Nonoperative therapies for combined modality treatment of hepatocellular cancer: expert consensus statement von Schwarz, Roderich E., Abou-Alfa, Ghassan K., Geschwind, Jeffrey F., Krishnan, Sunil, Salem, Riad, Venook, Alan P.

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Pancreaticoduodenectomy: Role of Interventional Radiologists in Managing Patients and Complications von Sohn, Taylor A, Yeo, Charles J, Cameron, John L, Geschwind, Jeffrey F, Mitchell, Sally E, Venbrux, Anthony C, Lillemoe, Keith D

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Pancreaticoduodenectomy von Sohn, Taylor A, Yeo, Charles J, Cameron, John L, Geschwind, Jeffrey F, Mitchell, Sally E, Venbrux, Anthony C, Lillemoe, Keith D

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De novo mutations in regulatory elements in neurodevelopmental disorders von Short, Patrick J., McRae, Jeremy F., Gallone, Giuseppe, Sifrim, Alejandro, Won, Hyejung, Geschwind, Daniel H., Wright, Caroline F., Firth, Helen V., FitzPatrick, David R., Barrett, Jeffrey C., Hurles, Matthew E.

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The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability von Singh, Tarjinder, Walters, James T R, Johnstone, Mandy, Curtis, David, Suvisaari, Jaana, Torniainen, Minna, Rees, Elliott, Iyegbe, Conrad, Blackwood, Douglas, McIntosh, Andrew M, Kirov, Georg, Geschwind, Daniel, Murray, Robin M, Di Forti, Marta, Bramon, Elvira, Gandal, Michael, Hultman, Christina M, Sklar, Pamela, Palotie, Aarno, Sullivan, Patrick F, O'Donovan, Michael C, Owen, Michael J, Barrett, Jeffrey C

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Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci von Sanders, Stephan J., He, Xin, Willsey, A. Jeremy, Ercan-Sencicek, A. Gulhan, Samocha, Kaitlin E., Cicek, A. Ercument, Murtha, Michael T., Bal, Vanessa H., Bishop, Somer L., Dong, Shan, Goldberg, Arthur P., Jinlu, Cai, Keaney, John F., Klei, Lambertus, Mandell, Jeffrey D., Moreno-De-Luca, Daniel, Poultney, Christopher S., Robinson, Elise B., Smith, Louw, Solli-Nowlan, Tor, Su, Mack Y., Teran, Nicole A., Walker, Michael F., Werling, Donna M., Beaudet, Arthur L., Cantor, Rita M., Fombonne, Eric, Geschwind, Daniel H., Grice, Dorothy E., Lord, Catherine, Lowe, Jennifer K., Mane, Shrikant M., Martin, Donna M., Morrow, Eric M., Talkowski, Michael E., Sutcliffe, James S., Walsh, Christopher A., Yu, Timothy W., Ledbetter, David H., Martin, Christa Lese, Cook, Edwin H., Buxbaum, Joseph D., Daly, Mark J., Devlin, Bernie, Roeder, Kathryn, State, Matthew W.

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Exceptionally low likelihood of Alzheimer’s dementia in APOE2 homozygotes from a 5,000-person neuropathological study von Reiman, Eric M., Arboleda-Velasquez, Joseph F., Quiroz, Yakeel T., Huentelman, Matthew J., Beach, Thomas G., Caselli, Richard J., Chen, Yinghua, Su, Yi, Myers, Amanda J., Hardy, John, Paul Vonsattel, Jean, Younkin, Steven G., Bennett, David A., De Jager, Philip L., Larson, Eric B., Crane, Paul K., Keene, C. Dirk, Kamboh, M. Ilyas, Kofler, Julia K., Duque, Linda, Gilbert, John R., Gwirtsman, Harry E., Buxbaum, Joseph D., Dickson, Dennis W., Frosch, Matthew P., Ghetti, Bernardino F., Lunetta, Kathryn L., Wang, Li-San, Hyman, Bradley T., Kukull, Walter A., Foroud, Tatiana, Haines, Jonathan L., Mayeux, Richard P., Pericak-Vance, Margaret A., Schneider, Julie A., Trojanowski, John Q., Farrer, Lindsay A., Schellenberg, Gerard D., Beecham, Gary W., Montine, Thomas J., Jun, Gyungah R.

