Linkage of frontotemporal dementia to chromosome 17 : Clinical and neuropathological characterization of phenotype von YAMAOKA, L. H, WELSH-BOHMER, K. A, PERICAK-VANCE, M. A, HULETTE, C. M, GASKELL, P. C, MURRAY, M, RIMMLER, J. L, ROSI HELMS, B, GUERRA, M, ROSES, A. D, SCHMECHEL, D. E

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Protective effect of apolipoprotein E type 2 allele for late onset Alzheimer disease von Corder, E. H, Saunders, A. M, Risch, N. J, Strittmatter, W. J, Schmechel, D. E, Gaskell, P. C, Rimmler, J. B, Locke, P. A, Conneally, P. M, Schmader, K. E, Small, G. W, Roses, A. D, Haines, J. L, Pericak-Vance, M. A

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Genetic basis for clinical expression in multiple sclerosis von BARCELLOS, L. F, OKSENBERG, J. R, HAUSER, S. L, GREEN, A. J, BUCHER, P, RIMMLER, J. B, SCHMIDT, S, GARCIA, M. E, LINCOLN, R. R, PERICAK-VANCE, M. A, HAINES, J. L

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A High-Density Screen for Linkage in Multiple Sclerosis von Sawcer, Stephen, Ban, Maria, Maranian, Mel, Yeo, Tai Wai, Compston, Alastair, Kirby, Andrew, Daly, Mark J, De Jager, Philip L, Walsh, Emily, Lander, Eric S, Rioux, John D, Hafler, David A, Ivinson, Adrian, Rimmler, Jacqueline, Gregory, Simon G, Schmidt, Silke, Pericak-Vance, Margaret A, Akesson, Eva, Hillert, Jan, Datta, Pameli, Oturai, Annette, Ryder, Lars P, Harbo, Hanne F, Spurkland, Anne, Myhr, Kjell-Morten, Laaksonen, Mikko, Booth, David, Heard, Robert, Stewart, Graeme, Lincoln, Robin, Barcellos, Lisa F, Hauser, Stephen L, Oksenberg, Jorge R, Kenealy, Shannon J, Haines, Jonathan L

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A Second-Generation Genomic Screen for Multiple Sclerosis von Kenealy, S.J., Babron, M.-C., Bradford, Y., Schnetz-Boutaud, N., Haines, J.L., Rimmler, J.B., Schmidt, S., Pericak-Vance, M.A., Barcellos, L.F., Lincoln, R.R., Oksenberg, J.R., Hauser, S.L., Clanet, M., Brassat, D., Edan, G., Yaouanq, J., Semana, G., Cournu-Rebeix, I., Lyon-Caen, O., Fontaine, B.

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Association of Polymorphisms in the Apolipoprotein E Region with Susceptibility to and Progression of Multiple Sclerosis von Schmidt, Silke, Barcellos, Lisa F., DeSombre, Karen, Rimmler, Jacqueline B., Lincoln, Robin R., Bucher, Patricia, Saunders, Ann M., Lai, Eric, Martin, Eden R., Vance, Jeffery M., Oksenberg, Jorge R., Hauser, Stephen L., Pericak-Vance, Margaret A., Haines, Jonathan L., Multiple Sclerosis Genetics Group

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Multiple susceptibility loci for multiple sclerosis von Haines, Jonathan L., Bradford, Yuki, Garcia, Melissa E., Reed, Allison D., Neumeister, Elizabeth, Pericak-Vance, Margaret A., Rimmler, Jacqueline B., Menold, Marissa M., Martin, Eden R., Oksenberg, Jorge R., Barcellos, Lisa F., Lincoln, Robin, Hauser, Stephen L.

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Linkage of the MHC to Familial Multiple Sclerosis Suggests Genetic Heterogeneity von Haines, Jonathan L., Terwedow, Henry A., Burgess, Katie, Pericak-Vance, Margaret A., Rimmler, Jackie B., Martin, Eden R., Oksenberg, Jorge R., Lincoln, Robin, Zhang, David Y., Banatao, Diosdado R., Gatto, Nicole, Goodkin, Donald E., Hauser, Stephen L.

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A complete genomic screen for multiple sclerosis underscores a role for the major histocompatability complex von Haines, J.L, Ter-Minassian, M, Bazyk, A, Gusella, J.F, Kim, D.J, Terwedow, H, PericakVance, M.A, Rimmler, J.B, Haynes, C.S, Roses, A.D, Lee, A, Shaner, B, Menold, M, Seboun, E, Fitoussi, R-P, Gartioux, C, Reyes, C, Ribierre, F, Gyapay, G, Weissenbach, J, Hauser, S.L, Goodkin, D.E, Lincoln, R, Usuku, K, Garcia-Merino, A, Gatto, N, Young, S, Oksenberg, J.R

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An autosomal genomic screen for dementia in an extended Amish family von Ashley-Koch, A.E., Shao, Y., Rimmler, J.B., Gaskell, P.C., Welsh-Bohmer, K.A., Jackson, C.E., Scott, W.K., Haines, J.L., Pericak-Vance, M.A.

