Ganglioside-induced differentiation-associated protein-1 is mutant in Charcot-Marie-Tooth disease type 4A/8q21 von Vance, Jeffery M, Baxter, Rachel V, Ben Othmane, Kamel, Rochelle, Julie M, Stajich, Jason E, Hulette, Christine, Dew-Knight, Susan, Hentati, Faycal, Ben Hamida, Mongi, Bel, S, Stenger, Judy E, Gilbert, John R, Pericak-Vance, Margaret A

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HLA-DR2 Dose Effect on Susceptibility to Multiple Sclerosis and Influence on Disease Course von Barcellos, L.F., Oksenberg, J.R., Begovich, A.B., Martin, E.R., Schmidt, S., Vittinghoff, E., Goodin, D.S., Pelletier, D., Lincoln, R.R., Bucher, P., Swerdlin, A., Pericak-Vance, M.A., Haines, J.L., Hauser, S.L.

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Mutation screening of spastin, atlastin, and REEP1 in hereditary spastic paraplegia von McCorquodale III, DS, Ozomaro, U, Huang, J, Montenegro, G, Kushman, A, Citrigno, L, Price, J, Speziani, F, Pericak-Vance, MA, Züchner, S

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Osteonecrosis of the jaw and bisphosphonates: A comparison with white phosphorus, radium, and osteopetrosis von Vance, Michael A.

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Mutations in the FUS/TLS Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis von Kwiatkowski, T.J. Jr, Bosco, D.A, LeClerc, A.L, Tamrazian, E, Vanderburg, C.R, Russ, C, Davis, A, Gilchrist, J, Kasarskis, E.J, Munsat, T, Valdmanis, P, Rouleau, G.A, Hosler, B.A, Cortelli, P, de Jong, P.J, Yoshinaga, Y, Haines, J.L, Pericak-Vance, M.A, Yan, J, Ticozzi, N, Siddique, T, McKenna-Yasek, D, Sapp, P.C, Horvitz, H.R, Landers, J.E, Brown, R.H. Jr

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Enhancing linkage analysis of complex disorders: an evaluation of high-density genotyping von Sawcer, Stephen J, Maranian, Mel, Singlehurst, Sara, Yeo, TaiWai, Compston, Alastair, Daly, Mark J, De Jager, Philip L, Gabriel, Stacey, Hafler, David A, Ivinson, Adrian J, Lander, Eric S, Rioux, John D, Walsh, Emily, Gregory, Simon G, Schmidt, Silke, Pericak-Vance, Margaret A, Barcellos, Lisa, Hauser, Stephen L, Oksenberg, Jorge R, Kenealy, Shannon J, Haines, Jonathan L

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Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A von Vance, Jeffery M, Züchner, Stephan, Mersiyanova, Irina V, Muglia, Maria, Bissar-Tadmouri, Nisrine, Rochelle, Julie, Dadali, Elena L, Zappia, Mario, Nelis, Eva, Patitucci, Alessandra, Senderek, Jan, Parman, Yesim, Evgrafov, Oleg, Jonghe, Peter De, Takahashi, Yuji, Tsuji, Shoij, Pericak-Vance, Margaret A, Quattrone, Aldo, Battologlu, Esra, Polyakov, Alexander V, Timmerman, Vincent, Schröder, J Michael

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Identification of Significant Association and Gene-Gene Interaction of GABA Receptor Subunit Genes in Autism von Ma, D.Q., Whitehead, P.L., Menold, M.M., Martin, E.R., Ashley-Koch, A.E., Mei, H., Ritchie, M.D., DeLong, G.R., Abramson, R.K., Wright, H.H., Cuccaro, M.L., Hussman, J.P., Gilbert, J.R., Pericak-Vance, M.A.

