The MYH9/APOL1 region and chronic kidney disease in European-Americans by O'Seaghdha, Conall M, Parekh, Rulan S, Hwang, Shih-Jen, Li, Man, Köttgen, Anna, Coresh, Josef, Yang, Qiong, Fox, Caroline S, Kao, W H Linda

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Electrophysiologic Substrate and Risk of Mortality in Incident Hemodialysis by Tereshchenko, Larisa G, Kim, Esther D, Oehler, Andrew, Meoni, Lucy A, Ghafoori, Elyar, Rami, Tejal, Maly, Maggie, Kabir, Muammar, Hawkins, Lauren, Tomaselli, Gordon F, Lima, Joao A, Jaar, Bernard G, Sozio, Stephen M, Estrella, Michelle, Kao, W H Linda, Parekh, Rulan S

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Polygenic Overlap Between Kidney Function and Large Artery Atherosclerotic Stroke by Holliday, Elizabeth G, Traylor, Matthew, Malik, Rainer, Bevan, Stephen, Maguire, Jane, Koblar, Simon A, Sturm, Jonathan, Hankey, Graeme J, Oldmeadow, Christopher, McEvoy, Mark, Sudlow, Cathie, Rothwell, Peter M, Coresh, Josef, Hamet, Pavel, Tremblay, Johanne, Turner, Stephen T, de Andrade, Mariza, Rao, Madhumathi, Schmidt, Reinhold, Crick, Peter A, Robino, Antonietta, Peralta, Carmen A, Jukema, J Wouter, Mitchell, Paul, Rosas, Sylvia E, Wang, Jie Jin, Scott, Rodney J, Dichgans, Martin, Mitchell, Braxton D, Kao, W.H Linda, Fox, Caroline S, Levi, Christopher, Attia, John, Markus, Hugh S

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Effects of Rare and Common Blood Pressure Gene Variants on Essential Hypertension: Results From the Family Blood Pressure Program, CLUE, and Atherosclerosis Risk in Communities Stu... by Nguyen, Khanh-Dung H, Pihur, Vasyl, Ganesh, Santhi K, Rakha, Ankit, Cooper, Richard S, Hunt, Steven C, Freedman, Barry I, Coresh, Joe, Kao, W.H Linda, Morrison, Alanna C, Boerwinkle, Eric, Ehret, Georg B, Chakravarti, Aravinda

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Genome-wide association study identifies common loci influencing circulating glycated hemoglobin (HbA1c ) levels in non-diabetic subjects: The Long Life Family Study (LLFS) by An, Ping, Miljkovic, Iva, Thyagarajan, Bharat, Kraja, Aldi T, Daw, E. Warwick, Pankow, James S, Selvin, Elizabeth, Kao, W.H. Linda, Maruthur, Nisa M, Nalls, Micahel A, Liu, Yongmei, Harris, Tamara B, Lee, Joseph H, Borecki, Ingrid B, Christensen, Kaare, Eckfeldt, John H, Mayeux, Richard, Perls, Thomas T, Newman, Anne B, Province, Michael A

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Associations between Genetic Variants in the NOS1AP (CAPON) Gene and Cardiac Repolarization in the Old Order Amish by Post, Wendy, Shen, Haiqing, Damcott, Coleen, Arking, Dan E., Kao, W. H. Linda, Sack, Paul A., Ryan, Kathleen A., Chakravarti, Aravinda, Mitchell, Braxton D., Shuldiner, Alan R.

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APOL1 Variants Associate with Increased Risk of CKD among African Americans by FOSTER, Meredith C, CORESH, Josef, FORNAGE, Myriam, ASTOR, Brad C, GRAMS, Morgan, FRANCESCHINI, Nora, BOERWINKLE, Eric, PAREKH, Rulan S, KAO, W. H. Linda

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Explaining the Racial Difference in AKI Incidence by GRAMS, Morgan E, MATSUSHITA, Kunihiro, YINGYING SANG, ESTRELLA, Michelle M, FOSTER, Meredith C, TIN, Adrienne, KAO, W. H. Linda, CORESH, Josef

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Genome-wide association analysis identifies variants associated with nonalcoholic fatty liver disease that have distinct effects on metabolic traits by 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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rs641738C>T near MBOAT7 is associated with liver fat, ALT and fibrosis in NAFLD: A meta-analysis by 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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Reliability of Urinary Albumin, Total Protein, and Creatinine Assays after Prolonged Storage: The Family Investigation of Nephropathy and Diabetes by Parekh, Rulan S, Kao, W H Linda, Meoni, Lucy A, Ipp, Eli, Kimmel, Paul L, La Page, Janine, Fondran, Carol, Knowler, William C, Klag, Michael J

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Reduced neutrophil count in people of African descent is due to a regulatory variant in the Duffy antigen receptor for chemokines gene by Reich, David, Nalls, Michael A, Kao, W H Linda, Akylbekova, Ermeg L, Tandon, Arti, Patterson, Nick, Mullikin, James, Hsueh, Wen-Chi, Cheng, Ching-Yu, Coresh, Josef, Boerwinkle, Eric, Li, Man, Waliszewska, Alicja, Neubauer, Julie, Li, Rongling, Leak, Tennille S, Ekunwe, Lynette, Files, Joe C, Hardy, Cheryl L, Zmuda, Joseph M, Taylor, Herman A, Ziv, Elad, Harris, Tamara B, Wilson, James G

