Genome-Wide Association Studies of Serum Magnesium, Potassium, and Sodium Concentrations Identify Six Loci Influencing Serum Magnesium Levels

por Meyer, Tamra E., Verwoert, Germaine C., Hwang, Shih-Jen, Glazer, Nicole L., Smith, Albert V., van Rooij, Frank J. A., Ehret, Georg B., Boerwinkle, Eric, Felix, Janine F., Leak, Tennille S., Harris, Tamara B., Yang, Qiong, Dehghan, Abbas, Aspelund, Thor, Katz, Ronit, Homuth, Georg, Kocher, Thomas, Rettig, Rainer, Ried, Janina S., Gieger, Christian, Prucha, Hanna, Pfeufer, Arne, Meitinger, Thomas, Coresh, Josef, Hofman, Albert, Sarnak, Mark J., Chen, Yii-Der Ida, Uitterlinden, André G., Chakravarti, Aravinda, Psaty, Bruce M., van Duijn, Cornelia M., Kao, W. H. Linda, Witteman, Jacqueline C. M., Gudnason, Vilmundur, Siscovick, David S., Fox, Caroline S., Köttgen, Anna
Publicado 2010

Genetic Association for Renal Traits among Participants of African Ancestry Reveals New Loci for Renal Function

por Liu, Ching-Ti, Garnaas, Maija K., Tin, Adrienne, Kottgen, Anna, Franceschini, Nora, Peralta, Carmen A., de Boer, Ian H., Lu, Xiaoning, Atkinson, Elizabeth, Ding, Jingzhong, Nalls, Michael, Shriner, Daniel, Coresh, Josef, Kutlar, Abdullah, Bibbins-Domingo, Kirsten, Siscovick, David, Akylbekova, Ermeg, Wyatt, Sharon, Astor, Brad, Mychaleckjy, Josef, Li, Man, Reilly, Muredach P., Townsend, Raymond R., Adeyemo, Adebowale, Zonderman, Alan B., de Andrade, Mariza, Turner, Stephen T., Mosley, Thomas H., Harris, Tamara B., Rotimi, Charles N., Liu, Yongmei, Kardia, Sharon L. R., Evans, Michele K., Shlipak, Michael G., Kramer, Holly, Flessner, Michael F., Dreisbach, Albert W., Goessling, Wolfram, Cupples, L. Adrienne, Kao, W. Linda, Fox, Caroline S.
Publicado 2011

Trans-ethnic Mendelian-randomization study reveals causal relationships between cardiometabolic factors and chronic kidney disease

por Zheng, Jie, Zhang, Yuemiao, Rasheed, Humaira, Walker, Venexia, Sugawara, Yuka, Li, Jiachen, Leng, Yue, Elsworth, Benjamin, Wootton, Robyn E, Fang, Si, Yang, Qian, Burgess, Stephen, Haycock, Philip C, Borges, Maria Carolina, Cho, Yoonsu, Carnegie, Rebecca, Howell, Amy, Robinson, Jamie, Thomas, Laurent F, Brumpton, Ben Michael, Hveem, Kristian, Hallan, Stein, Franceschini, Nora, Morris, Andrew P, Köttgen, Anna, Pattaro, Cristian, Wuttke, Matthias, Yamamoto, Masayuki, Kashihara, Naoki, Akiyama, Masato, Kanai, Masahiro, Matsuda, Koichi, Kamatani, Yoichiro, Okada, Yukinori, Walters, Robin, Millwood, Iona Y, Chen, Zhengming, Davey Smith, George, Barbour, Sean, Yu, Canqing, Åsvold, Bjørn Olav, Zhang, Hong, Gaunt, Tom R
Publicado 2021

Genome-wide studies reveal factors associated with circulating uromodulin and its relationships to complex diseases

por Li, Yong, Cheng, Yurong, Consolato, Francesco, Schiano, Guglielmo, Chong, Michael R., Pietzner, Maik, Nguyen, Ngoc Quynh H., Scherer, Nora, Biggs, Mary L., Kleber, Marcus E., Haug, Stefan, Göçmen, Burulça, Pigeyre, Marie, Sekula, Peggy, Steinbrenner, Inga, Schlosser, Pascal, Joseph, Christina B., Brody, Jennifer A., Grams, Morgan E., Hayward, Caroline, Schultheiss, Ulla T., Krämer, Bernhard K., Kronenberg, Florian, Peters, Annette, Seissler, Jochen, Steubl, Dominik, Then, Cornelia, Wuttke, Matthias, März, Winfried, Eckardt, Kai-Uwe, Gieger, Christian, Boerwinkle, Eric, Psaty, Bruce M., Coresh, Josef, Oefner, Peter J., Pare, Guillaume, Langenberg, Claudia, Scherberich, Jürgen E., Yu, Bing, Akilesh, Shreeram, Devuyst, Olivier, Rampoldi, Luca, Köttgen, Anna
Publicado 2022

