Rationalizing the diverse reactivity of [1.1.1]propellane through sigma-pi-delocalization von Sterling, AJ, Dürr, A, Smith, R, Anderson, EA, Duarte, F

Synthesis and applications of highly functionalized 1-halo-3-substituted bicyclo[1.1.1]pentanes von Caputo, D, Arroniz, C, Dürr, A, Mousseau, J, Stepan, A, Mansfield, S, Anderson, E

QUANTITATIVE ASSESSMENT OF BIOLOGICAL AND CLINICAL MANIFESTATIONS OF HUNTINGTON'S DISEASE BEFORE AND AFTER DIAGNOSIS-THE TRACK-HD STUDY von Lahiri, N, Tabrizi, S, Kennard, C, Durr, A, Leavitt, B, Fox, N, Roos, R

OCULOMOTOR DEFICITS IN PREMANIFEST AND EARLY HUNTINGTON'S DISEASE AND THEIR STRUCTURAL BRAIN CORRELATES: THE LONGITUDINAL TRACK-HD STUDY von Hicks, S, Scahill, R, Dumas, E, Durr, A, Blair, R, Levitt, B, Roos, R, Tabrizi, S, Kennard, C

OCULOMOTOR DEFICITS IN PRESYMPTOMATIC AND EARLY HUNTINGTON'S DISEASE AND THEIR STRUCTURAL BRAIN CORRELATES von Hicks, S, Rosas, H, Berna, C, Scahill, R, Durmas, E, Roos, R, Levitt, B, Tabrizi, S, Kennard, C, Durr, A

A computational cognitive biomarker for early-stage Huntington's disease von Wiecki, T, Antoniades, C, Stevenson, A, Kennard, C, Borowsky, B, Owen, G, Leavitt, B, Roos, R, Durr, A, Tabrizi, S, Frank, M

Biological and clinical changes in premanifest and early stage Huntington's disease in the TRACK-HD study: the 12-month longitudinal analysis. von Tabrizi, S, Scahill, R, Durr, A, Roos, R, Leavitt, B, Jones, R, Landwehrmeyer, G, Fox, N, Johnson, H, Hicks, S, Kennard, C, Craufurd, D, Frost, C, Langbehn, DR, Reilmann, R, Stout, J

Biological and clinical manifestations of Huntington's disease in the longitudinal TRACK-HD study: cross-sectional analysis of baseline data. von Tabrizi, S, Langbehn, DR, Leavitt, B, Roos, R, Durr, A, Craufurd, D, Kennard, C, Hicks, S, Fox, N, Scahill, R, Borowsky, B, Tobin, A, Rosas, H, Johnson, H, Reilmann, R, Landwehrmeyer, B, Stout, J

Potential endpoints for clinical trials in premanifest and early Huntington's disease in the TRACK-HD study: analysis of 24 month observational data von Tabrizi, S, Reilmann, R, Roos, R, Durr, A, Leavitt, B, Owen, G, Jones, R, Johnson, H, Craufurd, D, Hicks, S, Kennard, C, Landwehrmeyer, B, Stout, J, Borowsky, B, Scahill, R, Frost, C, Langbehn, DR

Potential endpoints for clinical trials in premanifest and early Huntington's disease in the TRACK-HD study: analysis of 24 month observational data. von Tabrizi, S, Reilmann, R, Roos, R, Durr, A, Leavitt, B, Owen, G, Jones, R, Johnson, H, Craufurd, D, Hicks, S, Kennard, C, Landwehrmeyer, B, Stout, J, Borowsky, B, Scahill, R, Frost, C, Langbehn, DR

Clinical impairment in premanifest and early Huntington's disease is associated with regionally specific atrophy. von Scahill, R, Hobbs, N, Say, M, Bechtel, N, Henley, S, Hyare, H, Langbehn, DR, Jones, R, Leavitt, B, Roos, R, Durr, A, Johnson, H, Lehéricy, S, Craufurd, D, Kennard, C, Hicks, S, Stout, J, Reilmann, R, Tabrizi, S

Clinical impairment in premanifest and early Huntington's disease is associated with regionally specific atrophy von Scahill, R, Hobbs, N, Say, M, Bechtel, N, Henley, S, Hyare, H, Langbehn, DR, Jones, R, Leavitt, B, Roos, R, Durr, A, Johnson, H, Lehéricy, S, Craufurd, D, Kennard, C, Hicks, S, Stout, J, Reilmann, R, Tabrizi, S

Autosomal recessive ataxias: a new gene - aprataxin - responsible for ataxia-ocular apraxia 1, and a new locus on 9q34 von Moreira, M, Klur, S, Barbot, C, Tachi, N, Bomont, P, Watanabe, M, Shoji, M, Warter, J, Aubourg, P, Durr, A, Nemeth, A, Amouri, R, Hentati, F, Alurkar, A, Divekar, D, Mendoca, P, Sequeiros, J, Coutinho, P, Koenig, M

