检索结果 - Laurie, Cecelia A.

Imputation-Based Genomic Coverage Assessments of Current Human Genotyping Arrays 由 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.

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GWASTools: an R/Bioconductor package for quality control and analysis of genome-wide association studies 由 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.

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

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Acquired Chromosomal Anomalies in Chronic Lymphocytic Leukemia (CLL) Patients Compared to >50,000 Quasi-normal Subjects 由 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.

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A Fully-Adjusted Two-Stage Procedure for Rank Normalization in Genetic Association Studies 由 Sofer, Tamar, Zheng, Xiuwen, Gogarten, Stephanie M., Laurie, Cecelia A., Grinde, Kelsey, Shaffer, John R., Shungin, Dmitry, O’Connell, Jeffrey R., Durazo-Arvizo, Ramon A., Raffield, Laura, Lange, Leslie, Musani, Solomon, Vasan, Ramachandran S., Cupples, L. Adrienne, Reiner, Alexander P., Laurie, Cathy C., Rice, Kenneth M.

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Genome-wide association of white blood cell counts in Hispanic/Latino Americans: the Hispanic Community Health Study/Study of Latinos 由 Jain, Deepti, Hodonsky, Chani J., Schick, Ursula M., Morrison, Jean V., Minnerath, Sharon, Brown, Lisa, Schurmann, Claudia, Liu, Yongmei, Auer, Paul L., Laurie, Cecelia A., Taylor, Kent D., Browning, Brian L., Papanicolaou, George, Browning, Sharon R., Loos, Ruth J. F., North, Kari E., Thyagarajan, Bharat, Laurie, Cathy C., Thornton, Timothy A., Sofer, Tamar, Reiner, Alexander P.

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Genome-Wide Association Study Reveals Multiple Loci Influencing Normal Human Facial Morphology 由 Shaffer, John R., Orlova, Ekaterina, Lee, Myoung Keun, Leslie, Elizabeth J., Raffensperger, Zachary D., Heike, Carrie L., Cunningham, Michael L., Hecht, Jacqueline T., Kau, Chung How, Nidey, Nichole L., Moreno, Lina M., Wehby, George L., Murray, Jeffrey C., Laurie, Cecelia A., Laurie, Cathy C., Cole, Joanne, Ferrara, Tracey, Santorico, Stephanie, Klein, Ophir, Mio, Washington, Feingold, Eleanor, Hallgrimsson, Benedikt, Spritz, Richard A., Marazita, Mary L., Weinberg, Seth M.

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Identification of paternal uniparental disomy on chromosome 22 and a de novo deletion on chromosome 18 in individuals with orofacial clefts 由 Oseni, Ganiyu O., Jain, Deepti, Mossey, Peter A., Busch, Tamara D., Gowans, Lord J.J., Eshete, Mekonen A., Adeyemo, Wasiu L., Laurie, Cecelia A., Laurie, Cathy C., Owais, Arwa, Olaitan, Peter B., Aregbesola, Babatunde S., Oginni, Fadekemi O., Bello, Saidu A., Donkor, Peter, Audu, Rosemary, Onwuamah, Chika, Obiri‐Yeboah, Solomon, Plange‐Rhule, Gyikua, Ogunlewe, Olugbenga M., James, Olutayo, Halilu, Taiye, Abate, Firke, Abdur‐Rahman, Lukman O., Oladugba, Abimbola V., Marazita, Mary L., Murray, Jeffrey C., Adeyemo, Adebowale A., Butali, Azeez

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

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Genome-wide association reveals contribution of MRAS to painful temporomandibular disorder in males 由 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