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Detection of High-Risk Paraneoplastic Antibodies against TRIM9 and TRIM67 Proteins von Bartley, Christopher M, Ngo, Thomas T, Do, Le Duy, Zekeridou, Anastasia, Dandekar, Ravi, Muñiz-Castrillo, Sergio, Alvarenga, Bonny D, Zorn, Kelsey C, Tubati, Asritha, Pinto, Anne-Laurie, Browne, Weston D, Hullett, Patrick W, Terrelonge, Mark, Schubert, Ryan D, Piquet, Amanda L, Yang, Binxia, Montalvo, Mayra, Kung, Andrew F, Mann, Sabrina A, Shah, Maulik P, Geschwind, Michael D, Gelfand, Jeffrey M, DeRisi, Joseph L, Pittock, Sean J, Honnorat, Jérôme, Pleasure, Samuel J, Wilson, Michael R

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Common genetic variants on 5p14.1 associate with autism spectrum disorders von Hakonarson, Hakon, Wang, Kai, Zhang, Haitao, Ma, Deqiong, Bucan, Maja, Glessner, Joseph T, Abrahams, Brett S, Salyakina, Daria, Imielinski, Marcin, Bradfield, Jonathan P, Sleiman, Patrick M. A, Kim, Cecilia E, Hou, Cuiping, Frackelton, Edward, Chiavacci, Rosetta, Takahashi, Nagahide, Sakurai, Takeshi, Rappaport, Eric, Lajonchere, Clara M, Munson, Jeffrey, Estes, Annette, Korvatska, Olena, Piven, Joseph, Sonnenblick, Lisa I, Alvarez Retuerto, Ana I, Herman, Edward I, Dong, Hongmei, Hutman, Ted, Sigman, Marian, Ozonoff, Sally, Klin, Ami, Owley, Thomas, Sweeney, John A, Brune, Camille W, Cantor, Rita M, Bernier, Raphael, Gilbert, John R, Cuccaro, Michael L, McMahon, William M, Miller, Judith, State, Matthew W, Wassink, Thomas H, Coon, Hilary, Levy, Susan E, Schultz, Robert T, Nurnberger, John I, Haines, Jonathan L, Sutcliffe, James S, Cook, Edwin H, Minshew, Nancy J, Buxbaum, Joseph D, Dawson, Geraldine, Grant, Struan F. A, Geschwind, Daniel H, Pericak-Vance, Margaret A, Schellenberg, Gerard D

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A statistical framework for cross-tissue transcriptome-wide association analysis von Hu, Yiming, Li, Mo, Lu, Qiongshi, Weng, Haoyi, Wang, Jiawei, Zekavat, Seyedeh M., Yu, Zhaolong, Li, Boyang, Gu, Jianlei, Muchnik, Sydney, Shi, Yu, Kunkle, Brian W., Mukherjee, Shubhabrata, Natarajan, Pradeep, Naj, Adam, Kuzma, Amanda, Zhao, Yi, Crane, Paul K., Lu, Hui, Zhao, Hongyu

