Search Results - "Nickerson, Debbie"

The All of Us Research Program: Data quality, utility, and diversity

Ramirez, Andrea H, Sulieman, Lina, Schlueter, David J, Halvorson, Alese, Qian, Jun, Ratsimbazafy, Francis, Loperena, Roxana, Mayo, Kelsey, Basford, Melissa, Deflaux, Nicole, Muthuraman, Karthik N, Natarajan, Karthik, Kho, Abel, Xu, Hua, Wilkins, Consuelo, Anton-Culver, Hoda, Boerwinkle, Eric, Cicek, Mine, Clark, Cheryl R, Cohn, Elizabeth, Ohno-Machado, Lucila, Schully, Sheri D, Ahmedani, Brian K, Argos, Maria, Cronin, Robert M, O’Donnell, Christopher, Fouad, Mona, Goldstein, David B, Greenland, Philip, Hebbring, Scott J, Karlson, Elizabeth W, Khatri, Parinda, Korf, Bruce, Smoller, Jordan W, Sodeke, Stephen, Wilbanks, John, Hentges, Justin, Mockrin, Stephen, Lunt, Christopher, Devaney, Stephanie A, Gebo, Kelly, Denny, Joshua C, Carroll, Robert J, Glazer, David, Harris, Paul A, Hripcsak, George, Philippakis, Anthony, Roden, Dan M, Program, the All of Us Research, Ahmedani, Brian, Johnson, Christine D Cole, Ahsan, Habib, Antoine-LaVigne, Donna, Singleton, Glendora, Topol, Eric, Baca-Motes, Katie, Steinhubl, Steven, Wade, James, Begale, Mark, Jain, Praduman, Sutherland, Scott, Lewis, Beth, Behringer, Melissa, Gharavi, Ali G, Bier, Louise, Brilliant, Murray H, Murali, Narayana, Hebbring, Scott Joseph, Farrar-Edwards, Dorothy, Burnside, Elizabeth, Drezner, Marc K, Taylor, Amy, Channamsetty, Veena, Montalvo, Wanda, Sharma, Yashoda, Chinea, Carmen, Jenks, Nancy, Thibodeau, Steve, Holmes, Beverly Wilson, Schlueter, Eric, Collier, Ever, Winkler, Joyce, Corcoran, John, D’Addezio, Nick, Daviglus, Martha, Winn, Robert, Roden, Dan, Denny, Joshua, Doheny, Kim, Nickerson, Debbie, Eichler, Evan, Jarvik, Gail, Funk, Gretchen

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Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program

Hu, Yao, Stilp, Adrienne M, McHugh, Caitlin P, Rao, Shuquan, Jain, Deepti, Zheng, Xiuwen, Lane, John, de Bellefon, Sébastian Méric, Raffield, Laura M, Chen, Ming-Huei, Yanek, Lisa R, Wheeler, Marsha, Yao, Yao, Ren, Chunyan, Broome, Jai, Moon, Jee-Young, de Vries, Paul S, Hobbs, Brian D, Sun, Quan, Surendran, Praveen, Brody, Jennifer A, Blackwell, Thomas W, Choquet, Hélène, Ryan, Kathleen, Duggirala, Ravindranath, Heard-Costa, Nancy, Wang, Zhe, Chami, Nathalie, Preuss, Michael H, Min, Nancy, Ekunwe, Lynette, Lange, Leslie A, Cushman, Mary, Faraday, Nauder, Curran, Joanne E, Almasy, Laura, Kundu, Kousik, Smith, Albert V, Gabriel, Stacey, Rotter, Jerome I, Fornage, Myriam, Lloyd-Jones, Donald M, Vasan, Ramachandran S, Smith, Nicholas L, North, Kari E, Boerwinkle, Eric, Becker, Lewis C, Lewis, Joshua P, Abecasis, Goncalo R, Hou, Lifang, O’Connell, Jeffrey R, Morrison, Alanna C, Beaty, Terri H, Kaplan, Robert, Correa, Adolfo, Blangero, John, Jorgenson, Eric, Psaty, Bruce M, Kooperberg, Charles, Walton, Russell T, Kleinstiver, Benjamin P, Tang, Hua, Loos, Ruth JF, Soranzo, Nicole, Butterworth, Adam S, Nickerson, Debbie, Rich, Stephen S, Mitchell, Braxton D, Johnson, Andrew D, Auer, Paul L, Li, Yun, Mathias, Rasika A, Lettre, Guillaume, Pankratz, Nathan, Laurie, Cathy C, Laurie, Cecelia A, Bauer, Daniel E, Conomos, Matthew P, Reiner, Alexander P, Consortium, NHLBI Trans-Omics for Precision Medicine

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The All of Us Research Program: Data quality, utility, and diversity

