Genetic Effects on Postprandial Variations of Inflammatory Markers in Healthy Individuals von Cheng, Yu‐Ching, Kao, Wen‐Hong L., Mitchell, Braxton D., Sharrett, A. Richey, Ryan, Kathleen A., Vogel, Robert A., Shuldiner, Alan R., Pollin, Toni I.

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Genome-Wide Association of Copy Number Polymorphisms and Kidney Function von Li, Man, Carey, Jacob, Cristiano, Stephen, Susztak, Katalin, Coresh, Josef, Boerwinkle, Eric, Kao, Wen Hong L, Beaty, Terri H, Köttgen, Anna, Scharpf, Robert B

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Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes von MORRIS, Andrew P, VOIGHT, Benjamin F, PROKOPENKO, Inga, HYUN MIN KANG, DINA, Christian, ESKOE, Tonu, FRASER, Ross M, KANONI, Stavroula, KUMAR, Ashish, LAGOU, Vasiliki, LANGENBERG, Claudia, LUAN, Jian'an, TESLOVICH, Tanya M, LINDGREN, Cecilia M, MÜLLER-NURASYID, Martina, PECHLIVANIS, Sonali, RAYNER, N. William, SCOTT, Laura J, WILTSHIRE, Steven, YENGO, Loic, KINNUNEN, Leena, ROSSIN, Elizabeth J, RAYCHAUDHURI, Soumya, FERREIRA, Teresa, JOHNSON, Andrew D, DIMAS, Antigones, LOOS, Ruthj F, VEDANTAM, Sailaja, HAN CHEN, FLOREZ, Jose C, FOX, Caroline, LIU, Ching-Ti, RYBIN, Denis, COUPER, David J, SEGRE, Ayellet V, KAO, Wen Hong L, MAN LI, CORNELIS, Marilyn C, KRAFT, Peter, QI SUN, VAN DAM, Rob M, STRINGHAM, Heather M, CHINES, Peter S, FISCHER, Krista, FONTANILLAS, Pierre, STEINTHORSDOTTIR, Valgerdur, HOLMEN, Oddgeir L, HUNT, Sarah E, JACKSON, Anne U, KONG, Augustine, LAWRENCE, Robert, MEYER, Julia, PERRY, John R. B, PLATOU, Carl G. P, POTTER, Simon, REHNBERG, Emil, STRAWBRIDGE, Rona J, KHAN, Hassan, GRALLERT, Harald, MAHAJAN, Anubha

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Sequence variation in IGF1R is associated with differences in insulin levels in nondiabetic Old Order Amish von Naj, Adam C., Kao, Wen-Hong L., O'Connell, Jeffrey R., Mitchell, Braxton D., Silver, Kristi D.

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Cytomegalovirus Infection and the Risk of Mortality and Frailty in Older Women: A Prospective Observational Cohort Study von Wang, George C., Kao, Wen Hong L., Murakami, Peter, Xue, Qian-Li, Chiou, Roger B., Detrick, Barbara, McDyer, John F., Semba, Richard D., Casolaro, Vincenzo, Walston, Jeremy D., Fried, Linda P.

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Genome-Wide Association Scan Identifies Variants near Matrix Metalloproteinase (MMP) Genes on Chromosome 11q21-22 Strongly Associated With Serum MMP-1 Levels von Cheng, Yu-Ching, Kao, Wen-Hong L, Mitchell, Braxton D, O'Connell, Jeffrey R, Shen, Haiqing, McArdle, Patrick F, Gibson, Quince, Ryan, Kathleen A, Shuldiner, Alan R, Pollin, Toni I

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Genome-wide association study for renal traits in the Framingham Heart and Atherosclerosis Risk in Communities Studies von Kottgen, Anna, Kao, Wen Hong L, Hwang, Shih-Jen, Boerwinkle, Eric, Yang, Qiong, Levy, Daniel, Benjamin, Emelia J, Larson, Martin G, Astor, Brad C, Coresh, Josef, Fox, Caroline S

