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Tracy Stockley
Tracy Stockley
Genome Diagnostics University Health Network
Verified email at uhn.ca
Title
Cited by
Cited by
Year
Molecular profiling for precision cancer therapies
ER Malone, M Oliva, PJB Sabatini, TL Stockley, LL Siu
Genome medicine 12, 1-19, 2020
5512020
Discordant KCNQ1OT1 imprinting in sets of monozygotic twins discordant for Beckwith–Wiedemann syndrome
R Weksberg, C Shuman, O Caluseriu, AC Smith, YL Fei, J Nishikawa, ...
Human Molecular Genetics 11 (11), 1317-1325, 2002
3882002
Molecular profiling of advanced solid tumors and patient outcomes with genotype-matched clinical trials: the Princess Margaret IMPACT/COMPACT trial
TL Stockley, AM Oza, HK Berman, NB Leighl, JJ Knox, FA Shepherd, ...
Genome medicine 8, 1-12, 2016
2432016
The clinical application of genome-wide sequencing for monogenic diseases in Canada: position statement of the Canadian College of Medical Geneticists
K Boycott, T Hartley, S Adam, F Bernier, K Chong, BA Fernandez, ...
Journal of Medical Genetics 52 (7), 431-437, 2015
2172015
The natural history of juvenile or subacute GM2 gangliosidosis: 21 new cases and literature review of 134 previously reported
GHB Maegawa, T Stockley, M Tropak, B Banwell, S Blaser, F Kok, ...
Pediatrics 118 (5), e1550-e1562, 2006
2072006
Pyrimethamine as a potential pharmacological chaperone for late-onset forms of GM2 gangliosidosis
GHB Maegawa, M Tropak, J Buttner, T Stockley, F Kok, JTR Clarke, ...
Journal of biological chemistry 282 (12), 9150-9161, 2007
1982007
CHARGE and Kabuki syndromes: gene-specific DNA methylation signatures identify epigenetic mechanisms linking these clinically overlapping conditions
DT Butcher, C Cytrynbaum, AL Turinsky, MT Siu, M Inbar-Feigenberg, ...
The American Journal of Human Genetics 100 (5), 773-788, 2017
1812017
Adavosertib plus gemcitabine for platinum-resistant or platinum-refractory recurrent ovarian cancer: a double-blind, randomised, placebo-controlled, phase 2 trial
S Lheureux, MC Cristea, JP Bruce, S Garg, M Cabanero, ...
The Lancet 397 (10271), 281-292, 2021
1452021
Heterogenous loss of mismatch repair (MMR) protein expression: a challenge for immunohistochemical interpretation and microsatellite instability (MSI) evaluation
AJ McCarthy, JM Capo‐Chichi, T Spence, S Grenier, T Stockley, ...
The Journal of Pathology: Clinical Research 5 (2), 115-129, 2019
1172019
Urinary globotriaosylceramide excretion correlates with the genotype in children and adults with Fabry disease
C Auray-Blais, D Cyr, A Ntwari, ML West, J Cox-Brinkman, DG Bichet, ...
Molecular genetics and metabolism 93 (3), 331-340, 2008
1172008
A classification system for clinical relevance of somatic variants identified in molecular profiling of cancer
MA Sukhai, KJ Craddock, M Thomas, AR Hansen, T Zhang, L Siu, ...
Genetics in Medicine 18 (2), 128-136, 2016
1102016
15q11.2 Duplication Encompassing Only the UBE3A Gene Is Associated with Developmental Delay and Neuropsychiatric Phenotypes
A Noor, L Dupuis, K Mittal, AC Lionel, CR Marshall, SW Scherer, ...
Human mutation 36 (7), 689-693, 2015
812015
Whole-exome sequencing and targeted copy number analysis in primary ciliary dyskinesia
CR Marshall, SW Scherer, MA Zariwala, L Lau, TA Paton, T Stockley, ...
G3: Genes, Genomes, Genetics 5 (8), 1775-1781, 2015
712015
Personalized risk assessment for prevention and early detection of breast cancer: integration and implementation (PERSPECTIVE I&I)
JD Brooks, H Nabi, IL Andrulis, AC Antoniou, J Chiquette, P Després, ...
Journal of personalized medicine 11 (6), 511, 2021
672021
Auditory responses in cochlear implant users with and without GJB2 deafness
EJ Propst, BC Papsin, TL Stockley, RV Harrison, KA Gordon
The Laryngoscope 116 (2), 317-327, 2006
662006
The mutational landscape of accelerated-and blast-phase myeloproliferative neoplasms impacts patient outcomes
CJ McNamara, T Panzarella, JA Kennedy, A Arruda, JO Claudio, ...
Blood advances 2 (20), 2658-2671, 2018
612018
Impact of genomic alterations on outcomes in myelofibrosis patients undergoing JAK1/2 inhibitor therapy
JY Spiegel, C McNamara, JA Kennedy, T Panzarella, A Arruda, T Stockley, ...
Blood advances 1 (20), 1729-1738, 2017
602017
Molecular characterization of gastric-type endocervical adenocarcinoma using next-generation sequencing
S Garg, TS Nagaria, B Clarke, O Freedman, Z Khan, J Schwock, ...
Modern Pathology 32 (12), 1823-1833, 2019
582019
Canavan disease: Carrier‐frequency determination in the Ashkenazi Jewish population and development of a novel molecular diagnostic assay
A Feigenbaum, R Moore, J Clarke, S Hewson, D Chitayat, PN Ray, ...
American Journal of Medical Genetics Part A 124 (2), 142-147, 2004
562004
Strategy for comprehensive molecular testing for Duchenne and Becker muscular dystrophies
TL Stockley, S Akber, N Bulgin, PN Ray
Genetic testing 10 (4), 229-243, 2006
552006
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