1. Association between the Lynch syndrome gene MSH2 and breast cancer susceptibility in a Canadian familial cancer registry. Issue 11 (4th August 2017) Authors: Goldberg, Mira; Bell, Kathleen; Aronson, Melyssa; Semotiuk, Kara; Pond, Greg; Gallinger, Steven; Zbuk, Kevin Journal: Journal of medical genetics Issue: Volume 54:Issue 11(2017) Page Start: 742 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Brief family history questionnaire to screen for Lynch syndrome in women with newly diagnosed non-serous, non-mucinous ovarian cancers. Issue 7 (10th January 2022) Authors: Kim, Soyoun Rachel; Tone, Alicia; Kim, Raymond; Cesari, Matthew; Clarke, Blaise; Hart, Tae; Aronson, Melyssa; Holter, Spring; Lytwyn, Alice; Maganti, Manjula; Oldfield, Leslie; Gallinger, Steven; Bernardini, Marcus Q; Oza, Amit M; Djordjevic, Bojana; Lerner-Ellis, Jordan; Van de Laar, Emily; Vicu... Journal: International journal of gynecological cancer Issue: Volume 32:Issue 7(2022) Page Start: 891 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Cancer Worry, Perceived Risk and Cancer Screening in First‐Degree Relatives of Patients with Familial Gastric Cancer. Issue 3 (22nd October 2015) Authors: Li, Jenny; Hart, Tae L.; Aronson, Melyssa; Crangle, Cassandra; Govindarajan, Anand Journal: Journal of genetic counseling Issue: Volume 25:Issue 3(2016) Page Start: 520 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Development and validation of a brief screening instrument for psychosocial risk associated with genetic testing: a pan-Canadian cohort study. Issue 3 (13th March 2013) Authors: Esplen, Mary Jane; Cappelli, Mario; Wong, Jiahui; Bottorff, Joan L; Hunter, Jon; Carroll, June; Dorval, Michel; Wilson, Brenda; Allanson, Judith; Semotiuk, Kara; Aronson, Melyssa; Bordeleau, Louise; Charlemagne, Nicole; Meschino, Wendy Journal: BMJ open Issue: Volume 3:Issue 3(2013) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Diagnostic criteria for constitutional mismatch repair deficiency (CMMRD): recommendations from the international consensus working group. Issue 4 (23rd February 2021) Authors: Aronson, Melyssa; Colas, Chrystelle; Shuen, Andrew; Hampel, Heather; Foulkes, William D; Baris Feldman, Hagit; Goldberg, Yael; Muleris, Martine; Wolfe Schneider, Kami; McGee, Rose B; Jasperson, Kory; Rangaswami, Arun; Brugieres, Laurence; Tabori, Uri Journal: Journal of medical genetics Issue: Volume 59:Issue 4(2022) Page Start: 318 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. DNA Mismatch Repair Status Predicts Need for Future Colorectal Surgery for Metachronous Neoplasms in Young Individuals Undergoing Colorectal Cancer Resection. Issue 7 (July 2015) Authors: Aronson, Melyssa; Holter, Spring; Semotiuk, Kara; Winter, Laura; Pollett, Aaron; Gallinger, Steven; Cohen, Zane; Gryfe, Robert Journal: Diseases of the colon & rectum Issue: Volume 58:Issue 7(2015:Jul.) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. DNAR-09. THE IMPACT OF MISMATCH REPAIR DEFICIENCY ON HIGH GRADE GLIOMAS IN CHILDREN, ADOLESCENTS AND YOUNG ADULTS; A REPORT FROM THE IRRDC AND THE GLIOMA TASKFORCE. (14th November 2022) Authors: Negm, Logine; Nobre, Liana; Bennett, Julie; Chung, Jiil; Fernandez, Nick; Johnson, Monique; Aronson, Melyssa; Zhang, Cindy; Komosa, Martin; Bianchi, Vanessa; Stengs, Lucie; Lim-Fat, Mary Jane; Keith, Julia; Tsang, Derek; Gao, Andrew; Munoz, David; Nguyen, Lananh; Das, Sunit; Levine, Adrian; Das, ... Journal: Neuro-oncology Issue: Volume 24(2022)Supplement 7 Page Start: vii92 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Evaluation of a decision aid for incidental genomic results, the Genomics ADvISER: protocol for a mixed methods randomised controlled trial. Issue 4 (26th April 2018) Authors: Shickh, Salma; Clausen, Marc; Mighton, Chloe; Casalino, Selina; Joshi, Esha; Glogowski, Emily; Schrader, Kasmintan A; Scheer, Adena; Elser, Christine; Panchal, Seema; Eisen, Andrea; Graham, Tracy; Aronson, Melyssa; Semotiuk, Kara M; Winter-Paquette, Laura; Evans, Michael; Lerner-Ellis, Jordan; Ca... Journal: BMJ open Issue: Volume 8:Issue 4(2018) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Exome and genome sequencing in adults with undiagnosed disease: a prospective cohort study. Issue 4 (24th June 2020) Authors: Shickh, Salma; Gutierrez Salazar, Mariana; Zakoor, Kathleen-Rose; Lázaro, Conxi; Gu, Jessica; Goltz, Jamie; Kleinman, Dakota; Noor, Abdul; Khalouei, Sam; Mighton, Chloe; Reble, Emma; Kodida, Rita; Bombard, Yvonne; DiTroia, Stephanie; Baxter, Samantha; Watkins, Nicholas; Care, Melanie; Adler, Arno... Journal: Journal of medical genetics Issue: Volume 58:Issue 4(2021) Page Start: 275 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Gastrointestinal Findings in the Largest Series of Patients With Hereditary Biallelic Mismatch Repair Deficiency Syndrome: Report from the International Consortium. (February 2016) Authors: Aronson, Melyssa; Gallinger, Steven; Cohen, Zane; Cohen, Shlomi; Dvir, Rina; Elhasid, Ronit; Baris, Hagit N; Kariv, Revital; Druker, Harriet; Chan, Helen; Ling, Simon C; Kortan, Paul; Holter, Spring; Semotiuk, Kara; Malkin, David; Farah, Roula; Sayad, Alain; Heald, Brandie; Kalady, Matthew F; Pen... Journal: American journal of gastroenterology Issue: Volume 111:Number 2(2016) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