Implication of FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)

por Riedhammer, Korbinian M., Nguyen, Thanh-Minh T., Koşukcu, Can, Calzada-Wack, Julia, Li, Yong, Saygılı, Seha, Wimmers, Vera, Kim, Gwang-Jin, Chrysanthou, Marialena, Bakey, Zeineb, Kraiger, Markus, Sanz-Moreno, Adrián, Amarie, Oana V, Rathkolb, Birgit, Klein-Rodewald, Tanja, Garrett, Lillian, Hölter, Sabine M., Seisenberger, Claudia, Haug, Stefan, Marschall, Susan, Wurst, Wolfgang, Fuchs, Helmut, Gailus-Durner, Valerie, Wuttke, Matthias, de Angelis, Martin Hrabe, Ćomić, Jasmina, Doğan, Özlem Akgün, Özlük, Yasemin, Taşdemir, Mehmet, Ağbaş, Ayşe, Canpolat, Nur, Ćalışkan, Salim, Weber, Ruthild, Bergmann, Carsten, Jeanpierre, Cecile, Saunier, Sophie, Lim, Tze Y., Hildebrandt, Friedhelm, Alhaddad, Bader, Wu, Kaman, Antony, Dinu, Matschkal, Julia, Schaaf, Christian, Renders, Lutz, Schmaderer, Christoph, Meitinger, Thomas, Heemann, Uwe, Köttgen, Anna, Arnold, Sebastian, Ozaltin, Fatih, Schmidts, Miriam, Hoefele, Julia
Publicado 2023

Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry

por Benjamin, Emelia J., Rice, Kenneth M., Arking, Dan E., Pfeufer, Arne, van Noord, Charlotte, Smith, Albert V., Schnabel, Renate B., Bis, Joshua C., Boerwinkle, Eric, Sinner, Moritz F., Dehghan, Abbas, Lubitz, Steven A., D’Agostino, Ralph B., Lumley, Thomas, Ehret, Georg B., Heeringa, Jan, Aspelund, Thor, Newton-Cheh, Christopher, Larson, Martin G., Marciante, Kristin D., Soliman, Elsayed Z., Rivadeneira, Fernando, Wang, Thomas J., Eiriksdottir, Gudny, Levy, Daniel, Psaty, Bruce M., Li, Man, Chamberlain, Alanna M., Hofman, Albert, Vasan, Ramachandran S., Harris, Tamara B., Rotter, Jerome I., Kao, W.H. Linda, Agarwal, Sunil K., Ch. Stricker, Bruno H., Wang, Ke, Launer, Lenore J., Smith, Nicholas L., Chakravarti, Aravinda, Uitterlinden, Andre G., Wolf, Philip A, Sotoodehnia, Nona, Kottgen, Anna, van Duijn, Cornelia M., Lunetta, Kathryn L., Heckbert, Susan R., Gudnason, Vilmundur, Alonso, Alvaro, Kaab, Stefan, Ellinor, Patrick T., Witteman, Jacqueline C.
Publicado 2009

Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium

por Ganesh, Santhi K., Zakai, Neil A., van Rooij, Frank J A., Soranzo, Nicole, Smith, Albert V., Nalls, Michael A., Chen, Ming-Huei, Kottgen, Anna, Glazer, Nicole L., Dehghan, Abbas, Kuhnel, Brigitte, Aspelund, Thor, Yang, Qiong, Tanaka, Toshiko, Jaffe, Andrew, Bis, Joshua C M., Verwoert, Germaine C., Teumer, Alexander, Fox, Caroline S., Guralnik, Jack M., Ehret, Georg B., Rice, Kenneth, Felix, Janine F., Rendon, Augusto, Eiriksdottir, Gudny, Levy, Daniel, Patel, Kushang V., Boerwinkle, Eric, Rotter, Jerome I., Hofman, Albert, Sambrook, Jennifer G., Hernandez, Dena, Zheng, Gang, Bandinelli, Stefania, Singleton, Andrew B., Coresh, Josef, Lumley, Thomas, Uitterlinden, André G., vanGils, Janine M., Launer, Lenore J., Cupples, L. Adrienne, Oostra, Ben A., Zwaginga, Jaap-Jan, Ouwehand, Willem H., Thein, Swee-Lay, Meisinger, Christa, Deloukas, Panos, Nauck, Matthias, Spector, Tim, Gieger, Christian, Gudnason, Vilmundur, van Duijn, Cornelia M., Psaty, Bruce M., Ferrucci, Luigi, Chakravarti, Aravinda, Greinacher, Andreas, O’Donnell, Christopher J., Witteman, Jacqueline C M., Furth, Susan, Cushman, Mary, Harris, Tamara B., Lin, Jing-Ping
Publicado 2009

