GIRL BORN WITHOUT LEGS AND WITHOUT ARMS: REPORT OF A CASE von LEVY, JULIUS L.

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Management of crushing chest injuries in children von Levy, Jr, J L

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Major abdominal trauma in children von Levy, Julius L., Linder, Lawrence H.

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Sacrococcygeal teratomas in infants von Levy, Julius L., Linder, Lawrence H.

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Etiology of "idiopathic" intussusception in infants von Levy, Jr, J L, Linder, L H

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Atresia of the small intestine von Linder, L H, Levy, Jr, J L

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Bilateral congenital diaphragmatic hernias through the foramina of Bochdalek von Levy, Julius L., Guynes, W.Allison, Louis, James E., Linder, Lawrence H.

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Sex-Specific Associations of Cardiovascular Risk Factors and Biomarkers With Incident Heart Failure von Suthahar, Navin, Lau, Emily S., Blaha, Michael J., Paniagua, Samantha M., Larson, Martin G., Psaty, Bruce M., Benjamin, Emelia J., Allison, Matthew A., Bartz, Traci M., Januzzi, James L., Levy, Daniel, Meems, Laura M.G., Bakker, Stephan J.L., Lima, Joao A.C., Cushman, Mary, Lee, Douglas S., Wang, Thomas J., deFilippi, Christopher R., Herrington, David M., Nayor, Matthew, Vasan, Ramachandran S., Gardin, Julius M., Kizer, Jorge R., Bertoni, Alain G., Allen, Norrina B., Gansevoort, Ron T., Shah, Sanjiv J., Gottdiener, John S., Ho, Jennifer E., de Boer, Rudolf A.

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The Association of Obesity and Cardiometabolic Traits With Incident HFpEF and HFrEF von Savji, Nazir, Meijers, Wouter C., Bartz, Traci M., Bhambhani, Vijeta, Cushman, Mary, Nayor, Matthew, Kizer, Jorge R., Sarma, Amy, Blaha, Michael J., Gansevoort, Ron T., Gardin, Julius M., Hillege, Hans L., Ji, Fei, Kop, Willem J., Lau, Emily S., Lee, Douglas S., Sadreyev, Ruslan, van Gilst, Wiek H., Wang, Thomas J., Zanni, Markella V., Vasan, Ramachandran S., Allen, Norrina B., Psaty, Bruce M., van der Harst, Pim, Levy, Daniel, Larson, Martin, Shah, Sanjiv J., de Boer, Rudolf A., Gottdiener, John S., Ho, Jennifer E.

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Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction von Do, Ron, Stitziel, Nathan O., Won, Hong-Hee, Jørgensen, Anders Berg, Duga, Stefano, Angelica Merlini, Pier, Kiezun, Adam, Farrall, Martin, Goel, Anuj, Zuk, Or, Guella, Illaria, Asselta, Rosanna, Lange, Leslie A., Peloso, Gina M., Auer, Paul L., Girelli, Domenico, Martinelli, Nicola, Farlow, Deborah N., DePristo, Mark A., Roberts, Robert, Stewart, Alexander F. R., Saleheen, Danish, Danesh, John, Epstein, Stephen E., Sivapalaratnam, Suthesh, Kees Hovingh, G., Kastelein, John J., Samani, Nilesh J., Schunkert, Heribert, Erdmann, Jeanette, Shah, Svati H., Kraus, William E., Davies, Robert, Nikpay, Majid, Johansen, Christopher T., Wang, Jian, Hegele, Robert A., Hechter, Eliana, Marz, Winfried, Kleber, Marcus E., Huang, Jie, Johnson, Andrew D., Li, Mingyao, Burke, Greg L., Gross, Myron, Liu, Yongmei, Assimes, Themistocles L., Heiss, Gerardo, Lange, Ethan M., Folsom, Aaron R., Taylor, Herman A., Olivieri, Oliviero, Hamsten, Anders, Clarke, Robert, Reilly, Dermot F., Yin, Wu, Rivas, Manuel A., Donnelly, Peter, Rossouw, Jacques E., Psaty, Bruce M., Herrington, David M., Wilson, James G., Rich, Stephen S., Bamshad, Michael J., Tracy, Russell P., Adrienne Cupples, L., Rader, Daniel J., Reilly, Muredach P., Spertus, John A., Cresci, Sharon, Hartiala, Jaana, Wilson Tang, W. H., Hazen, Stanley L., Allayee, Hooman, Reiner, Alex P., Carlson, Christopher S., Kooperberg, Charles, Jackson, Rebecca D., Boerwinkle, Eric, Lander, Eric S., Schwartz, Stephen M., Siscovick, David S., McPherson, Ruth, Tybjaerg-Hansen, Anne, Abecasis, Goncalo R., Watkins, Hugh, Nickerson, Deborah A., Ardissino, Diego, Sunyaev, Shamil R., O'Donnell, Christopher J., Altshuler, David, Gabriel, Stacey, Kathiresan, Sekar

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Predicting Heart Failure With Preserved and Reduced Ejection Fraction: The International Collaboration on Heart Failure Subtypes von Ho, Jennifer E, Enserro, Danielle, Brouwers, Frank P, Kizer, Jorge R, Shah, Sanjiv J, Psaty, Bruce M, Bartz, Traci M, Santhanakrishnan, Rajalakshmi, Lee, Douglas S, Chan, Cheeling, Liu, Kiang, Blaha, Michael J, Hillege, Hans L, van der Harst, Pim, van Gilst, Wiek H, Kop, Willem J, Gansevoort, Ron T, Vasan, Ramachandran S, Gardin, Julius M, Levy, Daniel, Gottdiener, John S, de Boer, Rudolf A, Larson, Martin G

