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Citation: Jr. Vaughan et al., Genetics of Parkinsonism: a review, ANN HUM GEN, 65, 2001, pp. 111-126

Authors: Periquet, M Lucking, CB Vaughan, JR Bonifati, V Durr, A De Michele, G Horstink, MW Farrer, M Illarioshkin, SN Pollak, P Borg, M Brefel-Courbon, C Denefle, P Meco, G Gasser, T Breteler, MMB Wood, NW Agid, Y Brice, A

Citation: M. Periquet et al., Origin of the mutations in the parkin gene in europe: Exon rearrangements are independent recurrent events, whereas point mutations may result from founder effects, AM J HU GEN, 68(3), 2001, pp. 617-626

Authors: Bandmann, O Vaughan, JR Holmans, P Marsden, CD Wood, NW

Citation: O. Bandmann et al., Detailed genotyping demonstrates association between the slow acetylator genotype for N-acetyltransferase 2 (NAT2) and familial Parkinson's disease, MOVEMENT D, 15(1), 2000, pp. 30-35

Authors: Morris, HR Vaughan, JR Datta, SR Bandopadhyay, R de Silva, HAR Schrag, A Cairns, NJ Burn, D Nath, U Lantos, PL Daniel, S Lees, AJ Quinn, NP Wood, NW

Citation: Hr. Morris et al., Multiple system atrophy/progressive supranuclear palsy: alpha-Synuclein, synphilin, tau, and APOE, NEUROLOGY, 55(12), 2000, pp. 1918-1920

Authors: Abbas, N Lucking, CB Ricard, S Durr, A Bonifati, V De Michele, G Bouley, S Vaughan, JR Gasser, T Marconi, R Broussolle, E Brefel-Courbon, C Harhangi, BS Oostra, AB Fabrizio, E Bohme, GA Pradier, L Wood, NW Filla, A Meco, G Denefle, P Agid, Y Brice, A

Citation: N. Abbas et al., A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe, HUM MOL GEN, 8(4), 1999, pp. 567-574

Authors: Harhangi, BS Farrer, MJ Lincoln, S Bonifati, V Meco, G De Michele, G Brice, A Durr, A Martinez, M Gasser, T Bereznai, B Vaughan, JR Wood, NW Hardy, J Oostra, BA Breteler, MMB

Citation: Bs. Harhangi et al., The lle93Met mutation in the ubiquitin carboxy-terminal-hydrolase-L1 gene is not observed in European cases with familial Parkinson's disease, NEUROSCI L, 270(1), 1999, pp. 1-4