Outpatient Varicose Vein Surgery with Transilluminated Powered Phlebectomy von Spitz, Gregory A., Braxton, Jeffrey M., Bergan, John J.

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Outpatient varicose vein surgery with transilluminated powered phlebectomy. Discussion von SPITZ, Gregory A, BRAXTON, Jeffrey M, BERGAN, John J

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Wafer-Scale Fabrication of Micro- to Nanoscale Bubble Swimmers and Their Fast Autonomous Propulsion by Ultrasound von McNeill, Jeffrey M, Nama, Nitesh, Braxton, Jesse M, Mallouk, Thomas E

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Molecular Findings Among Patients Referred for Clinical Whole-Exome Sequencing von Yang, Yaping, Muzny, Donna M, Xia, Fan, Niu, Zhiyv, Person, Richard, Ding, Yan, Ward, Patricia, Braxton, Alicia, Wang, Min, Buhay, Christian, Veeraraghavan, Narayanan, Hawes, Alicia, Chiang, Theodore, Leduc, Magalie, Beuten, Joke, Zhang, Jing, He, Weimin, Scull, Jennifer, Willis, Alecia, Landsverk, Megan, Craigen, William J, Bekheirnia, Mir Reza, Stray-Pedersen, Asbjorg, Liu, Pengfei, Wen, Shu, Alcaraz, Wendy, Cui, Hong, Walkiewicz, Magdalena, Reid, Jeffrey, Bainbridge, Matthew, Patel, Ankita, Boerwinkle, Eric, Beaudet, Arthur L, Lupski, James R, Plon, Sharon E, Gibbs, Richard A, Eng, Christine M

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Association of Cytochrome P450 2C19 Genotype With the Antiplatelet Effect and Clinical Efficacy of Clopidogrel Therapy von Shuldiner, Alan R, O’Connell, Jeffrey R, Bliden, Kevin P, Gandhi, Amish, Ryan, Kathleen, Horenstein, Richard B, Damcott, Coleen M, Pakyz, Ruth, Tantry, Udaya S, Gibson, Quince, Pollin, Toni I, Post, Wendy, Parsa, Afshin, Mitchell, Braxton D, Faraday, Nauder, Herzog, William, Gurbel, Paul A

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Genetic Variation in the Platelet Endothelial Aggregation Receptor 1 Gene Results in Endothelial Dysfunction von Fisch, Adam S, Yerges-Armstrong, Laura M, Backman, Joshua D, Wang, Hong, Donnelly, Patrick, Ryan, Kathleen A, Parihar, Ankita, Pavlovich, Mary A, Mitchell, Braxton D, O'Connell, Jeffrey R, Herzog, William, Harman, Christopher R, Wren, Jonathan D, Lewis, Joshua P

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Genome-wide association analysis identifies variants associated with nonalcoholic fatty liver disease that have distinct effects on metabolic traits von Speliotes, Elizabeth K, Yerges-Armstrong, Laura M, Wu, Jun, Hernaez, Ruben, Kim, Lauren J, Palmer, Cameron D, Gudnason, Vilmundur, Eiriksdottir, Gudny, Garcia, Melissa E, Launer, Lenore J, Nalls, Michael A, Clark, Jeanne M, Mitchell, Braxton D, Shuldiner, Alan R, Butler, Johannah L, Tomas, Marta, Hoffmann, Udo, Hwang, Shih-Jen, Massaro, Joseph M, O'Donnell, Christopher J, Sahani, Dushyant V, Salomaa, Veikko, Schadt, Eric E, Schwartz, Stephen M, Siscovick, David S, Voight, Benjamin F, Carr, J Jeffrey, Feitosa, Mary F, Harris, Tamara B, Fox, Caroline S, Smith, Albert V, Kao, W H Linda, Hirschhorn, Joel N, Borecki, Ingrid B

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Clinical Whole-Exome Sequencing for the Diagnosis of Mendelian Disorders von Yang, Yaping, Muzny, Donna M, Reid, Jeffrey G, Bainbridge, Matthew N, Willis, Alecia, Ward, Patricia A, Braxton, Alicia, Beuten, Joke, Xia, Fan, Niu, Zhiyv, Hardison, Matthew, Person, Richard, Bekheirnia, Mir Reza, Leduc, Magalie S, Kirby, Amelia, Pham, Peter, Scull, Jennifer, Wang, Min, Ding, Yan, Plon, Sharon E, Lupski, James R, Beaudet, Arthur L, Gibbs, Richard A, Eng, Christine M

