Targeted resequencing identifies defective variants of decoy receptor 3 in pediatric-onset inflammatory bowel disease von Cardinale, C J, Wei, Z, Panossian, S, Wang, F, Kim, C E, Mentch, F D, Chiavacci, R M, Kachelries, K E, Pandey, R, Grant, S F A, Baldassano, R N, Hakonarson, H

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Trans-ancestral genome-wide association study of longitudinal pubertal height growth and shared heritability with adult health outcomes von JP Bradfield, RL Kember, A Ulrich, Z Balkiyarova, A Alyass, IM Aris, JA Bell, KA Broadaway, Z Chen, JF Chai, NM Davies, D Fernandez-Orth, M Bustamante, R Fore, A Ganguli, A Heiskala, JJ Hottenga, C Íñiguez, S Kobes, J Leinonen, E Lowry, LP Lyytikainen, A Mahajan, N Pitkänen, TM Schnurr, CT Have, DP Strachan, E Thiering, S Vogelezang, KH Wade, CA Wang, A Wong, LA Holm, A Chesi, C Choong, M Cruz, P Elliott, S Franks, C Frithioff-Bøjsøe, WJ Gauderman, JT Glessner, V Gilsanz, K Griesman, RL Hanson, M Kaakinen, H Kalkwarf, A Kelly, J Kindler, M Kähönen, C Lanca, J Lappe, NR Lee, S McCormack, FD Mentch, JA Mitchell, N Mononen, H Niinikoski, E Oken, K Pahkala, X Sim, YY Teo, LJ Baier, T van Beijsterveldt, LS Adair, DI Boomsma, E de Geus, M Guxens, JG Eriksson, JF Felix, FD Gilliland, PM Biobank, T Hansen, Rebecca Hardy, MF Hivert, JC Holm, VWV Jaddoe, MR Järvelin, T Lehtimäki, DA Mackey, D Meyre, KL Mohlke, J Mykkänen, S Oberfield, CE Pennell, JRB Perry, O Raitakari, F Rivadeneira, SM Saw, S Sebert, JA Shepherd, M Standl, TIA Sørensen, NJ Timpson, M Torrent, G Willemsen, E Hypponen, C Power, MI McCarthy, RM Freathy, E Widén

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A genome-wide meta-analysis of six type 1 diabetes cohorts identifies multiple associated loci von Bradfield, Jonathan P, Qu, Hui-Qi, Wang, Kai, Zhang, Haitao, Sleiman, Patrick M, Kim, Cecilia E, Mentch, Frank D, Qiu, Haijun, Glessner, Joseph T, Thomas, Kelly A, Frackelton, Edward C, Chiavacci, Rosetta M, Imielinski, Marcin, Monos, Dimitri S, Pandey, Rahul, Bakay, Marina, Grant, Struan F A, Polychronakos, Constantin, Hakonarson, Hakon

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Common variants in MMP20 at 11q22.2 predispose to 11q deletion and neuroblastoma risk von Chang, Xiao, Zhao, Yan, Hou, Cuiping, Glessner, Joseph, McDaniel, Lee, Diamond, Maura A., Thomas, Kelly, Li, Jin, Wei, Zhi, Liu, Yichuan, Guo, Yiran, Mentch, Frank D., Qiu, Haijun, Kim, Cecilia, Evans, Perry, Vaksman, Zalman, Diskin, Sharon J., Attiyeh, Edward F., Sleiman, Patrick, Maris, John M., Hakonarson, Hakon

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GWAS of blood cell traits identifies novel associated loci and epistatic interactions in Caucasian and African-American children von Li, Jin, Glessner, Joseph T, Zhang, Haitao, Hou, Cuiping, Wei, Zhi, Bradfield, Jonathan P, Mentch, Frank D, Guo, Yiran, Kim, Cecilia, Xia, Qianghua, Chiavacci, Rosetta M, Thomas, Kelly A, Qiu, Haijun, Grant, Struan F A, Furth, Susan L, Hakonarson, Hakon, Sleiman, Patrick M A

