Chronic Kidney Disease Alters Vitamin A Homeostasis via Effects on Hepatic RBP4 Protein Expression and Metabolic Enzymes von Jing, J, Isoherranen, N, Robinson‐Cohen, C, Petrie, I, Kestenbaum, BR, Yeung, CK

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Does Secretory Clearance Follow Glomerular Filtration Rate in Chronic Kidney Diseases? Reconsidering the Intact Nephron Hypothesis von Chapron, A, Shen, DD, Kestenbaum, BR, Robinson‐Cohen, C, Himmelfarb, J, Yeung, CK

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Genetic Variants and Associations of 25-Hydroxyvitamin D Concentrations With Major Clinical Outcomes von Levin, Gregory P, Robinson-Cohen, Cassianne, de Boer, Ian H, Houston, Denise K, Lohman, Kurt, Liu, Yongmei, Kritchevsky, Stephen B, Cauley, Jane A, Tanaka, Toshiko, Ferrucci, Luigi, Bandinelli, Stefania, Patel, Kushang V, Hagström, Emil, Michaëlsson, Karl, Melhus, Håkan, Wang, Thomas, Wolf, Myles, Psaty, Bruce M, Siscovick, David, Kestenbaum, Bryan

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Genetic Variants Associated with Circulating Fibroblast Growth Factor 23 von Robinson-Cohen, Cassianne, Bartz, Traci M, Lai, Dongbing, Ikizler, T Alp, Peacock, Munro, Imel, Erik A, Michos, Erin D, Foroud, Tatiana M, Akesson, Kristina, Taylor, Kent D, Malmgren, Linnea, Matsushita, Kunihiro, Nethander, Maria, Eriksson, Joel, Ohlsson, Claes, Mellström, Daniel, Wolf, Myles, Ljunggren, Osten, McGuigan, Fiona, Rotter, Jerome I, Karlsson, Magnus, Econs, Michael J, Ix, Joachim H, Lutsey, Pamela L, Psaty, Bruce M, de Boer, Ian H, Kestenbaum, Bryan R

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Trans-ethnic association study of blood pressure determinants in over 750,000 individuals von Giri, Ayush, Hellwege, Jacklyn N., Keaton, Jacob M., Park, Jihwan, Qiu, Chengxiang, Warren, Helen R., Torstenson, Eric S., Kovesdy, Csaba P., Sun, Yan V., Wilson, Otis D., Robinson-Cohen, Cassianne, Roumie, Christianne L., Chung, Cecilia P., Birdwell, Kelly A., Damrauer, Scott M., DuVall, Scott L., Klarin, Derek, Cho, Kelly, Wang, Yu, Evangelou, Evangelos, Cabrera, Claudia P., Wain, Louise V., Shrestha, Rojesh, Mautz, Brian S., Akwo, Elvis A., Sargurupremraj, Muralidharan, Debette, Stéphanie, Boehnke, Michael, Scott, Laura J., Luan, Jian’an, Zhao, Jing-Hua, Willems, Sara M., Thériault, Sébastien, Shah, Nabi, Oldmeadow, Christopher, Almgren, Peter, Li-Gao, Ruifang, Verweij, Niek, Boutin, Thibaud S., Mangino, Massimo, Ntalla, Ioanna, Feofanova, Elena, Surendran, Praveen, Cook, James P., Karthikeyan, Savita, Lahrouchi, Najim, Liu, Chunyu, Sepúlveda, Nuno, Richardson, Tom G., Kraja, Aldi, Amouyel, Philippe, Farrall, Martin, Poulter, Neil R., Laakso, Markku, Zeggini, Eleftheria, Sever, Peter, Scott, Robert A., Langenberg, Claudia, Wareham, Nicholas J., Conen, David, Palmer, Colin Neil Alexander, Attia, John, Chasman, Daniel I., Ridker, Paul M., Melander, Olle, Mook-Kanamori, Dennis Owen, Harst, Pim van der, Cucca, Francesco, Schlessinger, David, Hayward, Caroline, Spector, Tim D., Jarvelin, Marjo-Riitta, Hennig, Branwen J., Timpson, Nicholas J., Wei, Wei-Qi, Smith, Joshua C., Xu, Yaomin, Matheny, Michael E., Siew, Edward E., Lindgren, Cecilia, Herzig, Karl-Heinz, Dedoussis, George, Denny, Joshua C., Psaty, Bruce M., Howson, Joanna M. M., Munroe, Patricia B., Newton-Cheh, Christopher, Caulfield, Mark J., Elliott, Paul, Gaziano, J. Michael, Concato, John, Wilson, Peter W. F., Tsao, Philip S., Velez Edwards, Digna R., Susztak, Katalin, O’Donnell, Christopher J., Hung, Adriana M., Edwards, Todd L.

