Public and Population Health Genomics

por Wise, A.L., Manolio, T.A.
Publicado 2016

The International Hundred Thousand Plus Cohort Consortium: integrating large-scale cohorts to address global scientific challenges

por Manolio, Teri A, Goodhand, Peter, Ginsburg, Geoffrey
Publicado 2020

eXclusionarY: 10 years later, where are the sex chromosomes in GWASs?

por Sun, Lei, Wang, Zhong, Lu, Tianyuan, Manolio, Teri A., Paterson, Andrew D.
Publicado 2023

Size matters: just how big is BIG?: Quantifying realistic sample size requirements for human genome epidemiology

por Burton, Paul R, Hansell, Anna L, Fortier, Isabel, Manolio, Teri A, Khoury, Muin J, Little, Julian, Elliott, Paul
Publicado 2009

Diabetes, gender, and left ventricular structure in African-Americans: the atherosclerosis risk in communities study

por Foppa, Murilo, Duncan, Bruce B, Arnett, Donna K, Benjamin, Emelia J, Liebson, Philip R, Manolio, Teri A, Skelton, Thomas N
Publicado 2006

Return of secondary findings in genomic sequencing: Military implications

por Hellwig, Lydia D., Turner, Clesson, Manolio, Teri A., Haigney, Mark, James, Cynthia A., Murray, Brittney, Szpisjak, Dale F., Muldoon, Sheila, Estrada‐Veras, Juvianee, Krokosky, Alyson, De Castro, Mauricio J.
Publicado 2018

A new statistic and its power to infer membership and phenotype in a genome-wide association study using genotype frequencies

por Jacobs, Kevin B., Yeager, Meredith, Wacholder, Sholom, Craig, David, Kraft, Peter, Hunter, David J., Paschal, Justin, Manolio, Teri A., Tucker, Margaret, Hoover, Robert N., Thomas, Gilles D., Chanock, Stephen J., Chatterjee, Nilanjan
Publicado 2009

Incidental genetic findings in randomized clinical trials: recommendations from the Genomics and Randomized Trials Network (GARNET)

por Bookman, Ebony B, Din-Lovinescu, Corina, Worrall, Bradford B, Manolio, Teri A, Bennett, Siiri N, Laurie, Cathy, Mirel, Daniel B, Doheny, Kimberly F, Anderson, Garnet L, Wehr, Kate, Weinshilboum, Richard, Chen, Donna T
Publicado 2013

Genetic Variants That Confer Resistance to Malaria Are Associated with Red Blood Cell Traits in African-Americans: An Electronic Medical Record-based Genome-Wide Association Study

por Ding, Keyue, de Andrade, Mariza, Manolio, Teri A., Crawford, Dana C., Rasmussen-Torvik, Laura J., Ritchie, Marylyn D., Denny, Joshua C., Masys, Daniel R., Jouni, Hayan, Pachecho, Jennifer A., Kho, Abel N., Roden, Dan M., Chisholm, Rex, Kullo, Iftikhar J.
Publicado 2013

The Next PAGE in Understanding Complex Traits: Design for the Analysis of Population Architecture Using Genetics and Epidemiology (PAGE) Study

por Matise, Tara C., Ambite, Jose Luis, Buyske, Steven, Carlson, Christopher S., Cole, Shelley A., Crawford, Dana C., Haiman, Christopher A., Heiss, Gerardo, Kooperberg, Charles, Marchand, Loic Le, Manolio, Teri A., North, Kari E., Peters, Ulrike, Ritchie, Marylyn D., Hindorff, Lucia A., Haines, Jonathan L.
Publicado 2011

Workshop proceedings: GWAS summary statistics standards and sharing

por MacArthur, Jacqueline A.L., Buniello, Annalisa, Harris, Laura W., Hayhurst, James, McMahon, Aoife, Sollis, Elliot, Cerezo, Maria, Hall, Peggy, Lewis, Elizabeth, Whetzel, Patricia L., Bahcall, Orli G., Barroso, Inês, Carroll, Robert J., Inouye, Michael, Manolio, Teri A., Rich, Stephen S., Hindorff, Lucia A., Wiley, Ken, Parkinson, Helen
Publicado 2021

