Pervasive sharing of genetic effects in autoimmune disease von Cotsapas, Chris, Voight, Benjamin F, Rossin, Elizabeth, Lage, Kasper, Neale, Benjamin M, Wallace, Chris, Abecasis, Gonçalo R, Barrett, Jeffrey C, Behrens, Timothy, Cho, Judy, De Jager, Philip L, Elder, James T, Graham, Robert R, Gregersen, Peter, Klareskog, Lars, Siminovitch, Katherine A, van Heel, David A, Wijmenga, Cisca, Worthington, Jane, Todd, John A, Hafler, David A, Rich, Stephen S, Daly, Mark J

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Two new Loci for body-weight regulation identified in a joint analysis of genome-wide association studies for early-onset extreme obesity in French and german study groups von Scherag, André, Dina, Christian, Hinney, Anke, Vatin, Vincent, Scherag, Susann, Vogel, Carla I G, Müller, Timo D, Grallert, Harald, Wichmann, H-Erich, Balkau, Beverley, Heude, Barbara, Jarvelin, Marjo-Riitta, Hartikainen, Anna-Liisa, Levy-Marchal, Claire, Weill, Jacques, Delplanque, Jérôme, Körner, Antje, Kiess, Wieland, Kovacs, Peter, Rayner, Nigel W, Prokopenko, Inga, McCarthy, Mark I, Schäfer, Helmut, Jarick, Ivonne, Boeing, Heiner, Fisher, Eva, Reinehr, Thomas, Heinrich, Joachim, Rzehak, Peter, Berdel, Dietrich, Borte, Michael, Biebermann, Heike, Krude, Heiko, Rosskopf, Dieter, Rimmbach, Christian, Rief, Winfried, Fromme, Tobias, Klingenspor, Martin, Schürmann, Annette, Schulz, Nadja, Nöthen, Markus M, Mühleisen, Thomas W, Erbel, Raimund, Jöckel, Karl-Heinz, Moebus, Susanne, Boes, Tanja, Illig, Thomas, Froguel, Philippe, Hebebrand, Johannes, Meyre, David

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A genome-wide association study of hypertension and blood pressure in African Americans von Adeyemo, Adebowale, Gerry, Norman, Chen, Guanjie, Herbert, Alan, Doumatey, Ayo, Huang, Hanxia, Zhou, Jie, Lashley, Kerrie, Chen, Yuanxiu, Christman, Michael, Rotimi, Charles

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Noisy splicing drives mRNA isoform diversity in human cells von Pickrell, Joseph K, Pai, Athma A, Gilad, Yoav, Pritchard, Jonathan K

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A comprehensive analysis of shared loci between systemic lupus erythematosus (SLE) and sixteen autoimmune diseases reveals limited genetic overlap von Ramos, Paula S, Criswell, Lindsey A, Moser, Kathy L, Comeau, Mary E, Williams, Adrienne H, Pajewski, Nicholas M, Chung, Sharon A, Graham, Robert R, Zidovetzki, Raphael, Kelly, Jennifer A, Kaufman, Kenneth M, Jacob, Chaim O, Vyse, Timothy J, Tsao, Betty P, Kimberly, Robert P, Gaffney, Patrick M, Alarcón-Riquelme, Marta E, Harley, John B, Langefeld, Carl D

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NRXN3 is a novel locus for waist circumference: a genome-wide association study from the CHARGE Consortium von Heard-Costa, Nancy L, Zillikens, M Carola, Monda, Keri L, Johansson, Asa, Harris, Tamara B, Fu, Mao, Haritunians, Talin, Feitosa, Mary F, Aspelund, Thor, Eiriksdottir, Gudny, Garcia, Melissa, Launer, Lenore J, Smith, Albert V, Mitchell, Braxton D, McArdle, Patrick F, Shuldiner, Alan R, Bielinski, Suzette J, Boerwinkle, Eric, Brancati, Fred, Demerath, Ellen W, Pankow, James S, Arnold, Alice M, Chen, Yii-Der Ida, Glazer, Nicole L, McKnight, Barbara, Psaty, Bruce M, Rotter, Jerome I, Amin, Najaf, Campbell, Harry, Gyllensten, Ulf, Pattaro, Cristian, Pramstaller, Peter P, Rudan, Igor, Struchalin, Maksim, Vitart, Veronique, Gao, Xiaoyi, Kraja, Aldi, Province, Michael A, Zhang, Qunyuan, Atwood, Larry D, Dupuis, Josée, Hirschhorn, Joel N, Jaquish, Cashell E, O'Donnell, Christopher J, Vasan, Ramachandran S, White, Charles C, Aulchenko, Yurii S, Estrada, Karol, Hofman, Albert, Rivadeneira, Fernando, Uitterlinden, André G, Witteman, Jacqueline C M, Oostra, Ben A, Kaplan, Robert C, Gudnason, Vilmundur, O'Connell, Jeffrey R, Borecki, Ingrid B, van Duijn, Cornelia M, Cupples, L Adrienne, Fox, Caroline S, North, Kari E

