Neonatal hyperoxia depletes pulmonary vein cardiomyocytes in adult mice via mitochondrial oxidation von Yee, Min, Cohen, Ethan David, Domm, William, Porter, Jr, George A, McDavid, Andrew N, O'Reilly, Michael A

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Neonatal hyperoxia inhibits proliferation and survival of atrial cardiomyocytes by suppressing fatty acid synthesis von Cohen, Ethan David, Yee, Min, Porter, George A., Ritzer, Erin, McDavid, Andrew N., Brookes, Paul S., Pryhuber, Gloria S., O'Reilly, Michael A.

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Quality Control Procedures for Genome‐Wide Association Studies von Turner, Stephen, Armstrong, Loren L., Bradford, Yuki, Carlson, Christopher S., Crawford, Dana C., Crenshaw, Andrew T., Andrade, Mariza, Doheny, Kimberly F., Haines, Jonathan L., Hayes, Geoffrey, Jarvik, Gail, Jiang, Lan, Kullo, Iftikhar J., Li, Rongling, Ling, Hua, Manolio, Teri A., Matsumoto, Martha, McCarty, Catherine A., McDavid, Andrew N., Mirel, Daniel B., Paschall, Justin E., Pugh, Elizabeth W., Rasmussen, Luke V., Wilke, Russell A., Zuvich, Rebecca L., Ritchie, Marylyn D.

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T Cell–Dependent Affinity Maturation and Innate Immune Pathways Differentially Drive Autoreactive B Cell Responses in Rheumatoid Arthritis von Lu, Daniel R., McDavid, Andrew N., Kongpachith, Sarah, Lingampalli, Nithya, Glanville, Jacob, Ju, Chia‐Hsin, Gottardo, Raphael, Robinson, William H.

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Intrinsic mitotic activity supports the human salivary gland acinar cell population von Ingalls, Matthew H., Hollomon, Andrew J., Newlands, Shawn D., McDavid, Andrew N., Ovitt, Catherine E.

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Neonatal Hyperoxia Activates Activating Transcription Factor 4 to Stimulate Folate Metabolism and Alveolar Epithelial Type 2 Cell Proliferation von Yee, Min, McDavid, Andrew N, Cohen, Ethan David, Huyck, Heidie L, Poole, Cory, Altman, Brian J, Maniscalco, William M, Deutsch, Gail H, Pryhuber, Gloria S, O'Reilly, Michael A

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Single-Cell Transcriptomic Profiling Identifies Molecular Phenotypes of Newborn Human Lung Cells von Bhattacharya, Soumyaroop, Myers, Jacquelyn A, Baker, Cameron, Guo, Minzhe, Danopoulos, Soula, Myers, Jason R, Bandyopadhyay, Gautam, Romas, Stephen T, Huyck, Heidie L, Misra, Ravi S, Dutra, Jennifer, Holden-Wiltse, Jeanne, McDavid, Andrew N, Ashton, John M, Al Alam, Denise, Potter, S Steven, Whitsett, Jeffrey A, Xu, Yan, Pryhuber, Gloria S, Mariani, Thomas J

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Pitfalls of merging GWAS data: lessons learned in the eMERGE network and quality control procedures to maintain high data quality von Zuvich, Rebecca L., Armstrong, Loren L., Bielinski, Suzette J., Bradford, Yuki, Carlson, Christopher S., Crawford, Dana C., Crenshaw, Andrew T., de Andrade, Mariza, Doheny, Kimberly F., Haines, Jonathan L., Hayes, M. Geoffrey, Jarvik, Gail P., Jiang, Lan, Kullo, Iftikhar J., Li, Rongling, Ling, Hua, Manolio, Teri A., Matsumoto, Martha E., McCarty, Catherine A., McDavid, Andrew N., Mirel, Daniel B., Olson, Lana M., Paschall, Justin E., Pugh, Elizabeth W., Rasmussen, Luke V., Rasmussen-Torvik, Laura J., Turner, Stephen D., Wilke, Russell A., Ritchie, Marylyn D.