The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphism. von Klebe, S, Golmard, J, Nalls, M, Saad, M, Singleton, AB, Bras, J, Hardy, J, Simon-Sanchez, J, Heutink, P, Kuhlenbäumer, G, Charfi, R, Klein, C, Hagenah, J, Gasser, T, Wurster, I, Lesage, S, Lorenz, D, Deuschl, G, Durif, F, Pollak, P, Damier, P, Tison, F, Durr, A, Amouyel, P, Lambert, J

Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease. von Keller, M, Saad, M, Bras, J, Bettella, F, Nicolaou, N, Simón-Sánchez, J, Mittag, F, Büchel, F, Sharma, M, Gibbs, JR, Schulte, C, Moskvina, V, Durr, A, Holmans, P, Kilarski, L, Guerreiro, R, Hernandez, D, Brice, A, Ylikotila, P, Stefánsson, H, Majamaa, K, Morris, H, Williams, N, Gasser, T, Heutink, P

Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis von Lin, K, Pulit, SL, Van Rheenen, W, Shatunov, A, Dekker, AM, McLaughlin, RL, Diekstra, FP, Van Der Spek, RAA, Võsa, U, De Jong, S, Robinson, MR, Yang, J, Fogh, I, Van Doormaal, PT, Tazelaar, GHP, Koppers, M, Blokhuis, AM, Sproviero, W, Jones, AR, Kenna, KP, Van Eijk, KR, Harschnitz, O, Schellevis, RD, Brands, WJ, Medic, J, Menelaou, A, Vajda, A, Ticozzi, N, Rogelj, B, Vrabec, K, Ravnik-Glavač, M, Koritnik, B, Zidar, J, Leonardis, L, Grošelj, LD, Millecamps, S, Salachas, F, Meininger, V, De Carvalho, M, Pinto, S, Mora, JS, Rojas-García, R, Polak, M, Chandran, S, Colville, S, Swingler, R, Morrison, KE, Shaw, PJ, Hardy, J, Orrell, RW, Pittman, A, Sidle, K, Fratta, P, Malaspina, A, Topp, S, Petri, S, Abdulla, S, Drepper, C, Sendtner, M, Meyer, T, Ophoff, RA, Staats, KA, Wiedau-Pazos, M, Lomen-Hoerth, C, Van Deerlin, VM, Trojanowski, JQ, Elman, L, McCluskey, L, Basak, AN, Tunca, C, Hamzeiy, H, Parman, Y, Meitinger, T, Lichtner, P, Radivojkov-Blagojevic, M, Andres, CR, Maurel, C, Bensimon, G, Landwehrmeyer, B, Brice, A, Payan, CAM, Saker-Delye, S, Dürr, A, Wood, NW, Tittmann, L, Lieb, W, Franke, A, Rietschel, M, Cichon, S, Nöthen, MM, Amouyel, P, Tzourio, C, Dartigues, J-F, Uitterlinden, AG, Rivadeneira, F, Estrada, K, Hofman, A, Curtis, C, Blauw, HM, Van Der Kooi, AJ, De Visser, M, Goris, A, Weber, M, Shaw, CE, Smith, BN, Pansarasa, O, Cereda, C, Del Bo, R, Comi, GP, D'Alfonso, S, Bertolin, C, Sorarù, G, Mazzini, L, Pensato, V, Gellera, C, Tiloca, C, Ratti, A, Calvo, A, Moglia, C, Brunetti, M, Arcuti, S, Capozzo, R, Zecca, C, Lunetta, C, Penco, S, Riva, N, Padovani, A, Filosto, M, Muller, B, Stuit, RJ, Registry, P, Slalom Group, Registry, S, Fals Sequencing Consortium, Slagen Consortium, Nnipps Study Group, Blair, I, Zhang, K, McCann, EP, Fifita, JA, Nicholson, GA, Rowe, DB, Pamphlett, R, Kiernan, MC, Grosskreutz, J, Witte, OW, Ringer, T, Prell, T, Stubendorff, B, Kurth, I, Hübner, CA, Leigh, PN, Casale, F, Chio, A, Beghi, E, Pupillo, E, Tortelli, R, Logroscino, G, Powell, J, Ludolph, AC, Weishaupt, JH, Robberecht, W, Van Damme, P, Franke, L, Pers, TH, Brown, RH, Glass, JD, Landers, JE, Hardiman, O, Andersen, PM, Corcia, P, Vourc'H, P, Silani, V, Wray, NR, Visscher, PM, De Bakker, PIW, Van Es, MA, Pasterkamp, RJ, Lewis, CM, Breen, G, Al-Chalabi, A, Van Den Berg, LH, Veldink, JH