Identification of novel genetic susceptibility loci for Behçet's disease using a genome-wide association study by Fei, Yiping, Webb, Ryan, Cobb, Beth L, Direskeneli, Haner, Saruhan-Direskeneli, Güher, Sawalha, Amr H

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A GWAS Study on Liver Function Test Using eMERGE Network Participants by Namjou, Bahram, Marsolo, Keith, Lingren, Todd, Ritchie, Marylyn D, Verma, Shefali S, Cobb, Beth L, Perry, Cassandra, Kitchner, Terrie E, Brilliant, Murray H, Peissig, Peggy L, Borthwick, Kenneth M, Williams, Marc S, Grafton, Jane, Jarvik, Gail P, Holm, Ingrid A, Harley, John B

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Detection of immunoglobulin response to COVID-19 vaccination using a novel rapid fingerstick assay by Cobb, Beth L., Sawalha, Amr H.

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GWAS and enrichment analyses of non-alcoholic fatty liver disease identify new trait-associated genes and pathways across eMERGE Network by Namjou, Bahram, Lingren, Todd, Huang, Yongbo, Parameswaran, Sreeja, Cobb, Beth L, Stanaway, Ian B, Connolly, John J, Mentch, Frank D, Benoit, Barbara, Niu, Xinnan, Wei, Wei-Qi, Carroll, Robert J, Pacheco, Jennifer A, Harley, Isaac T W, Divanovic, Senad, Carrell, David S, Larson, Eric B, Carey, David J, Verma, Shefali, Ritchie, Marylyn D, Gharavi, Ali G, Murphy, Shawn, Williams, Marc S, Crosslin, David R, Jarvik, Gail P, Kullo, Iftikhar J, Hakonarson, Hakon, Li, Rongling, Xanthakos, Stavra A, Harley, John B

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Clinical Performance of a Lateral Flow SARS-CoV-2 Total Antibody Assay by Cobb, Beth L, Lloyd, Matthew, Hock, Karl G, Farnsworth, Christopher W

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Two Functional Lupus-Associated BLK Promoter Variants Control Cell-Type- and Developmental-Stage-Specific Transcription by Guthridge, Joel M., Lu, Rufei, Sun, Harry, Sun, Celi, Wiley, Graham B., Dominguez, Nicolas, Macwana, Susan R., Lessard, Christopher J., Kim-Howard, Xana, Cobb, Beth L., Kaufman, Kenneth M., Kelly, Jennifer A., Langefeld, Carl D., Adler, Adam J., Harley, Isaac T.W., Merrill, Joan T., Gilkeson, Gary S., Kamen, Diane L., Niewold, Timothy B., Brown, Elizabeth E., Edberg, Jeffery C., Petri, Michelle A., Ramsey-Goldman, Rosalind, Reveille, John D., Vilá, Luis M., Kimberly, Robert P., Freedman, Barry I., Stevens, Anne M., Boackle, Susan A., Criswell, Lindsey A., Vyse, Tim J., Behrens, Timothy W., Jacob, Chaim O., Alarcón-Riquelme, Marta E., Sivils, Kathy L., Choi, Jiyoung, Joo, Young Bin, Bang, So-Young, Lee, Hye-Soon, Bae, Sang-Cheol, Shen, Nan, Qian, Xiaoxia, Tsao, Betty P., Scofield, R. Hal, Harley, John B., Webb, Carol F., Wakeland, Edward K., James, Judith A., Nath, Swapan K., Graham, Robert R., Gaffney, Patrick M.

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Phenome-wide association study (PheWAS) in EMR-linked pediatric cohorts, genetically links PLCL1 to speech language development and IL5-IL13 to Eosinophilic Esophagitis by Namjou, Bahram, Marsolo, Keith, Caroll, Robert J, Denny, Joshua C, Ritchie, Marylyn D, Verma, Shefali S, Lingren, Todd, Porollo, Aleksey, Cobb, Beth L, Perry, Cassandra, Kottyan, Leah C, Rothenberg, Marc E, Thompson, Susan D, Holm, Ingrid A, Kohane, Isaac S, Harley, John B

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Autoantibodies targeting glomerular annexin A2 identify patients with proliferative lupus nephritis by Caster, Dawn J., Korte, Erik A., Merchant, Michael L., Klein, Jon B., Wilkey, Daniel W., Rovin, Brad H., Birmingham, Dan J., Harley, John B., Cobb, Beth L., Namjou, Bahram, McLeish, Kenneth R., Powell, David W.

