GWASTools: an R/Bioconductor package for quality control and analysis of genome-wide association studies
GOGARTEN, Stephanie M, BHANGALE, Tushar, NELSON, Sarah C, RICE, Kenneth, SHEN, Jess, SWARNKAR, Rohit, WEIR, Bruce S, LAURIE, Cathy C, CONOMOS, Matthew P, LAURIE, Cecelia A, MCHUGH, Caitlin P, PAINTER, Ian, XIUWEN ZHENG, CROSSLIN, David R, LEVINE, David, LUMLEY, Thomas
Published in Bioinformatics (01.12.2012)
Published in Bioinformatics (01.12.2012)
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Genome-wide Association Study of Platelet Count Identifies Ancestry-Specific Loci in Hispanic/Latino Americans
Schick, Ursula M., Jain, Deepti, Hodonsky, Chani J., Morrison, Jean V., Davis, James P., Brown, Lisa, Sofer, Tamar, Conomos, Matthew P., Schurmann, Claudia, McHugh, Caitlin P., Nelson, Sarah C., Vadlamudi, Swarooparani, Stilp, Adrienne, Plantinga, Anna, Baier, Leslie, Bien, Stephanie A., Gogarten, Stephanie M., Laurie, Cecelia A., Taylor, Kent D., Liu, Yongmei, Auer, Paul L., Franceschini, Nora, Szpiro, Adam, Rice, Ken, Kerr, Kathleen F., Rotter, Jerome I., Hanson, Robert L., Papanicolaou, George, Rich, Stephen S., Loos, Ruth J.F., Browning, Brian L., Browning, Sharon R., Weir, Bruce S., Laurie, Cathy C., Mohlke, Karen L., North, Kari E., Thornton, Timothy A., Reiner, Alex P.
Published in American journal of human genetics (04.02.2016)
Published in American journal of human genetics (04.02.2016)
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Genome-wide association study of dental caries in the Hispanic Communities Health Study/Study of Latinos (HCHS/SOL)
Morrison, Jean, Laurie, Cathy C, Marazita, Mary L, Sanders, Anne E, Offenbacher, Steven, Salazar, Christian R, Conomos, Matthew P, Thornton, Timothy, Jain, Deepti, Laurie, Cecelia A, Kerr, Kathleen F, Papanicolaou, George, Taylor, Kent, Kaste, Linda M, Beck, James D, Shaffer, John R
Published in Human molecular genetics (15.02.2016)
Published in Human molecular genetics (15.02.2016)
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Imputation-based genomic coverage assessments of current human genotyping arrays
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
Published in G3 : genes - genomes - genetics (01.10.2013)
Published in G3 : genes - genomes - genetics (01.10.2013)
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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
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.
Published in HGG advances (08.07.2021)
Published in HGG advances (08.07.2021)
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Journal Article
Genetic Diversity and Association Studies in US Hispanic/Latino Populations: Applications in the Hispanic Community Health Study/Study of Latinos
Conomos, Matthew P., Laurie, Cecelia A., Stilp, Adrienne M., Gogarten, Stephanie M., McHugh, Caitlin P., Nelson, Sarah C., Sofer, Tamar, Fernández-Rhodes, Lindsay, Justice, Anne E., Graff, Mariaelisa, Young, Kristin L., Seyerle, Amanda A., Avery, Christy L., Taylor, Kent D., Rotter, Jerome I., Talavera, Gregory A., Daviglus, Martha L., Wassertheil-Smoller, Sylvia, Schneiderman, Neil, Heiss, Gerardo, Kaplan, Robert C., Franceschini, Nora, Reiner, Alex P., Shaffer, John R., Barr, R. Graham, Kerr, Kathleen F., Browning, Sharon R., Browning, Brian L., Weir, Bruce S., Avilés-Santa, M. Larissa, Papanicolaou, George J., Lumley, Thomas, Szpiro, Adam A., North, Kari E., Rice, Ken, Thornton, Timothy A., Laurie, Cathy C.
Published in American journal of human genetics (07.01.2016)
Published in American journal of human genetics (07.01.2016)
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Journal Article
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
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
Published in Human molecular genetics (01.07.2016)
Published in Human molecular genetics (01.07.2016)
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Journal Article
Genome-Wide Association Study Reveals Multiple Loci Influencing Normal Human Facial Morphology
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
Published in PLoS genetics (25.08.2016)
Published in PLoS genetics (25.08.2016)
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Journal Article
Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-Wide Meta-analysis
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
Published in Gastroenterology (New York, N.Y. 1943) (01.04.2013)
Published in Gastroenterology (New York, N.Y. 1943) (01.04.2013)
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Journal Article
A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3
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.
