Search Results - Wallace, Nora K

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    Inherited causes of clonal haematopoiesis in 97,691 whole genomes by Weinstock, Joshua S., Nandakumar, Satish K., Bao, Erik L., Szeto, Mindy D., Liao, Xiaotian, Nasser, Joseph, Laurie, Cecelia, Burugula, Bala Bharathi, Gibson, Christopher J., Lin, Amy E., Aguet, Francois, Ardlie, Kristin, Mitchell, Braxton D., Barnes, Kathleen C., Moscati, Arden, Redline, Susan, Psaty, Bruce M., Silverman, Edwin K., Weiss, Scott T., Palmer, Nicholette D., Vasan, Ramachandran S., Burchard, Esteban G., He, Jiang, Kaplan, Robert C., Smith, Nicholas L., Arnett, Donna K., Schwartz, David A., Guo, Xiuqing, Konkle, Barbara A., Custer, Brian, Peralta, Juan M., Gui, Hongsheng, Meyers, Deborah A., McGarvey, Stephen T., Chen, Ida Yii-Der, Shoemaker, M. Benjamin, Peyser, Patricia A., Broome, Jai G., Wang, Fei Fei, North, Kari E., Launer, Lenore J., Cade, Brian E., Bis, Joshua C., Cho, Michael H., Lasky-Su, Jessica, Bowden, Donald W., Cupples, L. Adrienne, Mak, Angel C. Y., Smith, Jennifer A., Kelly, Tanika N., Aslibekyan, Stella, Heckbert, Susan R., Tiwari, Hemant K., Yang, Ivana V., Heit, John A., Johnsen, Jill M., Curran, Joanne E., Wenzel, Sally E., Rao, Dabeeru C., Darbar, Dawood, Moon, Jee-Young, Tracy, Russell P., Buth, Erin J., Rafaels, Nicholas, Loos, Ruth J. F., Liu, Yongmei, Hou, Lifang, Lee, Jiwon, Kachroo, Priyadarshini, Freedman, Barry I., Levy, Daniel, Bielak, Lawrence F., Hixson, James E., Floyd, James S., Whitsel, Eric A., Ellinor, Patrick T., Irvin, Marguerite R., Fingerlin, Tasha E., Armasu, Sebastian M., Wheeler, Marsha M., Blangero, John, Williams, L. Keoki, Levy, Bruce D., Sheu, Wayne Huey-Herng, Roden, Dan M., Taylor, Kent D., Johnson, Andrew D., Auer, Paul L., Kooperberg, Charles, Laurie, Cathy C., Blackwell, Thomas W., Smith, Albert V., Lange, Ethan, Rotter, Jerome I., Kitzman, Jacob O., Lander, Eric S., Ebert, Benjamin L., Reiner, Alexander P., Jaiswal, Siddhartha, Kathiresan, Sekar

