Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits by Gilly, Arthur, Suveges, Daniel, Kuchenbaecker, Karoline, Pollard, Martin, Southam, Lorraine, Hatzikotoulas, Konstantinos, Farmaki, Aliki-Eleni, Bjornland, Thea, Waples, Ryan, Appel, Emil V. R., Casalone, Elisabetta, Melloni, Giorgio, Kilian, Britt, Rayner, Nigel W., Ntalla, Ioanna, Kundu, Kousik, Walter, Klaudia, Danesh, John, Butterworth, Adam, Barroso, Inês, Tsafantakis, Emmanouil, Dedoussis, George, Moltke, Ida, Zeggini, Eleftheria

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Estimating narrow-sense heritability using family data from admixed populations by Athanasiadis, Georgios, Speed, Doug, Andersen, Mette K, Appel, Emil V R, Grarup, Niels, Brandslund, Ivan, Jørgensen, Marit Eika, Larsen, Christina Viskum Lytken, Bjerregaard, Peter, Hansen, Torben, Albrechtsen, Anders

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Comparative Analyses of QTLs Influencing Obesity and Metabolic Phenotypes in Pigs and Humans by Pant, Sameer D, Karlskov-Mortensen, Peter, Jacobsen, Mette J, Cirera, Susanna, Kogelman, Lisette J A, Bruun, Camilla S, Mark, Thomas, Jørgensen, Claus B, Grarup, Niels, Appel, Emil V R, Galjatovic, Ehm A A, Hansen, Torben, Pedersen, Oluf, Guerin, Maryse, Huby, Thierry, Lesnik, Philipppe, Meuwissen, Theo H E, Kadarmideen, Haja N, Fredholm, Merete

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Author Correction: Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits by Gilly, Arthur, Suveges, Daniel, Kuchenbaecker, Karoline, Pollard, Martin, Southam, Lorraine, Hatzikotoulas, Konstantinos, Farmaki, Aliki-Eleni, Bjornland, Thea, Waples, Ryan, Appel, Emil V. R., Casalone, Elisabetta, Melloni, Giorgio, Kilian, Britt, Rayner, Nigel W., Ntalla, Ioanna, Kundu, Kousik, Walter, Klaudia, Danesh, John, Butterworth, Adam, Barroso, Inês, Tsafantakis, Emmanouil, Dedoussis, George, Moltke, Ida, Zeggini, Eleftheria

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The Ross recovery theorem with a regularised multivariate Markov chain by Maré, E., Van Appel, V.

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Re-analysis of public genetic data reveals a rare X-chromosomal variant associated with type 2 diabetes by Bonàs-Guarch, Sílvia, Guindo-Martínez, Marta, Miguel-Escalada, Irene, Grarup, Niels, Sebastian, David, Rodriguez-Fos, Elias, Sánchez, Friman, Planas-Fèlix, Mercè, Cortes-Sánchez, Paula, González, Santi, Timshel, Pascal, Pers, Tune H., Morgan, Claire C., Moran, Ignasi, Atla, Goutham, González, Juan R., Puiggros, Montserrat, Martí, Jonathan, Andersson, Ehm A., Díaz, Carlos, Badia, Rosa M., Udler, Miriam, Leong, Aaron, Kaur, Varindepal, Flannick, Jason, Jørgensen, Torben, Linneberg, Allan, Jørgensen, Marit E., Witte, Daniel R., Christensen, Cramer, Brandslund, Ivan, Appel, Emil V., Scott, Robert A., Luan, Jian’an, Langenberg, Claudia, Wareham, Nicholas J., Pedersen, Oluf, Zorzano, Antonio, Florez, Jose C, Hansen, Torben, Ferrer, Jorge, Mercader, Josep Maria, Torrents, David

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Genetic determinants of glycated hemoglobin levels in the Greenlandic Inuit population by Appel, Emil V R, Moltke, Ida, Jørgensen, Marit E, Bjerregaard, Peter, Linneberg, Allan, Pedersen, Oluf, Albrechtsen, Anders, Hansen, Torben, Grarup, Niels

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Prospective Studies Exploring the Possible Impact of an ID3 Polymorphism on Changes in Obesity Measures by Svendstrup, Mathilde, Appel, Emil V.R., Sandholt, Camilla H., Ahluwalia, Tarunveer S., Ängquist, Lars H., Thuesen, Betina H., Jørgensen, Marit E., Pedersen, Oluf, Grarup, Niels, Hansen, Torben, Sørensen, Thorkild I.A., Vestergaard, Henrik