Published in American journal of human genetics (07.04.2016)
Published in American journal of human genetics (07.04.2016)
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A fully adjusted two‐stage procedure for rank‐normalization in genetic association studies
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.
Published in Genetic epidemiology (01.04.2019)
Published in Genetic epidemiology (01.04.2019)
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Polygenic transcriptome risk scores for COPD and lung function improve cross-ethnic portability of prediction in the NHLBI TOPMed program
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
Published in American journal of human genetics (05.05.2022)
Published in American journal of human genetics (05.05.2022)
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Journal Article
Genome-wide association of white blood cell counts in Hispanic/Latino Americans: the Hispanic Community Health Study/Study of Latinos
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
Published in Human molecular genetics (15.03.2017)
Published in Human molecular genetics (15.03.2017)
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Whole Genome Analysis of Venous Thromboembolism: the Trans-Omics for Precision Medicine Program
Seyerle, Amanda A, Laurie, Cecelia A, Coombes, Brandon J, Jain, Deepti, Conomos, Matthew P, Brody, Jennifer, Chen, Ming-Huei, Gogarten, Stephanie M, Beutel, Kathleen M, Gupta, Namrata, Heckbert, Susan R, Jackson, Rebecca D, Johnson, Andrew D, Ko, Darae, Manson, JoAnn E, McKnight, Barbara, Metcalf, Ginger A, Morrison, Alanna C, Reiner, Alexander P, Sofer, Tamar, Tang, Weihong, Wiggins, Kerri L, Boerwinkle, Eric, de Andrade, Mariza, Gabriel, Stacey B, Gibbs, Richard A, Laurie, Cathy C, Psaty, Bruce M, Vasan, Ramachandran S, Rice, Ken, Kooperberg, Charles, Pankow, James S, Smith, Nicholas L, Pankratz, Nathan
Published in Circulation. Genomic and precision medicine (01.04.2023)
Published in Circulation. Genomic and precision medicine (01.04.2023)
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Journal Article
Correction: Corrigendum: Genome-wide association study of colorectal cancer identifies six new susceptibility loci
Schumacher, Fredrick R., Schmit, Stephanie L., Jiao, Shuo, Edlund, Christopher K., Wang, Hansong, Zhang, Ben, Hsu, Li, Huang, Shu-Chen, Fischer, Christopher P., Harju, John F., Idos, Gregory E., Lejbkowicz, Flavio, Manion, Frank J., McDonnell, Kevin, Melas, Marilena, Rennert, Hedy S., Shi, Wei, Thomas, Duncan C., Van Den Berg, David J., Hutter, Carolyn M., Aragaki, Aaron K., Butterbach, Katja, Caan, Bette J., Carlson, Christopher S., Chanock, Stephen J., Curtis, Keith R., Fuchs, Charles S., Gala, Manish, Giovannucci, Edward L., Gogarten, Stephanie M., Hayes, Richard B., Henderson, Brian, Hunter, David J., Jackson, Rebecca D., Kolonel, Laurence N., Kooperberg, Charles, Küry, Sébastien, LaCroix, Andrea, Laurie, Cathy C., Laurie, Cecelia A., Lemire, Mathieu, Levine, David, Ma, Jing, Makar, Karen W., Qu, Conghui, Taverna, Darin, Ulrich, Cornelia M., Wu, Kana, Kono, Suminori, West, Dee W., Berndt, Sonja I., Bezieau, Stephane, Brenner, Hermann, Campbell, Peter T., Chan, Andrew T., Chang-Claude, Jenny, Coetzee, Gerhard A., Conti, David V., Duggan, David, Figueiredo, Jane C., Fortini, Barbara K., Gallinger, Steven J., Gauderman, W. James, Giles, Graham, Green, Roger, Haile, Robert, Harrison, Tabitha A., Hoffmeister, Michael, Hopper, John L., Hudson, Thomas J., Jacobs, Eric, Iwasaki, Motoki, Jee, Sun Ha, Jenkins, Mark, Jia, Wei-Hua, Joshi, Amit, Li, Li, Lindor, Noralene M., Matsuo, Keitaro, Moreno, Victor, Mukherjee, Bhramar, Newcomb, Polly A., Potter, John D., Raskin, Leon, Rennert, Gad, Rosse, Stephanie, Severi, Gianluca, Schoen, Robert E., Seminara, Daniela, Shu, Xiao-Ou, Slattery, Martha L., Tsugane, Shoichiro, White, Emily, Xiang, Yong-Bing, Zanke, Brent W., Zheng, Wei, Le Marchand, Loic, Casey, Graham, Gruber, Stephen B., Peters, Ulrike
Published in Nature communications (26.10.2015)
Published in Nature communications (26.10.2015)
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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
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
Published in Molecular genetics & genomic medicine (01.11.2018)
Published in Molecular genetics & genomic medicine (01.11.2018)
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Acquired chromosomal anomalies in chronic lymphocytic leukemia patients compared with more than 50,000 quasi-normal participants
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
Published in Cancer genetics (01.01.2014)
Published in Cancer genetics (01.01.2014)
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Genetic analyses of diverse populations improves discovery for complex traits
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, Ambite, Jose Luis, 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, Le Marchand, Loic, Loos, Ruth J. F., Matise, Tara C., North, Kari E., Peters, Ulrike, Kenny, Eimear E., Carlson, Christopher S.