Common Variants in KCNN3 are Associated with Lone Atrial Fibrillation

por Ellinor, Patrick T., Lunetta, Kathryn L., Glazer, Nicole L., Pfeufer, Arne, Alonso, Alvaro, Chung, Mina K., Sinner, Moritz F., de Bakker, Paul I. W., Mueller, Martina, Lubitz, Steven A., Fox, Ervin, Darbar, Dawood, Smith, Nicholas L., Smith, Jonathan D., Schnabel, Renate B., Soliman, Elsayed Z., Rice, Kenneth M., Van Wagoner, David R., Beckmann, Britt-M., van Noord, Charlotte, Wang, Ke, Ehret, Georg B., Rotter, Jerome I., Hazen, Stanley L., Steinbeck, Gerhard, Smith, Albert V., Launer, Lenore J., Harris, Tamara B., Makino, Seiko, Nelis, Mari, Milan, David J., Perz, Siegfried, Esko, Tõnu, Köttgen, Anna, Moebus, Susanne, Newton-Cheh, Christopher, Li, Man, Möhlenkamp, Stefan, Wang, Thomas J., Kao, W.H. Linda, Vasan, Ramachandran S., Nöthen, Markus M., MacRae, Calum A., Stricker, Bruno H. Ch., Hofman, Albert, Uitterlinden, André G., Levy, Daniel, Boerwinkle, Eric, Metspalu, Andres, Topol, Eric J., Chakravarti, Aravinda, Gudnason, Vilmundur, Psaty, Bruce M., Roden, Dan M., Meitinger, Thomas, Wichmann, H.-Erich, Witteman, Jacqueline C.M., Barnard, John, Arking, Dan E., Benjamin, Emelia J., Heckbert, Susan R., Kääb, Stefan
Publicado 2010

Identification of a Sudden Cardiac Death Susceptibility Locus at 2q24.2 through Genome-Wide Association in European Ancestry Individuals

por Arking, Dan E., Junttila, M. Juhani, Goyette, Philippe, Huertas-Vazquez, Adriana, Eijgelsheim, Mark, Blom, Marieke T., Newton-Cheh, Christopher, Reinier, Kyndaron, Teodorescu, Carmen, Uy-Evanado, Audrey, Carter-Monroe, Naima, Kaikkonen, Kari S., Kortelainen, Marja-Leena, Boucher, Gabrielle, Lagacé, Caroline, Moes, Anna, Zhao, XiaoQing, Kolodgie, Frank, Rivadeneira, Fernando, Hofman, Albert, Witteman, Jacqueline C. M., Uitterlinden, André G., Marsman, Roos F., Pazoki, Raha, Bardai, Abdennasser, Koster, Rudolph W., Dehghan, Abbas, Hwang, Shih-Jen, Bhatnagar, Pallav, Post, Wendy, Hilton, Gina, Prineas, Ronald J., Li, Man, Köttgen, Anna, Ehret, Georg, Boerwinkle, Eric, Coresh, Josef, Kao, W. H. Linda, Psaty, Bruce M., Tomaselli, Gordon F., Sotoodehnia, Nona, Siscovick, David S., Burke, Greg L., Marbán, Eduardo, Spooner, Peter M., Cupples, L. Adrienne, Jui, Jonathan, Gunson, Karen, Kesäniemi, Y. Antero, Wilde, Arthur A. M., Tardif, Jean-Claude, O'Donnell, Christopher J., Bezzina, Connie R., Virmani, Renu, Stricker, Bruno H. C. h., Tan, Hanno L., Albert, Christine M., Chakravarti, Aravinda, Rioux, John D., Huikuri, Heikki V., Chugh, Sumeet S.
Publicado 2011

Association of omega 3 polyunsaturated fatty acids with incident chronic kidney disease: pooled analysis of 19 cohorts

por Ong, Kwok Leung, Marklund, Matti, Huang, Liping, Rye, Kerry-Anne, Hui, Nicholas, Pan, Xiong-Fei, Rebholz, Casey M, Kim, Hyunju, Steffen, Lyn M, van Westing, Anniek C, Geleijnse, Johanna M, Hoogeveen, Ellen K, Chen, Yun-Yu, Chien, Kuo-Liong, Fretts, Amanda M, Lemaitre, Rozenn N, Imamura, Fumiaki, Forouhi, Nita G, Wareham, Nicholas J, Birukov, Anna, Jäger, Susanne, Kuxhaus, Olga, Schulze, Matthias B, de Mello, Vanessa Derenji, Tuomilehto, Jaakko, Uusitupa, Matti, Lindström, Jaana, Tintle, Nathan, Harris, William S, Yamasaki, Keisuke, Hirakawa, Yoichiro, Ninomiya, Toshiharu, Tanaka, Toshiko, Ferrucci, Luigi, Bandinelli, Stefania, Virtanen, Jyrki K, Voutilainen, Ari, Jayasena, Tharusha, Thalamuthu, Anbupalam, Poljak, Anne, Bustamante, Sonia, Sachdev, Perminder S, Senn, Mackenzie K, Rich, Stephen S, Tsai, Michael Y, Wood, Alexis C, Laakso, Markku, Lankinen, Maria, Yang, Xiaowei, Sun, Liang, Li, Huaixing, Lin, Xu, Nowak, Christoph, Ärnlöv, Johan, Risérus, Ulf, Lind, Lars, Le Goff, Mélanie, Samieri, Cécilia, Helmer, Catherine, Qian, Frank, Micha, Renata, Tin, Adrienne, Köttgen, Anna, de Boer, Ian H, Siscovick, David S, Mozaffarian, Dariush, Wu, Jason HY
Publicado 2023