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Efficient Variant Set Mixed Model Association Tests for Continuous and Binary Traits in Large-Scale Whole-Genome Sequencing Studies von Chen, Han, Huffman, Jennifer E., Brody, Jennifer A., Wang, Chaolong, Lee, Seunggeun, Li, Zilin, Gogarten, Stephanie M., Sofer, Tamar, Bielak, Lawrence F., Bis, Joshua C., Blangero, John, Bowler, Russell P., Cade, Brian E., Cho, Michael H., Correa, Adolfo, Curran, Joanne E., de Vries, Paul S., Glahn, David C., Guo, Xiuqing, Johnson, Andrew D., Kardia, Sharon, Kooperberg, Charles, Lewis, Joshua P., Liu, Xiaoming, Mathias, Rasika A., Mitchell, Braxton D., O’Connell, Jeffrey R., Peyser, Patricia A., Post, Wendy S., Reiner, Alex P., Rich, Stephen S., Rotter, Jerome I., Silverman, Edwin K., Smith, Jennifer A., Vasan, Ramachandran S., Wilson, James G., Yanek, Lisa R., Redline, Susan, Smith, Nicholas L., Boerwinkle, Eric, Borecki, Ingrid B., Cupples, L. Adrienne, Laurie, Cathy C., Morrison, Alanna C., Rice, Kenneth M., Lin, Xihong

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Null Mutation in Human APOC3 Confers a Favorable Plasma Lipid Profile and Apparent Cardioprotection von Pollin, Toni I, Damcott, Coleen M, Shen, Haiqing, Ott, Sandra H, Shelton, John, Horenstein, Richard B, Post, Wendy, McLenithan, John C, Bielak, Lawrence F, Peyser, Patricia A, Mitchell, Braxton D, Miller, Michael, O'Connell, Jeffrey R, Shuldiner, Alan R

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New loci associated with kidney function and chronic kidney disease von Böger, Carsten A, Fuchsberger, Christian, Olden, Matthias, Glazer, Nicole L, Parsa, Afshin, Gao, Xiaoyi, Yang, Qiong, O'Connell, Jeffrey R, Li, Man, Tanaka, Toshiko, Isaacs, Aaron, Ketkar, Shamika, Dehghan, Abbas, Teumer, Alexander, Paré, Guillaume, Atkinson, Elizabeth J, Zeller, Tanja, Lohman, Kurt, Cornelis, Marilyn C, Probst-Hensch, Nicole M, Kronenberg, Florian, Tönjes, Anke, Hayward, Caroline, Aspelund, Thor, Eiriksdottir, Gudny, Rampersaud, Evadnie, Mitchell, Braxton D, Singleton, Andrew, Giallauria, Francesco, Metter, Jeffrey, de Boer, Ian H, Haritunians, Talin, Lumley, Thomas, Siscovick, David, Zillikens, M Carola, Oostra, Ben A, Feitosa, Mary, Province, Michael, de Andrade, Mariza, Turner, Stephen T, Schillert, Arne, Ziegler, Andreas, Schnabel, Renate B, Wilde, Sandra, Munzel, Thomas F, Leak, Tennille S, Klopp, Norman, Meisinger, Christa, Wichmann, H-Erich, Koenig, Wolfgang, Zgaga, Lina, Zemunik, Tatijana, Kolcic, Ivana, Hu, Frank B, Igl, Wilmar, Zaboli, Ghazal, Campbell, Harry, Ellinghaus, David, Aulchenko, Yurii S, Felix, Janine F, Rivadeneira, Fernando, Hofman, Albert, Imboden, Medea, Nitsch, Dorothea, Brandstätter, Anita, Stumvoll, Michael, Campbell, Susan, Endlich, Karlhans, Völzke, Henry, Nauck, Matthias, Völker, Uwe, Polasek, Ozren, Vitart, Veronique, Badola, Sunita, Parker, Alexander N, Ridker, Paul M, Blankenberg, Stefan, Liu, Yongmei, Curhan, Gary C, Franke, Andre, Paulweber, Bernhard, Prokopenko, Inga, Wang, Wei, Gudnason, Vilmundur, Shuldiner, Alan R, Coresh, Josef, Schmidt, Reinhold, Ferrucci, Luigi, Shlipak, Michael G, van Duijn, Cornelia M, Borecki, Ingrid, Gyllensten, Ulf, Wilson, James F, Witteman, Jacqueline C, Pramstaller, Peter P, Rettig, Rainer, Hastie, Nick, Kao, W H, Heid, Iris M, Fox, Caroline S

