Causal Associations Between Modifiable Risk Factors and the Alzheimer's Phenome by Andrews, Shea J., Fulton‐Howard, Brian, O'Reilly, Paul, Marcora, Edoardo, Goate, Alison M., Farrer, Lindsay A., Haines, Jonathan L., Mayeux, Richard, Naj, Adam C., Pericak‐Vance, Margaret A., Schellenberg, Gerard D., Wang, Li‐San

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A noise-reduction GWAS analysis implicates altered regulation of neurite outgrowth and guidance in autism by Hussman, John P, Chung, Ren-Hua, Griswold, Anthony J, Jaworski, James M, Salyakina, Daria, Ma, Deqiong, Konidari, Ioanna, Whitehead, Patrice L, Vance, Jeffery M, Martin, Eden R, Cuccaro, Michael L, Gilbert, John R, Haines, Jonathan L, Pericak-Vance, Margaret A

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Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalities by 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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Evaluation of copy number variations reveals novel candidate genes in autism spectrum disorder-associated pathways by GRISWOLD, Anthony J, DEQIONG MA, WRIGHT, Harry H, ABRAMSON, Ruth K, WILLIAMS, Scott M, MENON, Ramkumar, MARTIN, Eden R, HAINES, Jonathan L, GILBERT, John R, CUCCARO, Michael L, PERICAK-VANCE, Margaret A, CUKIER, Holly N, NATIONS, Laura D, SCHMIDT, Mike A, CHUNG, Ren-Hua, JAWORSKI, James M, SALYAKINA, Daria, KONIDARI, Loanna, WHITEHEAD, Patrice L

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Copy number variants in extended autism spectrum disorder families reveal candidates potentially involved in autism risk by Salyakina, Daria, Cukier, Holly N, Lee, Joycelyn M, Sacharow, Stephanie, Nations, Laura D, Ma, Deqiong, Jaworski, James M, Konidari, Ioanna, Whitehead, Patrice L, Wright, Harry H, Abramson, Ruth K, Williams, Scott M, Menon, Ramkumar, Haines, Jonathan L, Gilbert, John R, Cuccaro, Michael L, Pericak-Vance, Margaret A

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Report of the APOE4 National Institute on Aging/Alzheimer Disease Sequencing Project Consortium Working Group: Reducing APOE4 in Carriers is a Therapeutic Goal for Alzheimer's Dise... by Vance, Jeffery M, Farrer, Lindsay A, Huang, Yadong, Cruchaga, Carlos, Hyman, Bradley T, Pericak-Vance, Margaret A, Goate, Alison M, Greicius, Michael D, Griswold, Anthony J, Haines, Jonathan L, Tcw, Julia, Schellenberg, Gerard D, Tsai, Li-Huei, Herz, Joachim, Holtzman, David M

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Emergency Department Point-of-care Ultrasound in Out-of-Hospital and in-ED Cardiac Arrest by Gaspari, Romolo, Weekes, Anthony, Adhikari, Srikar, Noble, Vicki E, Nomura, Jason T, Theodoro, Daniel, Woo, Michael, Atkinson, Paul, Blehar, David, Brown, Samuel M, Caffery, Terrell, Douglass, Emily, Fraser, Jacqueline, Haines, Christine, Lam, Samuel, Lanspa, Michael, Lewis, Margaret, Liebmann, Otto, Limkakeng, Alexander, Lopez, Fernando, Platz, Elke, Mendoza, Michelle, Minnigan, Hal, Moore, Christopher, Novik, Joseph, Rang, Louise, Scruggs, Will, Raio, Christopher

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Polygenic Risk Score for Alzheimer's Disease in Caribbean Hispanics by Sariya, Sanjeev, Felsky, Daniel, Reyes‐Dumeyer, Dolly, Lali, Ricky, Lantigua, Rafael A., Vardarajan, Badri, Jiménez‐Velázquez, Ivonne Z., Haines, Jonathan L., Shellenberg, Gerard D., Pericak‐Vance, Margaret A, Paré, Guillaume, Mayeux, Richard, Tosto, Giuseppe

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Genetic variants and functional pathways associated with resilience to Alzheimer's disease by Dumitrescu, Logan, Mahoney, Emily R, Mukherjee, Shubhabrata, Lee, Michael L, Bush, William S, Engelman, Corinne D, Lu, Qiongshi, Fardo, David W, Trittschuh, Emily H, Mez, Jesse, Kaczorowski, Catherine, Hernandez Saucedo, Hector, Widaman, Keith F, Buckley, Rachel, Properzi, Michael, Mormino, Elizabeth, Yang, Hyun-Sik, Harrison, Tessa, Hedden, Trey, Nho, Kwangsik, Andrews, Shea J, Tommet, Doug, Hadad, Niran, Sanders, R Elizabeth, Ruderfer, Douglas M, Gifford, Katherine A, Moore, Annah M, Cambronero, Francis, Zhong, Xiaoyuan, Raghavan, Neha S, Vardarajan, Badri, Pericak-Vance, Margaret A, Farrer, Lindsay A, Wang, Li-San, Cruchaga, Carlos, Schellenberg, Gerard, Cox, Nancy J, Haines, Jonathan L, Keene, C Dirk, Saykin, Andrew J, Larson, Eric B, Sperling, Reisa A, Mayeux, Richard, Bennett, David A, Schneider, Julie A, Crane, Paul K, Jefferson, Angela L, Hohman, Timothy J

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Protective effect of complement factor B and complement component 2 variants in age-related macular degeneration by Spencer, Kylee L., Hauser, Michael A., Olson, Lana M., Schmidt, Silke, Scott, William K., Gallins, Paul, Agarwal, Anita, Postel, Eric A., Pericak-Vance, Margaret A., Haines, Jonathan L.

