Development and Validation of a Highly Sensitive e1a2 (p190) BCR-ABL Test to Determine Complete Molecular Response (Minimal Residual Disease Negative) As a Primary Endpoint for Pat... von Drafahl, Kristy, Smith, David C, Graham, Cristen, Glynn, Christine, Spittle, Cindy, Verrow, Scott, Rivera, Victor M., Srivastava, Shouryadeep, Hawkins, Kevin, Galderisi, Chad

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Discovery and prioritization of variants and genes for kidney function in >1.2 million individuals von Stanzick, Kira J., Li, Yong, Schlosser, Pascal, Gorski, Mathias, Wuttke, Matthias, Thomas, Laurent F., Rasheed, Humaira, Rowan, Bryce X., Graham, Sarah E., Vanderweff, Brett R., Patil, Snehal B., Robinson-Cohen, Cassiane, Gaziano, John M., O’Donnell, Christopher J., Willer, Cristen J., Hallan, Stein, Åsvold, Bjørn Olav, Gessner, Andre, Hung, Adriana M., Pattaro, Cristian, Köttgen, Anna, Stark, Klaus J., Heid, Iris M., Winkler, Thomas W.

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Causal relationships between NAFLD, T2D and obesity have implications for disease subphenotyping von Liu, Zhipeng, Zhang, Yang, Graham, Sarah, Wang, Xiaokun, Cai, Defeng, Huang, Menghao, Pique-Regi, Roger, Dong, Xiaocheng Charlie, Chen, Y. Eugene, Willer, Cristen, Liu, Wanqing

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Identification of cell type specific ACE2 modifiers by CRISPR screening von Sherman, Emily J, Mirabelli, Carmen, Tang, Vi T, Khan, Taslima G, Leix, Kyle, Kennedy, Andrew A, Graham, Sarah E, Willer, Cristen J, Tai, Andrew W, Sexton, Jonathan Z, Wobus, Christiane E, Emmer, Brian T

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Genome-scale CRISPR screening for modifiers of cellular LDL uptake von Emmer, Brian T, Sherman, Emily J, Lascuna, Paul J, Graham, Sarah E, Willer, Cristen J, Ginsburg, David

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Sex-specific and pleiotropic effects underlying kidney function identified from GWAS meta-analysis von Graham, Sarah E., Nielsen, Jonas B., Zawistowski, Matthew, Zhou, Wei, Fritsche, Lars G., Gabrielsen, Maiken E., Skogholt, Anne Heidi, Surakka, Ida, Hornsby, Whitney E., Fermin, Damian, Larach, Daniel B., Kheterpal, Sachin, Brummett, Chad M., Lee, Seunggeun, Kang, Hyun Min, Abecasis, Goncalo R., Romundstad, Solfrid, Hallan, Stein, Sampson, Matthew G., Hveem, Kristian, Willer, Cristen J.

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Exposure and risk factors for COVID-19 and the impact of staying home on Michigan residents von Wu, Kuan-Han H, Hornsby, Whitney E, Klunder, Bethany, Krause, Amelia, Driscoll, Anisa, Kulka, John, Bickett-Hickok, Ryan, Fellows, Austin, Graham, Sarah, Kaleba, Erin O, Hayek, Salim S, Shi, Xu, Sutton, Nadia R, Douville, Nicholas, Mukherjee, Bhramar, Jamerson, Kenneth, Brummett, Chad M, Willer, Cristen J

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Meta-analysis of sub-Saharan African studies provides insights into genetic architecture of lipid traits von Choudhury, Ananyo, Brandenburg, Jean-Tristan, Chikowore, Tinashe, Sengupta, Dhriti, Boua, Palwende Romuald, Crowther, Nigel J., Agongo, Godfred, Asiki, Gershim, Gómez-Olivé, F. Xavier, Kisiangani, Isaac, Maimela, Eric, Masemola-Maphutha, Matshane, Micklesfield, Lisa K., Nonterah, Engelbert A., Norris, Shane A., Sorgho, Hermann, Tinto, Halidou, Tollman, Stephen, Graham, Sarah E., Willer, Cristen J., Hazelhurst, Scott, Ramsay, Michèle