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Polygenic transcriptome risk scores for COPD and lung function improve cross-ethnic portability of prediction in the NHLBI TOPMed program 由 Hu, Xiaowei, Qiao, Dandi, Kim, Wonji, Moll, Matthew, Balte, Pallavi P., Lange, Leslie A., Bartz, Traci M., Kumar, Rajesh, Li, Xingnan, Yu, Bing, Cade, Brian E., Laurie, Cecelia A., Sofer, Tamar, Ruczinski, Ingo, Nickerson, Deborah A., Muzny, Donna M., Metcalf, Ginger A., Doddapaneni, Harshavardhan, Gabriel, Stacy, Gupta, Namrata, Dugan-Perez, Shannon, Cupples, L. Adrienne, Loehr, Laura R., Jain, Deepti, Rotter, Jerome I., Wilson, James G., Psaty, Bruce M., Fornage, Myriam, Morrison, Alanna C., Vasan, Ramachandran S., Washko, George, Rich, Stephen S., O’Connor, George T., Bleecker, Eugene, Kaplan, Robert C., Kalhan, Ravi, Redline, Susan, Gharib, Sina A., Meyers, Deborah, Ortega, Victor, Dupuis, Josée, London, Stephanie J., Lappalainen, Tuuli, Oelsner, Elizabeth C., Silverman, Edwin K., Barr, R. Graham, Thornton, Timothy A., Wheeler, Heather E., Cho, Michael H., Im, Hae Kyung, Manichaikul, Ani

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Assessing the contribution of rare variants to complex trait heritability from whole genome sequence data 由 Wainschtein, Pierrick, Jain, Deepti, Zheng, Zhili, Cupples, L. Adrienne, Shadyab, Aladdin H., McKnight, Barbara, Shoemaker, Benjamin M., Mitchell, Braxton D., Psaty, Bruce M., Kooperberg, Charles, Liu, Ching-Ti, Albert, Christine M., Roden, Dan, Chasman, Daniel I., Darbar, Dawood, Lloyd-Jones, Donald M., Arnett, Donna K., Regan, Elizabeth A., Boerwinkle, Eric, Rotter, Jerome I., O’Connell, Jeffrey R., Yanek, Lisa R., de Andrade, Mariza, Allison, Matthew A., McDonald, Merry-Lynn N., Chung, Mina K., Fornage, Myriam, Chami, Nathalie, Smith, Nicholas L., Ellinor, Patrick T., Vasan, Ramachandran S., Mathias, Rasika A., Loos, Ruth J.F., Rich, Stephen S., Lubitz, Steven A., Heckbert, Susan R., Redline, Susan, Guo, Xiuqing, Chen, Y.-D Ida, Laurie, Cecelia A., Hernandez, Ryan D., McGarvey, Stephen T., Goddard, Michael E., Laurie, Cathy C., North, Kari E., Lange, Leslie A., Weir, Bruce S., Yengo, Loic, Yang, Jian, Visscher, Peter M.

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A multi-ethnic genome-wide association study identifies novel loci for non-syndromic cleft lip with or without cleft palate on 2p24.2, 17q23 and 19q13 由 Leslie, Elizabeth J., Carlson, Jenna C., Shaffer, John R., Feingold, Eleanor, Wehby, George, Laurie, Cecelia A., Jain, Deepti, Laurie, Cathy C., Doheny, Kimberly F., McHenry, Toby, Resick, Judith, Sanchez, Carla, Jacobs, Jennifer, Emanuele, Beth, Vieira, Alexandre R., Neiswanger, Katherine, Lidral, Andrew C., Valencia-Ramirez, Luz Consuelo, Lopez-Palacio, Ana Maria, Valencia, Dora Rivera, Arcos-Burgos, Mauricio, Czeizel, Andrew E., Field, L. Leigh, Padilla, Carmencita D., Cutiongco-de la Paz, Eva Maria, C., Deleyiannis, Frederic, Christensen, Kaare, Munger, Ronald G., Lie, Rolv T., Wilcox, Allen, Romitti, Paul A., Castilla, Eduardo E., Mereb, Juan C., Poletta, Fernando A., Orioli, Iêda M., Carvalho, Flavia M., Hecht, Jacqueline T., Blanton, Susan H., Buxó, Carmen J., Butali, Azeez, Mossey, Peter A., Adeyemo, Wasiu L., James, Olutayo, Braimah, Ramat O., Aregbesola, Babatunde S., Eshete, Mekonen A., Abate, Fikre, Koruyucu, Mine, Seymen, Figen, Ma, Lian, de Salamanca, Javier Enríquez, Weinberg, Seth M., Moreno, Lina, Murray, Jeffrey C., Marazita, Mary L.