Genome-wide association study of PR interval

por Pfeufer, Arne, van Noord, Charlotte, Marciante, Kristin D., Arking, Dan E., Larson, Martin G., Smith, Albert Vernon, Tarasov, Kirill V., Müller, Martina, Sotoodehnia, Nona, Sinner, Moritz F., Verwoert, Germaine C., Li, Man, Kao, W.H. Linda, Köttgen, Anna, Coresh, Josef, Bis, Joshua C., Psaty, Bruce M., Rice, Kenneth, Rotter, Jerome I., Rivadeneira, Fernando, Hofman, Albert, Kors, Jan A., Stricker, Bruno H.C., Uitterlinden, André G., van Duijn, Cornelia M., Beckmann, Britt M., Sauter, Wiebke, Gieger, Christian, Lubitz, Steven A., Newton-Cheh, Christopher, Wang, Thomas J., Magnani, Jared W., Schnabel, Renate B., Chung, Mina K., Barnard, John, Smith, Jonathan D., Van Wagoner, David R., Vasan, Ramachandran S., Aspelund, Thor, Eiriksdottir, Gudny, Harris, Tamara B., Launer, Lenore J., Najjar, Samer S., Lakatta, Edward, Schlessinger, David, Uda, Manuela, Abecasis, Gonçalo R., Müller-Myhsok, Bertram, Ehret, Georg B., Boerwinkle, Eric, Chakravarti, Aravinda, Soliman, Elsayed Z., Lunetta, Kathryn L., Perz, Siegfried, Wichmann, H.-Erich, Meitinger, Thomas, Levy, Daniel, Gudnason, Vilmundur, Ellinor, Patrick T., Sanna, Serena, Kääb, Stefan, Witteman, Jacqueline C.M., Alonso, Alvaro, Benjamin, Emelia J., Heckbert, Susan R.
Publicado 2010

Stratifying Type 2 Diabetes Cases by BMI Identifies Genetic Risk Variants in LAMA1 and Enrichment for Risk Variants in Lean Compared to Obese Cases

por Perry, John R. B., Voight, Benjamin F., Yengo, Loïc, Amin, Najaf, Dupuis, Josée, Ganser, Martha, Grallert, Harald, Navarro, Pau, Li, Man, Qi, Lu, Steinthorsdottir, Valgerdur, Scott, Robert A., Almgren, Peter, Arking, Dan E., Aulchenko, Yurii, Balkau, Beverley, Benediktsson, Rafn, Bergman, Richard N., Boerwinkle, Eric, Bonnycastle, Lori, Burtt, Noël P., Campbell, Harry, Charpentier, Guillaume, Collins, Francis S., Gieger, Christian, Green, Todd, Hadjadj, Samy, Hattersley, Andrew T., Herder, Christian, Hofman, Albert, Johnson, Andrew D., Kottgen, Anna, Kraft, Peter, Labrune, Yann, Langenberg, Claudia, Manning, Alisa K., Mohlke, Karen L., Morris, Andrew P., Oostra, Ben, Pankow, James, Petersen, Ann-Kristin, Pramstaller, Peter P., Prokopenko, Inga, Rathmann, Wolfgang, Rayner, William, Roden, Michael, Rudan, Igor, Rybin, Denis, Scott, Laura J., Sigurdsson, Gunnar, Sladek, Rob, Thorleifsson, Gudmar, Thorsteinsdottir, Unnur, Tuomilehto, Jaakko, Uitterlinden, Andre G., Vivequin, Sidonie, Weedon, Michael N., Wright, Alan F., Hu, Frank B., Illig, Thomas, Kao, Linda, Meigs, James B., Wilson, James F., Stefansson, Kari, van Duijn, Cornelia, Altschuler, David, Morris, Andrew D., Boehnke, Michael, McCarthy, Mark I., Froguel, Philippe, Palmer, Colin N. A., Wareham, Nicholas J., Groop, Leif, Frayling, Timothy M., Cauchi, Stéphane
Publicado 2012

Whole genome sequence analyses of eGFR in 23,732 people representing multiple ancestries in the NHLBI trans-omics for precision medicine (TOPMed) consortium

por Lin, Bridget M, Grinde, Kelsey E, Brody, Jennifer A, Breeze, Charles E, Raffield, Laura M, Mychaleckyj, Josyf C, Thornton, Timothy A, Perry, James A, Baier, Leslie J, de las Fuentes, Lisa, Guo, Xiuqing, Heavner, Benjamin D, Hanson, Robert L, Hung, Yi-Jen, Qian, Huijun, Hsiung, Chao A, Hwang, Shih-Jen, Irvin, Margaret R, Jain, Deepti, Kelly, Tanika N, Kobes, Sayuko, Lange, Leslie, Lash, James P, Li, Yun, Liu, Xiaoming, Mi, Xuenan, Musani, Solomon K, Papanicolaou, George J, Parsa, Afshin, Reiner, Alex P, Salimi, Shabnam, Sheu, Wayne H-H, Shuldiner, Alan R, Taylor, Kent D, Smith, Albert V, Smith, Jennifer A, Tin, Adrienne, Vaidya, Dhananjay, Wallace, Robert B, Yamamoto, Kenichi, Sakaue, Saori, Matsuda, Koichi, Kamatani, Yoichiro, Momozawa, Yukihide, Yanek, Lisa R, Young, Betsi A, Zhao, Wei, Okada, Yukinori, Abecasis, Gonzalo, Psaty, Bruce M, Arnett, Donna K, Boerwinkle, Eric, Cai, Jianwen, Yii-Der Chen, Ida, Correa, Adolfo, Cupples, L Adrienne, He, Jiang, Kardia, Sharon LR, Kooperberg, Charles, Mathias, Rasika A, Mitchell, Braxton D, Nickerson, Deborah A, Turner, Steve T, Ramachandran, Vasan S, Rotter, Jerome I, Levy, Daniel, Kramer, Holly J, Köttgen, Anna, NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, TOPMed Kidney Working Group, Rich, Stephen S, Lin, Dan-Yu, Browning, Sharon R, Franceschini, Nora
Publicado 2021

