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. 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) ↗
3. Novel FH mutations in families with hereditary leiomyomatosis and renal cell cancer (HLRCC) and patients with isolated type 2 papillary renal cell carcinoma. Issue 4 (12th March 2011) Authors: Gardie, Betty; Remenieras, Audrey; Kattygnarath, Darouna; Bombled, Johny; Lefèvre, Sandrine; Perrier-Trudova, Victoria; Rustin, Pierre; Barrois, Michel; Slama, Abdelhamid; Avril, Marie-Françoise; Bessis, Didier; Caron, Olivier; Caux, Frédéric; Collignon, Patrick; Coupier, Isabelle; Cremin, Carol;... Journal: Journal of medical genetics Issue: Volume 48:Issue 4(2011) Page Start: 226 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. 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) ↗