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Patrick Shannon
Patrick Shannon
University of Toronto
Verified email at sinaihealthsystem.ca
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Cited by
Year
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
5962001
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
3571997
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
3382001
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
2562013
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
2412001
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
2072003
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
2031998
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
1902000
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
1741999
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
1732014
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
1692003
Critical illness–associated cerebral microbleeds
EM Fanou, JM Coutinho, P Shannon, TR Kiehl, MM Levi, ME Wilcox, ...
Stroke 48 (4), 1085-1087, 2017
1502017
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
1412007
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
1202006
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
1152004
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
1042007
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
1032002
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
992017
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
972006
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
972000
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