Impact of adding an IgG4 conjugate to routine direct immunofluorescence testing for subepithelial and intraepithelial autoimmune blistering disorders by Lehman, Julia S., Johnson, Emma F., Camilleri, Michael J., Gibson, Lawrence E., Comfere, Nneka I., Kalaaji, Amer N., Peters, Margot S., Cervenka, Derek J., Doppler, Joseph M., Lange, Colleen R., Miller, Cameron J., Wieland, Carilyn N.

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Indirect immunofluorescence testing for immunoglobulin (Ig)G4 and IgG increases test sensitivity over that of indirect immunofluorescence testing for IgG alone for pemphigoid and p... by Lehman, Julia S, Mohandesi, Nessa Aghazadeh, Agrawal, Shruti, Camilleri, Michael J, Cervenka, Derek J, Comfere, Nneka I, Johnson, Emma F, Kalaaji, Amer N, Lange, Colleen R, Shore, Carly J, Smith, Peyton, Wieland, Carilyn N, Gonzalez Guerrico, Anatilde M

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Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program by Taliun, Daniel, Kessler, Michael D., Carlson, Jedidiah, Taliun, Sarah A. Gagliano, Kang, Hyun Min, Pitsillides, Achilleas N., Emde, Anne-Katrin, Clarke, Wayne E., Shetty, Amol C., Wong, Quenna, Bobo, Dean M., Aguet, François, Albert, Christine, Aslibekyan, Stella, Barnard, John, Barr, R. Graham, Barwick, Lucas, Becker, Lewis C., Bielak, Lawrence F., Blangero, John, Bowden, Donald W., Burchard, Esteban G., Chalazan, Brandon, Chasman, Daniel I., Chen, Yii-Der Ida, Choi, Seung Hoan, Chung, Mina K., Curran, Joanne E., Daya, Michelle, Ellinor, Patrick T., Fatkin, Diane, Fingerlin, Tasha, Forer, Lukas, Franceschini, Nora, Germer, Soren, Gladwin, Mark T., Hall, Michael E., He, Jiang, Johnsen, Jill M., Johnson, Andrew D., Kardia, Sharon L. R., Klemmer, Robert, Kooperberg, Charles, Köttgen, Anna, Lange, Leslie A., Lin, Xihong, Lin, Keng-Han, Liu, Chunyu, Loos, Ruth J. F., Gerszten, Robert, Lunetta, Kathryn L., Mak, Angel C. Y., Manichaikul, Ani, Manning, Alisa K., Mathias, Rasika A., McManus, David D., McGarvey, Stephen T., Meigs, James B., Minear, Mollie A., Mitchell, Braxton D., Mohanty, Sanghamitra, Montasser, May E., Montgomery, Courtney, Morrison, Alanna C., Murabito, Joanne M., Natale, Andrea, Nelson, Sarah C., Palmer, Nicholette D., Pankratz, Nathan, Peyser, Patricia A., Post, Wendy S., Psaty, Bruce M., Rao, D. C., Reiner, Alexander P., Roden, Dan, Rotter, Jerome I., Schoenherr, Sebastian, Seo, Jeong-Sun, Sheu, Wayne H., Smith, Nicholas L., Smith, Jennifer A., Stilp, Adrienne M., Telen, Marilyn, Thornton, Timothy A., Tracy, Russell P., Van Den Berg, David J., Vasan, Ramachandran S., Vrieze, Scott, Weng, Lu-Chen, Zhao, Xutong, Boerwinkle, Eric, Gibbs, Richard, Rich, Stephen S., Silverman, Edwin K., Qasba, Pankaj, Gan, Weiniu, Zöllner, Sebastian, Wilson, James G., Laurie, Cathy C., Jaquish, Cashell E.