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Association of APOE polymorphism with chronic kidney disease in a nationally representative sample: a Third National Health and Nutrition Examination Survey (NHANES III) Genetic St... von Chu, Audrey Y, Parekh, Rulan S, Astor, Brad C, Coresh, Josef, Berthier-Schaad, Yvette, Smith, Michael W, Shuldiner, Alan R, Kao, Wen Hong L

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Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility von Below, Jennifer E, Horikoshi, Momoko, Johnson, Andrew D, Ng, Maggie C Y, Abecasis, Goncalo R, Been, Latonya F, Caulfield, Mark, Chang, Li-Ching, Chang, Tien-Jyun, Chang, Yi-Cheng, Chen, Chien-Hsiun, Chen, Han, Chidambaram, Manickam, Cho, Young Min, Collins, Francis S, Das, Debashish, Dedoussis, George, Dimas, Antigone S, Doney, Alex S F, Dorkhan, Mozhgan, Edkins, Sarah, Erbel, Raimund, Fontanillas, Pierre, Fox, Caroline, Froguel, Philippe, Gao, Yutang, Gieger, Christian, Gigante, Bruna, Grallert, Harald, Guiducci, Candace, Hamsten, Anders, Hattersley, Andrew T, Hayward, Caroline, Herder, Christian, Hofman, Albert, Holmen, Oddgeir L, Humphries, Steve E, Hydrie, Zafar I, Jackson, Anne U, Jia, Weiping, Kato, Norihiro, Kelly, Ann M, Khan, Hassan, Kim, Hyung-Lae, Kong, Augustine, Korpi-Hyövälti, Eeva, Kumar, Ashish, Laakso, Markku, Langenberg, Claudia, Li, Man, Li, Xinzhong, Li, Yun, Liang, Junbin, Liju, Samuel, Lind, Lars, Lindgren, Cecilia M, Lobbens, Stéphane, Lu, Wei, Luan, Jian'an, Lyssenko, Valeriya, Männistö, Satu, Meigs, James B, Meyer, Julia, Mohlke, Karen L, Musk, Bill, Nakamura, Jiro, Park, Kyong Soo, Rallidis, Loukianos, Rasheed, Asif, Rehnberg, Emil, Rudan, Igor, Rybin, Denis, Saaristo, Timo E, Sanghera, Dharambir K, Saramies, Jouko, Scott, Robert A, Shah, Nabi, Sim, Xueling, Sivapalaratnam, Suthesh, Stančáková, Alena, Steinthorsdottir, Valgerdur, Stirrups, Kathleen, Strawbridge, Rona J, Takeuchi, Fumihiko, Thorsteinsdottir, Unnur, Trip, Mieke D, Valladares-Salgado, Adan, Wang, Congrong, Wickremasinghe, Ananda R, Wu, Ying, Yamamoto, Ken, Yang, Mingyu, Young, Robin, Zhang, Fan, Zhang, Rong, Altshuler, David, Cho, Yoon Shin, Lee, Jong-Young, Teo, Yik Ying, Boehnke, Michael

