A Gimbal-Mounted Pressurization Chamber for Macroscopic and Microscopic Assessment of Ocular Tissues von Keyes, Joseph T, Yan, Dongmei, Rader, Jacob H, Utzinger, Urs, Vande Geest, Jonathan P

Volltext

The role of resting myocardial blood flow and myocardial blood flow reserve as a predictor of major adverse cardiovascular outcomes von Guerraty, Marie A, Rao, H Shanker, Anjan, Venkatesh Y, Szapary, Hannah, Mankoff, David A, Pryma, Daniel A, Rader, Daniel J, Dubroff, Jacob G

Volltext

Clinical Genetic Testing for Familial Hypercholesterolemia von Sturm, Amy C., Knowles, Joshua W., Gidding, Samuel S., Ahmad, Zahid S., Ahmed, Catherine D., Ballantyne, Christie M., Baum, Seth J., Bourbon, Mafalda, Carrié, Alain, Cuchel, Marina, de Ferranti, Sarah D., Defesche, Joep C., Freiberger, Tomas, Hershberger, Ray E., Hovingh, G. Kees, Karayan, Lala, Kastelein, Johannes Jacob Pieter, Kindt, Iris, Lane, Stacey R., Leigh, Sarah E., Linton, MacRae F., Mata, Pedro, Neal, William A., Nordestgaard, Børge G., Santos, Raul D., Harada-Shiba, Mariko, Sijbrands, Eric J., Stitziel, Nathan O., Yamashita, Shizuya, Wilemon, Katherine A., Ledbetter, David H., Rader, Daniel J.

Volltext

Clinical Genetic Testing for Familial Hypercholesterolemia: JACC Scientific Expert Panel von Sturm, Amy C, Knowles, Joshua W, Gidding, Samuel S, Ahmad, Zahid S, Ahmed, Catherine D, Ballantyne, Christie M, Baum, Seth J, Bourbon, Mafalda, Carrié, Alain, Cuchel, Marina, de Ferranti, Sarah D, Defesche, Joep C, Freiberger, Tomas, Hershberger, Ray E, Hovingh, G Kees, Karayan, Lala, Kastelein, Johannes Jacob Pieter, Kindt, Iris, Lane, Stacey R, Leigh, Sarah E, Linton, MacRae F, Mata, Pedro, Neal, William A, Nordestgaard, Børge G, Santos, Raul D, Harada-Shiba, Mariko, Sijbrands, Eric J, Stitziel, Nathan O, Yamashita, Shizuya, Wilemon, Katherine A, Ledbetter, David H, Rader, Daniel J

Volltext

Targeting the coronavirus nucleocapsid protein through GSK-3 inhibition von Liu, Xiaolei, Verma, Anurag, Garcia, Gustavo, Ramage, Holly, Lucas, Anastasia, Myers, Rebecca L., Michaelson, Jacob J., Coryell, William, Kumar, Arvind, Charney, Alexander W., Kazanietz, Marcelo G., Rader, Daniel J., Ritchie, Marylyn D., Berrettini, Wade H., Schultz, David C., Cherry, Sara, Damoiseaux, Robert, Arumugaswami, Vaithilingaraja, Klein, Peter S.

Volltext

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

Volltext

Folic Acid Intake from Fortification in United States Exceeds Predictions von Choumenkovitch, Silvina F., Selhub, Jacob, Rosenberg, Irwin H., Jacques, Paul F., Wilson, Peter W.F., Rader, Jeanne I.

Volltext

UTILIZING RUBIDIUM-82 CARDIAC POSITRON EMISSION TOMOGRAPHY REGIONAL MYOCARDIAL BLOOD FLOW TO DEVELOP NAIVE BAYES CLASSIFIER FOR CORONARY ARTERY DISEASE PREDICTION von Rao, H. Shanker, Guerraty, Marie, Dubroff, Jacob, Rader, Daniel

Volltext

Biomarkers of vitamin B-12 status in NHANES: a roundtable summary von YETLEY, Elizabeth A, PFEIFFER, Christine M, RANDY CURTIN, L, DURAZO-ARVIZU, Ramón A, ECKFELDT, John H, GREEN, Ralph, GREGORY, Jesse F, HOOFNAGLE, Andrew N, JACOBSEN, Donald W, JACQUES, Paul F, MOLLOY, Anne M, MASSARO, Joseph, PHINNEY, Karen W, MILLS, James L, NEXO, Ebba, RADER, Jeanne I, SELHUB, Jacob, SEMPOS, Christopher, SHANE, Barry, STABLER, Sally, STOVER, Patrick, TAMURA, Tsunenobu, TEDSTONE, Alison, FAZILI, Zia, THORPE, Susan J, COATES, Paul M, JOHNSON, Clifford L, FRANCES PICCIANO, Mary, LACHER, David A, BAILEY, Regan L, BLACKMORE, Sheena, BOCK, Jay L, BRODY, Lawrence C, CARMEL, Ralph

Volltext

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.

