Search Results - Sheu, Lawrence C.

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    Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility by Wessel, Jennifer, Chu, Audrey Y, Willems, Sara M, Dauriz, Marco, Raghavan, Sridharan, Hidalgo, Bertha, An, Ping, Lu, Yingchang, Ehm, Margaret G, Baldridge, Abigail S, Freitag, Daniel F, Garcia, Melissa E, Hara, Kazuo, Jakobsdottir, Johanna, Lange, Leslie A, Layton, Jill C, Li, Man, Morrison, Alanna C, Peters, Marjolein J, Southam, Lorraine, Stoiber, Marcus H, Strawbridge, Rona J, Varga, Tibor V, Barbieri, Caterina, Bombieri, Cristina, Bowden, Donald W, Burns, Sean M, Chen, Yuning, Chen, Yii-DerI, Cheng, Ching-Yu, Ehret, Georg B, Eiriksdottir, Gudny, Escher, Stefan A, Frånberg, Mattias, Gambaro, Giovanni, Goel, Anuj, Grove, Megan L, Karaleftheri, Maria, Kirkpatrick, Andrea, Kraja, Aldi T, Kuusisto, Johanna, Lange, Ethan M, Lee, I T, Lee, Wen-Jane, Leong, Aaron, Liao, Jiemin, Lindgren, Cecilia M, Malerba, Giovanni, Mamakou, Vasiliki, Maruthur, Nisa M, McLeod, Olga, Mohlke, Karen L, Muzny, Donna M, Renström, Frida, Rice, Ken, Sala, Cinzia F, Soranzo, Nicole, Speliotes, Elizabeth K, Stirrups, Kathleen, Thanopoulou, Anastasia, Traglia, Michela, Tsafantakis, Emmanouil, Javad, Sundas, Yanek, Lisa R, Becker, Diane M, Bis, Joshua C, Brown, James B, Ingelsson, Erik, Karter, Andrew J, Lorenzo, Carlos, Peloso, Gina M, Vaidya, Dhananjay, Varma, Rohit, Wagenknecht, Lynne E, Dedoussis, George, Deloukas, Panos, Franco, Oscar H, Gibbs, Richard A, Gudnason, Vilmundur, Hofman, Albert, Jansson, Jan-Håkan, Langenberg, Claudia, Launer, Lenore J, Levy, Daniel, Oostra, Ben A, Padmanabhan, Sandosh, Pankow, James S, Rudan, Igor, Schulze, Matthias B, Smith, Blair H, Walker, Mark, Wong, Tien Y, Laakso, Markku, Borecki, Ingrid B, van Duijn, Cornelia M, Waterworth, Dawn M, Loos, Ruth J.F., Meigs, James B, Scott, Robert A, Goodarzi, Mark O

    Published in Nature communications
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    Rare coding variants in RCN3 are associated with blood pressure by He, Karen Y, Kelly, Tanika N, Wang, Heming, Liang, Jingjing, Zhu, Luke, Cade, Brian E, Assimes, Themistocles L, Becker, Lewis C, Beitelshees, Amber L, Bielak, Lawrence F, Bress, Adam P, Brody, Jennifer A, Chang, Yen-Pei Christy, Chang, Yi-Cheng, de Vries, Paul S, Duggirala, Ravindranath, Fox, Ervin R, Franceschini, Nora, Furniss, Anna L, Gao, Yan, Guo, Xiuqing, Haessler, Jeffrey, Hung, Yi-Jen, Hwang, Shih-Jen, Irvin, Marguerite Ryan, Kalyani, Rita R, Liu, Ching-Ti, Liu, Chunyu, Martin, Lisa Warsinger, Montasser, May E, Muntner, Paul M, Mwasongwe, Stanford, Naseri, Take, Palmas, Walter, Reupena, Muagututi'a Sefuiva, Rice, Kenneth M, Sheu, Wayne H-H, Shimbo, Daichi, Smith, Jennifer A, Snively, Beverly M, Yanek, Lisa R, Zhao, Wei, Blangero, John, Boerwinkle, Eric, Chen, Yii-Der Ida, Correa, Adolfo, Cupples, L Adrienne, Curran, Joanne E, Fornage, Myriam, He, Jiang, Hou, Lifang, Kaplan, Robert C, Kardia, Sharon L R, Kenny, Eimear E, Kooperberg, Charles, Lloyd-Jones, Donald, Loos, Ruth J F, Mathias, Rasika A, McGarvey, Stephen T, Mitchell, Braxton D, North, Kari E, Peyser, Patricia A, Psaty, Bruce M, Raffield, Laura M, Rao, D C, Redline, Susan, Reiner, Alex P, Rich, Stephen S, Rotter, Jerome I, Taylor, Kent D, Tracy, Russell, Vasan, Ramachandran S, Morrison, Alanna C, Levy, Daniel, Chakravarti, Aravinda, Arnett, Donna K, Zhu, Xiaofeng

    Published in BMC genomics
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