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Genome-Wide Association Study for Coronary Artery Calcification With Follow-Up in Myocardial Infarction von O'DONNELL, Christopher J, KAVOUSI, Maryam, HOFFMANN, Udo, BIELAK, Lawrence F, QUNYUAN ZHANG, EIRIKSDOTTIR, Gudny, VAN DUIJN, Cornelia M, FOX, Caroline S, DE ANDRADE, Mariza, KRAJA, Aldi T, SIGURDSSON, Sigurdur, ELIAS-SMALE, Suzette E, SMITH, Albert V, MURABITO, Joanne M, LAUNER, Lenore J, VAN DER LUGT, Aad, KATHIRESAN, Sekar, KRESTIN, Gabriel P, HERRINGTON, David M, HOWARD, Timothy D, YONGMEI LIU, POST, Wendy, MITCHELL, Braxton D, KARDIA, Sharon L. R, O'CONNELL, Jeffrey R, HAIQING SHEN, SHULDINER, Alan R, ALTSHULER, David, ELOSUA, Roberto, SALOMAA, Veikko, SCHWARTZ, Stephen M, SISCOVICK, David S, VOIGHT, Benjamin F, BIS, Joshua C, FEITOSA, Mary F, GLAZER, Nicole L, PSATY, Bruce M, BOERWINKLE, Eric, HEISS, Gerardo, BLANKENBERG, Stefan, ZELLER, Tanja, WILD, Philipp S, SCHNABEL, Renate B, SCHILLERT, Arne, ZIEGLER, Andreas, HWANG, Shih-Jen, MIINZEL, Thomas F, WHITE, Charles C, ROTTER, Jerome I, NAILS, Michael, OUDKERK, Matthijs, JOHNSON, Andrew D, NEWMAN, Anne B, UITTERLINDEN, Andre G, MASSARO, Joseph M, CUNNINGHAM, Julie, SUN, Yan V, PROVINCE, Michael A, ASPELUND, Thor, DEHGHAN, Abbas

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A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation von Vujkovic, Marijana, Ramdas, Shweta, Lorenz, Kim M., Guo, Xiuqing, Darlay, Rebecca, Cordell, Heather J., He, Jing, Gindin, Yevgeniy, Chung, Chuhan, Myers, Robert P., Schneider, Carolin V., Park, Joseph, Lee, Kyung Min, Serper, Marina, Carr, Rotonya M., Kaplan, David E., Haas, Mary E., MacLean, Matthew T., Witschey, Walter R., Zhu, Xiang, Tcheandjieu, Catherine, Kember, Rachel L., Kranzler, Henry R., Verma, Anurag, Giri, Ayush, Klarin, Derek M., Sun, Yan V., Huang, Jie, Huffman, Jennifer E., Creasy, Kate Townsend, Hand, Nicholas J., Liu, Ching-Ti, Long, Michelle T., Yao, Jie, Budoff, Matthew, Tan, Jingyi, Li, Xiaohui, Lin, Henry J., Chen, Yii-Der Ida, Taylor, Kent D., Chang, Ruey-Kang, Krauss, Ronald M., Vilarinho, Silvia, Brancale, Joseph, Nielsen, Jonas B., Locke, Adam E., Jones, Marcus B., Verweij, Niek, Baras, Aris, Reddy, K. Rajender, Neuschwander-Tetri, Brent A., Schwimmer, Jeffrey B., Sanyal, Arun J., Chalasani, Naga, Ryan, Kathleen A., Mitchell, Braxton D., Gill, Dipender, Wells, Andrew D., Manduchi, Elisabetta, Saiman, Yedidya, Mahmud, Nadim, Miller, Donald R., Reaven, Peter D., Phillips, Lawrence S., Muralidhar, Sumitra, DuVall, Scott L., Lee, Jennifer S., Assimes, Themistocles L., Pyarajan, Saiju, Cho, Kelly, Edwards, Todd L., Damrauer, Scott M., Wilson, Peter W., Gaziano, J. Michael, O’Donnell, Christopher J., Khera, Amit V., Grant, Struan F. A., Brown, Christopher D., Tsao, Philip S., Saleheen, Danish, Lotta, Luca A., Bastarache, Lisa, Anstee, Quentin M., Daly, Ann K., Meigs, James B., Rotter, Jerome I., Lynch, Julie A., Rader, Daniel J., Voight, Benjamin F., Chang, Kyong-Mi

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Total Joint Arthroplasty Outcomes in Eligible Patients Versus Patients Who Failed to Meet at Least 1 Eligibility Criterion: A Single-Center Retrospective Analysis von Gauthier, Chase W., Bakaes, Yianni C., Kern, Elizabeth M., Kung, Justin E., Hopkins, Jeffrey S., Hamilton, Corey A., Bishop, Braxton C., March, Kyle A., Jackson, J. Benjamin

