The C-type lectin receptor CLEC4M binds, internalizes, and clears von Willebrand factor and contributes to the variation in plasma von Willebrand factor levels von Rydz, Natalia, Swystun, Laura L., Notley, Colleen, Paterson, Andrew D., Riches, J. Jacob, Sponagle, Kate, Boonyawat, Boonchai, Montgomery, Robert R., James, Paula D., Lillicrap, David

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Jnk1 activity is indispensable for appropriate cortical interneuron migration in the developing cerebral cortex von Riches, J Jacob, Reynolds, Kathryn

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Shwachman-Bodian Diamond syndrome is a multi-functional protein implicated in cellular stress responses von Ball, Heather L., Zhang, Bing, Riches, J. Jacob, Gandhi, Rikesh, Li, Jing, Rommens, Johanna M., Myers, Jeremy S.

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Autophagy variation within a cell population determines cell fate through selective degradation of Fap-1 von Gump, Jacob M., Staskiewicz, Leah, Morgan, Michael J., Bamberg, Alison, Riches, David W. H., Thorburn, Andrew

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Autologous Hematopoietic Stem Cell Transplantation vs Intravenous Pulse Cyclophosphamide in Diffuse Cutaneous Systemic Sclerosis: A Randomized Clinical Trial von van Laar, Jacob M, Farge, Dominique, Sont, Jacob K, Naraghi, Kamran, Marjanovic, Zora, Larghero, Jérôme, Schuerwegh, Annemie J, Marijt, Erik W. A, Vonk, Madelon C, Schattenberg, Anton V, Matucci-Cerinic, Marco, Voskuyl, Alexandre E, van de Loosdrecht, Arjan A, Daikeler, Thomas, Kötter, Ina, Schmalzing, Marc, Martin, Thierry, Lioure, Bruno, Weiner, Stefan M, Kreuter, Alexander, Deligny, Christophe, Durand, Jean-Marc, Emery, Paul, Machold, Klaus P, Sarrot-Reynauld, Francoise, Warnatz, Klaus, Adoue, Daniel F. P, Constans, Joël, Tony, Hans-Peter, Del Papa, Nicoletta, Fassas, Athanasios, Himsel, Andrea, Launay, David, Lo Monaco, Andrea, Philippe, Pierre, Quéré, Isabelle, Rich, Éric, Westhovens, Rene, Griffiths, Bridget, Saccardi, Riccardo, van den Hoogen, Frank H, Fibbe, Willem E, Socié, Gérard, Gratwohl, Alois, Tyndall, Alan

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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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Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes von Chauhan, Ganesh, Traylor, Matthew, Sargurupremraj, Muralidharan, Okada, Yukinori, Mishra, Aniket, Giese, Anne-Katrin, van der Laan, Sander W., Gretarsdottir, Solveig, Anderson, Christopher D., Almgren, Peter, Amouyel, Philippe, Bartz, Traci M., Benavente, Oscar R., Boncoraglio, Giorgio B., Butterworth, Adam S., Carrera, Caty, Chasman, Daniel I., Cotlarciuc, Ioana, Cruchaga, Carlos, de Bakker, Paul I. W., Duan, Qing, Gottesman, Rebecca F., Harris, Tamara B., Hassan, Ahamad, Havulinna, Aki S., Heckbert, Susan R., Hyacinth, Hyacinth I., Ikram, M. Arfan, Ingelsson, Erik, Jian, Xueqiu, Jukema, J. Wouter, Kanai, Masahiro, Keene, Keith L., Kissela, Brett M., Kleindorfer, Dawn O., Kooperberg, Charles, Lange, Leslie A., Langenberg, Claudia, Launer, Lenore J., Lemmens, Robin, Lewis, Cathryn M., Lin, Wei-Yu, Lorentzen, Erik, Magnusson, Patrik K., Meschia, James F., Mitchell, Braxton D., Mosley, Thomas H., Nalls, Michael A., O’Donnell, Martin J., Pulit, Sara L., Reiner, Alexander P., Ridker, Paul M., Rothwell, Peter M., Rotter, Jerome I., Sale, Michele M., Salomaa, Veikko, Sapkota, Bishwa R., Schmidt, Reinhold, Schmidt, Carsten O., Sharma, Pankaj, Slowik, Agnieszka, Sudlow, Cathie L. M., Tanislav, Christian, Thijs, Vincent N. S., Thorsteinsdottir, Unnur, Tiedt, Steffen, Trompet, Stella, Wareham, Nicholas J., Wassertheil-Smoller, Sylvia, Wilson, James G., Pastinen, Tomi, Ruusalepp, Arno, Koplev, Simon, Björkegren, Johan L. M., Codoni, Veronica, Civelek, Mete, Christophersen, Ingrid E., Roselli, Carolina, Ellinor, Patrick T., Kato, Norihiro, van der Harst, Pim, Elliott, Paul, Takeuchi, Fumihiko, Johnson, Andrew D., Sanghera, Dharambir K., Melander, Olle, Strbian, Daniel, Fernandez-Cadenas, Israel, Rolfs, Arndt, Hata, Jun, Woo, Daniel, Pare, Guillaume, Hopewell, Jemma C., Saleheen, Danish, Stefansson, Kari, Worrall, Bradford B., Seshadri, Sudha, Markus, Hugh S., Debette, Stephanie, Dichgans, Martin

