A NOVEL APPROACH FOR TRAINING RESUSCITATION TEAM LEADERS FOR IN-HOSPITAL CARDIAC ARRESTS: A GUIDE AND SIMULATION-BASED PROGRAM von OUD, LEE, E HEINS, JENNY, DAYTON, CHRISTOPHER L

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Exome Capture Reveals ZNF423 and CEP164 Mutations, Linking Renal Ciliopathies to DNA Damage Response Signaling von Chaki, Moumita, Airik, Rannar, Ghosh, Amiya K., Giles, Rachel H., Chen, Rui, Slaats, Gisela G., Wang, Hui, Hurd, Toby W., Zhou, Weibin, Cluckey, Andrew, Gee, Heon Yung, Ramaswami, Gokul, Hong, Chen-Jei, Hamilton, Bruce A., Červenka, Igor, Ganji, Ranjani Sri, Bryja, Vitezslav, Arts, Heleen H., van Reeuwijk, Jeroen, Oud, Machteld M., Letteboer, Stef J.F., Roepman, Ronald, Husson, Hervé, Ibraghimov-Beskrovnaya, Oxana, Yasunaga, Takayuki, Walz, Gerd, Eley, Lorraine, Sayer, John A., Schermer, Bernhard, Liebau, Max C., Benzing, Thomas, Le Corre, Stephanie, Drummond, Iain, Janssen, Sabine, Allen, Susan J., Natarajan, Sivakumar, O’Toole, John F., Attanasio, Massimo, Saunier, Sophie, Antignac, Corinne, Koenekoop, Robert K., Ren, Huanan, Lopez, Irma, Nayir, Ahmet, Stoetzel, Corinne, Dollfus, Helene, Massoudi, Rustin, Gleeson, Joseph G., Andreoli, Sharon P., Doherty, Dan G., Lindstrad, Anna, Golzio, Christelle, Katsanis, Nicholas, Pape, Lars, Abboud, Emad B., Al-Rajhi, Ali A., Lewis, Richard A., Omran, Heymut, Lee, Eva Y.-H.P., Wang, Shaohui, Sekiguchi, JoAnn M., Saunders, Rudel, Johnson, Colin A., Garner, Elizabeth, Vanselow, Katja, Andersen, Jens S., Shlomai, Joseph, Nurnberg, Gudrun, Nurnberg, Peter, Levy, Shawn, Smogorzewska, Agata, Otto, Edgar A., Hildebrandt, Friedhelm

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Penetrance estimate of LRRK2 p.G2019S mutation in individuals of non‐Ashkenazi Jewish ancestry von Lee, Annie J., Wang, Yuanjia, Alcalay, Roy N., Mejia‐Santana, Helen, Saunders‐Pullman, Rachel, Bressman, Susan, Corvol, Jean‐Christophe, Brice, Alexis, Lesage, Suzanne, Mangone, Graziella, Tolosa, Eduardo, Pont‐Sunyer, Claustre, Vilas, Dolores, Schüle, Birgitt, Kausar, Farah, Foroud, Tatiana, Berg, Daniela, Brockmann, Kathrin, Goldwurm, Stefano, Siri, Chiara, Asselta, Rosanna, Ruiz‐Martinez, Javier, Mondragón, Elisabet, Marras, Connie, Ghate, Taneera, Giladi, Nir, Mirelman, Anat, Marder, Karen

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Whole exome sequencing of intracranial aneurysm von Foroud, Tatiana

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CiliaCarta: An integrated and validated compendium of ciliary genes von van Dam, Teunis J P, Kennedy, Julie, van der Lee, Robin, de Vrieze, Erik, Wunderlich, Kirsten A, Rix, Suzanne, Dougherty, Gerard W, Lambacher, Nils J, Li, Chunmei, Jensen, Victor L, Leroux, Michel R, Hjeij, Rim, Horn, Nicola, Texier, Yves, Wissinger, Yasmin, van Reeuwijk, Jeroen, Wheway, Gabrielle, Knapp, Barbara, Scheel, Jan F, Franco, Brunella, Mans, Dorus A, van Wijk, Erwin, Képès, François, Slaats, Gisela G, Toedt, Grischa, Kremer, Hannie, Omran, Heymut, Szymanska, Katarzyna, Koutroumpas, Konstantinos, Ueffing, Marius, Nguyen, Thanh-Minh T, Letteboer, Stef J F, Oud, Machteld M, van Beersum, Sylvia E C, Schmidts, Miriam, Beales, Philip L, Lu, Qianhao, Giles, Rachel H, Szklarczyk, Radek, Russell, Robert B, Gibson, Toby J, Johnson, Colin A, Blacque, Oliver E, Wolfrum, Uwe, Boldt, Karsten, Roepman, Ronald, Hernandez-Hernandez, Victor, Huynen, Martijn A