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A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function von Porcu, Eleonora, Medici, Marco, Pistis, Giorgio, Volpato, Claudia B, Wilson, Scott G, Cappola, Anne R, Bos, Steffan D, Deelen, Joris, den Heijer, Martin, Freathy, Rachel M, Lahti, Jari, Liu, Chunyu, Lopez, Lorna M, Nolte, Ilja M, O'Connell, Jeffrey R, Tanaka, Toshiko, Trompet, Stella, Arnold, Alice, Bandinelli, Stefania, Beekman, Marian, Böhringer, Stefan, Brown, Suzanne J, Buckley, Brendan M, Camaschella, Clara, de Craen, Anton J M, Davies, Gail, de Visser, Marieke C H, Ford, Ian, Forsen, Tom, Frayling, Timothy M, Fugazzola, Laura, Gögele, Martin, Hattersley, Andrew T, Hermus, Ad R, Hofman, Albert, Houwing-Duistermaat, Jeanine J, Jensen, Richard A, Kajantie, Eero, Kloppenburg, Margreet, Lim, Ee M, Masciullo, Corrado, Mariotti, Stefano, Minelli, Cosetta, Mitchell, Braxton D, Nagaraja, Ramaiah, Netea-Maier, Romana T, Palotie, Aarno, Persani, Luca, Piras, Maria G, Psaty, Bruce M, Räikkönen, Katri, Richards, J Brent, Rivadeneira, Fernando, Sala, Cinzia, Sabra, Mona M, Sattar, Naveed, Shields, Beverley M, Soranzo, Nicole, Starr, John M, Stott, David J, Sweep, Fred C G J, Usala, Gianluca, van der Klauw, Melanie M, van Heemst, Diana, van Mullem, Alies, Vermeulen, Sita H, Visser, W Edward, Walsh, John P, Westendorp, Rudi G J, Widen, Elisabeth, Zhai, Guangju, Cucca, Francesco, Deary, Ian J, Eriksson, Johan G, Ferrucci, Luigi, Fox, Caroline S, Jukema, J Wouter, Kiemeney, Lambertus A, Pramstaller, Peter P, Schlessinger, David, Shuldiner, Alan R, Slagboom, Eline P, Uitterlinden, André G, Vaidya, Bijay, Visser, Theo J, Wolffenbuttel, Bruce H R, Meulenbelt, Ingrid, Rotter, Jerome I, Spector, Tim D, Hicks, Andrew A, Toniolo, Daniela, Sanna, Serena, Peeters, Robin P, Naitza, Silvia

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Whole-Genome Sequencing Association Analyses of Stroke and Its Subtypes in Ancestrally Diverse Populations From Trans-Omics for Precision Medicine Project von Hu, Yao, Haessler, Jeffrey W., Manansala, Regina, Wiggins, Kerri L., Moscati, Arden, Beiser, Alexa, Heard-Costa, Nancy L., Sarnowski, Chloe, Raffield, Laura M., Chung, Jaeyoon, Marini, Sandro, Anderson, Christopher D., Rosand, Jonathan, Xu, Huichun, Sun, Xiao, Kelly, Tanika N., Wong, Quenna, Lange, Leslie A., Rotter, Jerome I., Correa, Adolfo, Vasan, Ramachandran S., Seshadri, Sudha, Rich, Stephen S., Do, Ron, Loos, Ruth J.F., Longstreth, William T., Bis, Joshua C., Psaty, Bruce M., Tirschwell, David L., Assimes, Themistocles L., Silver, Brian, Liu, Simin, Jackson, Rebecca, Wassertheil-Smoller, Sylvia, Mitchell, Braxton D., Fornage, Myriam, Auer, Paul L., Reiner, Alex P., Kooperberg, Charles

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Analysis of rare genetic variation underlying cardiometabolic diseases and traits among 200,000 individuals in the UK Biobank von Jurgens, Sean J., Choi, Seung Hoan, Morrill, Valerie N., Chaffin, Mark, Pirruccello, James P., Halford, Jennifer L., Weng, Lu-Chen, Nauffal, Victor, Roselli, Carolina, Hall, Amelia W., Oetjens, Matthew T., Lagerman, Braxton, vanMaanen, David P., Aragam, Krishna G., Lunetta, Kathryn L., Haggerty, Christopher M., Lubitz, Steven A., Ellinor, Patrick T.