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Aortic progression and reintervention in patients with pathogenic variants after a thoracic aortic dissection von Norton, Elizabeth L., Hornsby, Whitney E., Wu, Xiaoting, Wolford, Brooke N., Graham, Sarah E., Willer, Cristen J., Yang, Bo

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Author Correction: Meta-analysis of sub-Saharan African studies provides insights into genetic architecture of lipid traits von Choudhury, Ananyo, Brandenburg, Jean-Tristan, Chikowore, Tinashe, Sengupta, Dhriti, Boua, Palwende Romuald, Crowther, Nigel J., Agongo, Godfred, Asiki, Gershim, Gómez-Olivé, F. Xavier, Kisiangani, Isaac, Maimela, Eric, Masemola-Maphutha, Matshane, Micklesfield, Lisa K., Nonterah, Engelbert A., Norris, Shane A., Sorgho, Hermann, Tinto, Halidou, Tollman, Stephen, Graham, Sarah E., Willer, Cristen J., Hazelhurst, Scott, Ramsay, Michèle

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Regulatory variants in TCF7L2 are associated with thoracic aortic aneurysm von Roychowdhury, Tanmoy, Lu, Haocheng, Hornsby, Whitney E., Crone, Bradley, Wang, Gao T., Guo, Dong-chuan, Sendamarai, Anoop K., Devineni, Poornima, Lin, Maoxuan, Zhou, Wei, Graham, Sarah E., Wolford, Brooke N., Surakka, Ida, Wang, Zhenguo, Chang, Lin, Zhang, Jifeng, Mathis, Michael, Brummett, Chad M., Melendez, Tori L., Shea, Michael J., Kim, Karen Meekyong, Deeb, G. Michael, Patel, Himanshu J., Eliason, Jonathan, Eagle, Kim A., Yang, Bo, Ganesh, Santhi K., Brumpton, Ben, Åsvold, Bjørn Olav, Skogholt, Anne Heidi, Hveem, Kristian, Pyarajan, Saiju, Klarin, Derek, Tsao, Philip S., Damrauer, Scott M., Leal, Suzanne M., Milewicz, Dianna M., Chen, Y. Eugene, Garcia-Barrio, Minerva T., Willer, Cristen J.

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Biobank-driven genomic discovery yields new insight into atrial fibrillation biology von Nielsen, Jonas B., Thorolfsdottir, Rosa B., Fritsche, Lars G., Zhou, Wei, Skov, Morten W., Graham, Sarah E., Herron, Todd J., McCarthy, Shane, Schmidt, Ellen M., Sveinbjornsson, Gardar, Surakka, Ida, Mathis, Michael R., Yamazaki, Masatoshi, Crawford, Ryan D., Gabrielsen, Maiken E., Skogholt, Anne Heidi, Holmen, Oddgeir L., Lin, Maoxuan, Wolford, Brooke N., Dey, Rounak, Dalen, Håvard, Sulem, Patrick, Chung, Jonathan H., Backman, Joshua D., Arnar, David O., Thorsteinsdottir, Unnur, Baras, Aris, O’Dushlaine, Colm, Holst, Anders G., Wen, Xiaoquan, Hornsby, Whitney, Dewey, Frederick E., Boehnke, Michael, Kheterpal, Sachin, Mukherjee, Bhramar, Lee, Seunggeun, Kang, Hyun M., Holm, Hilma, Kitzman, Jacob, Shavit, Jordan A., Jalife, José, Brummett, Chad M., Teslovich, Tanya M., Carey, David J., Gudbjartsson, Daniel F., Stefansson, Kari, Abecasis, Gonçalo R., Hveem, Kristian, Willer, Cristen J.

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Genome-wide association study of thoracic aortic aneurysm and dissection in the Million Veteran Program von Klarin, Derek, Devineni, Poornima, Sendamarai, Anoop K., Angueira, Anthony R., Graham, Sarah E., Shen, Ying H., Levin, Michael G., Pirruccello, James P., Surakka, Ida, Karnam, Purushotham R., Roychowdhury, Tanmoy, Li, Yanming, Wang, Minxian, Aragam, Krishna G., Paruchuri, Kaavya, Zuber, Verena, Shakt, Gabrielle E., Tsao, Noah L., Judy, Renae L., Vy, Ha My T., Verma, Shefali S., Rader, Daniel J., Do, Ron, Bavaria, Joseph E., Nadkarni, Girish N., Ritchie, Marylyn D., Burgess, Stephen, Guo, Dong-chuan, Ellinor, Patrick T., LeMaire, Scott A., Milewicz, Dianna M., Willer, Cristen J., Natarajan, Pradeep, Tsao, Philip S., Pyarajan, Saiju, Damrauer, Scott M.

