GRASP v2.0: an update on the Genome-Wide Repository of Associations between SNPs and phenotypes von Eicher, John D, Landowski, Christa, Stackhouse, Brian, Sloan, Arielle, Chen, Wenjie, Jensen, Nicole, Lien, Ju-Ping, Leslie, Richard, Johnson, Andrew D

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The additive blood pressure lowering effects of exercise intensity on post-exercise hypotension von Eicher, John D., BS, Maresh, Carl M., PhD, Tsongalis, Gregory J., PhD, Thompson, Paul D., MD, Pescatello, Linda S., PhD

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Alleles of a Polymorphic ETV6 Binding Site in DCDC2 Confer Risk of Reading and Language Impairment von Powers, Natalie R., Eicher, John D., Butter, Falk, Kong, Yong, Miller, Laura L., Ring, Susan M., Mann, Matthias, Gruen, Jeffrey R.

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Associations of prenatal nicotine exposure and the dopamine related genes ANKK1 and DRD2 to verbal language von Eicher, John D, Powers, Natalie R, Cho, Kelly, Miller, Laura L, Mueller, Kathryn L, Ring, Susan M, Tomblin, J Bruce, Gruen, Jeffrey R

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Integrative genomic analysis implicates limited peripheral adipose storage capacity in the pathogenesis of human insulin resistance von Lotta, Luca A, Gulati, Pawan, Day, Felix R, Payne, Felicity, Ongen, Halit, van de Bunt, Martijn, Gaulton, Kyle J, Eicher, John D, Sharp, Stephen J, Luan, Jian'an, De Lucia Rolfe, Emanuella, Stewart, Isobel D, Wheeler, Eleanor, Willems, Sara M, Adams, Claire, Yaghootkar, Hanieh, Forouhi, Nita G, Khaw, Kay-Tee, Johnson, Andrew D, Semple, Robert K, Frayling, Timothy, Perry, John R B, Dermitzakis, Emmanouil, McCarthy, Mark I, Barroso, Inês, Wareham, Nicholas J, Savage, David B, Langenberg, Claudia, O'Rahilly, Stephen, Scott, Robert A

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Fifteen new risk loci for coronary artery disease highlight arterial-wall-specific mechanisms von Howson, Joanna M M, Zhao, Wei, Barnes, Daniel R, Ho, Weang-Kee, Young, Robin, Paul, Dirk S, Waite, Lindsay L, Freitag, Daniel F, Fauman, Eric B, Salfati, Elias L, Sun, Benjamin B, Eicher, John D, Johnson, Andrew D, Sheu, Wayne H H, Nielsen, Sune F, Lin, Wei-Yu, Surendran, Praveen, Malarstig, Anders, Wilk, Jemma B, Tybjærg-Hansen, Anne, Rasmussen, Katrine L, Kamstrup, Pia R, Deloukas, Panos, Erdmann, Jeanette, Kathiresan, Sekar, Samani, Nilesh J, Schunkert, Heribert, Watkins, Hugh, Do, Ron, Rader, Daniel J, Johnson, Julie A, Hazen, Stanley L, Quyyumi, Arshed A, Spertus, John A, Pepine, Carl J, Franceschini, Nora, Justice, Anne, Reiner, Alex P, Buyske, Steven, Hindorff, Lucia A, Carty, Cara L, North, Kari E, Kooperberg, Charles, Boerwinkle, Eric, Young, Kristin, Graff, Mariaelisa, Peters, Ulrike, Absher, Devin, Hsiung, Chao A, Lee, Wen-Jane, Taylor, Kent D, Chen, Ying-Hsiang, Lee, I-Te, Guo, Xiuqing, Chung, Ren-Hua, Hung, Yi-Jen, Rotter, Jerome I, Juang, Jyh-Ming J, Quertermous, Thomas, Wang, Tzung-Dau, Rasheed, Asif, Frossard, Philippe, Alam, Dewan S, Majumder, Abdulla al Shafi, Di Angelantonio, Emanuele, Chowdhury, Rajiv, Chen, Yii-Der Ida, Nordestgaard, Børge G, Assimes, Themistocles L, Danesh, John, Butterworth, Adam S, Saleheen, Danish

