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. Cost Effectiveness Analysis of Genetic Testing for Breast and Ovarian Cancer Susceptibility Genes: BRCA1 and BRCA2. Issue 3 (8th April 2014) Authors: Kaldate, Rajesh; Huston, Alissa; McCoy, Heidi; Cardeiro, Dawn; Noyes, Katia Journal: Breast journal Issue: Volume 20:Issue 3(2014:May/Jun.) Page Start: 325 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Cost-Utility of a Prognostic Test Guiding Adjuvant Chemotherapy Decisions in Early-Stage Non-Small Cell Lung Cancer. (27th November 2015) Authors: Stenehjem, David D.; Bellows, Brandon K.; Yager, Kraig M.; Jones, Joshua; Kaldate, Rajesh; Siebert, Uwe; Brixner, Diana I. Journal: Oncologist Issue: Volume 21:Number 2(2016) Page Start: 196 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Cost‐Utility of a Prognostic Test Guiding Adjuvant Chemotherapy Decisions in Early‐Stage Non‐Small Cell Lung Cancer. (27th November 2015) Authors: Stenehjem, David D.; Bellows, Brandon K.; Yager, Kraig M.; Jones, Joshua; Kaldate, Rajesh; Siebert, Uwe; Brixner, Diana I. Journal: Oncologist Issue: Volume 21:Number 2(2016) Page Start: 196 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Frequency of mutations in individuals with breast cancer referred for BRCA1 and BRCA2 testing using next‐generation sequencing with a 25‐gene panel. Issue 1 (3rd September 2014) Authors: Tung, Nadine; Battelli, Chiara; Allen, Brian; Kaldate, Rajesh; Bhatnagar, Satish; Bowles, Karla; Timms, Kirsten; Garber, Judy E.; Herold, Christina; Ellisen, Leif; Krejdovsky, Jill; DeLeonardis, Kim; Sedgwick, Kristin; Soltis, Kathleen; Roa, Benjamin; Wenstrup, Richard J.; Hartman, Anne‐Renee Journal: Cancer Issue: Volume 121:Issue 1(2015) Page Start: 25 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Frequency of mutations in individuals with breast cancer referred for BRCA1 and BRCA2 testing using next‐generation sequencing with a 25‐gene panel. Issue 1 (3rd September 2014) Authors: Tung, Nadine; Battelli, Chiara; Allen, Brian; Kaldate, Rajesh; Bhatnagar, Satish; Bowles, Karla; Timms, Kirsten; Garber, Judy E.; Herold, Christina; Ellisen, Leif; Krejdovsky, Jill; DeLeonardis, Kim; Sedgwick, Kristin; Soltis, Kathleen; Roa, Benjamin; Wenstrup, Richard J.; Hartman, Anne‐Renee Journal: Cancer Issue: Volume 121:Issue 1(2015) Page Start: 25 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