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Efficient identification of rare variants in large populations: deep re-sequencing the CRP locus in the CARDIA study von Chen, Christina T L, McDavid, Andrew N, Kahsai, Orsalem J, Zebari, Ahmad S, Carlson, Christopher S

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Exceptionally low likelihood of Alzheimer’s dementia in APOE2 homozygotes from a 5,000-person neuropathological study von Reiman, Eric M., Arboleda-Velasquez, Joseph F., Quiroz, Yakeel T., Huentelman, Matthew J., Beach, Thomas G., Caselli, Richard J., Chen, Yinghua, Su, Yi, Myers, Amanda J., Hardy, John, Paul Vonsattel, Jean, Younkin, Steven G., Bennett, David A., De Jager, Philip L., Larson, Eric B., Crane, Paul K., Keene, C. Dirk, Kamboh, M. Ilyas, Kofler, Julia K., Duque, Linda, Gilbert, John R., Gwirtsman, Harry E., Buxbaum, Joseph D., Dickson, Dennis W., Frosch, Matthew P., Ghetti, Bernardino F., Lunetta, Kathryn L., Wang, Li-San, Hyman, Bradley T., Kukull, Walter A., Foroud, Tatiana, Haines, Jonathan L., Mayeux, Richard P., Pericak-Vance, Margaret A., Schneider, Julie A., Trojanowski, John Q., Farrer, Lindsay A., Schellenberg, Gerard D., Beecham, Gary W., Montine, Thomas J., Jun, Gyungah R.

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Novel Alzheimer Disease Risk Loci and Pathways in African American Individuals Using the African Genome Resources Panel: A Meta-analysis von Kunkle, Brian W, Schmidt, Michael, Klein, Hans-Ulrich, Naj, Adam C, Hamilton-Nelson, Kara L, Larson, Eric B, Evans, Denis A, De Jager, Phil L, Crane, Paul K, Buxbaum, Joe D, Ertekin-Taner, Nilufer, Barnes, Lisa L, Fallin, M. Daniele, Manly, Jennifer J, Go, Rodney C. P, Obisesan, Thomas O, Kamboh, M. Ilyas, Bennett, David A, Hall, Kathleen S, Goate, Alison M, Foroud, Tatiana M, Martin, Eden R, Wang, Li-San, Byrd, Goldie S, Farrer, Lindsay A, Haines, Jonathan L, Schellenberg, Gerard D, Mayeux, Richard, Pericak-Vance, Margaret A, Reitz, Christiane, Graff-Radford, Neill R, Martinez, Izri, Ayodele, Temitope, Logue, Mark W, Cantwell, Laura B, Jean-Francois, Melissa, Kuzma, Amanda B, Adams, L.D, Vance, Jeffery M, Cuccaro, Michael L, Chung, Jaeyoon, Mez, Jesse, Lunetta, Kathryn L, Jun, Gyungah R, Lopez, Oscar L, Hendrie, Hugh C, Reiman, Eric M, Kowall, Neil W, Leverenz, James B, Small, Scott A, Levey, Allan I, Golde, Todd E, Saykin, Andrew J, Starks, Takiyah D, Albert, Marilyn S, Hyman, Bradley T, Petersen, Ronald C, Sano, Mary, Wisniewski, Thomas, Vassar, Robert, Kaye, Jeffrey A, Henderson, Victor W, DeCarli, Charles, LaFerla, Frank M, Brewer, James B, Miller, Bruce L, Swerdlow, Russell H, Van Eldik, Linda J, Paulson, Henry L, Trojanowski, John Q, Chui, Helena C, Rosenberg, Roger N, Craft, Suzanne, Grabowski, Thomas J, Asthana, Sanjay, Morris, John C, Strittmatter, Stephen M, Kukull, Walter A