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Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci von Reschen, Michael E, Mahajan, Anubha, William Rayner, N, Scott, Laura J, Yengo, Loic, Wahl, Simone, Kestler, Hans, Chheda, Himanshu, Eisele, Lewin, Steinthorsdottir, Valgerdur, Chen, Han, Fuchsberger, Christian, Kwan, Phoenix, Thomsen, Soren K, Rundle, Jana K, van de Bunt, Martijn, Voight, Benjamin F, Abecasis, Gonçalo R, Baldassarre, Damiano, Carey, Jason, Chines, Peter S, Crenshaw, Andrew T, Edkins, Sarah, Eury, Elodie, Fontanillas, Pierre, Franks, Paul W, Gertow, Karl, Groves, Christopher J, Hassinen, Maija, Herder, Christian, Hreidarsson, Astradur B, Jackson, Anne U, Jonsson, Anna, Jørgensen, Marit E, Jørgensen, Torben, Kao, Wen-Hong L, Kerrison, Nicola D, Kinnunen, Leena, Kravic, Jasmina, Langford, Cordelia, Lichtner, Peter, Lindholm, Eero, Lobbens, Stéphane, Luan, Jian'an, Meyer, Julia, Mihailov, Evelin, Mühleisen, Thomas W, Navarro, Carmen, Oskolkov, Nikolay N, Pechlivanis, Sonali, Platou, Carl G P, Rybin, Denis, van der Schouw, Yvonne T, Sennblad, Bengt, Steinbach, Gerald, Storm, Petter, Sun, Qi, Thorand, Barbara, Tikkanen, Emmi, Trakalo, Joseph, Tremoli, Elena, Wood, Andrew R, Zeggini, Eleftheria, Birney, Ewan, Pasquali, Lorenzo, Pankow, James S, van Duijn, Cornelia, Sijbrands, Eric, Hu, Frank B, Thorsteinsdottir, Unnur, Stefansson, Kari, Lakka, Timo A, Rauramaa, Rainer, Stumvoll, Michael, Korpi-Hyövälti, Eeva, Kuusisto, Johanna, Metspalu, Andres, Jöcke, Karl-Heinz, Moebus, Susanne, Bergman, Richard N, Collins, Francis S, Mohlke, Karen L, Koistinen, Heikki, Tuomilehto, Jaakko, Deloukas, Panagiotis, Donnelly, Peter J, Frayling, Timothy M, Sladek, Rob, Froguel, Philippe, Hansen, Torben, Kathiresan, Sekar, Barroso, Inês, Langenberg, Claudia, Wareham, Nicholas J, O'Callaghan, Christopher A, Gloyn, Anna L, Altshuler, David, Boehnke, Michael, Teslovich, Tanya M, Morris, Andrew P

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Large-Scale Association Analysis Provides Insights into the Genetic Architecture and Pathophysiology of Type 2 Diabetes von Teslovich, Tanya M, Ferreira, Teresa, Segré, Ayellet V, Steinthorsdottir, Valgerdur, Strawbridge, Rona J, Grallert, Harald, Mahajan, Anubha, Kang, Hyun Min, Dina, Christian, Esko, Tonu, Fraser, Ross M, Kumar, Ashish, Lagou, Vasiliki, Luan, Jian’an, Lindgren, Cecilia M, Müller-Nurasyid, Martina, Pechlivanis, Sonali, Raychaudhuri, Soumya, Loos, Ruth J F, Vedantam, Sailaja, Chen, Han, Couper, David J, Li, Man, Cornelis, Marilyn, Kraft, Peter Elias, Chines, Peter S, Fischer, Krista, Jackson, Anne U, Lawrence, Robert, Rehnberg, Emil, Sivapalaratnam, Suthesh, Thorleifsson, Gudmar, Almgren, Peter, Atalay, Mustafa, Charpentier, Guillaume, Doney, Alex S F, Dorkhan, Mozhgan, Eury, Elodie, Gigante, Bruna, Herder, Christian, Hui, Jennie, Jonsson, Anna, Klopp, Norman, Kravic, Jasmina, Krjutškov, Kaarel, Langford, Cordelia, Leander, Karin, Männistö, Satu, Mirza, Ghazala, Mühleisen, Thomas W, Rallidis, Loukianos, Saramies, Jouko, Sigurðsson, Gunnar, Steinbach, Gerald, Thorand, Barbara, Trakalo, Joseph, Wennauer, Roman, Winckler, Wendy, Zabaneh, Delilah, Uitterlinden, Andre G, Hofman, Albert, Sijbrands, Eric, Abecasis, Goncalo R, Owen, Katharine R, Forouhi, Nita G, Syvänen, Ann-Christine, Eriksson, Johan G, Lyssenko, Valeriya, Isomaa, Bo, Hunter, David J, Shuldiner, Alan R, Barroso, Ines, Price, Jackie F, Wilson, James F, Pedersen, Nancy L, Khaw, Kay-Tee, Wareham, Nicholas J, Korpi-Hyövälti, Eeva, Laakso, Markku, Kuusisto, Johanna, Mohlke, Karen L, Bergman, Richard N, Tuomilehto, Jaakko, Boehm, Bernhard O, Gieger, Christian, Hveem, Kristian, Humphries, Steve E, Danesh, John, Salomaa, Veikko, Erbel, Raimund, Jöckel, Karl-Heinz, Peters, Annette, Illig, Thomas, Hattersley, Andrew T, Boerwinkle, Eric, Melander, Olle, Thorsteinsdottir, Unnur, Groop, Leif C, Pankow, James S, Altshuler, David Matthew