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Biomarkers of vascular calcification and mortality in patients with ESRD by Scialla, Julia J, Kao, W H Linda, Crainiceanu, Ciprian, Sozio, Stephen M, Oberai, Pooja C, Shafi, Tariq, Coresh, Josef, Powe, Neil R, Plantinga, Laura C, Jaar, Bernard G, Parekh, Rulan S

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Genetic variants at 2q24 are associated with susceptibility to type 2 diabetes by Qi, Lu, Cornelis, Marilyn C., Kraft, Peter, Stanya, Kristopher J., Linda Kao, W.H., Pankow, James S., Dupuis, Josée, Florez, Jose C., Fox, Caroline S., Paré, Guillaume, Sun, Qi, Girman, Cynthia J., Laurie, Cathy C., Mirel, Daniel B., Manolio, Teri A., Chasman, Daniel I., Boerwinkle, Eric, Ridker, Paul M., Hunter, David J., Meigs, James B., Lee, Chih-Hao, van Dam, Rob M., Hu, Frank B.

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Uromodulin Levels Associate with a Common UMOD Variant and Risk for Incident CKD by KÖTTGEN, Anna, HWANG, Shih-Jen, GUDNASON, Vilmundur, SHLIPAK, Michael G, QIONG YANG, CORESH, Josef, LEVY, Daniel, FOX, Caroline S, LARSON, Martin G, VAN EYK, Jennifer E, QIN FU, BENJAMIN, Emelia J, DEHGHAN, Abbas, GLAZER, Nicole L, LINDA KAO, W. H, HARRIS, Tamara B

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Pleiotropic genes for metabolic syndrome and inflammation by Kraja, Aldi T., Chasman, Daniel I., North, Kari E., Reiner, Alexander P., Yanek, Lisa R., Kilpeläinen, Tuomas O., Smith, Jennifer A., Dehghan, Abbas, Dupuis, Josée, Johnson, Andrew D., Feitosa, Mary F., Tekola-Ayele, Fasil, Chu, Audrey Y., Nolte, Ilja M., Dastani, Zari, Morris, Andrew, Pendergrass, Sarah A., Sun, Yan V., Ritchie, Marylyn D., Vaez, Ahmad, Lin, Honghuang, Ligthart, Symen, Marullo, Letizia, Rohde, Rebecca, Shao, Yaming, Ziegler, Mark A., Im, Hae Kyung, Schnabel, Renate B., Jørgensen, Torben, Jørgensen, Marit E., Hansen, Torben, Pedersen, Oluf, Stolk, Ronald P., Snieder, Harold, Hofman, Albert, Uitterlinden, Andre G., Franco, Oscar H., Ikram, M. Arfan, Richards, J. Brent, Rotimi, Charles, Wilson, James G., Lange, Leslie, Ganesh, Santhi K., Nalls, Mike, Rasmussen-Torvik, Laura J., Pankow, James S., Coresh, Josef, Tang, Weihong, Linda Kao, W.H., Boerwinkle, Eric, Morrison, Alanna C., Ridker, Paul M., Becker, Diane M., Rotter, Jerome I., Kardia, Sharon L.R., Loos, Ruth J.F., Larson, Martin G., Hsu, Yi-Hsiang, Province, Michael A., Tracy, Russell, Voight, Benjamin F., Vaidya, Dhananjay, O'Donnell, Christopher J., Benjamin, Emelia J., Alizadeh, Behrooz Z., Prokopenko, Inga, Meigs, James B., Borecki, Ingrid B.

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Genetic Variations in Nitric Oxide Synthase 1 Adaptor Protein Are Associated With Sudden Cardiac Death in US White Community-Based Populations by KAO, W. H. Linda, ARKING, Dan E, TOMASELLI, Gordon F, CORESH, Josef, SISCOVICK, David S, MARBAN, Eduardo, SPOONER, Peter M, BURKE, Gregory L, CHAKRAVARTI, Aravinda, POST, Wendy, REA, Thomas D, SOTOODEHNIA, Nona, PRINEAS, Ronald J, BISHE, Bryan, DOAN, Betty Q, BOERWINKLE, Eric, PSATY, Bruce M

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Meta-analysis of genome-wide association studies identifies six new Loci for serum calcium concentrations by 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

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Examination of Potential Modifiers of the Association of APOL1 Alleles with CKD Progression by Chen, Teresa K, Choi, Michael J, Kao, W H Linda, Astor, Brad C, Scialla, Julia J, Appel, Lawrence J, Li, Liang, Lipkowitz, Michael S, Wolf, Myles, Parekh, Rulan S, Winkler, Cheryl A, Estrella, Michelle M, Crews, Deidra C

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Nicotinic acetylcholine receptor genes on chromosome 15q25.1 are associated with nicotine and opioid dependence severity by Erlich, Porat M, Hoffman, Stuart N, Rukstalis, Margaret, Han, John J, Chu, Xin, Linda Kao, W. H, Gerhard, Glenn S, Stewart, Walter F, Boscarino, Joseph A

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