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Genome-wide association study in 79,366 European-ancestry individuals informs the genetic architecture of 25-hydroxyvitamin D levels von Jiang, Xia, O’Reilly, Paul F., Aschard, Hugues, Hsu, Yi-Hsiang, Richards, J. Brent, Dupuis, Josée, Ingelsson, Erik, Karasik, David, Pilz, Stefan, Berry, Diane, Kestenbaum, Bryan, Zheng, Jusheng, Luan, Jianan, Sofianopoulou, Eleni, Streeten, Elizabeth A., Lutsey, Pamela L., Yao, Lu, Tang, Weihong, Wallaschofski, Henri, Völzke, Henry, Zhou, Ang, Power, Chris, McCarthy, Mark I., Michos, Erin D., Boerwinkle, Eric, Weinstein, Stephanie J., Freedman, Neal D., Huang, Wen-Yi, Van Schoor, Natasja M., van der Velde, Nathalie, Groot, Lisette C. P. G. M. de, Enneman, Anke, Cupples, L. Adrienne, Booth, Sarah L., Vasan, Ramachandran S., Liu, Ching-Ti, Zhou, Yanhua, Ripatti, Samuli, Ohlsson, Claes, Vandenput, Liesbeth, Lorentzon, Mattias, Eriksson, Johan G., Shea, M. Kyla, Houston, Denise K., Kritchevsky, Stephen B., Liu, Yongmei, Lohman, Kurt K., Ferrucci, Luigi, Peacock, Munro, Gieger, Christian, Beekman, Marian, Slagboom, Eline, Deelen, Joris, Heemst, Diana van, Kleber, Marcus E., März, Winfried, de Boer, Ian H., Wood, Alexis C., Rotter, Jerome I., Rich, Stephen S., Robinson-Cohen, Cassianne, den Heijer, Martin, Jarvelin, Marjo-Riitta, Cavadino, Alana, Joshi, Peter K., Wilson, James F., Hayward, Caroline, Lind, Lars, Michaëlsson, Karl, Trompet, Stella, Zillikens, M. Carola, Uitterlinden, Andre G., Rivadeneira, Fernando, Broer, Linda, Zgaga, Lina, Theodoratou, Evropi, Farrington, Susan M., Timofeeva, Maria, Dunlop, Malcolm G., Valdes, Ana M., Tikkanen, Emmi, Lehtimäki, Terho, Lyytikäinen, Leo-Pekka, Kähönen, Mika, Raitakari, Olli T., Mikkilä, Vera, Ikram, M. Arfan, Sattar, Naveed, Jukema, J. Wouter, Wareham, Nicholas J., Langenberg, Claudia, Gundersen, Thomas E., Khaw, Kay-Tee, Butterworth, Adam S., Danesh, John, Spector, Timothy, Wang, Thomas J., Hyppönen, Elina, Kraft, Peter, Kiel, Douglas P.

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Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple Sclerosis von Manousaki, Despoina, Dudding, Tom, Haworth, Simon, Hsu, Yi-Hsiang, Liu, Ching-Ti, Medina-Gómez, Carolina, Voortman, Trudy, van der Velde, Nathalie, Melhus, Håkan, Robinson-Cohen, Cassianne, Cousminer, Diana L., Nethander, Maria, Vandenput, Liesbeth, Noordam, Raymond, Forgetta, Vincenzo, Greenwood, Celia M.T., Biggs, Mary L., Psaty, Bruce M., Rotter, Jerome I., Zemel, Babette S., Mitchell, Jonathan A., Taylor, Bruce, Lorentzon, Mattias, Karlsson, Magnus, Jaddoe, Vincent V.W., Tiemeier, Henning, Campos-Obando, Natalia, Franco, Oscar H., Utterlinden, Andre G., Broer, Linda, van Schoor, Natasja M., Ham, Annelies C., Ikram, M. Arfan, Karasik, David, de Mutsert, Renée, Rosendaal, Frits R., den Heijer, Martin, Wang, Thomas J., Lind, Lars, Orwoll, Eric S., Mook-Kanamori, Dennis O., Michaëlsson, Karl, Kestenbaum, Bryan, Ohlsson, Claes, Mellström, Dan, de Groot, Lisette C.P.G.M., Grant, Struan F.A., Kiel, Douglas P., Zillikens, M. Carola, Rivadeneira, Fernando, Sawcer, Stephen, Timpson, Nicholas J., Richards, J. Brent