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Practical considerations in genomic decision support: The eMERGE experience by Herr, Timothy M., Bielinski, Suzette J., Bottinger, Erwin, Brautbar, Ariel, Brilliant, Murray, Chute, Christopher G., Cobb, Beth L., Denny, Joshua C., Hakonarson, Hakon, Hartzler, Andrea L., Hripcsak, George, Kannry, Joseph, Kohane, Isaac S., Kullo, Iftikhar J., Lin, Simon, Manzi, Shannon, Marsolo, Keith, Overby, Casey Lynnette, Pathak, Jyotishman, Peissig, Peggy, Pulley, Jill, Ralston, James, Rasmussen, Luke, Roden, Dan M., Tromp, Gerard, Uphoff, Timothy, Weng, Chunhua, Wolf, Wendy, Williams, Marc S., Starren, Justin

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Harmonizing Clinical Sequencing and Interpretation for the eMERGE III Network by Venner, Eric, Muzny, Donna M., Abrams, Debra, Albertson-Junkans, Ladia, Ames, Darren C., Aronson, Samuel, Babb, Lawrence J., Balasubramanian, Adithya, Bastarache, Lisa, Behr, Meckenzie, Blout, Carrie, Bowser, Mark, Brilliant, Murray, Brodeur, Wendy, Caraballo, Pedro, Castro, Victor, Chisholm, Rex L., Chung, Wendy, Chute, Christopher G., City, Brittany, Connolly, John J., Crane, Paul, Crew, Katherine, De Andrade, Mariza, Denson, Shawn, Denny, Josh, DeSmet, Tim, Dikilitas, Ozan, Fullerton, Stephanie M., Gabriel, Stacey, Gainer, Vivian, Gharavi, Ali, Glazer, Andrew M., Goehringer, Jessica, Gordon, Adam S., Graham, Chet, Dayal, Jyoti, Hakonarson, Hakon, Harden, Maegan V., Harr, Margaret, Hayes, M. Geoffrey, Henrikson, Nora, Howell, Kayla M., Jiang, Yunyun, Joo, Yoonjung Yoonie, Justice, Anne E., Kalla, Sara E., Kalra, Divya, Kelly, Melissa A., Key, Dustin, Kiryluk, Krzysztof, Kullo, Iftikhar J., Larson, Eric B., Lin, Chiao-Feng, Linder, Jodell, Macbeth, Alyssa, Dinsmore, Michael J., Dodge, Sheila, Fasel, David, Fedotov, Alex, Feng, Qiping, McGowan, Michelle L., Meldrim, Jim, Mosley, Jonathan, Muniz, Jesse, Murdock, David R., Murugan, Mullai, Myers, Melanie F., Namjou, Bahram, Ni, Yizhao, Obeng, Aniwaa Owusu, Taylor, Casey Overby, Peterson, Josh F., Pratap, Siddharth, Prows, Cynthia A., Ralston, James D., Ramaprasan, Arvind, Rasmussen-Torvik, Laura, Schaid, Dan, Sengupta, Soumitra, Singh, Rajbir, Sleiman, Patrick M.A., Smoller, Jordan W., Stanaway, Ian B., Stroud, Mary, Tolwinski, Kasia, Van Driest, Sara L., Veenstra, David, Vicente, Gina, Wagner, Michael, Walunas, Theresa, Wells, Quinn, White, Peter S., Wiley, Ken L., Wilson, Michael W., Woolf, Betty, Yi, Victoria, Zhang, Ge, Zhang, Lan, Gibbs, Richard A.

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Horizons in Sjögren's syndrome genetics by Williams, Pamela H, Cobb, Beth L, Namjou, Bahram, Scofield, R Hal, Sawalha, Amr H, Harley, John B

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Genetic sex validation for sample tracking in next-generation sequencing clinical testing by Hu, Jianhong, Korchina, Viktoriya, Zouk, Hana, Harden, Maegan V, Murdock, David, Macbeth, Alyssa, Harrison, Steven M, Lennon, Niall, Kovar, Christie, Balasubramanian, Adithya, Zhang, Lan, Chandanavelli, Gauthami, Pasham, Divya, Rowley, Robb, Wiley, Ken, Smith, Maureen E, Gordon, Adam, Jarvik, Gail P, Sleiman, Patrick, Kelly, Melissa A, Bland, Harris T, Murugan, Mullai, Venner, Eric, Boerwinkle, Eric, Prows, Cynthia, Mahanta, Lisa, Rehm, Heidi L, Gibbs, Richard A, Muzny, Donna M