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Association of APOEpolymorphism with chronic kidney disease in a nationally representative sample: a Third National Health and Nutrition Examination Survey (NHANES III) Genetic Stu... von Chu, Audrey Y, Parekh, Rulan S, Astor, Brad C, Coresh, Josef, Berthier-Schaad, Yvette, Smith, Michael W, Shuldiner, Alan R, Kao, Wen Hong L

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Association of APOE polymorphism with chronic kidney disease in a nationally representative sample: a Third National Health and Nutrition Examination Survey von Chu, Audrey Y, Parekh, Rulan S, Astor, Brad C, Coresh, Josef, Berthier-Schaad, Yvette, Smith, Michael W, Shuldiner, Alan R, Kao, Wen Hong L

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Genome-Wide Association Study for Renal Traits in the Framingham Heart and Atherosclerosis Risk in Communities Studies von Kottgen, Anna, Kao, Wen Hong L, Hwang, Shih-Jen, Boerwinkle, Eric, Yang, Qiong, Benjamin, Emelia J, Larson, Martin G, Astor, Brad C, Coresh, Josef, Levy, Danielle Marie, Fox, Caroline

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Genome-wide association study for renal traits in the Framingham Heart and Atherosclerosis Risk in Communities Studies-0 von Kottgen, Anna, Hong L Kao, Wen, Hwang, Shih-Jen, Boerwinkle, Eric, Yang, Qiong, Levy, Daniel, J Benjamin, Emelia, G Larson, Martin, C Astor, Brad, Coresh, Josef, S Fox, Caroline

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Frailty and Cognitive Function in Incident Hemodialysis Patients von McAdams-DeMarco, Mara A, Tan, Jingwen, Salter, Megan L, Gross, Alden, Meoni, Lucy A, Jaar, Bernard G, Kao, Wen-Hong Linda, Parekh, Rulan S, Segev, Dorry L, Sozio, Stephen M

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Age and Sex Disparities in Discussions About Kidney Transplantation in Adults Undergoing Dialysis von Salter, Megan L., McAdams-Demarco, Mara A., Law, Andrew, Kamil, Rebecca J., Meoni, Lucy A., Jaar, Bernard G., Sozio, Stephen M., Linda Kao, Wen Hong, Parekh, Rulan S., Segev, Dorry L.

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Association Between Variants in or Near PNPLA3 , GCKR , and PPP1R3B With Ultrasound-Defined Steatosis Based on Data From the Third National Health and Nutrition Examination Survey von Hernaez, Ruben, McLean, Jody, Lazo, Mariana, Brancati, Frederick L, Hirschhorn, Joel N, Borecki, Ingrid B, Harris, Tamara B, Nguyen, Thutrang, Kamel, Ihab R, Bonekamp, Susanne, Eberhardt, Mark S, Clark, Jeanne M, Kao, Wen Hong Linda, Speliotes, Elizabeth K

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Interaction of FTO and Physical Activity Level on Adiposity in African‐American and European‐American Adults: The ARIC Study von Demerath, Ellen W., Lutsey, Pam L., Monda, Keri L., Linda‐Kao, Wen Hong, Bressler, Jan, Pankow, James S., North, Kari E., Folsom, Aaron R.

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Genome-wide association study for serum urate concentrations and gout among African Americans identifies genomic risk loci and a novel URAT1 loss-of-function allele von Tin, Adrienne, Woodward, Owen M., Kao, Wen Hong Linda, Liu, Ching-Ti, Lu, Xiaoning, Nalls, Michael A., Shriner, Daniel, Semmo, Mariam, Akylbekova, Ermeg L., Wyatt, Sharon B., Hwang, Shih-Jen, Yang, Qiong, Zonderman, Alan B., Adeyemo, Adebowale A., Palmer, Cameron, Meng, Yan, Reilly, Muredach, Shlipak, Michael G., Siscovick, David, Evans, Michele K., Rotimi, Charles N., Flessner, Michael F., Köttgen, Michael, Cupples, L. Adrienne, Fox, Caroline S., Köttgen, Anna

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