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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Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases von Li, Yun R, Li, Jin, Zhao, Sihai D, Bradfield, Jonathan P, Mentch, Frank D, Maggadottir, S Melkorka, Hou, Cuiping, Abrams, Debra J, Chang, Diana, Gao, Feng, Guo, Yiran, Wei, Zhi, Connolly, John J, Cardinale, Christopher J, Bakay, Marina, Glessner, Joseph T, Li, Dong, Kao, Charlly, Thomas, Kelly A, Qiu, Haijun, Chiavacci, Rosetta M, Kim, Cecilia E, Wang, Fengxiang, Snyder, James, Richie, Marylyn D, Flatø, Berit, Førre, Øystein, Denson, Lee A, Thompson, Susan D, Becker, Mara L, Guthery, Stephen L, Latiano, Anna, Perez, Elena, Resnick, Elena, Russell, Richard K, Wilson, David C, Silverberg, Mark S, Annese, Vito, Lie, Benedicte A, Punaro, Marilynn, Dubinsky, Marla C, Monos, Dimitri S, Strisciuglio, Caterina, Staiano, Annamaria, Miele, Erasmo, Kugathasan, Subra, Ellis, Justine A, Munro, Jane E, Sullivan, Kathleen E, Wise, Carol A, Chapel, Helen, Cunningham-Rundles, Charlotte, Grant, Struan F A, Orange, Jordan S, Sleiman, Patrick M A, Behrens, Edward M, Griffiths, Anne M, Satsangi, Jack, Finkel, Terri H, Keinan, Alon, Prak, Eline T Luning, Polychronakos, Constantin, Baldassano, Robert N, Li, Hongzhe, Keating, Brendan J, Hakonarson, Hakon

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genome-wide association study identifies KIAA0350 as a type 1 diabetes gene von HAKONARSON, Hakon, GRANT, Struan F. A, LAWSON, Margaret L, ROBINSON, Luke J, SKRABAN, Robert, YANG LU, CHIAVACCI, Rosetta M, STANLEY, Charles A, KIRSCH, Susan E, RAPPAPORT, Eric F, ORANGE, Jordan S, MONOS, Dimitri S, BRADFIELD, Jonathan P, DEVOTO, Marcella, QU, Hui-Qi, POLYCHRONAKOS, Constantin, MARCHAND, Luc, KIM, Cecilia E, GLESSNER, Joseph T, GRABS, Rosemarie, CASALUNOVO, Tracy, TABACK, Shayne P, FRACKELTON, Edward C

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A Genome-Wide Association Study Identifies a Locus for Nonsyndromic Cleft Lip with or without Cleft Palate on 8q24 von Grant, Struan F.A., PhD, Wang, Kai, PhD, Zhang, Haitao, PhD, Glaberson, Wendy, BA, Annaiah, Kiran, MSc, Kim, Cecilia E., BA, Bradfield, Jonathan P., BS, Glessner, Joseph T., MSc, Thomas, Kelly A., BA, Garris, Maria, BA, Frackelton, Edward C., BA, Otieno, F. George, MSc, Chiavacci, Rosetta M., BSN, Nah, Hyun-Duck, PhD, Kirschner, Richard E., MD, Hakonarson, Hakon, MD, PhD

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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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The Role of Obesity-associated Loci Identified in Genome-wide Association Studies in the Determination of Pediatric BMI von Zhao, Jianhua, Bradfield, Jonathan P., Li, Mingyao, Wang, Kai, Zhang, Haitao, Kim, Cecilia E., Annaiah, Kiran, Glessner, Joseph T., Thomas, Kelly, Garris, Maria, Frackelton, Edward C., Otieno, F. George, Shaner, Julie L., Smith, Ryan M., Chiavacci, Rosetta M., Berkowitz, Robert I., Hakonarson, Hakon, Grant, Struan F.A.

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Association analysis of the FTO gene with obesity in children of Caucasian and African ancestry reveals a common tagging SNP von Grant, Struan F A, Li, Mingyao, Bradfield, Jonathan P, Kim, Cecilia E, Annaiah, Kiran, Santa, Erin, Glessner, Joseph T, Casalunovo, Tracy, Frackelton, Edward C, Otieno, F George, Shaner, Julie L, Smith, Ryan M, Imielinski, Marcin, Eckert, Andrew W, Chiavacci, Rosetta M, Berkowitz, Robert I, Hakonarson, Hakon