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Inherited causes of clonal haematopoiesis in 97,691 whole genomes by Weinstock, Joshua S., Nandakumar, Satish K., Bao, Erik L., Szeto, Mindy D., Liao, Xiaotian, Nasser, Joseph, Laurie, Cecelia, Burugula, Bala Bharathi, Gibson, Christopher J., Lin, Amy E., Aguet, Francois, Ardlie, Kristin, Mitchell, Braxton D., Barnes, Kathleen C., Moscati, Arden, Redline, Susan, Psaty, Bruce M., Silverman, Edwin K., Weiss, Scott T., Palmer, Nicholette D., Vasan, Ramachandran S., Burchard, Esteban G., He, Jiang, Kaplan, Robert C., Smith, Nicholas L., Arnett, Donna K., Schwartz, David A., Guo, Xiuqing, Konkle, Barbara A., Custer, Brian, Peralta, Juan M., Gui, Hongsheng, Meyers, Deborah A., McGarvey, Stephen T., Chen, Ida Yii-Der, Shoemaker, M. Benjamin, Peyser, Patricia A., Broome, Jai G., Wang, Fei Fei, North, Kari E., Launer, Lenore J., Cade, Brian E., Bis, Joshua C., Cho, Michael H., Lasky-Su, Jessica, Bowden, Donald W., Cupples, L. Adrienne, Mak, Angel C. Y., Smith, Jennifer A., Kelly, Tanika N., Aslibekyan, Stella, Heckbert, Susan R., Tiwari, Hemant K., Yang, Ivana V., Heit, John A., Johnsen, Jill M., Curran, Joanne E., Wenzel, Sally E., Rao, Dabeeru C., Darbar, Dawood, Moon, Jee-Young, Tracy, Russell P., Buth, Erin J., Rafaels, Nicholas, Loos, Ruth J. F., Liu, Yongmei, Hou, Lifang, Lee, Jiwon, Kachroo, Priyadarshini, Freedman, Barry I., Levy, Daniel, Bielak, Lawrence F., Hixson, James E., Floyd, James S., Whitsel, Eric A., Ellinor, Patrick T., Irvin, Marguerite R., Fingerlin, Tasha E., Armasu, Sebastian M., Wheeler, Marsha M., Blangero, John, Williams, L. Keoki, Levy, Bruce D., Sheu, Wayne Huey-Herng, Roden, Dan M., Taylor, Kent D., Johnson, Andrew D., Auer, Paul L., Kooperberg, Charles, Laurie, Cathy C., Blackwell, Thomas W., Smith, Albert V., Lange, Ethan, Rotter, Jerome I., Kitzman, Jacob O., Lander, Eric S., Ebert, Benjamin L., Reiner, Alexander P., Jaiswal, Siddhartha, Kathiresan, Sekar

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Genome-Wide Association Study of Apparent Treatment-Resistant Hypertension in the CHARGE Consortium: The CHARGE Pharmacogenetics Working Group by Irvin, Marguerite R, Sitlani, Colleen M, Floyd, James S, Psaty, Bruce M, Bis, Joshua C, Wiggins, Kerri L, Whitsel, Eric A, Sturmer, Til, Stewart, James, Raffield, Laura, Sun, Fangui, Liu, Ching-Ti, Xu, Hanfei, Cupples, Adrienne L, Tanner, Rikki M, Rossing, Peter, Smith, Albert, Zilhão, Nuno R, Launer, Lenore J, Noordam, Raymond, Rotter, Jerome I, Yao, Jie, Li, Xiaohui, Guo, Xiuqing, Limdi, Nita, Sundaresan, Aishwarya, Lange, Leslie, Correa, Adolfo, Stott, David J, Ford, Ian, Jukema, J Wouter, Gudnason, Vilmundur, Mook-Kanamori, Dennis O, Trompet, Stella, Palmas, Walter, Warren, Helen R, Hellwege, Jacklyn N, Giri, Ayush, O'donnell, Christopher, Hung, Adriana M, Edwards, Todd L, Ahluwalia, Tarunveer S, Arnett, Donna K, Avery, Christy L