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Detection of immunoglobulin response to COVID-19 vaccination using a novel rapid fingerstick assay by Cobb, Beth L, Sawalha, Amr H

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Genetic sex validation for sample tracking in next-generation sequencing clinical testing by Hu, Jianhong, Harden, Maegan V, Balasubramanian, Adithya, Zhang, Lan, Chandanavelli, Gauthami, Rowley, Robb, Smith, Maureen E, Sleiman, Patrick, Kelly, Melissa A, Bland, Harris T, Albertson-Junkans, Ladia H, Almoguera, Berta, Aufox, Sharon, Babb, Lawrence J, Bangash, Hana, Bhoj, Elizabeth J, Bottinger, Erwin P, Bowen, Deborah J, Bowser, Mark, Brilliant, Murray, Buchanan, Adam H, Cagan, Andrew, Caraballo, Pedro J, Carey, David J, Chisholm, Rex L, City, Brittany B, Clayton, Ellen Wright, Cobb, Beth L, Crane, Paul K, Crew, Katherine D, Crosslin, David R, De Andrade, Mariza, Dikilitas, Ozan, Dufendach, Kevin R, Edwards, Todd L, Eng, Christine, Fullerton, Stephanie M, Gainer, Vivian S, Glessner, Joe T, Goehringer, Jessica M, Graham, Chet, Hartzler, Andrea L, Hebbring, Scott, Henrikson, Nora B, Hripcsak, George, Hsieh, Alexander L, Johnson, Darren K, Jones, Laney K, Jose, Sheethal, Josyula, Navya Shilpa, Justice, Anne E, Kaufman, Kenneth M, Keaton, Jacob M, Key, Dustin L, Khan, Atlas, Kirchner, H. Lester, Kitchner, Terrie, Kudalkar, Emily, Kuhn, Benjamin R, Lebo, Matthew S, Leppig, Kathleen A, Lin, Chiao-Feng, Linder, Jodell E, Lindor, Noralane M, Lingren, Todd, Liu, Cong, Luo, Yuan, Lynch, John, Malin, Bradley A, Mentch, Frank D, Miller, Erin M, Rasouly, Hila Milo, Nestor, Jordan, Ni, Yizhao, Obeng, Aniwaa Owusu, Pacyna, Joel E, Pisieczko, Cassandra, Rahm, Alanna K, Safarova, Maya S, Scrol, Aaron, Sengupta, Soumitra, Shaibi, Gabriel Q, Shang, Ning, Shen, Yufeng, Smoller, Jordan W, Stanaway, Ian B, Starren, Justin, Stone, Timoethia M, Tarczy-Hornoch, Peter, Varugheese, Matthew, Vazquez, Lyam, Veenstra, David L, Verbitsky, Miguel, Walunas, Theresa, Wehbe, Firas H, Wells, Quinn S, Williams, Janet, Woods, Laura Allison B, Wynn, Julia, Zhang, Yanfei

