Inflammatory profile discriminates clinical subtypes in LRRK2‐associated Parkinson's disease von Brockmann, K., Schulte, C., Schneiderhan‐Marra, N., Apel, A., Pont‐Sunyer, C., Vilas, D., Ruiz‐Martinez, J., Langkamp, M., Corvol, J.‐C., Cormier, F., Knorpp, T., Joos, T. O., Bernard, A., Gasser, T., Marras, C., Schüle, B., Aasly, J. O., Foroud, T., Marti‐Masso, J. F., Brice, A., Tolosa, E., Berg, D., Maetzler, W.

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Changes in actin dynamics and F-actin structure both in synaptoneurosomes of LRRK2(R1441G) mutant mice and in primary human fibroblasts of LRRK2(G2019S) mutation carriers von Caesar, M, Felk, S, Aasly, J.O, Gillardon, F

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Cerebrospinal fluid amyloid β and tau in LRRK2 mutation carriers von AASLY, J. O, SHI, M, KIM, H. M, LEVERENZ, J. B, GINGHINA, C, ARMALY, J, EDWARDS, K. L, SNAPINN, K. W, STOESSL, A. J, ZHANG, J, SOSSI, V, STEWART, T, JOHANSEN, K. K, WSZOLEK, Z. K, UITTI, R. J, HASEGAWA, K, YOKOYAMA, T, ZABETIAN, C. P

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Glucocerebrosidase gene mutations and Parkinson disease in the Norwegian population von TOFT, M, PIELSTICKER, L, ROSS, O. A, AASLY, J. O, FARRER, M. J

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Multicenter Analysis of Glucocerebrosidase Mutations in Parkinson's Disease von Sidransky, E, Nalls, M.A, Aasly, J.O, Aharon-Peretz, J, Annesi, G, Barbosa, E.R, Bar-Shira, A, Berg, D, Bras, J, Brice, A, Chen, C.-M, Clark, L.N, Condroyer, C, De Marco, E.V, Dürr, A, Eblan, M.J, Fahn, S, Farrer, M.J, Fung, H.-C, Gan-Or, Z, Gasser, T, Gershoni-Baruch, R, Giladi, N, Griffith, A, Gurevich, T, Januario, C, Kropp, P, Lang, A.E, Lee-Chen, G.-J, Lesage, S, Marder, K, Mata, I.F, Mirelman, A, Mitsui, J, Mizuta, I, Nicoletti, G, Oliveira, C, Ottman, R, Orr-Urtreger, A, Pereira, L.V, Quattrone, A, Rogaeva, E, Rolfs, A, Rosenbaum, H, Rozenberg, R, Samii, A, Samaddar, T, Schulte, C, Sharma, M, Singleton, A, Spitz, M, Tan, E.-K, Tayebi, N, Toda, T, Troiano, A.R, Tsuji, S, Wittstock, M, Wolfsberg, T.G, Wu, Y.-R, Zabetian, C.P, Zhao, Y, Ziegler, S.G

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Characterization of DCTN1 genetic variability in neurodegeneration von VILARINO-GÜELL, C, WIDER, C, UITTI, R. J, GRAFF-RADFORD, N. R, BOEVE, B. F, JOSEPHS, K. A, MILLER, B, BOYLAN, K. B, GWINN, K, ADLER, C. H, AASLY, J. O, HENTATI, F, SOTO-ORTOLAZA, A. I, DESTEE, A, KRYGOWSKA-WAJS, A, CHARTIER-HARLIN, M.-C, ROSS, O. A, RADEMAKERS, R, FARRER, M. J, COBB, S. A, KACHERGUS, J. M, KEELING, B. H, DACHSEL, J. C, HULIHAN, M. M, DICKSON, D. W, WSZOLEK, Z. K

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AN INDEPENDENT REPLICATION OF PARK16 IN ASIAN SAMPLES von VILARINO-GÜELL, C, ROSS, O. A, BARCIKOWSKA, M, LEE, M.-C, HENTATI, F, UITTI, R. J, WSZOLEK, Z. K, FARRER, M. J, WU, R.-M, AASLY, J. O, WHITE, L. R, RAJPUT, A, RAJPUT, A. H, LYNCH, T, KRYGOWSKA-WAJS, A, JASINSKA-MYGA, B, OPALA, G

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Association of the MAPT locus with Parkinson's disease von Wider, C., Vilariño-Güell, C., Jasinska-Myga, B., Heckman, M. G., Soto-Ortolaza, A. I., Cobb, S. A., Aasly, J. O., Gibson, J. M., Lynch, T., Uitti, R. J., Wszolek, Z. K., Farrer, M. J., Ross, O. A.

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PINK1 mutation heterozygosity and the risk of Parkinson’s disease von Toft, M, Myhre, R, Pielsticker, L, White, L R, Aasly, J O, Farrer, M J

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MEIS1 p.R272H in familial restless legs syndrome von Vilariño-Güell, C, Chai, H, Keeling, B H, Young, J E, Rajput, A, Lynch, T, Aasly, J O, Uitti, R J, Wszolek, Z K, Farrer, M J, Lin, S-C

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SNCA, MAPT, and GSK3B in Parkinson disease: a gene-gene interaction study von Wider, C., Vilariño-Güell, C., Heckman, M. G., Jasinska-Myga, B., Ortolaza-Soto, A. I., Diehl, N. N., Crook, J. E., Cobb, S. A., Bacon, J. A., Aasly, J. O., Gibson, J. M., Lynch, T., Uitti, R. J., Wszolek, Z. K., Farrer, M. J., Ross, O. A.

