Resultados da busca - Nelson, Sarah C.
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Recipient and donor genetic variants associated with mortality after allogeneic hematopoietic cell transplantation por Martin, Paul J., Levine, David M., Storer, Barry E., Nelson, Sarah C., Dong, Xinyuan, Hansen, John A.
Publicado em 2020Texto -
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Improved imputation accuracy in Hispanic/Latino populations with larger and more diverse reference panels: applications in the Hispanic Community Health Study/Study of Latinos (HCH... por Nelson, Sarah C., Stilp, Adrienne M., Papanicolaou, George J., Taylor, Kent D., Rotter, Jerome I., Thornton, Timothy A., Laurie, Cathy C.
Publicado em 2016Texto -
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Imputation-Based Genomic Coverage Assessments of Current Human Genotyping Arrays por Nelson, Sarah C., Doheny, Kimberly F., Pugh, Elizabeth W., Romm, Jane M., Ling, Hua, Laurie, Cecelia A., Browning, Sharon R., Weir, Bruce S., Laurie, Cathy C.
Publicado em 2013Texto -
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Genome-wide minor histocompatibility matching as related to the risk of graft-versus-host disease por Martin, Paul J., Levine, David M., Storer, Barry E., Warren, Edus H., Zheng, Xiuwen, Nelson, Sarah C., Smith, Anajane G., Mortensen, Bo K., Hansen, John A.
Publicado em 2017Texto -
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Genetic variants in sex hormone pathways and the risk of type 2 diabetes among African-American, Hispanic-American, and European-American postmenopausal women in the United States por GOTO, Atsushi, CHEN, Brian H., CHAN, Kei-hang K., LEE, Cathy, NELSON, Sarah C., CRENSHAW, Andrew, BOOKMAN, Ebony, MARGOLIS, Karen L., SALE, Michèle M., NG, Maggie C. Y., REINER, Alexander P., LIU, Simin
Publicado em 2018Texto -
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Consent for Use of Genetic Data among US Hispanics/Latinos: Results from the Hispanic Community Health Study/ Study of Latinos por Gonzalez, Sara, Strizich, Garrett, Isasi, Carmen R., Hua, Simin, Comas, Betsy, Sofer, Tamar, Thyagarajan, Bharat, Perreira, Krista M., Talavera, Gregory A., Daviglus, Martha L., Nelson, Sarah C., Giachello, Aida L., Schneiderman, Neil, Kaplan, Robert C
Publicado em 2021Texto -
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Comprehensive genetic analysis of the platelet activating factor acetylhydrolase (PLA2G7) gene and cardiovascular disease in case–control and family datasets por Sutton, Beth S., Crosslin, David R., Shah, Svati H., Nelson, Sarah C., Bassil, Anthony, Hale, A. Brent, Haynes, Carol, Goldschmidt-Clermont, Pascal J., Vance, Jeffery M., Seo, David, Kraus, William E., Gregory, Simon G., Hauser, Elizabeth R.
Publicado em 2008Texto -
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Genetic effects in the leukotriene biosynthesis pathway and association with atherosclerosis por Crosslin, David R., Shah, Svati H., Nelson, Sarah C., Haynes, Carol S., Connelly, Jessica J., Gadson, Shera, Goldschmidt-Clermont, Pascal J., Vance, Jeffery M., Rose, Jason, Granger, Chris B., Seo, David, Gregory, Simon G., Kraus, William E., Hauser, Elizabeth R.
Publicado em 2009Texto -
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GWASTools: an R/Bioconductor package for quality control and analysis of genome-wide association studies por Gogarten, Stephanie M., Bhangale, Tushar, Conomos, Matthew P., Laurie, Cecelia A., McHugh, Caitlin P., Painter, Ian, Zheng, Xiuwen, Crosslin, David R., Levine, David, Lumley, Thomas, Nelson, Sarah C., Rice, Kenneth, Shen, Jess, Swarnkar, Rohit, Weir, Bruce S., Laurie, Cathy C.
