Tracking clinical genetic services for newborns identified through newborn dried bloodspot screening in the United States—lessons learned

Por Livingston, Judith, Therrell, Bradford L., Mann, Marie Y., Anderson, Carolyn Stady, Christensen, Katherine, Gorski, Jerome L., Grange, Dorothy K., Peck, Dawn, Roberston, Margy, Rogers, Sharmini, Taylor, Maura, Kaye, Celia I.
Publicado em 2011

Implementing screening for Lynch syndrome among patients with newly diagnosed colorectal cancer: summary of a public health/clinical collaborative meeting

Por Bellcross, Cecelia A., Bedrosian, Sara R., Daniels, Elvan, Duquette, Debra, Hampel, Heather, Jasperson, Kory, Joseph, Djenaba A., Kaye, Celia, Lubin, Ira, Meyer, Laurence J., Reyes, Michele, Scheuner, Maren T., Schully, Sheri D., Senter, Leigha, Stewart, Sherri L., Pierre, Jeanette St., Westman, Judith, Wise, Paul, Yang, Vincent W., Khoury, Muin J.
Publicado em 2011

A framework for assessing outcomes from newborn screening: on the road to measuring its promise

Por Hinton, Cynthia F., Homer, Charles J., Thompson, Alexis A., Williams, Andrea, Hassell, Kathryn L., Feuchtbaum, Lisa, Berry, Susan A., Comeau, Anne Marie, Therrell, Bradford L., Brower, Amy, Harris, Katharine B., Brown, Christine, Monaco, Jana, Ostrander, Robert J., Zuckerman, Alan E., Kaye, Celia, Dougherty, Denise, Greene, Carol, Green, Nancy S.
Publicado no Mol Genet Metab (2016)