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Analysis commons, a team approach to discovery in a big-data environment for genetic epidemiology von Brody, Jennifer A, Morrison, Alanna C, Bis, Joshua C, O'Connell, Jeffrey R, Brown, Michael R, Huffman, Jennifer E, Ames, Darren C, Carroll, Andrew, Conomos, Matthew P, Gabriel, Stacey, Gibbs, Richard A, Gogarten, Stephanie M, Gupta, Namrata, Jaquish, Cashell E, Johnson, Andrew D, Lewis, Joshua P, Liu, Xiaoming, Manning, Alisa K, Papanicolaou, George J, Pitsillides, Achilleas N, Rice, Kenneth M, Salerno, William, Sitlani, Colleen M, Smith, Nicholas L, Heckbert, Susan R, Laurie, Cathy C, Mitchell, Braxton D, Vasan, Ramachandran S, Rich, Stephen S, Rotter, Jerome I, Wilson, James G, Boerwinkle, Eric, Psaty, Bruce M, Cupples, L Adrienne

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Identification of novel and rare variants associated with handgrip strength using whole genome sequence data from the NHLBI Trans-Omics in Precision Medicine (TOPMed) Program von Sarnowski, Chloé, Chen, Han, Biggs, Mary L, Wassertheil-Smoller, Sylvia, Bressler, Jan, Irvin, Marguerite R, Ryan, Kathleen A, Karasik, David, Arnett, Donna K, Cupples, L Adrienne, Fardo, David W, Gogarten, Stephanie M, Heavner, Benjamin D, Jain, Deepti, Kang, Hyun Min, Kooperberg, Charles, Mainous, Arch G, Mitchell, Braxton D, Morrison, Alanna C, O'Connell, Jeffrey R, Psaty, Bruce M, Rice, Kenneth, Smith, Albert V, Vasan, Ramachandran S, Windham, B Gwen, Kiel, Douglas P, Murabito, Joanne M, Lunetta, Kathryn L

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rs641738C>T near MBOAT7 is associated with liver fat, ALT and fibrosis in NAFLD: A meta-analysis von Teo, Kevin, Abeysekera, Kushala W.M., Adams, Leon, Aigner, Elmar, Anstee, Quentin M., Banales, Jesus M., Banerjee, Rajarshi, Basu, Priyadarshi, Berg, Thomas, Bhatnagar, Pallav, Buch, Stephan, Canbay, Ali, Caprio, Sonia, Chatterjee, Ankita, Ida Chen, Yii-Der, Chowdhury, Abhijit, Daly, Ann K., Datz, Christian, de Gracia Hahn, Dana, DiStefano, Johanna K., Dong, Jiawen, Duret, Amedine, Vreugdenhil, Anita, Alisi, Anna, Jańczyk, Wojciech, Baumann, Ulrich, van Mourik, Indra, Lacaille, Florence, Dabbas, Myriam, Kelly, Deirdre A., Nobili, Valerio, Fairey, Madison, Gerhard, Glenn S., Eiriksdottir, Gudny, Garcia, Melissa E., Harris, Tamara B., Kim, Lauren J., Launer, Lenore J., Nalls, Michael A., Smith, Albert V., Clark, Jeanne M., Hernaez, Ruben, Kao, W.H. Linda, Mitchell, Braxton D., Shuldiner, Alan R., Yerges-Armstrong, Laura M., Borecki, Ingrid B., Carr, J. Jeffrey, Feitosa, Mary F., Butler, Johannah L., Fox, Caroline S., Hirschhorn, Joel N., Hoffmann, Udo, Massaro, Joseph M., O'Donnell, Christopher J., Palmer, Cameron D., Sahani, Dushyant V., Speliotes, Elizabeth K., Guo, Xiuqing, Hampe, Jochen, Hickman, Matthew, Heintz, Lena, Hudert, Christian, Kelly, Matt, Krawczyk, Marcin, Langenberg, Claudia, Lavine, Joel, Li, Lin, Lim, Hong Kai, Loomba, Rohit, Luukkonen, Panu K., Melton, Phillip E., Mori, Trevor A., Palmer, Nicholette D., Parisinos, Constantinos A., Pillai, Sreekumar G., Qayyum, Faiza, Reichert, Matthias C., Romeo, Stefano, Rotter, Jerome I., Im, Yu Ri, Santoro, Nicola, Schafmayer, Clemens, Speliotes, Elizabeth K., Stender, Stefan, Stickel, Felix, Still, Christopher D., Strnad, Pavel, Taylor, Kent D., Tybjærg-Hansen, Anne, Umano, Giuseppina Rosaria, Utukuri, Mrudula, Valenti, Luca, Wagenknecht, Lynne E., Wareham, Nicholas J., Watanabe, Richard M., Wattacheril, Julia, Yki-Järvinen, Hannele, Young, Kendra A., Mann, Jake P.

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