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Follow-Up Analysis of Genome-Wide Association Data Identifies Novel Loci for Type 1 Diabetes von GRANT, Struan F. A, QU, Hui-Qi, ANNAIAH, Kiran, LAWSON, Margaret L, OTIENO, F. George, SANTA, Erin, SHANER, Julie L, SMITH, Ryan M, SKRABAN, Robert, IMIELINSKI, Marcin, CHIAVACCI, Rosetta M, GRUNDMEIER, Robert W, BRADFIELD, Jonathan P, STANLEY, Charles A, KIRSCH, Susan E, WAGGOTT, Daryl, PATERSON, Andrew D, MONOS, Dimitri S, POLYCHRONAKOS, Constantin, HAKONARSON, Hakon, MARCHAND, Luc, KIM, Cecilia E, GLESSNER, Joseph T, GRABS, Rosemarie, TABACK, Shayne P, FRACKELTON, Edward C, ECKERT, Andrew W

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An MRI study of neurological injury before and after congenital heart surgery von Mahle, William T, Tavani, Federica, Zimmerman, Robert A, Nicolson, Susan C, Galli, Kristin K, Gaynor, J William, Clancy, Robert R, Montenegro, Lisa M, Spray, Thomas L, Chiavacci, Rosetta M, Wernovsky, Gil, Kurth, C Dean

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A Novel Susceptibility Locus for Type 1 Diabetes on Chr12q13 Identified by a Genome-Wide Association Study von HAKONARSON, Hakon, QU, Hui-Qi, ECKERT, Andrew W, ANNAHIA, Kiran, LAWSON, Margaret L, OTIENO, F. George, SANTA, Erin, SHANER, Julie L, SMITH, Ryan M, ONYIAH, Chioma C, SKRABAN, Robert, CHIAVACCI, Rosetta M, BRADFIELD, Jonathan P, ROBINSON, Luke J, STANLEY, Charles A, KIRSCH, Susan E, DEVOTO, Marcella, MONOS, Dimitri S, GRANT, Struan F. A, POLYCHRONAKOS, Constantin, MARCHAND, Luc, KIM, Cecilia E, GLESSNER, Joseph T, GRABS, Rosemarie, CASALUNOVO, Tracy, TABACK, Shayne P, FRACKELTON, Edward C

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Use of intranasal fentanyl in children undergoing myringotomy and tube placement during halothane and sevoflurane anesthesia von GALINKIN, Jeffrey L, FAZI, Lisa M, CUY, Romulo M, CHIAVACCI, Rosetta M, KURTH, C. Dean, SHAH, Udayan K, JACOBS, Ian N, WATCHA, Mehernoor F

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ORMDL3 variants associated with asthma susceptibility in North Americans of European ancestry von Sleiman, Patrick M.A., PhD, Annaiah, Kiran, MSc, Imielinski, Marcin, MD, PhD, Bradfield, Jonathan P., BS, Kim, Cecilia E., BA, Frackelton, Edward C., BA, Glessner, Joseph T., MSc, Eckert, Andrew W., MSc, Otieno, F. George, MSc, Santa, Erin, BA, Thomas, Kelly, BA, Smith, Ryan M., BA, Glaberson, Wendy, BA, Garris, Maria, BA, Gunnlaugsson, Sigfus, BA, Chiavacci, Rosetta M., MSc, Allen, Julian, MD, Spergel, Jonathan, MD, PhD, Grundmeier, Robert, MD, PhD, Grunstein, Michael M., MD, PhD, Magnusson, Mark, MD, Bisgaard, Hans, MD, Grant, Struan F.A., PhD, Hakonarson, Hakon, MD, PhD

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Examination of Type 2 Diabetes Loci Implicates CDKAL1 as a Birth Weight Gene von JIANHUA ZHAO, MINGYAO LI, OTIENO, F. George, THOMAS, Kelly A, GARRIS, Maria, CUIPING HOU, FRACKELTON, Edward C, CHIAVACCI, Rosetta M, BERKOWITZ, Robert I, HAKONARSON, Hakon, GRANT, Struan F. A, BRADFIELD, Jonathan P, KAI WANG, HAITAO ZHANG, SLEIMAN, Patrick, KIM, Cecilia E, ANNAIAH, Kiran, GLABERSON, Wendy, GLESSNER, Joseph T

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Erratum: A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling von Li, Dong, Chang, Xiao, Connolly, John J., Tian, Lifeng, Liu, Yichuan, Bhoj, Elizabeth J., Robinson, Nora, Abrams, Debra, Li, Yun R., Bradfield, Jonathan P., Kim, Cecilia E., Li, Jin, Wang, Fengxiang, Snyder, James, Lemma, Maria, Hou, Cuiping, Wei, Zhi, Guo, Yiran, Qiu, Haijun, Mentch, Frank D., Thomas, Kelly A., Chiavacci, Rosetta M., Cone, Roger, Li, Bingshan, Sleiman, Patrick A., Hakonarson, Hakon

