Exact Inference for Hardy-Weinberg Proportions with Missing Genotypes: Single and Multiple Imputation

por Graffelman, Jan, Nelson, S., Gogarten, S. M., Weir, B. S.
Publicado 2015

Local Ancestry Inference in a Large US-Based Hispanic/Latino Study: Hispanic Community Health Study/Study of Latinos (HCHS/SOL)

por Browning, Sharon R., Grinde, Kelsey, Plantinga, Anna, Gogarten, Stephanie M., Stilp, Adrienne M., Kaplan, Robert C., Avilés-Santa, M. Larissa, Browning, Brian L., Laurie, Cathy C.
Publicado 2016

Genetic Associations with Plasma B12, B6, and Folate Levels in an Ischemic Stroke Population from the Vitamin Intervention for Stroke Prevention (VISP) Trial

por Keene, Keith L., Chen, Wei-Min, Chen, Fang, Williams, Stephen R., Elkhatib, Stacey D., Hsu, Fang-Chi, Mychaleckyj, Josyf C., Doheny, Kimberly F., Pugh, Elizabeth W., Ling, Hua, Laurie, Cathy C., Gogarten, Stephanie M., Madden, Ebony B., Worrall, Bradford B., Sale, Michele M.
Publicado 2014

Variant-specific inflation factors for assessing population stratification at the phenotypic variance level

por Sofer, Tamar, Zheng, Xiuwen, Laurie, Cecelia A., Gogarten, Stephanie M., Brody, Jennifer A., Conomos, Matthew P., Bis, Joshua C., Thornton, Timothy A., Szpiro, Adam, O’Connell, Jeffrey R., Lange, Ethan M., Gao, Yan, Cupples, L. Adrienne, Psaty, Bruce M., Rice, Kenneth M.
Publicado 2021

Recommendations on the use and reporting of race, ethnicity, and ancestry in genetic research: Experiences from the NHLBI TOPMed program

por Khan, Alyna T., Gogarten, Stephanie M., McHugh, Caitlin P., Stilp, Adrienne M., Sofer, Tamar, Bowers, Michael L., Wong, Quenna, Cupples, L. Adrienne, Hidalgo, Bertha, Johnson, Andrew D., McDonald, Merry-Lynn N., McGarvey, Stephen T., Taylor, Matthew R.G., Fullerton, Stephanie M., Conomos, Matthew P., Nelson, Sarah C.
Publicado 2022

Genome-Wide Meta-Analysis of Homocysteine and Methionine Metabolism Identifies Five One Carbon Metabolism Loci and a Novel Association of ALDH1L1 with Ischemic Stroke

por Williams, Stephen R., Yang, Qiong, Chen, Fang, Liu, Xuan, Keene, Keith L., Jacques, Paul, Chen, Wei-Min, Weinstein, Galit, Hsu, Fang-Chi, Beiser, Alexa, Wang, Liewei, Bookman, Ebony, Doheny, Kimberly F., Wolf, Philip A., Zilka, Michelle, Selhub, Jacob, Nelson, Sarah, Gogarten, Stephanie M., Worrall, Bradford B., Seshadri, Sudha, Sale, Michèle M.
Publicado 2014

Accounting for population structure in genetic studies of cystic fibrosis

por Kingston, Hanley, Stilp, Adrienne M., Gordon, William, Broome, Jai, Gogarten, Stephanie M., Ling, Hua, Barnard, John, Dugan-Perez, Shannon, Ellinor, Patrick T., Gabriel, Stacey, Germer, Soren, Gibbs, Richard A., Gupta, Namrata, Rice, Kenneth, Smith, Albert V., Zody, Michael C., Blackman, Scott M., Cutting, Garry, Knowles, Michael R., Zhou, Yi-Hui, Rosenfeld, Margaret, Gibson, Ronald L., Bamshad, Michael, Fohner, Alison, Blue, Elizabeth E.
Publicado 2022

