1. Burden of hereditary cancer susceptibility in unselected patients with pancreatic ductal adenocarcinoma referred for germline screening. (7th April 2020) Authors: Cremin, Carol; Lee, Michael Kuan‐Ching; Hong, Quan; Hoeschen, Carolyn; Mackenzie, Anna; Dixon, Katherine; McCullum, Mary; Nuk, Jennifer; Kalloger, Steve; Karasinska, Joanna; Scudamore, Charles; Kim, Peter T. W.; Donnellan, Fergal; Lam, Eric C. S.; Lim, Howard J.; Neben, Cynthia L.; Stedden, Will;... Journal: Cancer medicine Issue: Volume 9:Number 11(2020) Page Start: 4004 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Development and early‐stage evaluation of a patient portal to enhance familial communication about hereditary cancer susceptibility testing: A patient‐driven approach. (20th January 2023) Authors: Pollard, Samantha; Weymann, Deirdre; Loewen, Rosalie; Nuk, Jennifer; Sun, Sophie; Schrader, Kasmintan A.; Hessels, Chiquita; Regier, Dean A. Journal: Health expectations Issue: Volume 26:Number 2(2023) Page Start: 774 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Evaluation of out‐of‐pocket pay genetic testing in a publicly funded healthcare system. Issue 4 (5th January 2023) Authors: Grant, Peter; Cook, Courtney B.; Langlois, Sylvie; Nuk, Jennifer; Mung, SzeWing; Zhang, Qian; Lynd, Larry D.; Austin, Jehannine; Elliott, Alison M. Journal: Clinical genetics Issue: Volume 103:Issue 4(2023) Page Start: 424 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Genetic testing for hereditary cancer syndromes: patient recommendations for improved risk communication. (27th April 2020) Authors: Pollard, Samantha; Kalloger, Steve; Weymann, Deirdre; Sun, Sophie; Nuk, Jennifer; Schrader, Kasmintan A.; Regier, Dean A. Journal: Health expectations Issue: Volume 23:Number 4(2020) Page Start: 884 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Integrating Tumor Sequencing Into Clinical Practice for Patients With Mismatch Repair-Deficient Lynch Syndrome Spectrum Cancers. Issue 8 (16th August 2021) Authors: Dixon, Katherine; Asrat, Mary-Jill; Bedard, Angela C.; Binnington, Kristin; Compton, Katie; Cremin, Carol; Heidary, Nili; Lohn, Zoe; Lovick, Niki; McCullum, Mary; Mindlin, Allison; O'Loughlin, Melanie; Petersen, Tammy; Portigal-Todd, Cheryl; Scott, Jenna; St-Martin, Genevieve; Thompson, Jennifer;... Journal: Clinical and translational gastroenterology Issue: Volume 12:Issue 8(2021) Page Start: e00397 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Large‐scale group genetic counseling: Evaluation of a novel service delivery model in a Canadian hereditary cancer clinic. Issue 2 (1st October 2021) Authors: Lohn, Zoe; Fok, Alexandra; Richardson, Matthew; Derocher, Heather; Mung, Sze Wing; Nuk, Jennifer; Yuson, Jamie; Jevon, Mandy; A.Schrader, Kasmintan; Sun, Sophie Journal: Journal of genetic counseling Issue: Volume 31:Issue 2(2022) Page Start: 459 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Thorough in silico and in vitro cDNA analysis of 21 putative BRCA1 and BRCA2 splice variants and a complex tandem duplication in BRCA2 allowing the identification of activated cryptic splice donor sites in BRCA2 exon 11. Issue 4 (22nd January 2018) Authors: Baert, Annelot; Machackova, Eva; Coene, Ilse; Cremin, Carol; Turner, Kristin; Portigal‐Todd, Cheryl; Asrat, Marie Jill; Nuk, Jennifer; Mindlin, Allison; Young, Sean; MacMillan, Andree; Van Maerken, Tom; Trbusek, Martin; McKinnon, Wendy; Wood, Marie E.; Foulkes, William D.; Santamariña, Marta; de ... Journal: Human mutation Issue: Volume 39:Issue 4(2018) Page Start: 515 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