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Genetic sex validation for sample tracking in next-generation sequencing clinical testing by Hu, Jianhong, Harden, Maegan V, Balasubramanian, Adithya, Zhang, Lan, Chandanavelli, Gauthami, Rowley, Robb, Smith, Maureen E, Sleiman, Patrick, Kelly, Melissa A, Bland, Harris T, Albertson-Junkans, Ladia H, Almoguera, Berta, Aufox, Sharon, Babb, Lawrence J, Bangash, Hana, Bhoj, Elizabeth J, Bottinger, Erwin P, Bowen, Deborah J, Bowser, Mark, Brilliant, Murray, Buchanan, Adam H, Cagan, Andrew, Caraballo, Pedro J, Carey, David J, Chisholm, Rex L, City, Brittany B, Clayton, Ellen Wright, Cobb, Beth L, Crane, Paul K, Crew, Katherine D, Crosslin, David R, De Andrade, Mariza, Dikilitas, Ozan, Dufendach, Kevin R, Edwards, Todd L, Eng, Christine, Fullerton, Stephanie M, Gainer, Vivian S, Glessner, Joe T, Goehringer, Jessica M, Graham, Chet, Hartzler, Andrea L, Hebbring, Scott, Henrikson, Nora B, Hripcsak, George, Hsieh, Alexander L, Johnson, Darren K, Jones, Laney K, Jose, Sheethal, Josyula, Navya Shilpa, Justice, Anne E, Kaufman, Kenneth M, Keaton, Jacob M, Key, Dustin L, Khan, Atlas, Kirchner, H. Lester, Kitchner, Terrie, Kudalkar, Emily, Kuhn, Benjamin R, Lebo, Matthew S, Leppig, Kathleen A, Lin, Chiao-Feng, Linder, Jodell E, Lindor, Noralane M, Lingren, Todd, Liu, Cong, Luo, Yuan, Lynch, John, Malin, Bradley A, Mentch, Frank D, Miller, Erin M, Rasouly, Hila Milo, Nestor, Jordan, Ni, Yizhao, Obeng, Aniwaa Owusu, Pacyna, Joel E, Pisieczko, Cassandra, Rahm, Alanna K, Safarova, Maya S, Scrol, Aaron, Sengupta, Soumitra, Shaibi, Gabriel Q, Shang, Ning, Shen, Yufeng, Smoller, Jordan W, Stanaway, Ian B, Starren, Justin, Stone, Timoethia M, Tarczy-Hornoch, Peter, Varugheese, Matthew, Vazquez, Lyam, Veenstra, David L, Verbitsky, Miguel, Walunas, Theresa, Wehbe, Firas H, Wells, Quinn S, Williams, Janet, Woods, Laura Allison B, Wynn, Julia, Zhang, Yanfei

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GWAS and enrichment analyses of non-alcoholic fatty liver disease identify new trait-associated genes and pathways across eMERGE Network by Namjou, Bahram, Lingren, Todd, Huang, Yongbo, Parameswaran, Sreeja, Cobb, Beth L, Stanaway, Ian B, Connolly, John J, Mentch, Frank D, Benoit, Barbara, Niu, Xinnan, Wei, Wei-Qi, Carroll, Robert J, Pacheco, Jennifer A, Harley, Isaac T. W, Divanovic, Senad, Carrell, David S, Larson, Eric B, Carey, David J, Verma, Shefali, Ritchie, Marylyn D, Gharavi, Ali G, Murphy, Shawn, Williams, Marc S, Crosslin, David R, Jarvik, Gail P, Kullo, Iftikhar J, Hakonarson, Hakon, Li, Rongling, , Xanthakos, Stavra A, Harley, John B

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GWAS and enrichment analyses of non-alcoholic fatty liver disease identify new trait-associated genes and pathways across eMERGE Network by Namjou, Bahram, Lingren, Todd, Huang, Yongbo, Parameswaran, Sreeja, Cobb, Beth L, Stanaway, Ian B, Connolly, John J, Mentch, Frank D, Benoit, Barbara, Niu, Xinnan, Wei, Wei-Qi, Carroll, Robert J, Pacheco, Jennifer A, Harley, Isaac T. W, Divanovic, Senad, Carrell, David S, Larson, Eric B, Carey, David J, Verma, Shefali, Ritchie, Marylyn D, Gharavi, Ali G, Murphy, Shawn, Williams, Marc S, Crosslin, David R, Jarvik, Gail P, Kullo, Iftikhar J, Hakonarson, Hakon, Li, Rongling, , Xanthakos, Stavra A, Harley, John B

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A GWAS Study on Liver Function Test Using eMERGE Network Participants by Namjou, Bahram, Marsolo, Keith, Lingren, Todd, Ritchie, Marylyn D, Verma, Shefali S, Cobb, Beth L, Perry, Cassandra, Kitchner, Terrie E, Brilliant, Murray H, Peissig, Peggy L, Borthwick, Kenneth M, Williams, Marc S, Grafton, Jane, Jarvik, Gail P, Holm, Ingrid A, Harley, John B

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A GWAS Study on Liver Function Test Using eMERGE Network Participants by Namjou, Bahram, Marsolo, Keith, Lingren, Todd, Ritchie, Marylyn D, Verma, Shefali S, Cobb, Beth L, Perry, Cassandra, Kitchner, Terrie E, Brilliant, Murray H, Peissig, Peggy L, Borthwick, Kenneth M, Williams, Marc S, Grafton, Jane, Jarvik, Gail P, Holm, Ingrid A, Harley, John B

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Identification of novel genetic susceptibility loci for Behcet's disease using a genome-wide association study by Fei, Yiping, Webb, Ryan, Cobb, Beth L, Direskeneli, Haner, Saruhan-Direskeneli, Güher, Sawalha, Amr H

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