Multi-Omics Analysis Reveals a HIF Network and Hub Gene EPAS1 Associated with Lung Adenocarcinoma

por Wang, Zhaoxi, Wei, Yongyue, Zhang, Ruyang, Su, Li, Gogarten, Stephanie M., Liu, Geoffrey, Brennan, Paul, Field, John K., McKay, James D., Lissowska, Jolanta, Swiatkowska, Beata, Janout, Vladimir, Bolca, Ciprian, Kontic, Milica, Scelo, Ghislaine, Zaridze, David, Laurie, Cathy C., Doheny, Kimberly F., Pugh, Elizabeth K., Marosy, Beth A., Hetrick, Kurt N., Xiao, Xiangjun, Pikielny, Claudio, Hung, Rayjean J., Amos, Christopher I., Lin, Xihong, Christiani, David C.
Publicado 2018

GWAS of the electrocardiographic QT interval in Hispanics/Latinos generalizes previously identified loci and identifies population-specific signals

por Méndez-Giráldez, Raúl, Gogarten, Stephanie M., Below, Jennifer E., Yao, Jie, Seyerle, Amanda A., Highland, Heather M., Kooperberg, Charles, Soliman, Elsayed Z., Rotter, Jerome I., Kerr, Kathleen F., Ryckman, Kelli K., Taylor, Kent D., Petty, Lauren E., Shah, Sanjiv J., Conomos, Matthew P., Sotoodehnia, Nona, Cheng, Susan, Heckbert, Susan R., Sofer, Tamar, Guo, Xiuqing, Whitsel, Eric A., Lin, Henry J., Hanis, Craig L., Laurie, Cathy C., Avery, Christy L.
Publicado 2017

Identification of novel and rare variants associated with handgrip strength using whole genome sequence data from the NHLBI Trans-Omics in Precision Medicine (TOPMed) Program

por Sarnowski, Chloé, Chen, Han, Biggs, Mary L., Wassertheil-Smoller, Sylvia, Bressler, Jan, Irvin, Marguerite R., Ryan, Kathleen A., Karasik, David, Arnett, Donna K., Cupples, L. Adrienne, Fardo, David W., Gogarten, Stephanie M., Heavner, Benjamin D., Jain, Deepti, Kang, Hyun Min, Kooperberg, Charles, Mainous, Arch G., Mitchell, Braxton D., Morrison, Alanna C., O’Connell, Jeffrey R., Psaty, Bruce M., Rice, Kenneth, Smith, Albert V., Vasan, Ramachandran S., Windham, B. Gwen, Kiel, Douglas P., Murabito, Joanne M., Lunetta, Kathryn L.
Publicado 2021

Genome-wide association study of body fat distribution traits in Hispanics/Latinos from the HCHS/SOL

por Justice, Anne E, Young, Kristin, Gogarten, Stephanie M, Sofer, Tamar, Graff, Misa, Love, Shelly Ann M, Wang, Yujie, Klimentidis, Yann C, Cruz, Miguel, Guo, Xiuqing, Hartwig, Fernando, Petty, Lauren, Yao, Jie, Allison, Matthew A, Below, Jennifer E, Buchanan, Thomas A, Chen, Yii-Der Ida, Goodarzi, Mark O, Hanis, Craig, Highland, Heather M, Hsueh, Willa A, Ipp, Eli, Parra, Esteban, Palmas, Walter, Raffel, Leslie J, Rotter, Jerome I, Tan, Jingyi, Taylor, Kent D, Valladares, Adan, Xiang, Anny H, Sánchez-Johnsen, Lisa, Isasi, Carmen R, North, Kari E
Publicado 2021

Genome-wide association study and meta-analysis identify loci associated with ventricular and supraventricular ectopy

por Napier, Melanie D., Franceschini, Nora, Gondalia, Rahul, Stewart, James D., Méndez-Giráldez, Raúl, Sitlani, Colleen M., Seyerle, Amanda A., Highland, Heather M., Li, Yun, Wilhelmsen, Kirk C., Yan, Song, Duan, Qing, Roach, Jeffrey, Yao, Jie, Guo, Xiuqing, Taylor, Kent D., Heckbert, Susan R., Rotter, Jerome I., North, Kari E., Reiner, Alexander P., Zhang, Zhu-Ming, Tinker, Lesley F., Liao, Duanping, Laurie, Cathy C., Gogarten, Stephanie M., Lin, Henry J., Brody, Jennifer A., Bartz, Traci M., Psaty, Bruce M., Sotoodehnia, Nona, Soliman, Elsayed Z., Avery, Christy L., Whitsel, Eric A.
Publicado 2018

