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Author/Creator Chong, George

1. A homozygous PMS2 founder mutation with an attenuated constitutional mismatch repair deficiency phenotype. Issue 5 (17th February 2015)

Authors:
Li, Lili; Hamel, Nancy; Baker, Kristi; McGuffin, Michael J; Couillard, Martin; Gologan, Adrian; Marcus, Victoria A; Chodirker, Bernard; Chudley, Albert; Stefanovici, Camelia; Durandy, Anne; Hegele, Robert A; Feng, Bing-Jian; Goldgar, David E; Zhu, Jun; De Rosa, Marina; Gruber, Stephen B; Wimmer, ...
Journal:
Journal of medical genetics
Issue:
Volume 52:Issue 5(2015)
Page Start:
348
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

2. A randomized controlled trial comparing in-person and wiki-inspired nominal group techniques for engaging stakeholders in chronic kidney disease research prioritization. Issue 1 (December 2016)

Authors:
Elliott, Meghan; Straus, Sharon; Pannu, Neesh; Ahmed, Sofia; Laupacis, Andreas; Chong, George; Hillier, David; Huffman, Kate; Lei, Andrew; Villanueva, Berlene; Young, Donna; Tam-Tham, Helen; Donald, Maoliosa; Lillie, Erin; Manns, Braden; Hemmelgarn, Brenda
Journal:
BMC medical informatics and decision making
Issue:
Volume 16:Issue 1(2016)
Page Start:
1
Record Type:
Journal Article
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3. Data sharing to improve concordance in variant interpretation across laboratories: results from the Canadian Open Genetics Repository. Issue 6 (19th April 2021)

Authors:
Mighton, Chloe; Smith, Amanda C; Mayers, Justin; Tomaszewski, Robert; Taylor, Sherryl; Hume, Stacey; Agatep, Ron; Spriggs, Elizabeth; Feilotter, Harriet E; Semenuk, Laura; Wong, Henry; Lazo de la Vega, Lorena; Marshall, Christian R; Axford, Michelle M; Silver, Talia; Charames, George S; Di Gioacc...
Other Names:
author non-byline.; Agatep Ron author non-byline.; Ainsworth Peter author non-byline.; Akbari Mohammad R. author non-byline.; Aronson Melyssa author non-byline.; Basran Raveen author non-byline.; Blavier Andre author non-byline.; Blumenthal Andrea author non-byline.; Bombard Yvonne author non-by...
Journal:
Journal of medical genetics
Issue:
Volume 59:Issue 6(2022)
Page Start:
571
Record Type:
Journal Article
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5. Integrating NGS-derived mutational profiling in the diagnosis of multiple lung adenocarcinomas. (2021)

Authors:
Ezer, Nicole; Wang, Hangjun; Corredor, Andrea Gomez; Fiset, Pierre Olivier; Baig, Ayesha; van Kempen, Léon C.; Chong, George; Issac, Marianne S.M.; Fraser, Richard; Spatz, Alan; Riviere, Jean-Baptiste; Broët, Philippe; Spicer, Jonathan; Camilleri-Broët, Sophie
Journal:
Cancer treatment and research communications
Issue:
Number 29(2021)
Page Start:
Record Type:
Journal Article
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6. Oncology clinic-based germline genetic testing for exocrine pancreatic cancer enables timely return of results and unveils low uptake of cascade testing. Issue 8 (23rd September 2021)

Authors:
Wang, Yifan; Golesworthy, Bryn; Cuggia, Adeline; Domecq, Celine; Chaudhury, Prosanto; Barkun, Jeffrey; Metrakos, Peter; Asselah, Jamil; Bouganim, Nathaniel; Gao, Zu-Hua; Chong, George; Foulkes, William D; Zogopoulos, George
Journal:
Journal of medical genetics
Issue:
Volume 59:Issue 8(2022)
Page Start:
793
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