Ahmedani, Brian, Cole Johnson, Christine D., Ahsan, Habib, Antoine-LaVigne, Donna, Singleton, Glendora, Anton-Culver, Hoda, Topol, Eric, Baca-Motes, Katie, Steinhubl, Steven, Wade, James, Begale, Mark, Jain, Praduman, Sutherland, Scott, Lewis, Beth, Korf, Bruce, Behringer, Melissa, Gharavi, Ali G., Goldstein, David B., Hripcsak, George, Bier, Louise, Boerwinkle, Eric, Brilliant, Murray H., Murali, Narayana, Hebbring, Scott Joseph, Farrar-Edwards, Dorothy, Burnside, Elizabeth, Drezner, Marc K., Taylor, Amy, Channamsetty, Veena, Montalvo, Wanda, Sharma, Yashoda, Chinea, Carmen, Jenks, Nancy, Cicek, Mine, Thibodeau, Steve, Holmes, Beverly Wilson, Schlueter, Eric, Collier, Ever, Winkler, Joyce, Corcoran, John, D’Addezio, Nick, Daviglus, Martha, Winn, Robert, Wilkins, Consuelo, Roden, Dan, Denny, Joshua, Doheny, Kim, Nickerson, Debbie, Eichler, Evan, Jarvik, Gail, Funk, Gretchen, Philippakis, Anthony, Rehm, Heidi, Lennon, Niall, Kathiresan, Sekar, Gabriel, Stacey, Gibbs, Richard, Gil Rico, Edgar M., Glazer, David, Grand, Joannie, Greenland, Philip, Harris, Paul, Shenkman, Elizabeth, Hogan, William R., Igho-Pemu, Priscilla, Pollan, Cliff, Jorge, Milena, Okun, Sally, Karlson, Elizabeth W., Smoller, Jordan, Murphy, Shawn N., Ross, Margaret Elizabeth, Kaushal, Rainu, Winford, Eboni, Wallace, Febe, Khatri, Parinda, Kheterpal, Vik, Ojo, Akinlolu, Moreno, Francisco A., Kron, Irving, Peterson, Rachele, Menon, Usha, Lattimore, Patricia Watkins, Leviner, Noga, Obedin-Maliver, Juno, Lunn, Mitchell, Malik-Gagnon, Lynda, Mangravite, Lara, Marallo, Adria, Marroquin, Oscar, Visweswaran, Shyam, Reis, Steven, Marshall, Gailen, Jr., McGovern, Patrick, Mignucci, Deb, Moore, John, Munoz, Fatima, Talavera, Gregory, O'Connor, George T., O'Donnell, Christopher, Ohno-Machado, Lucila, Orr, Greg, Randal, Fornessa, Theodorou, Andreas A., Reiman, Eric, Roxas-Murray, Mercedita, Stark, Louisa, Tepp, Ronnie, Zhou, Alicia, Topper, Scott, Trousdale, Rhonda, Tsao, Phil, Weidman, Lisa, Weiss, Scott T., Wellis, David, Whittle, Jeffrey, Wilson, Amanda, Zuchner, Stephan, Zwick, Michael E., Ramirez, Andrea H., Sulieman, Lina, Schlueter, David J., Halvorson, Alese, Qian, Jun, Ratsimbazafy, Francis, Loperena, Roxana, Mayo, Kelsey, Basford, Melissa, Deflaux, Nicole, Muthuraman, Karthik N., Natarajan, Karthik, Kho, Abel, Xu, Hua, Clark, Cheryl R., Cohn, Elizabeth, Schully, Sheri D., Ahmedani, Brian K., Argos, Maria, Cronin, Robert M., O’Donnell, Christopher, Fouad, Mona, Hebbring, Scott J., Smoller, Jordan W., Sodeke, Stephen, Wilbanks, John, Hentges, Justin, Mockrin, Stephen, Lunt, Christopher, Devaney, Stephanie A., Gebo, Kelly, Denny, Joshua C., Carroll, Robert J., Harris, Paul A., Roden, Dan M.

Actionable exomic incidental findings in 6503 participants: challenges of variant classification

Amendola, Laura M, Dorschner, Michael O, Robertson, Peggy D, Salama, Joseph S, Hart, Ragan, Shirts, Brian H, Murray, Mitzi L, Tokita, Mari J, Gallego, Carlos J, Kim, Daniel Seung, Bennett, James T, Crosslin, David R, Ranchalis, Jane, Jones, Kelly L, Rosenthal, Elisabeth A, Jarvik, Ella R, Itsara, Andy, Turner, Emily H, Herman, Daniel S, Schleit, Jennifer, Burt, Amber, Jamal, Seema M, Abrudan, Jenica L, Johnson, Andrew D, Conlin, Laura K, Dulik, Matthew C, Santani, Avni, Metterville, Danielle R, Kelly, Melissa, Foreman, Ann Katherine M, Lee, Kristy, Taylor, Kent D, Guo, Xiuqing, Crooks, Kristy, Kiedrowski, Lesli A, Raffel, Leslie J, Gordon, Ora, Machini, Kalotina, Desnick, Robert J, Biesecker, Leslie G, Lubitz, Steven A, Mulchandani, Surabhi, Cooper, Greg M, Joffe, Steven, Richards, C Sue, Yang, Yaoping, Rotter, Jerome I, Rich, Stephen S, O’Donnell, Christopher J, Berg, Jonathan S, Spinner, Nancy B, Evans, James P, Fullerton, Stephanie M, Leppig, Kathleen A, Bennett, Robin L, Bird, Thomas, Sybert, Virginia P, Grady, William M, Tabor, Holly K, Kim, Jerry H, Bamshad, Michael J, Wilfond, Benjamin, Motulsky, Arno G, Scott, C Ronald, Pritchard, Colin C, Walsh, Tom D, Burke, Wylie, Raskind, Wendy H, Byers, Peter, Hisama, Fuki M, Rehm, Heidi, Nickerson, Debbie A, Jarvik, Gail P

