Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: implications for 22q11 deletion syndrome von Paylor, Richard, Glaser, Beate, Mupo, Annalisa, Ataliotis, Paris, Spencer, Corinne, Sobotka, Angela, Sparks, Chelsey, Choi, Chul-Hee, Oghalai, John, Curran, Sarah, Murphy, Kieran C, Monks, Stephen, Williams, Nigel, O'Donovan, Michael C, Owen, Michael J, Scambler, Peter J, Lindsay, Elizabeth

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The Moderating Role of Close Friends in the Relationship Between Conduct Problems and Adolescent Substance Use von Glaser, Beate, Ph.D, Shelton, Katherine H., Ph.D, van den Bree, Marianne B.M., Ph.D

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Genome-wide association study reveals multiple loci associated with primary tooth development during infancy von Pillas, Demetris, Hoggart, Clive J, Evans, David M, O'Reilly, Paul F, Sipilä, Kirsi, Lähdesmäki, Raija, Millwood, Iona Y, Kaakinen, Marika, Netuveli, Gopalakrishnan, Blane, David, Charoen, Pimphen, Sovio, Ulla, Pouta, Anneli, Freimer, Nelson, Hartikainen, Anna-Liisa, Laitinen, Jaana, Vaara, Sarianna, Glaser, Beate, Crawford, Peter, Timpson, Nicholas J, Ring, Susan M, Deng, Guohong, Zhang, Weihua, McCarthy, Mark I, Deloukas, Panos, Peltonen, Leena, Elliott, Paul, Coin, Lachlan J M, Smith, George Davey, Jarvelin, Marjo-Riitta

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Genetic variation in LIN28B is associated with the timing of puberty von Song, Kijoung, Vollenweider, Peter, Golding, Jean, Northstone, Kate, Mooser, Vincent, Khaw, Kay-Tee, Ness, Andrew R, Luan, Jian'an, McGeehin, Michael A, Glaser, Beate, Brage, Soren, Ong, Ken K, Barroso, Inês, Smith, George Davey, Andersen, Lars B, Gillson, Christopher J, Wong, Andrew, Loos, Ruth J, Li, Shengxu, Waeber, Gerard, Wareham, Nicholas J, Ring, Susan M, Rubin, Carol, Elks, Cathy E, Sims, Matthew A, Kuh, Diana, Waterworth, Dawn M, Bingham, Sheila A, Deloukas, Panagiotis, Strachan, David P, Zhao, Jing Hua, Ekelund, Ulf, Hardy, Rebecca, Marcus, Michele, Luben, Robert

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Comparison of Methods for Combining Case-Control and Family-Based Association Studies von Glaser, Beate, Holmans, Peter

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A genome-wide association study reveals variants in ARL15 that influence adiponectin levels von Richards, J Brent, Waterworth, Dawn, O'Rahilly, Stephen, Hivert, Marie-France, Loos, Ruth J F, Perry, John R B, Tanaka, Toshiko, Timpson, Nicholas John, Semple, Robert K, Soranzo, Nicole, Song, Kijoung, Rocha, Nuno, Grundberg, Elin, Dupuis, Josée, Florez, Jose C, Langenberg, Claudia, Prokopenko, Inga, Saxena, Richa, Sladek, Robert, Aulchenko, Yurii, Evans, David, Waeber, Gerard, Erdmann, Jeanette, Burnett, Mary-Susan, Sattar, Naveed, Devaney, Joseph, Willenborg, Christina, Hingorani, Aroon, Witteman, Jaquelin C M, Vollenweider, Peter, Glaser, Beate, Hengstenberg, Christian, Ferrucci, Luigi, Melzer, David, Stark, Klaus, Deanfield, John, Winogradow, Janina, Grassl, Martina, Hall, Alistair S, Egan, Josephine M, Thompson, John R, Ricketts, Sally L, König, Inke R, Reinhard, Wibke, Grundy, Scott, Wichmann, H-Erich, Barter, Phil, Mahley, Robert, Kesaniemi, Y Antero, Rader, Daniel J, Reilly, Muredach P, Epstein, Stephen E, Stewart, Alexandre F R, Van Duijn, Cornelia M, Schunkert, Heribert, Burling, Keith, Deloukas, Panos, Pastinen, Tomi, Samani, Nilesh J, McPherson, Ruth, Davey Smith, George, Frayling, Timothy M, Wareham, Nicholas J, Meigs, James B, Mooser, Vincent, Spector, Tim D

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Clear detection of ADIPOQ locus as the major gene for plasma adiponectin: Results of genome-wide association analyses including 4659 European individuals von Heid, Iris M, Henneman, Peter, Hicks, Andrew, Coassin, Stefan, Winkler, Thomas, Aulchenko, Yurii S, Fuchsberger, Christian, Song, Kijoung, Hivert, Marie-France, Waterworth, Dawn M, Timpson, Nicholas J, Richards, J. Brent, Perry, John R.B, Tanaka, Toshiko, Amin, Najaf, Kollerits, Barbara, Pichler, Irene, Oostra, Ben A, Thorand, Barbara, Frants, Rune R, Illig, Thomas, Dupuis, Josée, Glaser, Beate, Spector, Tim, Guralnik, Jack, Egan, Josephine M, Florez, Jose C, Evans, David M, Soranzo, Nicole, Bandinelli, Stefania, Carlson, Olga D, Frayling, Timothy M, Burling, Keith, Smith, George Davey, Mooser, Vincent, Ferrucci, Luigi, Meigs, James B, Vollenweider, Peter, Dijk, Ko Willems van, Pramstaller, Peter, Kronenberg, Florian, van Duijn, Cornelia M

