Glutamate receptor gene GRIN2A, coffee, and Parkinson disease von Hamza, Taye H, Hill-Burns, Erin M, Scott, William K, Vance, Jeffrey M, Factor, Stewart A, Zabetian, Cyrus P, Payami, Haydeh

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Admixture mapping identifies novel Alzheimer's disease risk regions in African Americans von Rajabli, Farid, Tosto, Giuseppe, Hamilton‐Nelson, Kara L., Kunkle, Brian W., Vardarajan, Badri N., Naj, Adam, Whitehead, Patrice G., Gardner, Olivia K., Bush, William S., Sariya, Sanjeev, Mayeux, Richard P., Farrer, Lindsay A., Cuccaro, Michael L., Vance, Jeffrey M., Griswold, Anthony J., Schellenberg, Gerard D., Haines, Jonathan L., Byrd, Goldie S., Reitz, Christiane, Beecham, Gary W., Pericak‐Vance, Margaret A., Martin, Eden R.

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Compound Heterozygosity for Loss-of-Function Lysyl-tRNA Synthetase Mutations in a Patient with Peripheral Neuropathy von McLaughlin, Heather M., Sakaguchi, Reiko, Liu, Cuiping, Igarashi, Takao, Pehlivan, Davut, Chu, Kristine, Iyer, Ram, Cruz, Pedro, Cherukuri, Praveen F., Hansen, Nancy F., Mullikin, James C., Biesecker, Leslie G., Wilson, Thomas E., Ionasescu, Victor, Nicholson, Garth, Searby, Charles, Talbot, Kevin, Vance, Jeffrey M., Züchner, Stephan, Szigeti, Kinga, Lupski, James R., Hou, Ya-Ming, Green, Eric D., Antonellis, Anthony

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Genome-wide linkage analyses of non-Hispanic white families identify novel loci for familial late-onset Alzheimer's disease von Kunkle, Brian W, Jaworski, James, Barral, Sandra, Vardarajan, Badri, Beecham, Gary W, Martin, Eden R, Cantwell, Laura S, Partch, Amanda, Bird, Thomas D, Raskind, Wendy H, DeStefano, Anita L, Carney, Regina M, Cuccaro, Michael, Vance, Jeffrey M, Farrer, Lindsay A, Goate, Alison M, Foroud, Tatiana, Mayeux, Richard P, Schellenberg, Gerard D, Haines, Jonathan L, Pericak-Vance, Margaret A

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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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Generation of disease-specific autopsy-confirmed iPSCs lines from postmortem isolated Peripheral Blood Mononuclear Cells von Belle, Kinsley, Shabazz, Francelethia S., Nuytemans, Karen, Davis, David A., Ali, Aleena, Young, Juan L., Scott, William K., Mash, Deborah C., Vance, Jeffrey M., Dykxhoorn, Derek M.

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Polymorphic variants in tenascin-C (TNC) are associated with atherosclerosis and coronary artery disease von Minear, Mollie A., Crosslin, David R., Sutton, Beth S., Connelly, Jessica J., Nelson, Sarah C., Gadson-Watson, Shera, Wang, Tianyuan, Seo, David, Vance, Jeffrey M., Sketch, Michael H., Haynes, Carol, Goldschmidt-Clermont, Pascal J., Shah, Svati H., Kraus, William E., Hauser, Elizabeth R., Gregory, Simon G.

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Human whole-exome genotype data for Alzheimer’s disease von Leung, Yuk Yee, Naj, Adam C., Chou, Yi-Fan, Valladares, Otto, Schmidt, Michael, Hamilton-Nelson, Kara, Wheeler, Nicholas, Lin, Honghuang, Gangadharan, Prabhakaran, Qu, Liming, Clark, Kaylyn, Kuzma, Amanda B., Lee, Wan-Ping, Cantwell, Laura, Nicaretta, Heather, Haines, Jonathan, Farrer, Lindsay, Seshadri, Sudha, Brkanac, Zoran, Cruchaga, Carlos, Pericak-Vance, Margaret, Mayeux, Richard P., Bush, William S., Destefano, Anita, Martin, Eden, Schellenberg, Gerard D., Wang, Li-San