BinomiRare: A robust test for association of a rare genetic variant with a binary outcome for mixed models and any case-control proportion

por Sofer, Tamar, Lee, Jiwon, Kurniansyah, Nuzulul, Jain, Deepti, Laurie, Cecelia A., Gogarten, Stephanie M., Conomos, Matthew P., Heavner, Ben, Hu, Yao, Kooperberg, Charles, Haessler, Jeffrey, Vasan, Ramachandran S., Cupples, L. Adrienne, Coombes, Brandon J., Seyerle, Amanda, Gharib, Sina A., Chen, Han, O’Connell, Jeffrey R., Zhang, Man, Gottlieb, Daniel J., Psaty, Bruce M., Longstreth, W.T., Rotter, Jerome I., Taylor, Kent D., Rich, Stephen S., Guo, Xiuqing, Boerwinkle, Eric, Morrison, Alanna C., Pankow, James S., Johnson, Andrew D., Pankratz, Nathan, Reiner, Alex P., Redline, Susan, Smith, Nicholas L., Rice, Kenneth M., Schifano, Elizabeth D.
Publicado 2021

Whole Genome Sequencing Based Analysis of Inflammation Biomarkers in the Trans-Omics for Precision Medicine (TOPMed) Consortium

por Jiang, Min-Zhi, Gaynor, Sheila M., Li, Xihao, Van Buren, Eric, Stilp, Adrienne, Buth, Erin, Wang, Fei Fei, Manansala, Regina, Gogarten, Stephanie M., Li, Zilin, Polfus, Linda M., Salimi, Shabnam, Bis, Joshua C., Pankratz, Nathan, Yanek, Lisa R., Durda, Peter, Tracy, Russell P., Rich, Stephen S., Rotter, Jerome I., Mitchell, Braxton D., Lewis, Joshua P., Psaty, Bruce M., Pratte, Katherine A., Silverman, Edwin K., Kaplan, Robert C., Avery, Christy, North, Kari, Mathias, Rasika A., Faraday, Nauder, Lin, Honghuang, Wang, Biqi, Carson, April P., Norwood, Arnita F., Gibbs, Richard A., Kooperberg, Charles, Lundin, Jessica, Peters, Ulrike, Dupuis, Josée, Hou, Lifang, Fornage, Myriam, Benjamin, Emelia J., Reiner, Alexander P., Bowler, Russell P., Lin, Xihong, Auer, Paul L., Raffield, Laura M.
Publicado 2023

Association of clonal hematopoiesis with chronic obstructive pulmonary disease

por Miller, Peter G., Qiao, Dandi, Rojas-Quintero, Joselyn, Honigberg, Michael C., Sperling, Adam S., Gibson, Christopher J., Bick, Alexander G., Niroula, Abhishek, McConkey, Marie E., Sandoval, Brittany, Miller, Brian C., Shi, Weiwei, Viswanathan, Kaushik, Leventhal, Matthew, Werner, Lillian, Moll, Matthew, Cade, Brian E., Barr, R. Graham, Correa, Adolfo, Cupples, L. Adrienne, Gharib, Sina A., Jain, Deepti, Gogarten, Stephanie M., Lange, Leslie A., London, Stephanie J., Manichaikul, Ani, O’Connor, George T., Oelsner, Elizabeth C., Redline, Susan, Rich, Stephen S., Rotter, Jerome I., Ramachandran, Vasan, Yu, Bing, Sholl, Lynette, Neuberg, Donna, Jaiswal, Siddhartha, Levy, Bruce D., Owen, Caroline A., Natarajan, Pradeep, Silverman, Edwin K., van Galen, Peter, Tesfaigzi, Yohannes, Cho, Michael H., Ebert, Benjamin L.
Publicado 2022