Published in Nature (London) (01.06.2019)
Published in Nature (London) (01.06.2019)
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Journal Article
Novel Common Genetic Susceptibility Loci for Colorectal Cancer
Schmit, Stephanie L, Edlund, Christopher K, Schumacher, Fredrick R, Gong, Jian, Harrison, Tabitha A, Huyghe, Jeroen R, Qu, Chenxu, Melas, Marilena, Van Den Berg, David J, Wang, Hansong, Tring, Stephanie, Plummer, Sarah J, Albanes, Demetrius, Alonso, M Henar, Amos, Christopher I, Anton, Kristen, Aragaki, Aaron K, Arndt, Volker, Barry, Elizabeth L, Berndt, Sonja I, Bezieau, Stéphane, Bien, Stephanie, Bloomer, Amanda, Boehm, Juergen, Boutron-Ruault, Marie-Christine, Brenner, Hermann, Brezina, Stefanie, Buchanan, Daniel D, Butterbach, Katja, Caan, Bette J, Campbell, Peter T, Carlson, Christopher S, Castelao, Jose E, Chan, Andrew T, Chang-Claude, Jenny, Chanock, Stephen J, Cheng, Iona, Cheng, Ya-Wen, Chin, Lee Soo, Church, James M, Church, Timothy, Coetzee, Gerhard A, Cotterchio, Michelle, Cruz Correa, Marcia, Curtis, Keith R, Duggan, David, Easton, Douglas F, English, Dallas, Feskens, Edith J M, Fischer, Rocky, FitzGerald, Liesel M, Fortini, Barbara K, Fritsche, Lars G, Fuchs, Charles S, Gago-Dominguez, Manuela, Gala, Manish, Gallinger, Steven J, Gauderman, W James, Giles, Graham G, Giovannucci, Edward L, Gogarten, Stephanie M, Gonzalez-Villalpando, Clicerio, Gonzalez-Villalpando, Elena M, Grady, William M, Greenson, Joel K, Gsur, Andrea, Gunter, Marc, Haiman, Christopher A, Hampe, Jochen, Harlid, Sophia, Harju, John F, Hayes, Richard B, Hofer, Philipp, Hoffmeister, Michael, Hopper, John L, Huang, Shu-Chen, Huerta, Jose Maria, Hudson, Thomas J, Hunter, David J, Idos, Gregory E, Iwasaki, Motoki, Jackson, Rebecca D, Jacobs, Eric J, Jee, Sun Ha, Jenkins, Mark A, Jia, Wei-Hua, Jiao, Shuo, Joshi, Amit D, Kolonel, Laurence N, Kono, Suminori, Kooperberg, Charles, Krogh, Vittorio, Kuehn, Tilman, Küry, Sébastien, LaCroix, Andrea, Laurie, Cecelia A, Lejbkowicz, Flavio, Lemire, Mathieu, Lenz, Heinz-Josef, Levine, David
Published in JNCI : Journal of the National Cancer Institute (01.02.2019)
Published in JNCI : Journal of the National Cancer Institute (01.02.2019)
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Detectable clonal mosaicism from birth to old age and its relationship to cancer
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
Published in Nature genetics (01.06.2012)
Published in Nature genetics (01.06.2012)
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