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Multiethnic meta-analysis identifies ancestry-specific and cross-ancestry loci for pulmonary function by Wyss, Annah B., Sofer, Tamar, Lee, Mi Kyeong, Terzikhan, Natalie, Nguyen, Jennifer N., Lahousse, Lies, Latourelle, Jeanne C., Smith, Albert Vernon, Bartz, Traci M., Gao, Wei, Ahluwalia, Tarunveer S., Tang, Wenbo, Oldmeadow, Christopher, Duan, Qing, de Jong, Kim, Wojczynski, Mary K., Wang, Xin-Qun, Noordam, Raymond, Hartwig, Fernando Pires, Jackson, Victoria E., Wang, Tianyuan, Obeidat, Ma’en, Hobbs, Brian D., Huan, Tianxiao, Gui, Hongsheng, Parker, Margaret M., Hu, Donglei, Mogil, Lauren S., Kichaev, Gleb, Jin, Jianping, Graff, Mariaelisa, Harris, Tamara B., Kalhan, Ravi, Heckbert, Susan R., Paternoster, Lavinia, Burkart, Kristin M., Liu, Yongmei, Holliday, Elizabeth G., Wilson, James G., Vonk, Judith M., Barr, R. Graham, de Mutsert, Renée, Menezes, Ana Maria Baptista, Adams, Hieab H. H., van den Berge, Maarten, Joehanes, Roby, Levin, Albert M., Liberto, Jennifer, Launer, Lenore J., Morrison, Alanna C., Sitlani, Colleen M., Celedón, Juan C., Kritchevsky, Stephen B., Scott, Rodney J., Christensen, Kaare, Rotter, Jerome I., Bonten, Tobias N., Wehrmeister, Fernando César, Bossé, Yohan, Xiao, Shujie, Oh, Sam, Franceschini, Nora, Brody, Jennifer A., Kaplan, Robert C., Lohman, Kurt, McEvoy, Mark, Province, Michael A., Rosendaal, Frits R., Taylor, Kent D., Nickle, David C., Williams, L. Keoki, Burchard, Esteban G., Wheeler, Heather E., Sin, Don D., Gudnason, Vilmundur, North, Kari E., Fornage, Myriam, Psaty, Bruce M., Myers, Richard H., O’Connor, George, Hansen, Torben, Laurie, Cathy C., Cassano, Patricia A., Sung, Joohon, Kim, Woo Jin, Attia, John R., Lange, Leslie, Boezen, H. Marike, Thyagarajan, Bharat, Rich, Stephen S., Mook-Kanamori, Dennis O., Horta, Bernardo Lessa, Uitterlinden, André G., Im, Hae Kyung, Cho, Michael H., Brusselle, Guy G., Gharib, Sina A., Dupuis, Josée, Manichaikul, Ani, London, Stephanie J.

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Global DNA methylation loss associated with mercury contamination and aging in the American alligator (Alligator mississippiensis) by Nilsen, Frances M., Parrott, Benjamin B., Bowden, John A., Kassim, Brittany L., Somerville, Stephen E., Bryan, Teresa A., Bryan, Colleen E., Lange, Ted R., Delaney, J. Patrick, Brunell, Arnold M., Long, Stephen E., Guillette, Louis J.

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Whole-exome sequencing study identifies four novel gene loci associated with diabetic kidney disease by Pan, Yang, Sun, Xiao, Mi, Xuenan, Huang, Zhijie, Hsu, Yenchih, Hixson, James E, Munzy, Donna, Metcalf, Ginger, Franceschini, Nora, Tin, Adrienne, Köttgen, Anna, Francis, Michael, Brody, Jennifer A, Kestenbaum, Bryan, Sitlani, Colleen M, Mychaleckyj, Josyf C, Kramer, Holly, Lange, Leslie A, Guo, Xiuqing, Hwang, Shih-Jen, Irvin, Marguerite R, Smith, Jennifer A, Yanek, Lisa R, Vaidya, Dhananjay, Chen, Yii-Der Ida, Fornage, Myriam, Lloyd-Jones, Donald M, Hou, Lifang, Mathias, Rasika A, Mitchell, Braxton D, Peyser, Patricia A, Kardia, Sharon L R, Arnett, Donna K, Correa, Adolfo, Raffield, Laura M, Vasan, Ramachandran S, Cupple, L Adrienne, Levy, Daniel, Kaplan, Robert C, North, Kari E, Rotter, Jerome I, Kooperberg, Charles, Reiner, Alexander P, Psaty, Bruce M, Tracy, Russell P, Gibbs, Richard A, Morrison, Alanna C, Feldman, Harold, Boerwinkle, Eric, He, Jiang, Kelly, Tanika N

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Deep-coverage whole genome sequences and blood lipids among 16,324 individuals by Natarajan, Pradeep, Peloso, Gina M., Zekavat, Seyedeh Maryam, Montasser, May, Ganna, Andrea, Chaffin, Mark, Khera, Amit V., Zhou, Wei, Bloom, Jonathan M., Engreitz, Jesse M., Ernst, Jason, O’Connell, Jeffrey R., Ruotsalainen, Sanni E., Alver, Maris, Manichaikul, Ani, Johnson, W. Craig, Perry, James A., Poterba, Timothy, Seed, Cotton, Surakka, Ida L., Esko, Tonu, Ripatti, Samuli, Salomaa, Veikko, Correa, Adolfo, Vasan, Ramachandran S., Kellis, Manolis, Neale, Benjamin M., Lander, Eric S., Abecasis, Goncalo, Mitchell, Braxton, Rich, Stephen S., Wilson, James G., Cupples, L. Adrienne, Rotter, Jerome I., Willer, Cristen J., Kathiresan, Sekar

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The human Y and inactive X chromosomes similarly modulate autosomal gene expression by San Roman, Adrianna K., Skaletsky, Helen, Godfrey, Alexander K., Bokil, Neha V., Teitz, Levi, Singh, Isani, Blanton, Laura V., Bellott, Daniel W., Pyntikova, Tatyana, Lange, Julian, Koutseva, Natalia, Hughes, Jennifer F., Brown, Laura, Phou, Sidaly, Buscetta, Ashley, Kruszka, Paul, Banks, Nicole, Dutra, Amalia, Pak, Evgenia, Lasutschinkow, Patricia C., Keen, Colleen, Davis, Shanlee M., Lin, Angela E., Tartaglia, Nicole R., Samango-Sprouse, Carole, Muenke, Maximilian, Page, David C.