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Common variants in the region around Osterix are associated with bone mineral density and growth in childhood von Timpson, Nicholas J., Tobias, Jon H., Richards, J. Brent, Soranzo, Nicole, Duncan, Emma L., Sims, Anne-Marie, Whittaker, Pamela, Kumanduri, Vasudev, Zhai, Guangju, Glaser, Beate, Eisman, John, Jones, Graeme, Nicholson, Geoff, Prince, Richard, Seeman, Ego, Spector, Tim D., Brown, Matthew A., Peltonen, Leena, Smith, George Davey, Deloukas, Panos, Evans, David M.

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A Variant in LIN28B Is Associated with 2D:4D Finger-Length Ratio, a Putative Retrospective Biomarker of Prenatal Testosterone Exposure von Medland, Sarah E., Zayats, Tetyana, Glaser, Beate, Nyholt, Dale R., Gordon, Scott D., Wright, Margaret J., Montgomery, Grant W., Campbell, Megan J., Henders, Anjali K., Timpson, Nicholas J., Peltonen, Leena, Wolke, Dieter, Ring, Susan M., Deloukas, Panos, Martin, Nicholas G., Smith, George Davey, Evans, David M.

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Functional Gene Group Analysis Reveals a Role of Synaptic Heterotrimeric G Proteins in Cognitive Ability von Ruano, Dina, Abecasis, Gonçalo R., Glaser, Beate, Lips, Esther S., Cornelisse, L. Niels, de Jong, Arthur P.H., Evans, David M., Smith, George Davey, Timpson, Nicolas J., Smit, August B., Heutink, Peter, Verhage, Matthijs, Posthuma, Danielle

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Dielectric breakdown simulations of an OLTC in a transformer von Wiesmüller, Maximilian, Glaser, Beate, Fuchs, Franz, Sterz, Oliver

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Obesity-susceptibility loci have a limited influence on birth weight: a meta-analysis of up to 28,219 individuals von Kilpeläinen, Tuomas O, den Hoed, Marcel, Ong, Ken K, Grøntved, Anders, Brage, Soren, Consortium, Early Growth Genetics, Jameson, Karen, Cooper, Cyrus, Khaw, Kay-Tee, Ekelund, Ulf, Wareham, Nicholas J, Loos, Ruth JF

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Strong evidence that GNB1L is associated with schizophrenia von Williams, Nigel M., Glaser, Beate, Norton, Nadine, Williams, Hywel, Pierce, Timothy, Moskvina, Valentina, Monks, Stephen, Del Favero, Jurgen, Goossens, Dirk, Rujescu, Dan, Giegling, Ina, Kirov, George, Craddock, Nicholas, Murphy, Kieran C., O'Donovan, Michael C., Owen, Michael J.

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No Association Between Schizophrenia and Polymorphisms in COMT in Two Large Samples von Williams, Hywel J., Glaser, Beate, Williams, Nigel M., Norton, Nadine, Zammit, Stanley, Macgregor, Stuart, Kirov, George K., Owen, Michael J., O'Donovan, Michael C.

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Analysis of ProDH, COMT and ZDHHC8 risk variants does not support individual or interactive effects on schizophrenia susceptibility von Glaser, Beate, Moskvina, Valentina, Kirov, George, Murphy, Kieran C., Williams, Hywel, Williams, Nigel, Owen, Michael J., O'Donovan, Michael C.

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Localization of Bipolar Susceptibility Locus by Molecular Genetic Analysis of the Chromosome 12q23-q24 Region in Two Pedigrees With Bipolar Disorder and Darier's Disease von Green, Elaine, Elvidge, Gareth, Jacobsen, Nick, Glaser, Beate, Jones, Ian, O'Donovan, Michael C., Kirov, George, Owen, Michael J., Craddock, Nick

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Analysis of copy number variation using quantitative interspecies competitive PCR von Williams, Nigel M, Williams, Hywel, Majounie, Elisa, Norton, Nadine, Glaser, Beate, Morris, Huw R, Owen, Michael J, O'Donovan, Michael C

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No Association Between the Putative Functional ZDHHC8 Single Nucleotide Polymorphism rs175174 and Schizophrenia in Large European Samples von Glaser, Beate, Schumacher, Johannes, Williams, Hywel J., Jamra, Rami Abou, Ianakiev, Nikolai, Milev, Radoi, Ohlraun, Stephanie, Schulze, Thomas G., Czerski, Piotr M., Hauser, Joanna, Jönsson, Erick G., Sedvall, Göran C., Klopp, Norman, Illig, Thomas, Becker, Tim, Propping, Peter, Williams, Nigel M., Cichon, Sven, Kirov, George, Rietschel, Marcella, Murphy, Kieran C., O’Donovan, Michael C., Nöthen, Markus M., Owen, Michael J.

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Linkage disequilibrium mapping of bipolar affective disorder at 12q23-q24 provides evidence for association at CUX2 and FLJ32356 von Glaser, Beate, Kirov, George, Green, Elaine, Craddock, Nick, Owen, Michael J.

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STATE ANALYSIS OF AN ON-LOAD TAP CHANGER von DOLLES, Markus, REHKOPF, Sebastian, ZINTL, Markus, GLASER, Beate

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