| Hereditary Early-Onset Parkinson's Disease Caused by Mutations in PINK1 EM Valente, PM Abou-Sleiman, V Caputo, MMK Muqit, K Harvey, ... Science 304 (5674), 1158-1160, 2004 | 4102 | 2004 |
| Kinase activity is required for the toxic effects of mutant LRRK2/dardarin E Greggio, S Jain, A Kingsbury, R Bandopadhyay, P Lewis, A Kaganovich, ... Neurobiology of Disease 23 (2), 329-341, 2006 | 834 | 2006 |
| GlyR α3: An Essential Target for Spinal PGE2-Mediated Inflammatory Pain Sensitization RJ Harvey, UB Depner, H Wassle, S Ahmadi, C Heindl, H Reinold, ... Science 304 (5672), 884-887, 2004 | 718 | 2004 |
| The mitochondrial protease HtrA2 is regulated by Parkinson's disease-associated kinase PINK1 H Plun-Favreau, K Klupsch, N Moisoi, S Gandhi, S Kjaer, D Frith, ... Nature Cell Biology 9 (11), 1243, 2007 | 573 | 2007 |
| Neuroligin 2 drives postsynaptic assembly at perisomatic inhibitory synapses through gephyrin and collybistin A Poulopoulos, G Aramuni, G Meyer, T Soykan, M Hoon, T Papadopoulos, ... Neuron 63 (5), 628-642, 2009 | 535 | 2009 |
| PINK1 cleavage at position A103 by the mitochondrial protease PARL E Deas, H Plun-Favreau, S Gandhi, H Desmond, S Kjaer, SHY Loh, ... Human Molecular Genetics 20 (5), 867-879, 2010 | 521 | 2010 |
| Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes JR Lemke, D Lal, EM Reinthaler, I Steiner, M Nothnagel, M Alber, ... Nature Genetics 45 (9), 1067, 2013 | 504 | 2013 |
| Mutations in α-tubulin cause abnormal neuronal migration in mice and lissencephaly in humans DA Keays, G Tian, K Poirier, GJ Huang, C Siebold, J Cleak, PL Oliver, ... Cell 128 (1), 45-57, 2007 | 476 | 2007 |
| Gephyrin: where do we stand, where do we go? JM Fritschy, RJ Harvey, G Schwarz Trends in Neurosciences 31 (5), 257-264, 2008 | 374 | 2008 |
| Highly effective SNP-based association mapping and management of recessive defects in livestock C Charlier, W Coppieters, F Rollin, D Desmecht, JS Agerholm, ... Nature Genetics 40 (4), 449, 2008 | 366 | 2008 |
| The GDP-GTP exchange factor collybistin: an essential determinant of neuronal gephyrin clustering K Harvey, IC Duguid, MJ Alldred, SE Beatty, H Ward, NH Keep, ... Journal of Neuroscience 24 (25), 5816-5826, 2004 | 320 | 2004 |
| Zinc-mediated inhibition of GABA-A receptors: discrete binding sites underlie subtype specificity AM Hosie, EL Dunne, RJ Harvey, TG Smart Nature Neuroscience 6 (4), 362, 2003 | 308 | 2003 |
| Large spectrum of lissencephaly and pachygyria phenotypes resulting from de novo missense mutations in tubulin alpha 1A (TUBA1A) K Poirier, DA Keays, F Francis, Y Saillour, N Bahi, S Manouvrier, ... Human Mutation 28 (11), 1055-1064, 2007 | 270 | 2007 |
| GRIN2B mutations in West syndrome and intellectual disability with focal epilepsy JR Lemke, R Hendrickx, K Geider, B Laube, M Schwake, RJ Harvey, ... Annals of Neurology 75 (1), 147-154, 2014 | 256 | 2014 |
| Glycine receptor autoimmune spectrum with stiff-man syndrome phenotype A McKeon, E Martinez-Hernandez, E Lancaster, JY Matsumoto, ... JAMA Neurology 70 (1), 44-50, 2013 | 240 | 2013 |
| Glycine transporters as novel therapeutic targets in schizophrenia, alcohol dependence and pain RJ Harvey, BK Yee Nature Reviews Drug Discovery 12 (11), 866-885, 2013 | 236 | 2013 |
| Mutations in the gene encoding GlyT2 (SLC6A5) define a presynaptic component of human startle disease MI Rees, K Harvey, BR Pearce, SK Chung, IC Duguid, P Thomas, ... Nature Genetics 38 (7), 801, 2006 | 236 | 2006 |
| Impaired GABAergic transmission and altered hippocampal synaptic plasticity in collybistin‐deficient mice T Papadopoulos, M Korte, V Eulenburg, H Kubota, M Retiounskaia, ... The EMBO Journal 26 (17), 3888-3899, 2007 | 222 | 2007 |
| The genetics of hyperekplexia: more than startle! RJ Harvey, M Topf, K Harvey, MI Rees Trends in Genetics 24 (9), 439-447, 2008 | 218 | 2008 |
| TUBA1A mutations cause wide spectrum lissencephaly (smooth brain) and suggest that multiple neuronal migration pathways converge on alpha tubulins RA Kumar, DT Pilz, TD Babatz, TD Cushion, K Harvey, M Topf, L Yates, ... Human Molecular Genetics 19 (14), 2817-2827, 2010 | 217 | 2010 |
Maya TopfProfessor @ Centre for Structural Systems Biology - HamburgVerified email at cssb-hamburg.de