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Mutation in the TRPC6 Cation Channel Causes Familial Focal Segmental Glomerulosclerosis von Winn, Michelle P, Conlon, Peter J, Lynn, Kelvin L, Farrington, Merry Kay, Creazzo, Tony, Hawkins, April F, Daskalakis, Nikki, Kwan, Shu Ying, Ebersviller, Seth, Burchette, James L, Pericak-Vance, Margaret A, Howell, David N, Vance, Jeffery M, Rosenberg, Paul B

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Complement Factor H Variant Increases the Risk of Age-Related Macular Degeneration von Haines, Jonathan L, Hauser, Michael A, Schmidt, Silke, Scott, William K, Olson, Lana M, Gallins, Paul, Spencer, Kylee L, Kwan, Shu Ying, Noureddine, Maher, Gilbert, John R, Schnetz-Boutaud, Nathalie, Agarwal, Anita, Postel, Eric A, Pericak-Vance, Margaret A

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Dissecting the role of Amerindian genetic ancestry and the ApoE ε4 allele on Alzheimer disease in an admixed Peruvian population von Marca-Ysabel, Maria Victoria, Rajabli, Farid, Cornejo-Olivas, Mario, Whitehead, Patrice G., Hofmann, Natalia K., Illanes Manrique, Maryenela Zaida, Veliz Otani, Diego Martin, Milla Neyra, Ana Karina, Castro Suarez, Sheila, Meza Vega, Maria, Adams, Larry D., Mena, Pedro R., Rosario, Isasi, Cuccaro, Michael L., Vance, Jeffery M., Beecham, Gary W., Custodio, Nilton, Montesinos, Rosa, Mazzetti Soler, Pilar E., Pericak-Vance, Margaret A.

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Mutations in the Novel Mitochondrial Protein REEP1 Cause Hereditary Spastic Paraplegia Type 31 von Züchner, Stephan, Wang, Gaofeng, Tran-Viet, Khanh-Nhat, Nance, Martha A., Gaskell, Perry C., Vance, Jeffery M., Ashley-Koch, Allison E., Pericak-Vance, Margaret A.

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Caspase-8, association with Alzheimer's Disease and functional analysis of rare variants von Rehker, Jan, Rodhe, Johanna, Nesbitt, Ryan R, Boyle, Evan A, Martin, Beth K, Lord, Jenny, Karaca, Ilker, Naj, Adam, Jessen, Frank, Helisalmi, Seppo, Soininen, Hilkka, Hiltunen, Mikko, Ramirez, Alfredo, Scherer, Martin, Farrer, Lindsay A, Haines, Jonathan L, Pericak-Vance, Margaret A, Raskind, Wendy H, Cruchaga, Carlos, Schellenberg, Gerard D, Joseph, Bertrand, Brkanac, Zoran

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Class II HLA interactions modulate genetic risk for multiple sclerosis von Moutsianas, Loukas, Jostins, Luke, Beecham, Ashley H, Dilthey, Alexander T, Xifara, Dionysia K, Ban, Maria, Shah, Tejas S, Patsopoulos, Nikolaos A, Alfredsson, Lars, Anderson, Carl A, Attfield, Katherine E, Baranzini, Sergio E, Barrett, Jeffrey, Binder, Thomas M C, Booth, David, Buck, Dorothea, Celius, Elisabeth G, Cotsapas, Chris, D'Alfonso, Sandra, Dendrou, Calliope A, Donnelly, Peter, Dubois, Bénédicte, Fontaine, Bertrand, Fugger, Lars, Goris, An, Gourraud, Pierre-Antoine, Graetz, Christiane, Hemmer, Bernhard, Hillert, Jan, Kockum, Ingrid, Leslie, Stephen, Lill, Christina M, Martinelli-Boneschi, Filippo, Oksenberg, Jorge R, Olsson, Tomas, Oturai, Annette, Saarela, Janna, Søndergaard, Helle Bach, Spurkland, Anne, Taylor, Bruce, Winkelmann, Juliane, Zipp, Frauke, Haines, Jonathan L, Pericak-Vance, Margaret A, Spencer, Chris C A, Stewart, Graeme, Hafler, David A, Ivinson, Adrian J, Harbo, Hanne F, Hauser, Stephen L, De Jager, Philip L, Compston, Alastair, McCauley, Jacob L, Sawcer, Stephen, McVean, Gil

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Mutations in the pleckstrin homology domain of dynamin 2 cause dominant intermediate Charcot-Marie-Tooth disease von Züchner, Stephan, Noureddine, Maher, Kennerson, Marina, Verhoeven, Kristien, Claeys, Kristl, Jonghe, Peter De, Merory, John, Oliveira, Sofia A, Speer, Marcy C, Stenger, Judith E, Walizada, Gina, Zhu, Danqing, Pericak-Vance, Margaret A, Nicholson, Garth, Timmerman, Vincent, Vance, Jeffery M