New Models for Large Prospective Studies: Is There a Better Way?

por Manolio, Teri A., Weis, Brenda K., Cowie, Catherine C., Hoover, Robert N., Hudson, Kathy, Kramer, Barnett S., Berg, Chris, Collins, Rory, Ewart, Wendy, Gaziano, J. Michael, Hirschfeld, Steven, Marcus, Pamela M., Masys, Daniel, McCarty, Catherine A., McLaughlin, John, Patel, Alpa V., Peakman, Tim, Pedersen, Nancy L., Schaefer, Catherine, Scott, Joan A., Sprosen, Timothy, Walport, Mark, Collins, Francis S.
Publicado 2012

Generalizability of Polygenic Risk Scores for Breast Cancer Among Women With European, African, and Latinx Ancestry

por Liu, Cong, Zeinomar, Nur, Chung, Wendy K., Kiryluk, Krzysztof, Gharavi, Ali G., Hripcsak, George, Crew, Katherine D., Shang, Ning, Khan, Atlas, Fasel, David, Manolio, Teri A., Jarvik, Gail P., Rowley, Robb, Justice, Ann E., Rahm, Alanna K., Fullerton, Stephanie M., Smoller, Jordan W., Larson, Eric B., Crane, Paul K., Dikilitas, Ozan, Wiesner, Georgia L., Bick, Alexander G., Terry, Mary Beth, Weng, Chunhua
Publicado 2021

Implementing genomic medicine in the clinic: the future is here

por Manolio, Teri A., Chisholm, Rex L., Ozenberger, Brad, Roden, Dan M., Williams, Marc S., Wilson, Richard, Bick, David, Bottinger, Erwin P., Brilliant, Murray H., Eng, Charis, Frazer, Kelly A., Korf, Bruce, Ledbetter, David H., Lupski, James R., Marsh, Clay, Mrazek, David, Murray, Michael F., O'Donnell, Peter H., Rader, Daniel J., Relling, Mary V., Shuldiner, Alan R., Valle, David, Weinshilboum, Richard, Green, Eric D., Ginsburg, Geoffrey S.
Publicado 2013

Genome-Wide Association Analysis of Ischemic Stroke in Young Adults

por Cheng, Yu-Ching, O’Connell, Jeffrey R., Cole, John W., Stine, O. Colin, Dueker, Nicole, McArdle, Patrick F., Sparks, Mary J., Shen, Jess, Laurie, Cathy C., Nelson, Sarah, Doheny, Kimberly F., Ling, Hua, Pugh, Elizabeth W., Brott, Thomas G., Brown, Robert D., Meschia, James F., Nalls, Michael, Rich, Stephen S., Worrall, Bradford, Anderson, Christopher D., Biffi, Alessandro, Cortellini, Lynelle, Furie, Karen L., Rost, Natalia S., Rosand, Jonathan, Manolio, Teri A., Kittner, Steven J., Mitchell, Braxton D.
Publicado 2011

Guidelines for investigating causality of sequence variants in human disease

por MacArthur, D. G., Manolio, T. A., Dimmock, D. P., Rehm, H. L., Shendure, J., Abecasis, G. R., Adams, D. R., Altman, R. B., Antonarakis, S. E., Ashley, E. A., Barrett, J. C., Biesecker, L. G., Conrad, D. F., Cooper, G. M., Cox, N. J., Daly, M. J., Gerstein, M. B., Goldstein, D. B., Hirschhorn, J. N., Leal, S. M., Pennacchio, L. A., Stamatoyannopoulos, J. A., Sunyaev, S. R., Valle, D., Voight, B. F., Winckler, W., Gunter, C.
Publicado 2014