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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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Glutamate Receptor Gene GRIN2A , Coffee, and Parkinson Disease: e1004774 von Hamza, Taye H, Hill-Burns, Erin M, Scott, William K, Vance, Jeffrey M, Factor, Stewart A, Zabetian, Cyrus P, Payami, Haydeh

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Genome-wide linkage analyses of non-Hispanic White families identifies novel loci for familial late-onset Alzheimer's disease von Kunkle, Brian W., Jaworski, James, Barral, Sandra, Vardarajan, Badri, Beecham, Gary W., Martin, Eden R., Cantwell, Laura S., Partch, Amanda, Bird, Thomas D., Raskind, Wendy H., DeStefano, Anita L., Carney, Regina M., Cuccaro, Michael, Vance, Jeffrey M., Farrer, Lindsay A., Goate, Alison M., Foroud, Tatiana, Mayeux, Richard P., Schellenberg, Gerard D., Haines, Jonathan L., Pericak-Vance, Margaret A.

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Family-based case-control study of MAOA and MAOB polymorphisms in Parkinson disease von Kang, Sun J., Scott, William K., Li, Yi-Ju, Hauser, Michael A., van der Walt, Joelle M., Fujiwara, Kenichiro, Mayhew, Gregory M., West, Sandra G., Vance, Jeffery M., Martin, Eden R.

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Relationship of genetic variability and depressive symptoms to adverse events after coronary artery bypass graft surgery von Phillips-Bute, Barbara, Mathew, Joseph P, Blumenthal, James A, Morris, Richard W, Podgoreanu, Mihai V, Smith, Michael, Stafford-Smith, Mark, Grocott, Hilary P, Schwinn, Debra A, Newman, Mark F

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Genetic Complexity and Parkinson's Disease von Scott, William K., Stajich, Jeffrey M., Yamaoka, Larry H., Speer, Marcy C., Vance, Jeffery M., Roses, Allen D., Pericak-Vance, Margaret A., Gasser, T., Müller-Myhsok, B., Wszolek, Z. K., Dürr, A., Vaughan, J. R., Bonifati, V., Meco, G., Bereznai, B., Oehlmann, R., Agid, Y., Brice, A., Wood, N., Polymeropoulos, Michael H.

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Mutations in the Pleckstrin Homology Domain of Dynamin 2 Cause Dominant Intermediate Charcot-Marie-Tooth Disease: LBS.002 von Zuchner, Stephan, Noureddine, Maher, Kennerson, Marina, Verhoeven, Kristien, Claeys, Kristl, De Jonghe, Peter, Merory, John, Oliveira, Sofia A., Speer, Marcy C., Stenger, Judith E., Walizada, Gina, Zhu, Danqing, Pericak-Vance, Margaret A., Nicholson, Garth, Timmerman, Vincent, Vance, Jeffrey M.

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Confirmation of linkage of oculopharyngeal muscular dystrophy to chromosome 14q11.2-q13 von STAJICH, J. M, GILCHRIST, J. M, PERICAK-VANCE, M. A, LENNON, F, LEE, A, YAMAOKA, L, HELMS, B, GASKELL, P. C, DONALD, L, ROSES, A. D, VANCE, J. M

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Isolation of Genomic DNA from Mammalian Cells von Gilbert, John R., Vance, Jeffrey M.

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Confirmation of linkage of oculopharyngel muscular dystrophy to chromosome 14q 11.2-q13 von Stajich, Jeffrey M., Lennon, Felicia, Lee, Arnold, Yamaoka, Larry, Helms, Barbara, Gaskell, Perry C., Roses, Allen D., Vance, Jeffrey M., Pericak-Vance, Margaret A., Gilchrist, James M., Donald, Lauren

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Ocular Motility in North Carolina Autosomal Dominant Ataxia von Small, Kent W., Pollock, Stephen C., Vance, Jeffrey M., Stajich, Jeff M., Pericak-Vance, Margaret

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GENETIC SUSCEPTIBILITY GENES FOR ASTHMA AND ATOPY AND ASTHMA-RELATED AND ATOPIC-RELATED PHENOTYPES von PERICAK-VANCE, MARGARET, A, VANCE, JEFFREY, M, HAINES, JONATHAN, L

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