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Genome-wide Modeling of Polygenic Risk Score in Colorectal Cancer Risk von Thomas, Minta, Sakoda, Lori C., Hoffmeister, Michael, Rosenthal, Elisabeth A., Lee, Jeffrey K., van Duijnhoven, Franzel J.B., Platz, Elizabeth A., Wu, Anna H., Dampier, Christopher H., de la Chapelle, Albert, Wolk, Alicja, Joshi, Amit D., Burnett-Hartman, Andrea, Gsur, Andrea, Lindblom, Annika, Castells, Antoni, Win, Aung Ko, Namjou, Bahram, Van Guelpen, Bethany, Tangen, Catherine M., He, Qianchuan, Li, Christopher I., Schafmayer, Clemens, Joshu, Corinne E., Ulrich, Cornelia M., Bishop, D. Timothy, Buchanan, Daniel D., Schaid, Daniel, Drew, David A., Muller, David C., Duggan, David, Crosslin, David R., Albanes, Demetrius, Giovannucci, Edward L., Larson, Eric, Qu, Flora, Mentch, Frank, Giles, Graham G., Hakonarson, Hakon, Hampel, Heather, Stanaway, Ian B., Figueiredo, Jane C., Huyghe, Jeroen R., Minnier, Jessica, Chang-Claude, Jenny, Hampe, Jochen, Harley, John B., Visvanathan, Kala, Curtis, Keith R., Offit, Kenneth, Li, Li, Le Marchand, Loic, Vodickova, Ludmila, Gunter, Marc J., Jenkins, Mark A., Slattery, Martha L., Lemire, Mathieu, Woods, Michael O., Song, Mingyang, Murphy, Neil, Lindor, Noralane M., Dikilitas, Ozan, Pharoah, Paul D.P., Campbell, Peter T., Newcomb, Polly A., Milne, Roger L., MacInnis, Robert J., Castellví-Bel, Sergi, Ogino, Shuji, Berndt, Sonja I., Bézieau, Stéphane, Thibodeau, Stephen N., Gallinger, Steven J., Zaidi, Syed H., Harrison, Tabitha A., Keku, Temitope O., Hudson, Thomas J., Vymetalkova, Veronika, Moreno, Victor, Martín, Vicente, Arndt, Volker, Wei, Wei-Qi, Chung, Wendy, Su, Yu-Ru, Hayes, Richard B., White, Emily, Vodicka, Pavel, Casey, Graham, Gruber, Stephen B., Schoen, Robert E., Chan, Andrew T., Potter, John D., Brenner, Hermann, Jarvik, Gail P., Corley, Douglas A., Peters, Ulrike, Hsu, Li

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A genome-wide association meta-analysis of diarrhoeal disease in young children identifies FUT2 locus and provides plausible biological pathways von Bustamante, Mariona, Standl, Marie, Bassat, Quique, Vilor-Tejedor, Natalia, Medina-Gomez, Carolina, Bonilla, Carolina, Ahluwalia, Tarunveer S, Bacelis, Jonas, Bradfield, Jonathan P, Tiesler, Carla M T, Rivadeneira, Fernando, Ring, Susan, Vissing, Nadja H, Fink, Nadia R, Jugessur, Astanand, Mentch, Frank D, Ballester, Ferran, Kriebel, Jennifer, Kiefte-de Jong, Jessica C, Wolsk, Helene M, Llop, Sabrina, Thiering, Elisabeth, Beth, Systke A, Timpson, Nicholas J, Andersen, Josefine, Schulz, Holger, Jaddoe, Vincent W V, Evans, David M, Waage, Johannes, Hakonarson, Hakon, Grant, Struan F A, Jacobsson, Bo, Bønnelykke, Klaus, Bisgaard, Hans, Davey Smith, George, Moll, Henriette A, Heinrich, Joachim, Estivill, Xavier, Sunyer, Jordi

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The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism von Hadley, Dexter, Wu, Zhi-liang, Kao, Charlly, Kini, Akshata, Mohamed-Hadley, Alisha, Thomas, Kelly, Vazquez, Lyam, Qiu, Haijun, Mentch, Frank, Pellegrino, Renata, Kim, Cecilia, Connolly, John, Glessner, Joseph, Hakonarson, Hakon

