1. Comprehensive sequencing of PALB2 in patients with breast cancer suggests PALB2 mutations explain a subset of hereditary breast cancer. Issue 7 (10th January 2014) Authors: Fernandes, Priscilla H.; Saam, Jennifer; Peterson, Jenny; Hughes, Elisha; Kaldate, Rajesh; Cummings, Shelly; Theisen, Aaron; Chen, Sonia; Trost, Jeffrey; Roa, Benjamin B. Journal: Cancer Issue: Volume 120:Issue 7(2014) Page Start: 963 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Comprehensive sequencing of PALB2 in patients with breast cancer suggests PALB2 mutations explain a subset of hereditary breast cancer. Issue 7 (10th January 2014) Authors: Fernandes, Priscilla H.; Saam, Jennifer; Peterson, Jenny; Hughes, Elisha; Kaldate, Rajesh; Cummings, Shelly; Theisen, Aaron; Chen, Sonia; Trost, Jeffrey; Roa, Benjamin B. Journal: Cancer Issue: Volume 120:Issue 7(2014) Page Start: 963 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. EP101/#503 Relevance of genomic instability score, tumor mutational burden, and tumor infiltrating lymphocytes as biomarkers in uterine serous carcinoma. (4th December 2022) Authors: Bloom, Elizabeth; Peters, Pamela; Whitaker, Regina; Previs, Rebecca; Strickland, Kyle; Timms, Kristen; Cummings, Shelly; Slavin, Thomas Journal: International journal of gynecological cancer Issue: Volume 32(2022)Supplement 3 Page Start: A89 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. EP176/#1052 Global assessment of BRCA1/2 genetic testing guidelines: investigating geographic and regional disparities in health equity for women and families at risk for hereditary ovarian cancer. (4th December 2022) Authors: Hughes, Brittany; Jorgensen, Kirsten; Cummings, Shelly; Alejandro Rauh-Hain, J; Eiken, Mary; Herzog, Thomas Journal: International journal of gynecological cancer Issue: Volume 32(2022)Supplement 3 Page Start: A119 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Pancreatic Ductal Carcinoma Risk Associated With Hereditary Cancer-Risk Genes. (21st April 2022) Authors: Gardiner, Anna; Kidd, John; Elias, Maria C; Young, Kayla; Mabey, Brent; Taherian, Nassim; Cummings, Shelly; Malafa, Mokenge; Rosenthal, Eric; Permuth, Jennifer B Journal: Journal of the National Cancer Institute Issue: Volume 114:Number 7(2022) Page Start: 996 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Response to Article: Langford et al. Racial and Ethnic Differences in Direct‐to‐Consumer Genetic Tests Awareness in HINTS 2007: Sociodemographic and Numeracy Correlates. J Genet Counsel (2012) 21:440–447. Issue 1 (25th October 2012) Authors: Cummings, Shelly Journal: Journal of genetic counseling Issue: Volume 22:Issue 1(2013) Page Start: 152 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Systematic mapping review of guidelines for BRCA1/2 genetic testing globally: investigating geographic and regional disparities in health equity for women and families at risk for hereditary ovarian cancer. Issue 2 (11th November 2022) Authors: Hughes, Brittany N; Jorgensen, Kirsten A; Cummings, Shelly; Morah, Damini; Krause, Kate; Rauh-Hain, Jose Alejandro; Herzog, Thomas J Journal: International journal of gynecological cancer Issue: Volume 33:Issue 2(2023) Page Start: 250 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. The emerging field of polygenic risk scores and perspective for use in clinical care. (3rd July 2020) Authors: Yanes, Tatiane; McInerney-Leo, Aideen M; Law, Matthew H; Cummings, Shelly Journal: Human molecular genetics Issue: Volume 29:Number R2(2020) Page Start: R165 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