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

Por Wise, Anastasia L., Gyi, Lin, Manolio, Teri A.
Publicado em 2013

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

Por Splinter, Kimberly, Hull, Sara Chandros, Holm, Ingrid A., McDonough, Tara L., Wise, Anastasia L., Ramoni, Rachel B.
Publicado no Clin Transl Sci (2017)

Genomic Medicine for Undiagnosed Diseases

Por Wise, Anastasia L., Manolio, Teri A., Mensah, George A., Peterson, Josh F., Roden, Dan M., Tamburro, Cecelia, Williams, Marc S., Green, Eric D.
Publicado no Lancet (2019)

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

Por Gahl, William A., Mulvihill, John J., Toro, Camilo, Markello, Thomas C., Wise, Anastasia L., Ramoni, Rachel B., Adams, David R., Tifft, Cynthia J.
Publicado no Mol Genet Metab (2016)

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

Por 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.
Publicado no COPD (2014)

The Undiagnosed Diseases Network: Accelerating Discovery about Health and Disease

Por 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.
Publicado no Am J Hum Genet (2017)

Characteristics of undiagnosed diseases network applicants: implications for referring providers

Por 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
Publicado no BMC Health Serv Res (2018)

A Common MUC5B Promoter Polymorphism and Pulmonary Fibrosis

Por 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.
Publicado em 2011

Strategic vision for improving human health at The Forefront of Genomics

Por 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.
Publicado no Nature (2020)

Effect of Genetic Diagnosis on Patients with Previously Undiagnosed Disease

Por 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.
Publicado no N Engl J Med (2018)

Newborn Sequencing in Genomic Medicine and Public Health

Por 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.
Publicado no Pediatrics (2017)