Polygenic Prediction of Weight and Obesity Trajectories from Birth to Adulthood von Khera, Amit V., Chaffin, Mark, Wade, Kaitlin H., Zahid, Sohail, Brancale, Joseph, Xia, Rui, Distefano, Marina, Senol-Cosar, Ozlem, Haas, Mary E., Bick, Alexander, Aragam, Krishna G., Lander, Eric S., Smith, George Davey, Mason-Suares, Heather, Fornage, Myriam, Lebo, Matthew, Timpson, Nicholas J., Kaplan, Lee M., Kathiresan, Sekar

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Genome-wide identification of DNA methylation QTLs in whole blood highlights pathways for cardiovascular disease von Huan, Tianxiao, Joehanes, Roby, Song, Ci, Peng, Fen, Guo, Yichen, Mendelson, Michael, Yao, Chen, Liu, Chunyu, Ma, Jiantao, Richard, Melissa, Agha, Golareh, Guan, Weihua, Almli, Lynn M., Conneely, Karen N., Keefe, Joshua, Hwang, Shih-Jen, Johnson, Andrew D., Fornage, Myriam, Liang, Liming, Levy, Daniel

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Epigenome-wide association study (EWAS) of BMI, BMI change and waist circumference in African American adults identifies multiple replicated loci von Demerath, Ellen W, Guan, Weihua, Grove, Megan L, Aslibekyan, Stella, Mendelson, Michael, Zhou, Yi-Hui, Hedman, Åsa K, Sandling, Johanna K, Li, Li-An, Irvin, Marguerite R, Zhi, Degui, Deloukas, Panos, Liang, Liming, Liu, Chunyu, Bressler, Jan, Spector, Tim D, North, Kari, Li, Yun, Absher, Devin M, Levy, Daniel, Arnett, Donna K, Fornage, Myriam, Pankow, James S, Boerwinkle, Eric

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Epigenome-wide association studies identify DNA methylation associated with kidney function von Chu, Audrey Y., Tin, Adrienne, Schlosser, Pascal, Ko, Yi-An, Qiu, Chengxiang, Yao, Chen, Joehanes, Roby, Grams, Morgan E., Liang, Liming, Gluck, Caroline A., Liu, Chunyu, Coresh, Josef, Hwang, Shih-Jen, Levy, Daniel, Boerwinkle, Eric, Pankow, James S., Yang, Qiong, Fornage, Myriam, Fox, Caroline S., Susztak, Katalin, Köttgen, Anna

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Polygenic Type 2 Diabetes Prediction at the Limit of Common Variant Detection von VASSY, Jason L, HIVERT, Marie-France, MEIGS, James B, PORNEALA, Bianca, DAURIZ, Marco, FLOREZ, Jose C, DUPUIS, Josée, SISCOVICK, David S, FORNAGE, Myriam, RASMUSSEN-TORVIK, Laura J, BOUCHARD, Claude

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Clonal hematopoiesis of indeterminate potential, DNA methylation, and risk for coronary artery disease von Uddin, M d Mesbah, Nguyen, Ngoc Quynh H., Yu, Bing, Brody, Jennifer A., Pampana, Akhil, Nakao, Tetsushi, Fornage, Myriam, Bressler, Jan, Sotoodehnia, Nona, Weinstock, Joshua S., Honigberg, Michael C., Nachun, Daniel, Bhattacharya, Romit, Griffin, Gabriel K., Chander, Varuna, Gibbs, Richard A., Rotter, Jerome I., Liu, Chunyu, Baccarelli, Andrea A., Chasman, Daniel I., Whitsel, Eric A., Kiel, Douglas P., Murabito, Joanne M., Boerwinkle, Eric, Ebert, Benjamin L., Jaiswal, Siddhartha, Floyd, James S., Bick, Alexander G., Ballantyne, Christie M., Psaty, Bruce M., Natarajan, Pradeep, Conneely, Karen N.