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CC-chemokine receptor 5 polymorphism and age of onset in familial multiple sclerosis von Barcellos, L. F., Schito, A. M., Rimmler, J. B., Vittinghoff, E., Shih, A., Lincoln, R., Callier, S., Elkins, M. K., Goodkin, D. E., Haines, J. L., Pericak-Vance, M. A., Hauser, S. L., Oksenberg, J. R.

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Apolipoprotein E, survival in Alzheimer's disease patients, and the competing risks of death and Alzheimer's disease von CORDER, E. H, SAUNDERS, A. M, GUSELLA, J. F, SMALL, G. W, ROSES, A. D, PERICAK-VANCE, M. A, HAINES, J. L, STRITTMATTER, W. J, SCHMECHEL, D. E, GASKELL, P. C, RIMMLER, J. B, LOCKE, P. A, CONNEALLY, P. M, SCHMADER, K. E, TANZI, R. E

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Genetic studies in Alzheimer's disease with an NACP/α-synuclein polymorphism von Xia, Yu, de Silva, H. A. Rohan, Rosi, Barbara L., Yamaoka, Larry H., Rimmler, Jacqueline B., Pericak-Vance, Margaret A., Roses, Allen D., Chen, Xiaohua, Masliah, Eliezer, Deteresa, Richard, Iwai, Akihiko, Sundsmo, Mary, Thomas, Ronald G., Hofstetter, C. Richard, Gregory, Ethan, Hansen, Lawrence A., Katzman, Robert, Thal, Leon J., Saitoh, Tsunao

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

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Linkage and association analysis of chromosome 19q13 in multiple sclerosis von PERICAK-VANCE, Margaret A, RIMMLER, Jacqueline B, MARTIN, Eden R, HAINES, Jonathan L, GARCIA, Melissa E, OKSENBERG, Jorge R, BARCELLOS, Lisa F, LINCOLN, Robin, GOODKIN, Donald E, HAUSER, Stephen L

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Alzheimer's disease and apolipoprotein e-4 allele in an amish population von Pericak-Vance, M. A., Johnson, C. C., Rimmler, J. B., Saunders, A. M., Robinson, L. C., D'Hondr, E. G., Jackson, C. E., Haines, J. L.

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Linkage analysis of candidate myelin genes in familial multiple sclerosis von Seboun, E, Oksenberg, J R, Rombos, A, Usuku, K, Goodkin, D E, Lincoln, R R, Wong, M, Pham-Dinh, D, Boesplug-Tanguy, O, Carsique, R, Fitoussi, R, Gartioux, C, Reyes, C, Ribierre, F, Faure, S, Fizames, C, Gyapay, G, Weissenbach, J, Dautigny, A, Rimmler, J B, Garcia, M E, Pericak-Vance, M A, Haines, J L, Hauser, S L

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Investigation of seven proposed regions of linkage in multiple sclerosis: an American and French collaborative study von PERICAK-VANCE, Margaret A, RIMMLER, Jackie B, LYON-CAEN, Olivier, FONTAINE, Bertrand, DUHAMEL, Emmanuelle, COPPIN, Helene, BRASSAT, David, ROTH, Marie-Paule, CLANET, Michel, ALIZADEH, Mehdi, YAOUANQ, Jacqueline, QUELVENNEC, Erwann, HAINES, Jonathan L, SEMANA, Gilbert, EDAN, Gilles, BABRON, Marie-Claude, GENIN, Emmanuelle, CLERGET-DARPOUX, Francoise, GARCIA, Melissa E, OKSENBERG, Jorge R, BARCELLOS, Lisa F, LINCOLN, Robin, HAUSER, Stephen L, COURNU-REBEIX, Isabelle, AZOULAY-CAYLA, Ariele

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Sequence variation in the transforming growth factor- beta 1 (TGFB1) gene and multiple sclerosis susceptibility von Green, A J, Barcellos, L F, Rimmler, J B, Garcia, ME, Caillier, S, Lincoln, R R, Bucher, P, Pericak-Vance, MA, Haines, J L, Hauser, S L, Oksenberg, J R

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Sequence variation in the transforming growth factor-β1 ( TGFB1) gene and multiple sclerosis susceptibility von Green, A.J, Barcellos, L.F, Rimmler, J.B, Garcia, M.E, Caillier, S, Lincoln, R.R, Bucher, P, Pericak-Vance, M.A, Haines, J.L, Hauser, S.L, Oksenberg, J.R

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