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Large-scale whole-exome sequencing association studies identify rare functional variants influencing serum urate levels von Tin, Adrienne, Li, Yong, Brody, Jennifer A., Nutile, Teresa, Chu, Audrey Y., Huffman, Jennifer E., Yang, Qiong, Chen, Ming-Huei, Robinson-Cohen, Cassianne, Macé, Aurélien, Liu, Jun, Demirkan, Ayşe, Sorice, Rossella, Sedaghat, Sanaz, Swen, Melody, Yu, Bing, Ghasemi, Sahar, Teumer, Alexanda, Vollenweider, Peter, Ciullo, Marina, Li, Meng, Uitterlinden, André G., Kraaij, Robert, Amin, Najaf, van Rooij, Jeroen, Kutalik, Zoltán, Dehghan, Abbas, McKnight, Barbara, van Duijn, Cornelia M., Morrison, Alanna, Psaty, Bruce M., Boerwinkle, Eric, Fox, Caroline S., Woodward, Owen M., Köttgen, Anna

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Mineral Metabolism Disturbances and Arteriovenous Fistula Maturation von Kubiak, R.W., Zelnick, L.R., Hoofnagle, A.N., Alpers, C.E., Terry, C.M., Shiu, Y.-T., Cheung, A.K., de Boer, I.H., Robinson-Cohen, C., Allon, M., Dember, L.M., Feldman, H.I., Himmelfarb, J., Huber, T.S., Roy-Chaudhury, P., Vazquez, M.A., Kusek, J.W., Beck, G.J., Imrey, P.B., Kestenbaum, B.

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B46 CRITICAL CARE: ICU EPIDEMIOLOGY AND OUTCOMES: Acute Kidney Injury Sub-Phenotypes Based On Creatinine Trajectory Identifies Critically Ill Patients At Increased Risk Of Death von Bhatraju, P, Mukherjee, P, Robinson-Cohen, C, Christie, J D, Meyer, N J, Matthay, M, Calfee, C S, O'Keefe, G, Christiani, D C, Himmelfarb, J, Wurfel, M M

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POS-437 Understanding Genetic and Clinical Determinants of Acquire Nephrotic Syndrome in Veterans (NephVA) in the Million Veteran Program (NephVA-MVP) von Fang, C.B., Chen, H.C., Bick, A., Chung, C., Tao, R., Katalin, S., Huffman, J., Robinson-Cohen, C., Siew, E., Hung, A.

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Large-scale whole-exome sequencing association studies identify rare functional variants influencing serum urate levels von Tin, A, Li, Y, Brody, JA, Nutile, T, Chu, AY, Huffman, JE, Yang, Q, Chen, M-H, Robinson-Cohen, C, Macé, A, Liu, J, Demirkan, A, Sorice, R, Sedaghat, S, Swen, M, Yu, B, Ghasemi, S, Teumer, A, Vollenweider, P, Ciullo, M, Li, M, Uitterlinden, AG, Kraaij, R, Amin, N, Van Rooij, J, Kutalik, Z, Dehghan, A, McKnight, B, Van Duijn, CM, Morrison, A, Psaty, BM, Boerwinkle, E, Fox, CS, Woodward, OM, Köttgen, A

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Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals von Winkler, T.W., Teumer, A., Thio, C.H.L., Li, M., Yang, Q., Nutile, T., Gunther, F., Parsa, A., Vries, A.P.J. de, Zonderman, A.B., Smith, A.V., Oldehinkel, A.J., Franke, A., Metspalu, A., Hicks, A.A., Tonjes, A., Peters, A., Ponte, B., Schottker, B., Brumpton, B., Jung, B., Ning, B., Hayward, C., Hartman, C.A., Heng, C.K., Cheng, C.Y., Willer, C.J., Toniolo, D., Waterworth, D.M., Montgomery, G.W., Snieder, H., Stringham, H.M., Schmidt, H., Tzoulaki, I., Olafsson, I., Martins, J., Cook, J.P., Halbritter, J., Felix, J.F., Divers, J., Kooner, J.S., Liu, J.J., Xu, J., Arnlov, J., Kuusisto, J., Jakobsdottir, J., Chambers, J.C., Gaziano, J.M., Marten, J., Jonas, J.B., Christensen, K., Matsuda, K., Strauch, K., Hveem, K., Wallentin, L., Raffield, L.M., Phillips, L.S., Ikram, M.A., Kleber, M.E., Francescatto, M., Concas, M.P., Piratsu, M., Laakso, M., Borst, M.H. de, Kavousi, M., Waldenberger, M., Boehnke, M., Stumvoll, M., Kastarinen, M., Martin, N.G., Pirastu, N., Hutri-Kahonen, N., Raitakari, O.T., Gasparini, P., Mishra, P.P., Magnusson, P.K.E., Elliott, P., Ridker, P.M., Joshi, P.K., Pramstaller, P.P., Vollenweider, P., Sim, R.Z.H., Burkhardt, R., Schmidt, R., Mutsert, R. de, Dam, R.M. van, Felicita, S.C., Padmanabhan, S., Vaccargiu, S., Hallan, S., Bakker, S.J.L., Lim, S.C., Lucae, S., Bergmann, S., Boutin, T.S., Bergler, T., Rabelink, T.J., Haller, T., Volker, U., Vitart