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Characterizing genetic risk at known prostate cancer susceptibility loci in African Americans von Haiman, Christopher A, Chen, Gary K, Blot, William J, Strom, Sara S, Berndt, Sonja I, Kittles, Rick A, Rybicki, Benjamin A, Isaacs, William B, Ingles, Sue A, Stanford, Janet L, Diver, W Ryan, Witte, John S, Chanock, Stephen J, Kolb, Suzanne, Signorello, Lisa B, Yamamura, Yuko, Neslund-Dudas, Christine, Thun, Michael J, Murphy, Adam, Casey, Graham, Sheng, Xin, Wan, Peggy, Pooler, Loreall C, Monroe, Kristine R, Waters, Kevin M, Le Marchand, Loic, Kolonel, Laurence N, Stram, Daniel O, Henderson, Brian E

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Differential allelic expression in the human genome: a robust approach to identify genetic and epigenetic cis-acting mechanisms regulating gene expression von Serre, David, Gurd, Scott, Ge, Bing, Sladek, Robert, Sinnett, Donna, Harmsen, Eef, Bibikova, Marina, Chudin, Eugene, Barker, David L, Dickinson, Todd, Fan, Jian-Bing, Hudson, Thomas J

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Genetic networks of liver metabolism revealed by integration of metabolic and transcriptional profiling von Ferrara, Christine T, Wang, Ping, Neto, Elias Chaibub, Stevens, Robert D, Bain, James R, Wenner, Brett R, Ilkayeva, Olga R, Keller, Mark P, Blasiole, Daniel A, Kendziorski, Christina, Yandell, Brian S, Newgard, Christopher B, Attie, Alan D

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A computational screen for regulators of oxidative phosphorylation implicates SLIRP in mitochondrial RNA homeostasis von Baughman, Joshua M, Nilsson, Roland, Gohil, Vishal M, Arlow, Daniel H, Gauhar, Zareen, Mootha, Vamsi K

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Identification of common genetic variation that modulates alternative splicing von Hull, Jeremy, Campino, Susana, Rowlands, Kate, Chan, Man-Suen, Copley, Richard R, Taylor, Martin S, Rockett, Kirk, Elvidge, Gareth, Keating, Brendan, Knight, Julian, Kwiatkowski, Dominic

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Fine-scale variation and genetic determinants of alternative splicing across individuals von Coulombe-Huntington, Jasmin, Lam, Kevin C L, Dias, Christel, Majewski, Jacek

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Ancient and recent positive selection transformed opioid cis-regulation in humans von Rockman, Matthew V, Hahn, Matthew W, Soranzo, Nicole, Zimprich, Fritz, Goldstein, David B, Wray, Gregory A

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Genome-wide expression of azoospermia testes demonstrates a specific profile and implicates ART3 in genetic susceptibility von Okada, Hiroyuki, Tajima, Atsushi, Shichiri, Kazuyoshi, Tanaka, Atsushi, Tanaka, Kenichi, Inoue, Ituro

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Deciphering normal blood gene expression variation--The NOWAC postgenome study von Dumeaux, Vanessa, Olsen, Karina S, Nuel, Gregory, Paulssen, Ruth H, Børresen-Dale, Anne-Lise, Lund, Eiliv

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Capturing the spectrum of interaction effects in genetic association studies by simulated evaporative cooling network analysis von McKinney, Brett A, Crowe, James E, Guo, Jingyu, Tian, Dehua

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Evaluation of candidate stromal epithelial cross-talk genes identifies association between risk of serous ovarian cancer and TERT, a cancer susceptibility "hot-spot" von Johnatty, Sharon E, Beesley, Jonathan, Chen, Xiaoqing, Macgregor, Stuart, Duffy, David L, Spurdle, Amanda B, deFazio, Anna, Gava, Natalie, Webb, Penelope M, Rossing, Mary Anne, Doherty, Jennifer Anne, Goodman, Marc T, Lurie, Galina, Thompson, Pamela J, Wilkens, Lynne R, Ness, Roberta B, Moysich, Kirsten B, Chang-Claude, Jenny, Wang-Gohrke, Shan, Cramer, Daniel W, Terry, Kathryn L, Hankinson, Susan E, Tworoger, Shelley S, Garcia-Closas, Montserrat, Yang, Hannah, Lissowska, Jolanta, Chanock, Stephen J, Pharoah, Paul D, Song, Honglin, Whitemore, Alice S, Pearce, Celeste L, Stram, Daniel O, Wu, Anna H, Pike, Malcolm C, Gayther, Simon A, Ramus, Susan J, Menon, Usha, Gentry-Maharaj, Aleksandra, Anton-Culver, Hoda, Ziogas, Argyrios, Hogdall, Estrid, Kjaer, Susanne K, Hogdall, Claus, Berchuck, Andrew, Schildkraut, Joellen M, Iversen, Edwin S, Moorman, Patricia G, Phelan, Catherine M, Sellers, Thomas A, Cunningham, Julie M, Vierkant, Robert A, Rider, David N, Goode, Ellen L, Haviv, Izhak, Chenevix-Trench, Georgia

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Adaptive evolution of conserved noncoding elements in mammals von Kim, Su Yeon, Pritchard, Jonathan K

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Linkage disequilibrium between two high-frequency deletion polymorphisms: implications for association studies involving the glutathione-S transferase (GST) genes von Zhao, Yongzhong, Marotta, Michael, Eichler, Evan E, Eng, Charis, Tanaka, Hisashi

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Forging links between human mental retardation-associated CNVs and mouse gene knockout models von Webber, Caleb, Hehir-Kwa, Jayne Y, Nguyen, Duc-Quang, de Vries, Bert B A, Veltman, Joris A, Ponting, Chris P

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