Large-scale pharmacogenomic study of sulfonylureas and the QT, JT, and QRS intervals: CHARGE Pharmacogenomics Working Group

por Floyd, James S, Sitlani, Colleen M, Avery, Christy L, Noordam, Raymond, Li, Xiaohui, Smith, Albert V, Gogarten, Stephanie M, Li, Jin, Broer, Linda, Evans, Daniel S, Trompet, Stella, Brody, Jennifer A, Stewart, James D, Eicher, John D, Seyerle, Amanda A, Roach, Jeffrey, Lange, Leslie A, Lin, Henry J, Kors, Jan A, Harris, Tamara B, Li-Gao, Ruifang, Sattar, Naveed, Cummings, Steven R, Wiggins, Kerri L, Napier, Melanie D, Stürmer, Til, Bis, Joshua C, Kerr, Kathleen F, Uitterlinden, André G, Taylor, Kent D, Stott, David J, de Mutsert, Renée, Launer, Lenore J, Busch, Evan L, Méndez-Giráldez, Raúl, Sotoodehnia, Nona, Soliman, Elsayed Z, Li, Yun, Duan, Qing, Rosendaal, Frits R, Slagboom, P Eline, Wilhelmsen, Kirk C, Reiner, Alexander P, Chen, Yii-Der I, Heckbert, Susan R, Kaplan, Robert C, Rice, Kenneth M, Jukema, J Wouter, Johnson, Andrew D, Liu, Yongmei, Mook-Kanamori, Dennis O, Gudnason, Vilmundur, Wilson, James G, Rotter, Jerome I, Laurie, Cathy C, Psaty, Bruce M, Whitsel, Eric A, Cupples, L Adrienne, Stricker, Bruno H
Publicado 2016

Detectable clonal mosaicism from birth to old age and its relationship to cancer

por Laurie, Cathy C., Laurie, Cecelia A., Rice, Kenneth, Doheny, Kimberly F., Zelnick, Leila R., McHugh, Caitlin P., Ling, Hua, Hetrick, Kurt N., Pugh, Elizabeth W., Amos, Chris, Wei, Qingyi, Wang, Li-e, Lee, Jeffrey E., Barnes, Kathleen C., Hansel, Nadia N., Mathias, Rasika, Daley, Denise, Beaty, Terri H., Scott, Alan F., Ruczinski, Ingo, Scharpf, Rob B., Bierut, Laura J., Hartz, Sarah M., Landi, Maria Teresa, Freedman, Neal D., Goldin, Lynn R., Ginsburg, David, Li, Jun, Desch, Karl C., Strom, Sara S., Blot, William J., Signorello, Lisa B., Ingles, Sue A., Chanock, Stephen J., Berndt, Sonja I., Le Marchand, Loic, Henderson, Brian E., Monroe, Kristine R, Heit, John A., de Andrade, Mariza, Armasu, Sebastian M., Regnier, Cynthia, Lowe, William L., Hayes, M. Geoffrey, Marazita, Mary L., Feingold, Eleanor, Murray, Jeffrey C., Melbye, Mads, Feenstra, Bjarke, Kang, Jae H., Wiggs, Janey L., Jarvik, Gail P., McDavid, Andrew N., Seshan, Venkatraman E., Mirel, Daniel B., Crenshaw, Andrew, Sharopova, Nataliya, Wise, Anastasia, Shen, Jess, Crosslin, David R., Levine, David M., Zheng, Xiuwen, Udren, Jenna I, Bennett, Siiri, Nelson, Sarah C., Gogarten, Stephanie M., Conomos, Matthew P., Heagerty, Patrick, Manolio, Teri, Pasquale, Louis R., Haiman, Christopher A., Caporaso, Neil, Weir, Bruce S.
Publicado 2012