Publicado em 2012Texto -
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Polymorphic variants in tenascin-C (TNC) are associated with atherosclerosis and coronary artery disease por Minear, Mollie A., Crosslin, David R., Sutton, Beth S., Connelly, Jessica J., Nelson, Sarah C., Gadson-Watson, Shera, Wang, Tianyuan, Seo, David, Vance, Jeffrey M., Sketch, Michael H., Haynes, Carol, Goldschmidt-Clermont, Pascal J., Shah, Svati H., Kraus, William E., Hauser, Elizabeth R., Gregory, Simon G.
Publicado em 2011Texto -
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Acquired Chromosomal Anomalies in Chronic Lymphocytic Leukemia (CLL) Patients Compared to >50,000 Quasi-normal Subjects por Laurie, Cathy C., Laurie, Cecelia A., Smoley, Stephanie A., Carlson, Erin E., Flinn, Ian, Fridley, Brooke L., Greisman, Harvey A., Gribben, John G., Jelinek, Diane F., Nelson, Sarah C., Paietta, Elisabeth, Schaid, Dan, Sun, Zhuoxin, Tallman, Martin S., Weinshilboum, Richard, Kay, Neil E., Shanafelt, Tait D.
Publicado em 2014Texto -
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Genome-wide association Scan of dental caries in the permanent dentition por Wang, Xiaojing, Shaffer, John R, Zeng, Zhen, Begum, Ferdouse, Vieira, Alexandre R, Noel, Jacqueline, Anjomshoaa, Ida, Cuenco, Karen T, Lee, Myoung-Keun, Beck, James, Boerwinkle, Eric, Cornelis, Marilyn C, Hu, Frank B, Crosslin, David R, Laurie, Cathy C, Nelson, Sarah C, Doheny, Kimberly F, Pugh, Elizabeth W, Polk, Deborah E, Weyant, Robert J, Crout, Richard, McNeil, Daniel W, Weeks, Daniel E, Feingold, Eleanor, Marazita, Mary L
Publicado em 2012Texto -
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Genetic variants associated with the white blood cell count in 13,923 subjects in the eMERGE Network por Crosslin, David R., McDavid, Andrew, Weston, Noah, Nelson, Sarah C., Zheng, Xiuwen, Hart, Eugene, de Andrade, Mariza, Kullo, Iftikhar J., McCarty, Catherine A., Doheny, Kimberly F., Pugh, Elizabeth, Kho, Abel, Hayes, M. Geoffrey, Pretel, Stephanie, Saip, Alexander, Ritchie, Marylyn D., Crawford, Dana C., Crane, Paul K., Newton, Katherine, Li, Rongling, Mirel, Daniel B., Crenshaw, Andrew, Larson, Eric B., Carlson, Chris S., Jarvik, Gail P.
Publicado em 2011Texto -
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Genome-wide association reveals contribution of MRAS to painful temporomandibular disorder in males por Smith, Shad B., Parisien, Marc, Bair, Eric, Belfer, Inna, Chabot-Doré, Anne-Julie, Gris, Pavel, Khoury, Samar, Tansley, Shannon, Torosyan, Yelizaveta, Zaykin, Dmitri V., Bernhardt, Olaf, de Oliveira Serrano, Priscila, Gracely, Richard H., Jain, Deepti, Järvelin, Marjo-Riitta, Kaste, Linda M., Kerr, Kathleen F., Kocher, Thomas, Lähdesmäki, Raija, Laniado, Nadia, Laurie, Cathy C., Laurie, Cecelia A., Männikkö, Minna, Meloto, Carolina B., Nackley, Andrea G., Nelson, Sarah C., Pesonen, Paula, Ribeiro-Dasilva, Margarete C., Rizzatti-Barbosa, Celia M., Sanders, Anne E., Schwahn, Christian, Sipilä, Kirsi, Sofer, Tamar, Teumer, Alexander, Mogil, Jeffrey S., Fillingim, Roger B., Greenspan, Joel D., Ohrbach, Richard, Slade, Gary D., Maixner, William, Diatchenko, Luda