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Duplicated antagonistic EPF peptides optimize grass stomatal initiation von Jangra, Raman, Brunetti, Sabrina C., Wang, Xutong, Kaushik, Pooja, Gulick, Patrick J., Foroud, Nora A., Wang, Shucai, Lee, Jin Suk

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Genome-wide association of familial late-onset Alzheimer's disease replicates BIN1 and CLU and nominates CUGBP2 in interaction with APOE von Wijsman, Ellen M, Pankratz, Nathan D, Choi, Yoonha, Rothstein, Joseph H, Faber, Kelley M, Cheng, Rong, Lee, Joseph H, Bird, Thomas D, Bennett, David A, Diaz-Arrastia, Ramon, Goate, Alison M, Farlow, Martin, Ghetti, Bernardino, Sweet, Robert A, Foroud, Tatiana M, Mayeux, Richard

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A novel ICK mutation causes ciliary disruption and lethal endocrine-cerebro-osteodysplasia syndrome von Oud, Machteld M, Bonnard, Carine, Mans, Dorus A, Altunoglu, Umut, Tohari, Sumanty, Ng, Alvin Yu Jin, Eskin, Ascia, Lee, Hane, Rupar, C Anthony, de Wagenaar, Nathalie P, Wu, Ka Man, Lahiry, Piya, Pazour, Gregory J, Nelson, Stanley F, Hegele, Robert A, Roepman, Ronald, Kayserili, Hülya, Venkatesh, Byrappa, Siu, Victoria M, Reversade, Bruno, Arts, Heleen H

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Whole genome association study of brain-wide imaging phenotypes for identifying quantitative trait loci in MCI and AD: A study of the ADNI cohort von Shen, Li, Kim, Sungeun, Risacher, Shannon L., Nho, Kwangsik, Swaminathan, Shanker, West, John D., Foroud, Tatiana, Pankratz, Nathan, Moore, Jason H., Sloan, Chantel D., Huentelman, Matthew J., Craig, David W., DeChairo, Bryan M., Potkin, Steven G., Jack, Clifford R., Weiner, Michael W., Saykin, Andrew J.

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Timeline to symptomatic Alzheimer's disease in people with Down syndrome as assessed by amyloid-PET and tau-PET: a longitudinal cohort study von Schworer, Emily K, Zammit, Matthew D, Wang, Jiebiao, Handen, Benjamin L, Betthauser, Tobey, Laymon, Charles M, Tudorascu, Dana L, Cohen, Annie D, Zaman, Shahid H, Ances, Beau M, Mapstone, Mark, Head, Elizabeth, Christian, Bradley T, Hartley, Sigan L, Aizenstein, Howard, Ances, Beau, Andrews, Howard, Bell, Karen, Birn, Rasmus, Brickman, Adam, Bulova, Peter, Cheema, Amrita, Chen, Kewei, Christian, Bradley, Clare, Isabel, Clark, Lorraine, Cohen, Ann, Constantino, John, Doran, Eric, Fagan, Anne, Feingold, Eleanor, Foroud, Tatiana, Handen, Benjamin, Harp, Jordan, Hartley, Sigan, Head, Elizabeth, Henson, Rachel, Hom, Christy, Honig, Lawrence, Ikonomovic, Milos, Johnson, Sterling, Jordan, Courtney, Kamboh, M. Ilyas, Keator, David, Klunk, William, Kofler, Julia, Kreisl, William, Krinsky-McHale, Sharon, Lai, Florence, Lao, Patrick, Laymon, Charles, Lee, Joseph, Lott, Ira, Lupson, Victoria, Mapstone, Mark, Mathis, Chester, Minhas, Davneet, Nadkarni, Neelesh, O'Bryant, Sid, Parisi, Melissa, Pang, Deborah, Petersen, Melissa, Price, Julie, Pulsifer, Margaret, Rafii, Michael, Reiman, Eric, Rizvi, Batool, Rosas, Diana, Ryan, Laurie, Schmitt, Frederick, Schupf, Nicole, Silverman, Wayne, Tudorascu, Dana, Tumuluru, Rameshwari, Tycko, Benjamin, Varadarajan, Badri, White, Desiree, Yassa, Michael, Zaman, Shahid, Zhang, Fan

