| α-Synuclein locus triplication causes Parkinson's disease AB Singleton, M Farrer, J Johnson, A Singleton, S Hague, J Kachergus, ... science 302 (5646), 841-841, 2003 | 5184 | 2003 |
| The Parkinson's disease protein DJ-1 is neuroprotective due to cysteine-sulfinic acid-driven mitochondrial localization RM Canet-Avilés, MA Wilson, DW Miller, R Ahmad, C McLendon, ... Proceedings of the National Academy of Sciences 101 (24), 9103-9108, 2004 | 1356 | 2004 |
| An in vitro model of Parkinson's disease: linking mitochondrial impairment to altered α-synuclein metabolism and oxidative damage TB Sherer, R Betarbet, AK Stout, S Lund, M Baptista, AV Panov, ... Journal of Neuroscience 22 (16), 7006-7015, 2002 | 744 | 2002 |
| Parkin protects against the toxicity associated with mutant α-synuclein: proteasome dysfunction selectively affects catecholaminergic neurons L Petrucelli, C O'Farrell, PJ Lockhart, M Baptista, K Kehoe, L Vink, P Choi, ... Neuron 36 (6), 1007-1019, 2002 | 707 | 2002 |
| α-Synuclein in blood and brain from familial Parkinson disease with SNCA locus triplication DW Miller, SM Hague, J Clarimon, M Baptista, K Gwinn-Hardy, ... Neurology 62 (10), 1835-1838, 2004 | 445 | 2004 |
| L166P mutant DJ-1, causative for recessive Parkinson's disease, is degraded through the ubiquitin-proteasome system PP Zhu, J Stadler, GR Klinefelter, C Blackstone, DW Miller, R Ahmad, ... Journal of Biological Chemistry 278 (38), 36588-36595, 2003 | 310 | 2003 |
| Mutant SOD1 alters the motor neuronal transcriptome: implications for familial ALS J Kirby, E Halligan, MJ Baptista, S Allen, PR Heath, H Holden, SC Barber, ... Brain 128 (7), 1686-1706, 2005 | 223 | 2005 |
| Co‐ordinate transcriptional regulation of dopamine synthesis genes by α‐synuclein in human neuroblastoma cell lines MJ Baptista, C O'Farrell, S Daya, R Ahmad, DW Miller, J Hardy, MJ Farrer, ... Journal of neurochemistry 85 (4), 957-968, 2003 | 220 | 2003 |
| Heterotrisomy, a significant contributing factor to ventricular septal defect associated with Down syndrome? M Baptista, U Fairbrother, C Howard, M Farrer, G Davies, D Trikka, ... Human genetics 107, 476-482, 2000 | 34 | 2000 |
| Parkin and 𝛂-Synuclein: Opponent Actions in The Pathogenesis of Parkinson’S Disease MJ Baptista, MR Cookson, DW Miller The Neuroscientist 10 (1), 63-72, 2004 | 32 | 2004 |
| Microarray analysis reveals induction of heat shock proteins mRNAs by the torsion dystonia protein, TorsinA MJ Baptista, C O'Farrell, J Hardy, MR Cookson Neuroscience letters 343 (1), 5-8, 2003 | 16 | 2003 |
| Dominant torsinA mutations in cellular systems. MJ Baptista, CA O'Farrell, MR Cookson Advances in neurology 94, 73-78, 2004 | 4 | 2004 |
| Triplication of the normal alpha synuclein gene is a cause of hereditary Parkinson’s disease A Singleton, M Farrer, J Johnson, A Singleton, S Hague, J Kachergus, ... American Journal of Human Genetics 73 (5), 184-184, 2003 | 4 | 2003 |
| Novel COL6AI variants and congenital heart defects (CHD) in Down Syndrome (DS) U Fairbrother, MJ Baptista, GE Davies, D Trikka, AM Kessling AMERICAN JOURNAL OF HUMAN GENETICS 73 (5), 515-515, 2003 | 2 | 2003 |
| Triplication of alpha-synuclein is causal of neuropathologically confirmed Parkinson's disease, diffuse Lewy body disease, and multiple system atrophy in a single kindred K Gwinn-Hardy, M Farrer, D Dickson, LW Jin, J Johnson, A Singleton, ... ANNALS OF NEUROLOGY 54 (6), 845-845, 2003 | | 2003 |
| Balon, N., Dupenloup, L., Blanc, F., Weiss, M., Rostain, J.-C., Nitrous oxide reverses the increase in striatal dopamine release produced by N-methyl-D-aspartate infusion in … MJ Baptista, C O’Farrell, J Hardy, MR Cookson, NR Basa, L Wang, ... Neuroscience Letters 343, 219-222, 2003 | | 2003 |
| PROTEIN SYNTHESIS, POST-TRANSLATION MODIFICATION, AND DEGRADATION-L166P Mutant D6J-1, Causative for Recessive Parkinson's Disease, Is Degraded through the Ubiquitin-Proteasome … DW Miller, R Ahmad, S Hague, MJ Baptista, R Canet-Aviles, C McLendon, ... Journal of Biological Chemistry 278 (38), 36588-36595, 2003 | | 2003 |
| Enzyme activity of GTP cyclohydrolase I mutations and their relevance to dopamine insufficiency. SM Hague, C Evey, M Baptista, M Cookson, J Hardy, A Singleton AMERICAN JOURNAL OF HUMAN GENETICS 71 (4), 513-513, 2002 | | 2002 |
| Microarray analysis of a cell culture model of early onset dystonia linked to torsin A mutations. MJ Baptista, C O'Farrell, R Ahmad, MR Cookson AMERICAN JOURNAL OF HUMAN GENETICS 71 (4), 391-391, 2002 | | 2002 |
| A central role for proteasome dysfunction in Parkinson's disease? MR Cookson, M Baptista, J Hardy, L Petrucelli, C O'Farrell, PJ Lockhart, ... NEUROBIOLOGY OF AGING 23 (1), S409-S410, 2002 | | 2002 |