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A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3 由 Leslie, Elizabeth J., Liu, Huan, Carlson, Jenna C., Shaffer, John R., Feingold, Eleanor, Wehby, George, Laurie, Cecelia A., Jain, Deepti, Laurie, Cathy C., Doheny, Kimberly F., McHenry, Toby, Resick, Judith, Sanchez, Carla, Jacobs, Jennifer, Emanuele, Beth, Vieira, Alexandre R., Neiswanger, Katherine, Standley, Jennifer, Czeizel, Andrew E., Deleyiannis, Frederic, Christensen, Kaare, Munger, Ronald G., Lie, Rolv T., Wilcox, Allen, Romitti, Paul A., Field, L. Leigh, Padilla, Carmencita D., Cutiongco-de la Paz, Eva Maria C., Lidral, Andrew C., Valencia-Ramirez, Luz Consuelo, Lopez-Palacio, Ana Maria, Valencia, Dora Rivera, Arcos-Burgos, Mauricio, Castilla, Eduardo E., Mereb, Juan C., Poletta, Fernando A., Orioli, Iêda M., Carvalho, Flavia M., Hecht, Jacqueline T., Blanton, Susan H., Buxó, Carmen J., Butali, Azeez, Mossey, Peter A., Adeyemo, Wasiu L., James, Olutayo, Braimah, Ramat O., Aregbesola, Babatunde S., Eshete, Mekonen A., Deribew, Milliard, Koruyucu, Mine, Seymen, Figen, Ma, Lian, de Salamanca, Javier Enríquez, Weinberg, Seth M., Moreno, Lina, Cornell, Robert A., Murray, Jeffrey C., Marazita, Mary L.

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Whole genome sequence analysis of pulmonary function and COPD in 19,996 multi-ethnic participants 由 Zhao, Xutong, Qiao, Dandi, Yang, Chaojie, Kasela, Silva, Kim, Wonji, Ma, Yanlin, Shrine, Nick, Batini, Chiara, Sofer, Tamar, Taliun, Sarah A. Gagliano, Sakornsakolpat, Phuwanat, Balte, Pallavi P., Prokopenko, Dmitry, Yu, Bing, Lange, Leslie A., Dupuis, Josée, Cade, Brian E., Lee, Jiwon, Gharib, Sina A., Daya, Michelle, Laurie, Cecelia A., Ruczinski, Ingo, Cupples, L. Adrienne, Loehr, Laura R., Bartz, Traci M., Morrison, Alanna C., Psaty, Bruce M., Vasan, Ramachandran S., Wilson, James G., Taylor, Kent D., Durda, Peter, Johnson, W. Craig, Cornell, Elaine, Guo, Xiuqing, Liu, Yongmei, Tracy, Russell P., Ardlie, Kristin G., Aguet, François, VanDenBerg, David J., Papanicolaou, George J., Rotter, Jerome I., Barnes, Kathleen C., Jain, Deepti, Nickerson, Deborah A., Muzny, Donna M., Metcalf, Ginger A., Doddapaneni, Harshavardhan, Dugan-Perez, Shannon, Gupta, Namrata, Gabriel, Stacey, Rich, Stephen S., O’Connor, George T., Redline, Susan, Reed, Robert M., Laurie, Cathy C., Daviglus, Martha L., Preudhomme, Liana K., Burkart, Kristin M., Kaplan, Robert C., Wain, Louise V., Tobin, Martin D., London, Stephanie J., Lappalainen, Tuuli, Oelsner, Elizabeth C., Abecasis, Goncalo R., Silverman, Edwin K., Barr, R. Graham, Cho, Michael H., Manichaikul, Ani