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The role of height-associated loci identified in genome wide association studies in the determination of pediatric stature von Zhao, Jianhua, Li, Mingyao, Bradfield, Jonathan P, Zhang, Haitao, Mentch, Frank D, Wang, Kai, Sleiman, Patrick M, Kim, Cecilia E, Glessner, Joseph T, Hou, Cuiping, Keating, Brendan J, Thomas, Kelly A, Garris, Maria L, Deliard, Sandra, Frackelton, Edward C, Otieno, F George, Chiavacci, Rosetta M, Berkowitz, Robert I, Hakonarson, Hakon, Grant, Struan F A

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Common variants at 5q22 associate with pediatric eosinophilic esophagitis von Verma, Ritu, Aceves, Seema, Collins, Margaret H, Liacouras, Chris, Sherrill, Joseph D, Martin, Lisa J, Thomas, Kelly, Sleiman, Patrick M A, Spergel, Jonathan M, Franciosi, James P, Grant, Struan F A, Annaiah, Kiran, Hakonarson, Hakon, Brown-Whitehorn, Terri, Putnam, Phil E, Cianferoni, Antonella, Rothenberg, Marc E, Kim, Cecilia, Glessner, Joseph, Frackelton, Edward, Blanchard, Carine, Abonia, J Pablo, Gober, Laura, Chiavacci, Rosetta M

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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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Common variants at five new loci associated with early-onset inflammatory bowel disease von Hakonarson, Hakon, Zhang, Haitao, Grand, Richard, Hou, Cuiping, Silverberg, Mark S, Muise, Aleixo, Stephens, Michael, Annese, Vito, Grundmeier, Robert, Russell, Richard K, Lee, Jessica, Daly, Mark, Griffiths, Anne, Heyman, Melvin B, Latiano, Anna, Kirschner, Barbara, Imielinski, Marcin, Baldassano, Robert N, Cucchiara, Salvatore, Grant, Struan F A, Flory, James H, Monos, Dimitri S, Saeed, Shehzad, Chiavacci, Rosetta M, Bradfield, Jonathan P, Dallapiccola, Bruno, Denson, Lee, Taylor, Kent, McGovern, Dermot, Dubinsky, Marla, Levine, Arie, Castro, Massimo, Abrams, Debra J, Kugathasan, Subra, Otieno, George, Walters, Thomas D, Frackelton, Edward C, Sleiman, Patrick, Van Limbergen, Johan, Wilson, David C, Essers, Jonah, Glessner, Joseph T, Stempak, Joanne, Guthery, Stephen L, Satsangi, Jack, Ferry, George D, Piccoli, David, Wang, Kai, Kim, Cecilia E

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High-resolution mapping and analysis of copy number variations in the human genome: a data resource for clinical and research applications von Shaikh, Tamim H, Gai, Xiaowu, Perin, Juan C, Glessner, Joseph T, Xie, Hongbo, Murphy, Kevin, O'Hara, Ryan, Casalunovo, Tracy, Conlin, Laura K, D'Arcy, Monica, Frackelton, Edward C, Geiger, Elizabeth A, Haldeman-Englert, Chad, Imielinski, Marcin, Kim, Cecilia E, Medne, Livija, Annaiah, Kiran, Bradfield, Jonathan P, Dabaghyan, Elvira, Eckert, Andrew, Onyiah, Chioma C, Ostapenko, Svetlana, Otieno, F George, Santa, Erin, Shaner, Julie L, Skraban, Robert, Smith, Ryan M, Elia, Josephine, Goldmuntz, Elizabeth, Spinner, Nancy B, Zackai, Elaine H, Chiavacci, Rosetta M, Grundmeier, Robert, Rappaport, Eric F, Grant, Struan F A, White, Peter S, Hakonarson, Hakon

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Variants of DENND1B Associated with Asthma in Children von Sleiman, Patrick M.A, Flory, James, Imielinski, Marcin, Bradfield, Jonathan P, Annaiah, Kiran, Willis-Owen, Saffron A.G, Wang, Kai, Rafaels, Nicholas M, Michel, Sven, Bonnelykke, Klaus, Zhang, Haitao, Kim, Cecilia E, Frackelton, Edward C, Glessner, Joseph T, Hou, Cuiping, Otieno, F. George, Santa, Erin, Thomas, Kelly, Smith, Ryan M, Glaberson, Wendy R, Garris, Maria, Chiavacci, Rosetta M, Beaty, Terri H, Ruczinski, Ingo, Orange, Jordan M, Allen, Julian, Spergel, Jonathan M, Grundmeier, Robert, Mathias, Rasika A, Christie, Jason D, von Mutius, Erika, Cookson, William O.C, Kabesch, Michael, Moffatt, Miriam F, Grunstein, Michael M, Barnes, Kathleen C, Devoto, Marcella, Magnusson, Mark, Li, Hongzhe, Grant, Struan F.A, Bisgaard, Hans, Hakonarson, Hakon

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