SLE non-coding genetic risk variant determines the epigenetic dysfunction of an immune cell specific enhancer that controls disease-critical microRNA expression von Hou, Guojun, Harley, Isaac T. W., Lu, Xiaoming, Zhou, Tian, Xu, Ning, Yao, Chao, Qin, Yuting, Ouyang, Ye, Ma, Jianyang, Zhu, Xinyi, Yu, Xiang, Xu, Hong, Dai, Dai, Ding, Huihua, Yin, Zhihua, Ye, Zhizhong, Deng, Jun, Zhou, Mi, Tang, Yuanjia, Namjou, Bahram, Guo, Ya, Weirauch, Matthew T., Kottyan, Leah C., Harley, John B., Shen, Nan

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Lupus enhancer risk variant causes dysregulation of IRF8 through cooperative lncRNA and DNA methylation machinery von Zhou, Tian, Zhu, Xinyi, Ye, Zhizhong, Wang, Yong-Fei, Yao, Chao, Xu, Ning, Zhou, Mi, Ma, Jianyang, Qin, Yuting, Shen, Yiwei, Tang, Yuanjia, Yin, Zhihua, Xu, Hong, Zhang, Yutong, Zang, Xiaoli, Ding, Huihua, Yang, Wanling, Guo, Ya, Harley, John B., Namjou, Bahram, Kaufman, Kenneth M., Kottyan, Leah C., Weirauch, Matthew T., Hou, Guojun, Shen, Nan

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Evaluation of the MC4R gene across eMERGE network identifies many unreported obesity-associated variants von Namjou, Bahram, Stanaway, Ian B., Lingren, Todd, Mentch, Frank D., Benoit, Barbara, Dikilitas, Ozan, Niu, Xinnan, Shang, Ning, Shoemaker, Ashley H., Carey, David J., Mirshahi, Tooraj, Singh, Rajbir, Nestor, Jordan G., Hakonarson, Hakon, Denny, Joshua C., Crosslin, David R., Jarvik, Gail P., Kullo, Iftikhar J., Williams, Marc S., Harley, John B.

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Projecting genetic associations through gene expression patterns highlights disease etiology and drug mechanisms von Pividori, Milton, Lu, Sumei, Li, Binglan, Su, Chun, Johnson, Matthew E., Wei, Wei-Qi, Feng, Qiping, Namjou, Bahram, Kiryluk, Krzysztof, Kullo, Iftikhar J., Luo, Yuan, Sullivan, Blair D., Voight, Benjamin F., Skarke, Carsten, Ritchie, Marylyn D., Grant, Struan F. A., Greene, Casey S.

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Variant level heritability estimates of type 2 diabetes in African Americans von Armstrong, Nicole D., Patki, Amit, Srinivasasainagendra, Vinodh, Ge, Tian, Lange, Leslie A., Kottyan, Leah, Namjou, Bahram, Shah, Amy S., Rasmussen-Torvik, Laura J., Jarvik, Gail P., Meigs, James B., Karlson, Elizabeth W., Limdi, Nita A., Irvin, Marguerite R., Tiwari, Hemant K.

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Haplotype-specific chromatin looping reveals genetic interactions of regulatory regions modulating gene expression in 8p23.1 von Saint Just Ribeiro, Mariana, Tripathi, Pulak, Namjou, Bahram, Harley, John B., Chepelev, Iouri

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Mendelian randomization analysis of plasma levels of CD209 and MICB proteins and the risk of varicose veins of lower extremities von Shadrina, Alexandra S, Elgaeva, Elizaveta E, Stanaway, Ian B, Jarvik, Gail P, Namjou, Bahram, Wei, Wei-Qi, Glessner, Joe, Hakonarson, Hakon, Suri, Pradeep, Tsepilov, Yakov A

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Electronic Health Record Based Algorithm to Identify Patients with Autism Spectrum Disorder von Lingren, Todd, Chen, Pei, Bochenek, Joseph, Doshi-Velez, Finale, Manning-Courtney, Patty, Bickel, Julie, Wildenger Welchons, Leah, Reinhold, Judy, Bing, Nicole, Ni, Yizhao, Barbaresi, William, Mentch, Frank, Basford, Melissa, Denny, Joshua, Vazquez, Lyam, Perry, Cassandra, Namjou, Bahram, Qiu, Haijun, Connolly, John, Abrams, Debra, Holm, Ingrid A, Cobb, Beth A, Lingren, Nataline, Solti, Imre, Hakonarson, Hakon, Kohane, Isaac S, Harley, John, Savova, Guergana