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Serum iron levels and the risk of Parkinson disease: a Mendelian randomization study von Pichler, Irene, Del Greco M, Fabiola, Gögele, Martin, Lill, Christina M, Bertram, Lars, Do, Chuong B, Eriksson, Nicholas, Foroud, Tatiana, Myers, Richard H, Nalls, Michael, Keller, Margaux F, Benyamin, Beben, Whitfield, John B, Pramstaller, Peter P, Hicks, Andrew A, Thompson, John R, Minelli, Cosetta

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Amyloid and tau‐PET in early‐onset AD: Baseline data from the Longitudinal Early‐onset Alzheimer's Disease Study (LEADS) von Cho, Hanna, Mundada, Nidhi S., Apostolova, Liana G., Carrillo, Maria C., Shankar, Ranjani, Amuiri, Alinda N., Zeltzer, Ehud, Windon, Charles C., Soleimani‐Meigooni, David N., Tanner, Jeremy A., Heath, Courtney Lawhn, Lesman‐Segev, Orit H., Aisen, Paul, Eloyan, Ani, Lee, Hye Sun, Hammers, Dustin B., Kirby, Kala, Dage, Jeffrey L., Fagan, Anne, Foroud, Tatiana, Grinberg, Lea T., Jack, Clifford R., Kramer, Joel, Kukull, Walter A., Murray, Melissa E., Nudelman, Kelly, Toga, Arthur, Vemuri, Prashanthi, Atri, Alireza, Day, Gregory S., Duara, Ranjan, Graff‐Radford, Neill R., Honig, Lawrence S., Jones, David T., Masdeu, Joseph, Mendez, Mario, Musiek, Erik, Onyike, Chiadi U., Riddle, Meghan, Rogalski, Emily J., Salloway, Stephen, Sha, Sharon, Turner, Raymond Scott, Wingo, Thomas S., Wolk, David A., Koeppe, Robert, Iaccarino, Leonardo, Dickerson, Bradford C., La Joie, Renaud, Rabinovici, Gil D.

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Greater Rupture Risk for Familial as Compared to Sporadic Unruptured Intracranial Aneurysms von BRODERICK, Joseph P, BROWN, Robert D, MEISSNER, Irene, FOROUD, Tatiana, MOOMAW, E. Charles J, SANDER CONNOLLY, E, SAUERBECK, Laura, HORNUNG, Richard, HUSTON, John, WOO, Daniel, ANDERSON, Craig, ROULEAU, Guy, KLEINDORFER, Dawn, FLAHERTY, Matthew L

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Genome-wide analysis reveals novel genes influencing temporal lobe structure with relevance to neurodegeneration in Alzheimer's disease von Stein, Jason L., Hua, Xue, Morra, Jonathan H., Lee, Suh, Hibar, Derrek P., Ho, April J., Leow, Alex D., Toga, Arthur W., Sul, Jae Hoon, Kang, Hyun Min, Eskin, Eleazar, Saykin, Andrew J., Shen, Li, Foroud, Tatiana, Pankratz, Nathan, Huentelman, Matthew J., Craig, David W., Gerber, Jill D., Allen, April N., Corneveaux, Jason J., Stephan, Dietrich A., Webster, Jennifer, DeChairo, Bryan M., Potkin, Steven G., Jack, Clifford R., Weiner, Michael W., Thompson, Paul M.

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Absence of C9ORF72 expanded or intermediate repeats in autopsy-confirmed Parkinson's disease von Nuytemans, Karen, Inchausti, Vanessa, Beecham, Gary W., Wang, Liyong, Dickson, Dennis W., Trojanowski, John Q., Lee, Virginia M.-Y., Mash, Deborah C., Frosch, Matthew P., Foroud, Tatiana M., Honig, Lawrence S., Montine, Thomas J., Dawson, Ted M., Martin, Eden R., Scott, William K., Vance, Jeffery M.

