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Speevak, Marsha D.
28  results:
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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