Volltext

ACCF/SCCT/ACR/AHA/ASE/ASNC/NASCI/SCAI/SCMR 2010 appropriate use criteria for cardiac computed tomography. A report of the American College of Cardiology Foundation Appropriate Use... von Taylor, Allen J, Cerqueira, Manuel, Hodgson, John McB, Mark, Daniel, Min, James, O'Gara, Patrick, Rubin, Geoffrey D, Kramer, Christopher M, Berman, Daniel, Brown, Alan, Chaudhry, Farooq A, Cury, Ricardo C, Desai, Milind Y, Einstein, Andrew J, Gomes, Antoinette S, Harrington, Robert, Hoffmann, Udo, Khare, Rahul, Lesser, John, McGann, Christopher, Rosenberg, Alan, Schwartz, Robert, Shelton, Marc, Smetana, Gerald W, Smith, Jr, Sidney C

Volltext

Biomarkers of folate status in NHANES: a roundtable summary von YETLEY, Elizabeth A, PFEIFFER, Christine M, RANDY CURTIN, L, DURAZO-ARVIZU, Ramón A, ECKFELDT, John H, GREEN, Ralph, GREGORY, Jesse F, HOOFNAGLE, Andrew N, JACOBSEN, Donald W, JACQUES, Paul F, MOLLOY, Anne M, MASSARO, Joseph, PHINNEY, Karen W, MILLS, James L, NEXO, Ebba, RADER, Jeanne I, SELHUB, Jacob, SEMPOS, Christopher, SHANE, Barry, PATRICK STOVER, Sally Stabler, TAMURA, Tsunenobu, TEDSTONE, Alison, THORPE, Susan J, FAZILI, Zia, COATES, Paul M, JOHNSON, Clifford L, PICCIANO, Mary Frances, LACHER, David A, BAILEY, Regan L, BLACKMORE, Sheena, BOCK, Jay L, BRODY, Lawrence C, CARMEL, Ralph

Volltext

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

Volltext

Inferring compound heterozygosity from large-scale exome sequencing data von Guo, Michael H., Francioli, Laurent C., Stenton, Sarah L., Goodrich, Julia K., Watts, Nicholas A., Singer-Berk, Moriel, Groopman, Emily, Darnowsky, Philip W., Solomonson, Matthew, Baxter, Samantha, Tiao, Grace, Neale, Benjamin M., Hirschhorn, Joel N., Rehm, Heidi L., Daly, Mark J., O’Donnell-Luria, Anne, Karczewski, Konrad J., MacArthur, Daniel G., Samocha, Kaitlin E.

Volltext

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

Volltext

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.

Volltext

Discovery of 318 new risk loci for type 2 diabetes and related vascular outcomes among 1.4 million participants in a multi-ethnic meta-analysis von Vujkovic, Marijana, Keaton, Jacob M., Lynch, Julie A., Miller, Donald R., Zhou, Jin, Tcheandjieu, Catherine, Huffman, Jennifer E., Assimes, Themistocles L., Lorenz, Kim, Zhu, Xiang, Hilliard, Austin T., Judy, Renae L., Huang, Jie, Lee, Kyung M., Klarin, Derek, Pyarajan, Saiju, Danesh, John, Melander, Olle, Rasheed, Asif, Mallick, Nadeem H., Hameed, Shahid, Qureshi, Irshad H., Afzal, Muhammad Naeem, Malik, Uzma, Jalal, Anjum, Abbas, Shahid, Sheng, Xin, Gao, Long, Kaestner, Klaus H., Susztak, Katalin, Sun, Yan V., DuVall, Scott L., Cho, Kelly, Lee, Jennifer S., Gaziano, J. Michael, Phillips, Lawrence S., Meigs, James B., Reaven, Peter D., Wilson, Peter W., Edwards, Todd L., Rader, Daniel J., Damrauer, Scott M., O’Donnell, Christopher J., Tsao, Philip S., Chang, Kyong-Mi, Voight, Benjamin F., Saleheen, Danish

Volltext

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

Volltext

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

Volltext

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.

Volltext