DNA methylation signature of chronic low-grade inflammation and its role in cardio-respiratory diseases

por Wielscher, Matthias, Mandaviya, Pooja R., Kuehnel, Brigitte, Joehanes, Roby, Mustafa, Rima, Robinson, Oliver, Zhang, Yan, Bodinier, Barbara, Walton, Esther, Mishra, Pashupati P., Schlosser, Pascal, Wilson, Rory, Tsai, Pei-Chien, Palaniswamy, Saranya, Marioni, Riccardo E., Fiorito, Giovanni, Cugliari, Giovanni, Karhunen, Ville, Ghanbari, Mohsen, Psaty, Bruce M., Loh, Marie, Bis, Joshua C., Lehne, Benjamin, Sotoodehnia, Nona, Deary, Ian J., Chadeau-Hyam, Marc, Brody, Jennifer A., Cardona, Alexia, Selvin, Elizabeth, Smith, Alicia K., Miller, Andrew H., Torres, Mylin A., Marouli, Eirini, Gào, Xin, van Meurs, Joyce B. J., Graf-Schindler, Johanna, Rathmann, Wolfgang, Koenig, Wolfgang, Peters, Annette, Weninger, Wolfgang, Farlik, Matthias, Zhang, Tao, Chen, Wei, Xia, Yujing, Teumer, Alexander, Nauck, Matthias, Grabe, Hans J., Doerr, Macus, Lehtimäki, Terho, Guan, Weihua, Milani, Lili, Tanaka, Toshiko, Fisher, Krista, Waite, Lindsay L., Kasela, Silva, Vineis, Paolo, Verweij, Niek, van der Harst, Pim, Iacoviello, Licia, Sacerdote, Carlotta, Panico, Salvatore, Krogh, Vittorio, Tumino, Rosario, Tzala, Evangelia, Matullo, Giuseppe, Hurme, Mikko A., Raitakari, Olli T., Colicino, Elena, Baccarelli, Andrea A., Kähönen, Mika, Herzig, Karl-Heinz, Li, Shengxu, Conneely, Karen N., Kooner, Jaspal S., Köttgen, Anna, Heijmans, Bastiaan T., Deloukas, Panos, Relton, Caroline, Ong, Ken K., Bell, Jordana T., Boerwinkle, Eric, Elliott, Paul, Brenner, Hermann, Beekman, Marian, Levy, Daniel, Waldenberger, Melanie, Chambers, John C., Dehghan, Abbas, Järvelin, Marjo-Riitta
Publicado 2022

Meta-Analysis of Genome-Wide Association Studies Identifies Six New Loci for Serum Calcium Concentrations

por O'Seaghdha, Conall M., Wu, Hongsheng, Yang, Qiong, Kapur, Karen, Guessous, Idris, Zuber, Annie Mercier, Köttgen, Anna, Stoudmann, Candice, Teumer, Alexander, Kutalik, Zoltán, Mangino, Massimo, Dehghan, Abbas, Zhang, Weihua, Eiriksdottir, Gudny, Li, Guo, Tanaka, Toshiko, Portas, Laura, Lopez, Lorna M., Hayward, Caroline, Lohman, Kurt, Matsuda, Koichi, Padmanabhan, Sandosh, Firsov, Dmitri, Sorice, Rossella, Ulivi, Sheila, Brockhaus, A. Catharina, Kleber, Marcus E., Mahajan, Anubha, Ernst, Florian D., Gudnason, Vilmundur, Launer, Lenore J., Mace, Aurelien, Boerwinckle, Eric, Arking, Dan E., Tanikawa, Chizu, Nakamura, Yusuke, Brown, Morris J., Gaspoz, Jean-Michel, Theler, Jean-Marc, Siscovick, David S., Psaty, Bruce M., Bergmann, Sven, Vollenweider, Peter, Vitart, Veronique, Wright, Alan F., Zemunik, Tatijana, Boban, Mladen, Kolcic, Ivana, Navarro, Pau, Brown, Edward M., Estrada, Karol, Ding, Jingzhong, Harris, Tamara B., Bandinelli, Stefania, Hernandez, Dena, Singleton, Andrew B., Girotto, Giorgia, Ruggiero, Daniela, d'Adamo, Adamo Pio, Robino, Antonietta, Meitinger, Thomas, Meisinger, Christa, Davies, Gail, Starr, John M., Chambers, John C., Boehm, Bernhard O., Winkelmann, Bernhard R., Huang, Jie, Murgia, Federico, Wild, Sarah H., Campbell, Harry, Morris, Andrew P., Franco, Oscar H., Hofman, Albert, Uitterlinden, Andre G., Rivadeneira, Fernando, Völker, Uwe, Hannemann, Anke, Biffar, Reiner, Hoffmann, Wolfgang, Shin, So–Youn, Lescuyer, Pierre, Henry, Hughes, Schurmann, Claudia, Munroe, Patricia B., Gasparini, Paolo, Pirastu, Nicola, Ciullo, Marina, Gieger, Christian, März, Winfried, Lind, Lars, Spector, Tim D., Smith, Albert V., Rudan, Igor, Wilson, James F., Polasek, Ozren, Deary, Ian J., Pirastu, Mario, Ferrucci, Luigi, Liu, Yongmei, Kestenbaum, Bryan, Kooner, Jaspal S., Witteman, Jacqueline C. M., Nauck, Matthias, Kao, W. H. Linda, Wallaschofski, Henri, Bonny, Olivier, Fox, Caroline S., Bochud, Murielle
Publicado 2013