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Genetic regulation of serum IgA levels and susceptibility to common immune, infectious, kidney, and cardio-metabolic traits von Liu, Lili, Khan, Atlas, Sanchez-Rodriguez, Elena, Zanoni, Francesca, Li, Yifu, Steers, Nicholas, Balderes, Olivia, Zhang, Junying, Krithivasan, Priya, LeDesma, Robert A., Fischman, Clara, Hebbring, Scott J., Harley, John B., Moncrieffe, Halima, Kottyan, Leah C., Namjou-Khales, Bahram, Walunas, Theresa L., Knevel, Rachel, Raychaudhuri, Soumya, Karlson, Elizabeth W., Denny, Joshua C., Stanaway, Ian B., Crosslin, David, Rauen, Thomas, Floege, Jürgen, Eitner, Frank, Moldoveanu, Zina, Reily, Colin, Knoppova, Barbora, Hall, Stacy, Sheff, Justin T., Julian, Bruce A., Wyatt, Robert J., Suzuki, Hitoshi, Xie, Jingyuan, Chen, Nan, Zhou, Xujie, Zhang, Hong, Hammarström, Lennart, Viktorin, Alexander, Magnusson, Patrik K. E., Shang, Ning, Hripcsak, George, Weng, Chunhua, Rundek, Tatjana, Elkind, Mitchell S. V., Oelsner, Elizabeth C., Barr, R. Graham, Ionita-Laza, Iuliana, Novak, Jan, Gharavi, Ali G., Kiryluk, Krzysztof

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909 Haplotype-specific chromatin looping reveals genetic interactions of regulatory regions modulating gene expression at the SLE susceptibility locus FAM167A-BLK von Ribeiro, Mariana Saint-Just, Tripathi, Pulak, Namjou, Bahram, Harley, John B, Chepelev, Iouri

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Identification of Four Novel Loci in Asthma in European American and African American Populations von Almoguera, Berta, Vazquez, Lyam, Mentch, Frank, Connolly, John, Pacheco, Jennifer A, Sundaresan, Agnes S, Peissig, Peggy L, Linneman, James G, McCarty, Catherine A, Crosslin, David, Carrell, David S, Lingren, Todd, Namjou-Khales, Bahram, Harley, John B, Larson, Eric, Jarvik, Gail P, Brilliant, Murray, Williams, Marc S, Kullo, Iftikhar J, Hysinger, Erik B, Sleiman, Patrick M A, Hakonarson, Hakon

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The effect of inversion at 8p23 on BLK association with lupus in Caucasian population von Namjou, Bahram, Ni, Yizhao, Harley, Isaac T W, Chepelev, Iouri, Cobb, Beth, Kottyan, Leah C, Gaffney, Patrick M, Guthridge, Joel M, Kaufman, Kenneth, Harley, John B

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Medical Records-Based Genetic Studies of the Complement System von Khan, Atlas, Shang, Ning, Petukhova, Lynn, Zhang, Jun, Shen, Yufeng, Hebbring, Scott J, Moncrieffe, Halima, Kottyan, Leah C, Namjou-Khales, Bahram, Knevel, Rachel, Raychaudhuri, Soumya, Karlson, Elizabeth W, Harley, John B, Stanaway, Ian B, Crosslin, David, Denny, Joshua C, Elkind, Mitchell S V, Gharavi, Ali G, Hripcsak, George, Weng, Chunhua, Kiryluk, Krzysztof

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Author Correction: Genetic regulation of serum IgA levels and susceptibility to common immune, infectious, kidney, and cardio-metabolic traits von Liu, Lili, Khan, Atlas, Sanchez-Rodriguez, Elena, Zanoni, Francesca, Li, Yifu, Steers, Nicholas, Balderes, Olivia, Zhang, Junying, Krithivasan, Priya, LeDesma, Robert A., Fischman, Clara, Hebbring, Scott J., Harley, John B., Moncrieffe, Halima, Kottyan, Leah C., Namjou-Khales, Bahram, Walunas, Theresa L., Knevel, Rachel, Raychaudhuri, Soumya, Karlson, Elizabeth W., Denny, Joshua C., Stanaway, Ian B., Crosslin, David, Rauen, Thomas, Floege, Jürgen, Eitner, Frank, Moldoveanu, Zina, Reily, Colin, Knoppova, Barbora, Hall, Stacy, Sheff, Justin T., Julian, Bruce A., Wyatt, Robert J., Suzuki, Hitoshi, Xie, Jingyuan, Chen, Nan, Zhou, Xujie, Zhang, Hong, Hammarström, Lennart, Viktorin, Alexander, Magnusson, Patrik K. E., Shang, Ning, Hripcsak, George, Weng, Chunhua, Rundek, Tatjana, Elkind, Mitchell S. V., Oelsner, Elizabeth C., Barr, R. Graham, Ionita-Laza, Iuliana, Novak, Jan, Gharavi, Ali G., Kiryluk, Krzysztof