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Death-associated protein kinase 1 variation and Parkinson's disease von Dachsel, J. C., Wider, C., Vilariño-Güell, C., Aasly, J. O., Rajput, A., Rajput, A. H., Lynch, T., Craig, D., Krygowska-Wajs, A., Jasinska-Myga, B., Opala, G., Barcikowska, M., Czyzewski, K., Wu, R. -M., Heckman, M. G., Uitti, R. J., Wszolek, Z. K., Farrer, M. J., Ross, O. A.

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Calbindin-1 association and Parkinson's disease von Soto-Ortolaza, A. I., Behrouz, B., Wider, C., Vilariño-Güell, C., Heckman, M. G., Aasly, J. O., Mark Gibson, J., Lynch, T., Jasinska-Myga, B., Krygowska-Wajs, A., Opala, G., Barcikowska, M., Czyzewski, K., Uitti, R. J., Wszolek, Z. K., Farrer, M. J., Ross, O. A.

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LRRK2 and Parkinson's disease in Norway von Toft, M, Haugarvoll, K, Ross, O A, Farrer, M J, Aasly, J O

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Clinical features of LRRK2-associated Parkinson's disease in central Norway von Aasly, Jan O., Toft, Mathias, Fernandez-Mata, Ignacio, Kachergus, Jennifer, Hulihan, Mary, White, Linda R., Farrer, Matthew

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Prevalence of haemochromatosis gene mutations in Parkinson’s disease von Aamodt, Anne Hege, Stovner, Lars Jacob, Thorstensen, Ketil, Lydersen, Stian, White, Linda R, Aasly, Jan O

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Mitochondrial impairment in patients with Parkinson disease with the G2019S mutation in LRRK2 von MORTIBOYS, Heather, JOHANSEN, Krisztina K, AASLY, Jan O, BANDMANN, Oliver

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A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants (vol 49, pg 721, 2012) von Sharma, M, Ioannidis, JP, Aasly, JO, Annesi, G, Brice, A, Bertram, L, Bozi, M, Barcikowska, M, Crosiers, D, Clarke, CE, Facheris, MF, Farrer, M, Garraux, G, Gispert, S, Auburger, G, Vilarino-Guell, C, Hadjigeorgiou, GM, Hicks, AA, Hattori, N, Jeon, BS, Jamrozik, Z, Krygowska-Wajs, A, Lesage, S, Lill, CM, Lin, JJ, Lynch, T, Lichtner, P, Lang, AE, Libioulle, C, Murata, M, Mok, V, Jasinska-Myga, B, Mellick, GD, Morrison, KE, Meitnger, T, Zimprich, A, Opala, G, Pramstaller, PP, Pichler, I, Park, SS, Quattrone, A, Rogaeva, E, Ross, OA, Stefanis, L, Stockton, JD, Satake, W, Silburn, PA, Strom, TM, Theuns, J, Tan, EK, Toda, T, Tomiyama, H, Uitti, RJ, Van Broeckhoven, C, Wirdefeldt, K, Wszolek, Z, Xiromerisiou, G, Yomono, HS, Yueh, KC, Zhao, Y, Gasser, T, Maraganore, D, Kruger, R

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Evaluation of the interaction between LRRK2 and PARK16 loci in determining risk of Parkinson’s disease: analysis of a large multi-center study von Wang, L., MS, Heckman, M.G., MS, Aasly, J.O., MD, Annesi, G., PhD, Bozi, M., MD, Chung, S.J., MD, Clarke, C., MD, Crosiers, D., MD, Eckstein, G., PhD, Garraux, G., MD, Hadjigeorgiou, G.M., MD, Hattori, N., MD, PhD, Jeon, B., MD, Kim, Y.J., MD PhD, Kubo, M, Lesage, S., PhD, Lin, J.J., MD, Lynch, T., MD, Lichtner, P., PhD, Mellick, G.D., PhD, Mok, V., MD, Morrison, K.E., MD, Quattrone, A., MD, Satake, W., MD PhD, Silburn, P.A., MD, Stefanis, L., MD, Stockton, J.D., MD, Tan, E.K., MD, Toda, T., MD PhD, Brice, A., MD, Van Broeckhoven, C., PhD, Uitti, R.J., MD, Wirdefeldt, K., MD PhD, Wszolek, Z., MD, Xiromerisiou, G., MD, Maraganore, D.M., MD, Gasser, T., MD, Krüger, R., MD, Farrer, M.J., PhD, Ross, O.A., PhD, Sharma, M., PhD

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Identification of the Genetic Basis for Complex Disorders by Use of Pooling-Based Genomewide Single-Nucleotide–Polymorphism Association Studies von Pearson, John V., Huentelman, Matthew J., Halperin, Rebecca F., Tembe, Waibhav D., Melquist, Stacey, Homer, Nils, Brun, Marcel, Szelinger, Szabolcs, Coon, Keith D., Zismann, Victoria L., Webster, Jennifer A., Beach, Thomas, Sando, Sigrid B., Aasly, Jan O., Heun, Reinhard, Jessen, Frank, Kölsch, Heike, Tsolaki, Magdalini, Daniilidou, Makrina, Reiman, Eric M., Papassotiropoulos, Andreas, Hutton, Michael L., Stephan, Dietrich A., Craig, David W.

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