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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Mechanisms of Disease: a molecular genetic update on hereditary axonal neuropathies von Züchner, Stephan, Vance, Jeffery M

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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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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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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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The Deacetylase HDAC6 Regulates Aggresome Formation and Cell Viability in Response to Misfolded Protein Stress von Kawaguchi, Yoshiharu, Kovacs, Jeffrey J, McLaurin, Adam, Vance, Jeffery M, Ito, Akihiro, Yao, Tso-Pang

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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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Axonal neuropathy with optic atrophy is caused by mutations in mitofusin 2 von Züchner, Stephan, De Jonghe, Peter, Jordanova, Albena, Claeys, Kristl G., Guergueltcheva, Velina, Cherninkova, Sylvia, Hamilton, Steven R., Van Stavern, Greg, Krajewski, Karen M., Stajich, Jeffery, Tournev, Ivajlo, Verhoeven, Kristien, Langerhorst, Christine T., de Visser, Marianne, Baas, Frank, Bird, Thomas, Timmerman, Vincent, Shy, Michael, Vance, Jeffery M.

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Mitochondrial Polymorphisms Significantly Reduce the Risk of Parkinson Disease von van der Walt, Joelle M., Nicodemus, Kristin K., Martin, Eden R., Scott, William K., Nance, Martha A., Watts, Ray L., Hubble, Jean P., Haines, Jonathan L., Koller, William C., Lyons, Kelly, Pahwa, Rajesh, Stern, Matthew B., Colcher, Amy, Hiner, Bradley C., Jankovic, Joseph, Ondo, William G., Allen Jr, Fred H., Goetz, Christopher G., Small, Gary W., Mastaglia, Frank, Stajich, Jeffrey M., McLaurin, Adam C., Middleton, Lefkos T., Scott, Burton L., Schmechel, Donald E., Pericak-Vance, Margaret A., Vance, Jeffery M.

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Glycyl tRNA Synthetase Mutations in Charcot-Marie-Tooth Disease Type 2D and Distal Spinal Muscular Atrophy Type V von Antonellis, Anthony, Ellsworth, Rachel E., Sambuughin, Nyamkhishig, Puls, Imke, Abel, Annette, Lee-Lin, Shih-Queen, Jordanova, Albena, Kremensky, Ivo, Christodoulou, Kyproula, Middleton, Lefkos T., Sivakumar, Kumaraswamy, Ionasescu, Victor, Funalot, Benoit, Vance, Jeffery M., Goldfarb, Lev G., Fischbeck, Kenneth H., Green, Eric D.

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Analysis of European mitochondrial haplogroups with Alzheimer disease risk von van der Walt, Joelle M, Dementieva, Yulia A, Martin, Eden R, Scott, William K, Nicodemus, Kristin K, Kroner, Charles C, Welsh-Bohmer, Kathleen A, Saunders, Ann M, Roses, Allen D, Small, Gary W, Schmechel, Donald E, Murali Doraiswamy, P, Gilbert, John R, Haines, Jonathan L, Vance, Jeffery M, Pericak-Vance, Margaret A

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Fibroblast Growth Factor 20 Polymorphisms and Haplotypes Strongly Influence Risk of Parkinson Disease von van der Walt, Joelle M., Noureddine, Maher A., Kittappa, Raja, Hauser, Michael A., Scott, William K., McKay, Ron, Zhang, Fengyu, Stajich, Jeffrey M., Fujiwara, Kenichiro, Scott, Burton L., Pericak-Vance, Margaret A., Vance, Jeffery M., Martin, Eden R.

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MFN2 mutation distribution and genotype/phenotype correlation in Charcot–Marie–Tooth type 2 von Verhoeven, Kristien, Claeys, Kristl G., Züchner, Stephan, Schröder, J. Michael, Weis, Joachim, Ceuterick, Chantal, Jordanova, Albena, Nelis, Eva, De Vriendt, Els, Van Hul, Matthias, Seeman, Pavel, Mazanec, Radim, Saifi, Gulam Mustafa, Szigeti, Kinga, Mancias, Pedro, Butler, Ian J., Kochanski, Andrzej, Ryniewicz, Barbara, De Bleecker, Jan, Van den Bergh, Peter, Verellen, Christine, Van Coster, Rudy, Goemans, Nathalie, Auer-Grumbach, Michaela, Robberecht, Wim, Milic Rasic, Vedrana, Nevo, Yoram, Tournev, Ivajlo, Guergueltcheva, Velina, Roelens, Filip, Vieregge, Peter, Vinci, Paolo, Moreno, Maria Teresa, Christen, H.-J., Shy, Michael E., Lupski, James R., Vance, Jeffery M., De Jonghe, Peter, Timmerman, Vincent

