Genome-wide association study identifies three novel loci in Fuchs endothelial corneal dystrophy

অনুযায়ী Afshari, Natalie A., Igo, Robert P., Morris, Nathan J., Stambolian, Dwight, Sharma, Shiwani, Pulagam, V. Lakshmi, Dunn, Steven, Stamler, John F., Truitt, Barbara J., Rimmler, Jacqueline, Kuot, Abraham, Croasdale, Christopher R., Qin, Xuejun, Burdon, Kathryn P., Riazuddin, S. Amer, Mills, Richard, Klebe, Sonja, Minear, Mollie A., Zhao, Jiagang, Balajonda, Elmer, Rosenwasser, George O., Baratz, Keith H, Mootha, V. Vinod, Patel, Sanjay V., Gregory, Simon G., Bailey-Wilson, Joan E., Price, Marianne O., Price, Francis W., Craig, Jamie E., Fingert, John H., Gottsch, John D., Aldave, Anthony J., Klintworth, Gordon K., Lass, Jonathan H., Li, Yi-Ju, Iyengar, Sudha K.
প্রকাশিত Nat Commun (2017)

Genome-Wide Association and Trans-ethnic Meta-Analysis for Advanced Diabetic Kidney Disease: Family Investigation of Nephropathy and Diabetes (FIND)

অনুযায়ী Iyengar, Sudha K., Sedor, John R., Freedman, Barry I., Kao, W. H. Linda, Kretzler, Matthias, Keller, Benjamin J., Abboud, Hanna E., Adler, Sharon G., Best, Lyle G., Bowden, Donald W., Burlock, Allison, Chen, Yii-Der Ida, Cole, Shelley A., Comeau, Mary E., Curtis, Jeffrey M., Divers, Jasmin, Drechsler, Christiane, Duggirala, Ravi, Elston, Robert C., Guo, Xiuqing, Huang, Huateng, Hoffmann, Michael Marcus, Howard, Barbara V., Ipp, Eli, Kimmel, Paul L., Klag, Michael J., Knowler, William C., Kohn, Orly F., Leak, Tennille S., Leehey, David J., Li, Man, Malhotra, Alka, März, Winfried, Nair, Viji, Nelson, Robert G., Nicholas, Susanne B., O’Brien, Stephen J., Pahl, Madeleine V., Parekh, Rulan S., Pezzolesi, Marcus G., Rasooly, Rebekah S., Rotimi, Charles N., Rotter, Jerome I., Schelling, Jeffrey R., Seldin, Michael F., Shah, Vallabh O., Smiles, Adam M., Smith, Michael W., Taylor, Kent D., Thameem, Farook, Thornley-Brown, Denyse P., Truitt, Barbara J., Wanner, Christoph, Weil, E. Jennifer, Winkler, Cheryl A., Zager, Philip G., Igo, Robert P., Hanson, Robert L., Langefeld, Carl D.
প্রকাশিত PLoS Genet (2015)

Rare and common variants in extracellular matrix gene Fibrillin 2 (FBN2) are associated with macular degeneration

অনুযায়ী Ratnapriya, Rinki, Zhan, Xiaowei, Fariss, Robert N., Branham, Kari E., Zipprer, David, Chakarova, Christina F., Sergeev, Yuri V., Campos, Maria M., Othman, Mohammad, Friedman, James S., Maminishkis, Arvydas, Waseem, Naushin H., Brooks, Matthew, Rajasimha, Harsha K., Edwards, Albert O., Lotery, Andrew, Klein, Barbara E., Truitt, Barbara J., Li, Bingshan, Schaumberg, Debra A., Morgan, Denise J., Morrison, Margaux A., Souied, Eric, Tsironi, Evangelia E., Grassmann, Felix, Fishman, Gerald A., Silvestri, Giuliana, Scholl, Hendrik P.N., Kim, Ivana K., Ramke, Jacqueline, Tuo, Jingsheng, Merriam, Joanna E., Merriam, John C., Park, Kyu Hyung, Olson, Lana M., Farrer, Lindsay A., Johnson, Matthew P., Peachey, Neal S., Lathrop, Mark, Baron, Robert V., Igo, Robert P., Klein, Ronald, Hagstrom, Stephanie A., Kamatani, Yoichiro, Martin, Tammy M., Jiang, Yingda, Conley, Yvette, Sahel, Jose-Alan, Zack, Donald J., Chan, Chi-Chao, Pericak-Vance, Margaret A., Jacobson, Samuel G., Gorin, Michael B., Klein, Michael L., Allikmets, Rando, Iyengar, Sudha K., Weber, Bernhard H., Haines, Jonathan L., Léveillard, Thierry, Deangelis, Margaret M., Stambolian, Dwight, Weeks, Daniel E., Bhattacharya, Shomi S., Chew, Emily Y., Heckenlively, John R., Abecasis, Gonçalo R., Swaroop, Anand
প্রকাশিত 2014