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Variants associated with Gaucher disease in multiple system atrophy von Mitsui, Jun, Matsukawa, Takashi, Sasaki, Hidenao, Yabe, Ichiro, Matsushima, Masaaki, Dürr, Alexandra, Brice, Alexis, Takashima, Hiroshi, Kikuchi, Akio, Aoki, Masashi, Ishiura, Hiroyuki, Yasuda, Tsutomu, Date, Hidetoshi, Ahsan, Budrul, Iwata, Atsushi, Goto, Jun, Ichikawa, Yaeko, Nakahara, Yasuo, Momose, Yoshio, Takahashi, Yuji, Hara, Kenju, Kakita, Akiyoshi, Yamada, Mitsunori, Takahashi, Hitoshi, Onodera, Osamu, Nishizawa, Masatoyo, Watanabe, Hirohisa, Ito, Mizuki, Sobue, Gen, Ishikawa, Kinya, Mizusawa, Hidehiro, Kanai, Kazuaki, Hattori, Takamichi, Kuwabara, Satoshi, Arai, Kimihito, Koyano, Shigeru, Kuroiwa, Yoshiyuki, Hasegawa, Kazuko, Yuasa, Tatsuhiko, Yasui, Kenichi, Nakashima, Kenji, Ito, Hijiri, Izumi, Yuishin, Kaji, Ryuji, Kato, Takeo, Kusunoki, Susumu, Osaki, Yasushi, Horiuchi, Masahiro, Kondo, Tomoyoshi, Murayama, Shigeo, Hattori, Nobutaka, Yamamoto, Mitsutoshi, Murata, Miho, Satake, Wataru, Toda, Tatsushi, Filla, Alessandro, Klockgether, Thomas, Wüllner, Ullrich, Nicholson, Garth, Gilman, Sid, Tanner, Caroline M., Kukull, Walter A., Stern, Mathew B., Lee, Virginia M.‐Y., Trojanowski, John Q., Masliah, Eliezer, Low, Phillip A., Sandroni, Paola, Ozelius, Laurie J., Foroud, Tatiana, Tsuji, Shoji

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Association of Long Runs of Homozygosity With Alzheimer Disease Among African American Individuals von Ghani, Mahdi, Reitz, Christiane, Cheng, Rong, Vardarajan, Badri Narayan, Jun, Gyungah, Sato, Christine, Naj, Adam, Rajbhandary, Ruchita, 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 A, 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, Lee, Joseph H, Schellenberg, Gerard D, St. George-Hyslop, Peter, Mayeux, Richard, Rogaeva, Ekaterina

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Characteristics of discordance between amyloid positron emission tomography and plasma amyloid-β 42/40 positivity von Pyun, Jung-Min, Park, Young Ho, Youn, Young Chul, Kang, Min Ju, Shim, Kyu Hwan, Jang, Jae-Won, You, Jihwan, Nho, Kwangsik, Kim, SangYun

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A Multiancestral Genome-Wide Exome Array Study of Alzheimer Disease, Frontotemporal Dementia, and Progressive Supranuclear Palsy von Chen, Jason A, Wang, Qing, Davis-Turak, Jeremy, Li, Yun, Karydas, Anna M, Hsu, Sandy C, Sears, Renee L, Chatzopoulou, Doxa, Huang, Alden Y, Wojta, Kevin J, Klein, Eric, Lee, Jason, Beekly, Duane L, Boxer, Adam, Faber, Kelley M, Haase, Claudia M, Miller, Josh, Poon, Wayne W, Rosen, Ami, Rosen, Howard, Sapozhnikova, Anna, Shapira, Jill, Varpetian, Arousiak, Foroud, Tatiana M, Levenson, Robert W, Levey, Allan I, Kukull, Walter A, Mendez, Mario F, Ringman, John, Chui, Helena, Cotman, Carl, DeCarli, Charles, Miller, Bruce L, Geschwind, Daniel H, Coppola, Giovanni

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Analysis of copy number variation in Alzheimer's disease in a cohort of clinically characterized and neuropathologically verified individuals von Swaminathan, Shanker, Huentelman, Matthew J, Corneveaux, Jason J, Myers, Amanda J, Faber, Kelley M, Foroud, Tatiana, Mayeux, Richard, Shen, Li, Kim, Sungeun, Turk, Mari, Hardy, John, Reiman, Eric M, Saykin, Andrew J

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