Rationalizing the diverse reactivity of [1.1.1]propellane through sigma-pi-delocalization by 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 by 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 by 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 by 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 by 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 by 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. by 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. by 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 by 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. by 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. by 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 by 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 by 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. by 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. by 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 by 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