Deletion of Pten in mouse brain causes seizures, ataxia and defects in soma size resembling Lhermitte-Duclos disease SA Backman, V Stambolic, A Suzuki, J Haight, A Elia, J Pretorius, ... Nature genetics 29 (4), 396-403, 2001 | 596 | 2001 |
Increase in proliferation and apoptosis of gastric epithelial cells early in the natural history of Helicobacter pylori infection. NL Jones, PT Shannon, E Cutz, H Yeger, PM Sherman The American journal of pathology 151 (6), 1695, 1997 | 357 | 1997 |
Astrocyte-specific expression of activated p21-ras results in malignant astrocytoma formation in a transgenic mouse model of human gliomas H Ding, L Roncari, P Shannon, X Wu, N Lau, J Karaskova, DH Gutmann, ... Cancer research 61 (9), 3826-3836, 2001 | 338 | 2001 |
Mutations in genes encoding the cadherin receptor-ligand pair DCHS1 and FAT4 disrupt cerebral cortical development S Cappello, MJ Gray, C Badouel, S Lange, M Einsiedler, M Srour, ... Nature genetics 45 (11), 1300-1308, 2013 | 256 | 2013 |
Neutrophil-mediated epithelial injury during transmigration: role of elastase HH Ginzberg, V Cherapanov, Q Dong, A Cantin, CAG McCulloch, ... American Journal of Physiology-Gastrointestinal and Liver Physiology 281 (3 …, 2001 | 241 | 2001 |
Descending vasomotor pathways in humans: correlation between axonal preservation and cardiovascular dysfunction after spinal cord injury JC Furlan, MG Fehlings, P Shannon, MD Norenberg, AV Krassioukov Journal of neurotrauma 20 (12), 1351-1363, 2003 | 207 | 2003 |
Axonal injury and the neuropathology of shaken baby syndrome P Shannon, CR Smith, J Deck, LC Ang, M Ho, L Becker Acta neuropathologica 95, 625-631, 1998 | 203 | 1998 |
Loss of neurofibromin is associated with activation of RAS/MAPK and PI3-K/AKT signaling in a neurofibromatosis 1 astrocytoma N Lau, MM Feldkamp, L Roncari, AH Loehr, P Shannon, DH Gutmann, ... Journal of Neuropathology & Experimental Neurology 59 (9), 759-767, 2000 | 190 | 2000 |
Measles inclusion-body encephalitis caused by the vaccine strain of measles virus A Bitnun, P Shannon, A Durward, PA Rota, WJ Bellini, C Graham, E Wang, ... Clinical Infectious Diseases 29 (4), 855-861, 1999 | 174 | 1999 |
Leiomodin-3 dysfunction results in thin filament disorganization and nemaline myopathy M Yuen, SA Sandaradura, JJ Dowling, AS Kostyukova, N Moroz, ... The Journal of clinical investigation 124 (11), 4693-4708, 2014 | 173 | 2014 |
Oligodendrogliomas result from the expression of an activated mutant epidermal growth factor receptor in a RAS transgenic mouse astrocytoma model H Ding, P Shannon, N Lau, X Wu, L Roncari, RL Baldwin, H Takebayashi, ... Cancer research 63 (5), 1106-1113, 2003 | 169 | 2003 |
Critical illness–associated cerebral microbleeds EM Fanou, JM Coutinho, P Shannon, TR Kiehl, MM Levi, ME Wilcox, ... Stroke 48 (4), 1085-1087, 2017 | 150 | 2017 |
Glioblastoma multiforme after stereotactic radiotherapy for acoustic neuroma: case report and review of the literature A Balasubramaniam, P Shannon, M Hodaie, N Laperriere, H Michaels, ... Neuro-oncology 9 (4), 447-453, 2007 | 141 | 2007 |
High-grade glioma formation results from postnatal pten loss or mutant epidermal growth factor receptor expression in a transgenic mouse glioma model Q Wei, L Clarke, DK Scheidenhelm, B Qian, A Tong, N Sabha, Z Karim, ... Cancer research 66 (15), 7429-7437, 2006 | 120 | 2006 |
Laforin preferentially binds the neurotoxic starch-like polyglucosans, which form in its absence in progressive myoclonus epilepsy EM Chan, CA Ackerley, H Lohi, L Ianzano, MA Cortez, P Shannon, ... Human molecular genetics 13 (11), 1117-1129, 2004 | 115 | 2004 |
Evaluation of subcortical white matter and deep white matter tracts in malformations of cortical development E Widjaja, S Blaser, E Miller, A Kassner, P Shannon, SH Chuang, ... Epilepsia 48 (8), 1460-1469, 2007 | 104 | 2007 |
Neuropathological changes in a mouse model of progressive myoclonus epilepsy: cystatin B deficiency and Unverricht-Lundborg disease P Shannon, LA Pennacchio, MK Houseweart, BA Minassian, RM Myers Journal of Neuropathology & Experimental Neurology 61 (12), 1085-1091, 2002 | 103 | 2002 |
CpG methylation, a parent-of-origin effect for maternal-biased transmission of congenital myotonic dystrophy L Barbé, S Lanni, A López-Castel, S Franck, C Spits, K Keymolen, ... The American Journal of Human Genetics 100 (3), 488-505, 2017 | 99 | 2017 |
Inner ear dysplasia is common in children with Down syndrome (trisomy 21) S Blaser, EJ Propst, D Martin, A Feigenbaum, AL James, P Shannon, ... The Laryngoscope 116 (12), 2113-2119, 2006 | 97 | 2006 |
Expression and regulation of neuropilin‐1 in human astrocytomas H Ding, X Wu, L Roncari, N Lau, P Shannon, A Nagy, A Guha International journal of cancer 88 (4), 584-592, 2000 | 97 | 2000 |