Pharmacogenomics Study of Thiazide Diuretics and QT Interval in Multi-Ethnic Populations: The Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE)

por Seyerle, Amanda A, Sitlani, Colleen M, Noordam, Raymond, Gogarten, Stephanie M, Li, Jin, Li, Xiaohui, Evans, Daniel S, Sun, Fangui, Laaksonen, Maarit A, Isaacs, Aaron, Kristiansson, Kati, Highland, Heather M, Stewart, James D, Harris, Tamara B, Trompet, Stella, Bis, Joshua C, Peloso, Gina M, Brody, Jennifer A, Broer, Linda, Busch, Evan L, Duan, Qing, Stilp, Adrienne M, O’Donnell, Christopher J, Macfarlane, Peter W, Floyd, James S, Kors, Jan A, Lin, Henry J, Li-Gao, Ruifang, Sofer, Tamar, Méndez-Giráldez, Raúl, Cummings, Steven R, Heckbert, Susan R, Hofman, Albert, Ford, Ian, Li, Yun, Launer, Lenore J, Porthan, Kimmo, Newton-Cheh, Christopher, Napier, Melanie D, Kerr, Kathleen F, Reiner, Alexander P, Rice, Kenneth M, Roach, Jeffrey, Buckley, Brendan M, Soliman, Elsayed Z, de Mutsert, Renée, Sotoodehnia, Nona, Uitterlinden, André G, North, Kari E, Lee, Craig R, Gudnason, Vilmundur, Stürmer, Til, Rosendaal, Frits R, Taylor, Kent D, Wiggins, Kerri L, Wilson, James G, Chen, Yii-Der I, Kaplan, Robert C, Wilhelmsen, Kirk, Cupples, L Adrienne, Salomaa, Veikko, van Duijn, Cornelia, Jukema, J Wouter, Liu, Yongmei, Mook-Kanamori, Dennis O, Lange, Leslie A, Vasan, Ramachandran S, Smith, Albert V, Stricker, Bruno H, Laurie, Cathy C, Rotter, Jerome I, Whitsel, Eric A, Psaty, Bruce M, Avery, Christy L
Publicado 2017

Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits—The Hispanic/Latino Anthropometry Consortium

por Fernández-Rhodes, Lindsay, Graff, Mariaelisa, Buchanan, Victoria L., Justice, Anne E., Highland, Heather M., Guo, Xiuqing, Zhu, Wanying, Chen, Hung-Hsin, Young, Kristin L., Adhikari, Kaustubh, Palmer, Nicholette D., Below, Jennifer E., Bradfield, Jonathan, Pereira, Alexandre C., Glover, LáShauntá, Kim, Daeeun, Lilly, Adam G., Shrestha, Poojan, Thomas, Alvin G., Zhang, Xinruo, Chen, Minhui, Chiang, Charleston W.K., Pulit, Sara, Horimoto, Andrea, Krieger, Jose E., Guindo-Martínez, Marta, Preuss, Michael, Schumann, Claudia, Smit, Roelof A.J., Torres-Mejía, Gabriela, Acuña-Alonzo, Victor, Bedoya, Gabriel, Bortolini, Maria-Cátira, Canizales-Quinteros, Samuel, Gallo, Carla, González-José, Rolando, Poletti, Giovanni, Rothhammer, Francisco, Hakonarson, Hakon, Igo, Robert, Adler, Sharon G., Iyengar, Sudha K., Nicholas, Susanne B., Gogarten, Stephanie M., Isasi, Carmen R., Papnicolaou, George, Stilp, Adrienne M., Qi, Qibin, Kho, Minjung, Smith, Jennifer A., Langefeld, Carl D., Wagenknecht, Lynne, Mckean-Cowdin, Roberta, Gao, Xiaoyi Raymond, Nousome, Darryl, Conti, David V., Feng, Ye, Allison, Matthew A., Arzumanyan, Zorayr, Buchanan, Thomas A., Ida Chen, Yii-Der, Genter, Pauline M., Goodarzi, Mark O., Hai, Yang, Hsueh, Willa, Ipp, Eli, Kandeel, Fouad R., Lam, Kelvin, Li, Xiaohui, Nadler, Jerry L., Raffel, Leslie J., Roll, Kathryn, Sandow, Kevin, Tan, Jingyi, Taylor, Kent D., Xiang, Anny H., Yao, Jie, Audirac-Chalifour, Astride, de Jesus Peralta Romero, Jose, Hartwig, Fernando, Horta, Bernando, Blangero, John, Curran, Joanne E., Duggirala, Ravindranath, Lehman, Donna E., Puppala, Sobha, Fejerman, Laura, John, Esther M., Aguilar-Salinas, Carlos, Burtt, Noël P., Florez, Jose C., García-Ortíz, Humberto, González-Villalpando, Clicerio, Mercader, Josep, Orozco, Lorena, Tusié-Luna, Teresa, Blanco, Estela, Gahagan, Sheila, Cox, Nancy J., Hanis, Craig, Butte, Nancy F., Cole, Shelley A., Comuzzie, Anthony G., Voruganti, V. Saroja, Rohde, Rebecca, Wang, Yujie, Sofer, Tamar, Ziv, Elad, Grant, Struan F.A., Ruiz-Linares, Andres, Rotter, Jerome I., Haiman, Christopher A., Parra, Esteban J., Cruz, Miguel, Loos, Ruth J.F., North, Kari E.
Publicado 2022