Publicado em 2019Texto -
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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 em 2012Texto -
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Genetic analyses of diverse populations improves discovery for complex traits por Wojcik, Genevieve L., Graff, Mariaelisa, Nishimura, Katherine K., Tao, Ran, Haessler, Jeffrey, Gignoux, Christopher R., Highland, Heather M., Patel, Yesha M., Sorokin, Elena P., Avery, Christy L., Belbin, Gillian M., Bien, Stephanie A., Cheng, Iona, Cullina, Sinead, Hodonsky, Chani J., Hu, Yao, Huckins, Laura M., Jeff, Janina, Justice, Anne E., Kocarnik, Jonathan M., Lim, Unhee, Lin, Bridget M., Lu, Yingchang, Nelson, Sarah C., Park, Sung-Shim L., Poisner, Hannah, Preuss, Michael H., Richard, Melissa A., Schurmann, Claudia, Setiawan, Veronica W., Sockell, Alexandra, Vahi, Karan, Verbanck, Marie, Vishnu, Abhishek, Walker, Ryan W., Young, Kristin L., Zubair, Niha, Acuña-Alonso, Victor, Luis Ambite, Jose, Barnes, Kathleen C., Boerwinkle, Eric, Bottinger, Erwin P., Bustamante, Carlos D., Caberto, Christian, Canizales-Quinteros, Samuel, Conomos, Matthew P., Deelman, Ewa, Do, Ron, Doheny, Kimberly, Fernández-Rhodes, Lindsay, Fornage, Myriam, Hailu, Benyam, Heiss, Gerardo, Henn, Brenna M., Hindorff, Lucia A., Jackson, Rebecca D., Laurie, Cecelia A., Laurie, Cathy C., Li, Yuqing, Lin, Dan-Yu, Moreno-Estrada, Andres, Nadkarni, Girish, Norman, Paul J., Pooler, Loreall C., Reiner, Alexander P., Romm, Jane, Sabatti, Chiara, Sandoval, Karla, Sheng, Xin, Stahl, Eli A., Stram, Daniel O., Thornton, Timothy A., Wassel, Christina L., Wilkens, Lynne R., Winkler, Cheryl A., Yoneyama, Sachi, Buyske, Steven, Haiman, Christopher A., Kooperberg, Charles, Marchand, Loic Le, Loos, Ruth J. F., Matise, Tara C., North, Kari E., Peters, Ulrike, Kenny, Eimear E., Carlson, Christopher S.
Publicado em 2019Texto -
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Rare coding variants in 35 genes associate with circulating lipid levels—A multi-ancestry analysis of 170,000 exomes por Hindy, George, Dornbos, Peter, Chaffin, Mark D., Liu, Dajiang J., Wang, Minxian, Selvaraj, Margaret Sunitha, Zhang, David, Park, Joseph, Aguilar-Salinas, Carlos A., Antonacci-Fulton, Lucinda, Ardissino, Diego, Arnett, Donna K., Aslibekyan, Stella, Atzmon, Gil, Ballantyne, Christie M., Barajas-Olmos, Francisco, Barzilai, Nir, Becker, Lewis C., Bielak, Lawrence F., Bis, Joshua C., Blangero, John, Boerwinkle, Eric, Bonnycastle, Lori L., Bottinger, Erwin, Bowden, Donald W., Bown, Matthew