Dissection of Genomewide-Scan Data in Extended Families Reveals a Major Locus and Oligogenic Susceptibility for Age-Related Macular Degeneration von Iyengar, Sudha K., Song, Danhong, Klein, Barbara E.K., Klein, Ronald, Schick, James H., Humphrey, Jennifer, Millard, Christopher, Liptak, Rachel, Russo, Karlie, Jun, Gyungah, Lee, Kristine E., Fijal, Bonnie, Elston, Robert C.

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Actionable druggable genome-wide Mendelian randomization identifies repurposing opportunities for COVID-19 von Gaziano, L, Giambartolomei, C, Pereira, AC, Gaulton, A, Posner, DC, Swanson, SA, Ho, Y-L, Iyengar, SK, Kosik, NM, Vujkovic, M, Gagnon, DR, Bento, AP, Barrio-Hernandez, I, Rönnblom, L, Hagberg, N, Lundtoft, C, Langenberg, C, Pietzner, M, Valentine, D, Gustincich, S, Tartaglia, GG, Allara, E, Surendran, P, Burgess, S, Zhao, JH, Peters, JE, Prins, BP, Angelantonio, ED, Devineni, P, Shi, Y, Lynch, KE, DuVall, SL, Garcon, H, Thomann, LO, Zhou, JJ, Gorman, BR, Huffman, JE, O'Donnell, CJ, Tsao, PS, Beckham, JC, Pyarajan, S, Muralidhar, S, Huang, GD, Ramoni, R, Beltrao, P, Danesh, J, Hung, AM, Chang, K-M, Sun, YV, Joseph, J, Leach, AR, Edwards, TL, Cho, K, Gaziano, JM, Butterworth, AS, Casas, JP, VA Million Veteran Program COVID-19 Science Initiative

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Genome-Wide Linkage Study of Retinal Vessel Diameters in the Beaver Dam Eye Study von Xing, Chao, Klein, Barbara E.K, Klein, Ronald, Jun, Gyungah, Lee, Kristine E, Iyengar, Sudha K

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Pleiotropic Effects of a Chromosome 3 Locus on Speech-Sound Disorder and Reading von Stein, Catherine M., Schick, James H., Gerry Taylor, H., Shriberg, Lawrence D., Millard, Christopher, Kundtz-Kluge, Amy, Russo, Karlie, Minich, Nori, Hansen, Amy, Freebairn, Lisa A., Elston, Robert C., Lewis, Barbara A., Iyengar, Sudha K.

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School-Age Follow-Up of Children With Childhood Apraxia of Speech von Lewis, Barbara A, Freebairn, Lisa A, Hansen, Amy J, Iyengar, Sudha K, Taylor, H. Gerry

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A Whole-Genome Screen of a Quantitative Trait of Age-Related Maculopathy in Sibships from the Beaver Dam Eye Study von Schick, James H., Iyengar, Sudha K., Klein, Barbara E., Klein, Ronald, Reading, Karlie, Liptak, Rachel, Millard, Christopher, Lee, Kristine E., Tomany, Sandra C., Moore, Emily L., Fijal, Bonnie A., Elston, Robert C.

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Genome-wide search for sarcoidosis susceptibility genes in African Americans von Iannuzzi, M C, Iyengar, S K, Gray-McGuire, C, Elston, R C, Baughman, R P, Donohue, J F, Hirst, K, Judson, M A, Kavuru, M S, Maliarik, M J, Moller, D R, Newman, L S, Rabin, D L, Rose, C S, Rossman, M D, Teirstein, A S, Rybicki, B A

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Identification of a Major Locus for Age-Related Cortical Cataract on Chromosome 6p12-q12 in the Beaver Dam Eye Study von Iyengar, Sudha K., Barbara E. K. Klein, Klein, Ronald, Jun, Gyungah, Schick, James H., Millard, Christopher, Liptak, Rachel, Russo, Karlie, Lee, Kristine E., Elston, Robert C., White, Raymond L.

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A Genetic Contribution to Intraocular Pressure: The Beaver Dam Eye Study von Duggal, Priya, Klein, Alison P, Lee, Kristine E, Iyengar, Sudha K, Klein, Ronald, Bailey-Wilson, Joan E, Klein, Barbara E. K

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The Family Investigation of Nephropathy and Diabetes (FIND): Design and methods von Knowler, William C., Coresh, Josef, Elston, Robert C., Freedman, Barry I., Iyengar, Sudha K., Kimmel, Paul L., Olson, Jane M., Plaetke, Rosemarie, Sedor, John R., Seldin, Michael F.

