Methylation differences in Alzheimer's disease neuropathologic change in the aged human brain von Lang, Anna-Lena, Eulalio, Tiffany, Fox, Eddie, Yakabi, Koya, Bukhari, Syed A, Kawas, Claudia H, Corrada, Maria M, Montgomery, Stephen B, Heppner, Frank L, Capper, David, Nachun, Daniel, Montine, Thomas J

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The GTEx Consortium atlas of genetic regulatory effects across human tissues von Aguet, Francois, Barbeira, Alvaro N., Bonazzola, Rodrigo, Brown, Andrew, Castel, Stephane E., Jo, Brian, Kasela, Silva, Kim-Hellmuth, Sarah, Liang, Yanyu, Parsana, Princy, Flynn, Elise, Fresard, Laure, Gamazon, Eric R., Hamel, Andrew R., He, Yuan, Hormozdiari, Farhad, Mohammadi, Pejman, Munoz-Aguirre, Manuel, Ardlie, Kristin G., Battle, Alexis, Bonazzola, Rodrigo, Brown, Christopher D., Cox, Nancy, Dermitzakis, Emmanouil T., Engelhardt, Barbara E., Garrido-Martin, Diego, Gay, Nicole R., Getz, Gad, Guigo, Roderic, Hamel, Andrew R., Handsaker, Robert E., He, Yuan, Hoffman, Paul J., Hormozdiari, Farhad, Im, Hae Kyung, Jo, Brian, Kasela, Silva, Kashin, Seva, Kim-Hellmuth, Sarah, Kwong, Alan, Lappalainen, Tuuli, Li, Xiao, Liang, Yanyu, MacArthur, Daniel G., Mohammadi, Pejman, Montgomery, Stephen B., Munoz-Aguirre, Manuel, Rouhana, John M., Hormozdiari, Farhad, Im, Hae Kyung, Kim-Hellmuth, Sarah, Ardlie, Kristin G., Getz, Gad, Guigo, Roderic, Im, Hae Kyung, Lappalainen, Tuuli, Montgomery, Stephen B., Im, Hae Kyung, Lappalainen, Tuuli, Lappalainen, Tuuli, Anand, Shankara, Gabriel, Stacey, Getz, Gad, Graubert, Aaron, Hadley, Kane, Handsaker, Robert E., Huang, Katherine H., Kashin, Seva, Li, Xiao, MacArthur, Daniel G., Meier, Samuel R., Nedzel, Jared L., Balliu, Brunilda, Conrad, Don, Cotter, Daniel J., Das, Sayantan, de Goede, Olivia M., Eskin, Eleazar, Eulalio, Tiffany Y., Ferraro, Nicole M., Garrido-Martin, Diego, Gay, Nicole R., Getz, Gad, Graubert, Aaron, Guigo, Roderic, Hadley, Kane, Hamel, Andrew R., Handsaker, Robert E., He, Yuan, Hoffman, Paul J., Hormozdiari, Farhad, Hou, Lei, Huang, Katherine H., Im, Hae Kyung, Jo, Brian, Kasela, Silva, Kashin, Seva, Kellis, Manolis, Kim-Hellmuth, Sarah, Kwong, Alan

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Single-cell epigenomic analyses implicate candidate causal variants at inherited risk loci for Alzheimer’s and Parkinson’s diseases von Corces, M. Ryan, Shcherbina, Anna, Kundu, Soumya, Gloudemans, Michael J., Frésard, Laure, Granja, Jeffrey M., Louie, Bryan H., Eulalio, Tiffany, Shams, Shadi, Bagdatli, S. Tansu, Mumbach, Maxwell R., Liu, Boxiang, Montine, Kathleen S., Greenleaf, William J., Kundaje, Anshul, Montgomery, Stephen B., Chang, Howard Y., Montine, Thomas J.