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Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder von Elia, Josephine, Glessner, Joseph T, Wang, Kai, Takahashi, Nagahide, Shtir, Corina J, Hadley, Dexter, Sleiman, Patrick M A, Zhang, Haitao, Kim, Cecilia E, Robison, Reid, Lyon, Gholson J, Flory, James H, Bradfield, Jonathan P, Imielinski, Marcin, Hou, Cuiping, Frackelton, Edward C, Chiavacci, Rosetta M, Sakurai, Takeshi, Rabin, Cara, Middleton, Frank A, Thomas, Kelly A, Garris, Maria, Mentch, Frank, Freitag, Christine M, Steinhausen, Hans-Christoph, Todorov, Alexandre A, Reif, Andreas, Rothenberger, Aribert, Franke, Barbara, Mick, Eric O, Roeyers, Herbert, Buitelaar, Jan, Lesch, Klaus-Peter, Banaschewski, Tobias, Ebstein, Richard P, Mulas, Fernando, Oades, Robert D, Sergeant, Joseph, Sonuga-Barke, Edmund, Renner, Tobias J, Romanos, Marcel, Romanos, Jasmin, Warnke, Andreas, Walitza, Susanne, Meyer, Jobst, Pálmason, Haukur, Seitz, Christiane, Loo, Sandra K, Smalley, Susan L, Biederman, Joseph, Kent, Lindsey, Asherson, Philip, Anney, Richard J L, Gaynor, J William, Shaw, Philip, Devoto, Marcella, White, Peter S, Grant, Struan F A, Buxbaum, Joseph D, Rapoport, Judith L, Williams, Nigel M, Nelson, Stanley F, Faraone, Stephen V, Hakonarson, Hakon

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Minority-centric meta-analyses of blood lipid levels identify novel loci in the Population Architecture using Genomics and Epidemiology von Hu, Yao, Graff, Mariaelisa, Haessler, Jeffrey, Buyske, Steven, Bien, Stephanie A, Tao, Ran, Highland, Heather M, Nishimura, Katherine K, Zubair, Niha, Lu, Yingchang, Verbanck, Marie, Hilliard, Austin T, Klarin, Derek, Damrauer, Scott M, Ho, Yuk-Lam, Wilson, Peter W. F, Chang, Kyong-Mi, Tsao, Philip S, Cho, Kelly, O'Donnell, Christopher J, Assimes, Themistocles L, Petty, Lauren E, Below, Jennifer E, Dikilitas, Ozan, Schaid, Daniel J, Kosel, Matthew L, Kullo, Iftikhar J, Rasmussen-Torvik, Laura J, Jarvik, Gail P, Feng, Qiping, Wei, Wei-Qi, Larson, Eric B, Mentch, Frank D, Almoguera, Berta, Sleiman, Patrick M, Raffield, Laura M, Correa, Adolfo, Martin, Lisa W, Daviglus, Martha, Matise, Tara C, Ambite, Jose Luis, Carlson, Christopher S, Do, Ron, Loos, Ruth J. F, Wilkens, Lynne R, Le Marchand, Loic, Haiman, Chris, Stram, Daniel O, Hindorff, Lucia A, North, Kari E, Kooperberg, Charles, Cheng, Iona, Peters, Ulrike, Barsh, Gregory S

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Common variants at 12q15 and 12q24 are associated with infant head circumference von Taal, H Rob, St Pourcain, Beate, Thiering, Elisabeth, Das, Shikta, Mook-Kanamori, Dennis O, Warrington, Nicole M, Kaakinen, Marika, Kreiner-Moeller, Eskil, Bradfield, Jonathan P, Freathy, Rachel M, Geller, Frank, Guxens, Monica, Cousminer, Diana L, Kerkhof, Marjan, Timpson, Nicholas J, Ikram, M Arfan, Beilin, Lawrence J, Boennelykke, Klaus, Buxton, Jessica L, Charoen, Pimphen, Chawes, Bo Lund Krogsgaard, Eriksson, Johan, Evans, David M, Hofman, Albert, Kemp, John P, Kim, Cecilia E, Klopp, Norman, Lahti, Jari, Lye, Stephen J, McMahon, George, Mentch, Frank D, Mueller-Nurasyid, Martina, O'Reilly, Paul F, Prokopenko, Inga, Rivadeneira, Fernando, Steegers, Eric A P, Sunyer, Jordi, Tiesler, Carla, Yaghootkar, Hanieh, nage, Myriam, Smith, Albert V, Seshadri, Sudha, Schmidt, Reinhold, Debette, Stephanie, Vrooman, Henri A, Sigurdsson, Sigurdur, Ropele, Stefan, Coker, Laura H, Longstreth, W T, et. al