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Prevalence of Pathogenic Transthyretin Gene Variants in the Rocky Mountain Region by Jacoby, Ellie, Quan, Dianna, Todd, Emily, Shortt, Jonathan, Smith, Harry, Rafaels, Nicholas, Crooks, Kristy

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Author Correction: TDP-43 loss and ALS-risk SNPs drive mis-splicing and depletion of UNC13A by Brown, Anna-Leigh, Wilkins, Oscar G., Keuss, Matthew J., Hill, Sarah E., Zanovello, Matteo, Lee, Weaverly Colleen, Bampton, Alexander, Lee, Flora C. Y., Masino, Laura, Qi, Yue A., Bryce-Smith, Sam, Gatt, Ariana, Hallegger, Martina, Fagegaltier, Delphine, Phatnani, Hemali, Newcombe, Jia, Gustavsson, Emil K., Seddighi, Sahba, Reyes, Joel F., Coon, Steven L., Ramos, Daniel, Schiavo, Giampietro, Fisher, Elizabeth M. C., Raj, Towfique, Secrier, Maria, Lashley, Tammaryn, Ule, Jernej, Buratti, Emanuele, Humphrey, Jack, Ward, Michael E., Fratta, Pietro

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Drug-Gene Interactions of Antihypertensive Medications and Risk of Incident Cardiovascular Disease: A Pharmacogenomics Study from the CHARGE Consortium by Bis, Joshua C, Sitlani, Colleen, Irvin, Ryan, Avery, Christy L, Smith, Albert Vernon, Sun, Fangui, Evans, Daniel S, Musani, Solomon K, Li, Xiaohui, Trompet, Stella, Krijthe, Bouwe P, Harris, Tamara B, Quibrera, P Miguel, Brody, Jennifer A, Demissie, Serkalem, Davis, Barry R, Wiggins, Kerri L, Tranah, Gregory J, Lange, Leslie A, Sotoodehnia, Nona, Stott, David J, Franco, Oscar H, Launer, Lenore J, Stürmer, Til, Taylor, Kent D, Cupples, L Adrienne, Eckfeldt, John H, Smith, Nicholas L, Liu, Yongmei, Wilson, James G, Heckbert, Susan R, Buckley, Brendan M, Ikram, M Arfan, Boerwinkle, Eric, Chen, Yii-Der Ida, de Craen, Anton J M, Uitterlinden, Andre G, Rotter, Jerome I, Ford, Ian, Hofman, Albert, Sattar, Naveed, Slagboom, P Eline, Westendorp, Rudi G J, Gudnason, Vilmundur, Vasan, Ramachandran S, Lumley, Thomas, Cummings, Steven R, Taylor, Jr, Herman A, Post, Wendy, Jukema, J Wouter, Stricker, Bruno H, Whitsel, Eric A, Psaty, Bruce M, Arnett, Donna

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Genome‐wide meta‐analysis of SNP and antihypertensive medication interactions on left ventricular traits in African Americans by Do, Anh N., Zhao, Wei, Baldridge, Abigail S., Raffield, Laura M., Wiggins, Kerri L., Shah, Sanjiv J., Aslibekyan, Stella, Tiwari, Hemant K., Limdi, Nita, Zhi, Degui, Sitlani, Colleen M., Taylor, Kent D., Psaty, Bruce M., Sotoodehnia, Nona, Brody, Jennifer A., Rasmussen‐Torvik, Laura J., Lloyd‐Jones, Donald, Lange, Leslie A., Wilson, James G., Smith, Jennifer A., Kardia, Sharon L. R., Mosley, Thomas H., Vasan, Ramachandran S., Arnett, Donna K., Irvin, Marguerite R.