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Polygenic Overlap Between C-Reactive Protein, Plasma Lipids, and Alzheimer Disease von Desikan, Rahul S, Schork, Andrew J, Wang, Yunpeng, Thompson, Wesley K, Dehghan, Abbas, Ridker, Paul M, Chasman, Daniel I, McEvoy, Linda K, Holland, Dominic, Chen, Chi-Hua, Karow, David S, Brewer, James B, Hess, Christopher P, Williams, Julie, Sims, Rebecca, O'Donovan, Michael C, Choi, Seung Hoan, Bis, Joshua C, Ikram, M Arfan, Gudnason, Vilmundur, DeStefano, Anita L, van der Lee, Sven J, Psaty, Bruce M, van Duijn, Cornelia M, Launer, Lenore, Seshadri, Sudha, Pericak-Vance, Margaret A, Mayeux, Richard, Haines, Jonathan L, Farrer, Lindsay A, Hardy, John, Ulstein, Ingun Dina, Aarsland, Dag, Fladby, Tormod, White, Linda R, Sando, Sigrid B, Rongve, Arvid, Witoelar, Aree, Djurovic, Srdjan, Hyman, Bradley T, Snaedal, Jon, Steinberg, Stacy, Stefansson, Hreinn, Stefansson, Kari, Schellenberg, Gerard D, Andreassen, Ole A, Dale, Anders M

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A meta-analysis of genomic screens in multiple sclerosis von The Transatlantic Multiple Sclerosis Genetics Cooperative

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Cigarette Smoking Strongly Modifies the Association of LOC387715 and Age-Related Macular Degeneration von Schmidt, Silke, Hauser, Michael A., Scott, William K., Postel, Eric A., Agarwal, Anita, Gallins, Paul, Wong, Frank, Chen, Yu Sarah, Spencer, Kylee, Schnetz-Boutaud, Nathalie, Haines, Jonathan L., Pericak-Vance, Margaret A.

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Network-Based Multiple Sclerosis Pathway Analysis with GWAS Data from 15,000 Cases and 30,000 Controls von Baranzini, Sergio E., Khankhanian, Pouya, Patsopoulos, Nikolaos A., Li, Michael, Stankovich, Jim, Cotsapas, Chris, Søndergaard, Helle Bach, Ban, Maria, Barizzone, Nadia, Bergamaschi, Laura, Booth, David, Buck, Dorothea, Cavalla, Paola, Celius, Elisabeth G., Comabella, Manuel, Comi, Giancarlo, Compston, Alastair, Cournu-Rebeix, Isabelle, D’alfonso, Sandra, Damotte, Vincent, Din, Lennox, Dubois, Bénédicte, Elovaara, Irina, Esposito, Federica, Fontaine, Bertrand, Franke, Andre, Goris, An, Gourraud, Pierre-Antoine, Graetz, Christiane, Guerini, Franca R., Guillot-Noel, Léna, Hafler, David, Hakonarson, Hakon, Hall, Per, Hamsten, Anders, Harbo, Hanne F., Hemmer, Bernhard, Hillert, Jan, Kemppinen, Anu, Kockum, Ingrid, Koivisto, Keijo, Larsson, Malin, Lathrop, Mark, Leone, Maurizio, Lill, Christina M., Macciardi, Fabio, Martin, Roland, Martinelli, Vittorio, Martinelli-Boneschi, Filippo, McCauley, Jacob L., Myhr, Kjell-Morten, Naldi, Paola, Olsson, Tomas, Oturai, Annette, Pericak-Vance, Margaret A., Perla, Franco, Reunanen, Mauri, Saarela, Janna, Saker-Delye, Safa, Salvetti, Marco, Sellebjerg, Finn, Sørensen, Per Soelberg, Spurkland, Anne, Stewart, Graeme, Taylor, Bruce, Tienari, Pentti, Winkelmann, Juliane, Zipp, Frauke, Ivinson, Adrian J., Haines, Jonathan L., Sawcer, Stephen, DeJager, Philip, Hauser, Stephen L., Oksenberg, Jorge R.

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Patterns of Brain Activation in People at Risk for Alzheimer's Disease von Bookheimer, Susan Y, Strojwas, Magdalena H, Cohen, Mark S, Saunders, Ann M, Pericak-Vance, Margaret A, Mazziotta, John C, Small, Gary W

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