    Published in Nature (London)
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    Behavioral Deficits at 18-22 Months of Age Are Associated with Early Cerebellar Injury and Cognitive and Language Performance in Children Born Extremely Preterm by Dempsey, Allison, Caplan, Michael S., Laptook, Abbot R., Vohr, Betty R., Hensman, Angelita M., Alksninis, Barbara, Cashore, Bill, Francis, Kim, Gingras, Dan, Walsh, Michele C., Newman, Nancy S., Zadell, Arlene, Yalcinkaya, Gulgun, Bulas, Dorothy, Foy, Katherine A., Freedman, Sharon F., Lohmeyer, Melody B., Carlton, David P., Adams-Chapman, Ira, Piazza, Anthony J., LaRossa, Maureen Mulligan, Higgins, Rosemary D., Sokol, Gregory M., Dusick, Anna M., Lemons, James A., Wilson, Leslie D., Hamer, Faithe, Cook, Ann B., Herron, Dianne E., Minnich, Heike M., Berberich, Mary Anne, Das, Abhik, Newman, Jamie E., Auman, Jeanette O'Donnell, Pickett, James W., Van Meurs, Krisa P., Stevenson, David K., Ball, M. Bethany, Pyle, Renee P., Weiss, Hali E., Frantz, Ivan D., McGowan, Elisabeth C., Brussa, Ana, Carlo, Waldemar A., Hopkins, Maria, Johnston, Kristen C., Patterson, Cryshelle S., Soong, Amanda, Vaucher, Yvonne E., Lukasik, Meghan, Pontillo, Deborah, Wilkes, James, Colaizy, Tarah T., Johnson, Karen J., Calejo, Maria, Frade Eguaras, Silvia M., Berkowits, Michelle Harwood, Hiriart-Fajardo, Sylvia, Mathews, Elaine O., Pierre, Helina, Stroerger, Alexandra, Ohls, Robin K., Lowe, Jean, Laroia, Nirupama, Myers, Gary J., Reubens, Linda J., Johnson, Julie Babish, Gelbard, Harris, Kushner, Emily, Wang, David, Salhab, Walid A., Heyne, Roy J., Allen, James, Guzman, Alicia, Hensley, Gaynelle, Hickman, Jackie F., Solis, Araceli, Torres, Lizette E., Kennedy, Kathleen A., Evans, Patricia W., Alaniz, Nora I., Harris, Beverly Foley, Jiminez, Margarita, McDavid, Georgia E., Morris, Brenda H., Reddoch, Stacy, Wright, Sharon L., Yoder, Bradley A., Baker, Shawna, Bird, Karie, Bullwinkle, Anna E., Burnett, Jill, Osborne, Karen A., Steele, R. Edison, Weaver-Lewis, Kimberlee, Peters, Nancy J., Chiu, Korinne, Goldstein, Donald J., Sood, Beena G., Johnson, Mary

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    Whole genome sequence analyses of eGFR in 23,732 people representing multiple ancestries in the NHLBI trans-omics for precision medicine (TOPMed) consortium by Lin, Bridget M, Grinde, Kelsey E, Brody, Jennifer A, Breeze, Charles E, Raffield, Laura M, Mychaleckyj, Josyf C, Thornton, Timothy A, Perry, James A, Baier, Leslie J, de las Fuentes, Lisa, Guo, Xiuqing, Heavner, Benjamin D, Hanson, Robert L, Hung, Yi-Jen, Qian, Huijun, Hsiung, Chao A, Hwang, Shih-Jen, Irvin, Margaret R, Jain, Deepti, Kelly, Tanika N, Kobes, Sayuko, Lange, Leslie, Lash, James P, Li, Yun, Liu, Xiaoming, Mi, Xuenan, Musani, Solomon K, Papanicolaou, George J, Parsa, Afshin, Reiner, Alex P, Salimi, Shabnam, Sheu, Wayne H-H, Shuldiner, Alan R, Taylor, Kent D, Smith, Albert V, Smith, Jennifer A, Tin, Adrienne, Vaidya, Dhananjay, Wallace, Robert B, Yamamoto, Kenichi, Sakaue, Saori, Matsuda, Koichi, Kamatani, Yoichiro, Momozawa, Yukihide, Yanek, Lisa R, Young, Betsi A, Zhao, Wei, Okada, Yukinori, Abecasis, Gonzalo, Psaty, Bruce M, Arnett, Donna K, Boerwinkle, Eric, Cai, Jianwen, Yii-Der Chen, Ida, Correa, Adolfo, Cupples, L Adrienne, He, Jiang, Kardia, Sharon LR, Kooperberg, Charles, Mathias, Rasika A, Mitchell, Braxton D, Nickerson, Deborah A, Turner, Steve T, Vasan, Ramachandran S, Rotter, Jerome I, Levy, Daniel, Kramer, Holly J, Köttgen, Anna, NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, TOPMed Kidney Working Group, Rich, Stephen S, Lin, Dan-Yu, Browning, Sharon R, Franceschini, Nora

    Published in EBioMedicine
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