eXclusion: Toward Integrating the X Chromosome in Genome-wide Association Analyses

Autor Wise, Anastasia L., Gyi, Lin, Manolio, Teri A.
Vydáno 2013

Implementing the Single Institutional Review Board Model: Lessons from the Undiagnosed Diseases Network

Autor Splinter, Kimberly, Hull, Sara Chandros, Holm, Ingrid A., McDonough, Tara L., Wise, Anastasia L., Ramoni, Rachel B.
Vydáno v Clin Transl Sci (2017)

Genomic Medicine for Undiagnosed Diseases

Autor Wise, Anastasia L., Manolio, Teri A., Mensah, George A., Peterson, Josh F., Roden, Dan M., Tamburro, Cecelia, Williams, Marc S., Green, Eric D.
Vydáno v Lancet (2019)

The NIH Undiagnosed Diseases Program and Network: Applications to modern medicine

Autor Gahl, William A., Mulvihill, John J., Toro, Camilo, Markello, Thomas C., Wise, Anastasia L., Ramoni, Rachel B., Adams, David R., Tifft, Cynthia J.
Vydáno v Mol Genet Metab (2016)

Cardiovascular Disease is Associated with COPD Severity and Reduced Functional Status and Quality of Life

Autor Black-Shinn, Jennifer L., Kinney, Gregory L., Wise, Anastasia L., Regan, Elizabeth A., Make, Barry, Krantz, Mori J., Barr, R. Graham, Murphy, James R., Lynch, David, Silverman, Edwin K., Crapo, James D., Hokanson, John E.
Vydáno v COPD (2014)

The Undiagnosed Diseases Network: Accelerating Discovery about Health and Disease

Autor Ramoni, Rachel B., Mulvihill, John J., Adams, David R., Allard, Patrick, Ashley, Euan A., Bernstein, Jonathan A., Gahl, William A., Hamid, Rizwan, Loscalzo, Joseph, McCray, Alexa T., Shashi, Vandana, Tifft, Cynthia J., Wise, Anastasia L.
Vydáno v Am J Hum Genet (2017)

Characteristics of undiagnosed diseases network applicants: implications for referring providers

Autor Walley, Nicole M., Pena, Loren D. M., Hooper, Stephen R., Cope, Heidi, Jiang, Yong-Hui, McConkie-Rosell, Allyn, Sanders, Camilla, Schoch, Kelly, Spillmann, Rebecca C., Strong, Kimberly, McCray, Alexa T., Mazur, Paul, Esteves, Cecilia, LeBlanc, Kimberly, Wise, Anastasia L., Shashi, Vandana
Vydáno v BMC Health Serv Res (2018)

A Common MUC5B Promoter Polymorphism and Pulmonary Fibrosis

Autor Seibold, Max A., Wise, Anastasia L., Speer, Marcy C., Steele, Mark P., Brown, Kevin K., Loyd, James E., Fingerlin, Tasha E., Zhang, Weiming, Gudmundsson, Gunnar, Groshong, Steve D., Evans, Christopher M., Garantziotis, Stavros, Adler, Kenneth B., Dickey, Burton F., du Bois, Roland M., Yang, Ivana V., Herron, Aretha, Kervitsky, Dolly, Talbert, Janet L., Markin, Cheryl, Park, Joungjoa, Crews, Anne L., Slifer, Susan H., Auerbach, Scott, Roy, Michelle G., Lin, Jia, Hennessy, Corinne E., Schwarz, Marvin I., Schwartz, David A.
Vydáno 2011

Strategic vision for improving human health at The Forefront of Genomics

Autor Green, Eric D., Gunter, Chris, Biesecker, Leslie G., Francesco, Valentina Di, Easter, Carla L., Feingold, Elise A., Felsenfeld, Adam L., Kaufman, David J., Ostrander, Elaine A., Pavan, William J., Phillippy, Adam M., Wise, Anastasia L., Dayal, Jyoti Gupta, Kish, Britny J., Mandich, Allison, Wellington, Christopher R., Wetterstrand, Kris A., Bates, Sarah A., Leja, Darryl, Vasquez, Susan, Gahl, William A., Graham, Bettie J., Kastner, Daniel L., Liu, Paul, Rodriguez, Laura Lyman, Solomon, Benjamin D., Bonham, Vence L., Brody, Lawrence C., Hutter, Carolyn M., Manolio, Teri A.
Vydáno v Nature (2020)

Effect of Genetic Diagnosis on Patients with Previously Undiagnosed Disease

Autor Splinter, Kimberly, Adams, David R., Bacino, Carlos A., Bellen, Hugo J., Bernstein, Jonathan A., Cheatle-Jarvela, Alys M., Eng, Christine M., Esteves, Cecilia, Gahl, William A., Hamid, Rizwan, Jacob, Howard J., Kikani, Bijal, Koeller, David M., Kohane, Isaac S., Lee, Brendan H., Loscalzo, Joseph, Luo, Xi, McCray, Alexa T., Metz, Thomas O., Mulvihill, John J., Nelson, Stanley F., Palmer, Christina G.S., Phillips, John A., Pick, Leslie, Postlethwait, John H., Reuter, Chloe, Shashi, Vandana, Sweetser, David A., Tifft, Cynthia J., Walley, Nicole M., Wangler, Michael F., Westerfield, Monte, Wheeler, Matthew T., Wise, Anastasia L., Worthey, Elizabeth A., Yamamoto, Shinya, Ashley, Euan A.
Vydáno v N Engl J Med (2018)

Newborn Sequencing in Genomic Medicine and Public Health

Autor Berg, Jonathan S., Agrawal, Pankaj B., Bailey, Donald B., Beggs, Alan H., Brenner, Steven E., Brower, Amy M., Cakici, Julie A., Ceyhan-Birsoy, Ozge, Chan, Kee, Chen, Flavia, Currier, Robert J., Dukhovny, Dmitry, Green, Robert C., Harris-Wai, Julie, Holm, Ingrid A., Iglesias, Brenda, Joseph, Galen, Kingsmore, Stephen F., Koenig, Barbara A., Kwok, Pui-Yan, Lantos, John, Leeder, Steven J., Lewis, Megan A., McGuire, Amy L., Milko, Laura V., Mooney, Sean D., Parad, Richard B., Pereira, Stacey, Petrikin, Joshua, Powell, Bradford C., Powell, Cynthia M., Puck, Jennifer M., Rehm, Heidi L., Risch, Neil, Roche, Myra, Shieh, Joseph T., Veeraraghavan, Narayanan, Watson, Michael S., Willig, Laurel, Yu, Timothy W., Urv, Tiina, Wise, Anastasia L.
Vydáno v Pediatrics (2017)