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Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease von Naj, Adam C, Jun, Gyungah, Beecham, Gary W, Wang, Li-San, Vardarajan, Badri Narayan, Buros, Jacqueline, Gallins, Paul J, Buxbaum, Joseph D, Crane, Paul K, Larson, Eric B, Bird, Thomas D, De Jager, Philip L, Schneider, Julie A, Younkin, Steven G, Cruchaga, Carlos, Kauwe, John S K, Nowotny, Petra, Hardy, John, Myers, Amanda J, Barmada, Michael M, Baldwin, Clinton T, Arnold, Steven E, Barber, Robert, Beach, Thomas, Bowen, James D, Boxer, Adam, Carlson, Chris S, Carney, Regina M, Carroll, Steven L, Clark, David G, Cummings, Jeffrey L, DeKosky, Steven T, Diaz-Arrastia, Ramon, Dickson, Dennis W, Faber, Kelley M, Fallon, Kenneth B, Farlow, Martin R, Ferris, Steven, Ganguli, Mary, Gearing, Marla, Ghetti, Bernardino, Gilbert, John R, Gilman, Sid, Glass, Jonathan D, Growdon, John H, Hamilton, Ronald L, Harrell, Lindy E, Head, Elizabeth, Honig, Lawrence S, Hulette, Christine M, Johnson, Nancy, Karydas, Anna, Kaye, Jeffrey A, Kim, Ronald, Lah, James J, Levey, Allan I, Lieberman, Andrew P, Mack, Wendy J, Marson, Daniel C, Martiniuk, Frank, Mash, Deborah C, McDavid, Andrew N, McKee, Ann C, Mesulam, Marsel, Miller, Bruce L, Miller, Carol A, Parisi, Joseph E, Perl, Daniel P, Peskind, Elaine, Rajbhandary, Ruchita A, Reisberg, Barry, Ringman, John M, Roberson, Erik D, Rosenberg, Roger N, Sano, Mary, Seeley, William, Shelanski, Michael L, Slifer, Michael A, Smith, Charles D, Sonnen, Joshua A, Spina, Salvatore, Tanzi, Rudolph E, Troncoso, Juan C, Weintraub, Sandra, Welsh-Bohmer, Kathleen A, Woltjer, Randall L, Cantwell, Laura B, Lunetta, Kathryn L, Kamboh, M Ilyas, Saykin, Andrew J, Reiman, Eric M, Morris, John C, Goate, Alison M, Blacker, Deborah, Tsuang, Debby W, Hakonarson, Hakon, Kukull, Walter A, Haines, Jonathan L, Pericak-Vance, Margaret A, Farrer, Lindsay A

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A novel Alzheimer disease locus located near the gene encoding tau protein von Jun, G, Ibrahim-Verbaas, C A, Vronskaya, M, Chung, J, Naj, A C, Kunkle, B W, Wang, L-S, Bis, J C, Bellenguez, C, Harold, D, Destefano, A L, Grenier-Boley, B, Sims, R, Smith, A V, Chouraki, V, Hamilton-Nelson, K L, Ikram, M A, Fievet, N, Martin, E R, Kamatani, Y, Valladares, O, Laza, A R, Zelenika, D, Choi, S-H, Boland, A, Becker, T, Kukull, W A, van der Lee, S J, Pasquier, F, Cruchaga, C, Beekly, D, Fitzpatrick, A L, Hanon, O, Gill, M, Gudnason, V, Campion, D, Love, S, Bennett, D A, Amin, N, Berr, C, Tsolaki, Magda, Buxbaum, J D, Lopez, O L, Deramecourt, V, Fox, N C, Cantwell, L B, Tárraga, L, Dufouil, C, Hardy, J, Crane, P K, Eiriksdottir, G, Hannequin, D, Clarke, R, Evans, D, Mosley, T H, Letenneur, L, Brayne, C, Maier, W, De Jager, P, Dartigues, J-F, Hampel, H, de Bruijn, R F A G, Tzourio, C, Pastor, P, Larson, E B, O'Donovan, M C, Montine, T J, Nalls, M A, Mead, S, Reiman, E M, Jonsson, P V, St George-Hyslop, P H, Boada, M, Passmore, P, Wendland, J R, Schmidt, R, Morgan, K, Powell, J F, Carasquillo, M, Jakobsdóttir, J, Kauwe, J S K, Rujescu, D, Nöthen, M M, Hofman, A, Jones, L, Haines, J L, Psaty, B M, Van Broeckhoven, C, Holmans, P, Launer, L J, Mayeux, R, Goate, A M, Escott-Price, V, Seshadri, S, Pericak-Vance, M A, Amouyel, P, Williams, J, van Duijn, C M, Schellenberg, G D, Farrer, L A

