1. "It's something I've committed to longer term": The impact of an immersion program for physicians on adoption of genomic medicine. Issue 3 (March 2021) Authors: Martyn, Melissa; McClaren, Belinda; Janinski, Monika; Lynch, Elly; Cunningham, Fiona; Gaff, Clara Journal: Patient education and counseling Issue: Volume 104:Issue 3(2021) Page Start: 480 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A novel approach to offering additional genomic findings—A protocol to test a two‐step approach in the healthcare system. Issue 2 (18th February 2019) Authors: Martyn, Melissa; Kanga‐Parabia, Anaita; Lynch, Elly; James, Paul A.; Macciocca, Ivan; Trainer, Alison H.; Halliday, Jane; Keogh, Louise; Wale, Janney; Winship, Ingrid; Bogwitz, Michael; Valente, Giulia; Walsh, Maie; Downie, Lilian; Amor, David; Wallis, Mathew; Cunningham, Fiona; Burgess, Matthew;... Journal: Journal of genetic counseling Issue: Volume 28:Issue 2(2019) Page Start: 388 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. A protocol for whole-exome sequencing in newborns with congenital deafness: a prospective population-based cohort. Issue 1 (14th September 2017) Authors: Downie, Lilian; Halliday, Jane L; Burt, Rachel A; Lunke, Sebastian; Lynch, Elly; Martyn, Melissa; Poulakis, Zeffie; Gaff, Clara; Sung, Valerie; Wake, Melissa; Hunter, Matthew; Saunders, Kerryn; Rose, Elizabeth; Rehm, Heidi L; Amor, David J Journal: BMJ paediatrics open Issue: Volume 1:Issue 1(2017) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. A transformative translational change programme to introduce genomics into healthcare: a complexity and implementation science study protocol. Issue 3 (5th March 2019) Authors: Taylor, Natalie; Best, Stephanie; Martyn, Melissa; Long, Janet C; North, Kathryn N; Braithwaite, Jeffrey; Gaff, Clara Journal: BMJ open Issue: Volume 9:Issue 3(2019) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Clinical audit of genetic testing and referral patterns for fragile X and associated conditions. Issue 6 (18th February 2016) Authors: Cotter, Megan; Archibald, Alison D.; McClaren, Belinda J.; Burgess, Trent; Francis, David; Hills, Louise; Martyn, Melissa; Oertel, Ralph; Slater, Howard; Cohen, Jonathan; Metcalfe, Sylvia A. Journal: American journal of medical genetics Issue: Volume 170:Issue 6(2016) Page Start: 1439 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Comprehensive evaluation of a prospective Australian patient cohort with suspected genetic kidney disease undergoing clinical genomic testing: a study protocol. Issue 8 (3rd August 2019) Authors: Jayasinghe, Kushani; Stark, Zornitza; Patel, Chirag; Mallawaarachchi, Amali; McCarthy, Hugh; Faull, Randall; Chakera, Aron; Sundaram, Madhivanan; Jose, Matthew; Kerr, Peter; Wu, You; Wardrop, Louise; Goranitis, Ilias; Best, Stephanie; Martyn, Melissa; Quinlan, Catherine; Mallett, Andrew J Journal: BMJ open Issue: Volume 9:Issue 8(2019) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Comprehensive evaluation of a prospective Australian patient cohort with suspected genetic kidney disease undergoing clinical genomic testing: a study protocol. Issue 8 (5th August 2019) Authors: Jayasinghe, Kushani; Stark, Zornitza; Patel, Chirag; Mallawaarachchi, Amali; McCarthy, Hugh; Faull, Randall; Chakera, Aron; Sundaram, Madhivanan; Jose, Matthew; Kerr, Peter; Wu, You; Wardrop, Louise; Goranitis, Ilias; Best, Stephanie; Martyn, Melissa; Quinlan, Catherine; Mallett, Andrew J Journal: BMJ open Issue: Volume 9:Issue 8(2019) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Exome Sequencing for Isolated Congenital Hearing Loss: A Cost‐Effectiveness Analysis. (31st December 2020) Authors: Downie, Lilian; Amor, David J.; Halliday, Jane; Lewis, Sharon; Martyn, Melissa; Goranitis, Ilias Journal: Laryngoscope Issue: Volume 131:Number 7(2021) Page Start: E2371 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Feasibility of Ultra-Rapid Exome Sequencing in Critically Ill Infants and Children With Suspected Monogenic Conditions in the Australian Public Health Care System. Issue 11 (November 2020) Authors: Lunke, Sebastian; Eggers, Stefanie; Wilson, Meredith; Patel, Chirag; Barnett, Christopher P.; Pinner, Jason; Sandaradura, Sarah A.; Buckley, Michael F.; Krzesinski, Emma I.; de Silva, Michelle G.; Brett, Gemma R.; Boggs, Kirsten; Mowat, David; Kirk, Edwin P.; Adès, Lesley C.; Akesson, Lauren S.; ... Journal: Obstetrical & gynecological survey Issue: Volume 75:Issue 11(2020) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Introducing Edna: A trainee chatbot designed to support communication about additional (secondary) genomic findings. Issue 4 (April 2021) Authors: Ireland, David; Bradford, DanaKai; Szepe, Emma; Lynch, Ella; Martyn, Melissa; Hansen, David; Gaff, Clara Journal: Patient education and counseling Issue: Volume 104:Issue 4(2021) Page Start: 739 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