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Erratum: Common variants at 12q15 and 12q24 are associated with infant head circumference von Taal, H Rob, St Pourcain, Beate, Thiering, Elisabeth, Das, Shikta, Mook-Kanamori, Dennis O, Warrington, Nicole M, Kaakinen, Marika, Kreiner-Møller, Eskil, Bradfield, Jonathan P, Freathy, Rachel M, Geller, Frank, Guxens, Mònica, Cousminer, Diana L, Kerkhof, Marjan, Timpson, Nicholas J, Ikram, M Arfan, Beilin, Lawrence J, Bønnelykke, Klaus, Buxton, Jessica L, Charoen, Pimphen, Chawes, Bo Lund Krogsgaard, Eriksson, Johan, Evans, David M, Hofman, Albert, Kemp, John P, Kim, Cecilia E, Klopp, Norman, Lahti, Jari, Lye, Stephen J, McMahon, George, Mentch, Frank D, Müller-Nurasyid, Martina, O'Reilly, Paul F, Prokopenko, Inga, Rivadeneira, Fernando, Steegers, Eric A P, Sunyer, Jordi, Tiesler, Carla, Yaghootkar, Hanieh, Breteler, Monique M B, Debette, Stéphanie, Fornage, Myriam, Gudnason, Vilmundur, Launer, Lenore J, van der Lugt, Aad, Mosley, Thomas H, Seshadri, Sudha, Smith, Albert V, Vernooij, Meike W, Blakemore, Alexandra I F, Chiavacci, Rosetta M, Feenstra, Bjarke, Fernandez-Banet, Julio, Grant, Struan F A, Hartikainen, Anna-Liisa, van der Heijden, Albert J, Iñiguez, Carmen, Lathrop, Mark, McArdle, Wendy L, Mølgaard, Anne, Newnham, John P, Palmer, Lyle J, Palotie, Aarno, Pouta, Annneli, Ring, Susan M, Sovio, Ulla, Standl, Marie, Uitterlinden, Andre G, Wichmann, H-Erich, Vissing, Nadja Hawwa, DeCarli, Charles, van Duijn, Cornelia M, McCarthy, Mark I, Koppelman, Gerard H, Estivill, Xavier, Hattersley, Andrew T, Melbye, Mads, Bisgaard, Hans, Pennell, Craig E, Widen, Elisabeth, Hakonarson, Hakon, Smith, George Davey, Heinrich, Joachim, Jarvelin, Marjo-Riitta, Jaddoe, Vincent W V

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Common variants at 12ql5 and 12q24 are associated with infant head circumference von TAAL, H. Rob, ST POURCAIN, Beate, GELLER, Frank, GUXENS, Monica, COUSMINER, Diana L, KERKHOF, Marjan, TIMPSON, Nicholas J, IKRAM, Marfan, BEILIN, Lawrence J, BONNELYKKE, Klaus, BUXTON, Jessica L, CHAROEN, Pimphen, THIERING, Elisabeth, CHAWES, Bo Lund Krogsgaard, ERIKSSON, Johan, EVANS, David M, HOFMAN, Albert, KEMP, John P, KIM, Cecilia E, KLOPP, Norman, LAHTI, Jari, LYE, Stephen J, MCMAHON, George, DAS, Shikta, MENTCH, Frank D, MÜLLER-NURASYID, Martina, O'REILLY, Paul F, PROKOPENKO, Inga, RIVADENEIRA, Fernando, STEEGERS, Eric A. P, SUNYER, Jordi, TIESLER, Carla, YAGHOOTKAR, Hanieh, BRETELER, Monique M. B, MOOK-KANAMORI, Dennis O, DEBETTE, Stephanie, FORNAGE, Myriam, GUDNASON, Vilmundur, LAUNER, Lenore J, DER LUGT, Aad Van, MOSLEY, Thomas H, SESHADRI, Sudha, SMITH, Albert V, VERNOOIJ, Meike W, BLAKEMORE, Alexandra I. F, WARRINGTON, Nicole M, CHIAVACCI, Rosetta M, FEENSTRA, Bjarke, FERNANDEZ-BANET, Julio, GRANT, Struan F. A, HARTIKAINEN, Anna-Liisa, DER HEIJDEN, Albert J.van, INIGUEZ, Carmen, LATHROP, Mark, MCARDLE, Wendyl, KAAKINEN, Marika, KREINER-MOLLER, Eskil, BRADFIELD, Jonathan P, FREATHY, Rachel M

