David M., Medland, Sarah E., Prom-Wormley, Elizabeth

Volltext