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Imputation and quality control steps for combining multiple genome-wide datasets von Verma, Shefali S, de Andrade, Mariza, Tromp, Gerard, Kuivaniemi, Helena, Pugh, Elizabeth, Namjou-Khales, Bahram, Mukherjee, Shubhabrata, Jarvik, Gail P, Kottyan, Leah C, Burt, Amber, Bradford, Yuki, Armstrong, Gretta D, Derr, Kimberly, Crawford, Dana C, Haines, Jonathan L, Li, Rongling, Crosslin, David, Ritchie, Marylyn D

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A GWAS Study on Liver Function Test Using eMERGE Network Participants von 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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47 Cross-ancestry GWAS meta-analysis of keloids discovers novel susceptibility loci in diverse populations von Greene, Catherine Anne, Hampton, Gabrielle, Jarvik, Gail P., Namjou-Khales, Bahram, Khan, Atlas, Luo, Yuan, Edwards, Todd L., Velez Edwards, Digna R., Hellwege, Jacklyn N.

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A phenome-wide association study to discover pleiotropic effects of PCSK9, APOB, and LDLR von Safarova, Maya S., Satterfield, Benjamin A., Fan, Xiao, Austin, Erin E., Ye, Zhan, Bastarache, Lisa, Zheng, Neil, Ritchie, Marylyn D., Borthwick, Kenneth M., Williams, Marc S., Larson, Eric B., Scrol, Aaron, Jarvik, Gail P., Crosslin, David R., Leppig, Kathleen, Rasmussen-Torvik, Laura J., Pendergrass, Sarah A., Sturm, Amy C., Namjou, Bahram, Shah, Amy Sanghavi, Carroll, Robert J., Chung, Wendy K., Wei, Wei-Qi, Feng, QiPing, Stein, C. Michael, Roden, Dan M., Manolio, Teri A., Schaid, Daniel J., Denny, Joshua C., Hebbring, Scott J., de Andrade, Mariza, Kullo, Iftikhar J.

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Osteopontin and systemic lupus erythematosus association: a probable gene-gender interaction von Han, Shizhong, Guthridge, Joel M, Harley, Isaac T W, Sestak, Andrea L, Kim-Howard, Xana, Kaufman, Kenneth M, Namjou, Bahram, Deshmukh, Harshal, Bruner, Gail, Espinoza, Luis R, Gilkeson, Gary S, Harley, John B, James, Judith A, Nath, Swapan K

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The eMERGE genotype set of 83,717 subjects imputed to ~40 million variants genome wide and association with the herpes zoster medical record phenotype von Stanaway, Ian B., Hall, Taryn O., Rosenthal, Elisabeth A., Palmer, Melody, Naranbhai, Vivek, Knevel, Rachel, Namjou‐Khales, Bahram, Carroll, Robert J., Kiryluk, Krzysztof, Gordon, Adam S., Linder, Jodell, Howell, Kayla Marie, Mapes, Brandy M., Lin, Frederick T.J., Joo, Yoonjung Yoonie, Hayes, M. Geoffrey, Gharavi, Ali G., Pendergrass, Sarah A., Ritchie, Marylyn D., Andrade, Mariza, Croteau‐Chonka, Damien C., Raychaudhuri, Soumya, Weiss, Scott T., Lebo, Matt, Amr, Sami S., Carrell, David, Larson, Eric B., Chute, Christopher G., Rasmussen‐Torvik, Laura Jarmila, Roy‐Puckelwartz, Megan J., Sleiman, Patrick, Hakonarson, Hakon, Li, Rongling, Karlson, Elizabeth W., Peterson, Josh F., Kullo, Iftikhar J., Chisholm, Rex, Denny, Joshua Charles, Jarvik, Gail P., Crosslin, David R.

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