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Investigating the genetic architecture of dementia with Lewy bodies: a two-stage genome-wide association study von Guerreiro, Rita, Ross, Owen A, Kun-Rodrigues, Celia, Hernandez, Dena G, Orme, Tatiana, Eicher, John D, Shepherd, Claire E, Parkkinen, Laura, Darwent, Lee, Heckman, Michael G, Scholz, Sonja W, Troncoso, Juan C, Pletnikova, Olga, Ansorge, Olaf, Clarimon, Jordi, Lleo, Alberto, Morenas-Rodriguez, Estrella, Clark, Lorraine, Honig, Lawrence S, Marder, Karen, Lemstra, Afina, Rogaeva, Ekaterina, St George-Hyslop, Peter, Londos, Elisabet, Zetterberg, Henrik, Barber, Imelda, Braae, Anne, Brown, Kristelle, Morgan, Kevin, Troakes, Claire, Al-Sarraj, Safa, Lashley, Tammaryn, Holton, Janice, Compta, Yaroslau, Van Deerlin, Vivianna, Serrano, Geidy E, Beach, Thomas G, Lesage, Suzanne, Galasko, Douglas, Masliah, Eliezer, Santana, Isabel, Pastor, Pau, Diez-Fairen, Monica, Aguilar, Miquel, Tienari, Pentti J, Myllykangas, Liisa, Oinas, Minna, Revesz, Tamas, Lees, Andrew, Boeve, Brad F, Petersen, Ronald C, Ferman, Tanis J, Escott-Price, Valentina, Graff-Radford, Neill, Cairns, Nigel J, Morris, John C, Pickering-Brown, Stuart, Mann, David, Halliday, Glenda M, Hardy, John, Trojanowski, John Q, Dickson, Dennis W, Singleton, Andrew, Stone, David J, Bras, Jose

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Imaging-genetics in dyslexia: Connecting risk genetic variants to brain neuroimaging and ultimately to reading impairments von Eicher, John D., Gruen, Jeffrey R.

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Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation von Chu, Audrey Y, Deng, Xuan, Fisher, Virginia A, Drong, Alexander, Zhang, Yang, Feitosa, Mary F, Liu, Ching-Ti, Weeks, Olivia, Choh, Audrey C, Duan, Qing, Dyer, Thomas D, Eicher, John D, Guo, Xiuqing, Heard-Costa, Nancy L, Kacprowski, Tim, Kent, Jack W, Lange, Leslie A, Liu, Xinggang, Lohman, Kurt, Lu, Lingyi, Mahajan, Anubha, O'Connell, Jeffrey R, Parihar, Ankita, Peralta, Juan M, Smith, Albert V, Zhang, Yi, Homuth, Georg, Kissebah, Ahmed H, Kullberg, Joel, Laqua, René, Launer, Lenore J, Nauck, Matthias, Olivier, Michael, Peyser, Patricia A, Terry, James G, Wojczynski, Mary K, Yao, Jie, Bielak, Lawrence F, Blangero, John, Borecki, Ingrid B, Bowden, Donald W, Carr, John Jeffrey, Czerwinski, Stefan A, Ding, Jingzhong, Friedrich, Nele, Gudnason, Vilmunder, Harris, Tamara B, Ingelsson, Erik, Johnson, Andrew D, Kardia, Sharon L R, Langefeld, Carl D, Lind, Lars, Liu, Yongmei, Mitchell, Braxton D, Morris, Andrew P, Mosley, Thomas H, Rotter, Jerome I, Shuldiner, Alan R, Towne, Bradford, Völzke, Henry, Wallaschofski, Henri, Wilson, James G, Allison, Matthew, Lindgren, Cecilia M, Goessling, Wolfram, Cupples, L Adrienne, Steinhauser, Matthew L, Fox, Caroline S

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Language Impairment and Dyslexia Genes Influence Language Skills in Children With Autism Spectrum Disorders von Eicher, John D., Gruen, Jeffrey R.

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A genome-wide association study identifies new loci for factor VII and implicates factor VII in ischemic stroke etiology von de Vries, Paul S., Sabater-Lleal, Maria, Huffman, Jennifer E., Marten, Jonathan, Song, Ci, Pankratz, Nathan, Bartz, Traci M., de Haan, Hugoline G., Delgado, Graciela E., Eicher, John D., Martinez-Perez, Angel, Ward-Caviness, Cavin K., Brody, Jennifer A., Chen, Ming-Huei, de Maat, Moniek P.M., Frånberg, Mattias, Gill, Dipender, Kleber, Marcus E., Rivadeneira, Fernando, Soria, José Manuel, Tang, Weihong, Tofler, Geoffrey H., Uitterlinden, André G., van Hylckama Vlieg, Astrid, Seshadri, Sudha, Boerwinkle, Eric, Davies, Neil M., Giese, Anne-Katrin, Ikram, M. Kamran, Kittner, Steven J., McKnight, Barbara, Psaty, Bruce M., Reiner, Alex P., Sargurupremraj, Muralidharan, Taylor, Kent D., Fornage, Myriam, Hamsten, Anders, März, Winfried, Rosendaal, Frits R., Souto, Juan Carlos, Dehghan, Abbas, Johnson, Andrew D., Morrison, Alanna C., O’Donnell, Christopher J., Smith, Nicholas L.