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Genome-wide Study of Atrial Fibrillation Identifies Seven Risk Loci and Highlights Biological Pathways and Regulatory Elements Involved in Cardiac Development von Nielsen, Jonas B., Fritsche, Lars G., Zhou, Wei, Teslovich, Tanya M., Holmen, Oddgeir L., Gustafsson, Stefan, Gabrielsen, Maiken E., Schmidt, Ellen M., Beaumont, Robin, Wolford, Brooke N., Lin, Maoxuan, Brummett, Chad M., Preuss, Michael H., Refsgaard, Lena, Bottinger, Erwin P., Graham, Sarah E., Surakka, Ida, Chu, Yunhan, Skogholt, Anne Heidi, Dalen, Håvard, Boyle, Alan P., Oral, Hakan, Herron, Todd J., Kitzman, Jacob, Jalife, José, Svendsen, Jesper H., Olesen, Morten S., Njølstad, Inger, Løchen, Maja-Lisa, Baras, Aris, Gottesman, Omri, Marcketta, Anthony, O’Dushlaine, Colm, Ritchie, Marylyn D., Wilsgaard, Tom, Loos, Ruth J.F., Frayling, Timothy M., Boehnke, Michael, Ingelsson, Erik, Carey, David J., Dewey, Frederick E., Kang, Hyun M., Abecasis, Gonçalo R., Hveem, Kristian, Willer, Cristen J.

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Genome-wide association study of cardiac troponin I in the general population von Moksnes, Marta R, Røsjø, Helge, Richmond, Anne, Lyngbakken, Magnus N, Graham, Sarah E, Hansen, Ailin Falkmo, Wolford, Brooke N, Gagliano Taliun, Sarah A, LeFaive, Jonathon, Rasheed, Humaira, Thomas, Laurent F, Zhou, Wei, Aung, Nay, Surakka, Ida, Douville, Nicholas J, Campbell, Archie, Porteous, David J, Petersen, Steffen E, Munroe, Patricia B, Welsh, Paul, Sattar, Naveed, Smith, George Davey, Fritsche, Lars G, Nielsen, Jonas B, Åsvold, Bjørn Olav, Hveem, Kristian, Hayward, Caroline, Willer, Cristen J, Brumpton, Ben M, Omland, Torbjørn

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Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction von Do, Ron, Stitziel, Nathan O., Won, Hong-Hee, Jørgensen, Anders Berg, Duga, Stefano, Angelica Merlini, Pier, Kiezun, Adam, Farrall, Martin, Goel, Anuj, Zuk, Or, Guella, Illaria, Asselta, Rosanna, Lange, Leslie A., Peloso, Gina M., Auer, Paul L., Girelli, Domenico, Martinelli, Nicola, Farlow, Deborah N., DePristo, Mark A., Roberts, Robert, Stewart, Alexander F. R., Saleheen, Danish, Danesh, John, Epstein, Stephen E., Sivapalaratnam, Suthesh, Kees Hovingh, G., Kastelein, John J., Samani, Nilesh J., Schunkert, Heribert, Erdmann, Jeanette, Shah, Svati H., Kraus, William E., Davies, Robert, Nikpay, Majid, Johansen, Christopher T., Wang, Jian, Hegele, Robert A., Hechter, Eliana, Marz, Winfried, Kleber, Marcus E., Huang, Jie, Johnson, Andrew D., Li, Mingyao, Burke, Greg L., Gross, Myron, Liu, Yongmei, Assimes, Themistocles L., Heiss, Gerardo, Lange, Ethan M., Folsom, Aaron R., Taylor, Herman A., Olivieri, Oliviero, Hamsten, Anders, Clarke, Robert, Reilly, Dermot F., Yin, Wu, Rivas, Manuel A., Donnelly, Peter, Rossouw, Jacques E., Psaty, Bruce M., Herrington, David M., Wilson, James G., Rich, Stephen S., Bamshad, Michael J., Tracy, Russell P., Adrienne Cupples, L., Rader, Daniel J., Reilly, Muredach P., Spertus, John A., Cresci, Sharon, Hartiala, Jaana, Wilson Tang, W. H., Hazen, Stanley L., Allayee, Hooman, Reiner, Alex P., Carlson, Christopher S., Kooperberg, Charles, Jackson, Rebecca D., Boerwinkle, Eric, Lander, Eric S., Schwartz, Stephen M., Siscovick, David S., McPherson, Ruth, Tybjaerg-Hansen, Anne, Abecasis, Goncalo R., Watkins, Hugh, Nickerson, Deborah A., Ardissino, Diego, Sunyaev, Shamil R., O'Donnell, Christopher J., Altshuler, David, Gabriel, Stacey, Kathiresan, Sekar

