Successful integration of newborn genetic testing into UK routine screening using prospective consent to determine eligibility for clinical trials

por Bendor-Samuel, Owen Martyn, Wishlade, Tabitha, Willis, Louise, Aley, Parvinder, Choi, Edward, Craik, Rachel, Mujadidi, Yama, Mounce, Ginny, Roseman, Fenella, De La Horra Gozalo, Arancha, Bland, James, Taj, Nazia, Smith, Ian, Ziegler, Anette-Gabriele, Bonifacio, Ezio, Winkler, Christiane, Haupt, Florian, Todd, John A, Servais, Laurent, Snape, Matthew D, Vatish, Manu
Publicado 2023

Genome-wide association study identifies a locus at 7p15.2 associated with endometriosis

por Painter, Jodie N., Anderson, Carl A., Nyholt, Dale R., Macgregor, Stuart, Lin, Jianghai, Lee, Sang Hong, Lambert, Ann, Zhao, Zhen Z., Roseman, Fenella, Guo, Qun, Gordon, Scott D., Wallace, Leanne, Henders, Anjali K., Visscher, Peter M., Kraft, Peter, Martin, Nicholas G., Morris, Andrew P., Treloar, Susan A., Kennedy, Stephen H., Missmer, Stacey A., Montgomery, Grant W., Zondervan, Krina T.
Publicado 2010