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Supplementary Material for: APOL1 G3 Variant Is Associated with Cardiovascular Mortality and Sudden Cardiac Death in Patients Receiving Maintenance Hemodialysis of European Ancestr... von T.-H., Schwantes-An, C., Robinson-Cohen, S., Liu, N., Zheng, M., Stedman, L., Wetherill, H.J., Edenberg, M., Vatta, T.M., Foroud, G.M., Chertow, S.M., Moe

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Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple Sclerosis von Manousaki, D., Dudding, T., Haworth, S., Hsu, Y.H., Liu, C.T., Medina-Gomez, C., Voortman, T., Velde, N. van der, Melhus, H., Robinson-Cohen, C., Cousminer, D.L., Nethander, M., Vandenput, L., Noordam, R., Forgetta, V., Greenwood, C.M.T., Biggs, M.L., Psaty, B.M., Rotter, J.I., Zemel, B.S., Mitchell, J.A., Taylor, B., Lorentzon, M., Karlsson, M., Jaddoe, V.V.W., Tiemeier, H., Campos-Obando, N., Franco, O.H., Utterlinden, A.G., Broer, L., Schoor, N.M. van, Ham, A.C., Ikram, M.A., Karasik, D., Mutsert, R. de, Rosendaal, F.R., Heijer, M. den, Wang, T.J., Lind, L., Orwoll, E.S., Mook-Kanamori, D.O., Michaelsson, K., Kestenbaum, B., Ohlsson, C., Mellstrom, D., Groot, L.C.P.G.M. de, Grant, S.F.A., Kiel, D.P., Zillikens, M.C., Rivadeneira, F., Sawcer, S., Timpson, N.J., Richards, J.B.

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Genome-wide association study in 79,366 European-ancestry individuals informs the genetic architecture of 25-hydroxyvitamin D levels von Jiang, X., O'Reilly, P.F., Aschard, H., Hsu, Y.H., Richards, J.B., Dupuis, J., Ingelsson, E., Karasik, D., Pilz, S., Berry, D., Kestenbaum, B., Zheng, J.S., Sofianopoulou, E., Albanes, D., Lutsey, P.L., Yao, L., Tang, W.H., Econs, M.J., Wallaschofski, H., Volzke, H., Zhou, A., Power, C., McCarthy, M.I., Michos, E.D., Boerwinkle, E., Weinstein, S.J., Freedman, N.D., Huang, W.Y., Schoor, N.M. van, Velde, N. van der, Groot, L.C.P.G.M. de, Enneman, A., Cupples, L.A., Booth, S.L., Vasan, R.S., Liu, C.T., Zhou, Y.H., Ripatti, S., Ohlsson, C., Vandenput, L., Lorentzon, M., Eriksson, J.G., Shea, M.K., Houston, D.K., Kritchevsky, S.B., Liu, Y.M., Lohman, K.K., Ferrucci, L., Peacock, M., Gieger, C., Beekman, M., Slagboom, E., Deelen, J., Heemst, D. van, Kleber, M.E., Marz, W., Boer, I.H. de, Wood, A.C., Rotter, J.I., Rich, S.S., Robinson-Cohen, C., Heijer, M. den, Jarvelin, M.R., Cavadino, A., Joshi, P.K., Wilson, J.F., Hayward, C., Lind, L., Michaelsson, K., Trompet, S., Zillikens, M.C., Uitterlinden, A.G., Rivadeneira, F., Broer, L., Zgaga, L., Campbell, H., Theodoratou, E., Farrington, S.M., Timofeeva, M., Dunlop, M.G., Tikkanen, E., Lehtimaki, T., Kahonen, M., Raitakari, O.T., Mikkila, V., Ikram, M.A., Sattar, N., Jukema, J.W., Wareham, N.J., Langenberg, C., Forouhi, N.G., Gundersen, T.E., Khaw, K.T., Butterworth, A.S., Danesh, J., Spector, T., Wang, T.J., Hypponen, E., Kraft, P., Kiel, D.P.