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Using genetic variation and environmental risk factor data to identify individuals at high risk for age-related macular degeneration by Spencer, Kylee L, Olson, Lana M, Schnetz-Boutaud, Nathalie, Gallins, Paul, Agarwal, Anita, Iannaccone, Alessandro, Kritchevsky, Stephen B, Garcia, Melissa, Nalls, Michael A, Newman, Anne B, Scott, William K, Pericak-Vance, Margaret A, Haines, Jonathan L

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Genome-wide association study identifies four novel loci associated with Alzheimer’s endophenotypes and disease modifiers by Deming, Yuetiva, Li, Zeran, Kapoor, Manav, Harari, Oscar, Del-Aguila, Jorge L., Black, Kathleen, Carrell, David, Cai, Yefei, Fernandez, Maria Victoria, Budde, John, Ma, Shengmei, Saef, Benjamin, Howells, Bill, Huang, Kuan-lin, Bertelsen, Sarah, Fagan, Anne M., Holtzman, David M., Morris, John C., Kim, Sungeun, Saykin, Andrew J., De Jager, Philip L., Albert, Marilyn, Moghekar, Abhay, O’Brien, Richard, Riemenschneider, Matthias, Petersen, Ronald C., Blennow, Kaj, Zetterberg, Henrik, Minthon, Lennart, Van Deerlin, Vivianna M., Lee, Virginia Man-Yee, Shaw, Leslie M., Trojanowski, John Q., Schellenberg, Gerard, Haines, Jonathan L., Mayeux, Richard, Pericak-Vance, Margaret A., Farrer, Lindsay A., Peskind, Elaine R., Li, Ge, Di Narzo, Antonio F., Kauwe, John S. K., Goate, Alison M., Cruchaga, Carlos

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Identifying X-chromosome variants associated with age-related macular degeneration by Grunin, Michelle, Igo, Jr, Robert P, Song, Yeunjoo E, Blanton, Susan H, Pericak-Vance, Margaret A, Haines, Jonathan L

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Drusen morphometrics on optical coherence tomography in eyes with age-related macular degeneration and normal aging by Oncel, Deniz, Corradetti, Giulia, Wakatsuki, Yu, Nittala, Muneeswar Gupta, Velaga, Swetha Bindu, Stambolian, Dwight, Pericak-Vance, Margaret A., Haines, Jonathan L., Sadda, SriniVas R.

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Male-specific epistasis between WWC1 and TLN2 genes is associated with Alzheimer's disease by Gusareva, Elena S., Twizere, Jean-Claude, Sleegers, Kristel, Dourlen, Pierre, Abisambra, Jose F., Meier, Shelby, Cloyd, Ryan, Weiss, Blaine, Dermaut, Bart, Bessonov, Kyrylo, van der Lee, Sven J., Carrasquillo, Minerva M., Katsumata, Yuriko, Cherkaoui, Majid, Asselbergh, Bob, Ikram, M. Arfan, Mayeux, Richard, Farrer, Lindsay A., Haines, Jonathan L., Pericak-Vance, Margaret A., Schellenberg, Gerard D., Sims, Rebecca, Williams, Julie, Amouyel, Philippe, van Duijn, Cornelia M., Ertekin-Taner, Nilüfer, Van Broeckhoven, Christine, Dequiedt, Franck, Fardo, David W., Lambert, Jean-Charles, Van Steen, Kristel

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Mitochondrial DNA polymorphism A4917G is independently associated with age-related macular degeneration by Canter, Jeffrey A, Olson, Lana M, Spencer, Kylee, Schnetz-Boutaud, Nathalie, Anderson, Brent, Hauser, Michael A, Schmidt, Silke, Postel, Eric A, Agarwal, Anita, Pericak-Vance, Margaret A, Sternberg, Jr, Paul, Haines, Jonathan L

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The PhenX Toolkit: Get the Most From Your Measures by Hamilton, Carol M., Strader, Lisa C., Pratt, Joseph G., Maiese, Deborah, Hendershot, Tabitha, Kwok, Richard K., Hammond, Jane A., Huggins, Wayne, Jackman, Dean, Pan, Huaqin, Nettles, Destiney S., Beaty, Terri H., Farrer, Lindsay A., Kraft, Peter, Marazita, Mary L., Ordovas, Jose M., Pato, Carlos N., Spitz, Margaret R., Wagener, Diane, Williams, Michelle, Junkins, Heather A., Harlan, William R., Ramos, Erin M., Haines, Jonathan

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Assessment of intraretinal hyperreflective foci using multimodal imaging in eyes with age‐related macular degeneration by Oncel, Deniz, Corradetti, Giulia, He, Ye, Ashrafkhorasani, Maryam, Nittala, Muneeswar Gupta, Stambolian, Dwight, Pericak‐Vance, Margaret A., Haines, Jonathan L., Sadda, Srinivas R.

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Examination of candidate exonic variants for association to Alzheimer disease in the Amish by D'Aoust, Laura N, Cummings, Anna C, Laux, Renee, Fuzzell, Denise, Caywood, Laura, Reinhart-Mercer, Lori, Scott, William K, Pericak-Vance, Margaret A, Haines, Jonathan L

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Blood-derived mitochondrial DNA copy number is associated with Alzheimer disease, Alzheimer-related biomarkers and serum metabolites by Tong, Tong, Zhu, Congcong, Farrell, John J, Khurshid, Zainab, Martin, Eden R, Pericak-Vance, Margaret A, Wang, Li-San, Bush, William S, Schellenberg, Gerard D, Haines, Jonathan L, Qiu, Wei Qiao, Lunetta, Kathryn L, Farrer, Lindsay A, Zhang, Xiaoling

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