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Speevak, Marsha D.
28
results:
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Online (28)
Mediatypes
Articles (Online) (23)
OpenAccess-fulltext (5)
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1
Neurodevelopmental functioning in probands and non‐proband ..:
Drmic, Irene E.
;
MacKinnon Modi, Bonnie
;
McConnell, Beth
...
American Journal of Medical Genetics Part A. 188 (2022) 10 - p. 2999-3008 , 2022
Link:
https://doi.org/10.1002/..
?
2
Prevalence of NTRK Fusions in Canadian Solid Tumour Cancer ..:
Silvertown, Joshua D.
;
Lisle, Connie
;
Semenuk, Laura
...
Molecular Diagnosis & Therapy. 27 (2022) 1 - p. 87-103 , 2022
Link:
https://doi.org/10.1007/..
?
3
A Pan-Canadian Validation Study for the Detection of EGFR T..:
Selvarajah, Shamini
;
Plante, Sophie
;
Speevak, Marsha
...
JTO Clinical and Research Reports. 2 (2021) 8 - p. 100212 , 2021
Link:
https://doi.org/10.1016/..
?
4
3. Standardizing recurrent copy number variant classificati..:
Andersen, Erica F.
;
Herriges, John
;
Coe, Bradley
...
Cancer Genetics. 252-253 (2021) - p. S1-S2 , 2021
Link:
https://doi.org/10.1016/..
?
5
Alpha-1-antitrypsin molecular testing in Canada: A seven ye..:
Mattman, Andre
;
Gilfix, Brian M.
;
Chen, Sharon Xuehui
...
Clinical Biochemistry. 81 (2020) - p. 27-33 , 2020
Link:
https://doi.org/10.1016/..
?
6
NullCanada: A novel α1-antitrypsin allele with in cis varia..:
Chen, Sharon
;
DeMarco, Mari L.
;
Estey, Mathew P.
...
Clinical Biochemistry. 79 (2020) - p. 23-27 , 2020
Link:
https://doi.org/10.1016/..
?
7
Data sharing as a national quality improvement program: rep..:
Lebo, Matthew S.
;
Zakoor, Kathleen-Rose
;
Chun, Kathy
...
Genetics in Medicine. 20 (2018) 3 - p. 294-302 , 2018
Link:
https://doi.org/10.1038/..
?
8
OTUD7A Regulates Neurodevelopmental Phenotypes in the 15q13..:
Uddin, Mohammed
;
Unda, Brianna K.
;
Kwan, Vickie
...
The American Journal of Human Genetics. 102 (2018) 2 - p. 278-295 , 2018
Link:
https://doi.org/10.1016/..
?
9
28. Dosage sensitivity curation of recurrent copy number va..:
Andersen, Erica
;
Burnside, Rachel
;
Coe, Bradley
...
Cancer Genetics. 224-225 (2018) - p. 61 , 2018
Link:
https://doi.org/10.1016/..
?
10
Molecular characterization of NRXN1 deletions from 19,263 c..:
Lowther, Chelsea
;
Speevak, Marsha
;
Armour, Christine M.
...
Genetics in Medicine. 19 (2017) 1 - p. 53-61 , 2017
Link:
https://doi.org/10.1038/..
?
11
Impact of IQ on the diagnostic yield of chromosomal microar..:
Lowther, Chelsea
;
Merico, Daniele
;
Costain, Gregory
...
Genome Medicine. 9 (2017) 1 - p. , 2017
Link:
https://doi.org/10.1186/..
?
12
Indexing Effects of Copy Number Variation on Genes Involved..:
Uddin, Mohammed
;
Pellecchia, Giovanna
;
Thiruvahindrapuram, Bhooma
...
Scientific Reports. 6 (2016) 1 - p. , 2016
Link:
https://doi.org/10.1038/..
?
13
Deletion of 15q11.2(BP1‐BP2) region: Further evidence for l..:
Hashemi, Bita
;
Bassett, Anne
;
Chitayat, David
...
American Journal of Medical Genetics Part A. 167 (2015) 9 - p. 2098-2102 , 2015
Link:
https://doi.org/10.1002/..
?
14
Evaluating EGFR Genotyping using HDx™ Reference Standards:
Speevak, Marsha
;
Murray, Chantal
BioTechniques. 58 (2015) 5 - p. 268-269 , 2015
Link:
https://doi.org/10.2144/..
?
15
Charcot–Marie–Tooth 1B caused by expansion of a familial my..:
Speevak, Marsha D.
;
Farrell, Sandra A.
European Journal of Medical Genetics. 56 (2013) 10 - p. 566-569 , 2013
Link:
https://doi.org/10.1016/..
1-15