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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Evaluating the role of the FUS/TLS-related gene EWSR1 in amyotrophic lateral sclerosis von COUTHOUIS, Julien, HART, Michael P, KIM, Cecilia E, FRACKELTON, Edward C, SOLSKI, Jennifer A, WILLIAMS, Kelly L, CLAY-FALCONE, Dana, ELMAN, Lauren, MCCLUSKEY, Leo, GREENE, Robert, HAKONARSON, Hakon, KALB, Robert G, ERION, Renske, LEE, Virginia M. Y, TROJANOWSKI, John Q, NICHOLSON, Garth A, BLAIR, Ian P, BONINI, Nancy M, VAN DEERLIN, Vivianna M, MOURELATOS, Zissimos, SHORTER, James, GITLER, Aaron D, KING, Oliver D, DIAZ, Zamia, NAKAYA, Tadashi, IBRAHIM, Fadia, KIM, Hyung-Jun, MOJSILOVIC-PETROVIC, Jelena, PANOSSIAN, Saarene

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Mutations in PDGFRB Cause Autosomal-Dominant Infantile Myofibromatosis von Martignetti, John A., Tian, Lifeng, Li, Dong, Ramirez, Maria Celeste M., Camacho-Vanegas, Olga, Camacho, Sandra Catalina, Guo, Yiran, Zand, Dina J., Bernstein, Audrey M., Masur, Sandra K., Kim, Cecilia E., Otieno, Frederick G., Hou, Cuiping, Abdel-Magid, Nada, Tweddale, Ben, Metry, Denise, Fournet, Jean-Christophe, Papp, Eniko, McPherson, Elizabeth W., Zabel, Carrie, Vaksmann, Guy, Morisot, Cyril, Keating, Brendan, Sleiman, Patrick M., Cleveland, Jeffrey A., Everman, David B., Zackai, Elaine, Hakonarson, Hakon

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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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Burden of potentially pathologic copy number variants is higher in children with isolated congenital heart disease and significantly impairs covariate-adjusted transplant-free surv... von Kim, Daniel Seung, BS, Kim, Jerry H., MD, MPH, Burt, Amber A., MS, Crosslin, David R., PhD, Burnham, Nancy, MSN, Kim, Cecilia E., BS, McDonald-McGinn, Donna M., MS, Zackai, Elaine H., MD, Nicolson, Susan C., MD, Spray, Thomas L., MD, Stanaway, Ian B., BS, Nickerson, Deborah A., PhD, Heagerty, Patrick J., PhD, Hakonarson, Hakon, MD, PhD, Gaynor, J. William, MD, Jarvik, Gail P., MD, PhD

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Genome-wide association identifies diverse causes of common variable immunodeficiency von Orange, Jordan S., MD, PhD, Glessner, Joseph T., MS, Resnick, Elena, MD, Sullivan, Kathleen E., MD, Lucas, Mary, MD, Ferry, Berne, MD, Kim, Cecilia E., BS, Hou, Cuiping, BS, Wang, Fengxiang, BS, Chiavacci, Rosetta, BSN, Kugathasan, Subra, MD, Sleasman, John W., MD, Baldassano, Robert, MD, Perez, Elena E., MD, Chapel, Helen, MD, Cunningham-Rundles, Charlotte, MD, Hakonarson, Hakon, MD, PhD

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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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Strong synaptic transmission impact by copy number variations in schizophrenia von Glessner, Joseph T., Reilly, Muredach P., Kim, Cecilia E., Takahashi, Nagahide, Albano, Anthony, Hou, Cuiping, Bradfield, Jonathan P., Zhang, Haitao, Sleiman, Patrick M. A., Flory, James H., Imielinski, Marcin, Frackelton, Edward C., Chiavacci, Rosetta, Thomas, Kelly A., Garris, Maria, Otieno, Frederick G., Davidson, Michael, Weiser, Mark, Reichenberg, Abraham, Davis, Kenneth L., Friedman, Joseph I., Cappola, Thomas P., Margulies, Kenneth B., Rader, Daniel J., Grant, Struan F. A., Buxbaum, Joseph D., Gur, Raquel E., Hakonarson, Hakon, Lupski, James R.

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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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Duplication of the SLIT3 locus on 5q35.1 predisposes to major depressive disorder von Glessner, Joseph T, Wang, Kai, Sleiman, Patrick M A, Zhang, Haitao, Kim, Cecilia E, Flory, James H, Bradfield, Jonathan P, Imielinski, Marcin, Frackelton, Edward C, Qiu, Haijun, Mentch, Frank, Grant, Struan F A, Hakonarson, Hakon

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Common variation in ISL1 confers genetic susceptibility for human congenital heart disease von Stevens, Kristen N, Hakonarson, Hakon, Kim, Cecilia E, Doevendans, Pieter A, Koeleman, Bobby P C, Mital, Seema, Raue, Jennifer, Glessner, Joseph T, Coles, John G, Moreno, Victor, Granger, Anne, Gruber, Stephen B, Gruber, Peter J

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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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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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Rare variants at 16p11.2 are associated with common variable immunodeficiency von Maggadottir, S. Melkorka, MD, Li, Jin, PhD, Glessner, Joseph T., PhD, Li, Yun Rose, PhD, Wei, Zhi, PhD, Chang, Xiao, PhD, Mentch, Frank D., PhD, Thomas, Kelly A., BA, Kim, Cecilia E., BS, Zhao, Yan, BS, Hou, Cuiping, BS, Wang, Fengxiang, PhD, Jørgensen, Silje F., MD, Perez, Elena E., MD, Sullivan, Kathleen E., MD, Orange, Jordan S., MD, PhD, Karlsen, Tom H., MD, PhD, Chapel, Helen, MD, Cunningham-Rundles, Charlotte, MD, Hakonarson, Hakon, MD, PhD

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17q12-21 variants interact with smoke exposure as a risk factor for pediatric asthma but are equally associated with early-onset versus late-onset asthma in North Americans of Euro... von Flory, James H., MD, MS, Sleiman, Patrick M., PhD, Christie, Jason D., MD, MS, Annaiah, Kiran, MSc, Bradfield, Jonathan, BS, Kim, Cecilia E., BA, Glessner, Joseph, MSc, Imielinski, Marcin, MD, PhD, Li, Hongzhe, PhD, Frackelton, Edward C., BA, Cuiping, Hou, PhD, Otieno, George, MSc, Thomas, Kelly, BA, Smith, Ryan, BA, Glaberson, Wendy, BA, Garris, Maria, BA, Chiavacci, Rosetta, MSc, Allen, Julian, MD, Spergel, Jonathan, MD, PhD, Grundmeier, Robert, MD, PhD, Grunstein, Michael, MD, PhD, Magnusson, Michael, MD, PhD, Grant, Struan F.A., PhD, Bønnelykke, Klaus, MD, Bisgaard, Hans, MD, Hakonarson, Hakon, MD, PhD

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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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Copy number variations in alternative splicing gene networks impact lifespan von Glessner, Joseph T, Smith, Albert Vernon, Panossian, Saarene, Kim, Cecilia E, Takahashi, Nagahide, Thomas, Kelly A, Wang, Fengxiang, Seidler, Kallyn, Harris, Tamara B, Launer, Lenore J, Keating, Brendan, Connolly, John, Sleiman, Patrick M A, Buxbaum, Joseph D, Grant, Struan F A, Gudnason, Vilmundur, Hakonarson, Hakon

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