The IGNITE network: a model for genomic medicine implementation and research

por Weitzel, Kristin Wiisanen, Alexander, Madeline, Bernhardt, Barbara A., Calman, Neil, Carey, David J., Cavallari, Larisa H., Field, Julie R., Hauser, Diane, Junkins, Heather A., Levin, Phillip A., Levy, Kenneth, Madden, Ebony B., Manolio, Teri A., Odgis, Jacqueline, Orlando, Lori A., Pyeritz, Reed, Wu, R. Ryanne, Shuldiner, Alan R., Bottinger, Erwin P., Denny, Joshua C., Dexter, Paul R., Flockhart, David A., Horowitz, Carol R., Johnson, Julie A., Kimmel, Stephen E., Levy, Mia A., Pollin, Toni I., Ginsburg, Geoffrey S.
Publicado 2016

The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and future

por Gottesman, Omri, Kuivaniemi, Helena, Tromp, Gerard, Faucett, W. Andrew, Li, Rongling, Manolio, Teri A., Sanderson, Saskia C., Kannry, Joseph, Zinberg, Randi, Basford, Melissa A., Brilliant, Murray, Carey, David J., Chisholm, Rex L., Chute, Christopher G., Connolly, John J., Crosslin, David, Denny, Joshua C., Gallego, Carlos J., Haines, Jonathan L., Hakonarson, Hakon, Harley, John, Jarvik, Gail P., Kohane, Isaac, Kullo, Iftikhar J., Larson, Eric B., McCarty, Catherine, Ritchie, Marylyn D., Roden, Dan M., Smith, Maureen E., Böttinger, Erwin P., Williams, Marc S.
Publicado 2013

Evaluation of the Metabochip Genotyping Array in African Americans and Implications for Fine Mapping of GWAS-Identified Loci: The PAGE Study

por Buyske, Steven, Wu, Ying, Carty, Cara L., Cheng, Iona, Assimes, Themistocles L., Dumitrescu, Logan, Hindorff, Lucia A., Mitchell, Sabrina, Ambite, Jose Luis, Boerwinkle, Eric, Buzkova, Petra, Carlson, Chris S., Cochran, Barbara, Duggan, David, Eaton, Charles B., Fesinmeyer, Megan D., Franceschini, Nora, Haessler, Jeffrey, Jenny, Nancy, Kang, Hyun Min, Kooperberg, Charles, Lin, Yi, Le Marchand, Loic, Matise, Tara C., Robinson, Jennifer G., Rodriguez, Carlos, Schumacher, Fredrick R., Voight, Benjamin F., Young, Alicia, Manolio, Teri A., Mohlke, Karen L., Haiman, Christopher A., Peters, Ulrike, Crawford, Dana C., North, Kari E.
Publicado 2012

Genetic Determinants of Lipid Traits in Diverse Populations from the Population Architecture using Genomics and Epidemiology (PAGE) Study

por Dumitrescu, Logan, Carty, Cara L., Taylor, Kira, Schumacher, Fredrick R., Hindorff, Lucia A., Ambite, José L., Anderson, Garnet, Best, Lyle G., Brown-Gentry, Kristin, Bůžková, Petra, Carlson, Christopher S., Cochran, Barbara, Cole, Shelley A., Devereux, Richard B., Duggan, Dave, Eaton, Charles B., Fornage, Myriam, Franceschini, Nora, Haessler, Jeff, Howard, Barbara V., Johnson, Karen C., Laston, Sandra, Kolonel, Laurence N., Lee, Elisa T., MacCluer, Jean W., Manolio, Teri A., Pendergrass, Sarah A., Quibrera, Miguel, Shohet, Ralph V., Wilkens, Lynne R., Haiman, Christopher A., Le Marchand, Loïc, Buyske, Steven, Kooperberg, Charles, North, Kari E., Crawford, Dana C.
Publicado 2011