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GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes von Franceschini, Nora, Giambartolomei, Claudia, de Vries, Paul S., Bis, Joshua C., Winkler, Thomas W., Graff, Misa, Kavousi, Maryam, Dale, Caroline, Hofer, Edith, van Leeuwen, Elisabeth M., Nolte, Ilja M., Lu, Lingyi, Pitkänen, Niina, Franzén, Oscar, Hwang, Shih-Jen, Musani, Solomon K., Schminke, Ulf, Palmas, Walter, Isaacs, Aaron, Correa, Adolfo, Zonderman, Alan B., Uitterlinden, André G., Wong, Andrew, Britton, Annie, Ruusalepp, Arno, Sennblad, Bengt, Hedblad, Bo, Pasaniuc, Bogdan, Penninx, Brenda W., Tzourio, Christophe, Fava, Cristiano, Baldassarre, Damiano, O’Leary, Daniel H., Tremoli, Elena, Schadt, Eric E., Ingelsson, Erik, Veglia, Fabrizio, Rivadeneira, Fernando, Beutner, Frank, Chauhan, Ganesh, Heiss, Gerardo, Snieder, Harold, Völzke, Henry, Markus, Hugh S., Deary, Ian J., Price, Jacqueline, Hopewell, Jemma C., Thiery, Joachim, Engmann, Jorgen, Rice, Kenneth, Taylor, Kent D., Dhana, Klodian, Lind, Lars, Holdt, Lesca M., Dörr, Marcus, Dichgans, Martin, Kivimaki, Mika, Melander, Olle, Raitakari, Olli, Franco, Oscar H., Rueda-Ochoa, Oscar L., Roussos, Panos, Whincup, Peter H., Giral, Philippe, Rauramaa, Rainer, Burkhardt, Ralph, Wannamethee, S. Goya, McLachlan, Stela, Trompet, Stella, Seshadri, Sudha, Kurl, Sudhir, Ring, Susan, Harris, Tamara B., Lehtimäki, Terho, Galesloot, Tessel E., Shah, Tina, Plagnol, Vincent, Rosamond, Wayne D., Post, Wendy, Zhu, Xiaofeng, Dehghan, Abbas, Seldenrijk, Adrie, Morrison, Alanna C., Hamsten, Anders, Psaty, Bruce M., Lawlor, Deborah A., Schmidt, Helena, Wilson, James F., Rotter, Jerome I., Wardlaw, Joanna M., Deanfield, John, Loeffler, Markus, Debette, Stéphanie, Humphries, Steve E., Völker, Uwe, Gudnason, Vilmundur, Hingorani, Aroon D., Björkegren, Johan L. M., Casas, Juan P., O’Donnell, Christopher J.