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GWAS of thyroid stimulating hormone highlights pleiotropic effects and inverse association with thyroid cancer von Zhou, Wei, Brumpton, Ben, Kabil, Omer, Gudmundsson, Julius, Thorleifsson, Gudmar, Weinstock, Josh, Zawistowski, Matthew, Nielsen, Jonas B., Chaker, Layal, Medici, Marco, Teumer, Alexander, Naitza, Silvia, Sanna, Serena, Schultheiss, Ulla T., Cappola, Anne, Karjalainen, Juha, Kurki, Mitja, Oneka, Morgan, Taylor, Peter, Fritsche, Lars G., Graham, Sarah E., Wolford, Brooke N., Overton, William, Rasheed, Humaira, Haug, Eirin B., Gabrielsen, Maiken E., Skogholt, Anne Heidi, Surakka, Ida, Davey Smith, George, Pandit, Anita, Roychowdhury, Tanmoy, Hornsby, Whitney E., Jonasson, Jon G., Senter, Leigha, Liyanarachchi, Sandya, Ringel, Matthew D., Xu, Li, Kiemeney, Lambertus A., He, Huiling, Netea-Maier, Romana T., Mayordomo, Jose I., Plantinga, Theo S., Hrafnkelsson, Jon, Hjartarson, Hannes, Sturgis, Erich M., Palotie, Aarno, Daly, Mark, Citterio, Cintia E., Arvan, Peter, Brummett, Chad M., Boehnke, Michael, de la Chapelle, Albert, Stefansson, Kari, Hveem, Kristian, Willer, Cristen J., Åsvold, Bjørn Olav

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Genome-wide meta-analysis of iron status biomarkers and the effect of iron on all-cause mortality in HUNT von Moksnes, Marta R., Graham, Sarah E., Wu, Kuan-Han, Hansen, Ailin Falkmo, Gagliano Taliun, Sarah A., Zhou, Wei, Thorstensen, Ketil, Fritsche, Lars G., Gill, Dipender, Mason, Amy, Cucca, Francesco, Schlessinger, David, Abecasis, Gonçalo R., Burgess, Stephen, Åsvold, Bjørn Olav, Nielsen, Jonas B., Hveem, Kristian, Willer, Cristen J., Brumpton, Ben M.

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A fast linkage method for population GWAS cohorts with related individuals von Zajac, Gregory J. M., Gagliano Taliun, Sarah A., Sidore, Carlo, Graham, Sarah E., Åsvold, Bjørn O., Brumpton, Ben, Nielsen, Jonas B., Zhou, Wei, Gabrielsen, Maiken, Skogholt, Anne H., Fritsche, Lars G., Schlessinger, David, Cucca, Francesco, Hveem, Kristian, Willer, Cristen J., Abecasis, Gonçalo R.

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Type 2 diabetes sex-specific effects associated with E167K coding variant in TM6SF2 von Fan, Yanbo, Wolford, Brooke N., Lu, Haocheng, Liang, Wenying, Sun, Jinjian, Zhou, Wei, Rom, Oren, Mahajan, Anubha, Surakka, Ida, Graham, Sarah E., Liu, Zhipeng, Kim, Hyunbae, Ramdas, Shweta, Fritsche, Lars G., Nielsen, Jonas B., Gabrielsen, Maiken Elvestad, Hveem, Kristian, Yang, Dongshan, Song, Jun, Garcia-Barrio, Minerva T., Zhang, Jifeng, Liu, Wanqing, Zhang, Kezhong, Willer, Cristen J., Chen, Y. Eugene

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