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Genome-wide meta-analysis of SNP-by9-ACEI/ARB and SNP-by-thiazide diuretic and effect on serum potassium in cohorts of European and African ancestry by Irvin, Marguerite R., Sitlani, Colleen M., Noordam, Raymond, Avery, Christie L., Bis, Joshua C., Floyd, James S., Li, Jin, Limdi, Nita A., Srinivasasainagendra, Vinodh, Stewart, James, de Mutsert, Renée, Mook-Kanamori, Dennis O., Lipovich, Leonard, Kleinbrink, Erica L., Smith, Albert, Bartz, Traci M., Whitsel, Eric A., Uitterlinden, Andre G., Wiggins, Kerri L., Wilson, James G., Zhi, Degui, Stricker, Bruno H., Rotter, Jerome I., Arnett, Donna K., Psaty, Bruce M., Lange, Leslie A.

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Multi-Site Clinical Assessment of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (MCAM): Design and Implementation of a Prospective/Retrospective Rolling Cohort Study by Unger, Elizabeth R, Lin, Jin-Mann S, Tian, Hao, Natelson, Benjamin H, Lange, Gudrun, Vu, Diana, Blate, Michelle, Klimas, Nancy G, Balbin, Elizabeth G, Bateman, Lucinda, Allen, Ali, Lapp, Charles W, Springs, Wendy, Kogelnik, Andreas M, Phan, Catrina C, Danver, Joan, Podell, Richard N, Fitzpatrick, Trisha, Peterson, Daniel L, Gottschalk, C Gunnar, Rajeevan, Mangalathu S

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Pharmacogenomics study of thiazide diuretics and QT interval in multi-ethnic populations: the cohorts for heart and aging research in genomic epidemiology by Seyerle, A A, Sitlani, C M, Noordam, R, Gogarten, S M, Li, J, Li, X, Evans, D S, Sun, F, Laaksonen, M A, Isaacs, A, Kristiansson, K, Highland, H M, Stewart, J D, Harris, T B, Trompet, S, Bis, J C, Peloso, G M, Brody, J A, Broer, L, Busch, E L, Duan, Q, Stilp, A M, O'Donnell, C J, Macfarlane, P W, Floyd, J S, Kors, J A, Lin, H J, Li-Gao, R, Sofer, T, Méndez-Giráldez, R, Cummings, S R, Heckbert, S R, Hofman, A, Ford, I, Li, Y, Launer, L J, Porthan, K, Newton-Cheh, C, Napier, M D, Kerr, K F, Reiner, A P, Rice, K M, Roach, J, Buckley, B M, Soliman, E Z, de Mutsert, R, Sotoodehnia, N, Uitterlinden, A G, North, K E, Lee, C R, Gudnason, V, Stürmer, T, Rosendaal, F R, Taylor, K D, Wiggins, K L, Wilson, J G, Chen, Y-DI, Kaplan, R C, Wilhelmsen, K, Cupples, L A, Salomaa, V, van Duijn, C, Jukema, J W, Liu, Y, Mook-Kanamori, D O, Lange, L A, Vasan, R S, Smith, A V, Stricker, B H, Laurie, C C, Rotter, J I, Whitsel, E A, Psaty, B M, Avery, C L

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Abstract MP80: Genome-wide Meta-analysis of SNP-by-antihypertensive Treatment Class Effect on Serum Potassium in Cohorts of European and African Ancestry From Cohorts for Heart and... by Irvin, Marguerite R, Zhi, Degui, Sitlani, Colleen, Limdi, Nita, Bis, Joshua A, Floyd, James, Avery, Christy, Whitsel, Eric, Lange, Leslie, Smith, Albert, Noordam, Raymond, Arnett, Donna, Psaty, Bruce

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Cre recombinase-dependent expression of a constitutively active mutant allele of the catalytic subunit of protein kinase A by Niswender, Colleen M., Willis, Brandon S., Wallen, Angela, Sweet, Ian R., Jetton, Thomas L., Thompson, Brian R., Wu, Chaodong, Lange, Alex J., McKnight, G. Stanley

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Genome-wide meta-analysis of SNP-by-ACEI/ARB and SNP-by-thiazide diuretic and effect on serum potassium in cohorts of European and African ancestry by Irvin, Marguerite R, Sitlani, Colleen M, Noordam, Raymond, Avery, Christie L, Bis, Joshua C, Floyd, James S, Li, Jin, Limdi, Nita A, Srinivasasainagendra, Vinodh, Stewart, James, de Mutsert, Renée, Mook-Kanamori, Dennis O, Lipovich, Leonard, Kleinbrink, Erica L, Smith, Albert, Bartz, Traci M, Whitsel, Eric A, Uitterlinden, Andre G, Wiggins, Kerri L, Wilson, James G, Zhi, Degui, Stricker, Bruno H, Rotter, Jerome I, Arnett, Donna K, Psaty, Bruce M, Lange, Leslie A

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