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The impact of sex on gene expression across human tissues von Oliva, Meritxell, Munoz-Aguirre, Manuel, Kim-Hellmuth, Sarah, Wucher, Valentin, Gewirtz, Ariel D. H., Cotter, Daniel J., Parsana, Princy, Kasela, Silva, Balliu, Brunilda, Vinuela, Ana, Castel, Stephane E., Mohammadi, Pejman, Aguet, Francois, Zou, Yuxin, Khramtsova, Ekaterina A., Skol, Andrew D., Garrido-Martin, Diego, Reverter, Ferran, Brown, Andrew, Evans, Patrick, Gamazon, Eric R., Payne, Anthony, Bonazzola, Rodrigo, Barbeira, Alvaro N., Hamel, Andrew R., Martinez-Perez, Angel, Soria, Jose Manuel, Pierce, Brandon L., Stephens, Matthew, Eskin, Eleazar, Dermitzakis, Emmanouil T., Segr, Ayellet, Im, Hae Kyung, Engelhardt, Barbara E., Ardlie, Kristin G., Montgomery, Stephen B., Battle, Alexis J., Lappalainen, Tuuli, Guigo, Roderic, Stranger, Barbara E.

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Determinants of telomere length across human tissues von Demanelis, Kathryn, Jasmine, Farzana, Chen, Lin S., Chernoff, Meytal, Tong, Lin, Delgado, Dayana, Zhang, Chenan, Shinkle, Justin, Sabarinathan, Mekala, Lin, Hannah, Ramirez, Eduardo, Oliva, Meritxell, Kim-Hellmuth, Sarah, Stranger, Barbara E., Lai, Tsung-Po, Aviv, Abraham, Ardlie, Kristin G., Aguet, Francois, Ahsan, Habibul, Doherty, Jennifer A., Kibriya, Muhammad G., Pierce, Brandon L.

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A Quantitative Proteome Map of the Human Body von Jiang, Lihua, Chan, Joanne, Fang, Huaying, Anand, Shankara, Gabriel, Stacey, Graubert, Aaron, Hadley, Kane, Huang, Katherine H., MacArthur, Daniel G., Meier, Samuel R., Segrè, Ayellet V., Balliu, Brunilda, Barbeira, Alvaro N., Battle, Alexis, Brown, Andrew, Brown, Christopher D., Castel, Stephane E., Conrad, Don, Cotter, Daniel J., Das, Sayantan, de Goede, Olivia M., Dermitzakis, Emmanouil T., Eskin, Eleazar, Eulalio, Tiffany Y., Garrido-Martín, Diego, Guigó, Roderic, He, Yuan, Hoffman, Paul J., Hormozdiari, Farhad, Im, Hae Kyung, Jo, Brian, Kasela, Silva, Kellis, Manolis, Kim-Hellmuth, Sarah, Li, Xin, Mohammadi, Pejman, Montgomery, Stephen B., Muñoz-Aguirre, Manuel, Nachun, Daniel C., Oliva, Meritxell, Parsana, Princy, Sabatti, Chiara, Skol, Andrew D., Stephens, Matthew, Strober, Benjamin J., Teran, Nicole A., Viñuela, Ana, Wang, Gao, Wucher, Valentin, Zou, Yuxin, Ferreira, Pedro G., Yeger-Lotem, Esti, Barcus, Mary E., Bradbury, Debra, Krubit, Tanya, McLean, Jeffrey A., Smith, Anna M., Sobin, Leslie, Tabor, David E., Brigham, Lori E., Gillard, Bryan M., Hasz, Richard, Johnson, Mark, Kopen, Gene, Moser, Michael T., Myer, Kevin, Shad, Saboor, Thomas, Jeffrey A., Washington, Michael, Rohrer, Daniel C., Valley, Dana R., Davis, David A., Mash, Deborah C., Mosavel, Maghboeba, Siminoff, Laura A., Flicek, Paul, Juettemann, Thomas, Powell, Conner C., Rosenbloom, Kate R., Ruffier, Magali, Sheppard, Dan, Taylor, Kieron, Akey, Joshua, Demanelis, Kathryn, Feinberg, Andrew P., Hansen, Kasper D., Kibriya, Muhammad G., Li, Jin Billy, Li, Qin, Linder, Sandra E., Pierce, Brandon L., Smith, Kevin S., Tang, Hua, Carithers, Latarsha J., Koester, Susan E., Little, A. Roger, Moore, Helen M., Rao, Abhi K., Vaught, Jimmie B., Volpi, Simona

