Detalhe da pesquisa
1.
Data sharing to improve concordance in variant interpretation across laboratories: results from the Canadian Open Genetics Repository.
J Med Genet
; 59(6): 571-578, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33875564
2.
Factors associated with return to work in patients with long-term disabilities due to neurological and neuropsychiatric disorders.
Neuropsychol Rehabil
; 29(9): 1313-1331, 2019 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-29125015
3.
Data sharing as a national quality improvement program: reporting on BRCA1 and BRCA2 variant-interpretation comparisons through the Canadian Open Genetics Repository (COGR).
Genet Med
; 20(3): 294-302, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-28726806
4.
Assessing the cost of implementing the 2011 Society of Obstetricians and Gynecologists of Canada and Canadian College of Medical Genetics practice guidelines on the detection of fetal aneuploidies.
Prenat Diagn
; 37(9): 916-923, 2017 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-28688121
5.
Virtual Reality-Induced Modification of Vestibulo-Ocular Reflex Gain in Posturography Tests.
J Clin Med
; 13(10)2024 May 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-38792284
6.
Visibility, impact, and applications of bibliometric software tools through citation analysis.
Scientometrics
; 128(7): 4007-4028, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37287881
7.
Retrospective testing of respiratory specimens for COVID-19 to assess for earlier SARS-CoV-2 infections in Alberta, Canada.
J Assoc Med Microbiol Infect Dis Can
; 6(1): 10-15, 2021 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-36340216
8.
The effect of subjective perception of cognition on emotional functioning in adults with long-term neurological and neuropsychiatric disorders.
Disabil Rehabil
; 42(22): 3135-3141, 2020 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-31006289
9.
Substance-Based Bibliometrics: Identifying Research Gaps by Counting and Analyzing Substances.
ACS Omega
; 4(1): 86-94, 2019 Jan 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-31459314
10.
Psychometric properties of the HI-FI problem checklist in a sample of adults with neurological and neuropsychiatric disorders: factors contributing to life satisfaction after long-term disability.
Disabil Rehabil
; 39(6): 608-618, 2017 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-26987650
11.
Chromosome 1q21.1 contiguous gene deletion is associated with congenital heart disease.
Circ Res
; 94(11): 1429-35, 2004 Jun 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-15117819
12.
Utility of the Community Integration Questionnaire in a sample of adults with neurological and neuropsychiatric disorders receiving prevocational training.
Disabil Rehabil
; 38(10): 1016-22, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-26289368
13.
Heteroduplex-based genotyping with microchip electrophoresis and dHPLC.
Genet Test
; 7(4): 283-93, 2003.
Artigo
em Inglês
| MEDLINE | ID: mdl-15000804
14.
Structural and spectroscopic demonstration of agostic C-C interactions in electron-deficient metallacyclobutanes and related cage complexes: possible implications for olefin polymerizations and metatheses.
J Am Chem Soc
; 127(47): 16426-35, 2005 Nov 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-16305228
15.
Integration of combined heteroduplex/restriction fragment length polymorphism analysis on an electrophoresis microchip for the detection of hereditary haemochromatosis.
Analyst
; 129(1): 25-31, 2004 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-14737579