Genomic variants, genes, and pathways of Alzheimer's disease: An overview von Naj, Adam C., Schellenberg, Gerard D.

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ODACH: a one-shot distributed algorithm for Cox model with heterogeneous multi-center data von Luo, Chongliang, Duan, Rui, Naj, Adam C., Kranzler, Henry R., Bian, Jiang, Chen, Yong

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Genetically regulated expression in late-onset Alzheimer’s disease implicates risk genes within known and novel loci von Chen, Hung-Hsin, Petty, Lauren E., Sha, Jin, Zhao, Yi, Kuzma, Amanda, Valladares, Otto, Bush, William, Naj, Adam C., Gamazon, Eric R., Below, Jennifer E.

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The unfolded protein response is activated in disease-affected brain regions in progressive supranuclear palsy and Alzheimer's disease von Stutzbach, Lauren D, Xie, Sharon X, Naj, Adam C, Albin, Roger, Gilman, Sid, Lee, Virginia M Y, Trojanowski, John Q, Devlin, Bernie, Schellenberg, Gerard D

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Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalities von Naj, Adam C, Beecham, Gary W, Martin, Eden R, Gallins, Paul J, Powell, Eric H, Konidari, Ioanna, Whitehead, Patrice L, Cai, Guiqing, Haroutunian, Vahram, Scott, William K, Vance, Jeffery M, Slifer, Michael A, Gwirtsman, Harry E, Gilbert, John R, Haines, Jonathan L, Buxbaum, Joseph D, Pericak-Vance, Margaret A

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Genotype Imputation in Genome‐Wide Association Studies von Naj, Adam C.

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The executive prominent / memory prominent spectrum in Alzheimer’s disease is highly heritable von Mez, Jesse, MD MS, Mukherjee, Shubhabrata, PhD, Thornton, Timothy, PhD, Fardo, David W., PhD, Trittschuh, Emily, PhD, Sutti, Sheila, MS, Sherva, Richard, PhD, Kauwe, John S., PhD, Naj, Adam C., PhD, Beecham, Gary W., PhD, Gross, Alden, PhD, Saykin, Andrew J., PsyD, Green, Robert C., MD MPH, Crane, Paul K., MD MPH

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FAM-MDR: a flexible family-based multifactor dimensionality reduction technique to detect epistasis using related individuals von Cattaert, Tom, Urrea, Víctor, Naj, Adam C, De Lobel, Lizzy, De Wit, Vanessa, Fu, Mao, Mahachie John, Jestinah M, Shen, Haiqing, Calle, M Luz, Ritchie, Marylyn D, Edwards, Todd L, Van Steen, Kristel

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Genetic heterogeneity: Challenges, impacts, and methods through an associative lens von Woodward, Alexa A., Urbanowicz, Ryan J., Naj, Adam C., Moore, Jason H.

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ALZHEIMER'S DISEASE SEQUENCING PROJECT: CASE-CONTROL ANALYSES von Naj, Adam C

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Association of SCARB1 Variants With Subclinical Atherosclerosis and Incident Cardiovascular Disease: The Multi-Ethnic Study of Atherosclerosis von Manichaikul, Ani, Naj, Adam C, Herrington, David, Post, Wendy, Rich, Stephen S, Rodriguez, Annabelle

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A haptoglobin (HP) structural variant alters the effect of APOE alleles on Alzheimer's disease von Bai, Haimeng, Naj, Adam C, Benchek, Penelope, Dumitrescu, Logan, Hohman, Timothy, Hamilton-Nelson, Kara, Kallianpur, Asha R, Griswold, Anthony J, Vardarajan, Badri, Martin, Eden R, Beecham, Gary W, Below, Jennifer E, Schellenberg, Gerard, Mayeux, Richard, Farrer, Lindsay, Pericak-Vance, Margaret A, Haines, Jonathan L, Bush, William S

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Early-Onset Alzheimer Disease and Candidate Risk Genes Involved in Endolysosomal Transport von Kunkle, Brian W, Vardarajan, Badri N, Naj, Adam C, Whitehead, Patrice L, Rolati, Sophie, Slifer, Susan, Carney, Regina M, Cuccaro, Michael L, Vance, Jeffery M, Gilbert, John R, Wang, Li-San, Farrer, Lindsay A, Reitz, Christiane, Haines, Jonathan L, Beecham, Gary W, Martin, Eden R, Schellenberg, Gerard D, Mayeux, Richard P, Pericak-Vance, Margaret A