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Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative 由 Little, Amarise, Hu, Yao, Sun, Quan, Jain, Deepti, Broome, Jai, Chen, Ming-Huei, Thibord, Florian, McHugh, Caitlin, Surendran, Praveen, Blackwell, Thomas W, Brody, Jennifer A, Bhan, Arunoday, Chami, Nathalie, de Vries, Paul S, Ekunwe, Lynette, Heard-Costa, Nancy, Hobbs, Brian D, Manichaikul, Ani, Moon, Jee-Young, Preuss, Michael H, Ryan, Kathleen, Wang, Zhe, Wheeler, Marsha, Yanek, Lisa R, Abecasis, Goncalo R, Almasy, Laura, Beaty, Terri H, Becker, Lewis C, Blangero, John, Boerwinkle, Eric, Butterworth, Adam S, Choquet, Hélène, Correa, Adolfo, Curran, Joanne E, Faraday, Nauder, Fornage, Myriam, Glahn, David C, Hou, Lifang, Jorgenson, Eric, Kooperberg, Charles, Lewis, Joshua P, Lloyd-Jones, Donald M, Loos, Ruth J F, Min, Yuan-I, Mitchell, Braxton D, Morrison, Alanna C, Nickerson, Deborah A, North, Kari E, O'Connell, Jeffrey R, Pankratz, Nathan, Psaty, Bruce M, Vasan, Ramachandran S, Rich, Stephen S, Rotter, Jerome I, Smith, Albert V, Smith, Nicholas L, Tang, Hua, Tracy, Russell P, Conomos, Matthew P, Laurie, Cecelia A, Mathias, Rasika A, Li, Yun, Auer, Paul L, Thornton, Timothy, Reiner, Alexander P, Johnson, Andrew D, Raffield, Laura M

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

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Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-wide Meta-analysis 由 Peters, Ulrike, Jiao, Shuo, Schumacher, Fredrick R., Hutter, Carolyn M., Aragaki, Aaron K., Baron, John A., Berndt, Sonja I., Bézieau, Stéphane, Brenner, Hermann, Butterbach, Katja, Caan, Bette J., Campbell, Peter T., Carlson, Christopher S., Casey, Graham, Chan, Andrew T., Chang-Claude, Jenny, Chanock, Stephen J., Chen, Lin S., Coetzee, Gerhard A., Coetzee, Simon G., Conti, David V., Curtis, Keith R., Duggan, David, Edwards, Todd, Fuchs, Charles S., Gallinger, Steven, Giovannucci, Edward L., Gogarten, Stephanie M., Gruber, Stephen B., Haile, Robert W., Harrison, Tabitha A., Hayes, Richard B., Henderson, Brian E., Hoffmeister, Michael, Hopper, John L., Hudson, Thomas J., Hunter, David J., Jackson, Rebecca D., Jee, Sun Ha, Jenkins, Mark A., Jia, Wei-Hua, Kolonel, Laurence N., Kooperberg, Charles, Küry, Sébastien, Lacroix, Andrea Z., Laurie, Cathy C., Laurie, Cecelia A., Le Marchand, Loic, Lemire, Mathieu, Levine, David, Lindor, Noralane M., Liu, Yan, Ma, Jing, Makar, Karen W., Matsuo, Keitaro, Newcomb, Polly A., Potter, John D., Prentice, Ross L., Qu, Conghui, Rohan, Thomas, Rosse, Stephanie A., Schoen, Robert E., Seminara, Daniela, Shrubsole, Martha, Shu, Xiao-Ou, Slattery, Martha L., Taverna, Darin, Thibodeau, Stephen N., Ulrich, Cornelia M., White, Emily, Xiang, Yongbing, Zanke, Brent W., Zeng, Yi-Xin, Zhang, Ben, Zheng, Wei, Hsu, Li

