Gene Expression and Genetic Variation in Response to Endoplasmic Reticulum Stress in Human Cells von Dombroski, Beth A., Nayak, Renuka R., Ewens, Kathryn G., Ankener, Wendy, Cheung, Vivian G., Spielman, Richard S.

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C9orf72 Hexanucleotide Repeat Expansion and Guam Amyotrophic Lateral Sclerosis–Parkinsonism-Dementia Complex von Dombroski, Beth A, Galasko, Douglas R, Mata, Ignacio F, Zabetian, Cyrus P, Craig, Ulla-Katrina, Garruto, Ralph M, Oyanagi, Kiyomitsu, Schellenberg, Gerard D

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Many human L1 elements are capable of retrotransposition von Sassaman, Donna M, Dombroski, Beth A, Moran, John V, Kimberland, Michelle L, Naas, Thierry P, DeBerardinis, Ralph J, Gabriel, Abram, Swergold, Gary D, Kazazian, Haig H

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High copy wildtype human 1N4R tau expression promotes early pathological tauopathy accompanied by cognitive deficits without progressive neurofibrillary degeneration von Wheeler, Jeanna M, McMillan, Pamela J, Hawk, Michele, Iba, Michiyo, Robinson, Linda, Xu, George J, Dombroski, Beth A, Jeong, Doori, Dichter, Marc A, Juul, Halvor, Loomis, Elaine, Raskind, Murray, Leverenz, James B, Trojanowski, John Q, Lee, Virginia M Y, Schellenberg, Gerard D, Kraemer, Brian C

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MAPT enhancer containing rs242557 regulates multiple neighboring genes in human microglial cell line von Das, Rueben G, Choi, Eirene, Jiang, Ming, Dombroski, Beth A., Schellenberg, Gerard D.

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Genetic Variations in EIF2AK3 are Associated with Neurocognitive Impairment in People Living with HIV von Akay-Espinoza, Cagla, Newton, Sarah E.B., Dombroski, Beth A., Kallianpur, Asha, Bharti, Ajay, Franklin, Donald R., Schellenberg, Gerard D., Heaton, Robert K., Grant, Igor, Ellis, Ronald J., Letendre, Scott L., Jordan-Sciutto, Kelly L.

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Association of common and rare variants with Alzheimer's disease in more than 13,000 diverse individuals with whole-genome sequencing from the Alzheimer's Disease Sequencing Projec... von Lee, Wan-Ping, Choi, Seung Hoan, Shea, Margaret G, Cheng, Po-Liang, Dombroski, Beth A, Pitsillides, Achilleas N, Heard-Costa, Nancy L, Wang, Hui, Bulekova, Katia, Kuzma, Amanda B, Leung, Yuk Yee, Farrell, John J, Lin, Honghuang, Kunkle, Brian W, Naj, Adam, Blue, Elizabeth E, Nusetor, Frederick, Wang, Dongyu, Boerwinkle, Eric, Bush, William S, Zhang, Xiaoling, De Jager, Philip L, Dupuis, Josée, Farrer, Lindsay A, Fornage, Myriam, Martin, Eden, Pericak-Vance, Margaret, Seshadri, Sudha, Wijsman, Ellen M, Wang, Li-San, Schellenberg, Gerard D, Destefano, Anita L, Haines, Jonathan L, Peloso, Gina M

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Isolation of an Active Human Transposable Element von Dombroski, Beth A., Mathias, Stephen L., Nanthakumar, Elizabeth, Scott, Alan F., Kazazian, Haig H.