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Methylome-wide association study provides evidence of particulate matter air pollution-associated DNA methylation von Gondalia, Rahul, Baldassari, Antoine, Holliday, Katelyn M., Justice, Anne E., Méndez-Giráldez, Raúl, Stewart, James D., Liao, Duanping, Yanosky, Jeff D., Brennan, Kasey J.M., Engel, Stephanie M., Jordahl, Kristina M., Kennedy, Elizabeth, Ward-Caviness, Cavin K., Wolf, Kathrin, Waldenberger, Melanie, Cyrys, Josef, Peters, Annette, Bhatti, Parveen, Horvath, Steve, Assimes, Themistocles L., Pankow, James S., Demerath, Ellen W., Guan, Weihua, Fornage, Myriam, Bressler, Jan, North, Kari E., Conneely, Karen N., Li, Yun, Hou, Lifang, Baccarelli, Andrea A., Whitsel, Eric A.

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Best practices and joint calling of the HumanExome BeadChip: the CHARGE Consortium von Grove, Megan L, Yu, Bing, Cochran, Barbara J, Haritunians, Talin, Bis, Joshua C, Taylor, Kent D, Hansen, Mark, Borecki, Ingrid B, Cupples, L Adrienne, Fornage, Myriam, Gudnason, Vilmundur, Harris, Tamara B, Kathiresan, Sekar, Kraaij, Robert, Launer, Lenore J, Levy, Daniel, Liu, Yongmei, Mosley, Thomas, Peloso, Gina M, Psaty, Bruce M, Rich, Stephen S, Rivadeneira, Fernando, Siscovick, David S, Smith, Albert V, Uitterlinden, Andre, van Duijn, Cornelia M, Wilson, James G, O'Donnell, Christopher J, Rotter, Jerome I, Boerwinkle, Eric

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Mitochondrial DNA copy number can influence mortality and cardiovascular disease via methylation of nuclear DNA CpGs von Castellani, Christina A., Longchamps, Ryan J., Sumpter, Jason A., Newcomb, Charles E., Lane, John A., Grove, Megan L., Bressler, Jan, Brody, Jennifer A., Floyd, James S., Bartz, Traci M., Taylor, Kent D., Wang, Penglong, Tin, Adrienne, Coresh, Josef, Pankow, James S., Fornage, Myriam, Guallar, Eliseo, O'Rourke, Brian, Pankratz, Nathan, Liu, Chunyu, Levy, Daniel, Sotoodehnia, Nona, Boerwinkle, Eric, Arking, Dan E.

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Identification of novel susceptibility methylation loci for pancreatic cancer in a two-phase epigenome-wide association study von Wang, Ziqiao, Lu, Yue, Fornage, Myriam, Jiao, Li, Shen, Jianjun, Li, Donghui, Wei, Peng

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Mutation of FOXC1 and PITX2 induces cerebral small-vessel disease von French, Curtis R, Seshadri, Sudha, Destefano, Anita L, Fornage, Myriam, Arnold, Corey R, Gage, Philip J, Skarie, Jonathan M, Dobyns, William B, Millen, Kathleen J, Liu, Ting, Dietz, William, Kume, Tsutomu, Hofker, Marten, Emery, Derek J, Childs, Sarah J, Waskiewicz, Andrew J, Lehmann, Ordan J

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Coronary heart disease and ischemic stroke polygenic risk scores and atherosclerotic cardiovascular disease in a diverse, population-based cohort study von Bebo, Allison, Jarmul, Jamie A, Pletcher, Mark J, Hasbani, Natalie R, Couper, David, Nambi, Vijay, Ballantyne, Christie M, Fornage, Myriam, Morrison, Alanna C, Avery, Christy L, de Vries, Paul S

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Interaction analysis of ancestry-enriched variants with APOE-ɛ4 on MCI in the Study of Latinos-Investigation of Neurocognitive Aging von Granot-Hershkovitz, Einat, Xia, Rui, Yang, Yunju, Spitzer, Brian, Tarraf, Wassim, Vásquez, Priscilla M., Lipton, Richard B., Daviglus, Martha, Argos, Maria, Cai, Jianwen, Kaplan, Robert, Fornage, Myriam, DeCarli, Charles, Gonzalez, Hector M., Sofer, Tamar