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Re-analysis of public genetic data reveals a rare X-chromosomal variant associated with type 2 diabetes by Bonàs Guarch, Sílvia, Guindo-Martínez, Marta, Miguel-Escalada, Irene, Grarup, Niels, Sebastián Muñoz, David, Rodriguez-Fos, Elias, Sánchez, Friman, Planas-Fèlix, Mercè, Cortes-Sánchez, Paula, González, Santi, Timshel, Pascal, Pers, Tune H, Morgan, Claire C, Moran, Ignasi, Atla, Goutham, González, Juan Ramón, Puiggros, Montserrat, Martí, Jonathan, Andersson, Ehm A, Díaz, Carlos, Badia, Rosa M, Udler, Miriam, Leong, Aaron, Kaur, Varindepal, Flannick, Jason, Jørgensen, Torben, Linneberg, Allan, Jørgensen, Marit E, Witte, Daniel R, Christensen, Cramer, Brandslund, Ivan, Appel, Emil V, Scott, Robert A, Luan, Jian'an, Langenberg, Claudia, Wareham, Nicholas J, Pedersen, Oluf, Zorzano Olarte, Antonio, Florez, Jose C, Hansen, Torben

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Publisher Correction: Re-analysis of public genetic data reveals a rare X-chromosomal variant associated with type 2 diabetes by Bonàs-Guarch, Sílvia, Guindo-Martínez, Marta, Miguel-Escalada, Irene, Grarup, Niels, Sebastian, David, Rodriguez-Fos, Elias, Sánchez, Friman, Planas-Fèlix, Mercè, Cortes-Sánchez, Paula, González, Santi, Timshel, Pascal, Pers, Tune H., Morgan, Claire C., Moran, Ignasi, Atla, Goutham, González, Juan R., Puiggros, Montserrat, Martí, Jonathan, Andersson, Ehm A., Díaz, Carlos, Badia, Rosa M., Udler, Miriam, Leong, Aaron, Kaur, Varindepal, Flannick, Jason, Jørgensen, Torben, Linneberg, Allan, Jørgensen, Marit E., Witte, Daniel R., Christensen, Cramer, Brandslund, Ivan, Appel, Emil V., Scott, Robert A., Luan, Jian’an, Langenberg, Claudia, Wareham, Nicholas J., Pedersen, Oluf, Zorzano, Antonio, Florez, Jose C, Hansen, Torben, Ferrer, Jorge, Mercader, Josep Maria, Torrents, David

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Natural history of amyotrophic lateral sclerosis in a database population Validation of a scoring system and a model for survival prediction by Haverkamp, Lanny J., Appel, Vicki, Appel, Stanley H.

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An Analysis of T-Cell Receptor Variable Region Gene Expression in Major Histocompatibility Complex Disparate Mice by Bill, Jerome, Appel, Virginia B., Palmer, Ed

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Rare and low-frequency coding variants alter human adult height by Wood, Andrew R., Kjaer, Troels R., Lu, Yingchang, Thorleifsson, Gudmar, Turcot, Valérie, Young, Kristin L., Rivas, Manuel A., Abecasis, Goncalo, Aben, Katja K., Allin, Kristine H., Blüher, Matthias, Bots, Michiel L., Brilliant, Murray H., Carey, David J., Chambers, John C., Chasman, Daniel I., Chen, Yii-Der Ida, Chu, Audrey Y., Collins, Francis S., Cook, James P., de Groot, Mark C. H., de Mutsert, Renée, Ebeling, Tapani, Evangelou, Evangelos, Feng, Shuang, Ford, Ian, Fornage, Myriam, Gandin, Ilaria, Gordon, Scott D., Gustafsson, Stefan, Hattersley, Andrew T., Heid, Iris M., Helgeland, Øyvind, Hewitt, Alex W., Hovingh, G. Kees, Hoyng, Carel B., Huang, Paul L., Hveem, Kristian, Ikram, M. Arfan, Jansson, Jan-Håkan, Jarvik, Gail P., Jiang, Xuejuan, Jukema, J. Wouter, Kitajima, Hidetoshi, Kluivers, Kirsten B., Kontto, Jukka, Kooner, Jaspal S., Kriebel, Jennifer, Kuusisto, Johanna, Langenberg, Claudia, Lee, I-Te, Li, Huaixing, Lin, Honghuang, Lophatananon, Artitaya, Lyytikäinen, Leo-Pekka, Madden, Pamela A. F., Männistö, Satu, Mazul, Angela L., Metspalu, Andres, Mook-Kanamori, Dennis O., Morgan, Anna, Morris, Andrew P., Müller-Nurasyid, Martina, Nalls, Mike A., Nielsen, Sune F., Njølstad, Pål R., Palmer, Colin N. A., Pasterkamp, Gerard, Pedersen, Oluf, Perola, Markus, Perry, James A., Person, Thomas N., Salomaa, Veikko, Samani, Nilesh J., Sandow, Kevin, Schmidt, Marjanka K., Segura-Lepe, Marcelo P., Sim, Xueling, Small, Kerrin S., Southam, Lorraine, Steinthorsdottir, Valgerdur, Stumvoll, Michael, Tansey, Katherine E., Tardif, Jean-Claude, Taylor, Kent D., Thompson, Deborah J., Tyrer, Jonathan P., Uitterlinden, André G., van Schoor, Natasja M., Vozzi, Diego, Wang, Shuai, Wang, Yiqin, Wilson, James G., Young, Robin, Willer, Cristen J., Liu, Dajiang J., North, Kari E., Kutalik, Zoltán, Loos, Ruth J. F., Deloukas, Panos