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A comparative study of structural variant calling in WGS from Alzheimer's disease families von Malamon, John S, Farrell, John J, Xia, Li Charlie, Dombroski, Beth A, Das, Rueben G, Way, Jessica, Kuzma, Amanda B, Valladares, Otto, Leung, Yuk Yee, Scanlon, Allison J, Lopez, Irving Antonio Barrera, Brehony, Jack, Worley, Kim C, Zhang, Nancy R, Wang, Li-San, Farrer, Lindsay A, Schellenberg, Gerard D, Lee, Wan-Ping, Vardarajan, Badri N

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COMPUTATIONAL IDENTIFICATION OF REGULATORY MECHANISMS AFFECTED BY NONCODING VARIANTS ASSOCIATED WITH LATE-ONSET ALZHEIMER'S DISEASE von Amlie-Wolf, Alexandre, Tang, Mitchell, King, Jessica, Dombroski, Beth A, Wang, Li-San, Schellenberg, Gerard D

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Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21 von Pulver, Ann E, Blouin, Jean-Louis, Dombroski, Beth A, Nath, Swapan K, Lasseter, Virginia K, Wolyniec, Paula S, Nestadt, Gerald, Thornquist, Mary, Ullrich, Gail, McGrath, John, Kasch, Laura, Lamacz, Malgorzata, Thomas, Marion G, Gehrig, Corinne, Radhakrishna, Uppala, Snyder, Sarah E, Balk, Katherine G, Neufeld, Karin, Swartz, Karen L, DeMarchi, Nicola, Papadimitriou, George N, Dikeos, Dimitris G, Stefanis, Costas N, Chakravarti, Aravinda, Childs, Barton, Housman, David E, Kazazian, Haig H, Antonarakis, Stylianos E

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Prediction of late-onset Alzheimer’s disease-associated enhancer elements von Tang, Mitchell, Kramer, Christian, Xu, George, Hawk, Michele, Hwang, Yih-Chii, Lin, Chiao-Feng, Kuksa, Pavel, Wang, Weixin, Dombroski, Beth A, Naj, Adam C, Wang, Li-San, Schellenberg, Gerald D

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Low-frequency variant imputation identifies rare variant candidate loci in a gwas of late-onset Alzheimer’s disease in the igap consortium von Kunkle, Brian W, Grenier-Boley, Benjamin, Vronskaya, Maria, Chouraki, Vincent, van der Lee, Sven J, Hamilton-Nelson, Kara L, Toeglhofer, A.M, Sims, Rebecca, Jakobsdottir, Johanna, Bis, Joshua C, Dombroski, Beth A, Martin, Eden R, Mayeux, Richard, Farrer, Lindsay A, van Duijn, Cornelia M, Haines, Jonathan L, Williams, Julie, Seshadri, Sudha, Amouyel, Philippe, Schellenberg, Gerard D, Pericak-Vance, Margaret A

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A new retrotransposable human L1 element from the LRE2 locus on chromosome 1q produces a chimaeric insertion von Holmes, Susan E, Dombroski, Beth A, Krebs, Claudia M, Boehm, Corinne D, Kazazian, Haig H

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ABCA7 deletion associated with Alzheimer's disease in african americans von Cukier, Holly N, Kunkle, Brian W, Rolati, Sophie, Hamilton-Nelson, Kara L, Kohli, Martin A, Dombroski, Beth A, Vardarajan, Badri N, Whitehead, Patrice L, Van Booven, Derek J, Martin, Eden R, Beecham, Gary W, Farrer, Lindsay A, Cuccaro, Michael L, Vance, Jeffery M, Mayeux, Richard, Gilbert, John R, Carney, Regina M, Byrd, Goldie S, Haines, Jonathan L, Schellenberg, Gerald D, Pericak-Vance, Margaret A, Lang, Rosalyn

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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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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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Is rs242561 a regulator of tau expression in adult mice? von DAS, Rueben G, Choi, Eirene, Sgourdou, Paraskevi, Bernard, Tia, Dombroski, Beth A., Schellenberg, Gerard D.

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RNA‐seq study on the effect of MAPT rs242557 deletion in HMC3 cells von Das, Rueben, Kuska, Pavel P., Lee, Wan‐Ping, Choi, Eirene, Jiang, Ming, Dombroski, Beth A., Schellenberg, Gerald D.

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EXPRESSION STUDY ON THE EFFECT OF DELETING A MAPT ENHANCER CONTAINING RS242557 IN MICE BRAIN von Das, Rueben G., Dombroski, Beth A., Bernard, Tia, Schellenberg, Gerard D.

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