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Genome-wide association study of plasma N6 polyunsaturated fatty acids within the cohorts for heart and aging research in genomic epidemiology consortium von Guan, Weihua, Steffen, Brian T, Lemaitre, Rozenn N, Wu, Jason H Y, Tanaka, Toshiko, Manichaikul, Ani, Foy, Millennia, Rich, Stephen S, Wang, Lu, Nettleton, Jennifer A, Tang, Weihong, Gu, Xiangjun, Bandinelli, Stafania, King, Irena B, McKnight, Barbara, Psaty, Bruce M, Siscovick, David, Djousse, Luc, Chen, Yii-Der Ida, Ferrucci, Luigi, Fornage, Myriam, Mozafarrian, Dariush, Tsai, Michael Y, Steffen, Lyn M

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Genetic risk factors underlying white matter hyperintensities and cortical atrophy von Patel, Yash, Shin, Jean, Sliz, Eeva, Tang, Ariana, Mishra, Aniket, Xia, Rui, Hofer, Edith, Rajula, Hema Sekhar Reddy, Wang, Ruiqi, Beyer, Frauke, Horn, Katrin, Riedl, Max, Yu, Jing, Völzke, Henry, Bülow, Robin, Völker, Uwe, Frenzel, Stefan, Wittfeld, Katharina, Van der Auwera, Sandra, Mosley, Thomas H., Bouteloup, Vincent, Lambert, Jean-Charles, Chêne, Geneviève, Dufouil, Carole, Tzourio, Christophe, Mangin, Jean-François, Gottesman, Rebecca F., Fornage, Myriam, Schmidt, Reinhold, Yang, Qiong, Witte, Veronica, Scholz, Markus, Loeffler, Markus, Roshchupkin, Gennady V., Ikram, M. Arfan, Grabe, Hans J., Seshadri, Sudha, Debette, Stephanie, Paus, Tomas, Pausova, Zdenka

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Longitudinal change in blood DNA epigenetic signature after smoking cessation von Keshawarz, Amena, Joehanes, Roby, Guan, Weihua, Huan, Tianxiao, DeMeo, Dawn L., Grove, Megan L., Fornage, Myriam, Levy, Daniel, O'Connor, George

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Association of blood pressure with cognitive function at midlife: a Mendelian randomization study von Sun, Daokun, Thomas, Emy A., Launer, Lenore J., Sidney, Stephen, Yaffe, Kristine, Fornage, Myriam

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Exosome miR-371b-5p promotes proliferation of lung alveolar progenitor type II cells by using PTEN to orchestrate the PI3K/Akt signaling von Quan, Yuan, Wang, Zhaohua, Gong, Ling, Peng, Xinmiao, Richard, Melissa A, Zhang, Junlan, Fornage, Myriam, Alcorn, Joseph L, Wang, Dachun

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Whole exome sequence-based association analyses of plasma amyloid-β in African and European Americans; the Atherosclerosis Risk in Communities-Neurocognitive Study von Simino, Jeannette, Wang, Zhiying, Bressler, Jan, Chouraki, Vincent, Yang, Qiong, Younkin, Steven G, Seshadri, Sudha, Fornage, Myriam, Boerwinkle, Eric, Mosley, Jr, Thomas H

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Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics von Hodonsky, Chani J., Baldassari, Antoine R., Bien, Stephanie A., Raffield, Laura M., Highland, Heather M., Sitlani, Colleen M., Wojcik, Genevieve L., Tao, Ran, Graff, Marielisa, Tang, Weihong, Thyagarajan, Bharat, Buyske, Steve, Fornage, Myriam, Hindorff, Lucia A., Li, Yun, Lin, Danyu, Reiner, Alex P., North, Kari E., Loos, Ruth J. F., Kooperberg, Charles, Avery, Christy L.

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