Genome-wide association study of kidney function decline in individuals of European descent

por Gorski, Mathias, Tin, Adrienne, Garnaas, Maija, McMahon, Gearoid M., Chu, Audrey Y., Tayo, Bamidele O., Pattaro, Cristian, Teumer, Alexander, Chasman, Daniel I., Chalmers, John, Hamet, Pavel, Tremblay, Johanne, Woodward, Marc, Aspelund, Thor, Eiriksdottir, Gudny, Gudnason, Vilmundur, Harris, Tammara B., Launer, Lenore J., Smith, Albert V., Mitchell, Braxton D., O'Connell, Jeffrey R., Shuldiner, Alan R., Coresh, Josef, Li, Man, Freudenberger, Paul, Hofer, Edith, Schmidt, Helena, Schmidt, Reinhold, Holliday, Elizabeth G., Mitchell, Paul, Wang, Jie Jin, de Boer, Ian H., Li, Guo, Siscovick, David S., Kutalik, Zoltan, Corre, Tanguy, Vollenweider, Peter, Waeber, Gérard, Gupta, Jayanta, Kanetsky, Peter A., Hwang, Shih-Jen, Olden, Matthias, Yang, Qiong, de Andrade, Mariza, Atkinson, Elizabeth J., Kardia, Sharon L.R., Turner, Stephen T., Stafford, Jeanette M., Ding, Jingzhong, Liu, Yongmei, Barlassina, Cristina, Cusi, Daniele, Salvi, Erika, Staessen, Jan A, Ridker, Paul M, Grallert, Harald, Meisinger, Christa, Müller-Nurasyid, Martina, Krämer, Bernhard K., Kramer, Holly, Rosas, Sylvia E., Nolte, Ilja M., Penninx, Brenda W., Snieder, Harold, Del Greco, Fabiola, Franke, Andre, Nöthlings, Ute, Lieb, Wolfgang, Bakker, Stephan J.L., Gansevoort, Ron T., van der Harst, Pim, Dehghan, Abbas, Franco, Oscar H., Hofman, Albert, Rivadeneira, Fernando, Sedaghat, Sanaz, Uitterlinden, André G., Coassin, Stefan, Haun, Margot, Kollerits, Barbara, Kronenberg, Florian, Paulweber, Bernhard, Aumann, Nicole, Endlich, Karlhans, Pietzner, Mike, Völker, Uwe, Rettig, Rainer, Chouraki, Vincent, Helmer, Catherine, Lambert, Jean-Charles, Metzger, Marie, Stengel, Benedicte, Lehtimäki, Terho, Lyytikäinen, Leo-Pekka, Raitakari, Olli, Johnson, Andrew, Parsa, Afshin, Bochud, Murielle, Heid, Iris M., Goessling, Wolfram, Köttgen, Anna, Kao, H. Linda, Fox, Caroline S., Böger, Carsten A.
Publicado 2014

Epigenome-wide association study of serum urate reveals insights into urate co-regulation and the SLC2A9 locus

por Tin, Adrienne, Schlosser, Pascal, Matias-Garcia, Pamela R., Thio, Chris H. L., Joehanes, Roby, Liu, Hongbo, Yu, Zhi, Weihs, Antoine, Hoppmann, Anselm, Grundner-Culemann, Franziska, Min, Josine L., Kuhns, Victoria L. Halperin, Adeyemo, Adebowale A., Agyemang, Charles, Ärnlöv, Johan, Aziz, Nasir A., Baccarelli, Andrea, Bochud, Murielle, Brenner, Hermann, Bressler, Jan, Breteler, Monique M. B., Carmeli, Cristian, Chaker, Layal, Coresh, Josef, Corre, Tanguy, Correa, Adolfo, Cox, Simon R., Delgado, Graciela E., Eckardt, Kai-Uwe, Ekici, Arif B., Endlich, Karlhans, Floyd, James S., Fraszczyk, Eliza, Gao, Xu, Gào, Xīn, Gelber, Allan C., Ghanbari, Mohsen, Ghasemi, Sahar, Gieger, Christian, Greenland, Philip, Grove, Megan L., Harris, Sarah E., Hemani, Gibran, Henneman, Peter, Herder, Christian, Horvath, Steve, Hou, Lifang, Hurme, Mikko A., Hwang, Shih-Jen, Kardia, Sharon L. R., Kasela, Silva, Kleber, Marcus E., Koenig, Wolfgang, Kooner, Jaspal S., Kronenberg, Florian, Kühnel, Brigitte, Ladd-Acosta, Christine, Lehtimäki, Terho, Lind, Lars, Liu, Dan, Lloyd-Jones, Donald M., Lorkowski, Stefan, Lu, Ake T., Marioni, Riccardo E., März, Winfried, McCartney, Daniel L., Meeks, Karlijn A. C., Milani, Lili, Mishra, Pashupati P., Nauck, Matthias, Nowak, Christoph, Peters, Annette, Prokisch, Holger, Psaty, Bruce M., Raitakari, Olli T., Ratliff, Scott M., Reiner, Alex P., Schöttker, Ben, Schwartz, Joel, Sedaghat, Sanaz, Smith, Jennifer A., Sotoodehnia, Nona, Stocker, Hannah R., Stringhini, Silvia, Sundström, Johan, Swenson, Brenton R., van Meurs, Joyce B. J., van Vliet-Ostaptchouk, Jana V., Venema, Andrea, Völker, Uwe, Winkelmann, Juliane, Wolffenbuttel, Bruce H. R., Zhao, Wei, Zheng, Yinan, Loh, Marie, Snieder, Harold, Waldenberger, Melanie, Levy, Daniel, Akilesh, Shreeram, Woodward, Owen M., Susztak, Katalin, Teumer, Alexander, Köttgen, Anna
Publicado 2021

Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction

por Sotoodehnia, Nona, Isaacs, Aaron, de Bakker, Paul I.W., Dörr, Marcus, Newton-Cheh, Christopher, Nolte, Ilja M., van der Harst, Pim, Müller, Martina, Eijgelsheim, Mark, Alonso, Alvaro, Hicks, Andrew A., Padmanabhan, Sandosh, Hayward, Caroline, Smith, Albert Vernon, Polasek, Ozren, Giovannone, Steven, Fu, Jingyuan, Magnani, Jared W., Marciante, Kristin D., Pfeufer, Arne, Gharib, Sina A., Teumer, Alexander, Li, Man, Bis, Joshua C., Rivadeneira, Fernando, Aspelund, Thor, Köttgen, Anna, Johnson, Toby, Rice, Kenneth, Sie, Mark P.S., Wang, Amanda Ying, Klopp, Norman, Fuchsberger, Christian, Wild, Sarah H., Leach, Irene Mateo, Estrada, Karol, Völker, Uwe, Wright, Alan F., Asselbergs, Folkert W., Qu, Jiaxiang, Chakravarti, Aravinda, Sinner, Moritz F., Kors, Jan A., Petersmann, Astrid, Harris, Tamara B., Soliman, Elsayed Z., Munroe, Patricia B., Psaty, Bruce M., Oostra, Ben A., Cupples, L. Adrienne, Perz, Siegfried, de Boer, Rudolf A., Uitterlinden, André G., Vözke, Henry, Spector, Timothy D., Liu, Fang-Yu, Boerwinkle, Eric, Dominiczak, Anna F., Rotter, Jerome I., van Herpen, Gé, Levy, Daniel, Wichmann, H.-Erich, van Gilst, Wiek H., Witteman, Jacqueline C.M., Kroemer, Heyo K., Kao, W.H. Linda, Heckbert, Susan R., Meitinger, Thomas, Hofman, Albert, Campbell, Harry, Folsom, Aaron R., van Veldhuisen, Dirk J., Schwienbacher, Christine, O’Donnell, Christopher J., Volpato, Claudia Beu, Caulfield, Mark J., Connell, John M., Launer, Lenore, Lu, Xiaowen, Franke, Lude, Fehrmann, Rudolf S.N., te Meerman, Gerard, Groen, Harry J.M., Weersma, Rinse K., van den Berg, Leonard H., Wijmenga, Cisca, Ophoff, Roel A., Navis, Gerjan, Rudan, Igor, Snieder, Harold, Wilson, James F., Pramstaller, Peter P., Siscovick, David S., Wang, Thomas J., Gudnason, Vilmundur, van Duijn, Cornelia M., Felix, Stephan B., Fishman, Glenn I., Jamshidi, Yalda, Stricker, Bruno H Ch, Samani, Nilesh J., Kääb, Stefan, Arking, Dan E.
Publicado 2010

Modulation of Genetic Associations with Serum Urate Levels by Body-Mass-Index in Humans

