Items where Author is "Conley, Yvette"

Article

Ratnapriya, Rinki and Zhan, Xiaowei and Fariss, Robert N. and Branham, Kari E. and Zipprer, David and Chakarova, Christina F. and Sergeev, Yuri V. and Campos, Maria M. and Othman, Mohammad and Friedman, James S. and Maminishkis, Arvydas and Waseem, Naushin H. and Brooks, Matthew and Rajasimha, Harsha K. and Edwards, Albert O. and Lotery, Andrew and Klein, Barbara E. and Truitt, Barbara J. and Li, Bingshan and Schaumberg, Debra A. and Morgan, Denise J. and Morrison, Margaux A. and Souied, Eric and Tsironi, Evangelia E. and Grassmann, Felix and Fishman, Gerald A. and Silvestri, Giuliana and Scholl, Hendrik P. N. and Kim, Ivana K. and Ramke, Jacqueline and Tuo, Jingsheng and Merriam, Joanna E. and Merriam, John C. and Park, Kyu Hyung and Olson, Lana M. and Farrer, Lindsay A. and Johnson, Matthew P. and Peachey, Neal S. and Lathrop, Mark and Baron, Robert V. and Igo, Robert P. and Klein, Ronald and Hagstrom, Stephanie A. and Kamatani, Yoichiro and Martin, Tammy M. and Jiang, Yingda and Conley, Yvette and Sahel, Jose-Alan and Zack, Donald J. and Chan, Chi-Chao and Pericak-Vance, Margaret A. and Jacobson, Samuel G. and Gorin, Michael B. and Klein, Michael L. and Allikmets, Rando and Iyengar, Sudha K. and Weber, Bernhard H. and Haines, Jonathan L. and Leveillard, Thierry and Deangelis, Margaret M. and Stambolian, Dwight and Weeks, Daniel E. and Bhattacharya, Shomi S. and Chew, Emily Y. and Heckenlively, John R. and Abecasis, Goncalo R. and Swaroop, Anand (2014) Rare and common variants in extracellular matrix gene Fibrillin 2 (FBN2) are associated with macular degeneration. HUMAN MOLECULAR GENETICS, 23 (21). pp. 5827-5837. ISSN 0964-6906, 1460-2083