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Detectable clonal mosaicism from birth to old age and its relationship to cancer von Laurie, Cathy C, Laurie, Cecelia A, Rice, Kenneth, Doheny, Kimberly F, Zelnick, Leila R, McHugh, Caitlin P, Ling, Hua, Hetrick, Kurt N, Pugh, Elizabeth W, Amos, Chris, Wei, Qingyi, Wang, Li-e, Lee, Jeffrey E, Barnes, Kathleen C, Hansel, Nadia N, Mathias, Rasika, Daley, Denise, Beaty, Terri H, Scott, Alan F, Ruczinski, Ingo, Scharpf, Rob B, Bierut, Laura J, Hartz, Sarah M, Landi, Maria Teresa, Freedman, Neal D, Goldin, Lynn R, Ginsburg, David, Li, Jun, Desch, Karl C, Strom, Sara S, Blot, William J, Signorello, Lisa B, Ingles, Sue A, Chanock, Stephen J, Berndt, Sonja I, Le Marchand, Loic, Henderson, Brian E, Monroe, Kristine R, Heit, John A, de Andrade, Mariza, Armasu, Sebastian M, Regnier, Cynthia, Lowe, William L, Hayes, M Geoffrey, Marazita, Mary L, Feingold, Eleanor, Murray, Jeffrey C, Melbye, Mads, Feenstra, Bjarke, Kang, Jae H, Wiggs, Janey L, Jarvik, Gail P, McDavid, Andrew N, Seshan, Venkatraman E, Mirel, Daniel B, Crenshaw, Andrew, Sharopova, Nataliya, Wise, Anastasia, Shen, Jess, Crosslin, David R, Levine, David M, Zheng, Xiuwen, Udren, Jenna I, Bennett, Siiri, Nelson, Sarah C, Gogarten, Stephanie M, Conomos, Matthew P, Heagerty, Patrick, Manolio, Teri, Pasquale, Louis R, Haiman, Christopher A, Caporaso, Neil, Weir, Bruce S

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Variants in the ATP-Binding Cassette Transporter (ABCA7), Apolipoprotein E ϵ4,and the Risk of Late-Onset Alzheimer Disease in African Americans von Reitz, Christiane, Jun, Gyungah, Naj, Adam, Rajbhandary, Ruchita, Vardarajan, Badri Narayan, Wang, Li-San, Valladares, Otto, Lin, Chiao-Feng, Larson, Eric B, Graff-Radford, Neill R, Evans, Denis, De Jager, Philip L, Crane, Paul K, Buxbaum, Joseph D, Murrell, Jill R, Raj, Towfique, Ertekin-Taner, Nilufer, Logue, Mark, Baldwin, Clinton T, Green, Robert C, Barnes, Lisa L, Cantwell, Laura B, Fallin, M. Daniele, Go, Rodney C. P, Griffith, Patrick, Obisesan, Thomas O, Manly, Jennifer J, Lunetta, Kathryn L, Kamboh, M. Ilyas, Lopez, Oscar L, Bennett, David A, Hendrie, Hugh, Hall, Kathleen S, Goate, Alison M, Byrd, Goldie S, Kukull, Walter A, Foroud, Tatiana M, Haines, Jonathan L, Farrer, Lindsay A, Pericak-Vance, Margaret A, Schellenberg, Gerard D, Mayeux, Richard

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Transethnic genome-wide scan identifies novel Alzheimer's disease loci von Jun, Gyungah R, Chung, Jaeyoon, Mez, Jesse, Barber, Robert, Beecham, Gary W, Bennett, David A, Buxbaum, Joseph D, Byrd, Goldie S, Carrasquillo, Minerva M, Crane, Paul K, Cruchaga, Carlos, De Jager, Philip, Ertekin-Taner, Nilufer, Evans, Denis, Fallin, M. Danielle, Foroud, Tatiana M, Friedland, Robert P, Goate, Alison M, Graff-Radford, Neill R, Hendrie, Hugh, Hall, Kathleen S, Hamilton-Nelson, Kara L, Inzelberg, Rivka, Kamboh, M. Ilyas, Kauwe, John S.K, Kukull, Walter A, Kunkle, Brian W, Kuwano, Ryozo, Larson, Eric B, Logue, Mark W, Manly, Jennifer J, Martin, Eden R, Montine, Thomas J, Mukherjee, Shubhabrata, Naj, Adam, Reiman, Eric M, Reitz, Christiane, Sherva, Richard, St. George-Hyslop, Peter H, Thornton, Timothy, Younkin, Steven G, Vardarajan, Badri N, Wang, Li-San, Wendlund, Jens R, Winslow, Ashley R, Haines, Jonathan, Mayeux, Richard, Pericak-Vance, Margaret A, Schellenberg, Gerard, Lunetta, Kathryn L, Farrer, Lindsay A