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Linkage analysis of candidate loci for end-stage renal disease due to diabetic nephropathy von IYENGAR, Sudha K, FOX, Katherine A, SEDOR, John R, SCHACHERE, Marlene, MANZOOR, Fauzia, SLAUGHTER, Mary E, COVIC, Adrian M, ORLOFF, S. Mohammed, HAYDEN, Patrick S, OLSON, Jane M, SCHELLING, Jeffrey R

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Mathematical Assumptions versus Biological Reality: Myths in Affected Sib Pair Linkage Analysis von Elston, Robert C., Song, Danhong, Iyengar, Sudha K.

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Dimensions of early speech sound disorders: A factor analytic study von Lewis, Barbara A., Freebairn, Lisa A., Hansen, Amy J., Stein, Catherine M., Shriberg, Lawrence D., Iyengar, Sudha K., Gerry Taylor, H.

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Variants in the Wilms' tumor gene are associated with focal segmental glomerulosclerosis in the African American population von Orloff, Mohammed S, Iyengar, Sudha K, Winkler, Cheryl A, Goddard, Katrina A. B, Dart, Richard A, Ahuja, Tejinder S, Mokrzycki, Michele, Briggs, William A, Korbet, Stephen M, Kimmel, Paul L, Simon, Eric E, Trachtman, Howard, Vlahov, David, Michel, Donna M, Berns, Jeffrey S, Smith, Michael C, Schelling, Jeffrey R, Sedor, John R, Kopp, Jeffrey B

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Genome-Wide Analyses Demonstrate Novel Loci That Predispose to Drusen Formation von Jun, Gyungah, Klein, Barbara E. K, Klein, Ronald, Fox, Katherine, Millard, Christopher, Capriotti, Jennifer, Russo, Karlie, Lee, Kristine E, Elston, Robert C, Iyengar, Sudha K

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Serum C-peptide concentrations poorly phenotype type 2 diabetic end-stage renal disease patients von Covic, Adrian M.C., Schelling, Jeffrey R., Constantiner, Marigel, Iyengar, Sudha K., Sedor, John R.

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Evidence for a Major Gene Influence on Tumor Necrosis Factor-α Expression in Tuberculosis: Path and Segregation Analysis von Stein, Catherine M., Nshuti, Lorna, Chiunda, Allan B., Boom, W. Henry, Elston, Robert C., Mugerwa, Roy D., Iyengar, Sudha K., Whalen, Christopher C.

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Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo von Ikram, MK, Sim, X, Jensen, RA, Cotch, MF, Hewitt, AW, Ikram, MA, Wang, JJ, Klein, R, Klein, BE, Breteler, MM, Cheung, N, Liew, G, Mitchell, P, Uitterlinden, AG, Rivadeneira, F, Hofman, A, De Jong, PT, Van Duijn, CM, Kao, L, Cheng, CY, Smith, AV, Glazer, NL, Lumley, T, McKnight, B, Psaty, BM, Jonasson, F, Eiriksdottir, G, Aspelund, T, Global BPgen Consortium, Harris, TB, Launer, LJ, Taylor, KD, Li, X, Iyengar, SK, Xi, Q, Sivakumaran, TA, Mackey, DA, Macgregor, S, Martin, NG, Young, TL, Bis, JC, Wiggins, KL, Heckbert, SR, Hammond, CJ, Andrew, T, Fahy, S, Attia, J, Holliday, EG, Scott, RJ, Islam, FM, Rotter, JI, McAuley, AK, Boerwinkle, E, Tai, ES, Gudnason, V, Siscovick, DS, Vingerling, JR, Wong, TY

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Kidney disease, genotype and the pathogenesis of vasculopathy von Hayden, Patrick S, Iyengar, Sudha K, Schelling, Jeffrey R, Sedor, John R

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The fa leptin receptor mutation and the heritability of respiratory frequency in a Brown Norway and Zucker intercross von Iyengar, Sudha K, Stein, Catherine M, Russo, Karlie, Erokwu, Bernadette O, Strohl, Kingman P

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