1. A Community Call to Action to Prioritize Inclusion and Enrollment of Women in HIV Cure-related Research. (15th December 2022) Authors: Campbell, Danielle M.; Cowlings, Portia D.; Tholanah, Martha; Robinson, Mallery Jenna; Graham, Gail; Aseru, Scovia; Dubé, Karine; Cohn, Susan E.; Bar, Katharine J.; Connick, Elizabeth; Mngqbisa, Rosie; Scully, Eileen P.; Stockman, Jamila K.; Gianella, Sara Journal: Journal of acquired immune deficiency syndromes Issue: Volume 91:Number 5(2022) Page Start: e12 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Atypical fibrodysplasia ossificans progressiva diagnosed by whole‐exome sequencing. (21st April 2015) Authors: Liu, Hao; Sawyer, Sarah L; Gos, Monika; Grynspan, David; Issa, Kheirie; Ramphal, Raveena; Rotaru, Carmen; Consortium, FORGE Canada; Majewski, Jacek; Boycott, Kym M; Graham, Gail; Bromwich, Matthew Journal: American journal of medical genetics Issue: Volume 167:Number 6(2015:Jun.) Page Start: 1337 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Blue Button use by patients to access and share health record information using the Department of Veterans Affairs' online patient portal. (16th April 2014) Authors: Turvey, Carolyn; Klein, Dawn; Fix, Gemmae; Hogan, Timothy P; Woods, Susan; Simon, Steven R; Charlton, Mary; Vaughan-Sarrazin, Mary; Zulman, Donna M; Dindo, Lilian; Wakefield, Bonnie; Graham, Gail; Nazi, Kim Journal: Journal of the American Medical Informatics Association Issue: Volume 21:Number 4(2014:Jul.) Page Start: 657 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Bridging clinical care and research in Ontario, Canada: Maximizing diagnoses from reanalysis of clinical exome sequencing data. Issue 3 (29th November 2022) Authors: Hartley, Taila; Soubry, Élisabeth; Acker, Meryl; Osmond, Matthew; Couse, Madeline; Gillespie, Meredith K.; Ito, Yoko; Marshall, Aren E.; Lemire, Gabrielle; Huang, Lijia; Chisholm, Caitlin; Eaton, Alison J.; Price, E. Magda; Dowling, James J.; Ramani, Arun K.; Mendoza‐Londono, Roberto; Costain, Gr... Journal: Clinical genetics Issue: Volume 103:Issue 3(2023) Page Start: 288 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. MG-123 Exonic and intronic NRXN1 deletions: Novel genotype-phenotype correlations. (4th December 2015) Authors: Lowther, Chelsea; Speevak, Marsha; Armour, Christine; Goh, Elaine; Graham, Gail; Li, Chumei; Zeesman, Susan; Nowaczyk, Malgorzata JM; Schultz, Lee-Anne; Morra, Antonella; Nicolson, Robert; Rajguru, Manjulata; Goobie, Sharan; Tarnopolsky, Mark A; Prasad, Chitra; Dick, Paul T; Hussain, Asmaa S; Gaz... Journal: Journal of medical genetics Issue: Volume 52(2015)Supplement 2 Page Start: A9 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Multiple neurofibromas as the presenting feature of familial atypical multiple malignant melanoma (FAMMM) syndrome. Issue 6 (23rd April 2013) Authors: Vanneste, Rachel; Smith, Erika; Graham, Gail Journal: American journal of medical genetics Issue: Volume 161:Issue 6(2013:Jun.) Page Start: 1425 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Similar values, different expectations: How do patients and providers view 'health' and perceive the healthcare experience?. (12th April 2022) Authors: Natafgi, Nabil; Ladeji, Olayinka; Blackwell, Shanikque; Hong, Yoon Duk; Graham, Gail; Cort, Marcia; Mullins, C. Daniel Journal: Health expectations Issue: Volume 25:Number 4(2022) Page Start: 1517 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