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Genomic analyses in African populations identify novel risk loci for cleft palate 由 Butali, Azeez, Mossey, Peter A, Adeyemo, Wasiu L, Eshete, Mekonen A, Gowans, Lord J J, Busch, Tamara D, Jain, Deepti, Yu, Wenjie, Huan, Liu, Laurie, Cecelia A, Laurie, Cathy C, Nelson, Sarah, Li, Mary, Sanchez-Lara, Pedro A, Magee, William P, Magee, Kathleen S, Auslander, Allyn, Brindopke, Frederick, Kay, Denise M, Caggana, Michele, Romitti, Paul A, Mills, James L, Audu, Rosemary, Onwuamah, Chika, Oseni, Ganiyu O, Owais, Arwa, James, Olutayo, Olaitan, Peter B, Aregbesola, Babatunde S, Braimah, Ramat O, Oginni, Fadekemi O, Oladele, Ayodeji O, Bello, Saidu A, Rhodes, Jennifer, Shiang, Rita, Donkor, Peter, Obiri-Yeboah, Solomon, Arthur, Fareed Kow Nanse, Twumasi, Peter, Agbenorku, Pius, Plange-Rhule, Gyikua, Oti, Alexander Acheampong, Ogunlewe, Olugbenga M, Oladega, Afisu A, Adekunle, Adegbayi A, Erinoso, Akinwunmi O, Adamson, Olatunbosun O, Elufowoju, Abosede A, Ayelomi, Oluwanifemi I, Hailu, Taiye, Hailu, Abiye, Demissie, Yohannes, Derebew, Miliard, Eliason, Steve, Romero-Bustillous, Miguel, Lo, Cynthia, Park, James, Desai, Shaan, Mohammed, Muiawa, Abate, Firke, Abdur-Rahman, Lukman O, Anand, Deepti, Saadi, Irfaan, Oladugba, Abimibola V, Lachke, Salil A, Amendt, Brad A, Rotimi, Charles N, Marazita, Mary L, Cornell, Robert A, Murray, Jeffrey C, Adeyemo, Adebowale A

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A System for Phenotype Harmonization in the National Heart, Lung, and Blood Institute Trans-Omics for Precision Medicine (TOPMed) Program 由 Stilp, Adrienne M, Emery, Leslie S, Broome, Jai G, Buth, Erin J, Khan, Alyna T, Laurie, Cecelia A, Wang, Fei Fei, Wong, Quenna, Chen, Dongquan, D’Augustine, Catherine M, Heard-Costa, Nancy L, Hohensee, Chancellor R, Johnson, William Craig, Juarez, Lucia D, Liu, Jingmin, Mutalik, Karen M, Raffield, Laura M, Wiggins, Kerri L, de Vries, Paul S, Kelly, Tanika N, Kooperberg, Charles, Natarajan, Pradeep, Peloso, Gina M, Peyser, Patricia A, Reiner, Alex P, Arnett, Donna K, Aslibekyan, Stella, Barnes, Kathleen C, Bielak, Lawrence F, Bis, Joshua C, Cade, Brian E, Chen, Ming-Huei, Correa, Adolfo, Cupples, L Adrienne, de Andrade, Mariza, Ellinor, Patrick T, Fornage, Myriam, Franceschini, Nora, Gan, Weiniu, Ganesh, Santhi K, Graffelman, Jan, Grove, Megan L, Guo, Xiuqing, Hawley, Nicola L, Hsu, Wan-Ling, Jackson, Rebecca D, Jaquish, Cashell E, Johnson, Andrew D, Kardia, Sharon L R, Kelly, Shannon, Lee, Jiwon, Mathias, Rasika A, McGarvey, Stephen T, Mitchell, Braxton D, Montasser, May E, Morrison, Alanna C, North, Kari E, Nouraie, Seyed Mehdi, Oelsner, Elizabeth C, Pankratz, Nathan, Rich, Stephen S, Rotter, Jerome I, Smith, Jennifer A, Taylor, Kent D, Vasan, Ramachandran S, Weeks, Daniel E, Weiss, Scott T, Wilson, Carla G, Yanek, Lisa R, Psaty, Bruce M, Heckbert, Susan R, Laurie, Cathy C

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