Imputation-Based Genomic Coverage Assessments of Current Human Genotyping Arrays

द्वारा 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.
प्रकाशित 2013

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

द्वारा 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.
प्रकाशित 2012

Genome-wide association study of dental caries in the Hispanic Communities Health Study/Study of Latinos (HCHS/SOL)

द्वारा 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.
में प्रकाशित Hum Mol Genet (2016)

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

द्वारा 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.
में प्रकाशित Nat Commun (2021)

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

द्वारा 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.
प्रकाशित 2014

A Fully-Adjusted Two-Stage Procedure for Rank Normalization in Genetic Association Studies

द्वारा 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.
में प्रकाशित Genet Epidemiol (2019)

Genome-wide association of white blood cell counts in Hispanic/Latino Americans: the Hispanic Community Health Study/Study of Latinos

द्वारा 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.
में प्रकाशित Hum Mol Genet (2017)

Genome-Wide Association Study Reveals Multiple Loci Influencing Normal Human Facial Morphology

द्वारा 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.
में प्रकाशित PLoS Genet (2016)

Identification of paternal uniparental disomy on chromosome 22 and a de novo deletion on chromosome 18 in individuals with orofacial clefts

द्वारा 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
में प्रकाशित Mol Genet Genomic Med (2018)

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

द्वारा 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.
में प्रकाशित HGG Adv (2021)

Genome-wide Association Study of Platelet Count Identifies Ancestry-Specific Loci in Hispanic/Latino Americans

द्वारा 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.
में प्रकाशित Am J Hum Genet (2016)

Genetic Diversity and Association Studies in US Hispanic/Latino Populations: Applications in the Hispanic Community Health Study/Study of Latinos

द्वारा 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.
में प्रकाशित Am J Hum Genet (2016)

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

द्वारा 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
में प्रकाशित Pain (2019)

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

द्वारा 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.
में प्रकाशित Hum Mol Genet (2016)

A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3

द्वारा 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.
में प्रकाशित Am J Hum Genet (2016)

Whole genome sequence analysis of pulmonary function and COPD in 19,996 multi-ethnic participants

द्वारा 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
में प्रकाशित Nat Commun (2020)

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

द्वारा 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.
प्रकाशित 2012

Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-wide Meta-analysis

द्वारा 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
प्रकाशित 2012

Genomic analyses in African populations identify novel risk loci for cleft palate

द्वारा 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
में प्रकाशित Hum Mol Genet (2019)

Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program

द्वारा Hu, Yao, Stilp, Adrienne M., McHugh, Caitlin P., Rao, Shuquan, Jain, Deepti, Zheng, Xiuwen, Lane, John, Méric de Bellefon, Sébastian, Raffield, Laura M., Chen, Ming-Huei, Yanek, Lisa R., Wheeler, Marsha, Yao, Yao, Ren, Chunyan, Broome, Jai, Moon, Jee-Young, de Vries, Paul S., Hobbs, Brian D., Sun, Quan, Surendran, Praveen, Brody, Jennifer A., Blackwell, Thomas W., Choquet, Hélène, Ryan, Kathleen, Duggirala, Ravindranath, Heard-Costa, Nancy, Wang, Zhe, Chami, Nathalie, Preuss, Michael H., Min, Nancy, Ekunwe, Lynette, Lange, Leslie A., Cushman, Mary, Faraday, Nauder, Curran, Joanne E., Almasy, Laura, Kundu, Kousik, Smith, Albert V., Gabriel, Stacey, Rotter, Jerome I., Fornage, Myriam, Lloyd-Jones, Donald M., Vasan, Ramachandran S., Smith, Nicholas L., North, Kari E., Boerwinkle, Eric, Becker, Lewis C., Lewis, Joshua P., Abecasis, Goncalo R., Hou, Lifang, O’Connell, Jeffrey R., Morrison, Alanna C., Beaty, Terri H., Kaplan, Robert, Correa, Adolfo, Blangero, John, Jorgenson, Eric, Psaty, Bruce M., Kooperberg, Charles, Walton, Russell T., Kleinstiver, Benjamin P., Tang, Hua, Loos, Ruth J.F., Soranzo, Nicole, Butterworth, Adam S., Nickerson, Debbie, Rich, Stephen S., Mitchell, Braxton D., Johnson, Andrew D., Auer, Paul L., Li, Yun, Mathias, Rasika A., Lettre, Guillaume, Pankratz, Nathan, Laurie, Cathy C., Laurie, Cecelia A., Bauer, Daniel E., Conomos, Matthew P., Reiner, Alexander P.
में प्रकाशित Am J Hum Genet (2021)