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Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis von Paternoster, L, Standl, M, Chen, CM, Ramasamy, A, Bonnelykke, K, Duijts, L, Ferreira, MA, Alves, AC, Thyssen, JP, Albrecht, E, Baurecht, H, Feenstra, B, Sleiman, PM, Hysi, P, Warrington, NM, Curjuric, I, Myhre, R, Curtin, JA, Groen-Blokhuis, MM, Kerkhof, M, Saaf, A, Franke, A, Ellinghaus, D, Folster-Holst, R, Dermitzakis, E, Montgomery, SB, Prokisch, H, Heim, K, Hartikainen, AL, Pouta, A, Pekkanen, J, Blakemore, AI, Buxton, JL, Kaakinen, M, Duffy, DL, Madden, PA, Heath, AC, Montgomery, GW, Thompson, PJ, Matheson, MC, Le Souef, P, St Pourcain, B, Smith, GD, Henderson, J, Kemp, JP, Timpson, NJ, Deloukas, P, Ring, SM, Wichmann, HE, Muller-Nurasyid, M, Novak, N, Klopp, N, Rodriguez, E, McArdle, W, Linneberg, A, Menne, T, Nohr, EA, Hofman, A, Uitterlinden, AG, Van Duijn, CM, Rivadeneira, F, De Jongste, JC, Van der Valk, RJ, Wjst, M, Jogi, R, Geller, F, Boyd, HA, Murray, JC, Kim, C, Mentch, F, March, M, Mangino, M, Spector, TD, Bataille, V, Pennell, CE, Holt, PG, Sly, P, Tiesler, CM, Thiering, E, Illig, T, Imboden, M, Nystad, W, Simpson, A, Hottenga, JJ, Postma, D, Koppelman, GH, Smit, HA, Soderhall, C, Chawes, B, Kreiner-Moller, E, Bisgaard, H, Melen, E, Boomsma, DI, Custovic, A, Jacobsson, B, Probst-Hensch, NM, Palmer, LJ, Glass, D, Hakonarson, H, Melbye, M

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A kinetic isotope effect study and transition state analysis of the S-adenosylmethionine synthetase reaction von Markham, G.D., Parkin, D.W., Mentch, F., Schramm, V.L.

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Author Correction: Trans-ancestral genome-wide association study of longitudinal pubertal height growth and shared heritability with adult health outcomes von Bradfeld, Jonathan P, Kember, Rachel L, Ulrich, Anna, Balkhiyarova, Zhanna, Alyass, Akram, Aris, Izzuddin M, Bell, Joshua A, Broadaway, K. Alaine, Chen, Zhanghua, Chai, Jin-Fang, Davies, Neil M, Fernandez-Orth, Dietmar, Bustamante, Mariona, Fore, Ruby, Ganguli, Amitavo, Heiskala, Anni, Hottenga, Jouke-Jan, Íñiguez, Carmen, Kobes, Sayuko, Leinonen, Jaakko, Lowry, Estelle, Lyytikainen, Leo-Pekka, Mahajan, Anubha, Pitkänen, Niina, Schnurr, Theresia M, Have, Christian Theil, Strachan, David P, Thiering, Elisabeth, Vogelezang, Suzanne, Wade, Kaitlin H, Wang, Carol A, Wong, Andrew, Holm, Louise Aas, Chesi, Alessandra, Choong, Catherine, Cruz, Miguel, Elliott, Paul, Franks, Steve, Frithiof-Bøjsøe, Christine, Gauderman, W. James, Gilsanz, Vicente, Griesman, Kendra, Hanson, Robert L, Kaakinen, Marika, Kalkwarf, Heidi, Kelly, Andrea, Kindler, Joseph, Kähönen, Mika, Lanca, Carla, Lappe, Joan, Lee, Nanette R, McCormack, Shana, Mentch, Frank D, Mitchell, Jonathan A, Mononen, Nina, Niinikoski, Harri, Oken, Emily, Pahkala, Katja, Sim, Xueling, Baier, Leslie J, van Beijsterveldt, Toos, Adair, Linda S, Boomsma, Dorret I, de Geus, Eco, Guxens, Mònica, Eriksson, Johan G, Felix, Janine F, Gilliland, Frank D, Hansen, Torben, Hardy, Rebecca, Holm, Jens-Christian, Jaddoe, Vincent W. V, Järvelin, Marjo-Riitta, Lehtimäki, Terho, Mackey, David A, Mohlke, Karen L, Mykkänen, Juha, Oberfeld, Sharon, Pennell, Craig E, Perry, John R. B, Raitakari, Olli, Rivadeneira, Fernando, Saw, Seang-Mei, Sebert, Sylvain, Shepherd, John A, Standl, Marie, Sørensen, Thorkild I. A, Timpson, Nicholas J, Torrent, Maties, Willemsen, Gonneke, Hypponen, Elina, Power, Chris, McCarthy, Mark I, Widén, Elisabeth, Hakonarson, Hakon, Prokopenko, Inga, Voight, Benjamin F, Zemel, Babette S, Grant, Struan F. A, Cousminer, Diana L

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Transition-state analysis of a Vmax mutant of AMP nucleosidase by the application of heavy-atom kinetic isotope effects von Parkin, David W, Mentch, Frank, Banks, Grace A, Horenstein, Benjamin A, Schramm, Vern L

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