Driving personalized medicine forward: the who, what, when, and how of educating the health-care workforce

por McCarthy, Jeanette J
Publicado 2014

Impact of gene variants on sex-specific regulation of human Scavenger receptor class B type 1 (SR-BI) expression in liver and association with lipid levels in a population-based st...

por Chiba-Falek, Ornit, Nichols, Marshall, Suchindran, Sunil, Guyton, John, Ginsburg, Geoffrey S, Barrett-Connor, Elizabeth, McCarthy, Jeanette J
Publicado 2010

Gene by Sex Interaction for Measures of Obesity in the Framingham Heart Study

por Benjamin, Ashlee M., Suchindran, Sunil, Pearce, Kaela, Rowell, Jennifer, Lien, Lillian F., Guyton, John R., McCarthy, Jeanette J.
Publicado 2011

Genome-Wide Association Study of Lp-PLA(2) Activity and Mass in the Framingham Heart Study

por Suchindran, Sunil, Rivedal, David, Guyton, John R., Milledge, Tom, Gao, Xiaoyi, Benjamin, Ashlee, Rowell, Jennifer, Ginsburg, Geoffrey S., McCarthy, Jeanette J.
Publicado 2010

Characterization of Serum Proteins Associated with IL28B Genotype among Patients with Chronic Hepatitis C

por Cyr, Derek D., Lucas, Joseph E., Thompson, J. Will, Patel, Keyur, Clark, Paul J., Thompson, Alexander, Tillmann, Hans L., McHutchison, John G., Moseley, M. Arthur, McCarthy, Jeanette J.
Publicado 2011

Metaprotein expression modeling for label-free quantitative proteomics

por Lucas, Joseph E, Thompson, J Will, Dubois, Laura G, McCarthy, Jeanette, Tillmann, Hans, Thompson, Alexander, Shire, Norah, Hendrickson, Ron, Dieguez, Francisco, Goldman, Phyllis, Schwarz, Kathleen, Patel, Keyur, McHutchison, John, Moseley, M Arthur
Publicado 2012

Characterization of the Poly-T Variant in the TOMM40 Gene in Diverse Populations

por Linnertz, Colton, Saunders, Ann M., Lutz, Michael W., Crenshaw, Donna M., Grossman, Iris, Burns, Daniel K., Whitfield, Keith E., Hauser, Michael A., McCarthy, Jeanette J., Ulmer, Megan, Allingham, Rand, Welsh-Bohmer, Kathleen A., Roses, Allen D., Chiba-Falek, Ornit
Publicado 2012

Artificial intelligence enables comprehensive genome interpretation and nomination of candidate diagnoses for rare genetic diseases

por De La Vega, Francisco M., Chowdhury, Shimul, Moore, Barry, Frise, Erwin, McCarthy, Jeanette, Hernandez, Edgar Javier, Wong, Terence, James, Kiely, Guidugli, Lucia, Agrawal, Pankaj B., Genetti, Casie A., Brownstein, Catherine A., Beggs, Alan H., Löscher, Britt-Sabina, Franke, Andre, Boone, Braden, Levy, Shawn E., Õunap, Katrin, Pajusalu, Sander, Huentelman, Matt, Ramsey, Keri, Naymik, Marcus, Narayanan, Vinodh, Veeraraghavan, Narayanan, Billings, Paul, Reese, Martin G., Yandell, Mark, Kingsmore, Stephen F.
Publicado 2021

Toward clinical genomics in everyday medicine: perspectives and recommendations

por Delaney, Susan K., Hultner, Michael L., Jacob, Howard J., Ledbetter, David H., McCarthy, Jeanette J., Ball, Michael, Beckman, Kenneth B., Belmont, John W., Bloss, Cinnamon S., Christman, Michael F., Cosgrove, Andy, Damiani, Stephen A., Danis, Timothy, Delledonne, Massimo, Dougherty, Michael J., Dudley, Joel T., Faucett, W. Andrew, Friedman, Jennifer R., Haase, David H., Hays, Tom S., Heilsberg, Stu, Huber, Jeff, Kaminsky, Leah, Ledbetter, Nikki, Lee, Warren H., Levin, Elissa, Libiger, Ondrej, Linderman, Michael, Love, Richard L., Magnus, David C., Martland, AnneMarie, McClure, Susan L., Megill, Scott E., Messier, Helen, Nussbaum, Robert L., Palaniappan, Latha, Patay, Bradley A., Popovich, Bradley W., Quackenbush, John, Savant, Mark J., Su, Michael M., Terry, Sharon F., Tucker, Steven, Wong, William T., Green, Robert C.
Publicado 2016