por Huffman, Jennifer E., Albrecht, Eva, Teumer, Alexander, Mangino, Massimo, Kapur, Karen, Johnson, Toby, Kutalik, Zoltán, Pirastu, Nicola, Pistis, Giorgio, Lopez, Lorna M., Haller, Toomas, Salo, Perttu, Goel, Anuj, Li, Man, Tanaka, Toshiko, Dehghan, Abbas, Ruggiero, Daniela, Malerba, Giovanni, Smith, Albert V., Nolte, Ilja M., Portas, Laura, Phipps-Green, Amanda, Boteva, Lora, Navarro, Pau, Johansson, Asa, Hicks, Andrew A., Polasek, Ozren, Esko, Tõnu, Peden, John F., Harris, Sarah E., Murgia, Federico, Wild, Sarah H., Tenesa, Albert, Tin, Adrienne, Mihailov, Evelin, Grotevendt, Anne, Gislason, Gauti K., Coresh, Josef, D'Adamo, Pio, Ulivi, Sheila, Vollenweider, Peter, Waeber, Gerard, Campbell, Susan, Kolcic, Ivana, Fisher, Krista, Viigimaa, Margus, Metter, Jeffrey E., Masciullo, Corrado, Trabetti, Elisabetta, Bombieri, Cristina, Sorice, Rossella, Döring, Angela, Reischl, Eva, Strauch, Konstantin, Hofman, Albert, Uitterlinden, Andre G., Waldenberger, Melanie, Wichmann, H-Erich, Davies, Gail, Gow, Alan J., Dalbeth, Nicola, Stamp, Lisa, Smit, Johannes H., Kirin, Mirna, Nagaraja, Ramaiah, Nauck, Matthias, Schurmann, Claudia, Budde, Kathrin, Farrington, Susan M., Theodoratou, Evropi, Jula, Antti, Salomaa, Veikko, Sala, Cinzia, Hengstenberg, Christian, Burnier, Michel, Mägi, Reedik, Klopp, Norman, Kloiber, Stefan, Schipf, Sabine, Ripatti, Samuli, Cabras, Stefano, Soranzo, Nicole, Homuth, Georg, Nutile, Teresa, Munroe, Patricia B., Hastie, Nicholas, Campbell, Harry, Rudan, Igor, Cabrera, Claudia, Haley, Chris, Franco, Oscar H., Merriman, Tony R., Gudnason, Vilmundur, Pirastu, Mario, Penninx, Brenda W., Snieder, Harold, Metspalu, Andres, Ciullo, Marina, Pramstaller, Peter P., van Duijn, Cornelia M., Ferrucci, Luigi, Gambaro, Giovanni, Deary, Ian J., Dunlop, Malcolm G., Wilson, James F., Gasparini, Paolo, Gyllensten, Ulf, Spector, Tim D., Wright, Alan F., Hayward, Caroline, Watkins, Hugh, Perola, Markus, Bochud, Murielle, Kao, W. H. Linda, Caulfield, Mark, Toniolo, Daniela, Völzke, Henry, Gieger, Christian, Köttgen, Anna, Vitart, Veronique
Publicado 2015

The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis

por Xie, Jingyuan, Liu, Lili, Mladkova, Nikol, Li, Yifu, Ren, Hong, Wang, Weiming, Cui, Zhao, Lin, Li, Hu, Xiaofan, Yu, Xialian, Xu, Jing, Liu, Gang, Caliskan, Yasar, Sidore, Carlo, Balderes, Olivia, Rosen, Raphael J., Bodria, Monica, Zanoni, Francesca, Zhang, Jun Y., Krithivasan, Priya, Mehl, Karla, Marasa, Maddalena, Khan, Atlas, Ozay, Fatih, Canetta, Pietro A., Bomback, Andrew S., Appel, Gerald B., Sanna-Cherchi, Simone, Sampson, Matthew G., Mariani, Laura H., Perkowska-Ptasinska, Agnieszka, Durlik, Magdalena, Mucha, Krzysztof, Moszczuk, Barbara, Foroncewicz, Bartosz, Pączek, Leszek, Habura, Ireneusz, Ars, Elisabet, Ballarin, Jose, Mani, Laila-Yasmin, Vogt, Bruno, Ozturk, Savas, Yildiz, Abdülmecit, Seyahi, Nurhan, Arikan, Hakki, Koc, Mehmet, Basturk, Taner, Karahan, Gonca, Akgul, Sebahat Usta, Sever, Mehmet Sukru, Zhang, Dan, Santoro, Domenico, Bonomini, Mario, Londrino, Francesco, Gesualdo, Loreto, Reiterova, Jana, Tesar, Vladimir, Izzi, Claudia, Savoldi, Silvana, Spotti, Donatella, Marcantoni, Carmelita, Messa, Piergiorgio, Galliani, Marco, Roccatello, Dario, Granata, Simona, Zaza, Gianluigi, Lugani, Francesca, Ghiggeri, GianMarco, Pisani, Isabella, Allegri, Landino, Sprangers, Ben, Park, Jin-Ho, Cho, BeLong, Kim, Yon Su, Kim, Dong Ki, Suzuki, Hitoshi, Amoroso, Antonio, Cattran, Daniel C., Fervenza, Fernando C., Pani, Antonello, Hamilton, Patrick, Harris, Shelly, Gupta, Sanjana, Cheshire, Chris, Dufek, Stephanie, Issler, Naomi, Pepper, Ruth J., Connolly, John, Powis, Stephen, Bockenhauer, Detlef, Stanescu, Horia C., Ashman, Neil, Loos, Ruth J. F., Kenny, Eimear E., Wuttke, Matthias, Eckardt, Kai-Uwe, Köttgen, Anna, Hofstra, Julia M., Coenen, Marieke J. H., Kiemeney, Lambertus A., Akilesh, Shreeram, Kretzler, Matthias, Beck, Lawrence H., Stengel, Benedicte, Debiec, Hanna, Ronco, Pierre, Wetzels, Jack F. M., Zoledziewska, Magdalena, Cucca, Francesco, Ionita-Laza, Iuliana, Lee, Hajeong, Hoxha, Elion, Stahl, Rolf A. K., Brenchley, Paul, Scolari, Francesco, Zhao, Ming-hui, Gharavi, Ali G., Kleta, Robert, Chen, Nan, Kiryluk, Krzysztof
Publicado 2020