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Genome-wide association study identifies novel loci for type 2 diabetes-attributed end-stage kidney disease in African Americans von Guan, Meijian, Keaton, Jacob M, Dimitrov, Latchezar, Hicks, Pamela J, Xu, Jianzhao, Palmer, Nicholette D, Ma, Lijun, Das, Swapan K, Chen, Yii-Der I, Coresh, Josef, Fornage, Myriam, Franceschini, Nora, Kramer, Holly, Langefeld, Carl D, Mychaleckyj, Josyf C, Parekh, Rulan S, Post, Wendy S, Rasmussen-Torvik, Laura J, Rich, Stephen S, Rotter, Jerome I, Sedor, John R, Thornley-Brown, Denyse, Tin, Adrienne, Wilson, James G, Freedman, Barry I, Bowden, Donald W, Ng, Maggie C Y

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Analysis of 6,515 exomes reveals the recent origin of most human protein-coding variants von Fu, Wenqing, O’Connor, Timothy D., Jun, Goo, Kang, Hyun Min, Abecasis, Goncalo, Leal, Suzanne M., Gabriel, Stacey, Rieder, Mark J., Altshuler, David, Shendure, Jay, Nickerson, Deborah A., Bamshad, Michael J., NHLBI Exome Sequencing Project, Akey, Joshua M.

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Examining the Acute Glycemic Effects of Different Types of Structured Exercise Sessions in Type 1 Diabetes in a Real-World Setting: The Type 1 Diabetes and Exercise Initiative (T1D... von Riddell, Michael C, Li, Zoey, Gal, Robin L, Calhoun, Peter, Jacobs, Peter G, Clements, Mark A, Martin, Corby K, Doyle Iii, Francis J, Patton, Susana R, Castle, Jessica R, Gillingham, Melanie B, Beck, Roy W, Rickels, Michael R

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The Ontogeny and Population Variability of Human Hepatic NADPH Dehydrogenase Quinone Oxido-Reductase 1 (NQO1) von Rougée, Luc R A, Riches, Zoe, Berman, Jacob M, Collier, Abby C

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Common variation in PHACTR1 is associated with susceptibility to cervical artery dissection von Debette, Stéphanie, Kamatani, Yoichiro, Metso, Tiina M, Kloss, Manja, Chauhan, Ganesh, Engelter, Stefan T, Pezzini, Alessandro, Thijs, Vincent, Markus, Hugh S, Dichgans, Martin, Wolf, Christiane, Dittrich, Ralf, Touzé, Emmanuel, Southerland, Andrew M, Samson, Yves, Abboud, Shérine, Béjot, Yannick, Caso, Valeria, Bersano, Anna, Gschwendtner, Andreas, Sessa, Maria, Cole, John, Lamy, Chantal, Medeiros, Elisabeth, Beretta, Simone, Bonati, Leo H, Grau, Armin J, Michel, Patrik, Majersik, Jennifer J, Sharma, Pankaj, Kalashnikova, Ludmila, Nazarova, Maria, Dobrynina, Larisa, Bartels, Eva, Guillon, Benoit, van den Herik, Evita G, Fernandez-Cadenas, Israel, Jood, Katarina, Nalls, Michael A, De Leeuw, Frank-Erik, Jern, Christina, Cheng, Yu-Ching, Werner, Inge, Metso, Antti J, Lichy, Christoph, Lyrer, Philippe A, Brandt, Tobias, Boncoraglio, Giorgio B, Wichmann, Heinz-Erich, Gieger, Christian, Johnson, Andrew D, Böttcher, Thomas, Castellano, Maurizio, Arveiler, Dominique, Ikram, M Arfan, Breteler, Monique M B, Padovani, Alessandro, Meschia, James F, Kuhlenbäumer, Gregor, Rolfs, Arndt, Worrall, Bradford B, Ringelstein, Erich-Bernd, Zelenika, Diana, Tatlisumak, Turgut, Lathrop, Mark, Leys, Didier, Amouyel, Philippe, Dallongeville, Jean