J., Brody, Jennifer A., Broome, Jai G., Burtt, Noël P., Cade, Brian E., Centeno-Cruz, Federico, Chan, Edmund, Chang, Yi-Cheng, Chen, Yii-Der I., Cheng, Ching-Yu, Choi, Won Jung, Chowdhury, Rajiv, Contreras-Cubas, Cecilia, Córdova, Emilio J., Correa, Adolfo, Cupples, L. Adrienne, Curran, Joanne E., Danesh, John, de Vries, Paul S., DeFronzo, Ralph A., Doddapaneni, Harsha, Duggirala, Ravindranath, Dutcher, Susan K., Ellinor, Patrick T., Emery, Leslie S., Florez, Jose C., Fornage, Myriam, Freedman, Barry I., Fuster, Valentin, Garay-Sevilla, Ma. Eugenia, García-Ortiz, Humberto, Germer, Soren, Gibbs, Richard A., Gieger, Christian, Glaser, Benjamin, Gonzalez, Clicerio, Gonzalez-Villalpando, Maria Elena, Graff, Mariaelisa, Graham, Sarah E., Grarup, Niels, Groop, Leif C., Guo, Xiuqing, Gupta, Namrata, Han, Sohee, Hanis, Craig L., Hansen, Torben, He, Jiang, Heard-Costa, Nancy L., Hung, Yi-Jen, Hwang, Mi Yeong, Irvin, Marguerite R., Islas-Andrade, Sergio, Jarvik, Gail P., Kang, Hyun Min, Kardia, Sharon L.R., Kelly, Tanika, Kenny, Eimear E., Khan, Alyna T., Kim, Bong-Jo, Kim, Ryan W., Kim, Young Jin, Koistinen, Heikki A., Kooperberg, Charles, Kuusisto, Johanna, Kwak, Soo Heon, Laakso, Markku, Lange, Leslie A., Lee, Jiwon, Lee, Juyoung, Lee, Seonwook, Lehman, Donna M., Lemaitre, Rozenn N., Linneberg, Allan, Liu, Jianjun, Loos, Ruth J.F., Lubitz, Steven A., Lyssenko, Valeriya, Ma, Ronald C.W., Martin, Lisa Warsinger, Martínez-Hernández, Angélica, Mathias, Rasika A., McGarvey, Stephen T., McPherson, Ruth, Meigs, James B., Meitinger, Thomas, Melander, Olle, Mendoza-Caamal, Elvia, Metcalf, Ginger A., Mi, Xuenan, Mohlke, Karen L., Montasser, May E., Moon, Jee-Young, Moreno-Macías, Hortensia, Morrison, Alanna C., Muzny, Donna M., Nelson, Sarah C., Nilsson, Peter M., O’Connell, Jeffrey R., Orho-Melander, Marju, Orozco, Lorena, Palmer, Colin N.A., Palmer, Nicholette D., Park, Cheol Joo, Park, Kyong Soo, Pedersen, Oluf, Peralta, Juan M., Peyser, Patricia A., Post, Wendy S., Preuss, Michael, Psaty, Bruce M., Qi, Qibin, Rao, D.C., Redline, Susan, Reiner, Alexander P., Revilla-Monsalve, Cristina, Rich, Stephen S., Samani, Nilesh, Schunkert, Heribert, Schurmann, Claudia, Seo, Daekwan, Seo, Jeong-Sun, Sim, Xueling, Sladek, Rob, Small, Kerrin S., So, Wing Yee, Stilp, Adrienne M., Tai, E. Shyong, Tam, Claudia H.T., Taylor, Kent D., Teo, Yik Ying, Thameem, Farook, Tomlinson, Brian, Tsai, Michael Y., Tuomi, Tiinamaija, Tuomilehto, Jaakko, Tusié-Luna, Teresa, Udler, Miriam S., van Dam, Rob M., Vasan, Ramachandran S., Viaud Martinez, Karine A., Wang, Fei Fei, Wang, Xuzhi, Watkins, Hugh, Weeks, Daniel E., Wilson, James G., Witte, Daniel R., Wong, Tien-Yin, Yanek, Lisa R., Kathiresan, Sekar, Rader, Daniel J., Rotter, Jerome I., Boehnke, Michael, McCarthy, Mark I., Willer, Cristen J., Natarajan, Pradeep, Flannick, Jason A., Khera, Amit V., Peloso, Gina M.