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Associations between endogenous sex hormones and FGF-23 among women and men in the Multi-Ethnic Study of Atherosclerosis von Ogunmoroti, Oluseye, Osibogun, Olatokunbo, Zhao, Di, Mehta, Rupal C, Ouyang, Pamela, Lutsey, Pamela L, Robinson-Cohen, Cassianne, Michos, Erin D

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Intermuscular adipose tissue accumulation is associated with higher tissue sodium in healthy individuals von Ertuglu, Lale A., Sahinoz, Melis, Alsouqi, Aseel, Deger, Serpil Muge, Guide, Andrew, Pike, Mindy, Robinson‐Cohen, Cassianne, Akwo, Elvis, Pridmore, Michael, Crescenzi, Rachelle, Madhur, Meena S., Kirabo, Annet, Harrison, David G., Luft, Friedrich C., Titze, Jens, Ikizler, T. Alp, Gamboa, Jorge L.

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Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals von Winkler, Thomas W., Gorski, Mathias, Stanzick, Kira J., Thomas, Laurent F., Hoppmann, Anselm, Cusi, Daniele, Li, Man, Li, Yong, Correa, Adolfo, Feresin, Agnese, de Vries, Aiko P. J., Rosenkranz, Alexander R., Franke, Andre, Metspalu, Andres, Podgornaia, Anna I., Brumpton, Ben, Smith, Blair H., Ning, Boting, Hayward, Caroline, Hartman, Catharina A., Wang, Chaolong, Sabanayagam, Charumathi, Schulz, Christina-Alexandra, Porteous, David J., Waterworth, Dawn M., Mascalzoni, Deborah, Mook-Kanamori, Dennis O., Hofer, Edith, Salvi, Erika, Guilianini, Franco, Ehret, Georg, Waeber, Gerard, Pistis, Giorgio, Nadkarni, Girish N., Delgado, Graciela E., Montgomery, Grant W., Snieder, Harold, Gao, He, Holm, Hilma, Kramer, Holly, Tzoulaki, Ioanna, Martins, Jade, Halbritter, Jan, Felix, Janine F., Divers, Jasmin, Xu, Jie, Ärnlöv, Johan, Jakobsdottir, Johanna, Gaziano, John M., Jonas, Jost B., Mychaleckyj, Josyf C., Endlich, Karlhans, Ho, Kevin, Strauch, Konstantin, Hveem, Kristian, Lind, Lars, Yerges-Armstrong, Laura M., Raffield, Laura M., Phillips, Lawrence S., Klaric, Lucija, Ising, Marcus, Kleber, Marcus E., Concas, Maria Pina, Orho-Melander, Marju, Perola, Markus, Biggs, Mary L., Boehnke, Michael, Kuokkanen, Mikko, Bochud, Murielle, Josyula, Navya Shilpa, Schupf, Nicole, Verweij, Niek, Mononen, Nina, Bansal, Nisha, Devuyst, Olivier, Gasparini, Paolo, Magnusson, Patrik K. E., Hamet, Pavel, Kovacs, Peter, Vollenweider, Peter, van der Harst, Pim, Dorajoo, Rajkumar, Sim, Ralene Z. H., Noordam, Raymond, Schmidt, Reinhold, de Mutsert, Renée, Padmanabhan, Sandosh, Kerr, Shona M., Vaccargiu, Simona, Patil, Snehal B., Bakker, Stephan J. L., Vogelezang, Suzanne, Ahluwalia, Tarunveer S., Rabelink, Ton J., Salomaa, Veikko, Jaddoe, Vincent W. V., Gao, Xin, Sim, Xueling, Yu, Zhi, Stark, Klaus J.

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Pharmacogenetic variants and risk of remdesivir‐associated liver enzyme elevations in Million Veteran Program participants hospitalized with COVID‐19 von Tuteja, Sony, Yu, Zhihong, Wilson, Otis, Chen, Hua‐Chang, Wendt, Frank, Chung, Cecilia P., Shah, Shailja C., Hunt, Christine M., Suzuki, Ayako, Chanfreau, Catherine, Gorman, Bryan R., Joseph, Jacob, Luoh, Shiuh‐Wen, Napolioni, Valerio, Robinson‐Cohen, Cassianne, Tao, Ran, Zhou, Jin, Chang, Kyong‐Mi, Hung, Adriana M.

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