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iDiabetes platform-enhanced phenotyping of patients with diabetes for precision diagnosis, prognosis and treatment: study protocol for a cluster-randomised controlled study in Tays... von Lin, YeunYi, Leith, Damien, Abbott, Michael, Barrett, Rachael, Bell, Samira, Croudace, Tim J, Cunningham, Scott, Dillon, John, Donnan, Peter, Farre, Albert, Hernández, Rodolfo, Lang, Chim, McKenzie, Stephanie, Mordi, Ify, Morrow, Susan, Munro, Cameron, Philip, Sam, Ryan, Mandy, Wake, Deborah, Wang, Huan, Win, Mya, Pearson, Ewan

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Serum magnesium and calcium levels in relation to ischemic stroke: Mendelian randomization study von Larsson, Susanna C, Boncoraglio, Giorgio B, Chauhan, Ganesh, Okada, Yukinori, van der Laan, Sander W, Gretarsdottir, Solveig, Anderson, Christopher D, Adams, Hieab HH, Almgren, Peter, Amouyel, Philippe, Bevan, Steve, Boncoraglio, Giorgio B, Cruchaga, Carlos, de Bakker, Paul IW, Hoed, Marcel den, Falcone, Guido J, Gustafsson, Stefan, Haessler, Jeffrey, Harris, Tamara B, Havulinna, Aki S, Heckbert, Susan R, Hsu, Fang-Chi, Jian, Xueqiu, Kissela, Brett M, Kubo, Michiaki, Lange, Leslie A, Langefeld, Carl D, Lemmens, Robin, Lewis, Cathryn M, Lin, Wei-Yu, Magnusson, Patrik K, Maguire, Jane, McArdle, Patrick F, Nalls, Michael A, Psaty, Bruce M, Rannikmäe, Kristiina, Reiner, Alexander P, Rost, Natalia S, Rothwell, Peter M, Sacco, Ralph L, Schmidt, Reinhold, Schminke, Ulf, Slowik, Agnieszka, Tanislav, Christian, Tatlisumak, Turgut, Taylor, Kent D, Trompet, Stella, Walters, Matthew, Wassertheil-Smoller, Sylvia, Yang, Qiong, Yusuf, Salim, Attia, John, Beiser, Alexa S, Cullell, Natalia, Dartigues, Jean-François, Delgado, Pilar, Gurpreet, Wander S, Hamsten, Anders, Ilinca, Andreea, Iwasaki, Motoki, Jackson, Rebecca D, Jood, Katarina, Kitazono, Takanari, Laurie, Cathy C, Li, Linxin, Lind, Lars, Liu, Yong Mei, Matsuda, Koichi, Minegishi, Naoko, Montaner, Joan, Norrving, Bo, Ogishima, Soichi, Parati, Eugenio A, Perola, Markus, Pileggi, Silvana, Rabionet, Raquel, Ribasés, Marta, Roquer, Jaume, Rudd, Anthony G, Sarin, Antti-Pekka, Satizabal, Claudia L, Sobue, Kenji, Tanno, Kozo, Valdimarsson, Einar M, Völzke, Henry, Wong, Quenna, Xu, Huichun, Longstreth, W T, Rolfs, Arndt, Hata, Jun, Woo, Daniel, Saleheen, Danish, Stefansson, Kari, Worrall, Bradford B, Kittner, Steven J, Seshadri, Sudha, Markus, Hugh S, Kamatani, Yoichiro, Debette, Stephanie, Dichgans, Martin

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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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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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2013 ACCF/ACR/ASE/ASNC/SCCT/SCMR Appropriate Utilization of Cardiovascular Imaging in Heart Failure: A Joint Report of the American College of Radiology Appropriateness Criteria Co... von Patel, Manesh R, White, Richard D, Abbara, Suhny, Bluemke, David A, Herfkens, Robert J, Picard, Michael, Shaw, Leslee J, Silver, Marc, Stillman, Arthur E, Udelson, James

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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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