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SNPing Away at Complex Diseases: Analysis of Single-Nucleotide Polymorphisms around APOE in Alzheimer Disease von Martin, Eden R., Lai, Eric H., Gilbert, John R., Rogala, Allison R., Afshari, A.J., Riley, John, Finch, K.L., Stevens, J.F., Livak, K.J., Slotterbeck, Brandon D., Slifer, Susan H., Warren, Liling L., Conneally, P. Michael, Schmechel, Donald E., Purvis, Ian, Pericak-Vance, Margaret A., Roses, Allen D., Vance, Jeffery M.

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Myotilin is mutated in limb girdle muscular dystrophy 1A von HAUSER, M. A, HORRIGAN, S. K, STAJICH, J. M, GASKELL, P. C, GILBERT, J. R, VANCE, J. M, PERICAK-VANCE, M. A, CARPEN, O, WESTBROOK, C. A, SPEER, M. C, SALMIKANGAS, P, TORIAN, U. M, VILES, K. D, DANCEL, R, TIM, R. W, TAIVAINEN, A, BARTOLONI, L, GILCHRIST, J. M

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SNPselector: a web tool for selecting SNPs for genetic association studies von Xu, Hong, Gregory, Simon G., Hauser, Elizabeth R., Stenger, Judith E., Pericak-Vance, Margaret A., Vance, Jeffery M., Züchner, Stephan, Hauser, Michael A.

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Glutathione S-transferase omega-1 modifies age-at-onset of Alzheimer disease and Parkinson disease von Li, Yi-Ju, Oliveira, Sofia A., Xu, Puting, Martin, Eden R., Stenger, Judith E., Scherzer, Clemens R., Hauser, Michael A., Scott, William K., Small, Gary W., Nance, Martha A., Watts, Ray L., Hubble, Jean P., Koller, William C., Pahwa, Rajesh, Stern, Mathew B., Hiner, Bradley C., Jankovic, Joseph, Goetz, Christopher G., Mastaglia, Frank, Middleton, Lefkos T., Roses, Allen D., Saunders, Ann M., Schmechel, Donald E., Gullans, Steven R., Haines, Jonathan L., Gilbert, John R., Vance, Jeffery M., Pericak-Vance, Margaret A.

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Parkin mutations and susceptibility alleles in late-onset Parkinson's disease von Oliveira, Sofia A., Scott, William K., Martin, Eden R., Nance, Martha A., Watts, Ray L., Hubble, Jean P., Koller, William C., Pahwa, Rajesh, Stern, Matthew B., Hiner, Bradley C., Ondo, William G., Allen Jr, Fred H., Scott, Burton L., Goetz, Christopher G., Small, Gary W., Mastaglia, Frank, Stajich, Jeffrey M., Zhang, Fengyu, Booze, Michael W., Winn, Michelle P., Middleton, Lefkos T., Haines, Jonathan L., Pericak-Vance, Margaret A., Vance, Jeffery M.

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Apolipoprotein E controls the risk and age at onset of Parkinson disease von LI, Y. J, HAUSER, M. A, PAHWA, R, STERN, M. B, HINER, B. C, JANKOVIC, J, GOETZ, C. G, SMALL, G. W, MASTAGLIA, F, HAINES, J. L, PERICAK-VANCE, M. A, VANCE, J. M, SCOTT, W. K, MARTIN, E. R, BOOZE, M. W, QIN, X. J, WALTER, J. W, NANCE, M. A, HUBBLE, J. P, KOLLER, W. C

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A Genomewide Scan for Early-Onset Coronary Artery Disease in 438 Families: The GENECARD Study von Hauser, Elizabeth R., Crossman, David C., Granger, Christopher B., Haines, Jonathan L., Jones, Christopher J.H., Mooser, Vincent, McAdam, Brendan, Winkelmann, Bernhard R., Wiseman, Alan H., Muhlestein, J. Brent, Bartel, Alan G., Dennis, Charles A., Dowdy, Elaine, Estabrooks, Susan, Eggleston, Karen, Francis, Sheila, Roche, Kath, Clevenger, Paula W., Huang, Liling, Pedersen, Bonnie, Shah, Svati, Schmidt, Silke, Haynes, Carol, West, Sandra, Asper, Donny, Booze, Michael, Sharma, Sanjay, Sundseth, Scott, Middleton, Lefkos, Roses, Allen D., Hauser, Michael A., Vance, Jeffery M., Pericak-Vance, Margaret A., Kraus, William E.

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