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Cell type-specific genetic regulation of gene expression across human tissues von Kim-Hellmuth, Sarah, Aguet, Francois, Oliva, Meritxell, Munoz-Aguirre, Manuel, Wucher, Valentin, Kasela, Silva, Castel, Stephane E., Hamel, Andrew R., Vinuela, Ana, Roberts, Amy L., Mangul, Serghei, Wen, Xiaoquan, Wang, Gao, Barbeira, Alvaro N., Garrido-Martin, Diego, Nadel, Brian, Zou, Yuxin, Bonazzola, Rodrigo, Quan, Jie, Brown, Andrew, Martinez-Perez, Angel, Soria, Jose Manuel, Getz, Gad, Dermitzakis, Emmanouil T., Small, Kerrin S., Stephens, Matthew, Xi, Hualin S., Im, Hae Kyung, Guig, Roderic, Segr, Ayellet, Stranger, Barbara E., Ardlie, Kristin G., Lappalainen, Tuuli

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Multi-Omic Profiling of Macrophages Lacking Tet2 or Dnmt3a Reveals Mechanisms of Hyper-Inflammation in Clonal Hematopoiesis von Rodrigues, Kameron B, Gopakumar, Jayakrishnan, Weng, Ziming, Mitchell, Shaneice Renee, Maurer, Margaret, Nachun, Daniel, Eulalio, Tiffany, Estrada, Dorothy, Mazumder, Thomas, Ma, Lisa, Montgomery, Stephen, Jaiswal, Siddhartha

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Transcriptomic signatures across human tissues identify functional rare genetic variation von Ferraro, Nicole M., Strober, Benjamin J., Einson, Jonah, Abell, Nathan S., Aguet, Francois, Barbeira, Alvaro N., Brandt, Margot, Bucan, Maja, Castel, Stephane E., Davis, Joe R., Greenwald, Emily, Hess, Gaelen T., Hilliard, Austin T., Kember, Rachel L., Kotis, Bence, Park, YoSon, Peloso, Gina, Ramdas, Shweta, Scott, Alexandra J., Smail, Craig, Tsang, Emily K., Zekavat, Seyedeh M., Ziosi, Marcello, Aradhana, Ardlie, Kristin G., Assimes, Themistocles L., Bassik, Michael C., Brown, Christopher D., Correa, Adolfo, Hall, Ira, Im, Hae Kyung, Li, Xin, Natarajan, Pradeep, Lappalainen, Tuuli, Mohammadi, Pejman, Montgomery, Stephen B., Battlett, Alexis

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Nonsense-mediated decay is highly stable across individuals and tissues von Teran, Nicole A., Nachun, Daniel C., Eulalio, Tiffany, Ferraro, Nicole M., Smail, Craig, Rivas, Manuel A., Montgomery, Stephen B.

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A vast resource of allelic expression data spanning human tissues von Castel, Stephane E., Aguet, Francois, Mohammadi, Pejman, Ardlie, Kristin G., Lappalainen, Tuuli

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Developing machine learning models to personalize care levels among emergency room patients for hospital admission von Nguyen, Minh, Corbin, Conor K, Eulalio, Tiffany, Ostberg, Nicolai P, Machiraju, Gautam, Marafino, Ben J, Baiocchi, Michael, Rose, Christian, Chen, Jonathan H

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Juvenile Shank3b deficient mice present with behavioral phenotype relevant to autism spectrum disorder von Balaan, Chantell, Corley, Michael J., Eulalio, Tiffany, Leite-ahyo, Ka’ahukane, Pang, Alina P.S., Fang, Rui, Khadka, Vedbar S., Maunakea, Alika K., Ward, Monika A.

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Single-cell epigenomic analyses implicate candidate causal variants at inherited risk loci for Alzheimer's and Parkinson's diseases von Corces, M Ryan, Shcherbina, Anna, Kundu, Soumya, Gloudemans, Michael J, Frésard, Laure, Granja, Jeffrey M, Louie, Bryan H, Eulalio, Tiffany, Shams, Shadi, Bagdatli, S Tansu, Mumbach, MAXWELL R, Liu, Boxiang, Montine, Kathleen S, Greenleaf, William J, Kundaje, Anshul, Montgomery, Stephen B, Chang, Howard Y, Montine, Thomas J

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