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Gene-centric meta-analyses for central adiposity traits in up to 57 412 individuals of European descent confirm known loci and reveal several novel associations

by Yoneyama, Sachiko, Guo, Yiran, Lanktree, Matthew B, Barnes, Michael R, Elbers, Clara C, Karczewski, Konrad J, Padmanabhan, Sandosh, Bauer, Florianne, Baumert, Jens, Beitelshees, Amber, Berenson, Gerald S, Boer, Jolanda M A, Burke, Gregory, Cade, Brian, Chen, Wei, Cooper-Dehoff, Rhonda M, Gaunt, Tom R, Gieger, Christian, Gong, Yan, Gorski, Mathias, Heard-Costa, Nancy, Johnson, Toby, Lamonte, Michael J, McDonough, Caitrin, Monda, Keri L, Onland-Moret, N Charlotte, Nelson, Christopher P, O'Connell, Jeffrey R, Ordovas, Jose, Peter, Inga, Peters, Annette, Shaffer, Jonathan, Shen, Haiqinq, Smith, Erin, Speilotes, Liz, Thomas, Fridtjof, Thorand, Barbara, Monique Verschuren, W M, Anand, Sonia S, Dominiczak, Anna, Davidson, Karina W, Hegele, Robert A, Heid, Iris, Hofker, Marten H, Huggins, Gordon S, Illig, Thomas, Johnson, Julie A, Kirkland, Susan, König, Wolfgang, Langaee, Taimour Y, McCaffery, Jeanne, Melander, Olle, Mitchell, Braxton D, Munroe, Patricia, Murray, Sarah S, Papanicolaou, George, Redline, Susan, Reilly, Muredach, Samani, Nilesh J, Schork, Nicholas J, Van Der Schouw, Yvonne T, Shimbo, Daichi, Shuldiner, Alan R, Tobin, Martin D, Wijmenga, Cisca, Yusuf, Salim, Hakonarson, Hakon, Lange, Leslie A, Demerath, Ellen W, Fox, Caroline S, North, Kari E, Reiner, Alex P, Keating, Brendan, Taylor, Kira C
Published in Human molecular genetics (01.05.2014)

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Whole-Exome Sequencing Identifies Rare and Low-Frequency Coding Variants Associated with LDL Cholesterol

by Lange, Leslie A., Schmidt, Ellen M., Bizon, Chris, Jun, Goo, Auer, Paul, Li, Kuo-ping, Locke, Adam, Rivas, Manuel A., Feitosa, Mary F., Zhang, Qunyuan, Huffman, Jennifer E., Crosby, Jacy, Robinson, Jennifer G., Crosslin, David R., Rosenthal, Elisabeth A., Tsai, Michael, Rieder, Mark J., Fox, Ervin R., van Duijn, Cornelia M., Taylor, Herman A., Loos, Ruth J.F., Ballantyne, Christie M., Reiner, Alexander P., Cupples, L. Adrienne, Kang, Hyun Min, Lettre, Guillaume, Rader, Daniel J., Reilly, Muredach P., Stoletzki, Nina, Barr, R. Graham, Benjamin, Emelia J., Carr, Jeff, Dupuis, Josée, Ellis, Jaclyn, Fornage, Myriam, Goff, David, Grody, Wayne, Heard-Costa, Nancy L., Levy, Daniel, Li, Dalin, Loria, Cay, Mackey, Rachel, Quinlan, Aaron R., Rice, Kenneth, Sanders, Jill P., Tracy, Russell P., Tsai, Michael Y., Wassel, Chrstina L., Watson, Karol, Wilson, Gregory, Wilson, James G., Zakai, Neil A., Nalls, Michael, Bamshad, Michael J., Accurso, Frank, Beaty, Terri, Caplan, Daniel, Chidekel, Aaron, Christiani, David C., De Paula, Alicia, Gutierrez, Hector, Hassoun, Paul M., Hiatt, Peter, Hummer, Laura K., Kim, Yoonhee, Lin, Xihong, Louie, Tin L., Mathias, Rasika A., McNamara, John, McNamara, Sharon, Nielson, Dennis, Orenstein, David, O’Sullivan, Brian, Passero, Mary Ann, Perkett, Elizabeth, Spencer, Terry, Tabor, Holly K., Weiss, Robert, Wigley, Fred, Wise, Robert A., Wurfel, Mark M., Eichler, Evan E., Fu, Wenqing, Smith, Joshua D., Tennessen, Jacob A., Peters, Ulrike, Brzyski, Robert, Curb, J. David, Eaton, Charles B., Heiss, Gerardo, Johnson, Karen C., Lasser, Norman, Lin, Dan-Yu, Logsdon, Benjamin A., Manson, JoAnn E., Martin, Lisa, Stein, Evan, Applebaum-Bowden, Deborah, Paltoo, Dina N., Sturcke, Anne
Published in American journal of human genetics (06.02.2014)

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