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Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease von Naj, Adam C, Jun, Gyungah, Beecham, Gary W, Wang, Li-San, Vardarajan, Badri Narayan, Buros, Jacqueline, Gallins, Paul J, Buxbaum, Joseph D, Crane, Paul K, Larson, Eric B, Bird, Thomas D, De Jager, Philip L, Schneider, Julie A, Younkin, Steven G, Cruchaga, Carlos, Kauwe, John S K, Nowotny, Petra, Hardy, John, Myers, Amanda J, Barmada, Michael M, Baldwin, Clinton T, Arnold, Steven E, Barber, Robert, Beach, Thomas, Bowen, James D, Boxer, Adam, Carlson, Chris S, Carney, Regina M, Carroll, Steven L, Clark, David G, Cummings, Jeffrey L, DeKosky, Steven T, Diaz-Arrastia, Ramon, Dickson, Dennis W, Faber, Kelley M, Fallon, Kenneth B, Farlow, Martin R, Ferris, Steven, Ganguli, Mary, Gearing, Marla, Ghetti, Bernardino, Gilbert, John R, Gilman, Sid, Glass, Jonathan D, Growdon, John H, Hamilton, Ronald L, Harrell, Lindy E, Head, Elizabeth, Honig, Lawrence S, Hulette, Christine M, Johnson, Nancy, Karydas, Anna, Kaye, Jeffrey A, Kim, Ronald, Lah, James J, Levey, Allan I, Lieberman, Andrew P, Mack, Wendy J, Marson, Daniel C, Martiniuk, Frank, Mash, Deborah C, McDavid, Andrew N, McKee, Ann C, Mesulam, Marsel, Miller, Bruce L, Miller, Carol A, Parisi, Joseph E, Perl, Daniel P, Peskind, Elaine, Rajbhandary, Ruchita A, Reisberg, Barry, Ringman, John M, Roberson, Erik D, Rosenberg, Roger N, Sano, Mary, Seeley, William, Shelanski, Michael L, Slifer, Michael A, Smith, Charles D, Sonnen, Joshua A, Spina, Salvatore, Tanzi, Rudolph E, Troncoso, Juan C, Weintraub, Sandra, Welsh-Bohmer, Kathleen A, Woltjer, Randall L, Cantwell, Laura B, Lunetta, Kathryn L, Kamboh, M Ilyas, Saykin, Andrew J, Reiman, Eric M, Morris, John C, Goate, Alison M, Blacker, Deborah, Tsuang, Debby W, Hakonarson, Hakon, Kukull, Walter A, Haines, Jonathan L, Pericak-Vance, Margaret A, Farrer, Lindsay A

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Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases von COPPOLA, Giovanni, CHINNATHAMBI, Subashchandrabose, LANE, Jessica R, KARYDAS, Anna M, KENET, Robert O, BIERNAT, Jacek, WANG, Li-San, COTMAN, Carl W, DECARLI, Charles S, LEVEY, Allan I, RINGMAN, John M, MENDEZ, Mario F, JIYONG LEE, Jason, CHUI, Helena C, LE BER, Isabelle, BRICE, Alexis, LUPTON, Michelle K, PREZA, Elisavet, LOVESTONE, Simon, POWELL, John, GRAFF-RADFORD, Neill, PETERSEN, Ronald C, BOEVE, Bradley F, DOMBROSKI, Beth A, LIPPA, Carol F, BIGIO, Eileen H, MACKENZIE, Ian, FINGER, Elizabeth, KERTESZ, Andrew, CASELLI, Richard J, GEARING, Marla, JUNCOS, Jorge L, GHETTI, Bernardino, SPINA, Salvatore, BAKER, Matt C, BORDELON, Yvette M, TOURTELLOTTE, Wallace W, FROSCH, Matthew P, VONSATTEL, Jean Paul G, ZAROW, Chris, BEACH, Thomas G, ALBIN, Roger L, LIEBERMAN, Andrew P, LEE, Virginia M, TROJANOWSKI, John Q, SOTO-ORTOLAZA, Alexandra I, VAN DEERLIN, Vivianna M, BIRD, Thomas D, GALASKO, Douglas R, MASLIAH, Eliezer, WHITE, Charles L, TRONCOSO, JuanC, HANNEQUIN, Didier, BOXER, Adam L, GESCHWIND, Michael D, KUMAR, Satish, LEE, Suzee E, KLEIN, Eric, HUANG, Alden Y, SEARS, Renee

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Assessment of the genetic variance of late-onset Alzheimer’s disease von Ridge, Perry G, Hoyt, Kaitlyn B, Boehme, Kevin, Mukherjee, Shubhabrata, Crane, Paul K, Haines, Jonathan L, Mayeux, Richard, Farrer, Lindsay A, Pericak-Vance, Margaret A, Schellenberg, Gerard D, Kauwe, John S.K