Inherited Causes of Clonal Hematopoiesis in 97,691 TOPMed Whole Genomes

por Bick, Alexander G., Weinstock, Joshua S., Nandakumar, Satish K., Fulco, Charles P., Bao, Erik L., Zekavat, Seyedeh M., Szeto, Mindy D., Liao, Xiaotian, Leventhal, Matthew J., Nasser, Joseph, Chang, Kyle, Laurie, Cecelia, Burugula, Bala Bharathi, Gibson, Christopher J., Lin, Amy E., Taub, Margaret A., Aguet, Francois, Ardlie, Kristin, Mitchell, Braxton D., Barnes, Kathleen C., Moscati, Arden, Fornage, Myriam, Redline, Susan, Psaty, Bruce M., Silverman, Edwin K., Weiss, Scott T., Palmer, Nicholette D., Vasan, Ramachandran S., Burchard, Esteban G., Kardia, Sharon L. R., He, Jiang, Kaplan, Robert C., Smith, Nicholas L., Arnett, Donna K., Schwartz, David A., Correa, Adolfo, de Andrade, Mariza, 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., Gogarten, Stephanie M., Wang, Fei Fei, Wong, Quenna, Montasser, May E., Daya, Michelle, Kenny, Eimear E., 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., Becker, Lewis C., Smith, Jennifer A., Kelly, Tanika N., Aslibekyan, Stella, Heckbert, Susan R., Tiwari, Hemant K., Yang, Ivana V., Heit, John A., Lubitz, Steven, Johnsen, Jill M., Curran, Joanne E., Wenzel, Sally E., Weeks, Daniel E., Rao, Dabeeru C., Darbar, Dawood, Moon, Jee-Young, Tracy, Russell P., Buth, Erin J., Rafaels, Nicholas, Loos, Ruth J.F., Durda, Peter, 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., Raffield, Laura M., Armasu, Sebastian M., Wheeler, Marsha M., Sabino, Ester C., Blangero, John, Williams, L. Keoki, Levy, Bruce D., Huey-Herng Sheu, Wayne, Roden, Dan M., Boerwinkle, Eric, Manson, JoAnn E., Mathias, Rasika A., Desai, Pinkal, Taylor, Kent D., Johnson, Andrew D., Auer, Paul L., Kooperberg, Charles, Laurie, Cathy C., Blackwell, Thomas W., Smith, Albert V., Zhao, Hongyu, Lange, Ethan, Lange, Leslie, Rich, Stephen S., Rotter, Jerome I., Wilson, James G., Scheet, Paul, Kitzman, Jacob O., Lander, Eric S., Engreitz, Jesse M., Ebert, Benjamin L., Reiner, Alexander P., Jaiswal, Siddhartha, Abecasis, Gonçalo, Sankaran, Vijay G., Kathiresan, Sekar, Natarajan, Pradeep
Publicado 2020