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Validated Reference Panel from Renewable Source of Genomic DNA Available for Standardization of Blood Group Genotyping

Arnoni, Carine P., de Paula Vendrame, Tatiane A., Bein, Gregor, Sachs, Ulrich J., Aravechia, Maria G., Bub, Carolina B., Bunce, Mike, Pye, David, Castilho, Lilian, de Macedo, Mayra D., Constanzo, Jessica, Chevrier, Marie-Claire, Desjardins, Nathalie, Corgier, Benjamin, da Silva, Nelly, Mailloux, Agnès, Delaney, Meghan, Teramura, Gayle, Harris, Samantha, Heidl, Sarah, Denomme, Gregory A., Bensing, Kathleen, Doescher, Andrea, Drnovsek, Tadeja D., Lukan, Anja, Flegel, Willy A., Srivastava, Kshitij, Frank, Rainer, König, Sabrina, Gassner, Christoph, Meyer, Stefan, Trost, Nadine, Hyland, Catherine, Liew, Yew-Wah, Roots, Naomi, Johnsen, Jill, Nickerson, Debbie, Wheeler, Marsha, Keller, Margaret, Horn, Trina, Keller, Jessica, Crottet, Sofia Lejon, Henny, Christine, Modan, Shirley, Ochoa, Gorka, Hoffman, Roser, Hellberg, Åsa, Nertsberg, Lis, Olsson, Martin L., Vrignaud, Cédric, Peyrard, Thierry, St-Louis, Maryse, Lavoie, Josée, Laflamme, Geneviève, Tani, Yoshihiko, Tanaka, Mitsunobu, Trinkle, Anthony, Goe, Stephanie, Westhoff, Connie, Vege, Sunitha, Wittig, Michael, Franke, Andre, Wu, Ping Chun, Volkova, Evgeniya, Sippert, Emilia, Liu, Meihong, Mercado, Teresita, Illoh, Orieji, Liu, Zhugong, Rios, Maria

Association Between Celiac Disease and Iron Deficiency in Caucasians, but not Non-Caucasians

Murray, Joseph A., McLachlan, Stela, Adams, Paul C., Eckfeldt, John H., Garner, Chad P., Vulpe, Chris D., Gordeuk, Victor R., Brantner, Tricia, Leiendecker-Foster, Catherine, Killeen, Anthony A., Acton, Ronald T., Barcellos, Lisa F., Nickerson, Debbie A., Beckman, Kenneth B., McLaren, Gordon D., McLaren, Christine E.

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Genome-Wide Association Study Identifies Genetic Loci Associated with Iron Deficiency

McLaren, Christine E., Garner, Chad P., Constantine, Clare C., McLachlan, Stela, Vulpe, Chris D., Snively, Beverly M., Gordeuk, Victor R., Nickerson, Debbie A., Cook, James D., Leiendecker-Foster, Catherine, Beckman, Kenneth B., Eckfeldt, John H., Barcellos, Lisa F., Murray, Joseph A., Adams, Paul C., Acton, Ronald T., Killeen, Anthony A., McLaren, Gordon D.

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Family-based exome sequencing and case-control analysis implicate CEP41 as an ASD gene

Patowary, Ashok, Won, So Yeon, Oh, Shin Ji, Nesbitt, Ryan R, Archer, Marilyn, Nickerson, Debbie, Raskind, Wendy H.^{Aff1, Aff4}, Bernier, Raphael, Lee, Ji Eun^{Aff2, Aff5}, Brkanac, Zoran^Aff1

eP098: Exome sequencing of >500 individuals with brain malformation phenotypes reveals marked genetic heterogeneity

Chen, Wei-Liang, Timms, Andrew, Pao, Emily, Chong, Jessica, Bamshad, Michael, Nickerson, Debbie, Doherty, Dan, Novotny, Edward, Saneto, Russell, Ellenbogen, Richard, Hauptman, Jason, Ojemann, Jeff, Dobyns, William, Aldinger, Kimberly, Mirzaa, Ghayda

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De novo variants in congenital diaphragmatic hernia identify MYRF as a new syndrome and reveal genetic overlaps with other developmental disorders.

Guo, Yicheng, Qi, Hongjian, Zhou, Xueya, Zhu, Na, Zhao, Haoquan, Kitaygorodsky, Alexander, Shen, Yufeng, Warner, Brad W., Mychaliska, George B., Potoka, Douglas, Wagner, Amy J., ElFiky, Mahmoud, Wilson, Jay M., High, Frances A., Longoni, Mauro, Donahoe, Patricia K., Nickerson, Debbie, Bamshad, Michael, Yu, Lan, Wynn, Julia

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