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A novel Alzheimer disease locus located near the gene encoding tau protein von Jun, G, Ibrahim-Verbaas, C A, Vronskaya, M, Chung, J, Naj, A C, Kunkle, B W, Wang, L-S, Bis, J C, Bellenguez, C, Harold, D, Destefano, A L, Grenier-Boley, B, Sims, R, Smith, A V, Chouraki, V, Hamilton-Nelson, K L, Ikram, M A, Fievet, N, Martin, E R, Kamatani, Y, Valladares, O, Laza, A R, Zelenika, D, Choi, S-H, Boland, A, Becker, T, Kukull, W A, van der Lee, S J, Pasquier, F, Cruchaga, C, Beekly, D, Fitzpatrick, A L, Hanon, O, Gill, M, Gudnason, V, Campion, D, Love, S, Bennett, D A, Amin, N, Berr, C, Tsolaki, Magda, Buxbaum, J D, Lopez, O L, Deramecourt, V, Fox, N C, Cantwell, L B, Tárraga, L, Dufouil, C, Hardy, J, Crane, P K, Eiriksdottir, G, Hannequin, D, Clarke, R, Evans, D, Mosley, T H, Letenneur, L, Brayne, C, Maier, W, De Jager, P, Dartigues, J-F, Hampel, H, de Bruijn, R F A G, Tzourio, C, Pastor, P, Larson, E B, O'Donovan, M C, Montine, T J, Nalls, M A, Mead, S, Reiman, E M, Jonsson, P V, St George-Hyslop, P H, Boada, M, Passmore, P, Wendland, J R, Schmidt, R, Morgan, K, Powell, J F, Carasquillo, M, Jakobsdóttir, J, Kauwe, J S K, Rujescu, D, Nöthen, M M, Hofman, A, Jones, L, Haines, J L, Psaty, B M, Van Broeckhoven, C, Holmans, P, Launer, L J, Mayeux, R, Goate, A M, Escott-Price, V, Seshadri, S, Pericak-Vance, M A, Amouyel, P, Williams, J, van Duijn, C M, Schellenberg, G D, Farrer, L A

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Novel Alzheimer Disease Risk Loci and Pathways in African American Individuals Using the African Genome Resources Panel: A Meta-analysis von Kunkle, Brian W, Schmidt, Michael, Klein, Hans-Ulrich, Naj, Adam C, Hamilton-Nelson, Kara L, Larson, Eric B, Evans, Denis A, De Jager, Phil L, Crane, Paul K, Buxbaum, Joe D, Ertekin-Taner, Nilufer, Barnes, Lisa L, Fallin, M. Daniele, Manly, Jennifer J, Go, Rodney C. P, Obisesan, Thomas O, Kamboh, M. Ilyas, Bennett, David A, Hall, Kathleen S, Goate, Alison M, Foroud, Tatiana M, Martin, Eden R, Wang, Li-San, Byrd, Goldie S, Farrer, Lindsay A, Haines, Jonathan L, Schellenberg, Gerard D, Mayeux, Richard, Pericak-Vance, Margaret A, Reitz, Christiane, Graff-Radford, Neill R, Martinez, Izri, Ayodele, Temitope, Logue, Mark W, Cantwell, Laura B, Jean-Francois, Melissa, Kuzma, Amanda B, Adams, L.D, Vance, Jeffery M, Cuccaro, Michael L, Chung, Jaeyoon, Mez, Jesse, Lunetta, Kathryn L, Jun, Gyungah R, Lopez, Oscar L, Hendrie, Hugh C, Reiman, Eric M, Kowall, Neil W, Leverenz, James B, Small, Scott A, Levey, Allan I, Golde, Todd E, Saykin, Andrew J, Starks, Takiyah D, Albert, Marilyn S, Hyman, Bradley T, Petersen, Ronald C, Sano, Mary, Wisniewski, Thomas, Vassar, Robert, Kaye, Jeffrey A, Henderson, Victor W, DeCarli, Charles, LaFerla, Frank M, Brewer, James B, Miller, Bruce L, Swerdlow, Russell H, Van Eldik, Linda J, Paulson, Henry L, Trojanowski, John Q, Chui, Helena C, Rosenberg, Roger N, Craft, Suzanne, Grabowski, Thomas J, Asthana, Sanjay, Morris, John C, Strittmatter, Stephen M, Kukull, Walter A