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Effects of Multiple Genetic Loci on Age at Onset in Late-Onset Alzheimer Disease: A Genome-Wide Association Study von Naj, Adam C, Jun, Gyungah, Reitz, Christiane, Kunkle, Brian W, Perry, William, Park, Yo Son, Beecham, Gary W, Rajbhandary, Ruchita A, Hamilton-Nelson, Kara L, Wang, Li-San, Kauwe, John S. K, Huentelman, Matthew J, Myers, Amanda J, Bird, Thomas D, Boeve, Bradley F, Baldwin, Clinton T, Jarvik, Gail P, Crane, Paul K, Rogaeva, Ekaterina, Barmada, M. Michael, Demirci, F. Yesim, Cruchaga, Carlos, Kramer, Patricia L, Ertekin-Taner, Nilufer, Hardy, John, Graff-Radford, Neill R, Green, Robert C, Larson, Eric B, St. George-Hyslop, Peter H, Buxbaum, Joseph D, Evans, Denis A, Schneider, Julie A, Lunetta, Kathryn L, Kamboh, M. Ilyas, Saykin, Andrew J, Reiman, Eric M, De Jager, Philip L, Bennett, David A, Morris, John C, Montine, Thomas J, Goate, Alison M, Blacker, Deborah, Tsuang, Debby W, Hakonarson, Hakon, Kukull, Walter A, Foroud, Tatiana M, Martin, Eden R, Haines, Jonathan L, Mayeux, Richard P, Farrer, Lindsay A, Schellenberg, Gerard D, Pericak-Vance, Margaret A

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Brain expression genome-wide association study (eGWAS) identifies human disease-associated variants von Zou, Fanggeng, Chai, High Seng, Younkin, Curtis S, Allen, Mariet, Crook, Julia, Pankratz, V Shane, Carrasquillo, Minerva M, Rowley, Christopher N, Nair, Asha A, Middha, Sumit, Maharjan, Sooraj, Nguyen, Thuy, Ma, Li, Malphrus, Kimberly G, Palusak, Ryan, Lincoln, Sarah, Bisceglio, Gina, Georgescu, Constantin, Kouri, Naomi, Kolbert, Christopher P, Jen, Jin, Haines, Jonathan L, Mayeux, Richard, Pericak-Vance, Margaret A, Farrer, Lindsay A, Schellenberg, Gerard D, Petersen, Ronald C, Graff-Radford, Neill R, Dickson, Dennis W, Younkin, Steven G, Ertekin-Taner, Nilüfer

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Novel late-onset Alzheimer disease loci variants associate with brain gene expression von ALLEN, Mariet, FANGGENG ZOU, MAHARJAN, Sooraj, NGUYEN, Thuy, LI MA, MALPHRUS, Kimberly G, PALUSAK, Ryan, LINCOLN, Sarah, BISCEGLIO, Gina, GEORGESCU, Constantin, SCHULTZ, Debra, RAKHSHAN, Fariborz, SENG CHAI, High, KOLBERT, Christopher P, JIN JEN, HAINES, Jonathan L, MAYEUX, Richard, PERICAK-VANCE, Margaret A, FARRER, Lindsay A, SCHELLENBERG, Gerard D, DISEASE, Alzheimer's, CONSORTIUM, Genetics, PETERSEN, Ronald C, YOUNKIN, Curtis S, GRAFF-RADFORD, Neill R, DICKSON, Dennis W, YOUNKIN, Steven G, ERTEKIN-TANER, Niliifer, CROOK, Julia, SHANE PANKRATZ, V, CARRASQUILLO, Minerva M, ROWLEY, Christopher N, NAIR, Asha A, MIDDHA, Sumit

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Manifestations of Alzheimer’s disease genetic risk in the blood are evident in a multiomic analysis in healthy adults aged 18 to 90 von Heath, Laura, Earls, John C., Magis, Andrew T., Kornilov, Sergey A., Lovejoy, Jennifer C., Funk, Cory C., Rappaport, Noa, Logsdon, Benjamin A., Mangravite, Lara M., Kunkle, Brian W., Martin, Eden R., Naj, Adam C., Ertekin-Taner, Nilüfer, Golde, Todd E., Hood, Leroy, Price, Nathan D.

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