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Four Susceptibility Loci for Gallstone Disease Identified in a Meta-analysis of Genome-Wide Association Studies von Joshi, Amit D, Andersson, Charlotte, Buch, Stephan, Stender, Stefan, Noordam, Raymond, Weng, Lu-Chen, Weeke, Peter E, Auer, Paul L, Boehm, Bernhard, Chen, Constance, Choi, Hyon, Curhan, Gary, Denny, Joshua C, De Vivo, Immaculata, Eicher, John D, Ellinghaus, David, Folsom, Aaron R, Fuchs, Charles, Gala, Manish, Haessler, Jeffrey, Hofman, Albert, Hu, Frank, Hunter, David J, Janssen, Harry L.A, Kang, Jae H, Kooperberg, Charles, Kraft, Peter, Kratzer, Wolfgang, Lieb, Wolfgang, Lutsey, Pamela L, Darwish Murad, Sarwa, Nordestgaard, Børge G, Pasquale, Louis R, Reiner, Alex P, Ridker, Paul M, Rimm, Eric, Rose, Lynda M, Shaffer, Christian M, Schafmayer, Clemens, Tamimi, Rulla M, Uitterlinden, André G, Völker, Uwe, Völzke, Henry, Wakabayashi, Yoshiyuki, Wiggs, Janey L, Zhu, Jun, Roden, Dan M, Stricker, Bruno H, Tang, Weihong, Teumer, Alexander, Hampe, Jochen, Tybjærg-Hansen, Anne, Chasman, Daniel I, Chan, Andrew T, Johnson, Andrew D

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Causal Effect of Plasminogen Activator Inhibitor Type 1 on Coronary Heart Disease von Song, Ci, Burgess, Stephen, Eicher, John D, O'Donnell, Christopher J, Johnson, Andrew D

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Replication and hematological characterization of human platelet reactivity genetic associations in men from the Caerphilly Prospective Study (CaPS) von Eicher, John D., Xue, Luting, Ben-Shlomo, Yoav, Beswick, Andrew D., Johnson, Andrew D.

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The regulatory element READ1 epistatically influences reading and language, with both deleterious and protective alleles von Powers, Natalie R, Eicher, John D, Miller, Laura L, Kong, Yong, Smith, Shelley D, Pennington, Bruce F, Willcutt, Erik G, Olson, Richard K, Ring, Susan M, Gruen, Jeffrey R

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Variants in the DYX2 locus are associated with altered brain activation in reading-related brain regions in subjects with reading disability von Cope, Natalie, Eicher, John D., Meng, Haiying, Gibson, Christopher J., Hager, Karl, Lacadie, Cheryl, Fulbright, Robert K., Constable, R. Todd, Page, Grier P., Gruen, Jeffrey R.

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GWAS analysis of handgrip and lower body strength in older adults in the CHARGE consortium von Matteini, Amy M., Tanaka, Toshiko, Karasik, David, Atzmon, Gil, Chou, Wen‐Chi, Eicher, John D., Johnson, Andrew D., Arnold, Alice M., Callisaya, Michele L., Davies, Gail, Evans, Daniel S., Holtfreter, Birte, Lohman, Kurt, Lunetta, Kathryn L., Mangino, Massimo, Smith, Albert V., Smith, Jennifer A., Teumer, Alexander, Yu, Lei, Arking, Dan E., Buchman, Aron S., Chibinik, Lori B., De Jager, Philip L., Evans, Denis A., Faul, Jessica D., Garcia, Melissa E., Gillham‐Nasenya, Irina, Gudnason, Vilmundur, Hofman, Albert, Hsu, Yi‐Hsiang, Ittermann, Till, Lahousse, Lies, Liewald, David C., Liu, Yongmei, Lopez, Lorna, Rivadeneira, Fernando, Rotter, Jerome I., Siggeirsdottir, Kristin, Starr, John M., Thomson, Russell, Tranah, Gregory J., Uitterlinden, André G., Völker, Uwe, Völzke, Henry, Weir, David R., Yaffe, Kristine, Zhao, Wei, Zhuang, Wei Vivian, Zmuda, Joseph M., Bennett, David A., Cummings, Steven R., Deary, Ian J., Ferrucci, Luigi, Harris, Tamara B., Kardia, Sharon L. R., Kocher, Thomas, Kritchevsky, Stephen B., Psaty, Bruce M., Seshadri, Sudha, Spector, Timothy D., Srikanth, Velandai K., Windham, B. Gwen, Zillikens, M. Carola, Newman, Anne B., Walston, Jeremy D., Kiel, Douglas P., Murabito, Joanne M.