Publicado em 2022Texto -
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Characterization of Large Structural Genetic Mosaicism in Human Autosomes por Machiela, Mitchell J., Zhou, Weiyin, Sampson, Joshua N., Dean, Michael C., Jacobs, Kevin B., Black, Amanda, Brinton, Louise A., Chang, I-Shou, Chen, Chu, Chen, Constance, Chen, Kexin, Cook, Linda S., Crous Bou, Marta, De Vivo, Immaculata, Doherty, Jennifer, Friedenreich, Christine M., Gaudet, Mia M., Haiman, Christopher A., Hankinson, Susan E., Hartge, Patricia, Henderson, Brian E., Hong, Yun-Chul, Hosgood, H. Dean, Hsiung, Chao A., Hu, Wei, Hunter, David J., Jessop, Lea, Kim, Hee Nam, Kim, Yeul Hong, Kim, Young Tae, Klein, Robert, Kraft, Peter, Lan, Qing, Lin, Dongxin, Liu, Jianjun, Le Marchand, Loic, Liang, Xiaolin, Lissowska, Jolanta, Lu, Lingeng, Magliocco, Anthony M., Matsuo, Keitaro, Olson, Sara H., Orlow, Irene, Park, Jae Yong, Pooler, Loreall, Prescott, Jennifer, Rastogi, Radhai, Risch, Harvey A., Schumacher, Fredrick, Seow, Adeline, Setiawan, Veronica Wendy, Shen, Hongbing, Sheng, Xin, Shin, Min-Ho, Shu, Xiao-Ou, VanDen Berg, David, Wang, Jiu-Cun, Wentzensen, Nicolas, Wong, Maria Pik, Wu, Chen, Wu, Tangchun, Wu, Yi-Long, Xia, Lucy, Yang, Hannah P., Yang, Pan-Chyr, Zheng, Wei, Zhou, Baosen, Abnet, Christian C., Albanes, Demetrius, Aldrich, Melinda C., Amos, Christopher, Amundadottir, Laufey T., Berndt, Sonja I., Blot, William J., Bock, Cathryn H., Bracci, Paige M., Burdett, Laurie, Buring, Julie E., Butler, Mary A., Carreón, Tania, Chatterjee, Nilanjan, Chung, Charles C., Cook, Michael B., Cullen, Michael, Davis, Faith G., Ding, Ti, Duell, Eric J., Epstein, Caroline G., Fan, Jin-Hu, Figueroa, Jonine D., Fraumeni, Joseph F., Freedman, Neal D., Fuchs, Charles S., Gao, Yu-Tang, Gapstur, Susan M., Patiño-Garcia, Ana, Garcia-Closas, Montserrat, Gaziano, J. Michael, Giles, Graham G., Gillanders, Elizabeth M., Giovannucci, Edward L., Goldin, Lynn, Goldstein, Alisa M., Greene, Mark H., Hallmans, Goran, Harris, Curtis C., Henriksson, Roger, Holly, Elizabeth A., Hoover, Robert N., Hu, Nan, Hutchinson, Amy, Jenab, Mazda, Johansen, Christoffer, Khaw, Kay-Tee, Koh, Woon-Puay, Kolonel, Laurence N., Kooperberg, Charles, Krogh, Vittorio, Kurtz, Robert C., LaCroix, Andrea, Landgren, Annelie, Landi, Maria Teresa, Li, Donghui, Liao, Linda M., Malats, Nuria, McGlynn, Katherine A., McNeill, Lorna H., McWilliams, Robert R., Melin, Beatrice S., Mirabello, Lisa, Peplonska, Beata, Peters, Ulrike, Petersen, Gloria M., Prokunina-Olsson, Ludmila, Purdue, Mark, Qiao, You-Lin, Rabe, Kari G., Rajaraman, Preetha, Real, Francisco X., Riboli, Elio, Rodríguez-Santiago, Benjamín, Rothman, Nathaniel, Ruder, Avima M., Savage, Sharon A., Schwartz, Ann G., Schwartz, Kendra L., Sesso, Howard D., Severi, Gianluca, Silverman, Debra T., Spitz, Margaret R., Stevens, Victoria L., Stolzenberg-Solomon, Rachael, Stram, Daniel, Tang, Ze-Zhong, Taylor, Philip R., Teras, Lauren R., Tobias, Geoffrey S., Viswanathan, Kala, Wacholder, Sholom, Wang, Zhaoming, Weinstein, Stephanie J., Wheeler, William, White, Emily, Wiencke, John K., Wolpin, Brian M., Wu, Xifeng, Wunder, Jay S., Yu, Kai, Zanetti, Krista A., Zeleniuch-Jacquotte, Anne, Ziegler, Regina G., de Andrade, Mariza, Barnes, Kathleen C., Beaty, Terri H., Bierut, Laura J., Desch, Karl C., Doheny, Kimberly F., Feenstra, Bjarke, Ginsburg, David, Heit, John A., Kang, Jae H., Laurie, Cecilia A., Li, Jun Z., Lowe, William L., Marazita, Mary L., Melbye, Mads, Mirel, Daniel B., Murray, Jeffrey C., Nelson, Sarah C., Pasquale, Louis R., Rice, Kenneth, Wiggs, Janey L., Wise, Anastasia, Tucker, Margaret, Pérez-Jurado, Luis A., Laurie, Cathy C., Caporaso, Neil E., Yeager, Meredith, Chanock, Stephen J.
Publicado em 2015Texto