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Prevalence and correlates of neuropsychological deficits in amyotrophic lateral sclerosis by Massman, P J, Sims, J, Cooke, N, Haverkamp, L J, Appel, V, Appel, S H

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Genetic insights into resting heart rate and its role in cardiovascular disease by van de Vegte, Yordi J., Eppinga, Ruben N., van der Ende, M. Yldau, Hagemeijer, Yanick P., Mahendran, Yuvaraj, Tan, Vanessa Y., Ntalla, Ioanna, Brody, Jennifer A., Lecoeur, Cecile, Hwang, Shih-Jen, Mononen, Nina, Auro, Kirsi, Jackson, Anne U., Zeng, Linyao, Nethander, Maria, Pechlivanis, Sonali, Qi, Lu, Zhao, Wei, Rizzi, Federica, Tanaka, Toshiko, Robino, Antonietta, Lange, Leslie, Zhang, Weihua, Guo, Xiuqing, Lin, Henry J., Noordam, Raymond, Milaneschi, Yuri, Schraut, Katharina E., den Hoed, Marcel, Trompet, Stella, van den Berg, Marten E., Pistis, Giorgio, Weiss, Stefan, Nolte, Ilja M., Lyytikäinen, Leo-Pekka, Iribarren, Carlos, Ring, Susan M., de Vries, Paul S., Sever, Peter, Linneberg, Allan, Bottinger, Erwin P., Sotoodehnia, Nona, Kolcic, Ivana, Gudbjartsson, Daniel F., Newton-Cheh, Christopher H., Nikus, Kjell, Salo, Perttu, Peyser, Patricia A., Schunkert, Heribert, Lorentzon, Mattias, Lahti, Jari, Rao, Dabeeru C., Cornelis, Marilyn C., Faul, Jessica D., Smith, Jennifer A., Concas, Maria Pina, Sinagra, Gianfranco, Delgado, Graciela E., Foco, Luisa, Melander, Olle, de Mutsert, Renée, de Geus, Eco J. C., Joshi, Peter K., Macfarlane, Peter W., Tan, Nicholas, Felix, Stephan B., Quek, Debra Q., Ingelsson, Martin, Raitakari, Olli T., Timpson, Nicholas J., Morrison, Alanna C., Heckbert, Susan R., Hayward, Caroline, Stefansson, Kari, Wareham, Nicholas J., van Duijn, Cornelia M., Feitosa, Mary F., Boehnke, Michael, Kardia, Sharon L. R., Ohlsson, Claes, Eriksson, Johan G., Moebus, Susanne, Cusi, Daniele, Girotto, Giorgia, Kääb, Stefan, Peters, Annette, März, Winfried, Smith, J. Gustav, Mook-Kanamori, Dennis O., Gyllensten, Ulf, Wilson, James F., Burgess, Stephen, Sundström, Johan, Lieb, Wolfgang, Eijgelsheim, Mark, Cheng, Ching-Yu, Dörr, Marcus, Wong, Tien-Yin, Riese, Harriette, Verweij, Niek

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Contributions of Ea(z) and Eb(z) MHC genes to lupus susceptibility in New Zealand mice by Vyse, T J, Rozzo, S J, Drake, C G, Appel, V B, Lemeur, M, Izui, S, Palmer, E, Kotzin, B L

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Genetic Analysis of the Imperfect Association of H-2 Haplotype with Lupus-Like Autoimmune Disease by Babcock, Susan K., Appel, Virginia B., Schiff, Marshall, Palmer, Ed, Kotzin, Brian L.

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Genome-wide association analysis identifies ancestry-specific genetic variation associated with acute response to metformin and glipizide in SUGAR-MGH by Li, Josephine H., Brenner, Laura N., Kaur, Varinderpal, Figueroa, Katherine, Schroeder, Philip, Huerta-Chagoya, Alicia, Udler, Miriam S., Leong, Aaron, Mercader, Josep M., Florez, Jose C.

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Thrombelastography-Based Monitoring for Massive Blood Loss During Elective Pediatric Surgery for Craniosynostosis Repair, a Pilot Study by Appel V, Inge M., Machotta, Andreas, Poley, Marten, Al, Maiwenn J

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P3630Genetic risk score of insulin resistance risk variants is associated with increased risk of coronary artery disease in patients referred to coronary angiography by Kuhr Skals, R, Lukacs Krogager, M, Rosenbaum Appel, E V, Schnurr, T M, Theil Have, C, Gislason, G, Enghusen, H, Koeber, L, Engstroem, T, Stender, S, Hansen, T, Grarup, N, Andersson, C, Torp-Pedersen, C, Weeke, P E

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