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Meta-analysis of rare and common exome chip variants identifies S1PR4 and other loci influencing blood cell traits von Pankratz, Nathan, Schick, Ursula M, Zhou, Yi, Zhou, Wei, Ahluwalia, Tarunveer Singh, Allende, Maria Laura, Auer, Paul L, Bork-Jensen, Jette, Brody, Jennifer A, Chen, Ming-Huei, Clavo, Vinna, Eicher, John D, Grarup, Niels, Hagedorn, Elliott J, Hu, Bella, Hunker, Kristina, Johnson, Andrew D, Leusink, Maarten, Lu, Yingchang, Lyytikäinen, Leo-Pekka, Manichaikul, Ani, Marioni, Riccardo E, Nalls, Mike A, Pazoki, Raha, Smith, Albert Vernon, van Rooij, Frank J A, Yang, Min-Lee, Zhang, Xiaoling, Zhang, Yan, Asselbergs, Folkert W, Boerwinkle, Eric, Borecki, Ingrid B, Bottinger, Erwin P, Cushman, Mary, de Bakker, Paul I W, Deary, Ian J, Dong, Liguang, Feitosa, Mary F, Floyd, James S, Franceschini, Nora, Franco, Oscar H, Garcia, Melissa E, Grove, Megan L, Gudnason, Vilmundur, Hansen, Torben, Harris, Tamara B, Hofman, Albert, Jackson, Rebecca D, Jia, Jia, Kähönen, Mika, Launer, Lenore J, Lehtimäki, Terho, Liewald, David C, Linneberg, Allan, Liu, Yongmei, Loos, Ruth J F, Nguyen, Vy M, Numans, Mattijs E, Pedersen, Oluf, Psaty, Bruce M, Raitakari, Olli T, Rich, Stephen S, Rivadeneira, Fernando, Di Sant, Amanda M Rosa, Rotter, Jerome I, Starr, John M, Taylor, Kent D, Thuesen, Betina Heinsbæk, Tracy, Russell P, Uitterlinden, Andre G, Wang, Jiansong, Wang, Judy, Dehghan, Abbas, Huo, Yong, Cupples, L Adrienne, Wilson, James G, Proia, Richard L, Zon, Leonard I, O'Donnell, Christopher J, Reiner, Alex P, Ganesh, Santhi K

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A comprehensive screening of copy number variability in dementia with Lewy bodies von Kun-Rodrigues, Celia, Orme, Tatiana, Carmona, Susana, Hernandez, Dena G., Ross, Owen A., Eicher, John D., Shepherd, Claire, Parkkinen, Laura, Darwent, Lee, Heckman, Michael G., Scholz, Sonja W., Troncoso, Juan C., Pletnikova, Olga, Dawson, Ted, Rosenthal, Liana, Ansorge, Olaf, Clarimon, Jordi, Lleo, Alberto, Morenas-Rodriguez, Estrella, Clark, Lorraine, Honig, Lawrence S., Marder, Karen, Lemstra, Afina, Rogaeva, Ekaterina, St. George-Hyslop, Peter, Londos, Elisabet, Zetterberg, Henrik, Barber, Imelda, Braae, Anne, Brown, Kristelle, Morgan, Kevin, Troakes, Claire, Al-Sarraj, Safa, Lashley, Tammaryn, Holton, Janice, Compta, Yaroslau, Van Deerlin, Vivianna, Serrano, Geidy E., Beach, Thomas G., Lesage, Suzanne, Galasko, Douglas, Masliah, Eliezer, Santana, Isabel, Pastor, Pau, Diez-Fairen, Monica, Aguilar, Miquel, Tienari, Pentti J., Myllykangas, Liisa, Oinas, Minna, Revesz, Tamas, Lees, Andrew, Boeve, Brad F., Petersen, Ronald C., Ferman, Tanis J., Escott-Price, Valentina, Graff-Radford, Neill, Cairns, Nigel J., Morris, John C., Pickering-Brown, Stuart, Mann, David, Halliday, Glenda M., Hardy, John, Trojanowski, John Q., Dickson, Dennis W., Singleton, Andrew, Stone, David J., Guerreiro, Rita, Bras, Jose

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Characterization of the DYX2 locus on chromosome 6p22 with reading disability, language impairment, and IQ von Eicher, John D., Powers, Natalie R., Miller, Laura L., Mueller, Kathryn L., Mascheretti, Sara, Marino, Cecilia, Willcutt, Erik G., DeFries, John C., Olson, Richard K., Smith, Shelley D., Pennington, Bruce F., Tomblin, J. Bruce, Ring, Susan M., Gruen, Jeffrey R.

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