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Predictors and outcomes of heart failure with mid‐range ejection fraction von Bhambhani, Vijeta, Kizer, Jorge R., Lima, Joao A.C., van der Harst, Pim, Bahrami, Hossein, Nayor, Matthew, de Filippi, Christopher R., Enserro, Danielle, Blaha, Michael J., Cushman, Mary, Wang, Thomas J., Gansevoort, Ron T., Fox, Caroline S., Gaggin, Hanna K., Kop, Willem J., Liu, Kiang, Vasan, Ramachandran S., Psaty, Bruce M., Lee, Douglas S., Brouwers, Frank P., Hillege, Hans L., Bartz, Traci M., Benjamin, Emelia J., Chan, Cheeling, Allison, Matthew, Gardin, Julius M., Januzzi, James L., Levy, Daniel, Herrington, David M., van Gilst, Wiek H., Bertoni, Alain G., Larson, Martin G., de Boer, Rudolf A., Gottdiener, John S., Shah, Sanjiv J., Ho, Jennifer E.

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Success and failure: a firsthand look into Uganda's most recent bednet distribution campaign von Zinszer, Kate, Stone, Jessie, Mpaata, Julius C, Muwanguzi, Sarah, Adler, Sasha, McGowan, Cheri L, Levy, Phillip D

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TGFB2 mutations cause familial thoracic aortic aneurysms and dissections associated with mild systemic features of Marfan syndrome von Boileau, Catherine, Guo, Dong-Chuan, Hanna, Nadine, Regalado, Ellen S, Detaint, Delphine, Gong, Limin, Varret, Mathilde, Prakash, Siddharth K, Li, Alexander H, d'Indy, Hyacintha, Braverman, Alan C, Grandchamp, Bernard, Kwartler, Callie S, Gouya, Laurent, Santos-Cortez, Regie Lyn P, Abifadel, Marianne, Leal, Suzanne M, Muti, Christine, Shendure, Jay, Gross, Marie-Sylvie, Rieder, Mark J, Vahanian, Alec, Nickerson, Deborah A, Michel, Jean Baptiste, Jondeau, Guillaume, Milewicz, Dianna M

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

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Rare and Coding Region Genetic Variants Associated With Risk of Ischemic Stroke: The NHLBI Exome Sequence Project von Auer, Paul L, Nalls, Mike, Meschia, James F, Worrall, Bradford B, Longstreth, W. T, Seshadri, Sudha, Kooperberg, Charles, Burger, Kathleen M, Carlson, Christopher S, Carty, Cara L, Chen, Wei-Min, Cupples, L. Adrienne, DeStefano, Anita L, Fornage, Myriam, Hardy, John, Hsu, Li, Jackson, Rebecca D, Jarvik, Gail P, Kim, Daniel S, Lakshminarayan, Kamakshi, Lange, Leslie A, Manichaikul, Ani, Quinlan, Aaron R, Singleton, Andrew B, Thornton, Timothy A, Nickerson, Deborah A, Peters, Ulrike, Rich, Stephen S

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Pathogenic Variants for Mendelian and Complex Traits in Exomes of 6,517 European and African Americans: Implications for the Return of Incidental Results von Tabor, Holly K., Auer, Paul L., Jamal, Seema M., Chong, Jessica X., Yu, Joon-Ho, Gordon, Adam S., Graubert, Timothy A., O’Donnell, Christopher J., Rich, Stephen S., Nickerson, Deborah A., Bamshad, Michael J.

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Quantifying rare, deleterious variation in 12 human cytochrome P450 drug-metabolism genes in a large-scale exome dataset von Gordon, Adam S, Tabor, Holly K, Johnson, Andrew D, Snively, Beverly M, Assimes, Themistocles L, Auer, Paul L, Ioannidis, John P A, Peters, Ulrike, Robinson, Jennifer G, Sucheston, Lara E, Wang, Danxin, Sotoodehnia, Nona, Rotter, Jerome I, Psaty, Bruce M, Jackson, Rebecca D, Herrington, David M, O'Donnell, Christopher J, Reiner, Alexander P, Rich, Stephen S, Rieder, Mark J, Bamshad, Michael J, Nickerson, Deborah A

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Common and rare von Willebrand factor (VWF) coding variants, VWF levels, and factor VIII levels in African Americans: the NHLBI Exome Sequencing Project von Johnsen, Jill M., Auer, Paul L., Morrison, Alanna C., Jiao, Shuo, Wei, Peng, Haessler, Jeffrey, Fox, Keolu, McGee, Sean R., Smith, Joshua D., Carlson, Christopher S., Smith, Nicholas, Boerwinkle, Eric, Kooperberg, Charles, Nickerson, Deborah A., Rich, Stephen S., Green, David, Peters, Ulrike, Cushman, Mary, Reiner, Alex P.

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Exome Sequencing and Genome-Wide Linkage Analysis in 17 Families Illustrate the Complex Contribution of TTN Truncating Variants to Dilated Cardiomyopathy von Norton, Nadine, Li, Duanxiang, Rampersaud, Evadnie, Morales, Ana, Martin, Eden R, Zuchner, Stephan, Guo, Shengru, Gonzalez, Michael, Hedges, Dale J, Robertson, Peggy D, Krumm, Niklas, Nickerson, Deborah A, Hershberger, Ray E

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