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Diffusion tensor imaging in preclinical and presymptomatic carriers of familial Alzheimer's disease mutations von Ringman, John M., O'Neill, Joseph, Geschwind, Daniel, Medina, Luis, Apostolova, Liana G., Rodriguez, Yaneth, Schaffer, Barbara, Varpetian, Arousiak, Tseng, Benjamin, Ortiz, Freddy, Fitten, Jaime, Cummings, Jeffrey L., Bartzokis, George

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Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel von Huang, Jie, Howie, Bryan, McCarthy, Shane, Memari, Yasin, Walter, Klaudia, Min, Josine L., Danecek, Petr, Malerba, Giovanni, Trabetti, Elisabetta, Zheng, Hou-Feng, Gambaro, Giovanni, Richards, J. Brent, Durbin, Richard, Timpson, Nicholas J., Marchini, Jonathan, Soranzo, Nicole

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Associations between Potentially Modifiable Risk Factors and Alzheimer Disease: A Mendelian Randomization Study von Østergaard, Søren D, Mukherjee, Shubhabrata, Sharp, Stephen J, Proitsi, Petroula, Lotta, Luca A, Day, Felix, Perry, John R B, Boehme, Kevin L, Walter, Stefan, Kauwe, John S, Gibbons, Laura E, Larson, Eric B, Powell, John F, Langenberg, Claudia, Crane, Paul K, Wareham, Nicholas J, Scott, Robert A

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Targeted Next-Generation Sequencing Analysis of 1,000 Individuals with Intellectual Disability von Grozeva, Detelina, Carss, Keren, Spasic-Boskovic, Olivera, Tejada, Maria-Isabel, Gecz, Jozef, Shaw, Marie, Corbett, Mark, Haan, Eric, Thompson, Elizabeth, Friend, Kathryn, Hussain, Zaamin, Hackett, Anna, Field, Michael, Renieri, Alessandra, Stevenson, Roger, Schwartz, Charles, Floyd, James A.B., Bentham, Jamie, Cosgrove, Catherine, Keavney, Bernard, Bhattacharya, Shoumo, Hurles, Matthew, Raymond, F. Lucy

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Transethnic genome-wide scan identifies novel Alzheimer's disease loci von Jun, Gyungah R, Chung, Jaeyoon, Mez, Jesse, Barber, Robert, Beecham, Gary W, Bennett, David A, Buxbaum, Joseph D, Byrd, Goldie S, Carrasquillo, Minerva M, Crane, Paul K, Cruchaga, Carlos, De Jager, Philip, Ertekin-Taner, Nilufer, Evans, Denis, Fallin, M. Danielle, Foroud, Tatiana M, Friedland, Robert P, Goate, Alison M, Graff-Radford, Neill R, Hendrie, Hugh, Hall, Kathleen S, Hamilton-Nelson, Kara L, Inzelberg, Rivka, Kamboh, M. Ilyas, Kauwe, John S.K, Kukull, Walter A, Kunkle, Brian W, Kuwano, Ryozo, Larson, Eric B, Logue, Mark W, Manly, Jennifer J, Martin, Eden R, Montine, Thomas J, Mukherjee, Shubhabrata, Naj, Adam, Reiman, Eric M, Reitz, Christiane, Sherva, Richard, St. George-Hyslop, Peter H, Thornton, Timothy, Younkin, Steven G, Vardarajan, Badri N, Wang, Li-San, Wendlund, Jens R, Winslow, Ashley R, Haines, Jonathan, Mayeux, Richard, Pericak-Vance, Margaret A, Schellenberg, Gerard, Lunetta, Kathryn L, Farrer, Lindsay A

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