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Reassessment of Risk Genotypes (GRN, TMEM106B, and ABCC9 Variants) Associated With Hippocampal Sclerosis of Aging Pathology von Nelson, Peter T, Wang, Wang-Xia, Partch, Amanda B, Monsell, Sarah E, Valladares, Otto, Ellingson, Sally R, Wilfred, Bernard R, Naj, Adam C, Wang, Li-San, Kukull, Walter A, Fardo, David W

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An association test of the spatial distribution of rare missense variants within protein structures identifies Alzheimer's disease-related patterns von Jin, Bowen, Capra, John A, Benchek, Penelope, Wheeler, Nicholas, Naj, Adam C, Hamilton-Nelson, Kara L, Farrell, John J, Leung, Yuk Yee, Kunkle, Brian, Vadarajan, Badri, Schellenberg, Gerard D, Mayeux, Richard, Wang, Li-San, Farrer, Lindsay A, Pericak-Vance, Margaret A, Martin, Eden R, Haines, Jonathan L, Crawford, Dana C, Bush, William S

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Corrigendum: An association test of the spatial distribution of rare missense variants within protein structures identifies Alzheimer's disease–related patterns von Jin, Bowen, Capra, John A., Benchek, Penelope, Wheeler, Nicholas, Naj, Adam C., Hamilton-Nelson, Kara L., Farrell, John J., Leung, Yuk Yee, Kunkle, Brian, Vadarajan, Badri, Schellenberg, Gerard D., Mayeux, Richard, Wang, Li-San, Farrer, Lindsay A., Pericak-Vance, Margaret A., Martin, Eden R., Haines, Jonathan L., Crawford, Dana C., Bush, William S.

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Detecting Familial Aggregation von Naj, Adam C., Beaty, Terri H.

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Quality control and integration of genotypes from two calling pipelines for whole genome sequence data in the Alzheimer's disease sequencing project von Naj, Adam C., Lin, Honghuang, Vardarajan, Badri N., White, Simon, Lancour, Daniel, Ma, Yiyi, Schmidt, Michael, Sun, Fangui, Butkiewicz, Mariusz, Bush, William S., Kunkle, Brian W., Malamon, John, Amin, Najaf, Choi, Seung Hoan, Hamilton-Nelson, Kara L., van der Lee, Sven J., Gupta, Namrata, Koboldt, Daniel C., Saad, Mohamad, Wang, Bowen, Nato, Alejandro Q., Sohi, Harkirat K., Kuzma, Amanda, Wang, Li-San, Cupples, L. Adrienne, van Duijn, Cornelia, Seshadri, Sudha, Schellenberg, Gerard D., Boerwinkle, Eric, Bis, Joshua C., Dupuis, Josée, Salerno, William J., Wijsman, Ellen M., Martin, Eden R., DeStefano, Anita L.

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LRP10 variants in progressive supranuclear palsy von Vergouw, Leonie J.M., Melhem, Shamiram, Donker Kaat, Laura, Chiu, Wang Z., Kuipers, Demy J.S., Breedveld, Guido, Boon, Agnita J.W., Wang, Li-San, Naj, Adam C., Mlynarksi, Elizabeth, Cantwell, Laura, Quadri, Marialuisa, Ross, Owen A., Dickson, Dennis W., Schellenberg, Gerard D., van Swieten, John C., Bonifati, Vincenzo, de Jong, Frank Jan

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Longitudinal change in memory performance as a strong endophenotype for Alzheimer's disease von Archer, Derek B., Eissman, Jaclyn M., Mukherjee, Shubhabrata, Lee, Michael L., Choi, Seo‐Eun, Scollard, Phoebe, Trittschuh, Emily H., Mez, Jesse B., Bush, William S., Kunkle, Brian W., Naj, Adam C., Gifford, Katherine A., Cuccaro, Michael L., Pericak‐Vance, Margaret A., Farrer, Lindsay A., Wang, Li‐San, Schellenberg, Gerard D., Mayeux, Richard P., Haines, Jonathan L., Jefferson, Angela L., Kukull, Walter A., Keene, C. Dirk, Saykin, Andrew J., Thompson, Paul M., Martin, Eden R., Bennett, David A., Barnes, Lisa L., Schneider, Julie A., Crane, Paul K., Dumitrescu, Logan, Hohman, Timothy J.

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